2-Sulfamoylbenzoic acid derivatives

Abstract

2-Sulfamoylbenzoic acid derivatives of general formula (I): 1

Description

TECHNICAL FIELD

[0001] The present invention relates to novel 2-sulfamoylbenzoic acid derivatives which have an antagonistic effect on both the leukotriene D4 (hereinafter referred to simply as LTD4) receptor and the thromboxane A2 (hereinafter referred to simply as TXA2) receptor, intermediates for their synthesis and their salts and medicines containing them.

BACKGROUND ART

[0002] For treatment of allergic diseases including bronchial asthma, anti-allergic agents such as histamine receptor antagonists and mediator release suppressants for mast cells and steroid drugs have been used, and for bronchial asthma, bronchodilators such as xanthine derivatives and stimulators for the β-sympathetic nerve receptor have been used as well.

[0003] In recent years, allergic diseases are recognized as allergic inflammations by their pathological profiles and have been found to be associated with various inflammatory cells and mediators. For example, bronchial asthma is characterized by increased sensitivity of the respiratory tract to various stimuli and defined as involving reversible stenosis of the respiratory tract, mucosal edema of the respiratory tract, mucous supersecretion and infiltration of inflammatory cells onto the walls of the respiratory tract.

[0004] Further, with respect to the related mediators, it is suggested that LTD4 not only has an intense bronchoconstrictor effect but also enhances the permeability of the respiratory tract vessels and mucus secretion, and that TXA2 not only has a potent bronchoconstrictor effect but also controls the sensitivity of the respiratory tract.

[0005] With the above-mentioned movements in research on treatment of allergic diseases, LTD4 receptor antagonists, TXA2 synthesis inhibitors and TXA2 receptor antagonists have been marketed and shown to be more effective than conventional anti-allergic agents.

[0006] However, because development of allergic diseases represented by bronchial asthma pathologically involves various mediators in parallel as mentioned above, antagonism against a receptor for a single mediator or inhibition of synthesis of a single mediator has its limit in terms of effect, and development of novel promising anti-allergic agents which show greater therapeutic effects by inhibiting both LTD4 and TXA2, major pathological mediators in allergy.

[0007] Compounds which have antagonistic effects on the receptors for both of the two mediators, LTD4 and TXA2, are disclosed in JP-A-3-258759, JP-A-4-154757, JP-A-4-154766, JP-A-5-262736, JP-A-5-279336, JP-A-6-41051 and WO96/11916. These compound are structurally different from the compounds of the present invention and are not expected to have satisfactory therapeutic effects as anti-allergic agents in view of the intensities of their antagonistic effects on the receptors for the major bronchoconstricting mediator LTD4 and the ratios of their antagonistic activities against the two mediators LTD4 and TXA2.

[0008] The present invention has been accomplished in view of the current situations in treatment of allergic diseases and research on their treatment with the aim of providing novel compounds which show potent antagonistic effects on the receptors for LTD4 and TXA2, which are the two major mediators in development of allergic diseases, and therefore are expected to have more excellent therapeutic effects and pharmaceuticals containing them as active ingredients.

DISCLOSURE OF THE INVENTION

[0009] In the above-mentioned movements in treatment of allergic diseases and research on their treatment, the present inventors have conducted extensive research with a view to attaining the above-mentioned object and, as a result, found out that the 2-sulfamoylbenzoic acid derivatives of the present invention have antagonistic effects on the receptors for the two mediators LTD4 and TXA2, which play important roles in development of allergic diseases, and have more excellent therapeutic effects than the above-mentioned receptor antagonists against a single mediator and inhibitors against synthesis of a single mediator. The present inventors have accomplished the present invention on the basis of this discovery.

[0010] Namely, the present invention provides 2-sulfamoylbenzoic acid derivatives represented by general formula (I): 2

[0011] (wherein R1 and R2 which may be the same or different, are hydrogen atoms, C3-8 cycloalkyl groups, optionally substituted C1-6 alkyl groups, optionally substituted aryl groups or form, together with the ring 3

[0012] a condensed ring represented by formula 4

[0013] which may be substituted with an optionally substituted C1-6 alkyl group, an amino group, a cyano group, a nitro group, a hydroxyl group, a halogen atom or a C1-5 alkoxy group, X is an oxygen atom, a nitrogen atom, a sulfur atom or —CH═CH—, R3 is an optionally substituted phenylsulfonylamino group, an optionally substituted phenylsulfonyl group or an optionally substituted phenylsulfoxide group, R4 is a hydrogen atom or an ester residue, n is an integer of from 2 to 6, A is —O—B—, —B—O—, —S—B—, —B—S— or —B—, and B is a C1-6 alkylene group or a C2-5 alkenylene group, provided that the cases wherein R1 is a C1-6 alkyl group, a C3-8 cycloalkyl group or a phenyl group, R2 is a hydrogen atom, A is a vinylene group, and X is a sulfur atom are excluded) or salts, hydrates or solvates thereof.

[0014] The present invention also provides, as useful intermediates for their synthesis, benzylamine derivatives represented by general formula (II): 5

[0015] (wherein R1 and R2 which may be the same or different, are hydrogen atoms, C3-8 cycloalkyl groups, optionally substituted C1-6 alkyl groups, optionally substituted aryl groups or form, together with the ring 6

[0016] a condensed ring represented by formula 7

[0017] which may be substituted with an optionally substituted C1-6 alkyl group, an amino group, a cyano group, a nitro group, a hydroxyl group, a halogen atom or a C1-5 alkoxy group, X is an oxygen atom, a nitrogen atom, a sulfur atom or —CH═CH—, R3 is an optionally substituted phenylsulfonylamino group, an optionally substituted phenylsulfonyl group or an optionally substituted phenylsulfoxide group, n is an integer of from 2 to 6, A is —O—B—, —B—O—, —S—B—, —B—S— or —B—, and B is a C1-6 alkylene group or a C2-5 alkenylene group, provided that the cases wherein R1 is a C1-6alkyl group, a C3-8 cycloalkyl group or a phenyl group, R2 is a hydrogen atom, A is a vinylene group, and X is a sulfur atom are excluded) or salts thereof, benzaldehyde derivatives represented by general formula (IIIa): 8

[0018] (wherein R1 and R2 which may be the same or different, are hydrogen atoms, C3-8 cycloalkyl groups, optionally substituted C1-6 alkyl groups, optionally substituted aryl groups or form, together with the ring 9

[0019] a condensed ring represented by formula 10

[0020] which may be substituted with an optionally substituted C1-6 alkyl group, an amino group, a cyano group, a nitro group, a hydroxyl group, a halogen atom or a C1-5 alkoxy group, A′ is —B′—O— or —B′—, and B′ is a C1-6 alkylene group) or salts thereof, benzonitrile derivatives represented by general formula (IV): 11

[0021] (wherein R1 and R2 which may be the same or different, are hydrogen atoms, C3-8 cycloalkyl groups, optionally substituted C1-6 alkyl groups, optionally substituted aryl groups or form, together with the ring 12

[0022] a condensed ring represented by formula 13

[0023] which may be substituted with an optionally substituted C1-6 alkyl group, an amino group, a cyano group, a nitro group, a hydroxyl group, a halogen atom or a C1-5 alkoxy group, and X is an oxygen atom, a nitrogen atom, a sulfur atom or —CH═CH—)or salts thereof and amine derivatives represented by general formula (V):

H2N—(CH2)n—R3

[0024] (wherein n is an integer of from 2 to 6, and R3 is an optionally substituted phenylsulfonylamino group, an optionally substituted phenylsulfonyl group or an optionally substituted phenylsulfoxide group) or salts thereof. The present invention further provides a pharmaceutical, anti-allergic agent and leukotriene and thromboxane A2 antagonistic agent containing a 2-sulfamoylbenzoic acid derivative represented by general formula (I) or a salt, hydrate or solvate thereof as an active ingredient.

[0025] In general formulae (I), (II), (IIIa), (IV) and (V) mentioned above, a “C3-8 cycloalkyl group” is a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group or a cyclooctyl group, preferably a cyclopropyl group or a cyclobutyl group.

[0026] A “C1-6 alkyl group” is a linear or branched alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a n-butyl group, an isobutyl group, a tert-butyl group, a n-pentyl group or a n-hexyl group, preferably an isopropyl group or a tert-butyl group.

[0027] An “optionally substituted aryl group” is a carbocyclic aryl group such as a phenyl group or a naphthyl group, which may have, as a substituent, a halogen atom such as a fluorine atom, a chlorine atom, a bromine atom or an iodine atom, a C1-6 alkyl group such as a methyl group or an ethyl group or a C1-5 alkoxy group such as a methoxy group or an ethoxy group, preferably a fluorine atom, a chlorine atom, a bromine atom, a methyl group or a methoxy group.

[0028] A “halogen atom” is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.

[0029] A “C1-5 alkoxy group” is a methoxy group, an ethoxy group, a n-propoxy group, a n-butoxy group, an isobutoxy group, a tert-butoxy group or a n-pentoxy group, preferably a methoxy group or an ethoxy group.

[0030] An “optionally substituted phenylsulfonylamino group”, an “optionally substituted phenylsulfonyl group” and an “optionally substituted phenylsulfoxide group” may have, as a substituent, a halogen atom such as a fluorine atom, a chlorine atom, a bromine atom or an iodine atom, a C1-6 alkyl group such as a methyl group or an ethyl group or a C1-5 alkoxy group such as a methoxy group or an ethoxy group, preferably a fluorine atom, a chlorine atom, a bromine atom, a methyl group or a methoxy group, at the ortho-position, meta-position, or para-position, preferably at the para-position.

[0031] An “ester residue” is an ester residue such as a C1-6 alkyl group, a benzyl group, a phenethyl group or a 1-naphthyl group or an ester group metabolically hydrolysable in vivo such as a lower alkanoyloxy lower alkyl group like an acetyloxymethyl group, a lower alkenoyl lower alkyl group like a vinylcarbonylmethyl group, a cycloalkylcabonyloxy lower alkyl group like a cyclopropylcarbonyloxymethyl group, a lower alkenoyloxy lower alkyl group like a vinylcaronyloxymethyl group, a lower alkoxy lower alkyl group like a methoxymethyl group, a lower alkoxy lower alkoxy lower alkyl group like a methoxymethoxymethyl group, a lower alkoxycarbonyloxy lower alkyl group like a methoxycarbonyloxymethylmethyl group, a benzoyloxy lower alkyl group like a benzoyloxymethyl group, a 2-oxotetrahydrofuan-5-yl group or a 2-oxo-5-(lower alkyl)-1,3-dioxolen-4-ylmethyl group. Herein, “lower” means a linear or branched carbon chain having a carbon number of 1 to 6.

[0032] A “C1-6 alkylene group” is a linear or branched alkylene group such as a methylene group, an ethylene group, a methylmethylene group, a trimethylene group, a propylene group, a dimethylmethylene group, a tetramethylene group, a 1-methyltrimethylene group, a 2-methyltrimethylene group, a 3-methyltrimethylene group, a 1-ethylethylene group, a 2-ethylethylene group, 2,2-dimethylethylene, 1,1-dimethylethylene, an ethylmethylmethylene group, a pentamethylene group, 1-methyltetramethylene, 2-methyltetramethylene, a 3-methyltetramethylene group, a 4-methyltetramethylene group, a 1,1-dimethyltrimethylene group, a 2,2-dimethyltrimethylene group, a 3,3-dimethyltrimethylene group, a 1,3-dimethyltrimethylene group, a 2,3-dimethyltrimethylene group, 1,2-dimethyltrimethylene, a 1,1,2-trimethylethylene group, a diethylmethylene group, a hexamethylene group, a 1-methylpentamethylene group, a 1,1-dimethyltetramethylene group or a 2,2-dimethyltetramethylene group, preferably a methylene group, an ethylene group, a propylene group, a methylmethylene group or a dimethylmethylene group.

[0033] A “C2-5 alkenylene group” is a vinylene group, a propenylene group or a butenylene group, preferably a vinylene group.

[0034] The present invention covers the racemic bodies, diastereomers and any optical isomers of compounds of the present invention represented by general formulae (I), (II), (IIIa), (IV) and (V) which have one or more asymmetric carbon atom. Further, the present invention also covers any geometrical isomers of the compounds of the present invention inclusive of the (E)-forms, (Z)-forms and mixtures thereof.

[0035] As salts of the compounds of the present invention represented by general formulae (I), (II), (IIIa), (IV) and (V), inorganic salts such hydrohalides such as hydrofluorides, hydrochlorides, hydrobromides and hydroiodides, nitrates, perchlorates, sulfates, phosphates and carbonates, lower alkylsulfonates such as methanesulfonates, trifluoromethanesulfonates and ethanesulfonates, arylsulfonates such as benzenesulfonates and p-toluenesulfonates, carboxylates such as acetates, fumarates, succinate, citrates, tartrates, oxalates and maleates, amino acid salts such as glycine salts, alanine salts, glutamates and aspartates and alkali metal salts such as sodium salts and potassium salts may be mentioned. As solvates, solvates with acetone, 2-butanol, 2-propanol, ethanol, ethyl acetate, tetrahydrofuran and diethyl ether may be mentioned.

[0036] The compounds of the present invention represented by general formulae (I), (II), (IIIa), (IV) and (V) can be produced by the processes described below.

[0037] [Process A] Process for producing the compounds of the present invention represented by general formulae (I) and (II) 14

[0038] (wherein R1, R2, X, R3, n and A are the same as defined above, and R4a is an ester residue.)

[0039] The first step is conventional reductive amination of an aldehyde represented by general formula (III) with an amine represented by general formula (V) and yields a benzylamine derivative represented by general formula (II).

[0040] This step is usually accomplished by in situ formation of an intermediary imine represented by general formula (II′) from the aldehyde represented by general formula (III) and the amine represented by general formula (V) followed by reduction with an appropriate reducing agent. For formation of the intermediary imine, as the reaction solvent, methanol, ethanol, isopropanol, benzene or toluene is preferable, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 20° C. to 140° C., and the reaction time is preferably from 1 to 24 hours. For reduction of the intermediary imine, as the reducing agent, for example, sodium borohydride or lithium aluminum hydride is preferable, though any usual reducing agent that can reduce an imino group to an amino group can be used without any particular restriction. With respect to the amounts of the respective reactants, the compound of general formula (V) is used preferably in an amount of 1 to 5 equivalents based on the compound of general formula (III), and the reducing agent is used preferably in an amount of from 1 to 5 equivalents based on the compound of general formula (III). The reaction solvent is preferably methanol, ethanol or isopropanol though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 70° C., and the reaction time is preferably from 30 minutes to 12 hours.

