Patent Application
20140371291
The present invention relates to a non-peptidic amide derivative having serine racemase inhibitory activity.
An N-methyl-D-aspartate (NMDA) receptor (hereinafter referred to as “NMDAR”) is one type of glutamate receptor.
The NMDAR has been considered to be a receptor that is involved in memory and learning. Therefore, the NMDAR has been one of the targets of Alzheimer-type dementia therapeutic agents.
D-serine is present in the mammalian brain, and is involved in control of the functions of the NMDAR as an endogenous coagonist.
D-serine is synthesized from L-serine by serine racemase (SR).
It has been known that an SR knock-out (KO) mouse shows a reduction in NMDA-induced neurodegeneration (see Non-patent Document 1), and a reduction in PTZ-induced epileptic seizure, for example.
Therefore, SR has been considered to be a new drug target for pathological conditions due to excessive nervous excitement. A dipeptide and the like have been known as an SR inhibitor (see Non-patent Document 2).
A dipeptide has a narrow concentration range that shows the SR inhibition effect, may have cellular toxicity, and does not have high specificity.
An object of the invention is to develop a novel SR inhibitor that exhibits sufficient activity and specificity.
Another object of the invention is to develop a novel candidate for a therapeutic agent for treating neurodegenerative diseases and hyperexcitable brain conditions.
The inventors of the invention synthesized novel low-molecular-weight compounds from structural information about a lead compound candidate for an SR inhibitor found by in silico screening based on three-dimensional structural information about SR, and evaluated the effects thereof on SR to find novel compounds having SR inhibitory activity. This finding has led to the completion of the invention.
The invention is described in detail below.
The terms used herein have the following meanings unless otherwise specified.
The term “halogen atom” used herein refers to a fluorine atom, a chlorine atom, a bromine atom, and an iodine atom. The term “alkyl group” used herein refers to a linear or branched alkyl group having 1 to 12 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, and hexyl. The term “lower alkyl group” used herein refers to a linear or branched alkyl group having 1 to 6 carbon atoms, such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, pentyl, and hexyl. The term “cycloalkyl group” used herein refers to a cycloalkyl group having 3 to 8 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. The term “aryl group” used herein refers to phenyl, naphthyl, indanyl, indenyl, and the like. The term “aralkyl group” used herein refers to an aryl-lower alkyl group such as benzyl, phenethyl, α-methylphenethyl, diphenylmethyl, and trityl. The term “alkoxy group” used herein refers to a linear or branched alkyloxy group having 1 to 12 carbon atoms, such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tert-butoxy, pentyloxy, hexyloxy, heptyloxy, and octyloxy. The term “lower alkoxy group” used herein refers to a linear or branched alkyloxy group having 1 to 6 carbon atoms, such as methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, tert-butoxy, pentyloxy, and hexyloxy. The term “alkylene group” used herein refers to a linear or branched alkylene group having 1 to 6 carbon atoms, such as methylene, ethylene, and propylene.
A group that protects a hydroxyl group may be an arbitrary group that can normally be used as a protecting group for a hydroxyl group. Examples of such a group include an acyl group such as benzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 4-bromobenzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, methoxycarbonyl, ethoxycarbonyl, tert-butoxycarbonyl, 1,1-dimethylpropoxycarbonyl, isopropoxycarbonyl, isobutyloxycarbonyl, diphenylmethoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2,2,2-tribromoethoxycarbonyl, 2-(trimethylsilyl)ethoxycarbonyl, 2-(phenylsulfonyl)ethoxycarbonyl, 2-(triphenylphosphonio)ethoxycarbonyl, 2-furfuryloxycarbonyl, 1-adamantyloxycarbonyl, vinyloxycarbonyl, allyloxycarbonyl, S-benzylthiocarbonyl, 4-ethoxy-1-naphthyloxycarbonyl, 8-quinolyloxycarbonyl, acetyl, formyl, chloroacetyl, dichloroacetyl, trichloroacetyl, trifluoroacetyl, methoxyacetyl, phenoxyacetyl, pivaloyl, and benzoyl; a lower alkyl group such as methyl, tert-butyl, 2,2,2-trichloroethyl, and 2-trimethylsilylethyl; a lower alkenyl group such as allyl; a lower aralkyl group such as benzyl, p-methoxybenzyl, 3,4-dimethoxybenzyl, diphenylmethyl, and trityl; an oxygen-containing/sulfur-containing heterocyclic group such as tetrahydrofuryl, tetrahydropyranyl, and tetrahydrothiopyranyl; a lower alkoxy/lower alkylthio-lower alkyl group such as methoxymethyl, methylthiomethyl, benzyloxymethyl, 2-methoxyethoxymethyl, 2,2,2-trichloroethoxymethyl, 2-(trimethylsilyl)ethoxymethyl, 1-ethoxyethyl, and 1-methyl-1-methoxyethyl; a lower alkyl/aryl-sulfonyl group such as methanesulfonyl and p-toluenesulfonyl; a substituted silyl group such as trimethylsilyl, triethylsilyl, triisopropylsilyl, diethylisopropylsilyl, tert-butyldimethylsilyl, tert-butyldiphenylsilyl, diphenylmethylsilyl, and tert-butylmethoxyphenylsilyl; and the like.
According to one aspect of the invention, there is provided a serine racemase inhibitor comprising one or more non-peptidic amide derivatives as an active ingredient, the one or more compounds being selected from a phenoxy(N-substituted carbamoylmethyl)acetamide derivative represented by a general formula [MM—1], an N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by a general formula [DR—1], an N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by a general formula [DR′—1], an N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by a general formula [LW—1], and a benzenesulfonamide derivative represented by a general formula [ED—1],
wherein R1m is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2m is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted cycloalkyl group, and Xm is an oxygen atom or a sulfur atom,
wherein R1d is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, Xd is an oxygen atom or an imino group, and nd is 0 or 1,
wherein R1d′ is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d′ is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, and Xd′ is an oxygen atom or an imino group,
wherein R1w is a substituted or unsubstituted styryl group, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted cyclohexylmethyl group, R2w is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and nw is 0, 1, or 2,
wherein R1e is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, R2e is a substituted or unsubstituted phenyl group or a substituted or unsubstituted tolylsulfonyl group, and Ae is an alkylene group or a phenylene group.
Another aspect of the invention provides novel non-peptidic amide derivatives having serine racemase inhibitory activity and respectively represented by the following general formulas.
A phenoxy(N-substituted carbamoylmethyl)acetamide derivative represented by the following general formula [MM—2].
wherein R1m is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2Am is an aryl group, an aralkyl group, or a cycloalkyl group that is optionally substituted with one or two atoms or substituents selected from a halogen atom, an alkyl group, an alkoxy group, a nitro group, and a hydroxyl group that is optionally protected, and Xm is an oxygen atom or a sulfur atom.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula [DR—1a].
wherein R1d is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, and Xd is an oxygen atom or an imino group.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula [DR—1b].
wherein R1d is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, and Read is a substituted or unsubstituted benzyl group or a substituted or unsubstituted arylacetamide group.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula [DR′—1].
wherein R1d′ is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d′ is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, and Xd′ is an oxygen atom or an imino group.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula [LW—1 d].
wherein R13w is a halogen atom, R12w, R14w, R15w, and R16w are independently atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a nitro group, and R2bw is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula [LW—1e].
wherein R2cw is a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and (1) R12w, R14w, and R16w are a hydrogen atom, and R13w and R15w are a halogen atom, or (2) R13w, R14w, and R15w are a hydrogen atom, and R12w and R16w are an alkoxy group.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula [LW—1g].
wherein R1aw is atoms or substituents selected from a halogen atom, an alkyl group, an alkoxy group, a nitro group, and a hydroxyl group that is optionally protected, and (1) R24w is a halogen atom, and R22w, R23w, R25w, and R26w are a hydrogen atom, or (2) R23w is an alkyl group, and R22w, R24w, R25w, and R26w are a hydrogen atom, or (3) R22w and R26w are a halogen atom, and R23w, R24w, and R25w are a hydrogen atom, or (4) R23w and R25w are a halogen atom, and R22w, R24w, and R26w are a hydrogen atom.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula [LW—1c].
wherein R2w is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and nw is 0, 1, or 2.
A benzenesulfonamide derivative represented by the following general formula [ED—1aa].
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, R21e is a hydrogen atom, a halogen atom, or an alkyl group, R22e is a hydrogen atom or a halogen atom, R23e is a hydrogen atom or a halogen atom, R24e is a hydrogen atom, an alkyl group, or an alkoxy group, Xe is an oxygen atom or a sulfur atom, and ne is 2 or 3, provided that a case where R11e is an alkyl group, R21e and R23e are a halogen atom, R22e and R24e are a hydrogen atom, Xe is an oxygen atom, and ne is 2 is excluded.
A benzenesulfonamide derivative represented by the following general formula [ED—1ab].
