【Technical Field】
The present disclosure relates to a method for chiral resolution of N-[4-(1-
aminoethyl)-phenyl]-sulfonamide derivatives.
【Background Art】
Recently, demand on stereochemically pure compounds is increasing rapidly.
One important use of these pure stereoisomers is as synthetic intermediates in the
pharmaceutical industry. For example, it is becoming gradually evident that
enantiopure drugs possess many advantages over racemic drug mixtures. The
advantages often include less side effects and better efficacies of the enantiopure
compounds [see, e.g., Stinson, S.C., Chem Eng News, Sept. 28, 1992, pp. 46-79].
For example, triadimenol can exist as four isomers. The (-)-(1S,2R)-isomer has
a stronger activity than the (+)-(1R,2R)-isomer and the (-)-(1S,2S)-isomer has a
stronger activity than the (+)-(1R,2S)-isomer. Among the four isomers of
dichlorobutrazol, the (1R,2R)-isomer is known to have stronger activity. Also, for
etaconazole, the (+)-(2S,4S)- and (-)-(2S,4R)-isomers are known to have better
fungicidal effect than others.
Therefore, if only one isomer having higher activity can be prepared selectively,
3
better effect can be achieved with less amount and, accordingly, environmental pollution
resulting from the use of the chemicals can be decreased. Especially for drugs, if one
of the isomers exhibits toxicity in human, it is very important to selectively prepare one
isomer only.
Accordingly, in medicine-, pharmacy- and biochemistry-related fields,
preparation of optically pure compounds for improving medicinal effect or preventing
side effects is a very important task.
However, still many drugs are used as racemic compounds with unavoidable
side effects owing to the existence of undesirable enantiomers (see, e.g., Nguyen, et al.,
Chiral Drugs: An Overview, Int. J. Biomed. Sci., 2 (2006) 85-100). A few techniques
are available for the preparative or analytical scale chiral separations. However, it
costs immense time and efforts to find out a separation technique suited for the
racemates of interest. Even if one should succeed in resolving an enantiomer, he will
then face the next difficulty, i.e., to enable the chiral resolution on an industrial scale.
For example, the efficacies of pure stereoisomers of vanilloid antagonists
including N-[4-(1-aminoethyl)-phenyl]-sulfonamide derivatives have been elucidated
[e.g., WO 2008-013414 A1, WO 2007-133637 A2, WO 2007-129188 A1, WO 2010-
010934 A1].
As a method for synthesizing single isomers of the N-[4-(1-aminoethyl)-phenyl]-
sulfonamide derivatives, asymmetric synthesis using the Ellman’s reagent is known.
For example, WO 2008-013414 A1, WO 2007-133637 A2, WO 2007-129188 A1 and
WO 2010-010934 A1 present a method of obtaining desired stereoisomers by
introducing the Ellman’s reagent and inducing asymmetric reduction using the same.
However, this method is disadvantageous in that a low-temperature reaction condition
should be maintained to achieve high optical purity (enantiomer excess, %ee). Also,
4
the process is dangerous because excessive generation of hydrogen and heat occurs
when the reaction is terminated. In addition, the disposal cost of the excessively
produced organic and inorganic wastes is also disadvantageous in terms of economy.
【Disclosure】
【Technical Problem】
Although asymmetric synthesis of N-[4-(1-aminoethyl)-phenyl]-sulfonamide
derivatives has been reported, a preparation method that can be utilized in commercial
scale has not been established as yet because of the problems in economy and safety.
Accordingly, the present disclosure is directed to solving the problems of the existing
asymmetric synthesis method and providing a novel method for chiral resolution of a
mixture of stereoisomers to an S or R compound having high optical purity.
【Technical Solution】
In an aspect, the present disclosure provides a method for resolving N-[4-(1-
aminoethyl)-phenyl]-sulfonamide derivatives of formula (I):
R6
R4
NH2
NH
S
O
O
R5
R1
R2
R7
R3
[Formula (I)]
to the respective compounds with high optical purity by using an O,O’-diacyltartaric acid
derivative (an example of chiral auxiliaries) and a soluble salt-forming acid (an example
of salt-forming compounds). In one embodiment, the present disclosure relates to a
method for resolving (R,S)-N-[4-(1-aminoethyl)-phenyl]-sulfonamide to N-[4-(1-
aminoethyl)-phenyl]-sulfonamide having high optical purity, including: (i) mixing an
5
(R,S)-N-[4-(1-aminoethyl)-phenyl]-sulfonamide derivative with an optically active O,O’-
diacyltartaric acid derivative (an example of chiral auxiliaries) and a soluble salt-forming
acid (an example of salt-forming compounds) in a polar protic solvent, and thereby
preparing an (R)- or (S)-N-[4-(1-aminoethyl)-phenyl]-sulfonamide diacyltartrate salt or a
solvate thereof with high optical purity, and (ii) liberating the resulting N-[4-(1-
aminoethyl)-phenyl]-sulfonamide salt or a solvate thereof with high optical purity by
using a base.
According to the method of the present disclosure, N-[4-(1-aminoethyl)-phenyl]-
sulfonamide derivatives can be easily resolved to the respective compounds having
high optical purity.
N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide is a general name
of a compound which has a structure of formula (II) as follows:
[Formula (II)]
and it is known as a useful intermediate product for manufacturing a compound
acting as a TRPV1 (transient receptor potential cation channel subfamily V member 1,
or capsaicin receptor or vanilloid receptor 1) antagonist.
As can be seen in formula (II), N-[4-(1-aminoethyl)-2,6-difluorophenyl]-
methanesulfonamide is a chiral compound wherein an amine group is bonded to an
asymmetric carbon atom (chiral center).
【Advantageous Effects】
In accordance with a method for chiral resolution according to an aspect of the
6
present disclosure, a mixture of stereoisomers, particularly a mixture of stereoisomers
of a compound wherein an amine group is bonded to an asymmetric carbon atom, can
be chirally resolved easily to a compound having high optical purity. This synthesis
method provides improved safety and economy over the asymmetric synthesis method
using the Ellman’s reagent. It allows for chiral resolution with comparable or better
optical purity and provides improved economy and environment friendliness through
collection and recycling of salts. Accordingly, this method can be advantageously used
in pharmaceutical and cosmetic fields where chiral resolution of compounds is desired.
In particular, the method according to the present disclosure allows for effective
preparation of desired stereoisomers with comparable or better optical purity as
compared to the existing asymmetric synthesis method using Ellman’s reagent. It is
also effective for large-scale production and provides economic advantages.
【Detailed Description of Invention】
In one aspect, the present disclosure provides a method for resolution of a
mixture of stereoisomers of compound,
comprising a step of mixing said mixture of stereoisomers of compound with
(i) a chiral auxiliary and
(ii) an auxiliary salt-forming compound
in the presence of a solvent,
thereby precipitating a diastereomeric salt of said chiral auxiliary (i) with the
compound. In one aspect, the method for resolution is related to a method for chiral
resolution.
In one aspect, the present disclosure provides a method for resolving a mixture
of stereoisomers of compound of formula (I),
7
R6
R4
NH2
NH
S
O
O
R5
R1
R2
R7
R3
(I)
comprising a step of mixing said mixture of stereoisomers of the compound of
formula (I) with
(i) a chiral auxiliary and
(ii) an auxiliary salt-forming compound
in the presence of a solvent,
thereby precipitating a diastereomeric salt of said chiral auxiliary (i) with the
compound of formula (I).
In an embodiment of the present disclosure, a method according to the present
invention provides a stereoisomer of the compound of formula (I) in enantiomeric
excess, specifically with high optical purity.
The term “in enantiomeric excess” in the present disclosure generally includes
any increase in the ratio of enantiomers, thus not only an enantiomeric excess
compared to a racemic mixture, but also an increase of one enantiomer over another
compared to a mixture wherein the ratio of enantiomers is not 1:1 (as in a racemate).
In some embodiments, the term in enantiomeric excess specifically corresponds to an
enantiomeric excess value (“%ee”) of at least 80%, or at least 90%, or at least 95% or
at least 96%, or at least 97%, or at least 98%, or at least 99%.
The term “high optical purity” in the present disclosure is a term well-understood
in the art. In some embodiments, the term “high optical purity” corresponds to an
enantiomeric excess value (“%ee”) of at least 80%, or at least 90%, or at least 95% or
at least 96%, or at least 97% or at least 98% or at least 99%.
In an aspect, the present disclosure provides a method for chiral resolution of a
8
mixture of stereoisomers, including mixing a mixture of stereoisomers with a soluble
salt-forming acid (an example of salt-forming compounds), and an optically active O,O'-
diacyltartaric acid derivative (an example of chiral auxiliaries).
The term ‘salt-forming compound’ in the present disclosure is not only a
compound to resolve a mixture of stereoisomers, but also a compound to help to
increase optical purity of the mixture of stereoisomers. The different solubility of the
salt formed with an enantiomer and a chiral auxiliary in the salt-forming compound is
used to help resolving the mixture of stereoisomers. A salt-forming compound may be
an acid or a salt thereof which are able to solubilize the mixture of stereoisomers to be
resolved. This salt-forming compound helps one enantiomer which does not form an
insoluble salt with the chiral auxiliary to remain soluble, thereby helping to obtaining a
non-soluble salt of another enantiomer in enantiomeric excess.