[0041] The second step is conventional sulfonamidation of the benzylamine derivative (II) obtained in the first step with a 2-chlorosulfonylbenzoic acid ester in the presence of a base and yields a 2-sulfamoylbenzoic acid derivative (Ia) which has an ester residue as R4 in general formula (I). The base may be either an aliphatic amine or an aromatic amine, preferably triethylamine or pyridine. With respect to the amounts of the respective reactants, the 2-chlorosulfonylbenzoic acid ester is used preferably in an amount of 1 to 3 equivalents based on the benzylamine derivative (II), and the base is used preferably in an amount of from 1 to 5 equivalents based on the benzylamine derivative (II). The reaction solvent is preferably chloroform, dichloromethane, 1,2-dichloroethane or 1,1,2,2-tetrachloroethane, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 100° C., and the reaction time is preferably from 30 minutes to 12 hours.

[0042] The third step is conventional hydrolysis of the compound of general formula (Ia) obtained in the second step and yields a compound of the present invention, wherein R4 is a hydrogen atom, represented by general formula (Ib). For this reaction, conventional hydrolysis in the presence of a base may be employed. The base is preferably a metal hydroxide or metal carbonate such as sodium hydroxide, potassium hydroxide, sodium carbonate or potassium carbonate. With respect to the amounts of the respective reactants, the base is used preferably in an amount of 1 to 50 equivalents based on the ester compound (Ia) . The reaction solvent is preferably water, methanol, ethanol, tetrahydrofuran or a mixture thereof though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 100° C., and the reaction time is preferably from 30 minutes to 24 hours.

[0043] A compound (Ia) of the present invention is also obtainable by esterification of a compound (Ib) of the present invention which comprises conversion of the compound (Ib) of the present invention into an acid halide with a halogenating agent such as thionyl chloride, oxalyl chloride or thionyl bromide followed by treatment with an alcohol in the presence or absence of a base. For formation of the acid halide, as the reaction solvent, dichloromethane, chloroform, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane or toluene is preferable, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 100° C., and the reaction time is preferably from 1 to 12 hours.

[0044] The base used for the esterification may be either an aliphatic amine or an aromatic amine, preferably triethylamine or pyridine. With respect to the amounts of the respective reactants, the alcohol is used preferably in an amount of from 1 to 10 equivalents based on the acid halide, and the base is used preferably in an amount of from 1 to 5 equivalents based on the acid halide. The reaction solvent may be dichloromethane, chloroform, 1,2-dichloroethane, 1,1,2,2-tetrachloroethane, toluene or the alcohol used for the esterification, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 80° C., and the reaction time is preferably from 30 minutes to 12 hours.

[0045] A compound (Ia) of the present invention is also obtainable from a compound (Ib) of the present invention through reaction with an alcohol using a condensing agent such as dicyclohexylcarbodiimide, 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide or 1,1′-carbonyldiimidazol. The condensing agent is used preferably in an amount of from 1 to 2 equivalents based on the compound (Ib) of the present invention. The reaction solvent is preferably N,N-dimethylformamide, dimethyl sulfoxide, tetrahydrofuran, dioxane, dichloromethane, chloroform or 1,2-dichloroethane though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 70° C., and the reaction time is preferably from 1 to 48 hours. In the cases of some types of reaction solvents, more than one equivalent of N-hydroxysuccinimide or N-hydroxybenzotriazole may be added beforehand so that the reaction proceeds smoothly.

[0046] [Process B] Process for producing the compounds (IIIb) of general formula (III) wherein X is a sulfur atom, and A is —CH2O— 15

[0047] (wherein R1 and R2 are the same as defined above except that they do not form a condensed ring, and Hal is a bromine atom or a chlorine atom.)

[0048] Firstly, a compound represented by formula (a) reacts with a compound (b) in the presence of a base to give a compound (c). The base used for the reaction is preferably a metal carbonate such as potassium carbonate or sodium carbonate or a metal hydride such as sodium hydride or potassium hydride. As the reaction solvent, N,N-dimethylformamide, dimethyl sulfoxide or acetone may be mentioned, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 0° C. to 100° C., and the reaction time is preferably from 30 minutes to 8 hours. Then, the resulting compound (c) reacts with O,O-diethyl dithiophosphate (d) to give a compound (e). For the reaction, O,O-diethyl dithiophosphate is used preferably in an amount of from 1 to 5 equivalents based on the compound (c). The reaction solvent is preferably water or a solvent mixture of an organic solvent/water, though there is no particular restriction unless the reaction is considerably inhibited, and as the organic solvent, dimethoxyethane, tetrahydrofuran or acetone is preferable. The reaction temperature is preferably from 25° C. to 100° C., and the reaction time is preferably from 30 minutes to 8 hours. The resulting compound (e) reacts with a bromoketone represented by formula (f) to give a compound represented by general formula (IIIb). With respect to the amounts of the respective reactants, the bromoketone represented by formula (f) is used preferably in an amount of from 1 to 2 equivalents based on the compound (e). The reaction solvent is preferably a lower alcohol such as methanol, ethanol or isopropanol though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 25° C. to 100° C., and the reaction time is preferably from 30 minutes to 24 hours.

[0049] [Process C] Process for producing the compounds (IIIc) of general formula (III) wherein A is —CH2O— 16

[0050] (wherein R1, R2, X and Hal are the same as defined above.)

[0051] A compound represented by formula (g) and a compound (b) undergo alkylation in the presence of a base to give a compound represented by general formula (IIIc). As the base used for the reaction, a metal carbonate such as potassium carbonate or sodium carbonate or a metal hydroxide such as sodium hydride or potassium hydride is preferable, and the base is used preferably in an amount of from 1 to 10 equivalents based on the compound (b). As the reaction solvent, N,N-dimethylformamide, dimethyl sulfoxide or acetone may be mentioned, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 30° C. to 100° C., and the reaction time is preferably from 30 minutes to 8 hours.

[0052] [Process D] Process for producing the compounds (IIId) of general formula (III) wherein A is an ethylene group and the compounds of the present invention represented by general formula (IV) 17

[0053] (wherein R1, R2, X and Hal are the same as defined above.)

[0054] A compound represented by formula (h) reacts with a compound (i) in the presence of a base to give a compound represented by formula (IV). As the base, an alkyl metal salt such as n-butyllithium, tert-butyllithium, lithium disiopropylamide or potassium tert-butoxide is preferably used. The base is used preferably in an amount of from 1 to 5 equivalents based on the compound of formula (h). As the reaction solvent, tetrahydrofuran, diethyl ether or toluene is preferable, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from −100° C. to 50° C., and the reaction time is preferably from 30 minutes to 12 hours. The subsequent reduction of the nitrile group in the resulting compound represented by general formula (IV) with a reducing agent affords a compound represented by general formula (IIId). The reducing agent is preferably a metal hydride, particularly diisopropylaluminum hydride, though any reducing agent that can reduce a nitrile group into an aldehyde group may be used without any no particular restriction, and used in an amount of from 1 to 2 equivalents based on the compound of general formula (IV). As the reaction solvent, tetrahydrofuran, diethyl ether or toluene may be mentioned, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from −100° C. to 50° C., and the reaction time is preferably from 30 minutes to 12 hours.

[0055] [Process E] Process for producing the compounds (IIId) of general formula (III) wherein A is an ethylene group 18

[0056] (wherein R1, R2 and X are the same as defined above.)

[0057] Catalytic hydrogenation of a compound represented by general formula (IIIe) in the presence of a catalyst affords a compound represented by general formula (IIld). As the hydrogenation catalyst, 5% palladium carbon, 10% palladium carbon, 30% palladium carbon, platinum oxide or Wilkinson's catalyst is preferable. The catalyst is used preferably in an amount of from {fraction (1/10)} to 1 time the weight of the compound (IIIe), and the hydrogen pressure is preferably from 1 to 5 atm. As the reaction solvent, methanol, ethanol, ethyl acetate or tetrahydrofuran is preferable, though there is no particular restriction unless the reaction is considerably inhibited. The reaction temperature is preferably from 25° C. to 70° C., and the reaction time is preferably from 1 to 72 hours.

[0058] [Process F] Process for producing the compounds (Va) of general formula (V) wherein R3 is an optionally substituted phenylsulfonyl group 19

[0059] (wherein n and Hal are the same as defined above, P is a protecting group, and Z is a hydrogen atom, a halogen atom, a C1-6 alkyl group or a C1-5 alkoxy group.)

[0060] An amino alcohol compound represented by formula (k) is converted into a compound of general formula (1) for protection of the amino group. The protection of the amino group can be accomplished by a conventional method using a protecting group such as a phthalimido group, a tert-butoxycarbonyl group or a benzyloxycarbonyl group. The resulting compound of formula (1) is converted into a compound of formula (m) by replacement of the hydroxyl group with a halogen atom. The halogenation can be accomplished conventionally by bromination using phosphorus tribromide or carbon tetrabromide/triphenylphosphine or chlorination using thionyl chloride or phosphorus pentachloride. The resulting compound of formula (m) reacts with a thiophenol of formula (n) to give a compound of formula (o). The substitution can be accomplished by using a base such as potassium carbonate or sodium hydride. The resulting compound of formula (o) is oxidized to a compound represented by formula (p) and then finally converted into a compound of general formula (Va) through deprotection. For the oxidation, an oxidizing agent such as metachloroperbenzoic acid may be used. For the deprotection, conventional methods may be used according to the protecting group.

[0061] [Process G] Process for producing the compounds (Vb) of general formula (V) wherein R3 is an optionally substituted phenylsulfonylamino group 20

[0062] (wherein n and Z are the same as defined above.)

[0063] A diamine compound represented by formula (q) reacts with a phenylsulfonyl chloride represented by formula (r) to give a compound of general formula (Vb). With respect to the amounts of the respective reactants, the diamine compound (q) is used preferably in an amount of from 1 to 20 equivalents based on the compound of formula (r). As the reaction solvent, chloroform, 1,2-dichloroethane, dichloromethane or 1,1,2,2-tetrachloroethane may be mentioned, though there is no particular restriction. The reaction temperature is preferably from 0° C. to 50° C., and the reaction time is preferably from 1 to 8 hours.

[0064] The compounds of the present invention and intermediates produced in the above-mentioned processes can be isolated in the forms of free compounds, salts, hydrates, solvates with various solvents such as ethanol or polymorphic crystals. Pharmaceutically acceptable salts of the compounds of the present invention are obtainable by conventional salt-forming reactions. Isolation can be accomplished through chemical techniques such as fractional extraction, crystallization and various types of fractional chromatography. Their optical isomers can be obtained as stereochemically pure isomers from appropriately selected starting materials or by racemic resolution of racemic compounds.

[0065] The 2-sulfamoylbenzoic acid derivatives of general formula (I) thus obtainable have an excellent anti-allergic effect by virtue of their antagonistic effects on both the LTD4 receptor and the TXA2 receptor and show excellent effects as preventive and therapeutic agents on allergic bronchial asthma, rhinitis and conjunctivitis, atopic dermatitis, gastroenteritis, colitis, vernal catarrh, nephritis and other allergic diseases. They are also useful as preventive and therapeutic agents for diseases associated with leukotrienes and TXA2 and widely applicable for prevention and treatment of ischemic heart and brain diseases, angina pectoris, inflammatory peptic ulcer and hepatopathy.

[0066] The 2-sulfamoylbenzoic acid derivatives of the present invention can be used by themselves or by using known drug formulations in various dosage forms, for example, for oral pharmaceuticals such as tablets, capsules, granules, fine granules, powders, liquids and syrups and for parenteral pharmaceuticals such as injections, nasal drops, eye drops, infusions, ointments, suppositories, inhalants, percutaneous pharmaceuticals and patches.

[0067] The dosages of the medicines of the present invention depend on the condition, age and body weight of the patient, the therapeutic effect and the mode and term of administration, but in the case of oral administration to an adult, they are usually administered in an amount of from 0.1 mg to 10 g per day.

BEST MODE FOR CARRYING OUT THE INVENTION

EXAMPLES

[0068] Now, the compounds of the present invention and their preparations will be described in further detail with reference to Examples. However, the present invention should not be restricted to these specific Examples. The H1-NMR spectra were obtained by means of a spectrometer, model JNM-EX270 (270 MHz, JEOL Ltd.) by using tetramethylsilane (TMS) as an internal standard, and the δ values were given in ppm. The DI-EI mass spectra were obtained by means of a spectrometer, model QP1000EX (Shimadzu Corporation) The FAB mass spectra were obtained by means of a high resolution mass spectrometer, model JMN-HX110A (JEOL Ltd.).

Example 1

[0069] Preparation of 3-[(4-isopropyl-2-thiazolyl)methoxy]benzaldehyde

[0070] 50 g (0.41 mol) of m-hydroxybenzaldehyde and 49 g (0.41 mol) of bromoacetonitrile were dissolved in 300 ml of N,N-dimethylformamide and stirred together with 85 g (0.62 mol) of potassium carbonate and 6.0 g (0.04 mol) of sodium iodide at room temperature for 1.5 hours. The solvent was distilled off in vacuo, and then water and ethyl acetate were added for extraction. The ethyl acetate layer was washed with saturated aqueous sodium chloride and dried over magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; chloroform) to give 58 g of 3-cyanomethoxybenzaldehyde in a yield of 88%.

[0071] 1 H-NMR(CDCl3):4.86 (2H, s) 7.25-7.30 (1H, m) 7.44-7.64 (3H, m) 10.01 (1H, s)

[0072] Then, 50 g (0.31 mol) of 3-cyanomethoxybenznaldehyde was dissolved in 500 ml of 1,2-dimethoxyethane and stirred together with 5.6 ml (0.31 mol) of water and 52 ml (0.31 mol) of O,O-diethyl dithiophosphate a: 70° C. for 3 hours. The solvent was distilled off in vacuo, and the residue was washed with ether and filtered off to give 31 g of 3-(thiocarbamoylmethoxy)benzaldehyde in a yield of 51%.

[0073] Mass (m/z):195(M+) 160 121

[0074] 1 H-NMR(CDCl3): 4.94 (2H, s) 7.20-7.29 (1H, m) 7.44-7.58 (3H, m) 7.97 (2H, br) 9.99 (1H, s)

[0075] Then, 32.9 g (0.38 mol) of methyl isopropyl ketone was dissolved in 291 ml of methanol and mixed with 2.9 ml of 25% HBr-AcOH under cooling with ice. 18.7 ml (0.36 mol) of bromine was added dropwise under cooling with ice, and the reaction solution was stirred for 2 hours. The reaction solution was stirred together with water at room temperature for 30 minutes and then together with 3-(thiocarbamoylmethoxy)benzaldehyde at room temperature for 5.5 hours. Water and saturated sodium hydrogen carbonate were added to adjust the pH to 8.0, and the reaction solution was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent, and the residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=20:1) to give 64.3 g of the title compound in a yield of 68%.