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, R25e and R26e are independently a hydrogen atom or an alkyl group, and ne is 2 or 3.
A benzenesulfonamide derivative represented by the following general formula [ED—1ba].
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, and R22e and R23e are independently a hydrogen atom or an alkyl group.
The scope of the invention includes any isomers (e.g., optical isomer, geometric isomer, and tautomer) of the non-peptidic amide derivatives respectively represented by the above general formulas, and also includes hydrates, solvates, and any crystalline forms thereof.
The non-peptidic amide derivatives respectively represented by the above general formulas may form a salt. Examples of such a salt include salts formed via an imino group or a hydroxyl group.
Salts of the DR compound and the ED compound may be salts with an alkali metal (e.g., sodium and potassium).
Examples of a preferable salt include a pharmacologically acceptable salt.
Examples of a preferable compound having serine racemase inhibitory activity include the following compounds.
A phenoxy(N-substituted carbamoylmethyl)acetamide derivative represented by the following general formula.
wherein R1am is a hydrogen atom, a halogen atom, an alkoxy group, or a hydroxyl group that is optionally protected, R1bm is a hydrogen atom or an alkyl group, R2am is a substituted or unsubstituted aryl group or a substituted or unsubstituted cycloalkyl group, Xm is an oxygen atom or a sulfur atom, and nm is 0 or 1.
Examples of a more preferable compound include the following compound.
A phenoxy(N-substituted carbamoylmethyl)acetamide derivative represented by the following general formula.
wherein R1am is a hydrogen atom, a halogen atom, an alkoxy group, or a hydroxyl group that is optionally protected, R1bm is a hydrogen atom or an alkyl group, and R2bm is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, a nitro group, and a hydroxyl group.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula.
wherein R1ad is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, R2bd is a substituted or unsubstituted aralkyl group, and nd is 0 or 1.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula.
wherein R1ad is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, and R2cd is a substituted or unsubstituted aryl group or a substituted or unsubstituted aralkyl group.
An N-(substituted)-2-(substituted sulfamoylamino)acetamide derivative represented by the following general formula.
wherein R1ad is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, and R2aad is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected.
wherein R1d′ is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d′ is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, and Xd′ is an oxygen atom or an imino group.
wherein R1aw is atoms or substituents selected from a halogen atom, an alkyl group, an alkoxy group, a nitro group, and a hydroxyl group that is optionally protected, R2w and R2aw are a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and nw is 0, 1, or 2.
Examples of a more preferable compound include the following compounds.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula.
wherein R13w is a halogen atom, R12w, R14w, R15w, and R16w are independently atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a nitro group, and R21w is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula.
wherein R2cw is a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and (1) R12w, R14w, and R16w are a hydrogen atom, and R13w and R15w are a halogen atom, or (2) R13w, R14w, and R15w are a hydrogen atom, and R12w and R16w are an alkoxy group.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula.
wherein (1) R12w, R14w, and R16w are a hydrogen atom, and R13w and R15w are a halogen atom, or (2) R13w, R14w, and R15w are a hydrogen atom, and R12w and R16w are an alkoxy group.
An N-[(acyl)hydrazinocarbothioyl]acetamide derivative represented by the following general formula.
wherein R1aw is atoms or substituents selected from a halogen atom, an alkyl group, an alkoxy group, a nitro group, and a hydroxyl group that is optionally protected, and (1) R24w is a halogen atom, and R22w, R23w, R25w, and R26w are a hydrogen atom, or (2) R23w is an alkyl group, and R22w, R24w, R25w, and R26w are a hydrogen atom, or (3) R22w and R26w are a halogen atom, and R23w, R24w, and R25w are a hydrogen atom, or (4) R23w and R25w are a halogen atom, and R22w, R24w, and R26w are a hydrogen atom.
A benzenesulfonamide derivative represented by the following general formula.
wherein R1e is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, R2e is a substituted or unsubstituted phenyl group or a substituted or unsubstituted tolylsulfonyl group, R2ae is a substituted or unsubstituted phenyl group, and ne is 2 or 3.
Examples of a more preferable compound include the following compounds.
A benzenesulfonamide derivative represented by the following general formula.
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, R21e is a hydrogen atom, a halogen atom, or an alkyl group, R22e is a hydrogen atom or a halogen atom, R23e is a hydrogen atom or a halogen atom, R24e is a hydrogen atom, an alkyl group, or an alkoxy group, Xe is an oxygen atom or a sulfur atom, and ne is 2 or 3, provided that a case where R11e is an alkyl group, R21e and R23e are a halogen atom, R22e and R24e are a hydrogen atom, Xe is an oxygen atom, and ne is 2 is excluded.
A benzenesulfonamide derivative represented by the following general formula.
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, R25e and R26e are independently a hydrogen atom or an alkyl group, and ne is 2 or 3.
A benzenesulfonamide derivative represented by the following general formula.
wherein R11e is a hydrogen atom, an alkyl group, or an alkoxy group, and R22e and R23e are independently a hydrogen atom or a halogen atom.
The non-peptidic amide derivatives may be produced using the following methods, for example.
wherein R1m is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2m is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted cycloalkyl group, and Xm is an oxygen atom or a sulfur atom.
The compound represented by the general formula [MM—1] can be produced by reacting the compound represented by the general formula [MM—4] with the compound represented by the general formula [MM—3] in the presence of a condensation agent.
A solvent used for the above reaction is not particularly limited as long as the solvent does not adversely affect the reaction. Examples of the solvent include halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as tetrahydrofuran; and amides such as N,N-dimethylformamide.
Examples of the condensation agent used for the above reaction include carbonyldiimidazole, 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC), and the like.
1-Hydroxybenzotriazole (HOBt) and 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine (HOOBt) may be used in combination as additives.
The condensation agent is used in a molar ratio of 1 or more (preferably 1 to 10) with respect to the compound represented by the general formula [3].
The above reaction is normally carried out at 0 to 200° C. (preferably 10 to 150° C.) for 10 minutes to 24 hours.
The compound represented by the general formula [MM—3] can be produced using a known method (see the following documents, for example).
The compound represented by the general formula [MM—4] can be produced using a known method (see the following documents, for example).
It is possible to use an arbitrary isomer (e.g., optical isomer, geometric isomer, or tautomer) of the compound represented by the general formula [MM—3] and the compound represented by the general formula [MM—4]. A hydrate, a solvate, or an arbitrary crystalline form thereof may be used.
These compounds may be used directly for the subsequent reaction without performing an isolation operation.
The compound represented by the general formula [MM—1] thus obtained can be isolated and purified using a normal method such as extraction, crystallization, distillation, and column chromatography.
wherein R1d is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, and a hydroxyl group that is optionally protected, R2d is a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, or a substituted or unsubstituted arylacetamide group, Xd is an oxygen atom or an imino group, and nd is 0 or 1.
The compound represented by the general formula [DR—1] or [DR′—1] can be produced by reacting the compound represented by the general formula [DR—3] with the compound represented by the general formula [DR—2] or [DR′—2] in the presence of a base.
A solvent used for the above reaction is not particularly limited as long as the solvent does not adversely affect the reaction. Examples of the solvent include halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as tetrahydrofuran; and the like.
Examples of the base used for the above reaction include organic bases such as diethylamine, triethylamine, and N,N-dimethyl-4-aminopyridine.
The base is used in a molar ratio of 0.1 to 2 with respect to the compound represented by the general formula [DR—3].
The above reaction is normally carried out at 0 to 200° C. (preferably 10 to 150° C.) for 10 minutes to 24 hours.
The compound represented by the general formula [DR—2] or [DR′—2] can be produced using a known method (see the following documents, for example).
The compound represented by the general formula [DR—3] can be produced using a known method (see the following document, for example).
It is possible to use an arbitrary isomer (e.g., optical isomer, geometric isomer, or tautomer) of the compound represented by the general formula [DR—2], the compound represented by the general formula [DR′—2], and the compound represented by the general formula [DR—3]. A hydrate, a solvate, or an arbitrary crystalline form thereof may be used.
These compounds may be used directly for the subsequent reaction without performing an isolation operation.
The compound represented by the general formula [DR—1] or [DR′—1] thus obtained can be isolated and purified using a normal method such as extraction, crystallization, distillation, and column chromatography.
wherein R1w is a substituted or unsubstituted styryl group, a substituted or unsubstituted benzyl group, or a substituted or unsubstituted cyclohexylmethyl group, R2w is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, and nw is 0, 1, or 2.
The compound represented by the general formula [LW—1] can be produced by reacting the compound represented by the general formula [LW—2] with the compound represented by the general formula [LW—3].
A solvent used for the above reaction is not particularly limited as long as the solvent does not adversely affect the reaction. Examples of the solvent include halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as tetrahydrofuran; and the like.
The above reaction is normally carried out at 0 to 200° C. (preferably 10 to 150° C.) for 10 minutes to 24 hours.
The compound represented by the general formula [LW—2] and the raw material compound can be produced using a known method (see the following documents, for example).