In an exemplary embodiment of the present disclosure, the soluble salt-forming
acid (an example of salt-forming compounds) may be selected from a group comprising
mandelic acid, camphorsulfonic acid, a stereoisomer thereof, and a combination thereof.
The term ‘chiral auxiliary’ in the present disclosure is well recognized by a person skilled
in the art and specifically means a chemical compound or unit that is temporarily
incorporated into an organic synthesis to control the stereochemical outcome of the
synthesis. The chirality of the chiral auxiliary can bias the stereoselectivity of one or
more subsequent reactions (see, e.g., chiral auxiliary, Wikipedia:
http://en.wikipedia.org/wiki/Chiral_auxiliary). In the present disclosure, the terms chiral
auxiliary and chiral acid may be used interchangeably.
In an exemplary embodiment of the present disclosure, the chiral auxiliary may
be an O,O'-diacyltartaric acid derivative. The chiral auxiliary may be selected from a
group consisting of 2,3-dibenzoyltartaric acid, O,O’-di-p-toluoyltartaric acid, a
9
stereoisomer thereof, and a combination thereof.
In an exemplary embodiment of the present disclosure, the 2,3-dibenzoyltartaric
acid may be (+)-2,3-dibenzoyl-D-tartaric acid or (-)-2,3-dibenzoyl-L-tartaric acid, which
are optical isomers of each other, and the O,O’-di-p-toluoyltartaric acid may be (+)-O,O’-
di-p-toluoyl-D-tartaric acid or (-)-O,O’-di-p-toluoyl-L-tartaric acid, which are optical
isomers of each other. Although the D and L forms of the tartaric acid derivative may
be used either alone or in combination, it is preferred that they are used alone without
being mixed with each other. When the D and L forms of the tartaric acid derivative
are used in combination in the method according to the present disclosure, a lower
optical purity may be obtained as compared to when the D or L form is used alone.
In an exemplary embodiment of the present disclosure, the mandelic acid may
be D-mandelic acid or L-mandelic acid, which are optical isomers of each other, or a
combination thereof, and the camphorsulfonic acid may be (1R)-(-)-10-camphorsulfonic
acid or (1S)-(+)-10-camphorsulfonic acid, which are optical isomers of each other, or a
combination thereof. As demonstrated in the Examples, the optical isomer form of the
mandelic acid or the camphorsulfonic acid has an insignificant effect on the optical
isomer form of the final product and the final product of high optical purity can be
obtained when the optical isomers of the mandelic acid or the camphorsulfonic acid are
used either alone or in combination.
In an exemplary embodiment of the present disclosure, the mixture of
stereoisomers may be a mixture of stereoisomers of a compound having an asymmetric
carbon atom. Specifically, in an exemplary embodiment of the present disclosure, the
compound having an asymmetric carbon atom may be one wherein an amine group is
bonded thereto. Specifically, in an exemplary embodiment of the present disclosure,
the compound may have, in addition to the amine group, a substituted or unsubstituted
10
phenyl group bonded to the asymmetric carbon atom. More specifically, in an
exemplary embodiment of the present disclosure, the compound having an asymmetric
carbon atom may be a compound of formula (I).
In an exemplary embodiment of the present disclosure, an R or S optical isomer
with high optical purity may be obtained from the mixture of stereoisomers.
In an exemplary embodiment of the present disclosure, when the chiral auxiliary
is selected from a group comprising (+)-2,3-dibenzoyl-D-tartaric acid and (+)-O,O’-di-ptoluoyl-
D-tartaric acid, and a combination thereof, an R enantiomer may be obtained in
high enantiomeric excess.
In an exemplary embodiment of the present disclosure, when the chiral auxiliary
is selected from a group comprising (-)-2,3-dibenzoyl-L-tartaric acid or (-)-O,O’-di-ptoluoyl-
L-tartaric acid, and a combination thereof, an S enantiomer may be obtained in
high enantiomeric excess.
In an exemplary embodiment of the present invention, the salt-forming
compound may be D-mandelic acid, L-mandelic acid, (1R)-(-)-10-camphorsulfonic acid
or (1S)-(+)-10-camphorsulfonic acid, or a combination thereof.
In an exemplary embodiment of the present disclosure, the compound wherein
an amine group is bonded to an asymmetric carbon atom may have a structure of
formula (I):
R6
R4
NH2
NH
S
O
O
R5
R1
R2
R7
R3
(I)
wherein
each of R1, R2, R3, R4, R5, R6 and R7 is independently any one selected from a
group consisting of H, -NH2, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group
11
and a halogen, and
R1 and R2 are different from each other.
In an exemplary embodiment of the present disclosure, the halogen may be at
least one selected from a group consisting of F, Cl, Br, and I, specifically from a group
consisting of F and Cl.
In an exemplary embodiment of the present disclosure, the R1 may be one
selected from a group consisting of a methyl group, an ethyl group, a propyl group, a
butyl group and a pentyl group, and the R2 may be hydrogen.
In an exemplary embodiment of the present disclosure, the R1 may be a methyl
group, the R3 and the R7 may be hydrogen, and each of the R4, the R5 and the R6 may
independently be one selected from a group consisting of F, Cl, Br, I and a C1-6 alkyl
group.
In an exemplary embodiment of the present disclosure, the R4 and the R6 may
be F, and the R5 may be a methyl group.
In an exemplary embodiment of the present disclosure, the compound may be
N-{4-[(1R/S)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
In an exemplary embodiment of the present disclosure, the solvent may be
added at an amount to achieve complete dissolution of all reactants.
In an exemplary embodiment of the present disclosure, the solvent may be a
polar protic solvent.
In an exemplary embodiment of the present disclosure, the polar protic solvent
may be one or more selected from a group consisting of water, a C1-14 alcohol, isopropyl
alcohol, acetic acid, nitromethane, propionic acid, formic acid and combinations thereof.
Specifically, the polar protic solvent may be one or more selected from a group
consisting of water, methanol, ethanol and isopropyl alcohol. More specifically, the
12
polar protic solvent may be methanol or isopropyl alcohol. More specifically, the polar
protic solvent may be isopropyl alcohol.
In an exemplary embodiment of the present disclosure, the polar protic solvent
may be used in an amount of 5-15 times, specifically 7-13 times, more specifically 9-11
times, more specifically 10 times, based on the total weight of the mixture of
stereoisomers (i.e. volume [solvent] / weight [stereoisomers], or (v/w)).
In an exemplary embodiment of the present disclosure, the mixing may be
performed at 40-70 ºC or at the boiling point of the solvent or solvent mixture. The
mixing may be performed for 1-4 hours. In an exemplary embodiment of the present
disclosure, the mixing may be performed by stirring under reflux.
In an exemplary embodiment of the present disclosure, the mixing may be
performed at a temperature of at least 30 ºC, at least 40 ºC, more specifically at least 50
ºC, or at the boiling point of the solvent or solvent mixture.
In an exemplary embodiment of the present disclosure, the mixing temperature
may be 30 ºC or higher, 40 ºC or higher, 50 ºC or higher, 60 ºC or higher or 70 ºC or
higher, or 70 ºC or lower, 60 ºC or lower, 50 ºC or lower, 40 ºC or lower or 30 ºC or
lower. The mixing temperature may be specifically 40-60 ºC, more specifically 45-55
ºC, more specifically 50 ºC.
In an exemplary embodiment of the present disclosure, the mixing time may be
1 hour or longer, 2 hours or longer, 3 hours or longer, 4 hours or longer or 5 hours or
longer, or 6 hours or shorter, 5 hours or shorter, 4 hours or shorter, 3 hours or shorter, 2
hours or shorter or 1 hour or shorter. The mixing time may be specifically 2-4 hours,
more specifically mixing time 2.5-3.5 hours, more specifically 3 hours.
In an exemplary embodiment of the present disclosure, the method may be
performed by reacting at a ratio of two molar equivalents of the compound having a
13
structure of formula (I) (comprising the R and S optical isomers in a given ratio) per one
molar equivalent of the chiral auxiliary. In an exemplary embodiment of the present
disclosure, the reacting may be performed according to Scheme 1.
[Scheme 1]
14
According to Scheme 1, two molecules of the compound of formula (I) which has
one optical activity are bound to one molecule of the chiral auxiliary to form an insoluble
15
salt, which can be precipitated. In contrast, the compound remaining unbound to the
chiral auxiliary is dissolved in the salt-forming compound and thus is not precipitated.
Through this reaction, the method according to the present disclosure can resolve a
compound having high optical purity from the mixture of stereoisomers. On the other
hand, if one molecule of the compound of formula (I) is bound to one molecule of the
chiral auxiliary to form a salt, the chiral resolution desired by the present disclosure is
not so good as compared to when two molecules are bound.
In an exemplary embodiment of the present disclosure, the molar equivalent of
the chiral auxiliary to the mixture of stereoisomers may be a molar equivalent for
reacting two molecules of the R- or S-form of the compound having a structure of
formula (I) with one molecule of the chiral auxiliary.
In an exemplary embodiment of the present disclosure, the molar equivalent
ratio of the chiral auxiliary to 1 molar equivalent of the mixture of stereoisomers may be
equal to or less than 0.5, 0.10-0.5, 0.15-0.5, 0.25-0.35, or 0.25.