[0076] 1 H-NMR(CDCl3): 1.33 (6H, d, J=6.9 Hz) 3.12 (1H,) 5.40 (2H, s) 6.92 (1H, d, J=0.99 Hz) 7.26-7.31 (1H, m) 7.47-7.54 (3H, m) 9.98 (1H, s)

[0077] Similarly, the compounds of Example 2 and 3 were prepared.

Example 2

[0078] 3-[(4-Cyclobutyl-2-thiazolyl)methoxy]benzaldehyde

[0079] Mass (m/z): 273(M+) 254 152

[0080] 1 H-NMR(CDCl3): 1.90-2.10 (2H, m) 2.20-2.43 (4H, m) 3.68 (1H, quint) 5.40 (2H, s) 6.94 (1H, s) 7.26-7.30 (1H, m) 7.47-7.54 (3H, m) 9.98 (1H, s)

Example 3

[0081] 3-[(4-Cyclopropyl-2-thiazolyl)methoxy]benzaldehyde

[0082] 1 H-NMR(CDCl3): 0.86-1.00 (4H, m) 2.06 (1H, m) 5.35 (2H, s) 6.87 (1H, s) 7.24-7.31 (1H, m) 7.44-7.53 (3H, m) 9.98 (1H, s)

Example 4

[0083] Preparation of 3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzonitrile

[0084] 766 mg (5 mmol) of 4-cyclobutyl-2-methylthiazole was dissolved in 15 ml of anhydrous tetrahydrofuran and mixed with 561 mg (5 mmol) of potassium tert-butoxide, and 3 ml (5 mmol) of n-butyllithium (1.68M hexane solution) was added dropwise at −78° C. After 3 hours of stirring at the same temperature, 1270 mg (6 mmol) of 3-bromomethylbenzonitrile in 3 ml anhydrous tetrahydrofuran was added dropwise, and the reaction solution was stirred for one hour and 40 minutes. After addition of saturated aqueous ammonium chloride, the reaction solution was extracted with diethyl ether twice, and the organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=4:1) to give 876 mg of the title compound as a yellow oily substance in a yield of 64%.

[0085] Mass (m/z): 268(M+)

[0086] 1 H-NMR(CDCl3): 1.84-2.11 (2H, m) 2.15-2.42 (4H, m) 3.11-3.19 (2H, m) 3.25-3.52 (2H, m) 3.57-3.70 (1H, m) 6.75 (lH,s) 7.35-7.52 (4H, m)

Example 5

[0087] Preparation of 3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzaldehyde

[0088] 875 mg (3.3 mmol) of 3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzonitrile was dissolved in 20 ml of toluene, and 3.6 ml (3.60 mmol) of 1.01M diisobutylaluminum hydride (toluene solution) was added at −78° C. The reaction solution was brought back to room temperature and stirred for 2 hours. The reaction solution was mixed with saturated aqueous ammonium chloride and 2N hydrochloric acid successively and stirred for 1 hour, and the organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=4:1) to give 792 mg of the title compound as a colorless oily substance in a yield of 89%.

[0089] Mass (m/z): 271 (M+) 242

[0090] 1 H-NMR(CDCl3): 1.84-2.42 (6H, m) 3.20 (2H, m) 3.32 (2H, m) 3.64 (1H, quint) 6.74 (1H, d, J=0.66 Hz) 7.47 (2H, m) 7.73 (2H, m) 9.99 (1H, s)

Example 6

[0091] Preparation of 3-[2-(2-quinolyl)ethyl]benzaldehyde

[0092] 5.5 g (21.2 mmol) of 3-[2-(2-quinolyl)ethenyl]benzaldehyde was dissolved in 500 ml and hydrogenated in the presence of 1.1 g of 10% palladium carbon at atmospheric pressure at room temperature for 10 hours under stirring. The 10% palladium carbon was filtered out through celite, and the filtrate was evaporated in vacuo. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=9:1) to give 2.8 g (10.7 mmol) of the title compound in a yield of 51%.

[0093] Mass (m/z): 261 (M+) 156

[0094] 1 H-NMR(CDCl3): 7.46-7.60 (3H, m) 7.65-7.91 (6H, m) 8.05-8.17 (3H, m) 10.07 (1H, s)

Example 7

[0095] Preparation of 5-(4-chlorophenylsulfonyl)pentanamine

[0096] 10 g (96.9 mmo)of 5-amino-1-pentanol was dissolved in 300 ml of toluene and refluxed together with 17.2 g (116 mmol) of phthalic anhydride at 120° C. for 24 hours. The solvent was distilled off in vacuo, and the residue was purified by silica gel column chromatography (eluent; chloroform) to give 16.6 g of 5-phthalimido-1-pentanol in a yield of 74%.

[0097] Mass (m/z): 233 (M+) 203 160

[0098] 1 H-NMR(CDCl3): 1.37-1.48 (2H, m) 1.58-1.78 (4H, m) 3.62-3.73 (4H, m) 7.68-7.74 (2H, m) 7.81-7.87 (2H, m)

[0099] Then, 16.2 g of 5-phthalimido-1-pentanol was dissolved in 350 ml of diethyl ether, and 4.3 ml of phosphorus tribromide was added dropwise at 0° C. The reaction solution was stirred at room temperature for 9 hours and neutralized with saturated aqueous sodium hydrogen carbonate, and the organic layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=9:1) to give 9.2 g of 1-bromo-5-phthalimidopentane in a yield of 45%.

[0100] Mass (m/z): 296 (M+) 216 160

[0101] 1 H-NMR(CDCl3): 1.44-1.55 (2H, m) 1.63-1.77 (2H, m) 1.86-2.00 (2H, m) 3.37-3.42 (2H, m) 3.67-3.73 (2H, m) 7.68-7.75 (2H, m) 7.81-7.88 (2H, m)

[0102] Then, 9.2 g (31 mmol) of 1-bromo-5-phthalimidopentane was dissolved in 100 ml of N,N-dimethylformamide and stirred together with 8.6 g (62 mmol) of potassium carbonate, 465 mg (3.1 mmol) of sodium iodide and 4.5 g (31 mmol) of 4-chlorothiophenol at room temperature for 15 hours. The solvent was distilled off in vacuo, and water and ethyl acetate were added for extraction. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was washed with hexane to give 9.6 g of 1-(4-chlorophenylthio)-5-phthalimidepentane in a yield of 86%.

[0103] Mass (m/z): 359 (M+) 216 160

[0104] 1 H-NMR(CDCl3): 1.47-1.51 (2H, m) 1.64-1.72 (4H, m) 2.88 (2H, t J=7.26 Hz) 3.68 (2H, t J=7.26 Hz) 7.23 (4H, s) 7.71-7.23 (2H, m) 7.82-7.86 (2H, m)

[0105] Then, 9.4 g (26.1 mmol) of 1-(4-chlorophenylthio)-5-phthalimidopentane was dissolved in 350 ml of 1,2-dichloroethane and stirred together with 9.9 g (57.4 mmol) of metachloroperbenzoic acid at room temperature for 18 hours. The reaction solution was washed with 5% sodium thiosulfate, 3% sodium hydrogen carbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vasuo for removal of the solvent to give 9.7 g of 1-(4-chlorophenylsulfonyl)-5-phthalimidopentane in a yield of 95%.

[0106] Mass (m/z): 391 (M+) 216 160

[0107] 1 H-NMR(CDCl3): 1.37-1.48 (2H, m) 1.61-1.81 (4H, m) 3.05-3.11 (2H, m) 3.62-3.93 (3H, m) 7.52-7.57 (2H, m) 7.69-7.75 (2H, m) 7.80-7.86 (2H, m)

[0108] Then, 4.0 g (10.2 mmol) of 1-(4-chlorophenylsulfonyl)-5-phthalimidopentane was dissolved in 120 ml of dichloromethane and 20 ml of ethanol and stirred together with 6 ml of 80% hydrazine hydrate at room temperature for 36 hours. The impurities were filtered out, and the filtrate was evaporated in vacuo to give 3.2 g of the title compound.

Example 8

[0109] Preparation of 4-(4-chlorophenylsulfonylamino)butanamine 26.4 g (0.3 mol) of 1,4-diaminobutane was dissolved in 100 ml of 1,2-dichloroethene and stirred together with 6.3 g (0.03 mmol) of 4-chlorophenylsulfonyl chloride at room temperature for 4 hours. After addition of chloroform, the reaction solution was filtered through celite, and the filtrate was washed with water three times and with saturated aqueous sodium chloride successively, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent to give 5.1 g of the title compound in a yield of 65%.

Example 9

[0110] Preparation of N-[4-(4-chlorobenzenesulfonylamino)butyl]-3-[(4-isopropyl-2-thiazolyl)methoxy]benzylamine (Compound No. 1a)

[0111] 2.27 g (8.69 mmol) of 3-[(4-isopropyl-2-thiazolyl)methoxy]benzaldehyde and 2.27 g (8.69 mmol) of 4-(4-chlorophenylsulfonylamino)butanamine were dissolved in 150 ml of ethanol and refluxed together with 4.0 g of molecular sieves 3A for 16 hours. The molecular sieves 3A was filtered out, and the filtrate was stirred together with 873 mg of sodium borohydride at room temperature for 3 hours. The reaction solution was evaporated in vacuo for removal of ethanol as the solvent and mixed with water and ethyl acetate for ethyl acetate extraction. The ethyl acetate layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; chloroform to chloroform:methanol=98:2) to give N-[4-(4-chlorobenzenesulfonylamino)butyl]-3-[(4-isopropyl-2-thiazolyl)methoxy]benzylamine (Compound No. 1a).

[0112] Compounds Nos. 2a to 90a were prepared similarly. The mass spectrum data are shown in Table 1.

TABLE 1
21
Com- pound No.	22	A	R3	n	FAB-MS (m/z)
1a	23	—CH2O—	24	4	508 (M+) 315 245
2a	25	—CH2O—	26	4	504 (M+) 330 258
3a	27	—CH2O—	28	4	566 (M+) 331 258
4a	29	—CH2O—	30	4	516 (M+) 330 258
5a	31	—CH2O—	32	4	500 (M+) 330 258
6a	33	—CH2O—	34	4	486 (M+) 330 258
7a	35	—CH2O—	36	3	506 (M+) 316 258
8a	37	—CH2O—	38	2	492 (M+) 302 258
9a	39	—CH2O—	40	2	536 (M+) 301 258
10a	41	—CH2O—	42	2	476 (M+) 302 258
11a	43	—CH2O—	44	2	458 (M+) 302 258
12a	45	—CH2O—	46	5	534 (M+) 344 258
13a	47	—CH2O—	48	4	520 (M+) 329 258
14a	49	—CH2O—	50	4	492 (M+) 318 246
15a	51	—CH2O—	52	4	552 (M+) 317 246
16a	53	—CH2O—	54	4	504 (M+) 319 246
17a	55	—CH2O—	56	4	488 (M+) 318 246
18a	57	—CH2O—	58	4	474 (M+) 318 246
19a	59	—CH2O—	60	4	542 (M+) 352 280
20a	61	—CH2O—	62	4	506 (M+) 316 244
21a	63	—CH2O—	64	4	490 (M+) 316 244
22a	65	—CH2O—	66	4	552 (M+) 317 244
23a	67	—CH2O—	68	4	472 (M+) 316 244
24a	69	—CH2O—	70	4	486 (M+) 316 244
25a	71	—CH2O—	72	4	502 (M+) 316 244
26a	73	—CH2O—	74	3	492 (M+) 302 244
27a	75	—CH2O—	76	2	478 (M+) 288 244
28a	77	—CH2O—	78	2	462 (M+) 288 244
29a	79	—CH2CH2—	80	4	518 (M+) 328 256
30a	81	—CH2CH2—	82	4	562 (M+) 327 256
31a	83	—CH2CH2—	84	4	485 (M+) 329 256
32a	85	—CH2CH2—	86	4	499 (M+) 329 256
33a	87	—CH2CH2—	88	4	490 (M+) 316 244
34a	89	—CH2CH2—	90	4	487 (M+) 317 244
35a	91	92	93	4	490 (M+) 316 244
36a	94	95	96	4	550 (M+) 315 244
37a	97	98	99	4	502 (M+) 316 244
38a	100	101	102	4	486 (M+) 316 244
39a	103	104	105	4	472 (M+) 316 244
40a	106	107	108	3	492 (M+) 302 244
41a	109	110	111	2	479 (M+) 289 244
42a	112	113	114	2	524 (M+) 289 278
43a	115	116	117	2	462 (M+) 288 244
44a	118	119	120	2	444 (M+) 288 244
45a	121	122	123	4	540 (M+) 350 278
46a	124	125	126	4	519 (M+) 345 278
47a	127	128	129	4	586 (M+) 351 278
48a	130	131	132	4	536 (M+) 350 278
49a	133	134	135	4	520 (M+) 350 278
50a	136	137	138	4	506 (M+) 350 278
51a	139	140	141	3	526 (M+) 336 278
52a	142	143	144	2	512 (M+) 322 278
53a	145	—CH2O—	146	4	494 (M+) 320 248
54a	147	—CH2O—	148	4	555 (M+) 322 248
55a	149	—CH2O—	150	4	506 (M+) 320 248
56a	151	—CH2O—	152	4	490 (M+) 320 248
57a	153	—CH2O—	154	4	476 (M+) 320 248
58a	155	—CH2O—	156	3	490 (M+) 300 248
59a	157	—CH2O—	158	2	482 (M+) 300 248
60a	159	—CH2O—	160	2	466 (M+) 292 248
61a	161	—CH2O—	162	2	526 (M+) 291 248
62a	163	—CH2O—	164	2	449 (M+) 293 248
63a	165	—CH2O—	166	5	537 (M+) 347 248
64a	167	—CH2O—	168	2	516 (M+) 326 282
65a	169	—CH2O—	170	4	546 (M+) 356 282
66a	171	—CH2CH2—	172	4	508 (M+) 318 246
67a	173	—CH2CH2—	174	4	492 (M+) 318 246
68a	175	—CH2CH2—	176	4	488 (M+) 318 246
69a	177	—CH2CH2—	178	4	504 (M+) 318 246
70a	179	—CH2CH2—	180	4	554 (M+) 319 246
71a	181	—CH2CH2—	182	2	480 (M+) 290 246
72a	183	—CH2CH2—	184	3	494 (M+) 304 246
73a	185	—CH2CH2—	186	5	522 (M+) 332 246
74a	187	—CH2CH2—	188	4	542 (M+) 352 280
75a	189	—HC2CH2—	190	4	526 (M+) 352 280
76a	191	—CH2CH2—	192	4	522 (M+) 352 280
77a	193	—CH2CH2—	194	4	538 (M+) 358 280
78a	195	—CH2CH2—	196	4	588 (M+) 353 280
79a	197	—CH2CH2—	198	2	515 (M+) 325 280
80a	199	—CH2CH2—	200	3	528 (M+) 338 280
81a	201	—CH2O—	202	5	519 (M+) 344 256
82a	203	—CH2O—	204	5	505 (M+) 330 244
83a	205	—CH2O—	206	5	507 (M+) 332 246
84a	207	208	209	5	505 (M+) 330 244
85a	210	211	212	5	539 (M+) 364 278
86a	213	—CH2CH2—	214	5	507 (M+) 328 280
87a	215	—CH2CH2—	216	5	541 (M+) 366 280
88a	217	—CH2O—	218	5	509 (M+) 334 248
89a	219	—CH2O—	220	4	510 (M+) 319
90a	221	222	223	4	506 (M+) 315

Example 10

[0113] Preparation of methyl [2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoate (Compound No. 1b)

[0114] 3.5 g (6.89 mmol) of the product in Example 9 (Compound 1a) was dissolved in 150 ml of 1,2-dichloroethane and stirred together with 1.4 ml (10.34 mmol) of triethylamine and 1.9 g (8.27 mmol) of methyl 2-chlorosulfonylbenzoate at room temperature for 4 hours. The 1,2-dichloroethane was distilled off in vacuo, and water and ethyl acetate were added. The ethyl acetate was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; chloroform) to give 3.5 g (4.95 mmol) of 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoate (Compound No. 1b) in a yield of 72%.