The compound represented by the general formula [LW—3] can be produced using a known method. For example, the compound represented by the general formula [LW—3] can be produced by reacting hydrazine monohydrate with a carboxylic acid ester.
wherein R2w is a substituted or unsubstituted aryl group, or a substituted or unsubstituted heterocyclic group that includes an oxygen atom or a sulfur atom as a ring atom, R′ is an alkyl group, and nw is 0, 1, or 2.
It is possible to use an arbitrary isomer (e.g., optical isomer, geometric isomer, or tautomer) of the compound represented by the general formula [LW—2] and the compound represented by the general formula [LW—3]. A hydrate, a solvate, or an arbitrary crystalline form thereof may be used.
These compounds may be used directly for the subsequent reaction without performing an isolation operation.
The compound represented by the general formula [LW—1] thus obtained can be isolated and purified using a normal method such as extraction, crystallization, distillation, and column chromatography.
wherein R1e is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, R2e is a substituted or unsubstituted phenyl group or a substituted or unsubstituted tolylsulfonyl group, and Ae is an alkylene group or a phenylene group.
The compound represented by the general formula [ED—1] can be produced by reacting the compound represented by the general formula [ED—2] with the compound represented by the general formula [ED—3].
A solvent used for the above reaction is not particularly limited as long as the solvent does not adversely affect the reaction. Examples of the solvent include halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as tetrahydrofuran; and the like.
The above reaction is normally carried out at 0 to 200° C. (preferably 10 to 100° C.) for 10 minutes to 24 hours.
The compound represented by the general formula [ED—2] and the raw material compound can be produced using a known method. For example, the compound represented by the general formula [ED—2] and the raw material compound can be produced by reacting the benzenesulfonyl chloride represented by the general formula [ED—4] with the diamine represented by the general formula [ED—5] under known conditions.
wherein R1e is atoms or substituents selected from a hydrogen atom, a halogen atom, an alkyl group, and an alkoxy group, and Ae is an alkylene group or a phenylene group.
It is possible to use an arbitrary isomer (e.g., optical isomer, geometric isomer, or tautomer) of the compound represented by the general formula [ED—2], the compound represented by the general formula [ED—3], the compound represented by the general formula [ED—4], and the compound represented by the general formula [ED—5]. A hydrate, a solvate, or an arbitrary crystalline form thereof may be used.
These compounds may be used directly for the subsequent reaction without performing an isolation operation.
The compound represented by the general formula [ED—1] thus obtained can be isolated and purified using a normal method such as extraction, crystallization, distillation, and column chromatography.
The compounds according to the invention may be mixed with various excipients and additives such as a solvent, an extender, a tonicity agent, a solubilizer, an emulsifier, a suspending agent, a thickener, an absorption promoter, a gelling/coagulation promoter, an optical stabilizer, a preservative, an emulsification/suspension/dispersion stabilizer, a coloring inhibitor, a defoamer, a soothing agent, a buffer, and a pH adjusting agent to prepare a drug preparation such as an injection or a suppository.
The preparation may be administered using an arbitrary method. The administration method is appropriately determined corresponding to the form of the preparation, the age, the sex, and other conditions of the patient, and the severity of the symptoms.
The dose of the effective component of the preparation is appropriately selected corresponding to the application, the age and the sex of the patient, the disease, and the like. The preparation is normally administered in an amount of 0.1 to 500 mg per day per adult at a time or several times a day.
The pharmacological action of the representative compounds according to the invention is described below.
The serine racemase (SR) activity inhibition effect of the compound was determined based on (1) the L-serine racemization reaction and (2) quantitative determination of D-serine produced (see below).
Recombinant SR (3.7 μg) that had been expressed by Escherichia coli and purified was reacted at 37° C. for 8 hours or more in 125 μL of a reaction mixture including 100 mM HEPES (pH: 8.0), 1 mM MgCl2, 10 μM PLP, 1 mM ATP, 20 mM L-serine, 5 mM DTT, and the compound (1 to 0.01 mM) dissolved in DMSO in accordance with the method proposed by Strisovsky et al. (Biochemistry, 44:13091-13100, 2005).
D-serine was quantitatively determined in accordance with the method proposed by Ito et al. (Analytical Biochemistry, 371: 167-172, 2007).
A solution including 25 μL of 100 mM HEPES (pH: 8.0), 20 μM PLP, and 2 μg of recombinant D-serine dehydratase 1 (Dsd1) was added to 25 μL of the reaction mixture (see (1)), and the mixture was reacted at 30° C. for 30 minutes.
In order to measure pyruvic acid produced from D-serine by Dsd1 using a colorimetric reaction, 50 μL of 0.05% DNP/2M HCl was added to 50 μL of the reaction solution, and the mixture was reacted at 30° C. for 5 minutes. After the addition of 100 μL of ethanol and 125 μL of 10 M NaOH, the mixture was sufficiently mixed, and reacted at room temperature for 10 minutes, and the absorbance at a wavelength of 515 nm was measured using a spectrophotometer.
The results are shown in Tables 1 and 2.
Note that each numerical value in parentheses in Tables 1 to 8 is the value of malonic acid (control).
The non-peptidic amide derivatives have serine racemase inhibitory activity. Therefore, the non-peptidic amide derivatives make it possible to adjust the activity of the NMDAR, and may be used as a novel therapeutic agent for treating neurodegenerative diseases and hyperexcitable brain conditions.
The invention is further described below by way of reference examples and examples.
Note that the invention is not limited to the following examples.
The abbreviations in the chemical structural formulas have the following meanings.
Me: methyl, Ph: phenyl, Bn: benzyl, Boc: butoxycarbonyl
Methyl bromoacetate (0.10 mL, 1 mmol) and potassium carbonate (207 mg, 1.5 mmol) were sequentially added to a dimethylformamide (3 mL) solution of a phenol compound (1.0 mmol) in an argon atmosphere, and the mixture was stirred at 80° C. overnight.
The reaction mixture was diluted with ethyl acetate (10 mL), and filtered through celite, and the solvent was evaporated.
The residue was purified by silica gel column chromatography (15 g, hexane:acetone=50:1 to 40:1) to obtain a methyl ester compound.
Reference: Synth. Commun., 2004, 34, 377-382.
Reference: Synth. Commun., 2004, 34, 377-382.
Reference: Lett. Org. Chem., 2011, 8, 234-241.
Reference: Org. Lett., 2010, 12, 4571-4575.
Reference: J. Am. Chem. Soc., 2007, 129, 3981-3929.
Reference: J. Am. Chem. Soc., 2007, 129, 3981-3929.
Reference: Lett. Org. Chem., 2011, 8, 234-241.
Triethylamine (0.21 mL, 1.5 mmol), N-(tert-butoxycarbonyl)glycine (175 mg, 1.0 mmol), EDC (192 mg, 1.0 mmol), and DMAP (12 mg, 0.1 mmol) were sequentially added to a methylene chloride (5 mL) solution of 2-methyl-4-methoxyaniline (0.13 mL, 1.0 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 5 hours.
After evaporating the solvent, the residue was purified by silica gel column chromatography (20 g, hexane:acetone=30:1 to 2:1) to obtain [(4-methoxy-2-methylphenylcarbamoyl)methyl]carbamic acid tert-butyl ester (290 mg) as a colorless oily substance.
1H-NMR (400 MHz, CDCl3): δ 1.48 (9H, s), 2.22 (3H, s), 3.78 (3H, s), 3.93 (2H, d, J=6.1 Hz), 5.21 (1H, br), 6.73-6.75 (2H, m), 7.59 (1H, d, J=9.3 Hz), 7.79 (1H, br)
13C-NMR (100 MHz, CDCl3): δ 17.85, 28.21, 45.09, 55.23, 80.32, 111.34, 115.82, 125.26, 128.09, 132.42, 156.44, 157.17, 168.34
IR (neat): 1680, 3290 cm−1
MS (EI): m/z 294 (M+)
Yield: 99%
The following compounds were obtained via a similar reaction.
Reference: Eur. J. Org. Chem., 2008, 23, 3976-3983.
Reference: Eur. J. Med. Chem., 1996, 31, 497-505.
Reference: J. Org. Chem., 2011, 76, 9278-9293.
Reference: J. Med. Chem., 2009, 52, 5005-5008.
Reference: Org. Lett., 2010, 12, 2718-2721.
1,1-Carbonylimidazole (1.38 g, 8.51 mmol) was added to a methylene chloride (10 mL) solution of N-(tert-butoxycarbonyl)glycine (1.36 g, 7.74 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 1 hour. After the addition of 2,6-difluoroaniline (0.78 mL, 7.74 mmol), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=6:1 to 3:1) to obtain [(2,6-difluorophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (1.73 g) as a colorless crystalline substance.
