Provided are heterocyclic amide compounds represented by formula (I), and an agricultural chemical, specincally a herbicide, which contains said compounds (in formula (1), Q represents an aromatic heterocycle indicated by any o f Q l to Q5, W represents an aromatic heterocycle indicated b y W-1, W-2, or W-3, X repre...

1112212345123412345Provided are a novel pest control agent composition and in particular a composition for a sterilising agent. A sterilising or bactericidal composition which contains: one or more compounds selected from oxime substituted amide compounds represented by formula (I) N oxides thereof and salts the...

An acyloxypyranone compound represented by formula (II) (wherein R represents an acyl group) is produced by causing an acylating agent and a hydrolase to act on hydroxypyranone represented by formula (I) in a hydrous organic solvent; an alkyne compound represented by formula (IV) is produced by causing an acetylene ...

The present invention relates to crystal forms of sulfonylurea compound and method for producing the same.. [Means of Solution] It has been found that a sulfonylurea compound of Formula (1): has two types of crystal polymorphisms and four types of pseudo crystal polymorphisms. A production method of each crystal ...

This invention relates to benzopyran derivatives of formula (I) or (II), or pharmaceutically acceptable salts thereof wherein R1 and R2 are independently of each other hydrogen atom. C1-6alkyl group or C6-14aryl group, R3 is hydrogen atom or Cusalkylcarbonyloxy group, or together with R4 forms a bond, R4 is hydrogen...

a1a2b1b2b3 Provided are a coating film having a function of inhibiting adhesion of biological matter; a production method for the coating film; a polymer obtained by polymerization of a specific monomer mixture; a coating film forming composition having a specific makeup; a production method for a copolymer containi...

To provide an insecticide, miticide, nematicide, molluscicide, disinfectant, or bactericide composition, and a pest control method. [Solution] An insecticide, miticide, nematicide, molluscicide, disinfectant, or bactericide composition containing one or two substances selected from 4-[5-(3,5-dichlorophenyl)-4,5-dihy...

A novel production method for producing 2 2 7 9 tetramethyl 2H pyrano[2 3 g]quinoline (compound (6)) that has a quinoline ring and a chromene ring using N (3 acetyl 4 hydroxyphenyl)butylamide (compound (1 )) that is commercially available as a raw material for medicines or the like as a starting raw material; and a ...

Provided is a novel method for producing a geminal difluoro compound. A novel production method for obtaining a geminal difluoro compound represented by formula (2) at a high yield by reacting a compound represented by formula (1) with a fluorinating agent in the presence of an N-chloroimide compound. (In the formul...

[Problem] To provide a method for producing a nitrogen- containing heterocyclic compound with high purity. [Solution] A method for producing a compound (A) of high purity, which comprises the step (a) and the step (b) described below. (a) a step wherein a mixture that contains the compound (A) and a compound (B) w...

[Problem] The present invention addresses the problem of providing a production method for synthesizing a nitrogenated heterocyclic N- oxide compound with high efficiency and in a safe manner. The present invention also addresses the problem of providing a novel N- oxide compound. [Solution] Provided is a method fo...

Provided is a novel method for producing an oligonucleotide using a nucleoside or oligonucleotide that is easy to isolate and has high storage stability. A method for producing an oligonucleotide including a step for carrying out H-phosphonation of the 5"-hydroxy group or 3"-hydroxy group of a nucleoside or oligonuc...

To provide a novel agricultural chemical and particularly an herbicide. [Solution] A ketone or oxime compound represented by formula (1) and a herbicide containing the same (in the formula: B represents B 1 B 2 or B 3; Q represents an oxygen atom =NOR etc.; R represents a hydrogen atom C C alkyl group etc.; R repres...

The purpose of the invention is to provide a novel organic amine salt or quaternary ammonium salt of the 3-{[((2E)-2-{1-[5-(4-t-butylphenyl)-4-hydroxy-3-thienyl]ethylidene}hydrazino)carbonothioyl]amino} benzoic acid represented by the formula shown below. The organic amine salt or quaternary ammonium salt has excell...

There is provided a novel pest control agent, particularly an insecticide or miticide. A substituted isoxazoline compound of General Formula (1): where A1, A2 and A3 independently are CH or N, etc., X1, X2 and X3 are independently are H, a halogen atom, etc., Y1 is H, etc., R1 is -C(O)Rla, -C(S)Rla, Rla is -C(R9)(R...