[0115] Compounds Nos. 2b to 90b were prepared similarly. The mass spectrum data are shown in Table 2.

TABLE 2
224
Com- pound No.	225	A	R3	n	FAB-MS (m/z)
1b	226	—CH2O—	227	4	706 (M+) 506
2b	228	—CH2O—	229	4	702 (M+)
3b	230	—CH2O—	231	4	764 (M+) 564
4b	232	—CH2O—	233	4	714 (M+) 514
5b	234	—CH2O—	235	4	698 (M+) 498
6b	236	—CH2O—	237	4	684 (M+) 484
7b	238	—CH2O—	239	3	704 (M+) 504
8b	240	—CH2O—	241	2	690 (M+) 490
9b	242	—CH2O—	243	2	734 (M+) 534
10b	244	—CH2O—	245	2	674 (M+) 474
11b	246	—CH2O—	247	2	656 (M+) 456
12b	248	—CH2O—	249	5	732 (M+) 532
13b	250	—CH2O—	251	4	718 (M+) 518
14b	252	—CH2O—	253	4	690 (M+) 490
15b	254	—CH2O—	255	4	750 (M+) 550
16b	256	—CH2O—	257	4	702 (M+) 502
17b	258	—CH2O—	259	4	686 (M+) 486
18b	260	—CH2O—	261	4	672 (M+) 472
19b	262	—CH2O—	263	4	740 (M+) 540
20b	264	—CH2O—	265	4	704 (M+) 504
21b	266	—CH2O—	267	4	684 (M+) 484
22b	268	—CH2O—	269	4	750 (M+) 550
23b	270	—CH2O—	271	4	670 (M+) 470
24b	272	—CH2O—	273	4	684 (M+) 484
25b	274	—CH2O—	275	4	700 (M+) 500
26b	276	—CH2O—	277	3	690 (M+) 490
27b	278	—CH2O—	279	2	676 (M+) 476
28b	280	—CH2O—	281	2	660 (M+) 460
29b	282	—CH2CH2—	283	4	716 (M+) 516
30b	284	—CH2CH2—	285	4	760 (M+) 562
31b	286	—CH2CH2—	287	4	683 (M+) 483
32b	288	—CH2CH2—	289	4	697 (M+) 497
33b	290	—CH2CH2—	291	4	688 (M+) 488
34b	292	—CH2CH2—	293	4	685 (M+) 485
35b	294	295	296	4	688 (M+) 488
36b	297	298	299	4	748 (M+) 548
37b	300	301	302	4	700 (M+) 500
38b	303	304	305	4	684 (M+) 484
39b	306	307	308	4	670 (M+) 470
40b	309	310	311	3	690 (M+) 490
41b	312	313	314	2	677 (M+) 477
42b	315	316	317	2	722 (M+) 522
43b	318	319	320	2	660 (M+) 460
44b	321	322	323	2	642 (M+) 442
45b	324	325	326	4	738 (M+) 538
46b	327	328	329	4	717 (M+) 517
47b	330	331	332	4	784 (M+) 584
48b	333	334	335	4	734 (M+) 534
49b	336	337	338	4	718 (M+) 518
50b	339	340	341	4	704 (M+) 504
518	342	343	344	3	724 (M+) 524
52b	345	346	347	2	710 (M+) 510
53b	348	—CH2O—	349	4	692 (M+) 492
54b	350	—CH2O—	351	4	753 (M+) 553
55b	352	—CH2O—	353	4	704 (M+) 504
56b	354	—CH2O—	355	4	688 (M+) 488
57b	356	—CH2O—	357	4	674 (M+) 474
58b	358	—CH2O—	359	3	688 (M+) 488
59b	360	—CH2O—	361	2	680 (M+) 480
60b	362	—CH2O—	363	2	664 (M+) 464
61b	364	—CH2O—	365	2	724 (M+) 524
62b	366	—CH2O—	367	2	657 (M+) 457
63b	368	—CH2O—	369	5	735 (M+) 535
64b	370	—CH2O—	371	2	714 (M+) 514
65b	372	—CH2O—	373	4	744 (M+) 544
66b	374	—CH2CH2—	375	4	706 (M+) 506
67b	376	—CH2CH2—	377	4	690 (M+) 490
68b	378	—CH2CH2—	379	4	686 (M+) 486
69b	380	—CH2CH2—	381	4	702 (M+) 502
70b	382	—CH2CH2—	383	4	752 (M+) 552
71b	384	—CH2CH2—	385	2	678 (M+) 478
72b	386	—CH2CH2—	387	3	692 (M+) 492
73b	388	—CH2CH2—	389	5	720 (M+) 520
74b	390	—CH2CH2—	391	4	740 (M+) 540
75b	392	—CH2CH2—	393	4	724 (M+) 524
76b	394	—CH2CH2—	395	4	720 (M+) 520
77b	396	—CH2CH2—	397	4	736 (M+) 536
78b	398	—CH2CH2—	399	4	786 (M+) 586
79b	400	—CH2CH2—	401	2	713 (M+) 513
80b	402	—CH2CH2—	403	3	726 (M+) 526
81b	404	—CH2O—	405	5	717 (M+) 517
82b	406	—CH2O—	407	5	703 (M+) 503
83b	408	—CH2O—	409	5	705 (M+) 505
84b	410	411	412	5	703 (M+) 503
85b	413	414	415	5	737 (M+) 537
86b	416	—CH2CH2—	417	5	705 (M+) 505
87b	418	—CH2CH2—	419	5	739 (M+) 539
88b	420	—CH2O—	421	5	707 (M+) 507
89b	422	—CH2O—	423	4	708 (M+) 509
90b	424	425	426	4	704 (M+) 505

Example b 11

[0116] Preparation of 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid (Compound No. 1)

[0117] 3.2 g (4.53 mmol) of the product in Example 10 (Compound No. 1b) was dissolved in 70 ml of methanol and 70 ml of tetrahydrofuran and stirred together with 50 ml of 1N sodium hydroxide at 80° C. for 3 hours. The reaction solution was evaporated in vacuo for removal of the solvent, mixed with water and neutralized with 1N hydrochloric acid, and the deposited precipitate was filtered off to give 2.7 g (3.9 mmol) of the title compound (Compound No. 1) in a yield of 86%.

[0118] Compounds Nos. 2 to 90 were prepared similarly. The mass spectrum data are shown in Table 3.