Yield: 78%
1H-NMR (400 MHz, CDCl3): δ 1.47 (9H, s), 4.00 (2H, d, J=4.6 Hz), 5.22 (1H, br), 6.96, (2H, t, J=8.1 Hz), 7.18-7.27 (1H, m), 7.74 (1H, br)
IR (KBr): 1684, 3281 cm−1
MS (EI): m/z 286 (M+)
Melting point: 119 to 120° C.
The following compounds were obtained via a similar reaction.
Yield: 98%
1H-NMR (400 MHz, CDCl3): δ 1.43 (9H, s), 2.31 (3H, s), 3.82 (2H, d, J=6.1 Hz), 4.46 (2H, d, J=5.6 Hz), 5.10 (1H, br), 6.22 (1H, br), 7.18-7.20 (4H, m)
Yield: 85%
1H-NMR (400 MHz, CDCl3): δ 1.43 (9H, s), 3.82 (2H, d, J=6.1 Hz), 4.41 (2H, d, J=5.9 Hz), 5.12 (1H, br), 6.50 (1H, br), 7.15 (2H, d, J=8.4 Hz), 7.45 (2H, d, J=8.4 Hz)
Yield: 93%
1H-NMR (400 MHz, CDCl3): δ 1.44 (9H, s), 3.80 (2H, d, J=6.1 Hz), 4.45 (2H, d, J=6.1 Hz), 5.07 (1H, br), 6.51 (1H, br), 7.20-7.29 (3H, m)
Yield: 89%
1H-NMR (400 MHz, CDCl3): δ 1.47 (9H, s), 3.90 (2H, d, J=6.1 Hz), 5.20 (1H, br), 7.16 (1H, t, J=8.1 Hz), 7.22-7.25 (1H, m), 7.39 (1H, d, J=8.1 Hz), 7.75 (1H, s), 8.25 (1H, br)
Yield: 92%
1H-NMR (400 MHz, CDCl3): δ 1.48 (9H, s), 3.94 (2H, d, J=5.9 Hz), 5.25 (1H, br), 7.47 (1H, t, J=7.9 Hz), 7.88 (1H, d, J=7.9 Hz), 7.94 (1H, d, J=7.9 Hz), 8.37 (1H, s), 8.67 (1H, br)
A Lawesson's reagent (50 mg, 0.12 mmol) was added to a THF (2 mL) solution of [(2,6-difluorophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (52 mg, 0.18 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight. After evaporating the solvent, the residue was purified by silica gel column chromatography (13 g, hexane:acetone=10:1 to 8:1) to obtain [(2,6-difluorophenylthiocarbamoyl)methyl]carbamic acid tert-butyl ester (23 mg) as a colorless crystalline substance.
Yield: 42%
1H-NMR (400 MHz, CDCl3): δ 1.55 (9H, s), 4.34 (2H, d, J=6.1 Hz), 5.40 (1H, br), 6.98 (2H, t, J=8.2 Hz), 7.30 (1H, t, J=8.2 Hz), 9.59 (1H, br)
1,1-Carbonylimidazole (1.38 g, 8.51 mmol) was added to a methylene chloride (10 mL) solution of N-(tert-butoxycarbonyl)glycine (1.36 g, 7.74 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 1 hour. After the addition of 2,6-difluoroaniline (0.78 mL, 7.74 mmol), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=6:1 to 3:1) to obtain [(2,6-difluorophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (1.73 g) as a colorless crystalline substance.
Yield: 78%
Melting point: 119 to 120° C.
1H-NMR (400 MHz, CDCl3): δ 1.47 (9H, s), 4.00 (2H, d, J=4.6 Hz), 5.22 (1H, br), 6.96, (2H, t, J=8.1 Hz), 7.18-7.27 (1H, m), 7.74 (1H, br)
The following compounds were obtained via a similar reaction.
Reference: J. Med. Chem., 2011, 54, 2738-2744.
Reference: ACS Chem. Neurosci., 2010, 1, 155-164.
Yield: 68%
Melting point: 118 to 119° C.
1H-NMR (400 MHz, CDCl3): δ 1.49 (9H, s), 3.98 (2H, d, J=5.6 Hz), 5.18 (1H, br), 6.99 (1H, td, J=8.1, 1.3 Hz), 7.32 (1H, td, J=8.1, 1.3 Hz), 7.54 (1H, dd, J=8.1, 1.3 Hz), 8.37 (1H, dd, J=8.1, 1.3 Hz), 8.47 (1H, br)
13C-NMR (100 MHz, CDCl3): δ 28.26, 45.49, 80.67, 113.38, 121.62, 125.33, 128.31, 132.23, 135.16, 156.04, 167.92
1,1-Carbonyldiimidazole (357 mg, 2.2 mmol) was added to a methylene chloride (5 mL) solution of N-(tert-butoxycarbonyl)glycine (350 mg, 2.0 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 1 hour. After the addition of benzyl alcohol (0.21 mL, 2.0 mmol), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (20 g, hexane:acetone=10:1) to obtain tert-butoxycarbonylaminoacetatic acid benzyl ester as a colorless oily substance (360 mg, 68%).
Several drops of concentrated hydrochloric acid were added to an ethanol (15 mL) solution of phenylacetic acid (770 mg, 5.00 mmol), and the mixture was refluxed with heating overnight.
A saturated sodium bicarbonate solution was added to the reaction mixture at 0° C. until the aqueous layer became neutral.
After evaporating ethanol, the organic layer was extracted with methylene chloride, dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain an ethyl ester compound (colorless crystals) (910 mg, 100%).
Hydrazine monohydrate (0.13 mL, 2.74 mmol) was added to an ethanol (2.0 mL) solution of the ethyl ester compound (500 mg, 2.74 mmol), and the mixture was refluxed with heating overnight.
The solvent was evaporated to obtain a hydrazide compound (colorless crystals).
1,1-Carbodiimidazole (488 mg, 3.01 mmol) was added to a methylene chloride (7 mL) solution of N-carbobenzoxyglycine (573 mg, 2.74 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 1 hour. After the addition of a methylene chloride (3 mL) solution of the hydrazide compound using a cannula, the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (20 g, methylene chloride:methanol=80:1 to 30:1) to obtain [N′-[2-(4-fluorophenyl)acetyl]hydrazinocarbamoylmethyl]carbamic acid butyl ester (colorless crystals) (840 mg).
Yield: 85%
Melting point: 185 to 186° C.
1H-NMR (400 MHz, CDCl3): δ 3.45 (2H, s), 3.65 (2H, d, J=5.9 Hz), 5.01 (2H, s), 7.12 (2H, t, J=8.7 Hz), 7.31 (2H, dd, J=8.7, 5.7 Hz), 7.33-7.34 (5H, m), 7.51 (1H, br), 9.92 (1H, br), 10.08 (1H, br)
Sulfuryl chloride (1.38 mL, 17.0 mmol) was added to dimethylformamide (1.55 mL, 20.0 mmol) at 0° C. in an argon atmosphere, and the mixture was stirred for 30 minutes.
After the addition of 4-methylstyrene (1.31 mL, 10.0 mmol), the mixture was stirred at 90° C. for 4 hours.
After returning the mixture to room temperature, ice water (25 mL) was added to the mixture.
The reaction mixture was filtered under suction, and washed with water to obtain 2-p-tolylethanesulfonyl chloride (1.134 g, 52%).
Methyl iodide (0.76 mL, 12.27 mmol) and potassium carbonate (2.26 g, 16.36 mmol) were sequentially added to an acetone (5 mL) solution of 4-hydroxybenzaldehyde (500 mg, 4.09 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
The reaction mixture was diluted with methylene chloride (10 mL), and filtered through celite, and the solvent was evaporated.
The residue was purified by silica gel column chromatography (20 g, hexane:acetone=50:1 to 30:1) to obtain 4-methoxybenzaldehyde (439 mg, yield: 79%).
The following compound was obtained via a similar reaction.
Reference: Bioorg. Med. Chem., 2004, 13, 433-441.
n-Butyllithium (2.45 mL, 4.00 mmol) was added to a tetrahydrofuran (10 mL) solution of 1,3,5-trichlorobenzene (724 mg, 4.00 mmol) at −78° C. in an argon atmosphere, and the mixture was stirred for 45 minutes.
After the addition of dimethylformamide (0.31 mL, 4.00 mmol) at −78° C., the mixture was stirred for 45 minutes.
After increasing the temperature of the mixture to −20° C., a saturated ammonium chloride solution (5 mL) was added to the mixture, followed by stirring for 5 minutes.
The organic layer was extracted with ethyl acetate, dried over sodium sulfate, and filtered, and the solvent was evaporated.
The residue was purified by silica gel column chromatography (15 g, hexane:acetone=50:1 to 40:1) to obtain a 2,4,6-trichlorobenzaldehyde compound (colorless crystals) (633 mg, 76%).
Malonic acid (156 mg, 1.50 mmol), pyridine (0.12 mL, 1.54 mmol), and aniline (0.01 mL, 0.12 mmol) were sequentially added to a toluene (5 mL) solution of 4-chlorobenzaldehyde (141 mg, 1.00 mmol), and the mixture was refluxed with heating overnight.
