Field of the Invention
The present invention relates to fused heterocyclic compounds represented
by the compounds of Formula (I) (as described herein); processes for their
preparation; pharmaceutical compositions comprising said compounds; and methods
of using said compounds for the treatment or prophylaxis of the diseases or
disorders mediated by GPR120 receptor.
Background of the Invention
Metabolic diseases or disorders are caused by an abnormal metabolic
process and may either be congenital due to an inherited enzyme abnormality or
acquired due to a disease of an endocrine organ or failure of a metabolically
important organ such as the liver or the pancreas.
Among the metabolic disorders, diabetes mellitus is the most prevalent and is
considered to be one of the five leading causes of death in the world (Diabetes Care,
vol. 27, 2004, pp.1 047-1 053). Diabetes mellitus is typically classified into two main
subtypes: Type 1 and Type 2 diabetes mellitus. Type 1 diabetes mellitus (otherwise
known as Insulin Dependent Diabetes Mellitus, IDDM), which generally occurs in
adolescents under 20 years of age, is an auto-immune disease causing an insulitis
with the subsequent destruction of insulin-producing -cells of the pancreas. Further,
in latent autoimmune diabetes in adults (LADA), -cells are destroyed due to
autoimmune attack. The subsequent lack of insulin leads to elevated levels of blood
and urine glucose (hyperglycemia). Although the exact trigger for this autoimmune
response is not known, patients with Type 1 diabetes have high levels of antibodies
against pancreatic beta cells (hereinafter "beta cells"). However, it cannot be
ascertained that all patients with high levels of these antibodies develop Type 1
diabetes. Type 2 diabetes mellitus or non-insulin-dependent diabetes mellitus
(NIDDM) is developed when human muscle, fat and liver cells are not able to
respond normally to insulin that body secretes. This inability to respond, otherwise
known as insulin resistance, may be due to restriction on the numbers of insulin
receptors on these cells, or a dysfunctional behaviour of signalling pathways within
the cells, or both. Initially, the -cells which are responsible for the production of
insulin, compensate for this insulin resistance by increasing their insulin secretion.
However, these cells gradually become unable to produce enough insulin to facilitate
the normal glucose homeostasis, causing the progression to Type 2 diabetes (Am J
Med. 108(6), Supplement 1, 2000, pp. 2S-8S). Type 2 diabetes (T2D) is
characterised by fasting hyperglycemia which occurs as an effect of the combined
lesions of insulin resistance and -cell dysfunction. There are two types of defects
associated with the -cells: the first component, an increase in the basal insulin
release which usually occurs in the presence of low, non-stimulatory glucose
concentrations. The second component is a failure to enhance the insulin release in
response to a hyperglycaemic challenge.
Obesity is another risk factor for developing metabolic diseases or disorders
such as diabetes, cardiovascular disorders, hypertension, hyperlipidemia and an
increased mortality. Diabetes caused by insulin resistance and obesity are part of the
"metabolic syndrome" which is defined as the linkage between several diseases
(also referred to as syndrome X, insulin-resistance syndrome, or deadly quartet).
These often occur in the same patients and are major risk factors for the
development of Type 2 diabetes and cardiovascular diseases (Frontiers in
Endocrinology, vol. 4, 201 3, pp. 1 - 11). It has been suggested that the control of
lipid levels and/or glucose levels is required to treat type 2 diabetes and
cardiovascular diseases. Even though lifestyle changes like exercise and healthy
diet are regarded as the most efficient ways to prevent and manage the disease,
pharmaceutical intervention is frequently necessary.
Current treatment options for diabetes, particularly T2D, include use of
hypoglycaemic agents and insulin. Metformin is one such hypoglycemic agent which
is used in the treatment of Type 2 diabetes. It is, in fact, one of the oldest drugs
used for the treatment of T2D and it still remains the drug of choice despite
associated gastrointestinal (Gl) side effects including anorexia, nausea, diarrhea and
vomiting commonly associated with it. In fact, metformin should be used with caution
in patients with renal impairment because of the slight risk of lactic acidosis.
Sulfonylureas (SUs) e.g. glimepiride, glipizide, are insulin secretagogues, which act
on -cells to increase insulin release, are commonly used in the treatment of Type 2
diabetes. However, use of sulfonylureas is also associated with adverse effects in
that they increase the risk of hypoglycaemia and lead to weight gain. Insulin
treatment which is chosen by patients carries the same side-effects.
Thiazolidinedione compounds e.g. rosiglitazone, pioglitazone, are insulin sensitizers
which bind to peroxisome proliferator-activated receptors (PPARs) in cells and
thereby increase the insulin sensitivity. Though, thiazolidinedione compounds have
also been widely used, the enhanced risks of cardiovascular disease and
hepatotoxicity have resulted in stringent limitations on their use. Relatively recently,
regulatory authorities approved new classes of anti-diabetic agents such as GLP-1
agonists (exenatide and liraglutide) and DPP-4 inhibitors (linagliptin and alogliptin).
It is a known fact that metabolic processes are regulated by fatty acids which
are important biological molecules that serve both as a source of energy and as
signalling molecules. Generally, it is believed that fatty acids produce their biological
effects through interacting with intracellular targets including, for example, the family
of peroxisome proliferator-activated receptors (PPARs). However, in the recent years
it has become clear that fatty acids also serve as agonists for a group of cell surface
G protein-coupled receptors (GPCRs). Free fatty acids (FFAs) have been
demonstrated to act as ligands of several GPCRs including GPR40 (FFAR1 ) ,
GPR43, GPR84, GPR1 19 and GPR1 20. One of the GPCR namely GPR40 facilitates
glucose-stimulated insulin secretion from pancreatic -cells, whereas the other
GPCR namely GPR120 regulates the secretion of glucagon-like peptide-1 (GLP-1) in
the intestine, as well as insulin sensitivity in macrophages. GPR1 0 is localized to
intestinal enteroendocrine cells, such as colonic L cells. Certain research studies
conducted relatively recently identified that loss-of-function of GPR120 human
variant is associated with obesity, diabetes and other insulin resistance, and related
metabolic disorders and also with inflammatory disorders. These findings establish
GPR1 20 as a potential target for the treatment of diabetes, other metabolic disorders
and also, inflammatory disorders (Trends Pharmacol Sci. vol. 32(9), 201 1 pp.543-
550).
Various patent documents describe compounds which are reported to be
GPR1 20 modulators. Examples of patent documents describing GPR120 modulators
include WO20081 03500, WO2009038204, WO201 0008831 , WO201 0048207,
WO201 0080537, WO20101 041 95, WO201 10721 32, WO201 3 139341 ,
WO201 3 185766, EP2125758A1 , US201 1065739 and US 8367708.
Thus, in view of the role of GPR120 receptor in potentiating metabolic
disorders such as diabetes and also, inflammatory disorders, there is need in the art
to develop compounds that act by modulating the GPR120 receptor pathways.
Summary of the Invention
In one aspect, the present invention relates to a compound of Formula (I) (as
described herein) or an isotopic form, a stereoisomer, a tautomer, a
pharmaceutically acceptable salt, a pharmaceutically acceptable solvate, a prodrug,
a polymorph, N-oxide, S-oxide, or a carboxylic acid isostere thereof.
In another aspect of the present invention, there is provided a process for the
preparation of the compound of Formula (I) or a pharmaceutically acceptable salt
thereof.
In a further aspect, the present invention relates to a pharmaceutical
composition comprising a therapeutically effective amount of a compound of Formula
(I) or a stereoisomer, a tautomer a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; and at least one pharmaceutically
acceptable carrier or excipient.
In a further aspect, the present invention relates to a pharmaceutical
composition comprising a therapeutically effective amount of a compound of Formula
(I) or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; and one further therapeutically active
agent and at least one pharmaceutically acceptable carrier or excipient.
In an aspect, the present invention relates to the compound of Formula (I) or a
stereoisomer, a tautomer, a pharmaceutically acceptable salt or a pharmaceutically
acceptable solvate thereof; for use as GPR120 agonist.
In another further aspect, the present invention relates to a method for
modulating GPR120 function in a cell, comprising contacting a cell with an effective
amount of a compound of Formula (I) or a stereoisomer, a tautomer, a
pharmaceutically acceptable salt or a pharmaceutically acceptable solvate thereof.
In yet another aspect, the present invention provides a compound of Formula
(I) or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; for use in the treatment or prophylaxis
of a disease or a disorder mediated by GPR120.
In yet another further aspect, the present invention provides a method for the
treatment or prophylaxis of a disease or a disorder mediated by GPR120, comprising
administering to a subject in need thereof; a therapeutically effective amount of the
compound of Formula (I) or a stereoisomer, a tautomer, a pharmaceutically
acceptable salt or a pharmaceutically acceptable solvate thereof.
In a still further aspect, the present invention relates to use of the compound
of Formula (I) or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; in the manufacture of a medicament,
for the treatment or prophylaxis of a disease or a disorder mediated by GPR120.
In another further aspect, the present invention relates to use of the
compound of Formula (I) or a stereoisomer, a tautomer, a pharmaceutically
acceptable salt or a pharmaceutically acceptable solvate thereof; in combination with
one further therapeutically active agent for the treatment or prophylaxis of a disease
or a disorder mediated by GPR1 20.
These and other objectives and advantages of the present invention will be
apparent to those skilled in the art from the following description.
Detailed Description of the Invention
In one aspect, the present invention relates to a compound of Formula (I),
Formula (I)
wherein,
Xi is -0-, -S- or -NR';
X2 is -0-, -S-, -N-, -NR'-, -CR'- or -CR'R"-;
Ring A is (C6-C 0)aryl or 5- to 10-membered heteroaryl;
Ring B is (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, (C6-Ci 0)aryl, 5- to 10-
membered heteroaryl or a saturated or partially unsaturated 3- to 11-membered
heterocyclyl ring containing one to four heteroatoms independently selected from the
group consisting of O, N and S;
R is hydrogen or (CrC 6)alkyl;
R2 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, hydroxy, cyano, nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7,
(C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl and (C6-Ci 0)aryl;
R3 and R4 at each occurrence are independently selected from the group
consisting of hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C(0)Rs, -C(0)NR5R6, -
S(0) R7, (C C6)alkyl, halo(C C6)alkyl, hydroxy, -0(CrC 6)alkyl, -(C3-C8)cycloalkyl,
(C6-Ci 0)aryl, -0(CrC 6)aryl, heterocyclyl and heteroaryl;
R5 and R6 at each occurrence are independently selected from the group
consisting of hydrogen, (CrC 6)alkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R7 is hydrogen, (C C6)alkyl or -NR5R6;
R' and R" at each occurrence are independently selected from the group
consisting of hydrogen, (C C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl and -
S(0) 2(Ci-C6)alkyl; or
R' and R" are taken together to form oxo, (C3-C8)cycloalkyl, (C5-
C8)cycloalkenyl, or 3- to 6-membered saturated or a partially unsaturated
heterocyclyl ring containing one or two heteroatoms independently selected from the
group consisting of O, N and S;
Ra and R at each occurrence are independently selected from the group
consisting of hydrogen, halogen and (CrC 6)alkyl;
n is an integer from 1 to 6;
p is an integer from 1 to 3;
q is an integer from 1 to 4;
t is an integer from 0 to 2;
represents presence or absence of a single bond;
wherein,
(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7, ( -C6)alkyl, halo(C C6)alkyl, -0(C
C 6)alkyl, (C6 -Cio)aryl, (C3-C8 )cycloalkyl, heterocyclyl and heteroaryl; wherein R5, R6,
R7 and t are as defined above;
-0(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R , (Ci-C6)alkyl, halo(Ci-C 6)alkyl, (C6-Ci 0)aryl,
(C3-C8)cycloalkyl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as
defined above;
(C3-C8)cycloalkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of oxo, halogen, hydroxy, cyano,
nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R , (Ci-C6)alkyl, halo(Ci-C 6)alkyl and
-0(CrC 6)alkyl; wherein R5, R6, R7 and t are as defined above;
(C5-C8)cycloalkenyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7, (C C6)alkyl, halo(C C6)alkyl and -0(C
C6)alkyl; wherein R5, R6, R7 and t are as defined above;
(C6 -Cio)aryl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro,
-C(0)R5, -C(0)OR5, -S(0) R7, -NR5R6, (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl,
halo(CrC 6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl, -O(C6-Ci 0)aryl, heterocyclyl and
heteroaryl, wherein R5, R6, R7 and t are as defined above;
heterocyclyl is a 3- to 11-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R5, -C(0)OR5, -S(0) R7, -NR5R6, (C C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above;
heteroaryl is a 5- to 10-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R5, -C(0)OR5, -S(0) R , -NR5R6, ( -C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above;
halogen is chlorine, bromine, iodine or fluorine;
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically acceptable salt,
a pharmaceutically acceptable solvate, a prodrug, a polymorph, N-oxide, S-oxide, or
a carboxylic acid isostere thereof.
Definitions
Unless otherwise indicated, the following definitions are set forth to illustrate
and define the meaning and scope of the various terms used to describe the
invention herein and the appended claims. These definitions should not be
interpreted in the literal sense as they are not intended to be general definitions and
are relevant only for this application.
The singular forms "a", "an" and "the" include plural aspects unless the
context clearly dictates otherwise. For instance, the terms "a", "an" and "the" refers to
"one or more" when used in the subject specification, including the claims. Thus, for
example, reference to "a compound" may include a plurality of such compounds, or
reference to "a disease" or "a disorder" includes a plurality of diseases or disorders.
Also, use of "(s)" as part of a term, includes reference to the term singly or in
plurality, for example, the term pharmaceutically acceptable salt(s) indicates a single
salt or more than one salt of the compound of formula (I).
The term "or" is generally employed in its sense including "and/or" unless the
content clearly dictates otherwise.
As used herein, the term "halogen" refers to chlorine, fluorine, bromine or
iodine atom.
As used herein, the term "(CrC 6)alkyl" or "alkyi" alone or as part of another
group, refers to the radical of saturated aliphatic groups, including straight or
branched-chain alkyi groups. A straight-chain or branched chain alkyi has six or
fewer carbon atoms in its backbone, for instance, CrC 6 for straight chain and C3-C6
for branched chain. As used herein, (CrC 6)alkyl refers to an alkyi group having from
1 to 6 carbon atoms. Representative examples of alkyi include, but are not limited
to, methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl, isopropyl, sec-butyl, isobutyl,
ferf-butyl, isopentyl, 2-methylbutyl and 3-methylbutyl.