In an exemplary embodiment of the present disclosure, the chiral auxiliary may
be used in an amount of 0.01 equivalent or more, 0.05 equivalent or more, 0.10
equivalent or more, 0.15 equivalent or more, 0.2 equivalent or more, 0.25 equivalent or
more, 0.3 equivalent or more, 0.35 equivalent or more, 0.4 equivalent or more, 0.45
equivalent or more, 0.5 equivalent or more, 0.55 equivalent or more or 0.6 equivalent or
more, or 0.6 equivalent or less, 0.55 equivalent or less, 0.5 equivalent or less, 0.45
equivalent or less, 0.4 equivalent or less, 0.35 equivalent or less, 0.3 equivalent or less,
0.25 equivalent or less, 0.2 equivalent or less, 0.15 equivalent or less, 0.10 equivalent
or less, 0.05 equivalent or less or 0.01 equivalent or less per 1 equivalent of the mixture
of stereoisomers.
In an exemplary embodiment of the present disclosure, the molar equivalent
16
ratio of the salt-forming compound to 1 molar equivalent of the mixture of stereoisomers
may be 0.50-1.5, 0.75-1.5, or 0.75-1.0.
Specifically, the salt-forming compound may be used in an amount of 0.5
equivalent or more, 0.55 equivalent or more, 0.6 equivalent or more, 0.65 equivalent or
more, 0.7 equivalent or more, 0.75 equivalent or more, 0.8 equivalent or more, 0.85
equivalent or more, 0.9 equivalent or more, 0.95 equivalent or more, 1.0 equivalent or
more, 1.05 equivalents or more, 1.1 equivalents or more, 1.15 equivalents or more, 1.2
equivalents or more, 1.25 equivalents or more, 1.3 equivalents or more, 1.35
equivalents or more, 1.4 equivalents or more, 1.45 equivalents or more, 1.5 equivalents
or more, 1.55 equivalents or more or 1.6 equivalents or more, or 1.6 equivalents or less,
1.55 equivalents or less, 1.5 equivalents or less, 1.45 equivalents or less, 1.4
equivalents or less, 1.35 equivalents or less, 1.3 equivalents or less, 1.25 equivalents or
less, 1.2 equivalents or less, 1.15 equivalents or less, 1.1 equivalents or less, 1.05
equivalents or less, 1.0 equivalent or less, 0.95 equivalent or less, 0.9 equivalent or less,
0.85 equivalent or less, 0.8 equivalent or less, 0.75 equivalent or less, 0.7 equivalent or
less, 0.65 equivalent or less, 0.6 equivalent or less, 0.55 equivalent or less, or 0.50
equivalent or less per 1 equivalent of the mixture of stereoisomers.
In an exemplary embodiment of the present disclosure, the molar equivalent
ratio of the chiral auxiliary and the salt-forming compound together to 1 molar equivalent
of the mixture of stereoisomers may be 0.6-2.0, 0.75-2.0, 0.8-2.0, 1.0-1.85, or 1.0-1.35.
Specifically, such molar equivalent ratio of the chiral auxiliary and the salt-forming
compound together may be a value that sums the molar equivalent of the chiral auxiliary
and the molar equivalent of the salt-forming compound described above.
In an exemplary embodiment of the present disclosure, when the salt-forming
compound and the chiral auxiliary are used in combination, a higher optical purity may
17
be obtained when the chiral auxiliary is used at a smaller equivalent ratio than the saltforming
compound per 1 equivalent of the racemic mixture.
In an exemplary embodiment of the present disclosure, a stereoisomer of the
compound with at least 96%, at least 97%, at least 98%, at least 99%, or 96% to 99%
enantiomeric excess obtained by a method according to the present invention is
provided. In another aspect, the present disclosure provides an R or S optical isomer
compound prepared by resolving a mixture of stereoisomers by the method according to
the present disclosure.
In an exemplary embodiment of the present disclosure, the stereoisomer may be
N-{4-[(1R)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide or N-{4-[(1S)-1-
aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
In the context of the present disclosure, an asymmetric carbon atom may refer
to a carbon atom that is attached to four different types of atoms, radicals or functional
groups. A compound having an asymmetric carbon atom exhibits optical rotation,
optical activity, or optical isomerism.
In the context of the present disclosure, a mixture of stereoisomers may refer to
a mixture of two enantiomers having optical activity. The mixing ratio may be 1:1
(corresponding to a racemic mixture) or, more generally, any ratio ranging from 1:10 to
10:1. In the context of the present disclosure, the mixture of stereoisomers may be an
artificially synthesized one or a mixture with an unknown ratio of an R optical isomer to
an S optical isomer. In accordance with the method of the present disclosure, the ratio
of one of the R or S optical isomers can be increased remarkably and the desired
optical isomer can be obtained with high optical purity regardless of the mixing ratio of
the mixture. Specifically, the mixture of stereoisomers to be resolved may be a 1:1
mixture of R and S optical isomers.
18
In the context of the present disclosure, N-[4-(1-aminoethyl)-2,6-difluorophenyl]-
methanesulfonamide refers to a compound of CAS No. 1202743-51-8 with a molecular
weight of 250.27 Da. It may be used interchangeably with INT-2 in the present
disclosure. It may also be a mixture of stereoisomers wherein R and S optical isomers
are mixed.
In the context of the present disclosure, N-{4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl}methanesulfonamide hydrochloride refers to a compound of CAS No.
956901-23-8 with a molecular weight of 286.73 Da and N-{4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl}methanesulfonamide refers to a compound of CAS No. 957103-01-4. In
the present disclosure, N-{4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl}methanesulfonamide may be used interchangeably with an R isomer of
INT-3.
In the context of the present disclosure, 3-(2-propyl-6-trifluoromethylpyridin-3-yl)-
acrylic acid refers to a compound of CAS No. 1005174-17-3 with a molecular weight of
259.22 Da.
In the context of the present disclosure, (R)-N-[1-(3,5-difluoro-4-
methanesulfonylaminophenyl)-ethyl]-3-(2-propyl-6-trifluoromethylpyridin-3-yl)-
acrylamide (PAC-14028) refers to a compound of CAS No. 1005168-10-4 with a
molecular weight of 491.47 Da.
In an exemplary embodiment of the present disclosure, the R or S optical isomer
of INT-3 may be obtained by a method including:
mixing INT-2 (N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide) with
the chiral auxiliary and the salt-forming compound;
adding to the mixture a polar protic solvent of 10 times based on the weight of
the INT-2 (v/w);
19
stirring the resulting mixture solution with the polar protic solvent added at 30-70
ºC for 1-4 hours under reflux;
cooling the mixture; and
obtaining a chiral acid salt of INT-3 by filtering the resulting solid.
In an exemplary embodiment of the present disclosure, the cooling may
performed at 15-30 ºC after the stirring under reflux.
In an exemplary embodiment of the present disclosure, the cooling may be
performed at a temperature of 10 ºC or higher, 15 ºC or higher, 20 ºC or higher, 22 ºC or
higher, 24 ºC or higher, 25 ºC or higher, 26 ºC or higher, 28 ºC or higher, 30 ºC or
higher or 35 ºC or higher, or 40 ºC or lower, 35 ºC or lower, 30 ºC or lower, 28 ºC or
lower, 26 ºC or lower, 25 ºC or lower, 24 ºC or lower, 22 ºC or lower, 20 ºC or lower, 15
ºC or lower, 10 ºC or lower or 5 ºC or lower.
In an exemplary embodiment of the present disclosure, the method may further
include a step of separating the chiral acid from the obtained chiral acid salt of INT-3.
Specifically, the separation may be performed by adding to the chiral acid salt of INT-3
water (5 times based on its weight) and 2 equivalents of a 28 vol% ammonia aqueous
solution, obtaining a suspension by stirring for 20-50 minutes, filtering the suspension
and obtaining an R or S optical isomer of INT-3 by removing excess water under
reduced pressure.
In another aspect, the present disclosure provides a method for chiral resolution
of a mixture of stereoisomers, including:
(1) a step of mixing a mixture of stereoisomers of a compound wherein an amine
group is bonded to an asymmetric carbon atom with a chiral auxiliary and a salt-forming
compound.
In an exemplary embodiment of the present disclosure, the compound may be
20
N-{4-[(1R/S)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
In an exemplary embodiment of the present disclosure, the chiral auxiliary in the
step (1) may be at least one selected from a group consisting of 2,3-dibenzoyltartaric
acid, O,O’-di-p-toluoyltartaric acid, stereoisomers thereof and a combination thereof.
In an exemplary embodiment of the present disclosure, the salt-forming
compound in the step (1) may be at least one selected from a group consisting of
mandelic acid, camphorsulfonic acid, stereoisomers thereof and a combination thereof.
In an exemplary embodiment of the present disclosure, the method may further
include, after the step (1): (2) a step of adding a solvent to the mixture of the step (1).
In an exemplary embodiment of the present disclosure, the solvent may be a
polar protic solvent.
In an exemplary embodiment of the present disclosure, the method may further
include: (3) a step of stirring the resulting mixture solution under reflux.