TABLE 3
427
Compound No.	428	A	R3	n	Physicochemical properties
1	429	—CH2O—	430	4	FAB-MS: (m/z) 692(M+) 508 458 246 1H NMR(CDCl3) 1.31(10H, m) 2.75(2H, br s) 3.15(2H, t J=6.8Hz) 4.40(2H, s) 5.33(2H, s) 6.81-6.91(4H,m) 7.15(1H, t J=7.8Hz) 7.38(2H, d J=7.38Hz) 7.51-7.64(3H, m) 7.71(2H, d J=8.58Hz) 7.90(1H, d J=7.26 Hz)
2	431	—CH2O—	432	4	FAB-MS: (m/z) 688(M+) 504 346 258 1H NMR(CDCl3) 1.33(4H, m) 1.88-2.12(2H, m) 2.17-2.43 (4H, m) 2.75(2H, br s) 3.14(2H, br t) 3.72(1H, quint) 4.40(2H, s) 5.12 (1H, br s) 5.37(2H, s) 6.81-6.90(2H, m) 6.95(1H, d J=0.7Hz) 7.08-7.14(3H, m) 7.54-7.68(3H, m) 7.80(2H, m) 7.94 (1H, d J=7.59Hz)
3	433	—CH2O—	434	4	FAB-MS: (m/z) 750(M++1) 670 564 1H NMR(CDCl3) 1.26(4H, m) 1.87-2.10(2H, m) 2.06-2.40 (4H, m) 2.71(2H, br s) 3.13(2H, br s) 3.65(1H, quint) 4.38(2H, s) 5.28 (2H, s) 5.68(1H, br s) 6.83(2H, m) 6.92 (1H, s) 7.14(1H, t J=7.9Hz) 7.45-7.50 (5H, m) 7.61(2H, d J=8.58Hz) 7.82 (1H, d J=7.59Hz)
4	435	—CH2O—	436	4	FAB-MS: (m/z) 700(M+) 516 365 240 1H NMR(CDCl3) 1.26(4H, m) 1.83-2.09(2H, m) 2.17-2.36 (4H, m) 1.83-2.09(2H, m) 2.17-2.36(4H, m) 3.11(2H, br s) 3.67(1H, quint) 3.79(3H, s) 4.35(2H, br s) 5.26 (2H, br s) 6.72-7.09(5H, m) 7.12(1H, br s) 7.26(1H, s) 7.30-7.90(6H, m)
5	437	—CH2O—	438	4	FAB-MS: (m/z) 684(M+) 645 500 1H NMR(CDCl3) 1.22-1.32(4H, m) 1.86-2.10(2H, m) 2.16-2.31(4H, m) 2.36(3H, s) 2.71(2H, br s) 3.13(2H, br s) 3.72(1H, quint) 4.38(2H, s) 5.29(2H, s) 6.81-6.92(4H, m) 7.10-7.21(3H, m) 7.44-7.59(3H, m) 7.65(2H, d J=8.25Hz) 7.87(1H, d J=7.59Hz)
6	439	—CH2O—	440	4	FAB-MS: (m/z) 670(M+) 486 346 1H NMR(CDCl3) 1.23-1.34(4H, m) 1.91-2.16(2H, m) 2.19-2.42(4H, m) 2.73(2H, br s) 3.13(2H, br s) 3.71(1H, quint) 4.39(2H, s) 5.11(1H, br s) 5.34(2H, s) 6.81-6.94 (4H, m) 7.13(1H, t J=7.76Hz) 7.41-7.65(6H, m) 7.78(2H, d J=6.93Hz) 7.92 (1H, d J=7.59Hz)
7	441	—CH2O—	442	3	FAB-MS: (m/z) 690(M+) 346 258 1H NMR(CDCl3) 1.41(2H, br s) 1.92-2.12(2H, m) 2.20-2.42(4H, m) 2.73(2H, br s) 3.22(2H, br s) 3.70(1H, quint) 4.38(2H, s) 5.33 (2H, s) 5.74(1H, br s) 6.80-6.94(4H, m) 7.14(1H, t) 7.35(2H, d J=8.58Hz) 7.52-7.60(3H, m) 7.69-(2H, d J=8.57 Hz) 7.85(1H, d J=7.26Hz)
8	443	—CH2O—	444	2	FAB-MS: (m/z) 676(M+) 492 458 1H NMR(CDCl3) 1.92-2.40(6H, m) 2.70(2H, br s) 3.26 (2H, br s) 3.71(1H, m) 4.34(2H, s) 5.40 (2H, s) 6.19(1H, br s) 6.77-6.97 (4H, m) 7.12(1H, m) 7.25-7.31(3H, m) 7.50-7.62(5H, m) 7.93(1H, d)
9	445	—CH2O—	446	2	FAB-MS: (m/z) 720(M+) 642 536 1H NMR(CDCl3) 1.85-2.13(2H, m) 2.15-2.44(4H, m) 2.70 (2H br s) 3.27(2H, t J=5.6Hz) 4.34 (2H, s) 5.42(2H, s) 6.16(1H, br s) 6.77(1H, d J=7.9Hz) 6.87-6.90(2H, m) 6.97(1H, s) 7.42-7.63(7H, m) 7.95(1H, d J=7.59Hz)
10	447	—CH2O—	448	2	FAB-MS: (m/z) 660(M+) 476 258 1H NMR(CDCl3) 1.85—2.43(4H, m) 2.71(2H, br s) 3.25 (2H, m) 3.74(1H, quint) 4.33(2H, s) 5.46(2H, s) 5.97(1H, br s) 6.77(1H, d J=7.58Hz) 6.85-6.92(2H, m) 6.98-7.15 (4H, m) 7.54-7.69(5H, m) 8.00(1H, d J=7.58Hz)
11	449	—CH2O—	450	2	FAB-MS: (m/z) 642(M+) 458 1H NMR(CDCl3) 1.89-2.43(6H, m) 2.73(2H, br s) 3.25 (2H, m) 3.74(1H, quint) 4.31(2H, s) 5.43(2H, s) 5.89(1H, br s) 6.77(1H, d J=7.58Hz) 6.89(2H, m) 6.97(1H, d J=0.66 Hz) 7.11(1H, t, J=7.92Hz) 7.35-7.70 (8H, m) 8.00(1H, d J=7.58Hz)
12	451	—CH2O—	452	5	FAB-MS: (m/z) 718(M+) 684 645 534 1H NMR(CDCl3) 1.05(2H, m) 1.27(4H, m) 1.85-2.45(6H, m) 2.78(2H, m) 3.10(2H, m) 3.73(1H, quint) 4.40(2H, s) 5.13(1H, br s) 5.37 (2H, s) 6.82-6.90(2H, m) 6.95(2H, d J=0.66Hz) 7.16(1H, m) 7.46(2H, m) 7.54-7.74(3H, m) 7.76(2H, dd J=1.98 6.93 Hz) 7.96(1H, m)
13	453	—CH2O—	454	4	FAB-MS: (m/z) 704(M+) 520 1H NMR(CDCl3) 1.30(4H, m) 1.90-2.08(2H, m) 2.16-2.39 (4H, m) 2.72(2H, br s) 3.14(2H, br s) 3.71(1H, quint) 4.40(2H, s) 5.22(1H, br s) 5.36(2H, s) 6.80-6.94(4H, m) 7.13(1H, d J=7.59Hz) 7.38(2H, d J=6.92Hz) 7.54-7.72(5H, m) 7.89(1H, d)
14	455	—CH2O—	456	4	FAB-MS: (m/z) 676(M+) 492 228 1H NMR(CDCl3) 1.31(10H, m) 2.77(2H, m) 3.14(3H, m) 4.43(2H, s) 5.14(1H, t J=5.78Hz) 5.37 (2H, s) 6.81-6.95(4H, m) 7.08-7.18 (3H, m) 7.53-7.70(3H, mk) 7.81-7.92(2H, m) 7.94(1H, d J=7.59Hz)
15	457	—CH2O—	458	4	FAB-MS: (m/z) 736(M+) 552 246 1H NMR(CDCl3) 1.31(10H, m) 2.74(2H, m) 3.14(3H, m) 4.41(2H, s) 5.35(2H, s) 5.25(1H, br S) 6.81-6.92(4H, m) 7.14(1H, t J=7.92 Hz) 7.51-7.81(7H, m) 7.90(1H, m)
16	459	—CH2O—	460	4	FAB-MS: (m/z) 688(M+) 504 1H NMR(CDCl3) 1.24-1.33(10H, m) 2.73(2H, m) 3.10-3.23(3H, m) 3.84(3H, s) 4.39(2H, s) 4.64(1H, br s) 4.92(1H, br s) 5.36(2H, s) 6.82-6.94(6H, m) 7.15(1H, t J=7.92Hz) 7.53-7.74(5H, m) 7.95(1H, d J=7.59Hz)
17	461	—CH2O—	462	4	FAB-MS: (m/z) 672(M+) 488 334 246 1H NMR(CDCl3) 1.09-1.33(10H, m) 2.39(3H, s) 2.72(2H, m) 3.11-3.22(3H, m) 4.40(1H, br s) 4.97(1H, br s) 5.36(2H, s) 5.59(1H, br s) 6.82-6.93(4H, m) 7.14(1H, t J=7.92 Hz) 7.25(2H, d J=8.24Hz) 7.52-7.68 (4H, m) 7.94(1H, d J=7.26Hz)
18	463	—CH2O—	464	4	FAB-MS: (m/z) 658(M+) 518 474 1H NMR(CDCl3) 1.25-1.33(10H, m) 2.76(2H, m) 3.11-3.18 (3H, s) 4.40(2H, s) 5.13(1H, br s) 5.34(2H, s) 6.82-6.93(4H, m) 7.15(1H, t J=7.92Hz) 7.43-7.67(6H, m) 7.79(2H, d J=6.93Hz) 7.93-1H, d J=7.59Hz)
19	465	—CH2O—	466	4	FAB-MS: (m/z) 726(M+) 542 1H NMR(CDCl3) 1.25-1.33(4H, m) 2.72(2H, br s) 3.17 (2H, m) 4.39(2H, s) 5.33(2H, s) 6.82-6.91(3H, m) 7.16(1H, m) 7.30-7.58(10H, m) 7.69(2H, dd J=6.75 1.8Hz) 7.83-7.87(3H, m)
20	467	—CH2O—	468	4	FAB-MS: (m/z) 690(M+) 504 1H NMR(CDCl3) 0.85-0.93(4H, m) 1.13(4H, d J=6.26Hz) 2.05(1H, br s) 2.68(2H, br s) 3.13 (2H, br s) 4.38(2H, s) 5.23(2H, s) 6.70-6.90(3H, m) 7.13(1H, br s) 7.30-7.90(8H, m)
21	469	—CH2O—	470	4	FAB-MS: (m/z) 674(M+) 490 353 244 1H NMR(CDCl3) 0.82-0.99(4H, m) 1.13(4H, d J=6.26Hz) 2.08(1H, m) 2.75(2H, br s) 3.12(2H, m) 4.40(2H, s) 5.23(1H, br s) 6.81-6.89(4H, m) 7.07-7.17(3H, m) 7.51-7.66(3H, m) 7.77—7.82(2H, m) 7.90(1H, d J=7.26Hz)
22	471	—CH2O—	472	4	FAB-MS: (m/z) 736(M++1) 550 244 246 1H NMR(CDCl3) 0.80-0.95(4H, m) 1.18-1.23(4H, m) 2.23 (1H, m) 2.62(2H, br s) 3.06(2H, br s) 4.33(2H, s) 5.17(2H, s) 6.88(4H, br s) 7.12(1H, m) 7.26-7.47(6H, m) 7.765 (2H, d J=8.58Hz) 7.63(1H, d J=7.92 Hz)
23	473	—CH2O—	474	4	FAB-MS: (M/Z) 656(M+) 472 332 1H NMR(CDCl3) 0.86-0.96(4H, m) 1.25(4H, m) 2.09(3H, m) 2.76(2H, br s) 3.15(2H, br s) 4.3 9(2H, s) 5.29(2H, s) 6.83-6.90(4H, m) 7.14(1H, m) 7.46-7.66(6H, m) 7.80 (2H, d J=7.26Hz) 7.93(1H, d J=7.26Hz)
24	475	—CH2O—	476	4	FAB-MS(m/z) 670(M+) 486 349 244 1H NMR(CDCl3) 0.81-0.94(4H, m) 1.24-1.32(4H, m) 2.02-2.12(1H, m) 2.37(3H, s) 2.73(2H, br s) 3.15(2H, m) 4.39(2H, s) 5.25(2H, s) 6.82-6.87(4H, m) 7.11-7.26(4H, m) 7.47-7.67(5H, m) 7.87(1H, d J=7.26 Hz)
25	477	—CH2O—	478	4	FAB-MS: (m/z) 686(M+) 1H NMR(CDCl3) 0.84-0.99(4H, m) 1.25-1.36(4H, m) 2.09 (1H, m) 2.74(2H, br s) 3.15(2H, d J=6.93Hz) 3.84(3H, s) 4.39(2H, s) 5.01 (1H, br s) 5.29(2H, s) 6.82-6.94(6H m) 7.15(1H, t J=7.92Hz) 7.52-7.75(5H, m) 7.93(1H, d J=7.59Hz)
26	479	—CH2O—	480	3	FAB-MS: (m/z) 676(M+) 493 318 244 1H NMR(CDCl3) 0.82-0.99(4H, m) 1.40(2H, d J=5.94Hz) 2.08(1H, m) 2.77(2H, br s) 3.26(2H, m) 4.38(2H, s) 5.28(1H, s) 5.66(1H, br s) 6.80-6.88(4H, m) 7.15(1H, m) 7.39 (2H, dd J=6.92 1.98Hz) 7.52-7.63 (3H, m) 7.71(2H, dd J=6.93 1.98Hz) 7.86 (1H, d J=7.26Hz)
27	481	—CH2O—	482	2	FAB-MS: (m/z) 662(M+) 478 341 1H NMR(CDCl3) 0.82-0.98(4H, m) 2.09(1H, m) 2.73(2H, br s) 3.30(2H, t J=5.75Hz) 4.35(2H, s) 5.36(2H, s) 6.02(1H, br s) 6.78-6.91(4H, m) 7.13(1H, t J=7.76Hz) 7.33 (2H, d J=8.58Hz) 7.53-7.67(5H, m) 7.96 (1H, d J=7.59Hz)
28	483	—CH2O—	484	2	FAB-MS: (m/z) 646(M+) 1H NMR(CDCl3) 0.82-0.97(4H, m) 2.09(1H, m) 2.74(2H, br s) 3.30(2H, t J=5.78Hz) 4.35(2H, s) 5.34(2H, s) 5.94(1H, br s) 6.78-6.89(4H, m) 7.00-7.16(3H, m) 7.53-7.65 (5H, m) 7.95(1H, d J=7.92Hz)
29	485	—CH2CH2—	486	4	FAB-MS: (m/z) 702(M+) 518 256 244 1H NMR(CDCl3) 1.20-1.40(4H, m) 1.82-2.41(6H, m) 2.75 (2H, br s) 3.01(2H, t) 3.14(2H, t) 3.31(2H, t) 3.66(1H, quint) 4.39(2H, s) 5.38(1H, br s) 6.77(1H, s) 7.02-7.17(4H, m) 7.50-7.65(3H, m) 7.71(2H, d J=8.58Hz) 7.38(2H, d J=8.57Hz) 7.90(1H, d J=7.26Hz)
30	487	—CH2CH2—	488	4	FAB-MS: (m/z) 748(M+) 670 564 1H NMR(CDCl3) 1.20-1.40(4H, m) 1.81-2.41(6H, m) 2.73 (2H, br s) 3.03(2H, m) 3.13(2H, m) 3.32(2H, m) 3.66(1H, quint) 4.39(2H, s) 5.38(1H, br s) 6.77(1H, s) 7.02-7.16(5H, m) 7.52-7.65(6H, m) 7.89(1H, d J=7.59Hz)
31	489	—CH2CH2—	490	4	FAB-MS: (m/z) 669(M+) 1H NMR(CDCl3) 0.82-0.99(4H, m) 1.40(2H, d J=5.94Hz) 2.08(1H, m) 2.77(2H, br s) 3.26(2H, m) 4.38(2H, s) 5.28(1H, s) 5.66(1H, br s) 6.80-6.88(4H, m) 7.15(1H, m) 7.39 (2H, dd J=6.92 19.98Hz) 7.52-7.63 (3H, m) 7.71(2H, dd J=6.93 1.98Hz) 7.86(1H d J=7.26Hz)