Furthermore, unless stated otherwise, the alkyi group can be unsubstituted
or substituted with one or more substituents, for example, from one to four
substituents, independently selected from the group consisting of halogen, hydroxy,
cyano, nitro, -NR5R6, -C(0)R5, -C(0)OR5, -C(0)NR5R6, -S(0) tR , (C C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-Ci 0)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl, heteroaryl and -C(0)NHS(0) R7, wherein R5, R6, R7 and t are as
defined above. Examples of substituted alkyi include, but are not limited to
hydroxymethyl, 2-chlorobutyl, trifluoromethyl, aminoethyl and benzyl.
As used herein, the term "halo(CrC 6)alkyl" or "haloalkyl" refers to alkyi groups
as defined above wherein one or more hydrogen atom of same or different carbon
atoms of the alkyi group are substituted with same or different halogens. A
monohalo(Ci-C 6)alkyl radical, for example, can have a chlorine, bromine, iodine or
fluorine atom. Dihalo or polyhalo(CrC 6)alkyl radicals can have two or more of the
same or different halogen atoms. Representative examples of halo(CrC 6)alkyl
include, but are not limited to, chloromethyl, dichloromethyl, trichloromethyl,
dichloroethyl, dichloropropyl, fluoromethyl, difluoromethyl, trifluoromethyl,
pentafluoroethyl, heptafluoropropyl, difluorochloromethyl, dichlorofluoromethyl,
difluoroethyl and difluoropropyl.
As used herein, the term "(CrC 6)alkoxy" or "alkoxy" refers to a (CrC 6)alkyl
having an oxygen radical attached thereto. The terms "(CrC 6)alkoxy" or "-0(CrC 6)-
alkyl" or alkoxy wherever used in this specification have the same meaning.
Representative examples of alkoxy groups include, but are not limited to, methoxy,
ethoxy, propoxy, isopropoxy, n-butoxy, isobutoxy and ferf-butoxy. Furthermore,
unless stated otherwise, the alkoxy groups can be unsubstituted or substituted with
one or more groups. A substituted alkoxy refers to a (CrC 6)alkoxy substituted with
one or more groups, particularly one to four groups independently selected from the
groups indicated above as the substituents for the alkyl group.
As used herein, the term "haloalkoxy" or "halo(CrC 6)alkoxy" refers to radicals
wherein one or more of the hydrogen atoms of same or different carbon atoms of the
alkoxy group are substituted with same or different halogens. Representative
examples of "haloalkoxy" or "halo(CrC 6)alkoxy" groups include, but are not limited
to, difluoromethoxy (OCHF2) , trifluoromethoxy (OCF3) and trifluorethoxy (OCH2CF3) .
As used herein, the term "(C3-C8)cycloalkyl" or "cycloalkyi" refers to a
saturated monocyclic hydrocarbon ring containing three to eight carbon atoms.
Representative (C3-C8 )cycloalkyl groups include, but are not limited to, cyclopropyl,
cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl. Unless stated
otherwise, (C3-C8)cycloalkyl can be unsubstituted or substituted with one or more
substituents, for example 1-5 substituents independently selected from the group
consisting of oxo, halogen, hydroxy, cyano, nitro, -NR5R6, -C(0)R 5, -C(0)NR 5R6, -
S(0) R7, (CrC 6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl, (C3-C8)cycloalkyl, (C6-
Cio)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above.
Cycloalkyi group comprises a saturated cycloalkyi ring system which does not
contain any double bond within the ring or a partially unsaturated cycloalkyi ring
system which may contain one or more double bonds within the ring system that is
stable, and do not form an aromatic ring system.
As used herein, the term "(C5-C8)cycloalkenyl" or "cycloalkenyl" refers to a
partially unsaturated monocyclic hydrocarbon ring containing five to eight carbon
atoms that is stable. The ring system contains at least one double bond and does not
form an aromatic ring system. A substituted "cycloalkenyl refers to a (C5-
Cs)cycloalkenyl substituted with one or more groups, for example 1-5 groups
selected from the groups indicated above as the substituents for the cycloalkyl
group.
The term "(C6-Ci 0)aryl " or "aryl" as used herein refers to monocyclic or bicyclic
hydrocarbon groups having 6 to 10 ring carbon atoms, wherein at least one
carbocyclic ring is having a electron system. Examples of (C6-Ci 0) aryl ring
systems include, but are not limited to, phenyl and naphthyl. Unless indicated
otherwise, aryl group can be unsubstituted or substituted with one or more
substituents, for example 1-4 substituents independently selected from the group
consisting of halogen, hydroxy, cyano, nitro, -C(0)R 5, -C(0)OR 5, -S(0) R7, -NR5R6,
(C C6)alkyl, halo(C C6)alkyl, -0 (C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl,
(C6-Ci 0)aryl , -O(C6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and t
are as defined above.
The aryl group can be substituted in any desired position. For example, in
monosubstituted phenyl, the substitutent may be located in the 2-position, the 3-
position, the 4-position or the 5-position. If the phenyl carries two substituents, they
can be located in 2,3-position, 2,4- position, 2,5-position, 2,6-position, 3,4-position or
3, 5-position. Representative examples of monosubstituted phenyl groups include,
but are not limited to, 3-trifluoromethylphenyl, 4-chlorophenyl and 4-cyanophenyl.
Examples of disubstituted phenyl groups include, but are not limited to, 4-methoxy-3-
trifluoromethylphenyl, 2-methoxy-5-trifluoromethylphenyl, xylene, 1,2-
dimethoxyphenyl and 2-fluoro-3-trifluoromethylphenyl.
As used herein, the term "-O(C6-Ci 0)aryl" refers to (C6-Ci 0)aryl group having
an oxygen radical attached thereto. The terms aryloxy or -O(C6-C 0)aryl wherever
used in this specification have the same meaning. Representative example includes,
but is not limited to, phenoxy. Furthermore, unless stated otherwise, the -0(C 6-
C 0)aryl group can be unsubstituted or substituted with one or more groups. A
substituted -O(C6-Ci 0)aryl refers to a (C6-Ci 0)aryl group having an oxygen radical
attached thereto and substituted with one or more groups, for example 1-5 groups
selected from the groups indicated above as the substituents for the (C6-Ci 0)aryl
group.
As used herein, the terms "heterocycle", "heterocyclyl" or "heterocyclic", refer
to a 3- to 11-membered, saturated or partially unsaturated monocyclic or bicyclic ring
system containing 1 to 4 heteroatoms independently selected from the group
consisting of oxygen, nitrogen and sulfur. Saturated heterocyclic ring systems do not
contain any double bond, whereas partially unsaturated heterocyclic ring systems
contains at least one double bond, but do not form an aromatic system containing a
heteroatom. The oxidized form of the ring nitrogen and sulfur atom contained in the
heterocyclyl to provide the corresponding N-oxide, S-oxide or S,S-dioxide is also
encompassed in the scope of the present invention. Representative examples of
heterocyclyls include, but are not limited to, oxetane, azetidine, thietane,
tetrahydrofuran, tetrahydrothiophene, pyrrolidine, dihydropyran, tetrahydropyran,
thio-dihydropyran, thio-tetrahydropyran, piperidine, piperazine, morpholine, 1,3-
oxazinane, 1,3-thiazinane, 4,5,6-tetrahydropyrimidine, 2,3-dihydrofuran,
dihydrothiene, dihydropyridine, tetrahydropyridine, isoxazolidine and pyrazolidine.
Furthermore, unless stated otherwise, the heterocyclyl groups can be
unsubstituted or substituted with one or more substituents independently selected
from the group consisting of halogen, hydroxy, cyano, nitro, -C(0)R 5, -C(0)OR 5, -
S(0) tR , -NR5R6, (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy,
(C3-C8)cycloalkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and t
are as defined above.
As used herein, the term "heteroaryl" refers to 5- to 10-membered monocyclic
or bicyclic aromatic ring system containing one to four identical or different
heteroatoms independently selected from the group consisting of oxygen, nitrogen
and sulfur atom. For instance, the heteroaryl ring can be 5- to 8-membered
monocyclic or bicyclic aromatic ring system or 5- to 6-membered monocyclic
aromatic ring system or 5-membered monocyclic aromatic ring system or 6-
membered monocyclic aromatic ring system. Representative examples of heteroaryl
include, but are not limited to, furan, pyrrole, thiophene, imidazole, oxazole, thiazole,
triazole, tetrazole, benzofuran, indole, benzoxazole, benzothiazole, isoxazole,
triazine, purine, pyridine, pyrazine, quinoline, isoquinoline, phenazine, oxadiazole,
pteridine, pyridazine, quinazoline, pyrimidine, isothiazole, quinoxaline
(benzopyrazine), tetrazole and pyrido[2,3-b]pyrazine. The oxidized form of the ring
nitrogen and sulfur atom contained in the heteroaryl to provide the corresponding Noxide,
S-oxide or S,S-dioxide is also encompassed in the scope of the present
invention.
Furthermore, unless stated otherwise, the heteroaryl groups can be
unsubstituted or substituted with one or more substituents, for example 1-4
substituents independently selected from the group consisting of halogen, hydroxy,
cyano, nitro, -C(0)R 5, -C(0)OFt 5, -S(0) F 7, -NR5R6, -C(0)NR 5R6, -S(0) NR5R6, (C
C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-
C 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above.
Representative examples of heteroaryl include, but are not limited to, pyrrole,
pyrazole, imidazole, isothiazole, pyrazine, furan, thiophene, triazole, benzothiazole,
benzofuran, indole, purine, pyridine, quinoline, isoquinoline, pyridazine, quinazoline,
pyrimidine and azocine.
The term "heteroatom" as used herein, includes nitrogen (N), oxygen (O) and
sulfur (S). Any heteroatom with unsatisfied valency is assumed to have a hydrogen
atom to satisfy the valency or when the heteroatom is N, it may be substituted with a
group selected from the group consisting of (Ci -C6 )alkyl, -C(0)(Ci -C6 )alkyl, -
C(0)0(C C6)alkyl and -S(0) 2(CrC 6)alkyl. Representative examples of (C C6)alkyl
groups include, but are not limited to, methyl, ethyl, propyl, butyl, pentyl, hexyl,
isopropyl and isobutyl.
As used herein, the term "isotopic forms" or "isotopically labelled forms" is a
general term used for isotopic forms of the compounds of Formula (I), wherein one
or more atoms of compounds of Formula (I) are replaced by their respective
isotopes. All isotopes of any particular atom or element as specified are
contemplated within the scope of the compounds of the invention. Examples of
isotopes that can be incorporated into the compounds disclosed herein include, but
are not limited to, isotopes of hydrogen such as H (deuterium or D) and 3H, carbon
such as 11C, 13C and 14C, nitrogen such as 13N and 15N, oxygen such as 150 , 1 0 and
180 , chlorine such as 36CI, fluorine such as 18F and sulfur such as 35S. Substitution
with heavier isotopes, for example, replacing one or more key carbon-hydrogen
bonds with carbon-deuterium bond may show certain therapeutic advantages,
resulting from longer metabolism cycles (e.g., increased in vivo half life or reduced
dosage requirements), improved safety or greater effectiveness and hence may be
preferred in certain circumstances.
Representative examples of isotopic forms of the compounds of Formula (I)
can include, without limitation, deuterated compounds of Formula (I). The term
"deuterated" as used herein, by itself or used to modify a compound or group, refers
to replacement of one or more hydrogen atom(s), which is attached to carbon(s),
with a deuterium atom . For example, the compounds of Formula (I) can include in
the definitions of one or more of the various variables R , R4, R5, R6 and R7 wherever
applicable, deuterium , deuterated-alkyl , deuterated-alkoxy, deuterated-cycloalkyl,
deuterated-heterocyclyl, deuterated-aryl, deuterated-heteroaryl and the like.
Within the context of the present invention and as used herein, the term
"stereoisomer" is a general term used for all isomers of individual compounds that
differ only in the orientation of their atoms in space. The term stereoisomer includes
mirror image isomers (enantiomers), mixtures of mirror image isomers (racemates,
racemic mixtures), geometric (cis/trans, syn/anti or E/Z) isomers, and isomers of
compounds with more than one chiral center that are not mirror images of one
another (diastereoisomers) .
As used herein, the term "tautomer" refers to the coexistence of two or more
compounds that differ from each other only in the position of one (or more) mobile
atoms and in electron distribution. For example, proton tautomers (also known as
prototropic tautomers) include interconversions via migration of a proton , such as
keto-enol and imine-enamine tautomers.
The term "pharmaceutically acceptable salt(s)" as used herein includes a salt
or salts of the active compounds i.e. the compounds of Formula (I) and are prepared
with suitable acids or bases, depending on the particular substituents found on the
compounds described herein.
As used herein, the term "solvate" or "solvates" describe a complex wherein
the compound of Formula (I) of the present invention , is coordinated with a
proportional amount of a solvent molecule. Specific solvates, wherein the solvent is
water, are referred to as hydrates.
As used herein, the term "prodrug" refers to a compound that is drug
precursor, which, when administered to a subject undergoes transformation through
metabolic process or chemical transformation in vivo to form an active compound, for
example, a prodrug after being brought to the physiological pH or through enzyme
action is converted to active compounds, that is, compound of Formula (I) of the
present invention . In context of the present invention prodrugs can be esters of the
compound of Formula (I), which on metabolism can form an active compound of
Formula (I).
As used herein, the term "polymorph" or "polymorphic form" or "polymorphs"
refer to crystals of the same compound that differs only in the arrangement and/or
conformation of the molecule in the crystal lattice.
As used herein, the term "N-oxide" refers to the oxide of the nitrogen atom of
a nitrogen-containing heteroaryl or heterocycle. N-oxide can be formed in the
presence of an oxidizing agent for example peroxide such as m-chloro-perbenzoic
acid or hydrogen peroxide. N-oxide refers to an amine oxide, also known as amine-
N-oxide, and is a chemical compound that contains N- 0 bond.