In an exemplary embodiment of the present disclosure, the stirring in the step
(3) may be performed for 30 minutes or longer, 1 hour or longer, 1.5 hours or longer, 2
hours or longer, 2.5 hours or longer, 3 hours or longer, 3.5 minutes or longer or 4 hours
or longer, or for 5 hours or shorter, 4.5 hours or shorter, 4 hours or shorter, 3.5 hours or
shorter, 3 hours or shorter, 3.5 hours or shorter, 3 hours or shorter, 2.5 hours or shorter,
2 hours or shorter, 1.5 hours or shorter, 1 hour or shorter or 30 minutes or shorter.
In an exemplary embodiment of the present disclosure, the stirring in the step
(3) may be performed at 20 ºC or higher, 25 ºC or higher, 30 ºC or higher, 35 ºC or
higher, 40 ºC or higher, 45 ºC or higher, 50 ºC or higher, 55 ºC or higher or 60 ºC or
higher, or at 70 ºC or lower, 65 ºC or lower, 60 ºC or lower, 55 ºC or lower, 50 ºC or
lower, 45 ºC or lower, 40 ºC or lower, 35 ºC or lower, 30 ºC or lower, 25 ºC or lower or
20 ºC or lower.
21
In an exemplary embodiment of the present disclosure, the method may further
include: (4) a step of cooling the mixture of the step (3).
In an exemplary embodiment of the present disclosure, the method may further
include: (5) a step of obtaining a diastereomer salt of the compound by filtering the
resulting solid. Specifically, in an exemplary embodiment of the present disclosure, the
diastereomer salt of the compound may be a diastereomer salt of INT-3.
In an exemplary embodiment of the present disclosure, the method may further
include: (6) a step of removing or separating a chiral acid from the obtained
diastereomer salt.
In an exemplary embodiment of the present disclosure, the step (6) may include:
1) a step of adding to the diastereomer salt of INT-3 water and an ammonia aqueous
solution. Specifically, in an exemplary embodiment of the present disclosure, the water
in the step (6) may be used in an amount of 2 times or more, 3 times or more, 4 times or
more, 5 times or more, 6 times or more or 7 times or more, or 7 times or less, 6 times or
less, 5 times or less, 4 times or less, 3 times or less or 2 times or less, based on the
weight of the diastereomer salt of INT-3. Specifically, in an exemplary embodiment of
the present disclosure, the ammonia aqueous solution in the step (6) may be a 20 vol%
or higher, 24 vol% or higher, 28 vol% or higher, 32 vol% or higher, 36 vol% or higher or
40 vol% or higher ammonia aqueous solution, or a 40 vol% or lower, 36 vol% or lower,
32 vol% or lower, 28 vol% or lower, 24 vol% or lower or 20 vol% or lower ammonia
aqueous solution. Specifically, in an exemplary embodiment of the present disclosure,
the ammonia aqueous solution in the step (6) may be used in an amount of 0.5
equivalent or more, 1 equivalent or more, 1.5 equivalents or more, 2 equivalents or
more, 2.5 equivalents or more or 3 equivalents or more, or 4 equivalents or less, 3.5
equivalents or less, 3 equivalents or less, 2.5 equivalents or less, 2 equivalents or less,
22
1.5 equivalents or less, 1 equivalent or less or 0.5 equivalent or less.
In an exemplary embodiment of the present disclosure, the step (6) may further
include, after the step 1): 2) a step of stirring the resulting mixture solution. Specifically,
in an exemplary embodiment of the present disclosure, the stirring in the step (6) may
be performed for 5 minutes or longer, 10 minutes or longer, 20 minutes or longer, 30
minutes or longer, 40 minutes or longer, 50 minutes or longer, 60 minutes or longer or
70 minutes or longer, or for 70 minutes or shorter, 60 minutes or shorter, 50 minutes or
shorter, 40 minutes or shorter, 30 minutes or shorter, 20 minutes or shorter or 10
minutes or shorter.
In an exemplary embodiment of the present disclosure, the step (6) may further
include: 3) a step of filtering the resulting suspension.
In an exemplary embodiment of the present disclosure, the step (6) may further
include: 4) a step of obtaining an R or S optical isomer of INT-3 by removing water from
the filtered suspension, specifically under reduced pressure.
In another aspect, the present invention provides a method for manufacturing a
compound of formula (IIIa) or (IIIb)
R6
R4
NH
NH
R1 O
N
CF3
S
O
O
R5
R7
R3
R2
(IIIa)
R6
R4
NH
NH R1 O
N
CF3
S
O
O
R5
R7
R3
R2
(IIIb)
wherein, each of R1, R2, R3, R4, R5, R6 and R7 is independently any one selected
from a group consisting of H, -NH2, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6
23
alkynyl group and a halogen, and
R1 and R2 are different from each other, comprising
Resolving, specifically chiral resolving, the mixture of stereoisomers of the
compound of formula (I) according to the method of present disclosure, and
converting the resulting stereoisomer to the compound of formula (IIIa) or (IIIb).
The converting step is described specifically also in Korean Patent Application No. 10-
2009-700433.
In an exemplary embodiment of the present disclosure, the compound of
formula (IIIa) may be (R)-N-[1-(3,5-difluoro-4-methanesulfonamino-phenyl)-ethyl]-3-(2-
propyl-6-trifluoromethyl-pyridine-3-yl)-acrylamide and the compound of formula (I) may
be N-{4-[(1R/S)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
In another exemplary embodiment of the present disclosure, the converting step
may comprise a step of coupling N-{4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl}methanesulfonamide (INT-3) with 3-(2-propyl-6-trifluoromethyl-pyridine-
3-yl)-acrylic acid (INT-7).
The R isomer compound resolved by the method according to the present
disclosure may be reacted with the substance described in Korean Patent Application
No. 10-2009-700433 to be used as an intermediate to prepare the novel drug described
in the patent application. Accordingly, in another aspect, the present disclosure relates
to a method for preparing the novel drug described in Korean Patent Application No. 10-
2009-700433 using the R isomer compound resolved by the method according to the
present disclosure or the novel drug prepared by the method.
In an exemplary embodiment of the present disclosure, (R)-N-[1-(3,5-difluoro-4-
methanesulfonylaminophenyl)-ethyl]-3-(2-propyl-6-trifluoromethyl-pridin-3-yl)-acrylamide
obtainable by the method of the present disclosure with at least of 96%, at least of 97%,
24
at least of 98%, at least of 99%, or 96%-99% of enantiomeric access is provided.
In another aspect, the present disclosure provides a TRPV1 antagonist
containing (R)-N-[1-(3,5-difluoro-4-methanesulfonylaminophenyl)-ethyl]-3-(2-propyl-6-
trifluoromethylpridin-3-yl)-acrylamide (PAC-14028) which is prepared by the method
according to the present disclosure as an effective ingredient. The TRPV1 antagonist
may be used in a pharmaceutical composition for preventing or treating the diseases
described below.
In a further aspect, the present disclosure relates to a pharmaceutical
composition containing (R)-N-[1-(3,5-difluoro-4-methanesulfonylaminophenyl)-ethyl]-3-
(2-propyl-6-trifluoromethylpyridin-3-yl)-acrylamide, an optical isomer thereof or a
pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier, for
preventing or treating a disease associated with the pathological stimulation and/or
aberrant expression of the vanilloid receptor selected from a group consisting of pain,
inflammatory disease of the joints, neuropathy, HIV-related neuropathy, nerve injury,
neurodegeneration, stroke, urinary incontinence, cystitis, stomach/duodenal ulcer,
irritable bowel syndrome (IBS) and inflammatory bowel disease (IBD), fecal urgency,
gastroesophageal reflux disease (GERD), Crohn’s disease, asthma, chronic obstructive
pulmonary disease, cough, neurotic/allergic/inflammatory skin disease, psoriasis,
pruritus, prurigo, skin irritation, inflammation of eye or mucous membrane, hyperacusis,
tinnitus, vestibular hypersensitivity, episodic vertigo, myocardial ischemia, hirsutism,
depilation, alopecia, rhinitis and pancreatitis.
In an exemplary embodiment of this aspect of the present disclosure, the pain
may be or be associated with a disease selected from a group consisting of
osteoarthritis, rheumatoid arthritis, ankylosing spondylitis, diabetic neuropathic pain,
post-operative pain, toothache, fibromyalgia, myofascial pain syndrome, back pain,
25
migraine and other types of headache.
In another aspect, the present disclosure provides a composition comprising: a
chiral auxiliary which is one or more selected from the group consisting of 2,3-
dibenzoyl-tartaric acid, O,O’-di-p-toluoyl-tartaric acid, a stereoisomer thereof, and a
combination thereof; and a salt-forming compound which is one or more selected from
the group consisting of mandelic acid, camphorsulfonic acid, a stereoisomer thereof,
and a combination thereof. In an aspect, the composition may be a chiral resolving
composition or a chiral resolving agent.
In an exemplary embodiment of the composition according to the present
invention, the molar equivalent ratio of the chiral auxiliary to 1 molar equivalent of a
mixture of stereoisomers which is to be resolved may be equal to or less than 0.5, or
0.15-0.5, 0.25-0.35, or 0.25.
In an exemplary embodiment of the composition according to the present
invention, the molar equivalent ratio of the salt-forming compound to 1 molar equivalent
a mixture of stereoisomers which is to be resolved may be 0.75-1.5.