32	491	—CH2CH2—	492	4	FAB-MS: (m/z) 683(M+) 1H NMR(CDCl3) 1.20-1.40(4H, m) 1.82-2.37(6H, m) 2.39 (3H, m) 2.72(2H, m) 3.01(2H, t) 3.13 (2H, t) 3.33(2H, t) 3.67(1H, quint) 4.38(2H, s) 6.76(1H, d J=0.66Hz) 7.04-7.26(7H, m) 7.51-7.68(4H, m) 7.92 (1H, d J=7.59Hz)
33	493	—CH2CH2—	494	4	FAB-MS: (m/z) 674(M+) 1H NMR(CDCl3) 1.28(10H, m) 2.70-2.78(2H, m) 2.99-3.66(4H, m) 3.34(2H, m) 4.39(2H, s) 5.21(1H, br t) 6.74(1H, s) 7.16(6H, m) .52-7.67(3H, m) 7.77-7.82(2H, m) 7.91(1H, d J=7.59Hz)
34	495	—CH2CH2—	496	4	FAB-MS: (m/z) 671(M+) 1H NMR(CDCl3) 1.28(10H, m) 2.39(3H, s) 2.68(2H, m) 2.99-3.19(4H, m) 3.34(2H, m) 4.38(2H, s) 5.00(1H, br t) 6.73(1H, s) 7.03-7.26(6H, m) 7.51-7.68(5H, m) 7.92(1H, d J=7.26Hz)
35	497	498	499	4	FAB-MS(m/z) 674(M+) 645 1H NMR(CDCl3) 1.23-1.35(4H, m) 2.65(2H, br s) 3.20 (2H, br s) 4.52(2H, s) 5.77(1H, br s) 6.81-7.05(3H, m) 7.15-7.17(2H, m) 7.39-7.95(13H, m) 8.25(2H, m)
36	500	501	502	4	FAB-MS: (m/z) 734(M+) 550 244 1H NMR(CDCl3) 1.22-1.33(4H, m) 2.63(2H, br s) 3.19 (2H, br s) 4.52(2H, s) 5.96(1H, br s) 7.05-7.16(2H, m) 7.38-7.93(16H, m) 8.25(2H, m)
37	503	504	505	4	FAB-MS: (m/z) 686(M+) 645 1H NMR(CDCl3) 1.22-1.35(4H, m) 2.66(2H, br s) 3.21 (2H, br s) 3.77(3H, s) 4.52(2H, s) 5.29 (1H, br s) 6.82(2H,m) 5.29(1H, br s) 6.82(2H, m) 7.19(2H, d J=4.62Hz) 7.40-7.94(14H, m) 8.25(2H, m)
38	506	507	508	4	FAB-MS: (m/z) 670(M+) 645 553 1H NMR(CDCl3) 1.19-1.32(4H, m) 2.31(3H, s) 2.63(2H, br s) 3.19(2H, br s) 4.50(2H, s) 5.44 (1H, br s) 7.26(4H, m) 7.39-7.78(13H, m) 7.87(1H, d J=7.92Hz) 8.24(2H, m)
39	509	510	511	4	FAB-MS: (m/z) 656(M+) 1H NMR(CDCl3) 1.20-1.32(4H, m) 2.64(2H, br s) 3.18 (2H, br s) 4.51(2H, s) 5.58(1H, br s) 7.12-7.92(19H, m) 8.24(2H, m)
40	512	513	514	3	FAB-MS: (m/z) 676(M+) 1H NMR(CDCl3) 1.25-1.33(2H, m) 2.63-2.70(2H, m) 3.10-3.21(4H, m) 3.50(2H, t J=7.92Hz) 4.34(2H, s) 6.17(1H, br s) 6.99-7.14 (3H, m) 7.26((4H, m) 7.39-7.78(13H, m) 7.87(1H, d J=7.92Hz) 8.24(2H, m)
41	515	516	517	2	FAB-MS: (m/z) 663(M+) 608 476 244 1H NMR(CDCl3) 2.75(2H, s) 3.30(2H, s) 4.48(2H, s) 5.98 (1H, br s) 7.13(2H, m) 7.43-7.93 (14H, m) 8.30(1H, d J=8.57Hz) 8.35(1H, d J=8.91Hz)
42	518	519	520	2	FAB-MS: (m/z) 708(M+) 522 244 1H NMR(CDCl3) 2.73(2H, s) 3.30(2H, s) 4.48(2H, s) 7.12(2H, s) 7.39—7.91(16H, m) 8.27(1H, d J=8.58Hz) 8.33(1H, d J=8.91Hz)
43	521	522	523	2	FAB-MS: (m/z) 646(M+) 460 244 1H NMR(CDCl3) 2.75(2H, s) 3.31(2H, s) 4.48(2H, s) 6.96(2H, s) 7.11(2H, d J=4.29Hz) 7.42-7.92(14H, m) 8.23(1H, d J=8.58Hz) 8.33(1H, d J=8.91Hz)
44	524	525	526	2	FAB-MS: (m/z) 628(M+) 483 1H NMR(CDCl3) 2.87(2H, dd J=12.2 5.94Hz) 3.37(2H, m) 4.00(3H, s) 4.45(2H, s) 7.22-7.75 (17H, m) 7.80(1H, d J=7.92Hz) 7.95(1H, dd J=6.1 1.5Hz) 8.09Hz(1H, d J=8.25 Hz) 8.16(1H, d J=8.9Hz)
45	527	528	529	4	FAB-MS: (m/z) 724(M+) 675 1H NMR(CDCl3) 1.21-1.40(4H, m) 2.68-2.72(2H, m) 3.22 (2H, br t J=6.93Hz) 4.50(2H, s) 5.59-5.64(1H, m) 7.18(2H, d J=4.95Hz) 7.30-7.72(14H, m) 7.89(1H, d J=7.59Hz) 8.13-8.17(2H, m)
46	530	531	532	4	FAB-MS(m/z) 708(M+) 1H NMR(CDCl3) 1.22-1.42(4H, m) 2.68-2.72(2H, m) 3.21 (2H, br t) 4.50(2H, s) 5.54-5.60(1H, m) 7.00-7.06(2H, m) 7.15-7.17(2H, m) 7.41(2H, dd J=1.98 8.58Hz) 7.47-7.78 (10H, m) 7.88(1H, d J=7.26Hz) 8.13-8.17(2H, m)
47	533	534	535	4	FAB-MS: (m/z) 768(M+) 1H NMR(CDCl3) 1.21-1.40(4H, m) 2.67-2.75(2H, m) 3.21 (2H, br t J=6.60Hz) 4.50(2H, s) 5.58-5.63(1H, m) 7.70(2H, J=4.62Hz) 7.38-7.66(12H, m) 7.71(2H, d J=8.9Hz) 7.88(1H, d J=7.26Hz) 8.13-8.17(2H, m)
48	536	537	538	4	FAB-MS: (m/z) 720(M+) 1H NMR(CDCl3) 1.21-1.41(4H, m) 2.67-2.74(2H, m) 3.23 (2H, br t J=6.93Hz) 3.78(3H, s) 4.50 (2H, s) 5.10-5.15(1H, m) 6.86(2H, d J=8.91Hz) 7.19-7.21(2H, m) 7.44(2H dd J=1.81 8.75Hz) 7.50-7.73(10H, m) 7.91(1H, d J=7.92Hz) 8.08-8.17(2H, m)
49	539	540	541	4	FAB-MS: (m/z) 704(M+) 1.20-1.41(4H, m) 2.32(3H, s) 2.67-2.70 (2H, m) 3.21(2H, br t J=6.93Hz) 4.49 (2H, s) 5.22-5.29(1H, m) 7.12-7.21 (4H, m) 7.41(2H, dd J=1.98 8.58Hz) 7.47-7.72(10H, m) 7.89(1H, d J=7.92Hz) 8.07-8.16(2H, m)
50	542	543	544	4	FAB-MS: (m/z) 704(M+) 1.20-1.41(4H, m) 2.32(3H, s) 2.67-2.75(2H, m) 3.21 (2H, br t H=6.93Hz) 4.50(2H, s) 5.30-5.37(1H, m) 7.06(1H, d J=6.27Hz) 7.18(2H, d J=4.62Hz) 7.36-7.75(14H, m) 7.90(1H, d J=7.92Hz) 8.13-8.16(2H, m)
51	545	546	547	3	FAB-MS: (m/z) 710(M+) 1H NMR(CDCl3) 1.46-1.53(2H, m) 2.51-2.60(2H, m) 3.22 (2H, br t J=7.09Hz) 4.48(2H, s) 7.25 (1H, d J=7.26Hz) 7.36-7.43(2H, m) 7.58-7.76(10H, m) 7.82(1H, d J=16.2Hz) 7.93(2H, d J=8.58Hz) 7.98-8.06(2H, m) 8.41(1H, d J=8.91Hz)
52	548	549	550	2	FAB-MS: (m/z) 696(M+) 1H NMR(CDCl3) 2.75-2.79(2H, m) 3.30-3.35(2H, m) 4.48 (2H, s) 7.14(2H, d J=4.29Hz) 7.25-7.29(2H, m) 7.42-7.64(10H, m) 7.70-7.77(2H, m) 7.90(1H, d J=7.59Hz) 8.22 (1H, d J=8.9Hz)
53	551	—CH2O—	552	4	FAB-MS: (m/z) 678(M+) 494 248 1H NMR(CDCl3) 1.10-1.28(4H, m) 2.62-2.68(2H, m) 3.07 (2H, br t J=6.60Hz) 4.37(2H, s) 5.36 (1H, br s) 5.42(1H, s) 6.78(1H, d J=7.58Hz) 6.91(1H, dd J=8.25Hz) 7.00-7.14(4H, m) 7.45-7.76(8H, m) 7.85(2H, t J=9.06Hz) 8.22(2H, t J=7.43Hz)
54	553	—CH2O—	554	4	FAB-MS: (m/z) 737(M+) 1H NMR(CDCl3) 1.08-1.28(4H, m) 2.58-2.66(2H, m) 3.00-3.10(2H, m) 4.34(2H, s) 5.33(2H, s) 6.77(1H, d J=7.25Hz) 6.88(1H, dd J=8.25Hz) 6.94(1H, s) 7.10(1H, t) J=7.75Hz) 7.30-7.80(12H, m) 8.12(1H, d J=8.92Hz) 8.17(1H, d J=8.25Hz)
55	555	—CH2O—	556	4	FAB-MS: (m/z) 690(M+) 1H NMR(CDCl3) 1.08-1.18(2H, m) 1.20-1.31(2H, m) 2.60-2.65(2H, m) 3.03(2H t J=6.95 Hz) 3.81(3H, s) 4.36(2H, s) 4.86 (1H, br s) 5.46(2H, s) 6.78(1H, d J=7.58Hz) 6.87-6.93(3H, m) 7.02(1H, s) 7.12(1H, t J=7.75Hz) 7.49-7.61(3H, m) 7.67-7.79(5H, m) 7.84(1H, d J=7.91Hz) 7.93(1H, d J=7.59 Hz) 8.24-8.29(2H, m)
56	557	—CH2O—	558	4	FAB-MS: (m/z) 674(M+) 1H NMR(CDCl3) 1.07-1.16(2H, m) 1.18-1.29(2H, m) 2.36(3H, s) 2.59-2.65(3H, m) 3.04(2H, t J=6.77Hz) 4.35(3H, s) 4.95-5.02(1H, m) 5.44(2H, s) 6.78(1H, d J=7.58Hz) 6.91(1H, dd J=7.92Hz) 7.01(1H, s) 7.11(1H, t J=7.76Hz) 7.19(2H, d J=7.92 Hz) 7.47-7.78(8H, m) 7.83(1H, d J=7.91Hz) 7.91(1H, d J=7.59Hz) 8.24(2H, d J=8.58Hz)
57	559	—CH2O—	560	4	FAB-MS: (m/z) 660(M+) 1H NMR(CDCl3) 1.05-1.15(2H, m) 1.17-1.29(2H, m) 2.60-2.67(2H, m) 3.02(2H, t J=6.93Hz) 4.35(2H, s) 4.94-4.98(1H, m) 5.50(2H, s) 6.78(1H, d J=7.58Hz) 6.93(1H, dd J=7.58Hz) 7.05(1H, s) 7.12(1H, t J=7.92Hz) 7.40-7.62(6H, m) 7.69-7.80 (5H, m) 7.85(1H, d J=7.92Hz) 7.95(1H, d J=7.92Hz) 8.27-8.32(2H, m)
58	561	—CH2O—	562	3	FAB-MS: (m/z) 674(M+) 539 1H NMR(CDCl3) 1.25-1.37(2H, m) 2.58-2.67(2H, m) 3.14(2H, t J=6.43Hz) 4.34(2H, s) 5.52 (2H, s) 6.55-6.63(1H, m) 6.77(1H, d J=7.58Hz) 6.93(1H, d J=7.91Hz) 7.01 (1H, m) 7.12(1H, t J=7.92Hz) 7.32(2H, d J=8.58Hz) 7.51-7.67(6H, m) 7.71-7.90(4H, m) 8.30(2H, d J=8.57Hz)
59	563	—CH2O—	564	2	FAB-MS: (m/z) 666(M+) 1H NMR(CDCl3) 2.66(2H, br s) 3.21(2H, br s) 4.32(2H, br s) 5.54(2H, br s) 6.75(1H, d J=6.93Hz) 6.91(1H, d J=8.58Hz) 7.00(21H, s) 7.10(1H, t J=7.75Hz) 7.24-7.27 (2H, m) 7.47-7.61(6H, m) 7.75-7.93 (4H, m) 8.26-8.43(2H, m)
60	565	—CH2O—	566	2	FAB-MS: (m/z) 650(M+) 1H NMR(CDCl3) 2.65-2.70(2H, m) 3.23(2H, br t) 4.33 (2H, s) 5.50(2H, s) 6.76(1H, d J=7.59 Hz) 6.89-7.00(4H, m) 7.10(1H, t J=7.75Hz) 7.42-7.62(6H, m) 7.73-7.92(4H, m) 8.23-8.32(2H, m)
61	567	—CH2O—	568	2	FAB-MS: (m/z) 710(M+) 1H NMR(CDCl3) 2.64-2.70(2H, m) 3.21(2H, t J=5.61Hz) 4.32(2H, s) 5.57(2H, s) 6.75(1H, d J=7.26Hz) 6.92(1H, dd J=2.31 8.24Hz) 7.01(1H, s) 7.11(1H, t J=7.92Hz) 7.46(4H, m) 7.49-7.65(4H, m) 7.77-7.95 (4H, m) 8.28-8.36(2H, m)
62	569	—CH2O—	570	2	FAB-MS: (m/z) 633(M+) 1H NMR(CDCl3) 2.65-2.70(2H, m) 3.18(2H, br t J=5.61 Hz) 4.29(2H, s 5.59(2H, s) 6.73(1H, d J=7.59Hz) 6.96(1H, dd J=1.98 8.25 Hz) 7.00(1H, s) 7.09(1H, t J=7.92Hz) 7.34(2H, t J=7.43Hz) 7.42-7.71(7H, m) 7.76-7.84(2H, m) 7.88(1H, d J=7.92 Hz) 7.98(1H, d J=7.59Hz) 8.33(1H, d J=8.91Hz) 8.34(1H, d J=8.25Hz)
63	571	—CH2O—	572	5	FAB-MS: (m/z) 721(M+) 1H NMR(CDCl3) 0.89-0.99(2H, m) 1.11-1.27(4H, m) 2.67-2.74(2H, m) 3.04(2H, t J=6.93Hz) 4.38(2H, s) 5.42(2H, s) 6.79(1H, d J=7.26Hz) 6.91(1H, dd J=1.65 8.25Hz) 7.02(1H, s) 7.13(1H, t J=7.92Hz)( 7.36(2H, d J=8.58Hz) 7.47-7.78(8H, m) 7.84(1H, d J=8.24Hz) 7.91(1H, d J=7.59 Hz) 8.24(2H, d J=8.58Hz)
64	573	—CH2O—	574	2	FAB-MS: (m/z) 700(M+) 1H NMR(CDCl3) 2.70-2.79(2H, m) 3.26(2H, t J=5.78Hz) 4.34(2H, s) 5.47(2H, s) 5.99-6.08 (1H, m) 6.78(1H, d J=7.58Hz) 6.91(1H, dd J=1.98 8.25Hz) 6.98(1H, s) 7.12 (1H, t J=7.92Hz) 7.28(2H, d J=8.58Hz) 7.50-7.81(8H, m) 7.93(1H, d J=7.26Hz) 8.21(1H, d J=1.98Hz) 8.27(1H, d J=8.58Hz)