As used herein, the term "S-oxide" refers to the oxide of the sulfur atom (Soxide)
or dioxide of the sulfur atom (S,S-dioxide) of a sulfur-containing heteroaryl or
heterocycle. S-oxide and S,S-dioxides can be formed in the presence of an oxidizing
agent for example peroxide such as m-chloro-perbenzoic acid or oxone.
As used herein, the term "carboxylic acid isostere" refers to a functional group
or a moiety that elicits similar physical, biological and/or chemical properties as a
carboxylic acid moiety. Representative examples of carboxylic acid isostere include,
but are not limited to:
; wherein R is hydrogen or (CrC 3)alkyl.
As used herein, the term "pharmaceutically acceptable" means that the
carrier, diluent, excipient, and/or salt must be compatible with the other ingredients of
the formulation, and not deleterious to the recipient thereof.
As used herein, the term "a disease or a disorder mediated by GPR1 20" or
"GPR1 20 mediated disease(s) or disorder(s)" refers to a disease or a disorder or a
condition characterized by inappropriate, for example, less than or greater than
normal, GPR120 activity. A GPR120-mediated disease or disorder may be
completely or partially mediated by inappropriate GPR1 20 activity.
The term "metabolic disorder" as used herein refers to a disorder relating to
abnormality of metabolism. Accordingly, in the context of the present invention all the
disorders relating to abnormality of metabolism are encompassed in the term
"metabolic disorders".
The term "metabolic syndrome " refers to a cluster of metabolic abnormalities
including abdominal obesity, insulin resistance, glucose intolerance, diabetes,
hypertension and dyslipidemia. These abnormalities are known to be associated with
an increased risk of vascular events.
The term "diabetes mellitus" or "diabetes" refers to a chronic disease or
disorder, which occurs when the pancreas does not produce enough insulin, or when
the body cannot effectively use the insulin it produces. This leads to an increased
concentration of glucose in the blood (hyperglycaemia). Two major forms of diabetes
are Type 1 diabetes (Insulin-dependent diabetes mellitus) and Type 2 diabetes (Noninsulin
dependent diabetes mellitus (NIDDM)). Type 1 diabetes is an autoimmune
disease in which the insulin-producing -cells of the pancreas are destroyed which
generally results in an absolute deficiency of insulin, the hormone that regulates
glucose utilization. Type 2 diabetes often occurs in the face of normal or even
elevated levels of insulin and can result from the inability of tissues to respond
appropriately to insulin. Other categories of diabetes include gestational diabetes (a
state of hyperglycemia which develops during pregnancy) and "other" rarer causes
(genetic syndromes, acquired processes such as pancreatitis, diseases such as
cystic fibrosis, exposure to certain drugs, viruses and unknown causes).
The term "cardiovascular disease" as used herein refers to any disease of
the heart or blood vessels. One or more diseases of heart encompassed in the term
"cardiovascular disease" is selected from, but are not limited to, angina, arrhythmia,
coronary artery disease (CAD), cardiomyopathy, myocardial infarction, heart failure,
hypertrophic cardiomyopathy, mitral regurgitation, mitral valve prolapse, pulmonary
stenosis, etc. The blood vessel disease encompassed in the term "cardiovascular
diseases", is selected from, but are not limited to, peripheral vascular disease, artery
disease, carotid artery disease, deep vein thrombosis, venous diseases,
atherosclerosis and the like.
The term "subject" as used herein refers to an animal, preferably a mammal,
and most preferably a human. The term "mammal" as used herein refers to warm
blooded vertebrate animals of the class 'mammalia', including humans,
characterized by a covering of hair on the skin and, in the female, milk-producing
mammary glands for nourishing the young. The term mammal includes animals such
as cat, dog, rabbit, bear, fox, wolf, monkey, deer, mouse, pig and human. In the
context of the present invention the phrase "a subject in need thereof" means a
subject (patient) in need of the treatment for the disease or disorder that is mediated
by GPR1 20. Alternatively, the phrase "a subject in need thereof" means a subject
(patient) diagnosed having a disease or a disorder that is mediated by GPR120.
As used herein, the terms "treatment", "treat" and "therapy" refer to alleviate,
slow the progression, attenuation, or cure of existing diseases or disorders (e.g.
diabetes). Treatment also includes curing, preventing development of or alleviating
to some extent, one or more of the symptoms of the diseases or disorders.
As used herein, the term "prophylaxis", used interchangeably with the terms
"prevention" or "preventing" means preventing or reducing the probability of the
occurrence of a clinical disease-state. Subjects are selected for preventative therapy
based on factors that are known to increase risk of suffering a clinical disease state
or a disorder compared to the general population. "Prophylaxis" therapies can be
divided into (a) primary prevention and (b) secondary prevention. Primary prevention
is defined as treatment in a subject that has not yet presented with a clinical disease
state or a disorder, whereas secondary prevention is defined as preventing a second
occurrence of the same or similar clinical disease state.
The term "pharmaceutically acceptable carrier" as used herein means a no n
toxic, inert, solid, semi-solid, diluent, encapsulating material or formulation auxiliary
of any type. Some examples of materials which can serve as pharmaceutically
acceptable carriers are sugars such as lactose, glucose, and sucrose; starches such
as corn starch and potato starch; cellulose and its derivatives such as sodium
carboxymethyl cellulose, ethyl cellulose and cellulose acetate; malt; gelatin; talc; as
well as other non-toxic compatible lubricants such as sodium lauryl sulfate and
magnesium stearate, as well as coloring agents, releasing agents, coating agents,
sweetening, flavoring and perfuming agents; preservatives and antioxidants can also
be present in the composition, according to the judgment of the formulator.
The term "compound(s) for use" as used herein embrace any one or more of
the following: (1) use of compound(s) of formula (I), (2) method of use of
compound(s) of formula (I), (3) use of formula (I) in the treatment of, (4) the use of
formula (I) for the manufacture of pharmaceutical composition / medicament for
treatment/treating or (5) method of treatment / treating / preventing a disease or a
disorder mediated by GPR120, comprising administering an effective amount of the
compound of formula (I) to a subject in need thereof.
As used herein, the term, "therapeutically effective amount" refers to an
amount of a compound of Formula (I) or a pharmaceutically acceptable salt thereof;
or a composition comprising a compound of Formula (I) or a salt thereof, effective in
producing the desired therapeutic response in a subject suffering from a disease or a
disorder or a disorder mediated by GPR1 20. An example of a disease or disorder
mediated by GPR1 20 is diabetes such as type 2 diabetes. Particularly, the term
"therapeutically effective amount" includes the amount of a compound (in the context
of the present invention, the compound of Formula (I) or a pharmaceutically
acceptable salt thereof), when administered that induces a positive modification in
the disease or disorder to be treated or is sufficient to prevent development of, or
alleviate to some extent one or more of the symptoms of the disease or disorder
being treated in a subject. In respect of the therapeutic amount of the compound,
consideration is also given that the amount of the compound used for the treatment
of a subject is low enough to avoid undue or severe side effects, within the scope of
sound medical judgment. The therapeutically effective amount of the compound or
composition will vary with the particular condition or disorder (in the context of the
present invention, the disease or disorder that is mediated by GPR120) being
treated, the age and physical condition of the subject, the severity of the condition or
disorder being treated or prevented, the duration of the treatment, the nature of
concurrent therapy, the specific compound or composition employed, the particular
pharmaceutically acceptable carrier utilized and other related factors.
Within the context of the present invention and as used herein
interchangeably throughout this application, the terms "compounds of Formula (I)"
and "compounds of the present invention" include all the isotopic forms,
stereoisomeric and tautomeric forms and mixtures thereof in all ratios, and their
pharmaceutically acceptable salts, solvates, polymorphs, prodrugs, carboxylic acid
isosteres, N-oxides and S-oxides. The compounds of Formula (I) are also referred to
as fused heterocyclic compounds. Further, in the context of the present invention,
reference to the compounds of Formula (I) includes reference to the compounds of
Formula (la) and/or the compounds of one or more embodiments of the present
invention as described herein. The compound(s) of the present invention can also be
referred to herein as "the active compound(s)" or "the active ingredient(s)".
As used herein, the term "GPR120 agonist(s)" refer to the compound(s) which
binds to, activates, increases, stimulates, potentiates, sensitizes or upregulates
GPR1 0 receptor and promotes insulin sensitization. In the context of the present
invention, the compounds of Formula (I) are provided for use as GPR120 agonists.
The term "optionally substituted" means "substituted or unsubstituted," and
therefore, the generic structural formulae described herein encompass compounds
that may or may not contain the specified optional substituent.
Embodiments
The invention encompasses all the compounds described by the Formula (I)
without limitation, however, for the purposes of further illustrations, preferred aspects
and elements of the invention are discussed herein in the form of the following
embodiments.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein is -0-.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -S-.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -NR'- and R' is as defined above.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -NR'- and R' is selected from the group consisting of
hydrogen, methyl, ethyl and propyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -O- and " " represents absence of bond.
In one embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -S- and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -NR'-; R' is as defined above and " " represents
absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -NR'-; R' is selected from the group consisting of
hydrogen, methyl, ethyl and propyl and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are independently selected from the
group consisting of hydrogen, (C C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl,
and -S(0) 2(CrC 6)alkyl; and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are independently selected from the
group consisting of hydrogen, methyl, ethyl and propyl; and " " represents
absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form oxo.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form (C3-
C8)cycloalkyl, (C5-C8)cycloalkenyl, or 3- to 6-membered saturated or a partially
unsaturated heterocyclyl ring containing one or two heteroatoms independently
selected from the group consisting of O, N and S and " " represents absence of
bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form (C3-
C8)cycloalkyl and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form
cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and " " represents absence of
bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form
cyclopropyl or cyclobutyl and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a 3- to 6-
membered saturated or a partially unsaturated heterocyclyl ring containing one or
two heteroatoms independently selected from the group consisting of O, N and S
and " " represents absence of bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a 3- to 6-
membered saturated or a partially unsaturated heterocyclyl ring containing an -Oatom.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a 3- to 6-
membered saturated or a partially unsaturated heterocyclyl ring containing a -Natom.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a 3- to 6-
membered saturated or a partially unsaturated heterocyclyl ring containing a -Satom.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a 3- or 4-
membered saturated or a partially unsaturated heterocyclyl ring containing one
heteroatom selected from the group consisting of O, N and S.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form a
saturated heterocyclyl ring selected from the group consisting of oxetane, thietane
and azetidine; wherein said oxetane, thietane and azetidine can be optionally
substituted.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'R"- and R' and R" are taken together to form
azetidine, wherein the nitrogen of azetidine can be optionally substituted with (C
C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl or -S(0) 2(CrC 6)alkyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -N-; and " " represents a single bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein X2 is -CR'-; wherein R' is selected from the group consisting of
hydrogen, methyl, ethyl and propyl and " " represents a single bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein is -0-, X2 is -O- and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -S- and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -NR'-; wherein R' is selected from the group
consisting of hydrogen, (C C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl and -
S(0) 2(CrC 6)alkyl; and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are independently
selected from the group consisting of hydrogen, (CrC 6)alkyl, -C(0)(CrC 6)alkyl, -
C(0)0(C C6)alkyl and -S(0) 2(C C6)alkyl; and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, or 3- to 6-membered saturated or a
partially unsaturated heterocyclyl ring containing one or two heteroatoms
independently selected from the group consisting of O, N and S and " "
represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form (C3-C8)cycloalkyl and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and " " represents
absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form cyclopropyl or cyclobutyl and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a saturated or a partially unsaturated 3- to 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S and " " represents absence of bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing an -O- atom.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing a -N- atom.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing a -S- atom.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a 3- or 4-membered saturated or a partially unsaturated heterocyclyl ring
containing a heteroatom selected from a group consisting of O, N and S.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form a saturated heterocyclyl ring selected from the group consisting of oxetane,
thietane and azetidine, wherein said oxetane, thietane and azetidine can be
optionally substituted.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together to
form azetidine; wherein the nitrogen of azetidine can be optionally substituted with
(Ci-C 6)alkyl, -C(0 )(Ci-C 6)alkyl, -C(0)0 (Ci-C 6)alkyl or -S(0 )2(Ci-C 6)alkyl.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein is -0-, X2 is -N-; and " " represents a single bond.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein is -0-, X2 is -CR'-; wherein R' is selected from the group
consisting of hydrogen, (Ci -C6)alkyl, -C(0 )(Ci -C6)alkyl, -C(0)0 (Ci -C6)alkyl and -
S(0 )2(Ci -C6)alkyl; and " " represents a single bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is (C6-Ci 0)aryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is phenyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is 5- to 10-membered heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is a 5- to 8-membered monocyclic heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is a 5- or 6-membered heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is phenyl or 6-membered heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is selected from the group consisting of phenyl, pyridyl,
pyridazinyl, pyrimidinyl and pyrazinyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is phenyl, X is -O- and X2 is -CR'-; wherein R' is
selected from the group consisting of hydrogen, (CrC 6)alkyl, -C(0 )(CrC 6)alkyl, -
C(0)0(C C6)alkyl and -S(0) 2(C C6)alkyl; and " " represents a single bond.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is (C3-C8)cycloalkyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is (Cs-Csjcycloalkenyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is cyclohexenyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is (C6 -Cio)aryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is phenyl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is 5- to 10-membered heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is 5- or 6-membered heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is saturated or partially unsaturated 3- to 11-membered
heterocyclyl ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is saturated 3- to 11-membered heterocyclyl ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is saturated 3- to 7-membered heterocyclyl ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is partially unsaturated 3- to 9-membered heterocyclyl
ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is partially unsaturated 5- to 11-membered heterocyclyl
ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is partially unsaturated 5- to 11-membered heterocyclyl
ring, wherein the ring is a bicyclic ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is
wherein is -0-, -S- or -NRX; Y2 at each occurrence is independently
selected from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2; Y 3 at
each occurrence is independently selected from -N- or -CR ; wherein Rx is hydrogen,
(CrC 6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl or -S(0) 2(Ci-C6)alkyl; R at each
occurrence is independently selected from the group consisting of hydrogen,
halogen, oxo, cyano, nitro, - NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7, (C C6)alkyl,
halo(Ci-C 6)alkyl, hydroxy, -0(Ci-C 6)alkyl, -(C3-C8)cycloalkyl, (C6-Ci 0)aryl, -0(Ci-
C6)aryl, heterocyclyl and heteroaryl.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is
wherein ring C is selected from the group consisting of (C3-C6)cycloalkyl, (C6-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Yi, Y2 and Y3 are as defined above.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is phenyl or 6-membered heteroaryl; and Ring B is
wherein Y2 at each occurrence is independently selected from a group consisting of
-0-, -S-, -NH-, -N(Ci-C 6)alkyl and -C(R )2; Yi, Y3 and R are as defined above.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring A is phenyl or 6-membered heteroaryl and Ring B is
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Yi, Y2 and Y3 are as defined above.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein R2 is hydrogen.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein Ra and R are hydrogen and n is as defined above.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein n is 2, 3 or 4.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein n is 3.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein R3 is halogen.