In an exemplary embodiment of the present invention, the molar equivalent ratio
of the salt forming compound to 1 molar equivalent of the chiral auxiliary in the
composition may be between 1.5 and 6, specifically between 3 and 6 (i.e. 3 to 6 moles
of the salt-forming compound for each mole of the chiral auxiliary).
In another aspect, the present disclosure provides a composition containing: a
chiral auxiliary; and a salt-forming compound.
In an exemplary embodiment of the present disclosure, the composition may
contain 0.10-0.5 equivalent of the chiral auxiliary per 1 equivalent of a mixture of
stereoisomers which is desired to be chirally resolved.
In an exemplary embodiment of the present disclosure, the composition may
26
contain 0.75-1.5 equivalent of the salt-forming compound per 1 equivalent of the mixture
of stereoisomers.
In another aspect, the present disclosure provides a resolving kit comprising a
chiral auxiliary; and a salt-forming compound.
In another aspect, the present disclosure provides a chiral resolving kit,
comprising: a chiral auxiliary which is one or more selected from the group consisting of
2,3-dibenzoyl-tartaric acid, O,O’-di-p-toluoyl-tartaric acid, a stereoisomer thereof, and a
combination thereof; and a salt-forming compound which is one or more selected from
the group consisting of mandelic acid, camphorsulfonic acid, a stereoisomer thereof,
and a combination thereof.
In an exemplary embodiment of the present disclosure, the chiral resolving kit
according the present invention may further comprise written instructions for using the
chiral auxiliary and the salt-forming compound, specifically for resolving a mixture of
stereoisomers of a compound of formula (I).
In an exemplary embodiment of the present invention, the molar equivalent ratio
of the chiral auxiliary to 1 equivalent of a mixture of stereoisomers which is to be
resolved may be equal to or less than 0.5, 0.15-0.5, 0.25-0.35, or 0.25.
In an exemplary embodiment of the present invention, the molar equivalent ratio
of the salt-forming compound to 1 equivalent of a mixture of stereoisomers which is to
be resolved may be 0.75-1.5.
In an exemplary embodiment of the present disclosure, the kit according the
present invention may further comprise written instructions for using the chiral auxiliary
and the salt-forming compound.
In an exemplary embodiment of the present disclosure, the written instructions
may contain instructions that the chiral auxiliary is used in amount of 0.10-0.5 equivalent
27
per 1 equivalent of the mixture of stereoisomers which is desired to be chirally resolved.
In an exemplary embodiment of the present disclosure, the written instructions
may contain instructions that the salt-forming compound is used in amount of 0.75-1.5
equivalent per 1 equivalent of the mixture of stereoisomers which is desired to be
chirally resolved.
In an exemplary embodiment of the chiral resolving kit according to the present
invention, the molar equivalent ratio of the salt forming compound to 1 molar equivalent
of the chiral auxiliary may be between 1.5 and 6, specifically between 3 and 6 (i.e. 3 to 6
moles of the salt-forming compound for each mole of the chiral auxiliary).
In an exemplary embodiment of the present disclosure, the written instructions
may contain instructions that the chiral auxiliary and the salt-forming compound are
mixed with the mixture of stereoisomers in a polar protic solvent.
In an exemplary embodiment of the present disclosure, the written instructions
may contain instructions about the method for resolving the mixture of stereoisomers
described in the present disclosure.
In another aspect, the present disclosure provides a use of the composition or
the kit according to present disclosure for chiral resolving of a mixture of stereoisomers.
Hereinafter, the present disclosure will be described in detail through the
following examples. However, the following examples are for illustrative purposes only,
and the scope of the present disclosure is not limited by these examples. Also, it will
be apparent to those of ordinary skill in the art that various changes and modifications
may be made thereto without departing from the scope of the present disclosure.
[Comparative Test Example 1] Measurement of optical purity for existing
asymmetric synthesis method
Asymmetric synthesis was performed according to Scheme 2.
28
[Scheme 2]
N-{2,6-Difluoro-4-[1-(2-methylpropane-2-sulfinylimino)-ethyl]-phenyl}-
methanesulfonamide (1 equivalent) was dissolved by adding tetrahydrofuran (THF) (20
29
mL) in an amount of 10 times based on its weight. After further dissolving NaBH4 (4
equivalents) in the resulting solution, reaction was performed for 10 hours at the
temperatures described in Table 1. Then, CH3OH was added dropwise until no
hydrogen gas evolution was observed.
The mixture was concentrated under reduced pressure and then purified by
chromatography to obtain N-{2,6-difluoro-4-[1-(2-methylpropane-2-sulfinylamino)-ethyl]-
phenyl}-methanesulfonamide. The mixture was stirred at room temperature for 30
minutes while adding excess 4 M HCl in dioxane dropwise and then concentrated under
reduced pressure. The resulting residue was purified by recrystallization in acetone to
obtain (R)-N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide hydrochloride.
Enantiomeric excess (ee%) of the obtained salt was measured in the same
manner as in the Test Example. The result is given in Table 1.
【Table 1】
Comparative
Example
Temperature during addition of
NaBH4 (ºC)
ee% (R isomer)
1-1 -48 96.2
1-2 -30 95.4
1-3 -20 95.2
1-4 -10 94.9
1-5 0 94.2
As seen from Table 1, to achieve optical activity of 96% or higher with the
existing method, the temperature should be maintained below -40 ºC continuously for
10 hours, whereas the same optical activity can be achieved through stirring and
purification at 50 ºC according to the present disclosure. Accordingly, it can be seen
30
that the method of the present disclosure is remarkably economical as compared to the
existing method. If the reaction is extended to the plant scale, it will be much easier to
maintain temperature at 50 ºC than at -40 ºC for 10 hours. Accordingly, the reaction
scale of the method of the present disclosure can be more easily extended as
compared to the existing method.
In addition, the existing method using 2-4 equivalents of sodium borohydride is
very dangerous because explosive hydrogen is generated in excess and also heat is
generated during the reaction. In contrast, the method of the present disclosure allows
for preparation of commercially useful stereoisomers with optical activity of 96% or more
without involving the excessive generation of explosive hydrogen or heat.
To conclude, the method of the present disclosure is more economical and safe
as compared to the existing method.
[Comparative Test Example 2] Measurement of optical purity for resolution using
one chiral resolving agent
N-[4-(1-Aminoethyl)-2,6-difluorophenyl]-methanesulfonamide (mixture of R and
S stereoisomers) was prepared according to the preparation method described in
Bioorganic & Medicinal Chemistry 15(18), 6043-6053; 2007. 1 equivalent of the
prepared N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide was mixed with 1
equivalent of the chiral auxiliary described in Tables 2 and 3. To the resulting mixture
was added a solvent (different solvents as described in the tables) of 10 times (vol.)
based on the weight of the N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide.
The resulting mixture solution was refluxed at 50 ºC for 3 hours and then cooled to 25
ºC. The resulting solid was filtered using a Büchner funnel to obtain each N-[4-(1-
aminoethyl)-2,6-difluorophenyl]-methanesulfonamide chiral acid salt. The obtained salt
is a once-resolved salt.
31
The obtained once-resolved N-[4-(1-aminoethyl)-2,6-difluorophenyl]-
methanesulfonamide salt was subjected to the above-described procedure of refluxing
after adding the solvent of 10 times based on weight, cooling and then filtering for 1 and
2 times to obtain twice-resolved and thrice-resolved N-[4-(1-aminoethyl)-2,6-
difluorophenyl]-methanesulfonamide salts.
After adding to each of the obtained N-[4-(1-aminoethyl)-2,6-difluorophenyl]-
methanesulfonamide chiral acid salts water of 5 times based on its weight and 2
equivalents of a 28 vol% ammonia aqueous solution, the mixture was stirred for 30
minutes. The resulting suspension was filtered using a Büchner funnel and excess
water was removed under reduced pressure to obtain N-[4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl]-methanesulfonamide or N-[4-[(1S)-1-aminoethyl]-2,6-difluorophenyl]-
methanesulfonamide (INT-3).
The optical purity (enantiomeric excess) of the obtained INT-3 was analyzed
using a chiral HPLC column (Shiseido Chiral CD-Ph, 4.6 mm x 250 mm, 5 μm). A
mixture solution of 0.5 mol/L sodium perchlorate and methanol (75 vol% : 25 vol%) was
used as a mobile phase and the optical purity (enantiomeric excess, ee%) of each chiral
acid salt was measured using the Waters e2695 Alliance HPLC system and calculated
according to Equation 1. And, the yield of reaction was calculated according to
Equation 2. The yield was calculated only for the thrice-resolved salt with the highest
optical activity.
The result is given in Tables 2 and 3.

1. Column temperature = 35 ºC
2. Flow rate = 0.5 mL/min
3. Detection wavelength = 220 nm
32
4. Rt (min) = 20.4 (R-enantiomer %), 18.9 (S-enantiomer %)
[Equation 1]
Enantiomeric excess (%ee) = ([Desired isomer] – [Opposite isomer]) / ([Desired
isomer] + [Opposite isomer]) x 100
[Equation 2]
Yield (%) = (Actual yield / Theoretical yield) x 100%
Actual yield: the amount of obtained product.
Theoretical yield: the maximum amount of product that can be obtained from the
given amount of reactant.
【Table 2】
Comp.
Ex.