11711221367n4567881Provided is a novel therapeutic agent for myeloma. A pyrazole compound represented by general formula (1) (In the formula: R represents a C1 6 alkyl an R substituted C1 6 alkyl a C1 6 haloalkyl a phenyl or a phenyl substituted by a number (a) of R or the like; R represents a hydrogen atom a C1 6 a...

An emulsifying pesticide composition that comprises (Z)-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-N-(methoxyiminomethyl)-2-methylbenzoic acid amide, a polar solvent, a nonpolar solvent and a surfactant. The content o f the polar solvent i s preferably 7.5-67.5 mass% relative t o the emulsif...

[Problem] To provide a novel triazinone compound which has an inhibitory. activity on a T-type voltage-dependent calcium channel and is useful particularly for the treatment of pain. [Solution] Provided is a novel triazinone compound represented by formula (I) (wherein each substituent is as defined in detail in t...

Provided is an efficient method for producing a 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative which is useful as a raw material of polyimide or the like. The present invention is a method for producing a 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative represented by...

As attached

Provided is a method for producing at high yield a cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative which is useful as a raw material of polyimide or the like. The present invention is a method for producing a 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride represented by formula (2) by...

To provide novel pesticides, especially insecticides or acaricides. A condensed heterocyclic compound represented by the formula (1) or its salt or an N-oxide thereof wherein 0 substituted with -S(O)nR1 is a ring represented by any one of 01 , 02 and 0 3, Q is a ring represented by any one of Q1 , Q2, Q3 and Q4, R1 ...

Provided is a novel pest control agent, particularly an insecticide or a miticide. A pyrazole derivative represented by general formula (1) and a pest control agent. In formula (1), A1 represents -N(O)m2 or -CR1; R1, R3, and R4 each independently represent a hydrogen atom, a halogen atom, C1-C6 alkyl, or the like; R...

Disclosed is a method for producing a tetrahydropyran compound represented by general formula (5) shown in the scheme. Accordingly, a tetrahydropyran derivative is obtained in high yield and with high selectivity without using a highly toxic reagent, and an industrially useful method for producing a tetrahydropyran ...

Disclosed is a novel process for producing a 2-aryl-3-hydroxy-4-substituted-carbonylthiophene compound, which is a compound useful as an intermediate for the production of a pharmaceutical agent or an agricultural agent or an intermediate for the production of the 2-aryl-3-hydroxy-4-substituted-carbonylthiophene com...

A process for the preparation of ß glycoside compounds represented by formula (3) characterized by reacting a cyclic alkene compound represented by formula (1) or (2) with a nucleophilic reagent in the presence of a transition metal catalyst.

To provide a novel tetracarboxylic acid dialkyt ester having alkyi groups on a cyclobutane ring, and a novel bis(chlorocarbonyl) compound obtained by chlorinating it, as well as processes for producing them. To further provide a process for producing specific isomers thereof.A tetracarboxylic acid dialkyl ester r...

The objective of the present invention is to provide a method for producing a compound represented by formula (1) or the like said compound being a 2 pyridone compound that is useful as a pharmaceutical product or a pharmaceutical intermediate with high yield. A method for producing a 2 pyridone compound represented...

Disclosed is a method for producing a ß dihydrofuran deriving compound or a ß tetrahydrofuran deriving compound represented by formula (1) or (4) which is characterized by having a dialkyl dicarbonate a diaralkyl dicarbonate or a halide act on a diol compound represented by formula (2) or (3). Also disclosed is a me...

There is provided an inexpensive and efficient method for producing an 0-[l-(2-hydroxypropyl)]oxime compound with an extremely high purity which is suitable as an intermediate for pharmaceuticals, agrochemicals, or electronic materials, for example.  An industrially useful method for producing the 0-[l-(2-hydroxypro...

To provide a novel method for producing a 2-azaadamantane compound from a bicyclocarbamate compound......

A novel method for producing a stereoselective epoxyketone compound is provided. A method for producing an epoxyketone compound represented by the formula (1) as represented by the following scheme whereby it is possible to obtain an epoxyketone derivative in good yield and at high selectivity and to provide an indu...

From the compound represented by formula (3), the optically active alcohol compound represented by formula (8) can be produced with high selectivity and in high yields, and an industrially useful production method and an intermediate of the compound can be provided. (In the formula , R represents a hydrogen atom , a...