In an embodiment, the present invention encompasses a compound of
Formula (I), wherein R3 is F, CI or Br.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein R3 is F.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la);
Formula (la)
Wherein,
Xi is -0-, -S- or -NR';
X2 is -0-, -S-, -N-, -NR'-, -CR'- or -CR
Ring A is phenyl or 6-membered heteroaryl;
Ring B is (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, (C6-Ci 0)aryl, 5- to 10-membered
heteroaryl or a saturated or partially unsaturated 3- to 11-membered heterocyclyl
ring containing one to four heteroatoms independently selected from the group
consisting of O, N and S;
R is hydrogen or (CrC 6)alkyl;
R2 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, hydroxy, cyano, nitro, -NR5R6, -C (0)R 5, -C (0)NR 5R6, -S(0) R7,
(C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl and (C6-Ci 0)aryl;
R3 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C (0)R 5, -C (0)NR 5R6, -S(0) R7, (Ci -
C6)alkyl, halo(CrC 6)alkyl, hydroxy and -0(C C6)alkyl;
R4 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C (0)R 5, -C (0)NR 5R6, -S(0) R , (C
C6)alkyl, halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, (C 3-C8)cycloalkyl, (C6 -Ci 0)aryl, -
0(CrC 6)aryl, heterocyclyl and heteroaryl;
R5 and R6 at each occurrence are independently selected from the group consisting
of hydrogen, (CrC 6)alkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R is hydrogen, (CrC 6)alkyl or -NR5R6;
R' and R" at each occurrence are independently selected from the group consisting
of hydrogen, (CrC 6)alkyl, -C (0)(C C6)alkyl, -C (0)0(C C6)alkyl and -S (0) 2 (C
C6)alkyl; or
R' and R" are taken together to form oxo, (C3-C8 )cycloalkyl, (Cs-C ^cycloalkenyl, or
3- to 6-membered saturated or a partially unsaturated heterocyclyl ring containing
one or two heteroatoms independently selected from the group consisting of O, N
and S;
Ra and R at each occurrence are independently selected from the group consisting
of hydrogen, halogen and (CrC 6)alkyl;
n is an integer from 1 to 6;
p is an integer from 1 to 3;
q is an integer from 1 to 4;
t is an integer from 0 to 2;
represents presence or absence of a single bond;
wherein,
(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
N R5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) tR (Ci-C 6)alkyl, halo(C C6)alkyl, -0(C
C6)alkyl, (C3-C8)cycloalkyl, (C6-C 0)aryl, heterocyclyl and heteroaryl; wherein R5 , R6 ,
R7 and t are as defined above;
-0(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
N R5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) tR ( -C6)alkyl, halo(C C 6)alkyl, (C6-C 0)aryl,
(C3-C8)cycloalkyl, and heterocyclyl; wherein R5 , R6 , R7 and t are as defined above;
(C3-C8)cycloalkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of oxo, halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) R , (C C6)alkyl, halo(CrC 6)alkyl and -
0(CrC 6)alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C5-C8)cycloalkenyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
N R5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) R7 , (C C6)alkyl, halo(C C6)alkyl and -0(C
C6)alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C6-Ci 0)aryl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro,
-C (0)R 5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl,
halo(CrC 6)alkoxy, (C3-C 8)cycloalkyl, (C6-Ci 0)aryl, -O(C6-Ci 0)aryl, heterocyclyl and
heteroaryl, wherein R5 , R6 , R7 and t are as defined above;
heterocyclyl is a 3- to 11-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C (0) R5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5 , R6 , R7 and t are as defined above;
heteroaryl is a 5- to 10-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C (0)R 5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C 6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5 , R6 , R7 and t are as defined above;
halogen is chlorine, bromine, iodine or fluorine;
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically acceptable salt,
a pharmaceutically acceptable solvate, a prodrug, a polymorph, N-oxide, S-oxide, or
a carboxylic acid isostere thereof.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-.
In an embodiment, the compound of Formula (I) encompasses a compound
of Formula (la); wherein X is -S-.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -NR'- and R' is as defined above.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -NR'- and R' is selected from the group consisting of
hydrogen, methyl, ethyl and propyl.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X2 is -O- and " " represents absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X2 is -S- and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -NR'-; R' is as defined above and " "
represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -NR'-; R' is selected from the group
consisting of hydrogen, methyl, ethyl and propyl and " " represents absence of
bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are independently
selected from the group consisting of hydrogen, (CrC 6)alkyl, -C(0)(CrC 6)alkyl, -
C(0)0(C C6)alkyl, and -S(0) 2(C C6)alkyl; and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are independently
selected from the group consisting of hydrogen, methyl, ethyl and propyl; and " "
represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form oxo.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, or 3- to 6-membered saturated or a
partially unsaturated heterocyclyl ring containing one or two heteroatoms
independently selected from the group consisting of O, N and S and " "
represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form (C3-C8)cycloalkyl and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and " " represents
absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form cyclopropyl or cyclobutyl and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing an -O- atom.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing a -N- atom.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing a -S- atom.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a 3- or 4-membered saturated or a partially unsaturated heterocyclyl ring
containing one heteroatom selected from the group consisting of O, N and S.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form a saturated heterocyclyl ring selected from the group consisting of oxetane,
thietane and azetidine, wherein said oxetane, thietane and azetidine can be
optionally substituted.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'R"- and R' and R" are taken together to
form azetidine, wherein the nitrogen of azetidine can be optionally substituted with
(CrC 6alkyl), -C(0)(C C6alkyl), -C(0)0(C C6alkyl) or -S(0) 2(CrC 6alkyl).
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -N-; and " " represents a single bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X2 is -CR'-; wherein R' is selected from the group
consisting of hydrogen, methyl, ethyl and propyl and " " represents a single bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -NR'-; wherein R' is selected from the group
consisting of hydrogen, (C C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl and -
S(0) 2(CrC 6)alkyl; and " " represents absence of bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are
independently selected from the group consisting of hydrogen, (CrC 6)alkyl, -
C(0)(C C6)alkyl, -C(0)0(C C6)alkyl and -S(0) 2(C C6)alkyl; and " " represents
absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, or 3- to 6-membered saturated or a
partially unsaturated heterocyclyl ring containing one or two heteroatoms
independently selected from the group consisting of O, N and S and " "
represents absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form (C3-C8)cycloalkyl and " " represents absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl and " " represents
absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S and " " represents absence of bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing an -O- atom.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form a 3- to 6-membered saturated or a partially unsaturated heterocyclyl ring
containing a -N- atom.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form 3- or 4-membered saturated or a partially unsaturated heterocyclyl ring
containing a heteroatom selected from a group of O, N and S.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein is -0-, X2 is -CR'R"-; R' and R" are taken together to form a
saturated heterocyclyl ring independently selected from the group consisting of
oxetane, thietane and azetidine, wherein said oxetane, thietane and azetidine can be
optionally substituted.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein X is -0-, X2 is -CR'R"-; wherein R' and R" are taken together
to form azetidine; wherein the nitrogen of azetidine can be optionally substituted with
(CrC 6)alkyl, -C(0 )(Ci -C6)alkyl, -C (0 )0 (Ci -C6)alkyl or -S(0 )2 (Ci -C6)alkyl.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein is -0-, X2 is -N-; and " " represents a single bond.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la); wherein is -0-, X2 is -CR'-; wherein R' is selected from the group
consisting of hydrogen, (Ci-C 6)alkyl, -C(0)(Ci-C 6)alkyl, -C(0)0(Ci-C 6)alkyl and -
S(0) 2(Ci-C 6)alkyl; and " " represents a single bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein R4 at each occurrence is independently selected
from the group consisting of hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C(0)R 5,
-C(0)NR 5R6, -S(0) R7, (C C6)alkyl, halo(C C6)alkyl, (C3-C8)cycloalkyl, hydroxy,
-0(CrC 6)alkyl and -0(Ci-C 6)aryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is phenyl ring.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is 6-membered heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is selected from the group consisting of
pyridyl, pyridazinyl, pyrimidinyl and pyrazinyl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is 6-membered heteroaryl, X is -O- and
X2 is -CR'-; wherein R' is selected from the group consisting of hydrogen, (C
C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(Ci-C 6)alkyl and -S(0) 2(C C6)alkyl; and " "
represents a single bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is phenyl, X is -O- and X2 is -CR'-;
wherein R' is selected from the group consisting of hydrogen, (CrC 6)alkyl, -
C(0)(C C6)alkyl, -C(0)0(Ci-C 6)alkyl and -S(0) 2(C C6)alkyl; and " " represents a
single bond.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B phenyl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is 5- to 10-membered heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is 5- or 6-membered heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is saturated or partially unsaturated 3- to
11-membered heterocyclyl ring.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is saturated 3- to 11-membered
heterocyclyl ring.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is saturated 3- to 7-membered
heterocyclyl ring.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is partially unsaturated 3- to 9-membered
heterocyclyl ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is partially unsaturated 5- to 11-membered heterocyclyl
ring.
In another embodiment, the present invention encompasses a compound of
Formula (I), wherein ring B is partially unsaturated 5- to 11-membered heterocyclyl
ring, wherein the ring is a bicyclic ring.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring B is
wherein is -0-, -S- or -NR X; Y 2 at each occurrence is independently
selected from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2 ; Y 3 at
each occurrence is independently selected from -N- or -CR ; wherein Rx is hydrogen,
(CrC 6)alkyl, -C (0)(Ci -C6)alkyl, -C (0)0(Ci -C 6)alkyl or -S(0) 2 (Ci -C 6)alkyl; R at each
occurrence is independently selected from the group consisting of hydrogen,
halogen , oxo, cyano, nitro, - NR5R6, -C(0)R 5, -C(0)NR 5R6, -S(0) tR , (C C6)alkyl,
halo(Ci -C6)alkyl, hydroxy, -0(C C6)alkyl, -(C3-C8)cycloalkyl, (C6-Ci 0)aryl , -0(C
C6)aryl , heterocyclyl and heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein ring B is
wherein ring C is selected from the group consisting of (C3-Ce)cycloalkyl, (Ce-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Y , Y2 and Y3 are as defined above.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein R2, Ra and R are hydrogen.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein ring A is phenyl or 6-membered heteroaryl and
ring B is
wherein is -0-, -S- or -NRX; Y2 at each occurrence is independently
selected from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2; Y3 at
each occurrence is independently selected from -N- or -CR ; wherein Rx is hydrogen,
(CrC 6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl or -S(0) 2(C C6)alkyl ; R at each
occurrence is independently selected from the group consisting of hydrogen,
halogen , oxo, cyano, nitro, - NR5R6, -C(0)R 5, -C(0)NR 5R6, -S(0) R7, (C C6)alkyl,
halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, -(C3-C8)cycloalkyl, (C6-Ci 0)aryl, -0(C
C6)aryl, heterocyclyl and heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is phenyl and ring B is
wherein Y Y2 and Y3 are as defined above.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is phenyl or 6-membered heteroaryl and
wherein ring C is selected from the group consisting of (C3-C6)cycloalkyl, (C6-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6- membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Yi, Y2 and Y3 are as defined above.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la); wherein ring A is phenyl and ring B is
wherein ring C is selected from the group consisting of (C3-C6)cycloalkyl, (C6-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Y , Y2 and Y3 are as defined above.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein is -O- and X2 is -CR'-; wherein R' is selected
from the group consisting of hydrogen, (Ci -C6)alkyl, -C(0)(Ci -C6)alkyl , -C(0)0(Ci -
B is
wherein is -0-, -S- or -NRX; Y2 at each occurrence is independently selected
from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2; Y3 at each
occurrence is independently selected from -N- or -CR ; wherein Rx is hydrogen, ( -
C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(Ci-C 6)alkyl or -S(0) 2(C C6)alkyl ; R at each
occurrence is independently selected from the group consisting of hydrogen,
halogen , oxo, cyano, nitro, - NR5R6, -C(0)R 5, -C(0)NR 5R6, -S(0) R7, (Ci -C6)alkyl,
halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, -(C3-C8)cycloalkyl, (C6-Ci 0)aryl , -0(C
C6)aryl , heterocyclyl and heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein X is -O- and X2 is -CR'-; wherein R' is selected
from the group consisting of hydrogen, (CrC 6)alkyl, -C(0)(CrC 6)alkyl , -C(0)0(C
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Y , Y2 and Y3 are as defined above.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein is -O- and X2 is -CR'-; wherein R' is selected
from the group consisting of hydrogen, (Ci -C6)alkyl, -C(0)(Ci -C6)alkyl , -C(0)0(Ci -
C6)alkyl and -S(0) 2(Ci -C6)alkyl ; and " " represents a single bond ; ring A is phenyl
and ring B is
wherein is -0-, -S- or -NRX; Y2 at each occurrence is independently
selected from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2; Y3 at
each occurrence is independently selected from -N- or -CR ; wherein Rx is hydrogen,
(CrC 6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl or -S(0) 2(C C6)alkyl ; R at each
occurrence is independently selected from the group consisting of hydrogen,
halogen , oxo, cyano, nitro, - NR5R6, -C(0)R 5, -C(0)NR 5R6, -S(0) R7, (C C6)alkyl,
halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, -(C3-C8)cycloalkyl, (C6-Ci 0)aryl , -0(C
C6)aryl , heterocyclyl and heteroaryl.