Chiral
auxiliary
Solvent
%ee (R enantiomer) Yield of
thriceresolved
salt
Onceresolved
Twiceresolved
Thriceresolved
2-1
(+)-2,3-Dibenzoyl-
Dtartaric
acid
Water
(H2O)
40.1 77.5 91 15
2-2 Methanol 68.4 84.2 97 9
2-3 Ethanol 44.2 78.4 94 11
2-4
Isopropyl
alcohol
36.9 68.1 92.1 17
2-5 Butanol 24.7 56.9 88.0 17
【Table 3】
33
Comp.
Ex.
Chiral
auxiliary
Solvent
%ee (R enantiomer) Yield of
thriceresolved
salt
Onceresolved
Twiceresolved
Thriceresolved
3-1
O,O′-Di-ptoluoyl-
Dtartaric
acid
Water (H2O) 38 71.5 75.4 16
3-2 Methanol 63.2 79.2 96.1 4
3-3 Ethanol 41.2 71.5 91 10
3-4
Isopropyl
alcohol
35.6 62.3 89.2 15
3-5 Butanol 21.5 49.3 80.0 14
As can be seen from Tables 2 and 3, when only dibenzoyltartaric acid or
ditoluoyltartaric acid was used, an optical isomer of higher purity could be obtained as
the number of resolutions increased. In particular, the purity was the highest when
methanol or ethanol was used. However, when the resolution was performed less than
3 times, the purity was very low as compared to a commercially useful purity of at least
96% ee.
In addition, the isomer yield was very low, such as below 20% when only
dibenzoyltartaric acid or ditoluoyltartaric acid was used, regardless of the solvent.
[Test Example 1] Measurement of optical purity for different chiral auxiliary and
auxiliary salt-forming compound and mixing ratios thereof
N-[4-(1-Aminoethyl)-2,6-difluorophenyl]-methanesulfonamide (mixture of
stereoisomers of R and S isomers) was prepared according to the preparation method
described in Bioorganic & Medicinal Chemistry 15(18), 6043-6053; 2007. 1 equivalent
34
of the prepared N-[4-(1-aminoethyl)-2,6-difluorophenyl]-methanesulfonamide was mixed
with the chiral auxiliary and the auxiliary salt-forming compound described in Tables 4-8
of the equivalents described in the tables. To the resulting mixture was added a
solvent (different solvents described in Tables 4-8) of 10 times based on the weight of
the methanesulfonamide compound. The resulting mixture solution was refluxed at 50
ºC for 3 hours and then cooled to 25 ºC. The resulting solid was filtered using a
Büchner funnel to obtain each INT-3 chiral acid salt.
After adding to each of the obtained N-[4-(1-aminoethyl)-2,6-difluorophenyl]-
methanesulfonamide chiral acid salts water of 5 times based on its weight and 2
equivalents of a 28 vol% ammonia aqueous solution, the mixture was stirred for 30
minutes. The resulting suspension was filtered using a Büchner funnel and excess
water was removed under reduced pressure to obtain N-[4-[(1R)-1-aminoethyl]-2,6-
difluorophenyl]-methanesulfonamide or N-[4-[(1S)-1-aminoethyl]-2,6-difluorophenyl]-
methanesulfonamide (INT-3).
The optical purity (enantiomeric excess) of the obtained INT-3 was analyzed
using a chiral HPLC column (Shiseido Chiral CD-Ph, 4.6 mm x 250 mm, 5 μm). A
mixture solution of 0.5 mol/L sodium perchlorate and methanol (75 vol% : 25 vol%) was
used as a mobile phase and the optical purity (enantiomeric excess, ee%) of each chiral
acid salt was measured using the Waters e2695 Alliance HPLC system.
The result is given in Tables 4-8. Table 4 shows the result of testing whether
the optical purity and yield of INT-3 are affected by the optical activity of mandelic acid
which is one of the auxiliary salt-forming compounds. Table 5 shows the result when
2,3-dibenzoyltartaric acid and mandelic acid were used. Table 6 shows the result when
2,3-dibenzoyltartaric acid and camphorsulfonic acid were used. Table 7 shows the
result when di-p-toluoyltartaric acid and mandelic acid were used. Table 8 shows the
35
result when ditoluoyltartaric acid and camphorsulfonic acid were used. Each table
shows the result of obtaining the chiral acid salt using different solvents.

1. Column temperature = 35 ºC
2. Flow rate = 0.5 mL/min
3. Detection wavelength = 220 nm
4. Rt (min) = 20.4 (R-enantiomer %), 18.9 (S-enantiomer %)
The optical purity was calculated according to Equation 1, and the reaction yield
was calculated according to Equation 2.
The camphorsulfonic acid, the mandelic acid, the 2,3-dibenzoyltartaric acid and
the O,O’-di-p-toluoyltartaric acid used in the experiments were purchased from Sigma
Aldrich.
【Table 4】
Ex.
Combination of the chiral auxiliary
and salt-forming compound
(Equivalents)
Solvent
ee% (R
isomer)
Yield
(%)
(+)-2,3-
Dibenzoyl-Dtartaric
acid
Mandelic acid
D D L
D+L
(1:1)
Ex. 1-1 0.25 1.0 Water 88.0 41
36
Methanol 99.3 16
Ethanol 98.5 25
Isopropyl
alcohol
99.1 41
Ex. 1-2 0.25 1.0
Water 88.1 40
Methanol 99.4 15
Ethanol 98.9 24
Isopropyl
alcohol
99.2 42
Ex. 1-3 0.25 1.0
Water 88.2 41
Methanol 99.4 17
Ethanol 98.9 24
Isopropyl
alcohol
99.1 42
【Table 5】
Ex.
Combination of the
chiral auxiliary and saltforming
compound
(Equivalents) Solvent ee% (R isomer)
(+)-2,3-
dibenzoyl-Dtartaric
acid
D/Lmandelic
acid
Yield
(%)
2-1 0.25 1 Water 88.2 40
37
2-2 0.35 1 84.5 45
2-3 0.5 1 56.3 21
2-4 1 1 30 80
2-5 0.25 1
Methanol
99.4 15
2-6 0.35 1 98.1 16
2-7 0.5 1 - -
2-8 1 1 - -
2-9 0.25 1
Ethanol
98.9 24
2-10 0.35 1 98.1 25
2-11 0.5 1 66.4 40
2-12 1 1 10 71
2-13 0.25 1
Isopropyl
alcohol
99.1 41
2-14 0.35 1 98.7 42
2-15 0.5 1 97.4 21
2-16 1 1 15 82
2-17 0.25 0.75 99.1 42
2-18 0.25 1.5 99.2 38
2-19 0.35 0.75 98.7 40
2-20 0.35 1.5 98.6 32
38
2-21 0.5 0.75 96.9 24
2-22 0.5 1.5 96.1 16
*For mandelic acid, the same result was obtained for D and L isomers.
【Table 6】
Ex.
Combination of the chiral auxiliary and
salt-forming compound (Equivalents)
Solvent
ee% (R
isomer)
(+)-2,3-
Dibenzoyl-Dtartaric
acid
(R,S)-10-Camphorsulfonic
acid
Yield
(%)
3-1 0.25 1
Water
88.5 39
3-2 0.35 1 84.7 42
3-3 0.5 1 60.0 19
3-4 1 1 32 75
3-5 0.25 1
Methanol
99.2 13
3-6 0.35 1 98.5 16
3-7 0.5 1 97.3 9
3-8 1 1 - -
3-9 0.25 1
Ethanol
98.5 21
3-10 0.35 1 98.5 24
39
3-11 0.5 1 66.5 39
3-12 1 1 15 68
3-13 0.25 1
Isopropyl
alcohol
99.0 40
3-14 0.35 1 98.9 41
3-15 0.5 1 97.1 25
3-16 1 1 16 81
3-17 0.25 0.75 98.3 40
3-18 0.25 1 98.8 38
3-19 0.25 1.5 99.1 38
3-20 0.35 0.75 97.1 41
3-21 0.35 1 97.9 39
3-22 0.35 1.5 98.7 34
*For camphorsulfonic acid, the same result was obtained for R and S isomers.
【Table 7】
Ex.
Combination of the chiral
auxiliary and salt-forming
compound (Equivalents)
Solvent
ee% (R
(+)-O,O’-Di-p- isomer)
toluoyl-Dtartaric
acid
D/L-Mandelic
acid
Yield
(%)
40
4-1 0.25 1
Water
79.2 38
4-2 0.35 1 75.3 41
4-3 0.5 1 49.1 22
4-4 1 1 21 79
4-5 0.25 1
Methanol
97.5 14
4-6 0.35 1 96.2 15
4-7 0.5 1 - -
4-8 1 1 - -
4-9 0.25 1
Ethanol
97.1 21
4-10 0.35 1 96.5 24
4-11 0.5 1 56 39
4-12 1 1 11 68
4-13 0.25 1
Isopropyl alcohol
98.1 38
4-14 0.35 1 96.9 37
4-15 0.5 1 96.1 21
4-16 1 1 14 79
4-17 0.25 0.75 98 40
4-18 0.25 1.5 98.5 35
4-19 0.35 0.75 96.5 39
41
4-20 0.35 1.5 97 31
4-21 0.5 0.75 96.1 24
4-22 0.5 1.5 96.5 14
*For mandelic acid, the same result was obtained for D and L isomers.