65	575	—CH2O—	576	4	FAB-MS: (m/z) 730(M+) 1H NMR(CDCl3) 1.18-1.36(4H, m) 2.68-2.74(2H, m) 3.13(2H, t J=6.76Hz) 4.39(2H, s) 6.80 (1H, d J=7.59Hz) 6.90(1H, dd J=7.92Hz) 6.97(1H, m) 7.14(1H t J=7.92Hz) 7.35(2H, d J=8.58Hz) 7.48-7.70(7H, m) 7.76(1H, d J=8.58Hz) 7.88(1H, d J=7.26 Hz) 8.14(1H, d J=1.65Hz) 8.20(1H, d J=8.58Hz)
66	577	—CH2CH2—	578	4	FAB-MS: (m/z) 692(M+) 600 508 246 1H NMR(CDCl3) 1.10-1.30(4H, m) 3.60-2.68(2H, m) 3.05-3.13(4H, m) 3.44(2H, t J=7.92Hz) 4.38(2H, s) 5.74-5.81(1H, m) 7.01-7.11(3H, m) 7.26-7.37(4H, m) 7.46(1H, t d J=1.32-7.5Hz) 7.53-7.68(5H, m) 7.72-7.88(3H, m) 8.22(1H, d J=8.25Hz) 8.34(1H, d J=8.58Hz)
67	579	—CH2CH2—	580	4	FAB-MS: (m/z) 676(M+) 492 246 1H NMR(CDCl3) 1.14-1.30(4H, m) 2.59-2.67(2H, m) 3.08-3.13(4H, m) 3.44(2H, t J=7.92Hz) 4.38(2H, s) 5.60-5.70(1H, m) 6.99-7.13(5H, m) 7.26(1H, s) 7.35(1H, d J=8.58Hz) 7.43-7.64(4H, m) 7.71-7.88(5H, m) 8.21(1H, d J=8.58Hz) 8.34(1H, d J=8.58Hz)
68	581	—CH2CH2—	582	4	MS: (m/z) 672(M+) 488 246 1H NMR(CDCl3) 1.10-1.30(4H, m) 2.34(3H, s) 2.59-2.65(2H, m) 3.04-3.12(4H, m) 3.42(2H, t J=7.75Hz) 4.37(2H, s) 5.25-5.32(1H, m) 7.00-7.12(3H, s) 7.17(2H, d J=7.92Hz) 7.25(1H, d J=7.59Hz) 7.32(1H, d J=8.58Hz) 7.42-7.64(6H, m) 7.71-7.81(2H, m) 7.87(1H, d J=7.26Hz) 8.18 1H, d J=8.58Hz) 8.34(1H, d J=8.25Hz)
69	583	—CH2CH2—	584	4	FAB-MS: (m/z) 688(M+) 596 504 246 1H NMR(CDCl3) 1.09-1.33(4H, m) 2.59-2.68(2H, m) 3.04-3.12(4H, m) 3.42(2H, t J=7.75Hz) 3.79(3H, s) 4.37(2H, s) 6.85(2H, d J=8.91Hz) 7.00-7.12(3H, m) 7.25(1H, d J=6.27Hz) 7.32(1H, d J=8.58Hz) 7.42-7.58(3H, m) 7.62-7.81(5H, m) 7.88 (1H, d J=7.26Hz) 8.18(1H, d J=8.58Hz) 8.24(1H, d J=8.58Hz)
70	585	—CH2CH2—	586	4	FAB-MS: (m/z) 736(M+) 552 246 1H NMR(CDCl3) 1.11-1.29(4H, m) 2.58-2.64(2H, m) 3.07-3.12(4H, m) 3.43(2H, t J=7.75Hz) 4.37(2H, s) 5.78-5.82(1H, m) 7.01-7.13(3H, m) 7.25(1H, d J=2.97Hz) 7.34 (1H, d J=8.54Hz) 7.42-7.47(3H, m) 7.512-7.62(5H, m) 7.71-7.87(3H, m) 8.21 (1H, d J=8.58Hz) 8.33(1H, d J=8.58Hz)
71	587	—CH2CH2—	588	2	FAB-MS: (m/z) 664(M+) 480 246 1H NMR(CDCl3) 2.57-2.69(2H, m) 2.99-3.07(2H, m) 3.10-3.18(2H, m) 3.18-3.27(2H, m) 4.41 (2H, m) 7.00-7.04(1H, m) 7.09(1H, br s) 7.18-7.21(2H, m) 7.41(1H, d J=8.25 Hz) 7.52-7.79(9H, m) 7.85-8.00(3H, m) 8.25(1H, d J=8.58Hz)
72	589	—CH2CH2—	590	3	FAB-MS: (m/z) 578(M+) 1H NMR(CDCl3) 1.25-1.33(2H, m) 2.63-2.70(2H, m) 3.10-3.21(4H, m) 3.50(2H, t J=7.92Hz) 4.34(2H, s) 6.17-6.24(1H, m) 6.99-7.14(3H, m) 7.26-7.33(3H, m) 7.40(1H, d J=8.58Hz) 7.48(1H, td J=7.59 1.54Hz) 7.56-7.67(5H, m) 7.79-7.88(3H, m) 8.27(1H, d J=8.58Hz) 8.42(1H, d J=8.58Hz)
73	591	—CH2CH2—	592	5	FAB-MS: (m/z) 706(M+) 672 1H NMR(CDCl3) 0.89-1.01(2H, m) 1.09-1.25(4H, m) 2.64-2.72(2H, m) 3.02-3.14(4H, m) 3.47 (2H, t J=7.75Hz) 4.38(2H, s) 5.63-5.70(1H, m) 7.00-7.13(3H, m) 7.26-7.29 (1H, m) 7.36(2H, d J=7.26Hz) 7.44-7.83(9H, m) 7.91(1H, d J=7.26Hz) 8.23 (1H, d J=8.58Hz) 8.41(1H, d J=8.58Hz)
74	593	—CH2CH2—	594	4	FAB-MS: (m/z) 726(M+) 542 383 280 1H NMR(CDCl3) 1.18-1.35(4H, m) 2.69(2H, br d J=4.62 Hz) 3.05-3.13(4H, m) 3.35(2H, t J=7.67Hz) 4.37(1H, s) 5.42-5.50(1H, m) 7.01-7.15(3H, m) 7.20(1H, m) 7.28-7.36(3H, m) 7.44-7.74(7H, m) 7.87(1H, d J=7.59Hz) 8.11(1H, d J=8.58Hz) 8.21 (1H, d J=1.32Hz)
75	595	—CH2CH2—	596	4	FAB-MS: (m/z) 710(M+) 526 228 1H NMR(CDCl3) 1.19-1.37(4H, m) 2.70(2H, br d J=4.95 Hz) 3.05-3.15(4H, m) 3.36(2H, br t J=7.76Hz) 4.38(2H, s) 5.35-5.42(1H, m) 7.02-7.15(5H, m) 7.21(1H, s) 7.23 1H, d J=8.25Hz) 7.44-7.78(7H, m) 7.87 (1H, d J=7.59Hz) 8.12(1H, d J=8.25Hz) 8.21(1H, s)
76	597	—CH2CH2—	598	4	FAB-MS: (m/z) 706(M+) 614 522 349 1H NMR(CDCl3) 1.15-1.38(4H, m) 2.37(3H, s) 2.67-2.73(2H, m) 3.05-3.13(4H, m) 3.34(2H, t 7.92Hz) 4.37(2H, s) 5.05-5.13(1H, m) 7.01-7.14(3H, m) 7.20-7.30(4H, m) 7.44-7.69(6H, m) 7.72(1H, d J=8.58Hz) 7.90(1H, d J=7.92Hz) 8.05(1H, d J=8.25Hz) 8.20(1H, d J=1.98Hz)
77	599	—CH2CH2—	600	4	FAB-MS: (m/z) 722(M+) 688 538 1H NMR(CDCl3) 1.15-1.39(4H, m) 2.63-2.71(2H, m) 3.04-3.13(4H, m) 3.34(2H, t J=7.92Hz) 3.80(3H, s) 4.37(2H, s) 6.88(2H, d J=8.91Hz) 7.01-7.14(3H, m) 7.19(1H, s) 7.28(1H, d J=8.58Hz) 7.43-7.73(7H, m) 7.88(1H, d J=7.59Hz) 8.09(1H, d J=8.58Hz) 8.21(1H, d J=1.65Hz)
78	601	—CH2CH2—	602	4	FAB-MS: (m/z) 770(M+) 1H NMR(CDCl3) 1.12-1.32(4H, m) 2.65-2.72(2H, m) 3.05-3.15(4H, m) 3.35(2H, t J=7.92Hz) 4.38(2H, s) 7.02-7.15(3H, m) 7.20(1H, s) 7.30(1H, d J=8.58Hz) 7.45-7.53 (4H, m) 7.56-7.66(4H, m) 7.73(1H, d J=8.58Hz) 7.86(1H, d J=7.26Hz) 8.12 (1H, d J=8.25Hz) 8.21(1H, d J=1.98Hz
79	603	—CH2CH2—	604	2	FAB-MS: (m/z) 699(M+) 1H NMR(CDCl3) 2.70-2.77(2H, m) 3.10(2H, t J=7.75Hz) 3.23-3.28(2H, m) 3.43(2H, t J=7.91 Hz) 4.35(2H, s) 6.99-7.13(3H, m) 7.26-7.29(3H, m) 7.36(1H, d J=8.58Hz) 7.48-7.54(4H, m) 7.57-7.64(2H, m) 7.76 (1H, d J=8.91Hz) 7.91(1H, d J=7.92Hz) 8.18(1H, d J=8.58Hz) 8.26(1H, d J=1.65Hz)
80	605	—CH2CH2—	606	3	FAB-MS: (m/z) 712(M+) 528 1H NMR(CDCl3) 1.28-1.38(2H, m) 2.68-2.75(2H, m) 3.09(2H, t J=7.76Hz) 3.20-3.25(2H, m) 3.39(2H, t J=7.92Hz) 4.35(2H, s) 5.86 (1H, br t) 7.00-7.15(3H, m) 7.25-7.26 (2H, m) 7.33(2H, d J=8.58Hz) 7.48-7.56(2H, m) 7.59-7.68(4H, m) 7.76(1H, d J=8.91Hz) 7.86((1H, d J=7.92Hz) 8.17(1H, d J=8.58Hz) 8.27(1H, d)
81	607	—CH2O—	608	5	FAB-MS: (m/z) 703(M+) 669 519 1H NMR(CDCl3) 1.11-1.19(2H, m) 1.25-1.36(2H, m) 1.47-1.58(2H, m) 1.85-2.13(2H, m) 2.17-2.31(2H, m) 2.34-2.45(2H, m) 2.87-2.96(2H, m) 3.10(2H, t J=7.26Hz) 3.74 (1H, quint J=8.49Hz) 4.39(2H, s) 5.38 (2H, s) 6.80-6.88(2H, m) 6.94-6.96 (2H, m) 7.13(1H, t J=7.92Hz) 7.50-7.70 (5H, m) 7.79(2H, d J=8.58Hz) 7.96(1H, d J=7.59Hz)
82	609	—CH2O—	610	5	FAB-MS: (m/z) 689(M+) 655 505 244 1H NMR(CDCl3) 0.83-0.91(2H, m) 0.91-1.00(2H, m) 1.14-1.22(2H, m) 1.26-1.38(2H, m) 1.51-1.62(2H, m) 2.07-2.17(1H, m) 2.91-2.97(2H, m) 3.12(2H, t J=7.26Hz) 4.39 (2H, s) 5.30(2H, s) 6.81-6.88(3H, m) 6.93(1H, br s) 7.15(1H, t J=7.92Hz) 7.52(2H, d J=8.57Hz) 7.56-7.71(3H, m_ 7.81(2H, d J=8.58Hz) 7.95(1H, d J=7.59Hz)
83	611	—CH2O—	612	5	FAB-MS: (m/z) 691(M+) 657 507 473 1H NMR(CDCl3) 1.11-1.19(2H, m) 1.26-1.33(8H, m) 1.47-1.59(2H, m) 2.88-2.94(2H, m) 3.08-3.13(2H, m) 3.19(1H, quint J=6.93Hz) 4.39(2H, s) 5.38(2H, s) 6.81-6.88 (2H, s) 6.93(1H, s) 6.95(1H, br s) 7.13 (1H, t J=7.92Hz) 7.52(2H, d J=8.58Hz) 7.56-7.70(3H, m) 7.79(2H, d J=8.58 Hz) 7.96(1H, d J=7.59Hz)
84	613	614	615	5	FAB-MS: (m/z) 689(M+) 244 1H NMR(CDCl3) 1.18-1.11(2H, m) 1.22-1.39(2H, m) 1.42-1.50(2H, m) 2.78-2.84(2H, m) 3.20 (2H, br t J=6.78Hz) 4.50(2H, s) 7.14-7.16(2H, s) 7.42-7.82(15H, m) 7.91(1H, d J=7.26Hz) 8.22-8.27(2H, m)
85	616	617	618	5	FAB-MS: (m/z) 723(M+) 1H NMR(CDCl3) 1.17-1.23(2H, m) 1.24-1.37(2H, m) 1.42-1.55(2H, m) 2.82-2.87(2H, m) 3.21 (2H, br t J=6.93Hz) 4.50(2H, s) 7.17-7.22(2H, m) 7.42-7.88(14H, m) 7.91 (1H, d J=7.59Hz) 8.13-8.16(2H, m)
86	619	—CH2CH2—	620	5	FAB-MS: (m/z) 691(M+) 507 1H NMR(CDCl3) 1.05-1.15(2H, m) 1.21-1.32(2H, m) 1.41-1.51(2H, m) 2.81-2.88(2H, m) 3.01-3.18(4H, m) 3.37-3.45(2H, m) 4.37(2H, s) 6.97-7.07(3H, m) 7.26-7.31(2H, m) 7.47-7.61(5H, m) 7.67-7.82(5H, m) 7.92(1H, d J=7.26Hz) 8.16(1H, d J=8.25Hz) 8.36(1H, d J=8.25Hz)
87	621	—CH2CH2—	622	5	FAB-MS: (m/z) 725(M+) 1H NMR(CDCl3) 1.08-1.18(2H, m) 1.22-1.23(2H, m) 1.45-1.56(2H, m) 2.85-2.91(2H, m) 3.04-3.12(4H, m) 3.38(2H, t J=7.76Hz) 4.38(2H, s) 6.99-7.15(3H, m) 7.20-7.28 (2H, m) 7.44-7.68(5H, m) 7.68-7.83 (4H, m) 7.92(1H, d J=6.93Hz) 8.08(1H, d J=8.58Hz) 8.24(1H, d J=1.65Hz)
88	623	—CH2O—	624	5	FAB-MS: (m/z) 693(M+) 1H NMR(CDCl3) 0.95-1.06(2H, m) 1.16-1.27(2H, m) 1.37-1.49(2H, m) 2.81-2.86(2H, m) 3.01 (2H, t J=7.43Hz) 4.35(2H, s) 5.46(2H, s) 6.77(1H, d J=7.58Hz) 6.90(1H, dd J=1.82 8.08Hz) 7.03(1H, s) 7.11(1H, t J=7.76Hz) 7.47-7.64(5H, m) 7.69-7.80(5H, m) 7.85(1H, d J=7.91Hz) 7.96(1H, dd J=1.49 7.76Hz) 8.25-8.31 (2H, m)
89	625	—CH2O—	626	4	FAB-MS: (m/z) 694(M+) 510 248 1H NMR(CDCl3) 1.10-1.27(4H, m) 2.61-2.68(2H, m) 3.07 (2H, br t J=6.93Hz) 4.37(2H, s) 5.44 (2H, s) 6.78(1H, d J=7.25Hz) 6.91(1H, d J=8.24Hz) 7.00(1H, s) 7.09-7.15 (1H, m) 7.32 (2H, d J=8.91Hz) 7.46-6.78 (8H, m) 7.82-7.89(2H, m) 8.21-8.26(2H, m)
90	627	628	629	4	FAB-MS: (m/z) 690(M+) 506 244 1H NMR(CDCl3) 1.20-1.39(4H, m) 2.60-2.67(2H, m) 3.15-3.21(2H, m) 4.51(2H, s) 5.98-6.02(1H, br s) 7.03-7.17(2H, m) 7.25-7.31(2H, m) 7.36(1H, d J=7.26Hz) 7.43-7.79(12H, m) 7.86(1H, d J=7.59Hz) 8.23-8.30 (2H, m)