In another embodiment, the compound of Formula (I) encompasses a
compound of Formula (la) ; wherein X is -O- and X2 is -CR'-; wherein R' is selected
from the group consisting of hydrogen, (Ci -Ce)alkyl, -C(0)(Ci -C6)alkyl, -C(0)0(Ci -
C6)alkyl and -S(0) 2(C C6)alkyl ; and " " represents a single bond ; ring A is phenyl
and ring B is
wherein ring C is selected from the group consisting of (C3-C6)cycloalkyl, (C6-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl ring
containing one or two heteroatoms independently selected from the group consisting
of O, N and S; and Y Y2 and Y3 are as defined above.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la) ; wherein n is 2, 3 or 4.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la) ; wherein n is 3.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la) ; wherein R3 is halogen .
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la) ; wherein R3 is F, CI or Br.
In an embodiment, the compound of Formula (I) encompasses a compound of
Formula (la) ; wherein R3 is F.
Representative compounds of the present invention include:
4-(2-(2-(5-Cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic acid;
4-(2-(5-Fluoro-2-(5-(1 -methylcyclopropyl)thiophen-2-yl)phenyl)benzofuran-5-
yl)butanoic acid;
4-(2-(2-(5-Cyclopropylthiazol-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic acid;
4-(2-(2-(5,6-Dihydro-4H-cyclopenta[d]thiazol-2-yl)-5-fluorophenyl)benzofuran-5-
yl)butanoic acid;
4-(2-(5-Fluoro-2-(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)phenyl)benzofuran-5-
yl)butanoic acid;
4-(2-(5-Fluoro-2-(isoindolin-5-yl)phenyl)benzofuran-5-yl)butanoic acid;
4-(2-(2-(5,7-Dihydrofuro[3,4-b]pyridin-3-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic
acid; and
4-(2-(2-(6,7-Dihydro-5H-cyclopenta[b]pyridin-3-yl)-5-fluorophenyl)benzofuran-5-
yl)butanoic acid
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically acceptable salt,
a pharmaceutically acceptable solvate, a prodrug, a polymorph, N-oxide, S-oxide, or
a carboxylic acid isostere thereof.
In another aspect of the present invention, there is provided a process for the
preparation of the compounds of Formula (I) or pharmaceutically acceptable salts
thereof.
The compounds of Formula (I) can be prepared by various methods including
using methods well known to a person skilled in the art. Examples of processes for
the preparation of a compound of Formula (I) are described below and illustrated in
the following scheme but are not limited thereto. It will be appreciated by persons
skilled in the art that within the process described herein, the order of the synthetic
steps employed may be varied and will depend inter alia on factors such as the
nature of functional groups present in a particular substrate and the protecting group
strategy (if any) to be adopted. Clearly, such factors will also influence the choice of
reagents such as bases, solvents or coupling agents to be used in the reaction
steps.
The reagents, reactants and intermediates used in the following processes
are either commercially available or can be prepared according to standard
procedures known in the art, for instance those reported in the literature references.
Scheme 1
(wherein is (C -C )alkyl) (wherein is hydrogen)
In one embodiment, there is provided a processes for the preparation of the
compound of Formula (I), wherein
X is -0-;
X2 is -CR'-;
Ring A is (C6-Ci 0)aryl or 5- to 10-membered heteroaryl;
Ring B is (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, (C6-Ci 0)aryl, 5- to 10-membered
heteroaryl or a saturated or partially unsaturated 3- to 11-membered heterocyclyl
ring containing one to four heteroatoms independently selected from the group
consisting of O, N and S;
R is hydrogen or (CrC 6)alkyl;
R2 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, hydroxy, cyano, nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7,
(C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl and (C6-Ci 0)aryl;
R3 and R4 at each occurrence are independently selected from the group consisting
of hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7,
(C C6)alkyl, halo(C C6)alkyl, hydroxy, -0(CrC 6)alkyl, (C3-C8)cycloalkyl, (C6-
C 0)aryl, -0(CrC 6)aryl, heterocyclyl and heteroaryl;
R5 and R6 are independently selected from the group consisting of hydrogen, (C
C6)alkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R is hydrogen, (CrC 6)alkyl or -NR5R6;
R' and R" are independently selected from the group consisting of hydrogen, (Ci-
C6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl and -S(0)2(CrC 6)alkyl; or
R' and R" are taken together to form oxo, (C3-C8)cycloalkyl, (C5-
C8)cycloalkenyl, or 3- to 6-membered saturated or a partially unsaturated
heterocyclyl ring containing one or two heteroatoms independently selected from the
group consisting of O, N and S;
Ra and R at each occurrence are independently selected from the group consisting
of hydrogen, halogen and (CrC 6)alkyl;
n is an integer from 1 to 6;
p is an integer from 1 to 3;
q is an integer from 1 to 4;
t is an integer from 0 to 2;
represents presence or absence of a single bond;
wherein,
(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R , (Ci-C6)alkyl, halo(Ci-C 6)alkyl, -0(CiC
6)alkyl, (C3-C8)cycloalkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6,
R7 and t are as defined above;
-0(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0)tR ( -C6)alkyl, halo(Ci-C 6)alkyl, (C3-
C8)cycloalkyl, (C6-Ci 0)aryl and heterocyclyl; wherein R5, R6, R7 and t are as defined
above;
(C3-C8)cycloalkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of oxo, halogen, hydroxy, cyano,
nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7, (C C6)alkyl, halo(CrC 6)alkyl and -
0(Ci-C6)alkyl; wherein R5, R6, R7 and t are as defined above;
(C5-C8)cycloalkenyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro, -
NR5R6, -C(0)R5, -C(0)NR5R6, -S(0)tR , (C C6)alkyl, halo(C C6)alkyl and -0(C
C6)alkyl; wherein R5, R6, R7 and t are as defined above;
(C6-Ci 0)aryl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano, nitro,
-C(0)R5, -C(0)OR5, -S(0) R7, -NR5R6, (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl,
halo(CrC 6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl, -O(C6-Ci 0)aryl, heterocyclyl and
heteroaryl, wherein R5, R6, R7 and t are as defined above;
heterocyclyl is a 3- to 11-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R5, -C(0)OR5, -S(0) R , -NR5R6, (Ci-C6)alkyl,
halo(C C6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above;
heteroaryl is a 5- to 10-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R5, -C(0)OR5, -S(0) R7, -NR5R6, (C C6)alkyl,
halo(Ci-C 6)alkyl, -0(Ci-C 6)alkyl, halo(Ci-C 6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl,
heterocyclyl and heteroaryl; wherein R5, R6, R7 and t are as defined above;
halogen is chlorine, bromine, iodine or fluorine;
wherein said process consists the reaction steps as depicted in the above
Scheme 1. The reactions steps of the process are described below:
Step 1a:
This process step involves reacting dioxaborolan derivative (compound (1)
wherein R3, Ring A and q are as defined above) with compound (2) (wherein R4,
Ring B and q are as defined above) in a solvent such as dichloromethane, THF,
toluene, acetonitrile, dioxane, water or a mixture thereof, in the presence of a base
selected from potassium hydroxide (KOH), sodium hydroxide (NaOH), potassium
carbonate (K2C0 3) or sodium carbonate (Na2C0 3) and a palladium catalyst, such as
palladium tetrakistriphenylphosphine [Pd(PPh3)4] or [ 1 , 1 -
bis(diphenylphosphino)ferrocene]dichloropalladium(ll), at a temperature ranging from
100 to 120 C for a time period ranging from 5 to 15 minutes, to obtain the
compound (3), (wherein Ring A, Ring B, R3, R4 and q are as defined above).
Step 1b:
In this process step, the compound (3) is subjected to Seyferth-Gilbert
homologation (Synthetic Communications 2008, 39 (2), 299-310). Compound (3) is
treated with dimethyl (1-diazo-2-oxopropyl)phosphonate in the presence of a base
such as dry potassium carbonate in a solvent selected from methanol, ethanol,
isopropyl alcohol or mixture thereof to obtain the compound (4), (wherein Ring A,
Ring B, R3, R4 and q are as defined above).
Step 1c:
In this process step, the compound (4) is subjected to Sonogashira coupling
(Org. Process Res. ound (4) is treated with a
compound of formula is (CrC 6)alkyl; Ra, R and
n are as defined above), in the presence of copper(l) iodide, a base such as
triethylamine, palladium catalyst such as bis(triphenylphosphine)palladium(ll)
dichloride and a solvent selected from dioxane, DMF, toluene, THF or acetonitrile to
obtain the compound of Formula (I) (wherein R is (Ci -C6 )alkyl).
Step 1d:
The compound of Formula (I) (obtained in Step 1c), is taken in a solvent
selected from THF, ethanol, MeOH, water or a mixture thereof, and hydrolyzed using
a base selected from NaOH, KOH, Lithium hydroxide (LiOH) or barium hydroxide
(Ba(OH)2) , to obtain the compound of Formula (I) (wherein is hydrogen).
The compounds of Formula (I) can be converted into their pharmaceutically
acceptable salts by following procedure known to persons skilled in the art.
The pharmaceutically acceptable salts of the compounds of Formula (I) are
prepared with relatively non-toxic acids or bases, depending on the particular
substituents found on the compounds described herein. When the compounds of
Formula (I) of the present invention contain an acidic group they can form an
addition salt with a suitable base. For example, pharmaceutically acceptable base
addition salts of the compounds of the present invention may include their alkali
metal salts such as sodium, potassium, calcium, magnesium, ammonium or an
organic base addition salt. Examples of pharmaceutically acceptable organic base
addition salts of the compounds of the present invention include those derived from
organic bases like lysine, arginine, guanidine, diethanolamine, metformin or other
organic bases known to a person skilled in the art.
When the compounds of Formula (I) of the present invention contain one or
more basic groups, they can form an addition salt with an inorganic or an organic
acid. Examples of pharmaceutically acceptable acid addition salts include those
derived from inorganic acids like boric acid, perchloric acid, hydrochloric acid,
hydrobromic acid, hydrofluoric acid, hydriodic acid, nitric acid, carbonic acid,
monohydrogencarbonic acid, phosphoric acid, monohydrogenphosphoric acid,
dihydrogenphosphoric acid, sulfuric acid, monohydrogensulfuric acid, phosphorous
acids or other inorganic acids known to the person skilled in the art. Furthermore,
examples of pharmaceutically acceptable acid addition salts include the salts derived
from organic acids such as acetic acid, propionic acid, isobutyric acid, oxalic acid,
malic acid acid, tartaric acid, citric acid, ascorbic, maleic acid, malonic acid, benzoic
acid, succinic acid, suberic acid, fumaric acid, mandelic acid, phthalic acid,
benzenesulfonic acid, toluenesulfonic acid, methanesulfonic acid, glucuronic acid,
galacturonic acid, naphthoic acid, camphoric acid or other organic acids known to
the person skilled in the art. Certain specific compounds of the present invention
contain both basic and acidic functionalities that allow the compounds to be
converted into either base or acid addition salts.
The pharmaceutically acceptable salts of the present invention can be
synthesized from the subject compound i.e. the compound of Formula (I) which
contains a basic or acidic moiety by conventional chemical methods. Generally, the
pharmaceutically acceptable salts are prepared by contacting the free base or acid
(the compounds of formula (I)) with a desired salt-forming inorganic or organic acid
or a base in a suitable solvent or dispersant or by anion exchange or cation
exchange with other salts. Suitable solvents are, for example, ethyl acetate, ethers,
alcohols, acetone, or mixtures of these solvents.
In an embodiment of the present invention, the compound of Formula (I) or
the compound of Formula (la) is provided as a pharmaceutically acceptable salt.
Those skilled in the art will recognize that the compounds of Formula (I) of
the present invention contain asymmetric or chiral centres, and therefore exist in
different stereoisomeric forms, as racemic mixtures of enantiomers, mixtures of
diastereomers or enantiomerically or optically pure compounds. The term "chiral"
refers to molecules which have the property of non-superimposability of the mirror
image cohort, while the term "achiral" refers to molecules which are superimposable
on their mirror image partner. It is intended that all stereoisomeric forms of the
compounds of the invention, including but not limited to, diastereomers and
enantiomers, as well as mixtures thereof such as racemic mixtures, geometric
isomers form part of the present invention.
When the compounds of Formula (I) of the present invention contain one
chiral centre, the compounds exist in two enantiomeric forms and the present
invention includes both enantiomers and mixtures of enantiomers, such as the
specific 50:50 mixture referred to as a racemic mixtures. The enantiomers can be
resolved by methods known to those skilled in the art, such as formation of
diastereoisomeric salts which may be separated, for example, by crystallization (see,
CRC Handbook of Optical Resolutions via Diastereomeric Salt Formation by David
Kozma (CRC Press, 2001 )); formation of diastereoisomeric derivatives or complexes
which may be separated, for example, by crystallization, gas-liquid or liquid
chromatography; selective reaction of one enantiomer with an enantiomer-specific
reagent, for example enzymatic esterification; or gas-liquid or liquid chromatography
in a chiral environment, for example on a chiral support for example silica with a
bound chiral ligand or in the presence of a chiral solvent. It will be appreciated that
where the desired enantiomer is converted into another chemical entity by one of the
separation procedures described above, a further step is required to liberate the
desired enantiomeric form. Alternatively, specific enantiomers may be synthesized
by asymmetric synthesis using optically active reagents, substrates, catalysts or
solvents, or by converting one enantiomer into the other by asymmetric
transformation. Designation of a specific absolute configuration at a chiral carbon of
the compounds of the invention is understood to mean that the designated
enantiomeric form of the compounds is in enantiomeric excess (ee) or in other words
is substantially free from the other enantiomer. For example, the "R" forms of the
compounds are substantially free from the "S" forms of the compounds and are,
thus, in enantiomeric excess of the "S" forms. Conversely, "S" forms of the
compounds are substantially free of "R" forms of the compounds and are, thus, in
enantiomeric excess of the "R" forms. Enantiomeric excess, as used herein, is the
presence of a particular enantiomer at greater than 50%. In a particular embodiment
when a specific absolute configuration is designated, the enantiomeric excess of
depicted compounds is at least about 90%. When a compound of Formula (I) of the
present invention has two or more chiral carbons it can have more than two optical
isomers and can exist in diastereoisomeric forms. For example, when there are two
chiral carbons, the compound can have up to 4 optical isomers and 2 pairs of
enantiomers ((S,S)/(R,R) and (R,S)/(S,R)). The pairs of enantiomers (e.g.,
(S,S)/(R,R)) are mirror image stereoisomers of one another. The stereoisomers that
are not mirror-images (e.g., (S,S) and (R,S)) are diastereomers. The
diastereoisomeric pairs may be separated by methods known to those skilled in the
art, for example chromatography or crystallization and the individual enantiomers
within each pair may be separated as described above. The present invention
includes each diastereoisomer of such compounds and mixtures thereof.