There is provided a production method of a 2-hydroxyaryl aldehyde compound. A production method of a 2-hydroxyaryl aldehyde compound that is characterized by comprising reacting a hydroxyaryl compound with paraformaldehyde in the presence of magnesium chloride and an amine compound of Formula (a): where R9 is a C...

To produce a bisaminophenylurea as the desired product with high purity in high yield with a high volume efficiency with a small amount of by-products.  A (nitrophenyl)alkylamine hydrohalide represented by the formula (1) and a carbonyl compound represented by the formula (2) are subjected to a condensation reacti...

It is intended to provide a sustained-release pharmaceutical preparation with absorbability not dependent on pH. The sustained-release preparation is characterized by containing 4-bromo-6-[3-(4-chlorophenyl)propoxy]-5-(3-pyridylmethylamino)-3(2H)-pyridazinone or a salt thereof, as a pharmaceutically active ingredien...

There is provided a process for efficiently producing an anti form of an optically active p-hydroxy-a-aminocarboxylic acid derivative that is useful as an intermediate for Pharmaceuticals and agrochemicals. The process for producing optically active β-hydroxy-a-aminocarboxylic acid derivative of formula (2) or...

A method for producing aminobenzopyran compound of formula (2) Characterized by reducing a nitro group on 2,2-dimethyl 2H-1-benzopyran compound of formula (1) with 2 to 5 molar amount of hydrazine in the presence of a metal catalyst of the kind such as herein described.

Disclosed is a method for producing a succinimide compound. Specifically disclosed is a method for producing a succinimide compound represented by the formula (3) below (wherein R5 represents a straight chain, branched or cyclic alkyl group having 1-12 carbon atoms or the like) by reacting an aminomalonic a...

A novel process for producing an optically active (E)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-5-hy-droxy-3-oxohept-6-enoic acid ester represented by the formula (III), which is an important intermediate for medicines. It comprises reacting a l,3-bis(trimethylsilyloxy)-l-alkoxybuta-l,3-diene represented by ...

There is provided a process for producing an acetylene compound useful as an intermediate of Pharmaceuticals, from 4-nitrofluorobenzene, in industrially and economically advantageous manner. Concretely, it is a method for producing an acetylene compound of formula (3) characterized by reacting 4-nitrofluorob...

The present invention provides compounds useful for prevention, treatment or alleviation of diseases against which activation of the thrombopoietin receptor is effective. A compound represented by the formula (1): wherein A, B, R1, L1, R2, L2, L3, Y, L4, R3 and X are the same as defined in the description, a tautome...

A compound represented by the formula (1): wherein A, B, R1, L1, R2, L2, L3, Y, L4, R3 and X are the same as defined in the description, a tautomer, prodrug or pharmaceutically acceptable salt of the compound or a solvate thereof.

A method for producing a drug substance of crystalline pitavastatin calcium excellent in stability, is presented. In the production of a compound (pitavastatin calcium) represented by the formula (1): The water content is adjusted to a level of from 5 to 15%, and the crystal form is controlled to be crystal form A, ...

There is provided a T-type calcium channel blocker that is optically active 1,4-dihydropyridine compound, a pharmaceutically acceptable salt thereof or a solvate thereof, of formula (1) wherein R1 and R2 are independently of each other C1-6 alkyl group or R1 and R2 together form -CR5R6-CR7R8-, -CR6R6-CR7R8-CR9...

By a production method of a quinoline compound represented by the formula (I), which comprises reacting quinolinecarbaldehyde represented by the formula (II) with an imine compound represented by the formula (III) and then subjecting the resulting compound to hydrolysis, a quinoline compound useful as a synthetic in...

Abstract "Crystalline Forms Of Pitavastatin Calcium" The present invention is directed to new crystalline forms of Pitavastatin hemicaicium salt, referred to hereinafter as polymorphic Forms A, B, C, D, E and F, as well as the amorphous form. Furthermore, the present invention is directed to processes for the prep...

There is provided a novel method for producing an optically active succinimide compound which is a useful compound utilized as an intermediate raw material for pharmaceutical products or the like.  The method for producing an optically active succinimide compound of formula (2) comprises processing a racemic compoun...