Example 12

[0119] Preparation of ethyl 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazoyl)methoxy]benzyl}}sulfamoylbenzoate (Compound No. 1c)

[0120] 2.15 g (3.11 mmol) of 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid (Compound No. 1) was mixed with 16 ml of 1,2-dichloroethane and 0.41 ml (4.7 mmol) of oxalyl chloride and stirred in the presence of a catalytic amount of N,N-dimethylmamide at room temperature. The reaction solution was evaporated in vacuo for removal of the solvent and stirred together with 12 ml of ethanol, 12 ml of 1,2-dichloroethane and 0.65 ml (4.66 mmol) of triethylamine at room temperature for 1 hour. The reaction solution was mixed with water and saturated aqueous sodium hydrogen carbonate for neutralization and then extracted with chloroform. The chloroform layer was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; n-hexane:ethyl acetate=3:1) to give 1.42 g of the title compound in a yield of 63.5%.

[0121] 1 H-NMR(CDCl3): 1.23-1.41 (13H, m) 2.82 (2H, m) 3.06-3.17 (3H, m) 4.38-4.45 (4H, m) 4.83 (1H, t) 5.26 (2H, s) 6.90 (4H, d J=0.66 Hz) 7.22 (1H, m) 7.45 (2H, d J=1.98 6.6 Hz) 7.51-7.65 (3H, m) 7.74 (2H, d J=1.98 6.6 Hz) 7.83 (1H, m)

[0122] Similarly, the compounds of Examples 13 and 14 were prepared.

Example 13

[0123] Preparation of ethyl 2-{N-[4-(4-methylbenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoate (Compound No. 5c)

[0124] 1 H-NMR(CDCl3): 1.22-1.41 (7H, m) 1.84-2.39 (6H, m) 2.41(3H, s) 2.80(2H, m) 3.16 (2H, m) 3.67 (1H, quint) 4.37-4.45 (4H, m) 4.61 (1H, t J=6.27 Hz) 5.27 (2H, s) 6.88-6.92 (4H, m) 7.22-7.29 (3H, m) 7.50-7.62 (3H, m) 7.68 (2H, d J=8.24 Hz) 7.82 (1h, d J=7.25 Hz)

Example 14

[0125] Preparation of ethyl 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[4-cyclobutyl-2-thiazolyl)ethyl]benzyl}}sulfamoylbenzoate (Compound No. 29c)

[0126] 1 H-NMR(CDCl3): 1.21.41 (7H, m) 1.87-2.39 (6H, m) 2.80 (2H, m) 3.14 (2H, br s) 3.22 (2H, m) 4.40 (4H, m) 5.04 (1H, t J=5.94 Hz) 6.75 (1H, s) 7.08 (3H, m) 7.20 (1H, m) 7.45 (2H, dd J=6.6 1.98 Hz) 7.51-7.65 (3H, m) 7.73 (2H, d J=8.25 Hz) 7.82 (1H, d J=8.24 Hz)

Example 15

[0127] Preparation of 5-{2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylphenyl}-1H-tetrazole 630

[0128] 3.5 g (6.4 mmol) of the hydrochloride of the product in Example 9 (Compound 1a) was dissolved in 75 ml of 1,2-dichloroethane and stirred together with 2.7 ml of triethylamine and 1.7 g (1.3 eq) of 2-chlorosulfonylbenzonitrile at room temperature overnight. The organic layer was washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and evaporated in vacuo for removal of the solvent. The residue was purified by silica gel column chromatography (eluent; chloroform to chloroform:methanol=99:1) to give 3.9 g of 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzonitrile (Compound No. 91b) in a yield of 89%.

[0129] FAB=MS (m/z): 673(M+)

[0130] 1 H-NMR(CDCl3): 1.32 (6H, d, J=6.93 Hz),1.42 (4H, m),2.85 (2H, m), 3.11 (1H, m), 3.29 (2H, m), 4.42 (2H, m), 4.62 (1H, m), 5.29 (2H, s), 6.84-6.89 (3H, m), 6.91 (1H, s), 7.22 (1H, m), 7.47 (2H, dd, J=8.58, 1.82 Hz), 7.65-7.78 (4H, m), 7.88 (1H, dd, J=1.98, 7.26 Hz), 8.07 (1H, m)

[0131] 3.8 g (5.6 mmol) of the above-mentioned product (Compound No. 91b) was dissolved in 100 ml of toluene and stirred together with 3.7 ml (5.0 eq) of trimethylsilyl azide and 702 mg (0.5 eq) of dibutyltin oxide under heating at 70° C. for 28 hours. The solvent was distilled off in vacuo, and 50 ml of 1N sodium hydroxide and 50 ml of water were added to the residue. The insolubles were filtered out, and the filtrate was washed with 100 ml of ether. The aqueous layer was acidified with 6N hydrochloric acid and extracted with chloroform. The solvent was distilled off in vacuo, and the residue was purified by silica gel column chromatography (eluent; chloroform to chloroform:methanol=99:1-95:5) to give 3.1 g of an oily substance in a yield of 78%. The oily substance was dissolved in 8.4 ml of 1N sodium hydroxide and 50 ml of water and acidified (pH 3.0) with 1N hydrochloric acid, and the deposited precipitate was filtered off to give 2.4 g of the title compound (Compound No. 91).

[0132] FAB-MS (m/z): 716(M+)

[0133] 1 H-NMR(CDCl3): 1.16 (4H, m), 1.27 (6H, d, J=6.93 Hz),2.73 (2H, m), 2.87 (2H, m), 3.07 (1H, m), 4.08 (2H, s), 5.30 (2H, m), 6.74-6.91 (4H, m), 7.20 (1H, t, J=7.76 Hz), 7.46 (2H, m), 7.68-7.80 (4H, m), 7.97 (1H, dd, J=1.65, 7.32 Hz), 8.08 (1H, dd, J=1.65, 5.66 Hz)

TEST EXAMPLES

[0134] Next, the excellent antagonistic effects on the receptors for both mediators LTD4 and TXA2 and anti-allergic effects of the 2-sulfamoylbenzoic acid derivatives of the present invention will be demonstrated by referring to Test Examples.

[0135] Compounds of the present invention were tested on the LTD4 inhibitory effects, TXA2 inhibitory effects and antiasthmatic effects. The test procedures and the test results were as follows.

Test Example 1

LTD4 Antagonistic Effects

[0136] Guinea pigs were bled to death, and the ilea were excised and made into ileum preparations. The ileum preparations were suspended with a 1 g load in Magnus tubes filled with 2 ml Tyrode solution maintained at 37° C. under aeration with a 95% O2-5% CO2 gas mixture, and LTD4-induced constrictions were isotonically recorded.

[0137] After equilibration of the tonuses of the ilea, constrictive responses to cumulative addition of 0.05-3.5 ng/ml LTD4 were observed. After the constrictive responses reached equilibrium, LTD4 was added again cumulatively 5 minutes after pre-treatment with a test substance to induce constriction. The pA2 values were calculated in accordance with Van Rossum's method. The results are shown below in Table 4.

Test Example 2

TXA2 Antagonistic Effects

[0138] Guinea pigs were bled to death, and the tracheae were excised and made into tracheal muscle strips in accordance with Takagi et al. The strips were suspended with a 1 g load in Magnus tubes filled with 2 ml Tyrode solution maintained at 37° C. under aeration with a 95% O2-5% CO2 gas mixture, and U-46619-induced constrictions were isotonically recorded.

[0139] After equilibration of the tonuses of the strips, constrictive responses to cumulative addition of 10−10-10−7M U-46619 were observed. After the constrictive responses reached equilibrium, U-46619 was added again cumulatively 5 minutes after pre-treatment with a test substance to induce constriction. The pA2 values were calculated in accordance with Van Rossum's method. The results are shown below in Table 4.

[0140] These results demonstrate the excellent antagonistic effects of compounds of the present invention on the receptors for both mediators LTD4 and TXA2.

TABLE 4
Results of Test Examples 1 and 2
Compound	LTD4 inhibitory	TXA2 inhibitory
No.	effect (pA2)	effect (pAp)
1	9.73	8.30
2	9.59	7.99
3	9.26	8.12
13	9.92	7.90
14	9.92	8.06
15	9.47	8.03
16	10.03	7.99
17	9.80	7.97
20	9.43	8.17
21	9.65	7.99
22	9.45	8.31
24	9.65	8.17
29	9.92	7.90
53	9.82	8.69
54	9.71	7.90
55	9.82	8.78
71	9.12	8.40
72	9.58	8.05
91	9.05	7.73

Test Example 3

Antiasthmatic Effects

[0141] The antiasthmatic effects were evaluated by the immediate asthmatic responses of passively sensitized guinea pigs. The previous day, the guinea pigs were sensitized by intravenous injections of a 10-fold diluted anti-DNP-ovalbumin guinea pig serum (guinea pig PCA titer; X1024) on the ears. The day of the test, after pre-treatment with pyrilamine (10 mg/kg i.p.), normal airway resitances were measured with a double flow plethysmograph in accordance with Pennock et al. The test substances (3 mg/kg) in DMSO were dissolved in 50% normal guinea pig serum-saline and intravenously injected from the ear vein 5 minutes before inhalation of the antigen. Immediate asthmatic responses were induced by 3 minutes of inhalational exposure to 1% ovalbumin in saline as the antigen from an ultrasonic neblizer, and the airway resistances were measured 5 minutes (4 to 6 minutes) after the inhalation. The results are expressed by the inhibition rates given by the following expression:

[0142] Inhibition rate (%)=(1−(A−B)/(C−D))×100

[0143] wherein A: the airway resistance with a test substance after inhalation of the antigen,

[0144] B: the airway resistance with a test substance before inhalation of the antigen,

[0145] C: the airway resistance with a control after inhalation of the antigen,

[0146] D: the airway resistance with a control before inhalation of the antigen.

[0147] The results are shown below in Table 5. These results demonstrate the excellent antiasthmatic effects of compounds of the present invention.

TABLE 5
Results of Test Example 3
Compound No. Antiasthmatic effect Inhibition rate (%)
1            53.5
24           40.5
38           59.5
70           54.0

Acute Toxicity Test

[0148] Compounds Nos. 1, 5 and 29 were administeredto ICR mice intravenously in an amount of 100 mg/kg and orally in an amount of 1000 mg/kg, but none of the mice died.

FORMULATION EXAMPLES

[0149] Now, formulation examples using compounds of the present invention will be given below. However, the present invention is by no means restricted by these formulations.

Formulation Example 1

[0150] Tablets each containing 100 mg of an active ingredient were prepared in accordance with the following formulation.

(Ingredients)         (mg)
Compound No. 1        100
Lactose               30
Corn starch           40
Crystalline cellulose 15
Methylcellulose       3
Magnesium stearate    2

Formulation Example 2

[0151] A capsule drug was prepared by encapsulating 190 mg of an ingredient mixture containing 100 mg of an active ingredient in accordance with the following formulation.

(Ingredients)         (mg)
Compound No. 1        100
Lactose               50
Corn starch           30
Crystalline cellulose 8
Magnesium stearate    2

INDUSTRIAL APPLICABILITY

[0152] The novel 2-sulfamoylbenzoic acid derivatives represented by general formula (I) of the present invention are both an antagonistic effect on the LTD4 receptor and an antagonistic effect on the TXA2 receptor and show an excellent antiasthmatic effect. Therefore, the compounds of the present invention are useful as anti-allergic agents for treatment and prevention of various allergic diseases such as allergic bronchial asthma.

Claims

1. A 2-sulfamoylbenzoic acid derivative represented by general formula (I):

2. The 2-sulfamoylbenzoic acid derivative according to claim 1 or a salt, hydrate or solvate thereof, wherein in general formula (I), X is a sulfur atom, and A is —CH2O— or an ethylene group.

3. The 2-sulfamoylbenzoic acid derivative according to claim 2 or a salt, hydrate or solvate thereof, wherein in general formula (I), R1 and R2 which may be the same or different, are hydrogen atoms, C3-8 cycloalkyl groups, optionally substituted C1-6 alkyl groups or optionally substituted aryl groups.

4. 2-{N-[4-(4-Chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methylbenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methoxybenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-bromobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-fluorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-bromobenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-fluorobenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(benzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methylbenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxylbernzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methoxybenzenesulfonylamino)butyl]-N-{3-[(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-(4-cyclopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-(5-(4-chlorobenzenesulfonyl)pentyl]-N-{3-[2-(4-cyclobutyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-fluorobenzenesulfonylamino)butyl]-N-{3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzyl}}sulfamoylbenzoic acid and 2-{N-[4-(4-bromobenzenesulfonylamino)butyl]-N-{3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzyl}}sulfamoylbenzoic acid, or salts, hydrates or solvates thereof.

5. The 2-sulfamoylbenzoic acid derivative according to claim 1 or a salt, hydrate or solvate thereof, wherein in general formula (I), X is —CH═CH—, and A is —CH2O—, an ethylene group or a vinylene group.

6. The 2-sulfamoylbenzoic acid derivative according to claim 5 or a salt, hydrate or solvate thereof, wherein in general formula (I), R1 and R2 form together with the ring

7. 2-{N-[4-(4-Chlorobenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-bromobenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-fluorobenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methylbenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methoxybenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(benzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-bromobenzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-fluorobenzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl) ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methylbenzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-methoxybenzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(benzenesulfonylamino)butyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-quinolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(7-chloro-2-quinolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-(2-quinolyl)ethenyl]benzyl}}sulfamoylbenzoic acid and 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[(7-chloro-2-quinolyl)ethenyl]benzyl}}sulfamoylbenzoic acid, or salts, hydrates or solvates thereof.

8. 2-{N-[4-(4-Chlorobenzenesulfonylamino)butyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[(4-isopropyl-2-thiazolyl)methoxy]benzyl}}sulfamoylbenzoic acid, 2-{N-[4-(4-chlorobenzenesulfonylamino)butyl]-N-{3-[2-(4-cyclobutyl-2-thiazolyl)ethyl]benzyl}}sulfamoylbenzoic acid, 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[2-(7-chloro-2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid and 2-{N-[5-(4-chlorobenzenesulfonylamino)pentyl]-N-{3-[2-(2-quinolyl)ethyl]benzyl}}sulfamoylbenzoic acid, or salts, hydrates or solvates thereof.

9. A benzylamine derivative represented by general formula (II):

10. A benzaldehyde derivative represented by general formula (IIIa):

11. A benzonitrile derivative represented by general formula (IV):

12. An amine derivative represented by general formula (V):

13. A pharmaceutical containing the 2-sulfamoylbenzoic acid derivative according to claim 1 or a salt, hydrate or solvate thereof as an active ingredient.

14. An anti-allergic agent containing the 2-sulfamoylbenzoic acid derivative according to claim 1 or a salt, hydrate or solvate thereof as an active ingredient.

15. A leukotriene and thromboxane A2 antagonistic agent containing the 2-sulfamoylbenzoic acid derivative according to claim 1 or a salt, hydrate or solvate thereof as an active ingredient.