The isotopically labelled forms of compounds of Formula (I), can be
prepared by conventional techniques known to those skilled in the art or by
processes analogous to those described above or in the subsequent section on
examples by using a corresponding isotopically labelled reagent in place of the nonlabelled
reagent.
In one embodiment, the compounds of Formula (I) exists as tautomers, and
it is intended to encompass all the tautomeric forms of the compounds within the
scope of the present invention.
Furthermore, the present invention includes all the solvates of the
compounds of Formula (I), for example, hydrates and the solvates formed with other
solvents of crystallisation, selected from alcohols such as methanol, ethanol, 1-
propanol or 2-propanol, ethers such as diethyl ether, isopropyl ether or
tetrahydrofuran, esters such as methyl acetate or ethyl acetate, ketone such as
acetone or their mixtures thereof. Certain compounds of the present invention can
exist in unsolvated forms as well as solvated forms, including hydrated forms.
It is also intended to encompass various polymorphs of the compounds of
Formula (I) within the scope of the present invention. Various polymorphs of the
compounds of the present invention can be prepared by standard crystallisation
procedures known in the art. The crystallisation technique employed can utilize
various solvents or their mixtures, temperature conditions and various modes of
cooling, ranging from very fast to very slow cooling. The presence of polymorphs can
be determined by IR (Infra-red) spectroscopy, solid probe NMR (Nuclear Magnetic
Resonance) spectroscopy, differential scanning calorimetry, powder X-ray diffraction
or such other standard techniques.
Furthermore, the present invention also includes prodrugs of the compounds
of Formula (I). The prodrugs of the compounds of the present invention are
derivatives of the aforesaid compounds of the invention which upon administration to
a subject in need thereof undergoes chemical conversion by metabolic or chemical
processes to release the parent drug in vivo from which the prodrug is derived. The
preferred prodrugs are pharmaceutically acceptable ester derivatives e.g., alkyl
esters, cycloalkyl esters, alkenyl esters, benzyl esters, mono- or di-substituted alkyl
esters convertible by solvolysis under physiological conditions to the parent
carboxylic acid, and those conventionally used in the art.
The present invention also relates to carboxylic acid isosteres of the
compounds of Formula (I).
The present invention also relates to N-oxide derivatives of the compounds
of Formula (I).
The present invention also relates to S-oxide derivatives of the compounds
of Formula (I).
In one aspect of the present invention, i.e. the compounds of Formula (I) are
GPR1 0 agonists.
In an embodiment of the present invention, the compounds of Formula (I)
find use in the treatment or prophylaxis of a disease or a disorder mediated by
GPR1 20.
In another aspect, the present invention relates to a method for the treatment
or prophylaxis of a disease or a disorder mediated by GPR120, comprising
administering to a subject in need thereof, a therapeutically effective amount of a
compound of Formula (I) or a stereoisomer, a tautomer, a pharmaceutically
acceptable salt or a pharmaceutically acceptable solvate thereof.
In an embodiment, the present invention relates to use of the compound of
Formula (I) or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; for the treatment or prophylaxis of a
disease or a disorder mediated by GPR1 20.
According to one embodiment, the present invention relates to use of the
compounds of Formula (I) or a stereoisomer, a tautomer, a pharmaceutically
acceptable salt or a pharmaceutically acceptable solvate thereof; in the manufacture
of a medicament for the treatment or prophylaxis of a disease or a disorder mediated
by GPR120.
In an embodiment of the invention, the disease or disorder mediated by
GPR1 20 is selected from the group consisting of diabetes, obesity, hyperglycemia,
glucose intolerance, insulin resistance, hyperinsulinemia, hypercholesterolemia,
hypertension, hyperlipoproteinemia, hyperlipidemia, hypertriglyceridemia,
dyslipidemia, metabolic syndrome, cardiovascular disease, atherosclerosis, kidney
disease, polycystic ovary syndrome, ketoacidosis, thrombotic disorders, diabetic
nephropathy, diabetic neuropathy, diabetic retinopathy, sexual dysfunction, fatty liver
development, dermatopathy, dyspepsia, hypoglycemia, cancer, edema and a
disorder related to glucose levels such as pancreatic beta cell regeneration.
In an embodiment of the invention, the disease or disorder mediated by
GPR1 20 is selected from the group consisting of diabetes, obesity, insulin
resistance, hyperglycemia, glucose intolerance, hypercholesterolemia,
hypertriglyceridemia, dyslipidemia, hyperlipoproteinemia, hyperinsulinemia,
atherosclerosis, diabetic nephropathy, diabetic neuropathy, diabetic retinopathy,
metabolic syndrome, hypertension and pancreatic beta cell degeneration.
In an embodiment of the invention, the disease or disorder mediated by
GPR1 20 is selected from the group consisting of diabetes, obesity, insulin
resistance, hyperglycemia, glucose intolerance, metabolic syndrome and pancreatic
beta cell degeneration.
In an embodiment, the disease or disorder mediated by GPR1 0 is Type 2
diabetes.
In an embodiment, the disease or disorder mediated by GPR1 0 is a
metabolic disorder which refers to one or more diseases or disorders as identified
above.
In an embodiment, the disease or disorder mediated by GPR120 is an
inflammatory disorder.
Accordingly, the present invention relates to a method for the treatment or
prophylaxis of a metabolic disorder, comprising administering to a subject in need
thereof a therapeutically amount of a compound of Formula (I) or a stereoisomer, a
tautomer, or a pharmaceutically acceptable salt or a pharmaceutically acceptable
solvate thereof.
In an embodiment, the present invention provides use of the compound of
Formula (I) or a stereoisomer, a tautomer or a pharmaceutically acceptable salt
thereof for the treatment or prophylaxis of a metabolic disorder.
According to one embodiment, the present invention relates to use of the
compounds of Formula (I) or pharmaceutically acceptable salts thereof in the
manufacture of a medicament, for the treatment or prophylaxis of a metabolic
disorder.
In one embodiment, the metabolic disorder is selected from the group
consisting of diabetes, obesity, cardiovascular disease, hypertension, ketoacidosis,
insulin resistance, glucose intolerance, hyperglycemia, hypertriglyceridemia,
polycystic ovary syndrome, hypercholesterolemia, hyperlipoproteinemia,
dyslipidemia, metabolic syndrome, hyperlipidemia, diabetic nephropathy, diabetic
neuropathy, diabetic retinopathy, edema and related disorders associated with
abnormal plasma lipoprotein, triglycerides and pancreatic beta cell degeneration.
In an embodiment, the metabolic disorder is selected from the group
consisting of diabetes, obesity, insulin resistance, hyperglycemia, glucose
intolerance, hypercholesterolemia, hypertriglyceridemia, dyslipidemia,
hyperlipoproteinemia, hyperinsulinemia, atherosclerosis, diabetic nephropathy,
diabetic neuropathy, diabetic retinopathy, metabolic syndrome, hypertension and
pancreatic beta cell degeneration.
In an embodiment, the metabolic disorder is selected from the group
consisting of diabetes, obesity, insulin resistance, glucose intolerance, dyslipidemia,
hyperinsulinemia, metabolic syndrome and pancreatic beta cell degeneration.
In an embodiment, the metabolic disorder is Type 2 diabetes.
Pharmaceutical compositions
Furthermore, the present invention relates to pharmaceutical compositions
that contain a therapeutically effective amount of at least one compound of Formula
(I) or its pharmaceutically acceptable salt in addition to a customary
pharmaceutically acceptable carrier, and to a process for the production of a
pharmaceutical composition, which includes bringing at least one compound of
Formula (I), into a suitable administration form using a pharmaceutically suitable and
physiologically tolerable excipient and, if appropriate, further suitable active
compounds, additives or auxiliaries.
According to one embodiment, the present invention relates to a
pharmaceutical composition comprising the compounds of Formula (I) or
pharmaceutically acceptable salts thereof and one or more pharmaceutically
acceptable excipients; for use as GPR1 0 agonists.
According to another embodiment, the present invention relates to a
pharmaceutical composition comprising the compounds of Formula (I) or
pharmaceutically acceptable salts thereof and one or more pharmaceutically
acceptable excipients; for use in the treatment or prophylaxis of a disease or a
disorder mediated by GPR120.
It is further intended to include within the scope of the present invention the
use of the compounds of Formula (I) or its pharmaceutically acceptable salts thereof
in combination with at least one therapeutically active agent.
According to one embodiment, the present invention provides a
pharmaceutical composition, comprising a therapeutically effective amount of a
compound of Formula (I) or a pharmaceutically acceptable salt thereof and at least
one further therapeutically active agent, together with a pharmaceutically acceptable
carrier.
In an embodiment, the present invention relates to use of the compound of
Formula (I) or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; in combination with a further
therapeutically active agent, in the treatment or prophylaxis of a disease or a
disorder mediated by GPR120.
The therapeutically active agent that can be used in combination with one or
more of the compounds of Formula (I) is selected from the compounds or active
substances known to be used in the treatment of diabetes and other conditions or
disorders such as obesity, insulin resistance, hyperglycemia, glucose intolerance,
hypercholesterolemia, hypertriglyceridemia, dyslipidemia, hyperlipoproteinemia,
hyperinsulinemia or atherosclerosis. According to the present invention, the
therapeutically active agent, used in combination with the compounds of Formula (I)
of the present invention, include, but are not limited to, insulin, sulfonylureas,
biguanidines, meglitinides, oxadiazolidinediones, thiazolidinediones, glucosidase
inhibitors, inhibitors of glycogen phosphorylase, glucagon antagonists, HMGCoA
reductase inhibitor, GLP-1 (Glucogen-like peptide-1 ) agonists, potassium channel
openers, inhibitors of dipeptidylpeptidase IV (DPP-IV), diglyceride acyltransferase
(DGAT) inhibitor, insulin sensitizers, modulators of glucose uptake, modulators of
glucose transport and modulators of glucose reabsorption, modulators of the
sodium-dependent glucose transporter 1 or 2 (SGLT1 , SGLT2), compounds which
alter lipid metabolism such as antihyperlipidemic active ingredients and antilipidemic
active ingredients, PPARgamma agonists and agents with combined PPARalpha
and gamma activity and active ingredients which act on the ATP-dependent
potassium channel of the beta cells.
In an embodiment, the compound of Formula (I) can be used in combination
with a PPAR gamma agonist selected from the group consisting of rosiglitazone,
pioglitazone and rivoglitazone.
In an embodiment, the compound of Formula (I) can be used in combination
with a HMGCoA reductase inhibitor selected from the group consisting of
simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin and
rosuvastatin.
In an embodiment, the compound of Formula (I) can be used in combination
with a sulfonylurea selected from the group consisting of tolbutamide, glibenclamide,
glipizide and glimepiride.
In another embodiment, the compound of the Formula (I) can be used in
combination with a meglitinide selected from the group consisting of repaglinide,
nateglinide and mitiglinide.
In another embodiment, the compound of the Formula (I) can be used in
combination with GLP-1 agonist selected from the group consisting of exenatide,
liraglutide, taspoglutide albiglutide and lixisenatide.
In another embodiment, the compound of the Formula (I) can be used in
combination with DPP-IV inhibitor selected from the group consisting of alogliptin,
gemigliptin, linagliptin, saxagliptin, sitagliptin and vildagliptin.
Accordingly, in an embodiment the further therapeutically active agent that
can be used in combination with one or more compounds of Formula (I)
encompassed in the present invention, can be selected from one or more of the
agents including, but not limited to, insulin, rosiglitazone, pioglitazone, rivoglitazone,
simvastatin, fluvastatin, pravastatin, lovastatin, atorvastatin, cerivastatin,
rosuvastatin, tolbutamide, glibenclamide, glipizide, glimepiride, repaglinide,
nateglinide, mitiglinide, exenatide, liraglutide, taspoglutide albiglutide, lixisenatide,
alogliptin, gemigliptin, linagliptin, saxagliptin, sitagliptin, vildagliptin and the like.
The pharmaceutical compositions according to the present invention are
prepared in a manner known and familiar to one skilled in the art. Pharmaceutically
acceptable inert inorganic and/or organic carriers and/or additives can be used in
addition to the compounds of Formula (I) and/or their pharmaceutically acceptable
salts. For the production of pills, tablets, coated tablets and hard gelatin capsules it is
possible to use, for example, lactose, corn starch or derivatives thereof, gum arabic,
magnesia or glucose, etc. Carriers for soft gelatin capsules and suppositories are, for
example, fats, waxes, natural or hardened oils, etc. Suitable carriers for the
production of solutions, for example injection solutions, or of emulsions or syrups
are, for example, water, physiological sodium chloride solution or alcohols, for
example, ethanol, propanol or glycerol, sugar solutions, such as glucose solutions or
mannitol solutions, or a mixture of the various solvents which have been mentioned.
Further, the pharmaceutical composition of the present invention also
contains additives such as, for example, fillers, antioxidants, emulsifiers,
preservatives, flavours, solubilisers or colourants. The pharmaceutical composition
of the present invention can also contain two or more compounds of Formula (I) or a
stereoisomer, a tautomer, pharmaceutically acceptable salt or a pharmaceutically
acceptable solvate thereof. The pharmaceutical compositions can also contain one
or more other therapeutically or prophylactically active agents.
The pharmaceutical composition can contain about 1 to 99%, for example,
about 10 to 80%, by weight of the compound of Formula (I) or a stereoisomer, a
tautomer, pharmaceutically acceptable salt or a pharmaceutically acceptable solvate
thereof.