A 10% hydrochloric acid aqueous solution was added to the mixture until the aqueous layer became acidic. The organic layer was extracted with ethyl acetate, dried over sodium sulfate, and filtered, and the solvent was evaporated.
The residue was purified by silica gel column chromatography (20 g, methylene chloride:methanol=100:1 to 40:1) to obtain 3-(4-chlorophenyl)acrylic acid (colorless crystals) (162 mg, 89%).
Reference: J. Org. Chem., 2008, 73, 5766-5775.
The following compounds were obtained via a similar reaction.
Reference: Org. Biomol. Chem., 2009, 7, 4062-4066.
Reference: Chem. Eur. J., 2000, 6, 3386-3390.
Reference: Synth. Commun., 1980, 10, 37-42.
Reference: Synth. Commun., 2002,32, 195-201.
Reference: J. Med. Chem., 1993, 36, 2381-2389.
Reference: J. Org. Chem., 1995, 60, 1981-1984.
Reference: J. Org. Chem., 1999, 64, 3975-3978.
(1) Triethyl phosphonoacetate (0.66 mL, 3.32 mmol) was added to a tetrahydrofuran (5 mL) solution of sodium hydride (133 mg, 3.32 mmol) in an argon atmosphere, and the mixture was stirred for 30 minutes. After the addition of a tetrahydrofuran (5 mL) solution of 2,4,6-trichlorobenzaldehyde (580 mg, 2.77 mmol) using a cannula, the mixture was stirred at room temperature overnight.
After evaporating the solvent, water (10 mL) was added to the mixture. The organic layer was extracted with methylene chloride, dried over sodium sulfate, and filtered, and the solvent was evaporated.
The residue was purified by silica gel column chromatography (15 g, hexane:acetone=90:1 to 80:1) to obtain 3-(2,4,6-trichlorophenyl)acrylic acid ethyl ester (colorless oil) (751 mg, 97%).
(2) Lithium hydroxide monohydrate (226 mg, 5.38 mmol) was added to a methanol-water (3:1) solution (20 mL) of 3-(2,4,6-trichlorophenyl)acrylic acid ethyl ester (751 mg, 2.69 mmol) in an argon atmosphere, and the mixture was refluxed with heating for 2 hours.
After evaporating the solvent, a 10% hydrochloric acid aqueous solution was added to the mixture until the aqueous layer became acidic. The organic layer was extracted with ethyl acetate, dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain 3-(2,4,6-trichlorophenyl)acrylic acid (colorless crystals) (654 mg, 97%).
1H-NMR (400 MHz, CDCl3): δ 6.64 (1H, d, J=16.2 Hz), 7.41 (2H, s), 7.82 (1H, d, J=16.2 Hz)
The following compounds were obtained via a similar reaction.
Thionyl chloride (0.05 mL, 0.66 mmol) was added to a methylene chloride (3 mL) solution of 3-(4-chlorophenyl)acrylic acid (100 mg, 0.55 mmol) in an argon atmosphere, and the mixture was stirred at room temperature overnight.
After evaporating the solvent, methylene chloride (3 mL) was added to the mixture. After the sequential addition of ammonium thiocyanate (63 mg, 0.82 mmol) and PEG-400 (one drop), the mixture was stirred at room temperature for 2 hours.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=50:1 to 40:1) to obtain 3-(4-chlorophenyl)acryloyl isothiocyanate (colorless crystals) (105 mg, 85%).
1H-NMR (400 MHz, CDCl3) δ: 6.48 (1H, d, J=16.1 Hz), 7.41 (2H, d, J=8.7 Hz), 7.50 (2H, d, J=8.7 Hz), 7.72 (1H, d, J=15.6 Hz); Yield: 85%.
The following compounds were obtained via a similar reaction.
1H-NMR (400 MHz, CDCl3) δ: 6.74 (1H, d, J=16.1 Hz), 7.43 (2H, s), 7.85 (1H, d, J=16.1 Hz)
Yield: 80%
1H-NMR (400 MHz, CDCl3) δ: 6.43 (1H, d, J=15.8 Hz), 7.13 (2H, t, J=8.6 Hz), 7.57 (2H, dd, J=8.6, 5.3 Hz), 7.73 (1H, d, J=15.8 Hz)
Yield: 88%
1H-NMR (400 MHz, CDCl3) δ: 3.84 (3H, s), 3.88 (3H, s), 6.42-6.53 (3H, m), 7.46 (1H, d, J=16.1 Hz), 8.00 (1H, d, J=16.1 Hz)
Yield: 73%
1H-NMR (400 MHz, CDCl3) δ: 6.45 (1H, d, J=15.8 Hz), 7.58-7.62 (3H, m), 7.74 (1H, s)
Yield: 63%
1H-NMR (400 MHz, CDCl3) δ: 1.25 (6H, d, J=7.1 Hz), 2.93 (1H, sept, J=7.1 Hz), 6.45 (1H, d, J=15.7 Hz), 7.27 (2H, d, J=8.2 Hz), 7.48 (2H, d, J=8.2 Hz), 7.73 (1H, d, J=15.7 Hz)
Yield: 79%
1H-NMR (400 MHz, CDCl3): δ 6.47 (1H, d, J=15.6 Hz), 7.33 (1H, t, J=7.4 Hz), 7.41 (2H, t, J=7.4 Hz), 7.55-7.61 (6H, m), 7.74 (1H, d, J=15.6 Hz)
Yield: 83%
1H-NMR (400 MHz, CDCl3) δ: 3.89 (6H, s), 6.55 (2H, d, J=8.5 Hz), 6.99 (1H, d, J=15.9 Hz), 7.32 (1H, t, J=8.5 Hz), 8.23 (1H, d, J=15.9 Hz)
Yield: 27%
1H-NMR (400 MHz, CDCl3): δ 6.74-6.79 (3H, m), 7.78 (1H, d, J=16.1 Hz)
Yield: 67%
1H-NMR (400 MHz, CDCl3) δ: 6.57 (1H, d, J=15.9 Hz), 7.66-7.71 (4H, m), 7.78 (1H, d, J=15.9 Hz)
Yield: 85%
Reference: Chem. Pep. Chem. Zvesti, 1974, 28, 693-696.
Reference: Chem. Pep. Chem. Zvesti, 1969, 23, 173-180.
Ammonium thiocyanate (114 mg, 1.50 mmol) and PEG-400 (three drops) were sequentially added to a methylene chloride (5 mL) solution of acetyl chloride (155 mg, 1 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 2 hours.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=50:1 to 40:1) to obtain phenylacetyl isothiocyanate (colorless crystals) (132 mg, 75%).
The following compounds were obtained via a similar reaction.
Reference: Bioorg. Med. Chem. Lett., 2008, 18, 1945-1951.
Reference: J. Org. Chem., 2008, 73, 2096-2104.
Thionyl chloride (0.15 mL, 2.00 mmol) was added to a benzene (5 mL) solution of (2,6-difluorophenyl)acetic acid (172 mg, 1.00 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, methylene chloride (5 mL) was added to the mixture. After the sequential addition of ammonium thiocyanate (114 mg, 1.50 mmol) and PEG-400 (four drops), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=50:1 to 40:1) to obtain (2,6-difluorophenyl)acetyl isothiocyanate (colorless crystals) (105 mg, 49%).
Thionyl chloride (0.15 mL, 2.00 mmol) was added to a benzene (5 mL) solution of cyclohexylacetic acid (142 mg, 1.00 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, methylene chloride (5 mL) was added to the mixture. After the sequential addition of ammonium thiocyanate (114 mg, 1.50 mmol) and PEG-400 (four drops), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=80:1 to 70:1) to obtain (cyclohexyl)acetyl isothiocyanate (colorless crystals) (120 mg, 66%).
Thionyl chloride (0.29 mL, 4.00 mmol) was added to a methylene chloride (5 mL) solution of 2-thiopheneacetic acid (284 mg, 2.00 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, methylene chloride (5 mL) was added to the mixture. After the sequential addition of thioammonium cyanide (228 mg, 3.00 mmol) and polyethylene glycol (PEG-400, six drops), the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=100:1) to obtain thiophen-2-ylacetyl chloride (colorless crystals) (133 mg, 36%).
2 mL of a methylene chloride solution of the sulfonyl chloride compound 4a (1.0 mmol) was added to 5 mL of a methylene chloride solution of the diamine compound 5a (5.0 mmol) at 0° C. in an argon atmosphere using a cannula, and the mixture was stirred at room temperature for 3 hours.
10 mL of water was added to the mixture.
The organic layer was extracted with methylene chloride, dried over sodium sulfate, dried, and filtered.
The solvent was evaporated to obtain the amine compound 2a.
The following compound was obtained via a similar reaction.
Reference: Zh. Obshch. Khim., 1962, 32, 887-892.