【Table 8】
Ex.
Combination of the chiral
auxiliary and salt-forming
compound (Equivalents)
Solvent
ee% (R
(+)-O,O’-Di-p- isomer)
toluoyl-Dtartaric
acid
(R,S)-10-
Camphorsulfonic
acid
Yield
(%)
5-1 0.25 1
Water
79.0 35
5-2 0.35 1 77.2 39
5-3 0.5 1 51.2 20
5-4 1 1 21.5 75
5-5 0.25 1
Methanol
98.1 16
5-6 0.35 1 96.5 15
5-7 0.5 1 97.0 8
5-8 1 1 - -
5-9 0.25 1 Ethanol 97.5 22
42
5-
10
0.35 1 96.1 23
5-
11
0.5 1 61 35
5-
12
1 1 13 71
5-
13
0.25 1
Isopropyl alcohol
98.2 34
5-
14
0.35 1 97.0 35
5-
15
0.5 1 96.5 25
5-
16
1 1 17 75
5-
17
0.25 0.75 96.5 38
5-
18
0.25 1 97.1 35
5-
19
0.25 1.5 97.5 34
5- 0.35 0.75 96.5 39
43
20
5-
21
0.35 1 97.9 39
5-
22
0.35 1.5 97.1 34
*For camphorsulfonic acid, the same result was obtained for R and S isomers.
From Table 4, it can be seen that the optical activity of the mandelic acid which
acts as a soluble salt-forming compound does not affect optical resolution. Specifically,
almost the same result was obtained when D or L mandelic acid or a mixture thereof
was used. Accordingly, it can be seen that the tartaric acid derivative such as
dibenzoyltartaric acid plays an important role in optical resolution.
From Tables 5-8, it can be seen that, when diacyltartaric acid is used for the
optical resolution, 2 equivalents (molecules) of N-[4-(1-aminoethyl)-phenyl]-
methanesulfonamide and 1 equivalent (molecule) of diacyltartaric acid form a salt in a
polar solvent such as water, methanol, ethanol and isopropyl alcohol, as described in
Scheme 1.
Also, from Tables 5-8, it can be seen that, when diacyltartaric acid was used in
an amount of 0.25 equivalent, 0.35 equivalent, 0.5 equivalent and 1 equivalent for given
equivalents of mandelic acid and camphorsulfonic acid, the optical purity was highest
when 0.25 equivalent was used, followed by 0.35 equivalent and 0.5 equivalent. When
1 equivalent of diacyltartaric acid was used, the optical purity was very low.
Accordingly, it can be seen that, in a polar solvent such as water, methanol,
ethanol and isopropyl alcohol, 2 equivalents (molecules) of N-[4-(1-aminoethyl)-phenyl]-
methanesulfonamide and 1 equivalent (molecule) of diacyltartaric acid form a salt which
44
can be selectively resolved.
Specifically, referring to Table 5 and Table 6 wherein 2,3-dibenzoyl-D-tartaric
acid and mandelic acid or camphorsulfonic acid were used, optical purity was low as
89% ee or lower when water was used as the solvent. When methanol or ethanol was
used, the optical purity was 96% ee or higher when 0.25 equivalent or 0.35 equivalent
of tartaric acid was used, but the yield was 25% or lower. However, the yield is 2 times
or higher as compared to when only 2,3-dibenzoyl-D-tartaric acid was used (see Table
2). In particular, when the solvent was methanol and mandelic acid was used, the
resolution did not occur when 0.5 equivalent of dibenzoyl-D-tartaric acid was used but
the resolution did occur when camphorsulfonic acid was used. When the solvent was
isopropyl alcohol, optical purity of 96% ee or higher could be obtained when 0.25
equivalent, 0.35 equivalent or 0.5 equivalent of tartaric acid was used and the yield was
also 20% or higher. Particularly, when 0.25 equivalent or 0.35 equivalent of tartaric
acid was used, the yield was 40% or higher.
Based on these results, experiment was performed in isopropyl alcohol with the
equivalent of tartaric acid fixed while varying the equivalent of mandelic acid or
camphorsulfonic acid (Examples 2-17 through 2-22 and Examples 3-17 through 3-22).
As a result, when 0.5 equivalent or less of tartaric acid was used, the R isomer could be
obtained with high optical purity of 96% ee or higher and high yield when 0.75-1.5
equivalent of mandelic acid or camphorsulfonic acid was used. In particular, the
isomer could be obtained with high optical purity of 96% ee or higher and the highest
yield of 42% in Example 2-17.
Referring to Tables 7 and 8 wherein O,O’-di-p-toluoyltartaric acid and mandelic
acid or camphorsulfonic acid was used, optical purity was low as 80% ee or lower when
water was used as the solvent. When methanol or ethanol was used, the optical purity
45
was 96% ee or higher when 0.25 equivalent or 0.35 equivalent of tartaric acid was used,
but the yield was 25% or lower. Yet, this yield is 2 times or higher as compared to
when only O,O’-di-p-toluoyltartaric acid was used (see Table 3). In addition, the optical
resolution did occur in methanol when camphorsulfonic acid was used, when 0.5
equivalent of di-p-toluoyltartaric acid was used. When the solvent was isopropyl
alcohol, optical purity of 96% ee or higher could be obtained when 0.25 equivalent, 0.35
equivalent or 0.5 equivalent of tartaric acid was used and the yield was also 20% or
higher. Particularly, when 0.25 equivalent or 0.35 equivalent of tartaric acid was used,
the yield was 34% or higher.
In Examples 4-17 through 4-22 and Examples 5-17 through 5-22, experiment
was performed in isopropyl alcohol with the equivalent of tartaric acid fixed while varying
the equivalent of mandelic acid or camphorsulfonic acid. As a result, when 0.5
equivalent or less of tartaric acid was used, the R isomer could be obtained with high
optical purity of 96% ee or higher and high yield when 0.75-1.5 equivalent of mandelic
acid or camphorsulfonic acid was used. In particular, the isomer could be obtained
with high optical purity of 96% ee or higher and the highest yield of 40% in Example 4-
17.
To conclude, an R isomer with high optical purity of 96% ee or higher could be
obtained when 0.25-0.5 equivalent of diacyltartaric acid and 0.75-1.5 equivalent of
mandelic acid or camphorsulfonic acid were used. Especially, the isomer could be
obtained with higher yield when the solvent was isopropyl alcohol. In addition, when
the solvent was isopropyl alcohol, the isomer with high optical purity of 96% ee or higher
could be obtained with a yield of 30% or higher by using 0.25-0.35 equivalent of
diacyltartaric acid and 0.75-1.5 equivalent of mandelic acid or camphorsulfonic acid.
It will be obvious to those skilled in the art that N-{4-[(1S)-1-aminoethyl]-2,6-
46
difluorophenyl}methanesulfonamide will be obtained when the 2,3-dibenzoyltartaric acid
or the O,O’-di-p-toluoyltartaric acid is an L isomer.
Accordingly, an R or S optical isomer of high optical purity can be obtained by
the method according to the present disclosure.
[Test Example 2] Preparation of (R)-N-[1-(3,5-difluoro-4-
methanesulfonylaminophenyl)-ethyl]-3-(2-propyl-6-trifluoromethylpyridin-3-yl)-
acrylamide
(R)-N-[1-(3,5-Difluoro-4-methanesulfonylaminophenyl)-ethyl]-3-(2-propyl-6-
trifluoromethylpyridin-3-yl)-acrylamide was prepared using the N-{4-[(1R)-1-aminoethyl]-
2,6-difluorophenyl}methanesulfonamide prepared according to the present disclosure,
according to the method described in Korean Patent Application No. 10-2009-700433.
Specifically, N-{4-[(1R)-1-aminoethyl]-2,6-difluorophenyl} methanesulfonamide
hydrochloride (62 mg, 0.22 mmol) was reacted with 3-(2-propyl-6-trifluoromethylpyridin-
3-yl)-acrylic acid (56 mg, 0.22 mmol). The product was purified by crystallizing in ether
to obtain the target compound (81 mg, 73%).
1H NMR (300 MHz, DMSO-d6): δ 9.50 (bs, 1H), 8.81 (d, 1H, J = 7.8 Hz), 8.16 (d,
1H, J = 8.4 Hz), 7.80 (d, 1H, J = 7.8 Hz), 7.67 (d, 1H, J = 15.6 Hz), 7.18 (d, 2H, J = 7.2
Hz), 6.76 (d, 1H, J = 15.6 Hz), 5.04 (m, 1H), 3.05 (s, 3H), 2.91 (m, 2H), 1.65 (m, 2H),
1.41 (d, 3H, J = 6.9 Hz), 0.92 (t, 3H, J = 7.2 Hz).
ESI [M+H]+: 492.
Accordingly, the R isomer of the compound having a structure of formula (I),
which has been resolved by the method according to the present disclosure, may be
47
used as an intermediate to prepare various novel compounds that can act as TRPV1
antagonists using the substance or the method described in Korean Patent Application
No. 10-2009-700433.
Hereinafter, formulation examples of the composition according to the present
disclosure will be described. However, the following examples are for illustrative
purposes only and it will be apparent to those of ordinary skill in the art that the scope of
the present disclosure is not limited by the examples.