The amount of the active ingredient i.e. the compound of Formula (I) or a
stereoisomer, a tautomer, pharmaceutically acceptable salt in the pharmaceutical
compositions can, for example, vary from about 1 to 500 mg. In case of higher body
weight of the subject in need of the treatment, the pharmaceutical composition may
contain the compound of Formula (I) or a stereoisomer, a tautomer,
pharmaceutically acceptable salt or a pharmaceutically acceptable solvate thereof; in
an amount ranging from 5 mg to 1000 mg. The desirable dosage of the compounds
of Formula (I) can be selected over a wide range. The daily dosage to be
administered is selected to achieve the desired therapeutic effect in subjects being
treated for metabolic disorders. A dosage of about 0.05 to 50 mg/kg/day of the
compounds of Formula (I) or a stereoisomer, a tautomer, pharmaceutically
acceptable salt or a pharmaceutically acceptable solvate thereof may be
administered. In case of higher body weight of the mammal in need of the treatment,
a dosage of about 0.1 to 100 mg/kg/day of the compound of Formula (I) or a
stereoisomer, a tautomer, pharmaceutically acceptable salt or a pharmaceutically
acceptable solvate thereof may be administered. If required, higher or lower daily
dosages can also be administered. Actual dosage levels of the active ingredients in
the pharmaceutical composition of this present invention can be varied so as to
obtain an amount of the active ingredient, which is effective to achieve the desired
therapeutic response for a particular subject (patient), composition, and mode of
administration without being toxic to the subject. The selected dosage level can be
readily determined by a skilled medical practitioner in the light of the relevant
circumstances, including the condition (diseases or disorder) to be treated, the
chosen route of administration depending on a number of factors, such as age,
weight and physical health and response of the individual patient, pharmacokinetics,
severity of the disease and the like, factors known in the medical art.
The pharmaceutical compositions according to the present invention can be
administered orally, for example in the form of pills, tablets, coated tablets, capsules,
granules or elixirs. Administration, however, can also be carried out rectally, for
example in the form of suppositories, or parenterally, for example intravenously,
intramuscularly or subcutaneously, in the form of injectable sterile solutions or
suspensions, or topically, for example in the form of solutions or transdermal
patches, or in other ways, for example in the form of aerosols or nasal sprays.
It is understood that modifications that do not substantially affect the activity of
the various embodiments of this invention are included within scope of the invention
disclosed herein. Accordingly, the following examples are intended to illustrate but
not to limit scope of the present invention.
Experimental
Nomenclature of the compounds exemplified in the present invention is
derived from Chemdraw Ultra version 9.0.1 CambridgeSoft Corporation, Cambridge.
Reagents were purchased from commercial suppliers such as Combi-Blocks
Inc., CA; and CombiPhos Catalysts, Inc. and were used as such.
Unless otherwise stated all temperatures are in degree Celsius. Also, in the
examples and elsewhere, abbreviations have the following meanings:
The abbreviations and terms that are used herein:
Example 1
4-(2-(2-(5-Cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic
(Compound 1)
Step 1a
Synthesis of 2-(5-cyclopropylthiophen-2-yl)-5-fluorobenzaldehyde
Potassium carbonate (851 mg, 6.1 5 mmol) was added to a solution of 5-
fluoro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzaldehyde (commercial
source, 923 mg, 3.69 mmol) and 2-bromo-5-cyclopropylthiophene (commercial
source, 500 mg, 2.462 mmol) in dioxane : water (4:1) (4 mL) and the mixture was
degassed with argon for 2 to 3 minutes. To the resulting solution, palladium tetrakis
triphenylphosphine (35.6 mg, 0.123 mmol) was added and the mixture was again
degassed with argon for 2 to 3 minutes. The mixture was then heated at 110 C for
10 minutes in microwave. After completion of reaction, the compound was extracted
with EtOAc, dried over sodium sulfate, concentrated and purified by column
chromatography (silica gel column/ EtOAc and PET as eluent) to obtain the title
compound (248 mg, 1.007 mmol) as colorless thick liquid. Yield: 40.9 %; 1H NMR
(300 MHz, CDCI3) : 10.14 (s, 1H), 7.67 (dd, J= 3, 9 Hz, 1H), 7.52 (dd, J= 5.1 , 8.4
Hz, 1H), 7.33 (d, J= 83, 8.1 Hz, 1H), 6.82 (dd, J= 3.3, 5.1 Hz, 2H), 2.17-2.08 (m, 1H),
1. 1 0-1 .03 (m, 2H), 0.82-0.77 (m, 2H); HPLC: 95.67%, MS: (m/z) 247 (M+1 ) .
Step 1b
Synthesis of 2-cyclopropyl-5-(2-ethynyl-4-fluorophenyl)thiophene
Dimethyl(1-diazo-2-oxopropyl)phosphonate (4680 mg, 2.436 mmol) was added
slowly to the reaction mixture of 2-(5-cyclopropylthiophen-2-yl)-5-fluorobenzaldehyde
(compound of Step 1a, 500 mg, 2.030 mmol) and dry potassium carbonate (561 mg,
4.06 mmol) in methanol. After completion of the reaction, solvent was evaporated,
extracted with EtOAc, dried over sodium sulfate and purified by column
chromatography to obtain the title compound (430 mg, 1.768 mmol ) as pale yellow
liquid. Yield: 87 %; 1H NMR (300 MHz, CDCI3) : 7.46-7.41 (m, 1H), 7.36 (d, J = 3.6
Hz, 1H), 7.29-7.26 (m, 1H), 7.10-7.03 (m, 1H), 6.76 (d, J = 3.6 Hz, 1H), 3.29 (s, 1H),
2.1 5-2.07 (m,1 H), 1.07-1 .00 (m, 2H), 0.82-0.77 (m, 2H); HPLC: 99.63%; MS: (m/z)
243.0 (M + H).
Step 1c
Synthesis of methyl 4-(2-(2-(5-cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-
5-yl)butanoate
To a solution of methyl 4-(4-hydroxy-3-iodophenyl)butanoate (0.1 g, 0.312 mmol)
and copper(l) iodide (2.97 mg, 0.01 6 mmol) in DMF ( 1 .5 mL) was added
Pd(PPh3)2CI2 (8.77 mg, 0.012 mmol), copper(l) iodide (2.97 mg, 0.01 6 mmol) and
triethylamine (0.087 mL, 0.625 mmol) under nitrogen atmosphere. The reaction
mixture was stirred for 10 minutes, followed by addition of 2-cyclopropyl-5-(2-ethynyl-
4-fluorophenyl)thiophene (compound of step 1b, 0.1 5 1 g, 0.625 mmol) to the
reaction mixture at RT. The reaction mixture was then heated to 60 °C for 2 hours
and then stirred overnight at RT. After completion of reaction, the reaction mixture
was filtered through celite bed®. The residue was concentrated and purified by
column chromatography to obtain the title compound as pale yellow semisolid.
1H NMR (300 MHz, CDCI3) : 7.70-7.69 (m, 1H), 7.41 -7.37 (m, 2H), 7.13-7.02 (m,
2H), 6.76 (d, J = 3.3 Hz, 1H), 6.74 (d, J = 3.6 Hz, 1H), 6.22 (m, 1H), 3.68 (s, 3H),
2.72 (t, J = 7.2 Hz, 2H), 2.35 (t, J = 7.5 Hz, 2H), 2.15-2.08 (m,1 H), 2.01-1 .94 (m, 2H),
1.07 (m, 2H), 0.81-0.77 (m, 2H); HPLC: 99.76%; MS: (m/z) 435.1 (M + H), 457.1 (M
+ Na).
Step l d
Synthesis of 4-(2-(2-(5-cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-5-
yl)butanoic acid
To a solution of methyl 4-(2-(2-(5-cyclopropylthiophen-2-yl)-5-
fluorophenyl)benzofuran-5-yl)butanoate (compound of step 1c, 40 mg, 0.092 mmol)
in THF:MeOH (4:1) (4 mL) was added lithium hydroxide hydrate ( 19.31 mg, 0.460
mmol) then the mixture was allowed to stir at RT for 2 to 3 hours. After completion of
the reaction, the solvent was removed. The reaction mixture was neutralized with
saturated ammonium chloride, extracted with EtOAc, dried over sodium sulfate and
concentrated to obtain the title compound as off-white solid. 1H NMR (300 MHz,
DMSO-de): 12.04 (bs, 1H), 7.65-7.61 (m, 1H), 7.55-7.50 (m, 1H), 7.44 (d, J =
8.7Hz, 1H), 7.40 (s, 1H), 7.36-7.30 (m, 1H), 7.15 (d, J = 7.2Hz, 1H), 6.82 (d, J = 3.6
Hz, 1H), 6.78 (d, J = 3.3Hz, 1H), 6.51 (s, 1H), 2.68 (t, J = 7.2 Hz, 2H), 2.21 (t, J = 7.5
Hz, 2H), 2.1 5-2.07 (m,1 H), 14.87-1 .77 (m, 2H), 1.01 -0.95 (m, 2H), 0.68-0.63 (m, 2H);
HPLC: 98.84%; MS: (m/z) 421 . 1 (M + H).
Example 2
4-(2-(5-Fluoro-2-(5-(1 -methylcyclopropyl)thiophen-2-yl)phenyl)benzofuran-5-
yl)butanoic acid (Compound 2)
Step 2a
Synthesis of 5-fluoro-2-(5-(1 -methylcyclopropyl)thiophen-2-yl)benzaldehyde
The title compound was prepared in an analogous manner as the compound
of Step 1a of Example 1, by using 2-bromo-5-(1-methylcyclopropyl)thiophene
instead of 2-bromo-5-cyclopropylthiophene. 1H NMR (300 MHz, CDCI3) : 10.16 (s,
1H), 7.68-7.64 (m, 1H), 7.54-7.46 (m, 2H), 7.39-7.31 (m, 1H), 6.83-6.80 (m, 1H),
2.1 7-2.08 (m, 1H), 1.53 (s, 3H), 1.03-1 .00 (m, 2H), 0.99-0.91 (m, 2H); HPLC:
80.84%, MS: (m/z) 261 .0 (M + 1).
Step 2b
Synthesis of 2-(2-ethynyl-4-fluorophenyl)-5-(1 -methylcyclopropyl)thiophene
The title compound was prepared in an analogous manner as the compound
of Step 1b of Example 1, by using 5-fluoro-2-(5-(1-methylcyclopropyl)thiophen-2-
yl)benzaldehyde (compound of step 2a) instead of 2-(5-cyclopropylthiophen-2-yl)-5-
fluorobenzaldehyde. 1H NMR (300 MHz, CDCI3) : 7.47-7.42 (m, 1H), 7.38 (d, J =
3.6 Hz, 1H), 7.31-7.26 (m, 1H), 7.1 1-7.03 (m, 1H), 6.76 (d, J = 3.6 Hz, 1H), 3.29 (s,
1H), 1.52 (m, 3H), 1.02-0.94 (m, 2H), 0.90-0.82 (m, 2H) ; HPLC: 90.34%; MS: (m/z)
257.1 (M + H).
Step 2c
Synthesis of methyl 4-(2-(5-fluoro-2-(5-(1-methylcyclopropyl)thiophen-2-
yl)phenyl)benzofuran-5-yl)butanoate
The title compound was prepared in an analogous manner as the compound
of Step 1c of Example 1, by using 2-(2-ethynyl-4-fluorophenyl)-5-(1-
methylcyclopropyl)thiophene (compound of step 2b) instead of 2-cyclopropyl-5-(2-
ethynyl-4-fluorophenyl)thiophene. 1H NMR (500 MHz, CDCI3) : 7.70-7.66 (m, 1H),
7.42-7.34 (m, 3H), 7.17-7.02 (m, 2H), 6.75-6.72 (m, 2H), 6.21 (s, 1H), 3.68 (s, 3H),
2.72 (t, J = 7.5 Hz, 2H), 2.33 (t, J = 7.5 Hz, 2H), 2.04-2.30 (m, 2H), 1.53 (s, 3H),
0.98-0.95 (m, 2H), 0.93-0.89 (m, 2H); HPLC: 98.47%; MS: (m/z) 449.1 (M + H).
Step 2d
Synthesis of 4-(2-(5-fluoro-2-(5-(1-methylcyclopropyl)thiophen-2-
yl)phenyl)benzofuran-5-yl)butanoic acid
The title compound was prepared in an analogous manner as the compound of Step
1d of Example 1, by using methyl 4-(2-(5-fluoro-2-(5-(1-methylcyclopropyl)thiophen2-
yl)phenyl)benzofuran-5-yl)butanoate (Compound of step 2c) instead of methyl 4-
(2-(2-(5-cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoate.
1HNMR (300 MHz, CDCI3) : 7.70-7.66 (m, 1H), 7.42-7.35 (m, 2H), 7.1 7-7.02 (m,
3H), 6.74-6.73 (m, 2H), 6.22 (s, 1H), 2.75 (t, J = 7.2 Hz, 2H), 2.39 (t, J = 7.5 Hz,
2H), 2.05-1 .98 (m, 2H), 1.52 (s, 3H), 0.98-0.95 (m, 2H), 0.92-0.89 (m, 2H); HPLC:
93.82%; M:S (m/z) 435.1 (M + H).
Pharmacological assays
Representative compounds of Formula (I) of the present invention (referred to
as test compounds) were tested for their activity using the assays and the methods
described below:
Beta () arrestin 2 Interaction Assay (BRET assay) was performed using
CHO-K1 cells stably expressing the GPR1 20L receptor using -galactosidase (Beta
gal) enzyme fragment complementation assay. The measurement of GPR120
activation upon agonist activation was directly provided by -arrestin recruitment.
One day before the -arrestin 2 assay, CHO-K1 cells were seeded and incubated
overnight at 37 C in a 5% C0 2 humidified atmosphere. Cells were treated with the
test compounds in the various concentrations ranging from 30to 1nM and
incubated for 2 hours for GPCR (GPR1 20) activation. Extent of Arrestin recruitment
was measured by adding detection reagents for Beta gal complementation assay
and was further incubated for 1 hour. The chemi-luminescent signal was detected on
Polar Star (BMG Labtech). The dose-response curve was analyzed using Sigma
Plot/ Graph Pad. The EC50 (concentration of the test compounds where 50% of
compounds' maximal activity is observed) values were calculated from the doseresponse
curve.
The EC50 values for the test compounds varied between 10 nM and 10 .