Reference: Zh. Obshch. Khim., 1962, 32, 887-892.
Reference: J. Med. Chem., 1982, 25, 1286-1292.
Reference: Chin. J. Chem., 2011, 29, 2081-2085.
Reference: J. Med. Chem., 2012, 55, 4457-4478.
Pyridine (0.149 mL, 1.85 mmol) was added to 3 mL of a tetrahydrofuran solution of o-phenylenediamine (500 mg, 4.62 mmol) in an argon atmosphere. After the addition of 2 mL of a tetrahydrofuran solution of toluenesulfonyl chloride (294 mg, 1.54 mmol) at 0° C. using a cannula, the mixture was stirred at room temperature for 4 hours.
5 mL of water was added to the mixture.
The organic layer was extracted with methylene chloride, washed with 5 mL of a saturated sodium chloride solution, dried over sodium sulfate, and filtered.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=10:1) to obtain N-(2-aminophenyl)-4-methylbenzenesulfonamide (colorless crystals) (218 mg, 54%).
Reference: Angew. Chem. Int. Ed., 2007, 46, 7247-7250.
Pyridine (0.1 mL, 1.80 mmol) was added to a tetrahydrofuran (3 mL) solution of phenylenediamine (487 mg, 4.50 mmol) in an argon atmosphere. After the addition of a tetrahydrofuran (2 mL) solution of 4-chlorobenzenesulfonyl chloride (317 mg, 1.50 mmol) at 0° C. using a cannula, the mixture was stirred at room temperature for 4 hours.
After evaporating the solvent, water (5 mL) was added to the mixture. The organic layer was extracted with methylene chloride, washed with a saturated sodium chloride solution (5 mL), dried over sodium sulfate, and filtered, and the solvent was evaporated.
The residue was recrystallized from ethanol-water to obtain 2-p-tolylethanesulfonyl acid(2-aminophenyl)amide (384 mg, 91%) as a colorless crystalline substance.
1H-NMR (400 MHz, CDCl3): δ 2.36 (3H, s), 4.15 (2H, br), 5.95 (1H, br), 6.65 (td, J=8.1, 1.5 Hz), 6.76 (1H, dd, J=8.1, 1.5 Hz), 6.79 (1H, d, J=15.4 Hz), 6.99 (1H, dd, J=8.1, 1.5 Hz), 7.07 (1H, td, J=8.1, 1.5 Hz), 7.18 (2H, d, J=8.2 Hz), 7.32 (2H, d, J=8.2 Hz), 7.38 (1H, d, J=15.4 Hz)
The following compound was obtained via a similar reaction.
(1) Lithium hydroxide monohydrate (52 mg, 1.23 mmol) was added to a methanol-water (3:1) solution (4 mL) of phenoxyacetic acid methyl ester (102 mg, 0.61 mmol), and the mixture was refluxed with heating for 2 hours.
After evaporating the solvent, a 10% hydrochloric acid aqueous solution was added to the mixture until the aqueous layer became acidic, followed by extraction with ethyl acetate.
The organic layer was dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain phenoxyacetic acid (92 mg) as a colorless crystalline substance.
(2) Trifluoroacetic acid (0.6 mL, 8.08 mmol) was added to a methylene chloride (3.5 mL) solution of [(4-methoxy-2-methylphenylcarbamoyl)methyl]carbamic acid tert-butyl ester (236 mg, 0.80 mmol) in an argon atmosphere, and the mixture was stirred at room temperature overnight.
A saturated sodium bicarbonate solution was added to the reaction mixture at 0° C. until the aqueous layer became basic, followed by extraction with methylene chloride.
The organic layer was dried over potassium carbonate, and filtered, and the solvent was evaporated to obtain 2-amino-N-(4-methoxy-2-methylphenyl)acetamide (146 mg) as a colorless crystalline substance.
(3) 1,1-Carbonyldiimidazole (92 mg, 0.57 mmol) was added to a methylene chloride (5 mL) solution of phenoxyacetic acid (78 mg, 0.52 mmol) in an argon atmosphere, and the mixture was stirred at room temperature for 1 hour. After the addition of a methylene chloride (2 mL) solution of 2-amino-N-(4-methoxy-2-methylphenyl)acetamide (100 mg, 0.52 mmol) using a cannula, the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=5:1 to 3:1) to obtain N-[(4-methoxy-2-methylphenylcarbamoyl)methyl]-2-phenoxyacetamide (113 mg) as a colorless crystalline substance.
Yield: 67%
Melting point: 165 to 166° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 2.19 (3H, s), 3.76 (3H, s), 4.16 (2H, d, J=5.9 Hz), 4.57 (2H, s), 6.72 (2H, m), 6.92 (2H, d, J=7.6 Hz), 7.01 (1H, t, J=7.6 Hz), 7.30 (2H, t, J=7.6 Hz), 7.38 (1H, br), 7.52 (1H, d, J=9.5 Hz), 7.62 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 17.95, 42.06, 55.09, 66.86, 111.15, 114.74, 115.32, 121.20, 126.67, 128.81, 129.50, 134.03, 156.83, 157.68, 167.49, 168.21
IR (KBr): 1668, 3258 cm−1
MS (EI): m/z 328 (M+)
The following compounds were obtained in the same manner as in Example 1.
Yield: 80%
Melting point: 170 to 171° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 2.20 (3H, s), 3.76 (3H, s), 4.16 (2H, d, J=5.6 Hz), 4.53 (2H, s), 6.71-6.73 (2H, m), 6.85 (2H, d, J=9.0 Hz), 7.24-7.27 (2H, m), 7.35 (1H, br), 7.50 (1H, d, J=9.5 Hz), 7.56 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 17.95, 42.03, 55.09, 67.10, 111.15, 115.32, 116.55, 124.91, 126.68, 128.80, 129.23, 134.05, 156.57, 156.83, 167.45, 167.91
IR (KBr): 1666, 3267 cm−1
MS (EI): m/z 362 (M+)
Yield: 69%
Melting point: 159 to 160° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): 2.19 (3H, s), 3.76 (3H, s), 4.16 (2H, d, J=5.6 Hz), 4.52 (2H, s), 6.71-6.73 (2H, m), 6.81 (2H, d, J=8.8 Hz), 7.36 (1H, br), 7.40 (2H, d, J=8.8 Hz), 7.50 (1H, d, J=9.5 Hz), 7.59 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 17.95, 55.10, 67.03, 100.08, 111.16, 112.63, 115.32, 117.07, 126.69, 128.79, 132.12, 134.05, 156.83, 157.02, 167.44, 167.88
IR (KBr): 1663, 3273 cm−1
MS (EI): m/z 406 (M+)
Yield: 78%
Melting point: 205 to 206° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.13 (2H, d, J=5.6 Hz), 4.54 (2H, s), 6.86 (2H, d, J=9.0 Hz), 7.24-7.28 (3H, m), 7.27 (2H, d, J=9.0 Hz), 7.61 (2H, d, J=8.8 Hz), 7.98 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.42, 67.05, 86.74, 116.56, 121.33, 124.95, 129.23, 137.39, 138.62, 156.52, 167.52, 167.94
IR (KBr): 1663, 3294 cm−1
MS (EI): m/z 444 (M+)
Yield: 91%
Melting point: 211 to 212° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.13 (2H, d, J=5.6 Hz), 4.53 (2H, s), 6.81 (2H, d, J=8.8 Hz), 7.24-7.30 (3H, m), 7.41 (2H, d, J=8.8 Hz), 7.61 (2H, d, J=8.8 Hz), 7.98 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.43, 66.99, 86.75, 112.69, 117.08, 121.34, 132.14, 137.40, 138.63, 156.98, 167.53, 167.93
IR (KBr): 1661, 3290 cm−1
MS (EI): m/z 488 (M+)
Yield: 82%