A novel production method of quinolinecarbaldehydes (IV), which includes reacting aminobenzophenones (I) with β-ketoaldehyde derivative (II) inthe presenhce of an acid togive quinolinecarbaldehyde derivative (III), and then hydrolyzing the quinolineecarbaldehyde derivative and a method of producing novel β-ketoaldeh...

A drug for inhibiting vascular intimal hyperplasia which is effective in the prevention of restenosis after percutaneous transluminal coronary angioplasty (PTCA) and stent placement in a blood vessel or effective ' in treatments for the progress thereof. The drug for inhibiting vascular intimal hyperplasia contains ...

TO BE FILLED

There is provided a process for producing oxirane compound comprising treating with hydrogen peroxide in the presence of either an olefin oxidation catalyst prepared from an organic compound or a polymer compound of formula (1) a tungstic acid compound, a phosphoric acid, hydrogen peroxide and a quaternary ammonium...

Disclosed is a method for easily producing a 2-azaadamantane with high yield. Specifically disclosed is a method for producing a 2-azaadamantane represented by the formula (1) below, wherein a compound represented by the formula (2) below is cyclized in the presence of an acid.

To provide a novel method for producing an isothiocyanate compound having a carboxyl group(s) from the corresponding amino compound having a carboxyl group(s). A method for producing an isothiocyanate compound which has a carboxyl group(s) and is represented by the formula (2). And the method comprises reacting a...

There is provided a novel pesticide, particularly an insecticide or an acaricide. A substituted isoxazoline compound of formula (1) or a salt thereof:wherein A1, A2and A3 independently of one another are carbon atom or nitrogen atom, G is benzene ring, etc., L is -CH2-, -C(CH3)-, -CH(CN)-, etc., X is halogen atom,...

[PROBLEMS] To provide an efficient process for producing an optically active chromene oxide compound which is an important intermediate for a benzopyran compound effective in the treatment of arrhythmia. [MEANS FOR SOLVING PROBLEMS] The process for producing an optically active chromene oxide compound comprises us...

A compound represented by the formula (I) (wherein R1, R2, R3 and R4 are as defined in the description), a tautomer, prodrug or pharmaceutically acceptable salt of the compound or a solvate thereof.

The present invention relates to the pharmaceutical useful for the prevention and the treatment of diabetic complications such as diabetic nephropathy, diabetic neuropathy, diabetic retinopathy and diabetic angiopathy among others, and to the prophylaxis and/or treatment drug for diabetic complications with the comp...

[Problems] To provide a novel herbicide composition and a weeding method. [Means for solving problems] A herbicide composition comprising compound (A) represented by the general formula (1) and at least one compound selected from dymron, dimepiperate and esprocarb. A weeding method comprising applying the compoun...

2122m2Provided is an inexpensive simple and efficient method for preparing from a starting material a nitro compound constituting a diamine precursor compound which is a starting material for producing a polyamic acid and/or polyimide. Compound (1) is reacted according to reaction formula (1) with di tert butyl ...

A novel process for producing an optically active (E)-7-[2-cyclopropyl-4-(4-fluorophenyl)quinolin-3-yl]-5-hydroxy-3-oxohept-6-enoic acid ester represented by the formula (III), which is an important intermediate for medicines. It comprises reacting a 1,3-bis(trimethylsilyloxy)-1-alkoxybuta-1,3-diene represented by t...

[Problem] To provide a stable high water content W/O type emulsion gel. [Solution] A W/O type emulsion gel which comprises a gel forming agent comprising a compound represented by formula (1) or (2) (wherein R1 and R3 independently represent a linear or branched alkyl group having 1 to 20 carbon atoms a cyclic alky...

A neutrophilia inhibitor effective in treatments for the incidence or progress of acute infectious diseases, collagen disease, chronic obstructive pulmonary disease (COPD), chronic bronchitis, pulmonary emphysema, small airway diseases, gout, Cushing syndrome, myelofibrosis, tumorous neutrophilia, polycythemia vera,...

This invention relates to benzopyran com-pounds of formula (I) wherein X is NR6, Y is a bond, SO or SO2, Z is C1-4alkyl group or phenyl group, W is hydrogen atom, hydroxy group, C1-6 alkoxy group, a halogen atom, (I) C1-4alkyl group or C1-6alkylsulfonylamino group, Rl and R2 are independently of each other C1-3alkyl...