Conclusion:
The EC50 values determined for the test compounds by BRET assay is
indicative of GPR120 agonist activity of the compounds of the present invention.
im
Formula (I)
wherein,
X i is -0-, -S- or -NR';
X2 is -0-, -S-, -N-, -NR'-, -CR'- or -CR'R"-;
Ring A is (C6-Ci 0)aryl or 5- to 10-membered heteroaryl;
Ring B is (C3-C8 )cycloalkyl, (Cs -C^cycloalkenyl, (C6-Cio )aryl, 5- to 10-
membered heteroaryl or a saturated or partially unsaturated 3- to 11-
membered heterocyclyl ring containing one to four heteroatoms independently
selected from the group consisting of O, N and S;
R is hydrogen or (CrC 6)alkyl;
R2 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, hydroxy, cyano, nitro, -NR5R6, -C(0)Rs, -C(0)NR 5R6, -
S(0) R7, (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl and (C6-Ci 0)aryl;
R3 and R4 at each occurrence are independently selected from the group
consisting of hydrogen, halogen, oxo, cyano, nitro, - NR5R6, -C(0)R 5, -
C(0)NR 5R6, -S(0) R7, (C C6)alkyl, halo(C C6)alkyl, hydroxy, -0(C C6)alkyl,
(C3-C8)cycloalkyl, (C6-Ci 0)aryl, -O (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R5 and R6 are independently selected from the group consisting of hydrogen,
(CrC 6)alkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R is hydrogen, (CrC 6)alkyl or -NR5R6;
R' and R" are independently selected from the group consisting of hydrogen,
(Ci -C6)alkyl, -C(0)(Ci -C6)alkyl, -C(0)0(Ci -C6)alkyl and -S (0) 2 (Ci -C6)alkyl; or
R' and R" are taken together to form oxo, (C3-C8)cycloalkyl, (C5-
C8)cycloalkenyl, or 3- to 6-membered saturated or a partially unsaturated
heterocyclyl ring containing one or two heteroatoms independently selected
from the group consisting of O, N and S;
Ra and R at each occurrence are independently selected from the group
consisting of hydrogen, halogen and (CrC 6)alkyl;
n is an integer from 1 to 6;
p is an integer from 1 to 3;
q is an integer from 1 to 4;
t is an integer from 0 to 2;
represents presence or absence of a single bond;
wherein,
(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) tR , (C C6)alkyl, halo(C C6)alkyl, -
0(CrC 6)alkyl, (C3-C 8)cycloalkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
wherein R5 , R6 , R7 and t are as defined above;
-0(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0) R5 , -C (0)NR 5R6 , -S (0) tR , (C C6)alkyl, halo(C C6)alkyl,
(C3-C8)cycloalkyl, (C6-Ci 0)aryl and heterocyclyl; wherein R5 , R6 , R7 and t are
as defined above;
(C3-C 8)cycloalkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of oxo, halogen, hydroxy,
cyano, nitro, -NR 5R6 , -C (0)R 5 , -C (0)N R5R6 , -S (0) R7 , (C C6)alkyl, halo(C
C6)alkyl and -0(CrC 6)alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C5-C8)cycloalkenyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) t R7 , (Ci -C6)alkyl, halo(Ci -C6)alkyl
and -0(CrC 6)alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C6-Ci 0)aryl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro,
-C(0)R 5, -C(0)OR 5, -S(0) tR -NR5R6, (C C6)alkyl, halo(C C6)alkyl, -0(C
C6)alkyl, halo(C C6)alkoxy, (C3-C8)cycloalkyl, (C6-Ci 0)aryl, -0(C 6-Cio)aryl,
heterocyclyl and heteroaryl, wherein R5, R6, R7 and t are as defined above;
heterocyclyl is a 3- to 11-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R 5, -C(0)OR 5, -S(0) tR , -NR5R6, (C
C6)alkyl, halo(C C6)alkyl, -0(Ci-C 6)alkyl, halo(C C6)alkoxy, (C3-
C8)cycloalkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and
t are as defined above;
heteroaryl is a 5- to 10-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C(0)R 5, -C(0)OR 5, -S(0) tR7, -NR5R6, (C
C6)alkyl, halo(Ci-C 6)alkyl, -0(C C6)alkyl, halo(C C6)alkoxy, (C3-
C8)cycloalkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5, R6, R7 and
t are as defined above;
halogen is chlorine, bromine, iodine or fluorine;
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically
acceptable salt, a pharmaceutically acceptable solvate, a prodrug, a
polymorph, N-oxide, S-oxide, or a carboxylic acid isostere thereof.
2. The compound according to claim 1, represented by Formula la
Formula (la)
wherein,
Xi is -0-, -S- or -NR';
X2 is -0-, -S-, -N-, -NR'-, -CR'- or -CR'R"-;
Ring A is phenyl or 6-membered heteroaryl;
Ring B is (C3-C8)cycloalkyl, (C5-C8)cycloalkenyl, (C6-Ci 0)aryl, 5- to 10-
membered heteroaryl or a saturated or partially unsaturated 3- to 11-
membered heterocyclyl ring containing one to four heteroatoms independently
selected from the group consisting of O, N and S;
R is hydrogen or (CrC 6)alkyl;
R2 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, hydroxy, cyano, nitro, -NR5R6, -C(0)Rs, -C(0)NR5R6, -
S(0) R7, (C C6)alkyl, halo(C C6)alkyl, -0(C C6)alkyl and (C6-Ci 0)aryl;
R3 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -
S(0) R , (C C6)alkyl, halo(C C6)alkyl, hydroxy and -0(C C6)alkyl;
R4 at each occurrence is independently selected from the group consisting of
hydrogen, halogen, oxo, cyano, nitro, -NR5R6, -C(0)Rs, -C(0)NR5R6, -
S(0) R , (C C6)alkyl, halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, (C3-
C8)cycloalkyl, (C6-Ci 0)aryl, -0(CrC 6)aryl, heterocyclyl and heteroaryl;
R5 and R6 at each occurrence are independently selected from the group
consisting of hydrogen, (CrC 6)alkyl, (C6-Ci 0)aryl, heterocyclyl and heteroaryl;
R is hydrogen, (CrC 6)alkyl or -NR5R6;
R' and R" at each occurrence are independently selected from the group
consisting of hydrogen, (CrC 6)alkyl, -C(0)(C C6)alkyl, -C(0)0(C C6)alkyl
and -S(0) 2(CrC 6)alkyl; or
R' and R" are taken together to form oxo, (C3-C8)cycloalkyl, (C5-
C8)cycloalkenyl, or 3- to 6-membered saturated or a partially unsaturated
heterocyclyl ring containing one or two heteroatoms independently selected
from the group consisting of O, N and S;
Ra and R at each occurrence are independently selected from the group
consisting of hydrogen, halogen and (CrC 6)alkyl;
n is an integer from 1 to 6;
p is an integer from 1 to 3;
q is an integer from 1 to 4;
t is an integer from 0 to 2;
represents presence or absence of a single bond;
wherein,
(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR5R6, -C(0)R5, -C(0)NR5R6, -S(0) R7, (C C6)alkyl, halo(C C6)alkyl, -
0(CrC 6)alkyl, (C 3-C 8)cycloalkyl, (C 6-Ci 0)aryl, heterocyclyl and heteroaryl;
wherein R5 , R6 , R7 and t are as defined above;
-0(CrC 6)alkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) R , (Ci -C 6)alkyl, halo(Ci -C 6)alkyl,
(C 6-Ci 0)aryl, (C 3-C8)cycloalkyl, and heterocyclyl; wherein R5 , R6 , R7 and t are
as defined above;
(C 3-C 8)cycloalkyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of oxo, halogen, hydroxy,
cyano, nitro, -NR 5R6 , -C (0)R 5 , -C (0)N R5R6 , -S (0) R7 , (C C 6)alkyl, halo(C
C 6)alkyl and -0(Ci -C6 )alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C 5-C 8)cycloalkenyl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro, -NR 5R6 , -C (0)R 5 , -C (0)NR 5R6 , -S (0) t R , (C C 6)alkyl, halo(C C 6)alkyl
and -0(CrC 6)alkyl; wherein R5 , R6 , R7 and t are as defined above;
(C 6-Ci 0)aryl is unsubstituted or substituted with one or more groups
independently selected from the group consisting of halogen, hydroxy, cyano,
nitro,
-C (0)R 5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C C 6)alkyl, halo(C C 6)alkyl, -0(C
C 6)alkyl, halo(C C 6)alkoxy, (C3-C 8)cycloalkyl, (C 6-Ci 0)aryl, -O(C6-Ci 0)aryl,
heterocyclyl and heteroaryl, wherein R5 , R6 , R7 and t are as defined above;
heterocyclyl is a 3- to 11-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C (0)R 5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C
C 6)alkyl, halo(C C 6)alkyl, -0(CrC 6)alkyl, halo(C C 6)alkoxy, (C 3-
C 8)cycloalkyl, (C 6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5 , R6 , R7 and
t are as defined above;
heteroaryl is a 5- to 10-membered ring, which is unsubstituted or substituted
with one or more groups independently selected from the group consisting of
halogen, hydroxy, cyano, nitro, -C (0)R 5 , -C (0)OR 5 , -S (0) R7 , -NR 5R6 , (C
C 6)alkyl, halo(CrC 6)alkyl, -0(C C 6)alkyl, halo(C C 6)alkoxy, (C 3-
C 8)cycloalkyl, (C 6-Ci 0)aryl, heterocyclyl and heteroaryl; wherein R5 , R6 , R7 and
t are as defined above;
halogen is chlorine, bromine, iodine or fluorine;
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically
acceptable salt, a pharmaceutically acceptable solvate, a prodrug, a
polymorph, N-oxide, S-oxide, or a carboxylic acid isostere thereof.
3. The compound according to claim 2, wherein ring A is phenyl, X is -O- and X2
is -CR'-; wherein R' is selected from the group consisting of hydrogen, (C
C6)alkyl, -C(0)(d-C 6)alkyl, -C(0)0(C C6)alkyl and -S(0) 2(CrC 6)alkyl; and "-
—-" represents a single bond.
4. The compound according to claim 2, wherein ring B is
wherein - is -0-, -S- or -NRX; Y2 at each occurrence is independently
selected from a group consisting of -0-, -S-, -NH-, -N(CrC 6)alkyl and -C(R )2;
Y3 at each occurrence is independently selected from -N- or -CR ; wherein Rx
is hydrogen, (Ci-C 6)alkyl, -C(0)(Ci-C 6)alkyl, -C(0)0(Ci-C 6)alkyl or -S(0) 2(Ci-
C6)alkyl; R at each occurrence is independently selected from the group
consisting of hydrogen, halogen, oxo, cyano, nitro, - NR5R6, -C(0)R 5, -
C(0)NR 5R6, -S(0) R7, (C C6)alkyl, halo(C C6)alkyl, hydroxy, -0(C C6)alkyl, -
(C3-C8)cycloalkyl, (C6-Ci 0)aryl, -0(CrC 6)aryl, heterocyclyl and heteroaryl.
5. The compound according to claim 2, wherein ring B is
wherein ring C is selected from the group consisting of (C3-C6)cycloalkyl, (C6-
C 0)aryl, 5- or 6-membered heteroaryl and 5- or 6-membered heterocyclyl
ring containing one or two heteroatoms independently selected from the group
consisting of O, N and S; and Y Y2 and Y3 are as defined above.
6. The compound according to claim 2, wherein R4 at each occurrence is
independently selected from the group consisting of hydrogen, halogen, oxo,
cyano, nitro, -NR5R6, -C(0)R 5, -C(0)NR 5R6, -S(0) R7, (C C6)alkyl, halo(C
C6)alkyl, (C3-C8)cycloalkyl, hydroxy, -0(C C6)alkyl and -0(CrC 6)aryl.
7. The compound according to any one of claims 1 to 6 is selected from the
group consisting of:
4-(2-(2-(5-Cyclopropylthiophen-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic
acid;
4-(2-(5-Fluoro-2-(5-(1-methylcyclopropyl)thiophen-2-yl)phenyl)benzofuran-5-
yl)butanoic acid;
4-(2-(2-(5-Cyclopropylthiazol-2-yl)-5-fluorophenyl)benzofuran-5-yl)butanoic
acid;
4-(2-(2-(5,6-Dihydro-4H-cyclopenta[d]thiazol-2-yl)-5-fluorophenyl)benzofuran-
5-yl)butanoic acid;
4-(2-(5-Fluoro-2-(4,5,6,7-tetrahydrobenzo[d]thiazol-2-yl)phenyl)benzofuran-5-
yl)butanoic acid;
4-(2-(5-Fluoro-2-(isoindolin-5-yl)phenyl)benzofuran-5-yl)butanoic acid;
4-(2-(2-(5,7-Dihydrofuro[3,4-b]pyridin-3-yl)-5-fluorophenyl)benzofuran-5-
yl)butanoic acid; and
4-(2-(2-(6,7-Dihydro-5H-cyclopenta[b]pyridin-3-yl)-5-fluorophenyl)benzofuran-
5-yl)butanoic acid
or an isotopic form, a stereoisomer, a tautomer, a pharmaceutically
acceptable salt, a pharmaceutically acceptable solvate, a prodrug, a
polymorph, N-oxide, S-oxide, or a carboxylic acid isostere thereof.
8. A pharmaceutical composition comprising a therapeutically effective amount
of a compound of Formula (I) according to claim 1, or a stereoisomer, a
tautomer, a pharmaceutically acceptable salt or a pharmaceutically
acceptable solvate thereof; and at least one pharmaceutically acceptable
carrier or excipient.
9. A method for the treatment or prophylaxis of a disease or a disorder mediated
by GPR1 0 comprising administering to a subject in need thereof; a
therapeutically effective amount of compound of Formula (I) according to
claim 1, or a stereoisomer, a tautomer, a pharmaceutically acceptable salt or
a pharmaceutically acceptable solvate thereof.
10. The method according to claim 9, wherein the disease or disorder mediated
by GPR120 is a metabolic disorder.
11.The method according to claim 9, wherein the disease or disorder mediated
by GPR1 20 is an inflammatory disorder.
12. A compound according to any one of claims 1 to 7 or a stereoisomer, a
tautomer, a pharmaceutically acceptable salt or a pharmaceutically
acceptable solvate thereof; for use in the treatment or prophylaxis of a
disease or a disorder mediated by GPR1 20.
13. The use of the compound according to any one of claims 1 to 7 or a
stereoisomer, a tautomer, a pharmaceutically acceptable salt or a
pharmaceutically acceptable solvate thereof; in the manufacture of a
medicament, for the treatment or prophylaxis of a disease or a disorder
mediated by GPR120.