Melting point: 169 to 170° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 2.22 (3H, s), 3.78 (3H, s), 4.18 (2H, d, J=5.6 Hz), 4.54 (2H, s), 6.74-6.75 (2H, m), 6.89 (2H, dd, J=8.9, 4.1 Hz), 7.01 (2H, t, J=8.9 Hz), 7.38 (1H, br), 7.54 (1H, d, J=9.8 Hz), 7.59 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 17.93, 42.03, 55.08, 67.48, 111.14, 115.31, 115.82 (d, J=22.3 Hz), 116.12 (d, J=8.3 Hz), 126.67, 128.81, 134.03, 154.05 (d, J=2.5 Hz), 156.82, 156.84 (d, J=236.5 Hz), 167.47, 168.09
IR (KBr): 3260, 1666 cm−1
MS (EI): m/z 346 (M+)
Yield: 96%
Melting point: 190 to 191° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.17 (2H, d, J=4.9 Hz), 4.55 (2H, s), 6.90 (2H, dd, J=8.8, 4.0 Hz), 7.02 (2H, t, J=8.8 Hz), 7.12 (1H, br), 7.29 (2H, d, J=8.5 Hz), 7.38 (1H, br), 7.63 (2H, d, J=8.5 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 42.41, 67.44, 86.73, 115.85 (d, J=23.2 Hz), 116.14 (d, J=8.3 Hz), 121.34, 137.39, 138.64, 154.02 (d, J=2.5 Hz), 156.87 (d, J=236.6 Hz), 167.55, 168.13
IR (KBr): 3312, 1672 cm−1
MS (EI): m/z 428 (M+)
Yield: 97%
Melting point: 213 to 214° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.13 (2H, d, J=5.9 Hz), 4.53 (2H, s), 6.82 (2H, d, J=8.9 Hz), 7.00 (2H, d, J=8.5 Hz), 7.31 (1H, br), 7.40-7.44 (2H, m), 7.41 (2H, d, J=8.9 Hz), 7.95 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.28, 66.98, 112.65, 115.28 (d, J=22.3 Hz), 117.07, 120.90 (d, J=7.4 Hz), 132.11, 135.18 (d, J=2.5 Hz), 156.99, 157.96 (d, J=239.8 Hz), 167.24, 167.88
IR (KBr): 3389, 1657 cm−1
MS (EI): m/z 380 (M+)
Yield: 96%
Melting point: 202 to 203° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.14 (2H, d, J=5.9 Hz), 4.53 (2H, s), 6.88 (2H, dd, J=9.3, 4.1 Hz), 6.98-7.02 (4H, m), 7.34 (1H, br), 7.43 (2H, dd, J=9.0, 4.6 Hz), 7.99 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.30, 67.44, 115.33 (d, J=22.3 Hz), 115.87 (d, J=23.2 Hz), 116.14 (d, J=8.3 Hz), 120.92 (d, J=7.4 Hz), 135.22 (d, J=1.7 Hz), 154.04 (d, J=1.7 Hz), 156.88 (d, J=236.5 Hz), 158.00 (d, J=239.0 Hz), 167.32, 168.16
IR (KBr): 3296, 1672 cm−1
MS (EI): m/z 320 (M+)
Yield: 92%
Melting point: 192 to 193° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.15 (2H, d, J=5.6 Hz), 4.53 (2H. s), 6.88 (2H, dd, J=8.9, 4.3 Hz), 7.00 (2H, t, J=8.9 Hz), 7.38 (2H, d, J=9.1 Hz), 7.39 (1H, br), 7.42 (2H, d, J=9.1 Hz), 8.22 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.40, 67.40, 114.83, 115.85 (d, J=23.2 Hz), 116.12 (d, J=8.3 Hz), 121.05, 131.56, 138.20, 154.01 (d, J=2.5 Hz), 156.85 (d, J=236.6 Hz), 167.59, 168.16
IR (KBr): 1686, 3256 cm−1
MS (EI): m/z 380 (M+)
Yield: 79%
Melting point: 190 to 191° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 3.79 (3H, s), 4.15 (2H, d, J=5.6 Hz), 4.55 (2H, s), 6.84 (2H, d, J=9.0 Hz), 6.86 (2H, d, J=8.9 Hz), 7.34 (1H, br), 7.38 (2H, d, J=9.0 Hz), 7.43 (2H, d, J=8.9 Hz), 7.78 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.22, 55.12, 66.98, 112.66, 113.85, 117.07, 120.73, 131.91, 132.14, 155.21, 156.99, 166.80, 167.84
IR (KBr): 1655, 3261 cm−1
MS (EI): m/z 392 (M+)
Yield: 84%
Melting point: 185 to 186° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 3.80 (3H, s), 4.16 (2H, d, J=5.6 Hz), 4.55 (2H, s), 6.86-6.92 (2H, m), 6.87 (2H, d, J=8.9 Hz), 7.02 (2H, t, J=8.5 Hz), 7.38 (1H, br), 7.39 (2H, d, J=8.9 Hz), 7.80 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.24, 55.14, 67.45, 113.87, 115.88 (d, J=23.2 Hz), 116.15 (d, J=7.4 Hz), 120.76, 131.96, 154.05 (d, J=1.7 Hz), 155.24, 156.88 (d, J=236.5 Hz) 166.86, 168.10
IR (KBr): 1659, 3279 cm−1
MS (EI): m/z 332 (M+)
Yield: 78%
Melting point: 210 to 211° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 1.12-1.19 (3H, m), 1.31-1.38 (3H, m), 1.53-1.61 (1H, m), 1.67-1.75 (2H, m), 1.88-1.93 (2H, m), 3.76 (1H, br), 3.96 (2H, d, J=5.4 Hz), 4.51 (2H, s), 5.64 (1H, br), 6.83 (2H, d, J=9.1 Hz), 7.42 (2H, d, J=9.1 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 24.53, 25.17, 32.37, 41.59, 47.53, 66.94, 112.63, 117.03, 132.14, 156.97, 167.19, 167.56
IR (KBr): 1653, 3290 cm−1
MS (EI): m/z 370 (M+)
Yield: 91%
Melting point: 184 to 185° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 1.12-1.18 (3H, m), 1.31-1.40 (3H, m), 1.53-1.64 (1H, m), 1.67-1.75 (2H, m), 1.85-1.95 (2H, m), 3.78 (1H, br), 3.96 (2H, d, J=5.4 Hz), 4.50 (2H, s), 5.68 (1H, br), 6.89 (2H, dd, J=8.8, 4.3 Hz), 7.01 (2H, t, J=8.8 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 24.56, 25.20, 32.40, 41.61, 47.59, 67.42, 115.88 (d, J=23.2 Hz), 116.11 (d, J=8.3 Hz), 154.03 (d, J=1.7 Hz), 156.88 (d, J=236.5 Hz), 167.27, 167.83
IR (KBr): 1653, 3292 cm−1
MS (EI): m/z 308 (M+)
Yield: 100%
Melting point: 173 to 174° C.
1H-NMR (400 MHz, CDCl3): δ 4.22 (2H, d, J=1.5 Hz), 4.53 (2H, s), 6.81 (2H, d, J=9.0 Hz), 6.95 (2H, t, J=8.4 Hz), 7.04 (1H, br), 7.21-7.24 (1H, m), 7.40 (2H, d, J=9.0 Hz), 7.50 (1H, br)
IR (KBr): 1661, 3261 cm−1
Yield: 98%
Melting point: 195 to 196° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.02 (2H, d, J=5.4 Hz), 4.44 (2H, d, J=5.9 Hz), 4.48 (2H, s), 6.12 (1H, br), 6.79 (2H, d, J=9.1 Hz), 6.98 (1H, br), 7.24-7.35 (5H, m), 7.38 (2H, d, J=9.1 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 41.80, 41.99, 66.99, 112.61, 117.04, 126.73, 127.15, 128.21, 132.13, 139.30, 156.99, 167.80, 168.55
IR (KBr): 1653, 3277 cm−1
MS (EI): m/z 376 (M+)
Yield: 88%
Melting point: 165 to 166° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.03 (2H, d, J=5.6 Hz), 4.45 (2H, d, J=5.6 Hz), 4.48 (2H, s), 6.16 (1H, br), 6.85 (2H, dd, J=8.9, 4.1 Hz), 6.97 (2H, t, J=8.9 Hz), 7.09 (1H, br), 7.22-7.35 (5H, m)
IR (KBr): 1655, 3263 cm−1
Yield: 94%
Melting point: 143 to 144° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 2.21 (3H, s), 3.76 (3H, s), 3.78 (3H, s), 4.17 (2H, d, J=6.1 Hz), 4.53 (2H, s), 6.73-6.75 (2H, m), 6.84 (2H, d, J=9.5 Hz), 6.88 (2H, d, J=9.5 Hz), 7.39 (1H, br), 7.53 (1H, d, J=9.5 Hz), 7.64 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 17.95, 42.01, 55.08, 55.33, 67.61, 111.14, 114.56, 115.31, 115.72, 126.66, 128.81, 134.02, 151.70, 153.82, 156.80, 167.49, 168.41
IR (KBr): 1660, 3273 cm−1
MS (EI): m/z 358 (M+)
Yield: 70%
Melting point: 115 to 116° C.
1H-NMR (400 MHz, CDCl3): δ 2.21 (3H, s), 3.78-3.81 (6H, m), 4.18 (2H, d, J=5.9 Hz), 4.57 (2H, s), 6.51-6.53 (2H, m), 6.58 (1H, d, J=7.8 Hz), 6.73-6.75 (2H, m), 7.21 (1H, t, J=7.8 Hz), 7.38 (1H, br), 7.52 (1H, d, J=9.5 Hz), 7.65 (1H, br)
IR (KBr): 1659, 3331 cm−1
Yield: 68%
Melting point: 184 to 185° C.