An isoxazoline-substituted benzamide compound of formula (1) or a salt thereof: wherein A1, A2and A3 independently of one another are carbon atom or nitrogen atom, G is benzene ring, etc., X is halogen atom, C1C6haioalkyl, etc., Y ia halogen atm, C1-C6alkyl, etc., R1 is C1C12alkyl arbitrarily substituted with R16, ...

There is provided a novel herbicide.  A pyrazole sulfonylurea compound of formula (1): (Figure Remove)wherein R1 is C^alkyl, etc., R2 is hydrogen atom, C^alkyl, C^haloalkyl, etc., R3, R4, R5 and R6 independently of one another are hydrogen atom, C^alkyl, etc., with a proviso that at least one of R3, R4, R5 an...

[PROBLEMS] To provide an efficient process for producing an optically active epoxy compound. [MEANS FOR SOLVING PROBLEMS] The process for producing an optically active epoxy compound comprises asymmetrically epoxidizing an unsaturated compound with an oxidizing agent in the presence of an optically active titaniu...

To provide a method for producing an alicyclic tetracarboxylic acid such as bicyclo[3.3.0]octane-2-exo-4-exo-6-endo-8-endo-tetracarboxylic acid of high purity with high productivity. A method for producing an alicyclic tetracarboxylic acid  which comprises adding a compound represented by the following formula [A]...

There is provided a novel intermediate for producing pesticides. A method for producing 1,3-bis(substituted phenyl)-3-substituted-3-hydroxypropan-1 -one compound of Formula (3) comprises reacting an aromatic ketone compound of Formula (4) and a substituted acetophenone compound of Formula (5) as starting raw materia...

Provided is an inducing agent for megakaryocytes and/or platelets from pluripotent stem cells the inducing agent being useful in treating diseases involving thrombopenia. A method for producing megakaryocytes and/or platelets the method comprising: separating hematopoietic progenitor cells and cells that form a sept...

To provide a novel tetracarboxylic acid dialkyl ester having alkyl groups on a cyclobutane ring, and a novel bis(Ghlorocarbonyl) compound obtained by chlorinating it, as well as processes for producing them.  To further provide a process for producing specific isomers thereof. A tetra carboxylic acid dialkyl ester ...

To provide crystal forms of (3R, 4S)-7-hydroxymethyl-2,2,9-trimethyl-4-(phenethylamino)-3,4-dihydro-2H-pyrano[2,3-g]quinolin-3-ol that are excellent as a drug, and production methods thereof [MEANS FOR SOLVING THE PROBLEMS] Production methods including crystallizing (3R, 4S)-7-hydroxymethyl-2,2,9-trimethyl-4-(phene...

The purpose of the present invention is to provide a method for manufacturing optically active 5hydroxy 3-ketoesters with high yield and high stereoselectivity that can be used as a pharmaceutical intermediate. The purpose of the present invention is also to provide a manufacturing intermediate for a novel pharmaceu...

Provided is a novel pest control agent, particularly a fungicide and nematicide. An oxime-substituted amide compound represented by formula (I) [where G represents a structure represented by G 1-1 or the like; G2 represents a structure represented by G 2-2 or the like; W represents an oxygen atom or the like; X ...

Novel tricyclic pyrimidine compounds and tricyclic pyridine compounds having JAK inhibitory activities are provided. A tricyclic heterocyclic compound represented by the formula (I): wherein the rings A and B X Y R R R L L L and n are as defined in the description.

[Problem] To provide an external skin preparation solid substrate exhibiting high breaking strength and excellent thermal stability and usable as a stick shaped substrate or the like. [Solution] An external skin preparation solid substrate containing: a lipid peptide type compound comprising one or more types select...

To provide a novel tetracarboxylic acid dialkyi ester having alkyl groups on a cyclobutane ring, and a novel bis(chlorocarbonyl) compound obtained by chlorinating it, as well as processes for producing them. To further provide a process for producing specific isomers thereof.A tetracarboxylic acid dialkyi ester r...

Provided are a diamine compound useful as a material for a polyimide polymer for producing a liquid crystal alignment film or the like and a novel method for producing an intermediate of the diamine compound. A compound represented by formula (C) is obtained by causing p fluoronitrobenzene (D) and 4 (aminomethyl)pip...

Provided is a novel noxious organism control agent particularly an insecticide or a miticide. A condensed heterocyclic compound represented by formula (1) [wherein D substituted by S(O)R represents a ring represented by D1 D2 or D3; Q represents a ring represented by Q1 Q2 Q3 or Q4; R represents a (C C) alkyl group...