[Formulation Example 1] Amorphous chiral resolving agent compositions
An amorphous solid chiral resolving agent containing at least one of 0.15-0.5
equivalent of 2,3-dibenzoyltartaric acid and O,O’-di-p-toluoyltartaric acid; and at least
one of 0.75-1.5 equivalent of mandelic acid and camphorsulfonic acid, per 1 equivalent
of a mixture of stereoisomers.
[Formulation Example 2] Crystallized chiral resolving agent compositions
A crystallized solid chiral resolving agent containing at least one of 0.15-0.5
equivalent of 2,3-dibenzoyltartaric acid and O,O’-di-p-toluoyltartaric acid; and at least
one of 0.75-1.5 equivalent of mandelic acid and camphorsulfonic acid, per 1 equivalent
of a mixture of stereoisomers.

【CLAIMS】
1. A method for chiral resolution of a mixture of stereoisomers of a
compound of formula (I),
R6
R4
NH2
NH
S
O
O
R5
R1
R2
R7
R3
(I)
wherein each of R1, R2, R3, R4, R5, R6 and R7 is independently any one selected
from a group consisting of H, -NH2, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6
alkynyl group and a halogen, and R1 and R2 are different from each other,
comprising mixing said mixture of stereoisomers of the compound of formula (I)
with
(i) a chiral auxiliary; and
(ii) an auxiliary salt-forming compound
in the presence of a solvent, thereby precipitating a diastereomeric salt of said
chiral auxiliary (i) with the compound of formula (I) in enantiomeric excess.
2. The method according to claim 1, wherein the chiral auxiliary is one or
more selected from a group consisting of 2,3-dibenzoyltartaric acid, O,O’-di-ptoluoyltartaric
acid, a stereoisomer thereof, and a combination thereof and the auxiliary
salt-forming compound is one or more selected from a group consisting of mandelic
acid, camphorsulfonic acid, a stereoisomer thereof, and a combination thereof.
3. The method according to claim 1, wherein R2 is hydrogen and an R
enantiomer of the compound of formula (I) is obtained in enantiomeric excess when the
49
chiral auxiliary is selected from a group consisting of the (+)-2,3-dibenzoyl-D-tartaric
acid, (+)-O,O’-di-p-toluoyl-D-tartaric acid and a combination thereof.
4. The method according to claim 1, wherein R2 is hydrogen and an S
enantiomer of the compound of formula (I) is obtained in enantiomeric excess when the
chiral auxiliary is selected from a group consisting of the (-)-2,3-dibenzoyl-L-tartaric acid,
(-)-O,O’-di-p-toluoyl-L-tartaric acid and a combination thereof.
5. The method according to claim 1, wherein the auxiliary salt-forming
compound is D-mandelic acid, L-mandelic acid, (1R)-(-)-10-camphorsulfonic acid, (1S)-
(+)-10-camphorsulfonic acid or a combination thereof.
6. The method according to claim 1, wherein the halogen is one or more
selected from a group consisting of F, Cl, Br, and I
7. The method according to claim 6, wherein R1 is selected from a group
consisting of methyl, ethyl, propyl, butyl and pentyl and R2 is hydrogen.
8. The method according to claim 7, wherein R1 is methyl, R2, R3 and R7
are hydrogen, and R4, R5 and R6 are independently selected from a group consisting of
F, Cl, methyl, ethyl, and propyl.
9. The method according to claim 8, wherein the compound of formula (I) is
N-{4-[(1R/S)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
50
10. The method according to claim 1, wherein the solvent is one or more
selected from a group consisting of water, a C1-14 alcohol, acetic acid, nitromethane,
propionic acid, formic acid and a combination thereof.
11. The method according to claim 10, wherein the solvent is one or more
selected from a group consisting of water, methanol, ethanol and isopropyl alcohol.
12. The method according to claim 11, wherein the solvent is methanol,
isopropyl alcohol or a combination thereof.
13. The method according to claim 1, wherein the solvent is added at an
amount to achieve complete dissolution of all reactants.
14. The method according to claim 13, wherein the solvent is added at an
amount of 5-15 times (v/w) of based on the total weight of the mixture of stereoisomers
of the compound of formula (I).
15. The method according to claim 1, wherein the mixing is performed at 40-
70 ºC or at the boiling point of the solvent or solvent mixture.
16. The method according to any one of claims 1 to 15, wherein the molar
equivalent ratio of the chiral auxiliary to 1 molar equivalent of the mixture of
stereoisomers is 0.10-0.5.
17. The method according to claim 16, wherein the molar equivalent ratio of
51
the chiral auxiliary to 1 molar equivalent of the mixture of stereoisomers is 0.2-0.3.
18. The method according to any one of claims 1 to 15, wherein the molar
equivalent ratio of the auxiliary salt-forming compound to 1 molar equivalent of the
mixture of stereoisomers is 0.5-1.5.
19. The method according to claim 18, wherein the molar equivalent ratio of
the auxiliary salt-forming compound to 1 molar equivalent of the mixture of
stereoisomers is 0.75-1.5.
20. The method according to any one of claims 1 to 15, wherein the molar
equivalent ratio of the chiral auxiliary and the auxiliary salt-forming compound together
to 1 molar equivalent of the mixture of stereoisomers is 0.75-2.0.
21. A stereoisomer of the compound of the formula (I) with 96-99% of
enantiomeric excess obtained by the method according to claim 16.
22. The stereoisomer according to claim 21, wherein the stereoisomer is N-
{4-[(1R)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide or N-{4-[(1S)-1-
aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
23. A method for preparing a compound of formula (IIIa) or (IIIb)
52
R6
R4
NH
NH
R1 O
N
CF3
S
O
O
R5
R7
R3
R2
(IIIa)
R6
R4
NH
NH
R1 O
N
CF3
S
O
O
R5
R7
R3
R2
(IIIb)
wherein, each of R1, R2, R3, R4, R5, R6 and R7 is independently any one selected
from a group consisting of H, -NH2, a C1-6 alkyl group, a C2-6 alkenyl group, a C2-6
alkynyl group and a halogen, and R1 and R2 are different from each other, comprising
resolving the mixture of stereoisomers of the compound of formula (I) according
to the method of any one of claims 1 to 16, and
converting the resulting stereoisomer to the compound of formula (IIIa) or (IIIb).
24. The method according to claim 23, wherein the compound of formula
(IIIa) is (R)-N-[1-(3,5-difluoro-4-methanesulfonamino-phenyl)-ethyl]-3-(2-propyl-6-
trifluoromethyl-pyridine-3-yl)-acrylamide and the compound of formula (I) is N-{4-
[(1R/S)-1-aminoethyl]-2,6-difluorophenyl}methanesulfonamide.
25. The method according to claim 23, wherein said converting the resulting
stereoisomer to the compound of formula (IIIa) or (IIIb) comprises coupling N-{4-[(1R)-1-
aminoethyl]-2,6-difluorophenyl}methanesulfonamide (INT-3) with 3-(2-propyl-6-
trifluoromethyl-pyridine-3-yl)-acrylic acid (INT-7).
26. (R)-N-[1-(3,5-difluoro-4-methanesulfonylaminophenyl)-ethyl]-3-(2-propyl53
6-trifluoromethyl-pridin-3-yl)-acrylamide obtained by the method according to claim 23
with 96-99% of enantiomeric access.
27. A composition comprising a chiral auxiliary and an auxiliary salt-forming
compound, wherein the chiral auxiliary is one or more selected from a group consisting
of 2,3-dibenzoyl-tartaric acid, O,O’-di-p-toluoyl-tartaric acid, a stereoisomer thereof and
a combination thereof, and the auxiliary salt-forming compound is one or more selected
from a group consisting of mandelic acid, camphorsulfonic acid, a stereoisomer thereof
and a combination thereof.
28. The composition according to claim 27, wherein the composition
comprises 0.10-0.5 molar equivalent of the chiral auxiliary based on 1 molar equivalent
of a mixture of stereoisomers which is to be resolved.
29. The composition according to claim 27, wherein the composition
comprises 0.75-1.5 molar equivalents of the auxiliary salt-forming compound based on
1 molar equivalent of a mixture of stereoisomers which is to be resolved.
30. A chiral resolving kit, comprising: a chiral auxiliary which is one or more
selected from a group consisting of 2,3-dibenzoyl-tartaric acid, O,O’-di-p-toluoyl-tartaric
acid, a stereoisomer thereof and a combination thereof; and an auxiliary salt-forming
compound which is one or more selected from a group consisting of mandelic acid,
camphorsulfonic acid, a stereoisomer thereof, or a combination thereof.
31. The kit according to claim 30, wherein the molar equivalent ratio of the
54
chiral auxiliary to 1 molar equivalent of a mixture of stereoisomers which is to be
resolved is 0.10-0.5.
32. The kit according to claim 30, wherein the molar equivalent ratio of the
auxiliary salt-forming compound to 1 molar equivalent of a mixture of stereoisomers
which is to be resolved is 0.75-1.5.
33. The kit according to claim 30, wherein the kit further comprises written
instructions for using the chiral auxiliary and the auxiliary salt-forming compound to
resolve a mixture of stereoisomers.
34. The kit according to claim 30, wherein the kit is for resolving a mixture of
stereoisomers of a compound of formula (I) in claim 1.