Provided is a method for producing a 1,3-di-substituted-cyclobutane-1,2,3,4-tetracarboxylic acid (2) and a dianhydride (3) of the acid with high selectivity and high yield. A 1,3-di-substituted-cyclobutane-1,2,3,4-tetracarboxylic acid (2) is produced through step (a) of producing a crystal (1) that is composed of an...

Provided is an efficient method for producing a 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative which is useful as a raw material of polyimide or the like. The present invention is a method for producing a 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative represented by...

1212 Provided is a method for obtaining cyclobutanetetracarboxylic acid and/or a dianhydride thereof by using as the raw material the residue remaining after a target substance generated in a process for producing a cyclobutanetetracarboxylic acid derivative or the like has been separated. A method for: producing ...

Provided is an efficient method for producing a 1 3 dialkyl 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride derivative which is useful as a raw material of polyimide or the like. The present invention is a method for producing a 1 3 dialkyl 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 dianhydride d...

Provided is an efficient method for producing a high purity 1 3 dialkyl 1 2 3 4 cyclobutane tetracarboxylic acid 1 2:3 4 di anhydride which is a raw material of a polyimide or the like. The present invention is a method for producing a 1 3 dialkyl cyclobutane 1 2 3 4 tetracarboxylic acid 1 2:3 4 di anhydride by he...

Substituted alkenylbenzene compound of formula (4): wherein X1 to X4 are as herein described as in the specification and claims.

2-Cyclopropyl-4-(4'-fluorophenyl)quinoline-3-carboxyaldehyde useful as a material, for pharmaceutical products, can be obtained by reacting 3-cyclopropyl-3- oxopropanenitrile with 2-amino-4'-fluorobenzophenone to obtain 2-cyclopropyl-4-(4'-fluorophenyl)quinoline-3-carbonitrile, and reducing it...

This invention discloses a process for producing a C1-C4alkyl ester of 3,5-dihydroxy-6-heptenoic acid, whichcomprises a step of contacting a 3,5-dihydroxy-6-heptenoicacid derivative of the formula (1): wherein R is a C1-4 alkyl group, with a C1-4 alcohol-containing solvent...

To provide novel pyridazinone compounds, which inhibit the purinergic P2X7 receptor and are useful for prevention, therapy and improvement of inflammatory and immunological diseases. A compound represented by the formula (I) (wherein R1, R2, Q, X, Y and Z are the same as defined in the description), a tautomer, pr...

2-Pyridone compounds represented by general formula [1], tautomers or stereoisomer thereof, pharmaceutically acceptable salts of the same, or solvates thereof have excellent GK-activating activity and therefore are useful as drugs.  In general formula [1], A is a benzene ring or a pyridine ring; X is a structure rep...

To provide a liquid pesticide composition containing a novel isoxazoline-substituted benzamide compound. [Solution] A liquid pesticide composition containing: (a) (Z)-4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazole-3-yl]-N-(methoxyiminomethyl)-2-methyl benzoic acid amide as a pesticide active ingred...

Provided is a novel tricyclic compound which has JAK inhibitory activity and is especially useful for prophylaxis, treatment or amelioration of autoimmune diseases, inflammatory diseases and allergic diseases. A novel tricyclic compound which is represented by formula (I), formula (II) or formula (III) (wherein each...

The present invention provides a copolymer or the like obtained by polymerizing a monomer mixture including at least compounds represented by formulas (A) (B) and (C) (in the formulas Ta,Tb Tb,Ua1,Ua2,Ub1,Ub2 and Ub3 Qa,Qb and Qc Ra,Rb and Rb An and m are as defined in the description and claims). The copolymer of t...

To provide a process for simply and efficiently producing, from an inexpensive starting material, a nitro compound being a precursor compound for a diamine as a starting material for producing a polyamic acid and/or a polyimide.  In accordance with the reaction formula (1), compound 1 (wherein R1 is -CH2COOR or-CH2P...

A compound  represented by  the  formula.  (1) : 5 wherein a is a nitrogen atom or cr4. B is an oxygen atom, a sulfur atom or NS9  (provided that when A is a nitrogenatom,  B is not NH) ,  R1  is  a C2_14 aryl  group,  L1  is  a bond,CR10R11, an oxygen atom, a sulfur atom or NR1...