1H-NMR (400 MHz, CDCl3): δ 4.22 (2H, d, J=1.0 Hz), 4.54 (2H, s), 6.86 (2H, d, J=9.0 Hz), 6.96 (2H, t, J=8.2 Hz), 7.22-7.26 (1H, m), 7.26 (2H, d, J=9.0 Hz), 7.30 (1H, br), 7.50 (1H, br)
IR (KBr): 1663, 3261 cm−1
Yield: 84%
Melting point: 164 to 165° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): 4.25 (2H, d, J=3.2 Hz), 4.55 (2H, s), 6.89-7.01 (9H, m), 7.05 (1H, t, J=7.4 Hz), 7.29 (2H, t, J=7.4 Hz), 7.37 (1H, br), 7.60 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 41.58, 67.36, 111.88 (dd, J=17.8, 5.4 Hz), 114.19 (t, J=16.5 Hz), 116.14, 117.47, 120.58, 122.73, 128.06 (t, J=10.3 Hz), 129.92, 150.06, 154.04, 157.73 (dd, J=248.1, 5.8 Hz), 157.82, 167.91, 168.26
IR (KBr): 1665, 3273 cm−1
Yield: 82%
Melting point: 161 to 162° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 2.33 (3H, s), 4.25 (2H, s), 4.57 (2H, s), 6.74 (1H, d, J=8.3 Hz), 6.77 (1H, s), 6.83 (1H, d, J=8.3 Hz), 6.97 (2H, t, J=7.9 Hz), 7.19 (1H, t, J=7.9 Hz), 7.20-7.27 (1H, m), 7.38 (1H, br), 7.61 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 21.09, 41.56, 66.80, 111.87 (dd, J=19.0, 5.8 Hz), 114.19 (t, J=16.5 Hz), 115.44, 121.97, 128.04 (t, J=9.9 Hz), 128.21, 129.25, 139.03, 157.69, 157.73 (dd, J=248.1, 5.8 Hz), 167.88, 168.30
IR (KBr): 1680, 3258 cm−1
Yield: 95%
Melting point: 164 to 165° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 3.74 (3H, s), 4.23 (2H, s), 4.52 (2H, s), 6.82 (2H, d, J=9.1 Hz), 6.86 (2H, d, J=9.1 Hz), 6.95 (2H, t, J=8.1 Hz), 7.24-7.25 (1H, m), 7.36 (1H, br), 7.61 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 41.54, 55.35, 67.60, 111.88 (dd, J=17.8, 5.4 Hz), 114.19 (t, J=17.0 Hz), 114.59, 115.75, 128.04 (t, J=12.0 Hz), 151.73, 153.85, 157.72 (dd, J=249.4, 6.2 Hz), 167.90, 168.46
IR (KBr): 1666, 3271 cm−1
Yield: 34%
Melting point: 194 to 195° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 4.27 (2H, s), 4.54 (2H, s), 6.89 (2H, dd, J=9.1, 4.3 Hz), 6.95-7.03 (4H, m), 7.22-7.26 (1H, m), 7.39 (1H, br), 7.67 (1H, br)
IR (KBr): 1663, 3261 cm−1
Yield: 66%
Melting point: 174 to 175° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 4.57 (2H, s), 4.59 (2H. s), 6.84 (2H, d, J=9.0 Hz), 7.00 (2H, t, J=7.7 Hz), 7.33 (1H, t, J=7.7 Hz), 7.43 (2H, d, J=9.0 Hz), 7.62 (1H, br), 9.46 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 48.89, 67.03, 112.11 (dd, J=18.2, 4.1 Hz), 112.63, 116.18 (t, J=16.5 Hz), 117.09, 129.74 (t, J=9.5 Hz), 132.12, 156.99, 157.49 (dd, J=250.6, 5.8 Hz), 167.99, 203.40
IR (KBr): 1670, 3020, 3207 cm−1
Yield: 75%
Melting point: 160 to 161° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 3.74 (3H, s), 4.54 (2H, s), 4.57 (2H, d, J=6.1 Hz), 6.83 (2H, d, J=9.5 Hz), 6.87 (2H, d, J=9.5 Hz), 6.98 (2H, t, J=8.1 Hz), 7.31 (1H, t, J=8.1 Hz), 7.57 (1H, br), 9.45 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 48.90, 55.35, 67.64, 112.13 (dd, J=18.6, 4.5 Hz), 114.58, 115.75, 116.21 (t, J=16.5 Hz), 129.75 (t, J=9.9 Hz), 151.71, 153.83, 157.52 (dd, J=249.8, 5.0 Hz), 168.53, 203.48
IR (KBr): 1670, 3007, 3182 cm−1
Yield: 47%
Melting point: 174 to 175° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 2.30 (3H, s), 4.01 (2H, d, J=5.4 Hz), 4.44 (2H, d, J=5.6 Hz), 4.46 (2H, s), 6.06 (1H, br), 6.79 (2H, d, J=9.1 Hz), 7.14-7.24 (5H, m), 7.38 (2H, d, J=9.1 Hz)
IR (KBr): 1649, 3275 cm−1
Yield: 76%
Melting point: 208 to 209° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 4.04 (2H, d, J=5.4 Hz), 4.41 (2H, d, J=6.1 Hz), 4.50 (2H, s), 6.26 (1H, br), 6.81 (2H, d, J=9.0 Hz), 7.14 (2H, d, J=8.5 Hz), 7.20-7.35 (1H, m), 7.41 (2H, d, J=9.0 Hz), 7.46 (2H, d, J=8.5 Hz)
IR (KBr): 1655, 3271 cm−1
Yield: 85%
Melting point: 179 to 180° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 4.02 (2H, d, J=5.6 Hz), 4.45 (2H, d, J=5.9 Hz), 4.50 (2H, s), 6.30 (1H, br), 6.81 (2H, d, J=9.0 Hz), 7.19-7.26 (3H, m), 7.41 (2H, d, J=9.0 Hz), 7.79 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 35.60, 41.79, 66.96, 112.64, 117.02, 118.38 (d, J=24.8 Hz), 120.07 (d, J=9.1 Hz), 125.62 (d, J=14.9 Hz), 127.37 (d, J=3.3 Hz), 131.04 (d, J=5.0 Hz), 132.12, 156.96, 159.81 (d, J=249.8 Hz), 167.89, 168.86
IR (KBr): 1661, 3279 cm−1
Yield: 70%
Melting point: 227 to 228° C.
1H-NMR (400 MHz, CDCl3): δ 4.13 (2H, d, J=5.9 Hz), 4.53 (2H, s), 6.81 (2H, d, J=9.1 Hz), 7.16 (1H, t, J=8.1 Hz), 7.22-7.35 (2H, m), 7.37 (1H, d, J=8.1 Hz), 7.41 (2H, d, J=9.1 Hz), 7.74 (1H, s), 8.18 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.45, 66.97, 112.71, 117.08, 117.90, 121.48, 121.57, 125.93, 130.80, 132.15, 140.37, 156.98, 167.77, 168.00
IR (KBr): 1661, 3281 cm−1
Yield: 73%
Melting point: 174 to 175° C.
1H-NMR (400 MHz, CDCl3): δ 3.75 (3H, s), 4.16 (2H, d, J=5.6 Hz), 4.53 (2H, s), 6.83 (2H, d, J=9.3 Hz), 6.87 (2H, d, J=9.3 Hz), 7.16 (1H, t, J=7.8 Hz), 7.22-7.24 (1H, m), 7.39 (1H, d, J=7.8 Hz), 7.40 (1H, br), 7.74 (1H, s), 8.33 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.43, 55.36, 67.59, 114.60, 115.77, 117.90, 121.48, 121.57, 125.92, 130.81, 140.41, 151.70, 153.87, 167.83, 168.53
IR (KBr): 1663, 3312 cm−1
Yield: 71%
Melting point: 205 to 206° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 4.14 (2H, d, J=5.9 Hz), 4.54 (2H, s), 6.82 (2H, d, J=9.0 Hz), 7.09 (1H, d, J=8.3 Hz), 7.21-7.28 (2H, m), 7.30 (1H, d, J=8.3 Hz), 7.41 (2H, d, J=9.0 Hz), 7.61 (1H, s), 8.10 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.42, 66.95, 112.70, 117.07, 117.49, 118.60, 123.01, 130.47, 132.14, 133.08, 140.23, 156.97, 167.77, 167.99
IR (KBr): 1661, 3281 cm−1
Yield: 77%
Melting point: 197 to 198° C.
1H-NMR (400 MHz, CDCl3): δ 4.22 (2H, d, J=5.9 Hz), 4.58 (2H, s), 6.84 (2H, d, J=8.7 Hz), 7.41 (1H, br), 7.42 (2H, d, J=8.7 Hz), 7.48 (1H, t, J=8.5 Hz), 7.90 (1H, d, J=8.5 Hz), 7.96 (1H, d, J=8.5 Hz), 8.39 (1H, s), 8.76 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 42.51, 66.95, 112.69, 113.22, 117.06, 117.81, 125.08, 130.20, 132.13, 139.91, 147.92, 156.96, 168.07, 168.21
IR (KBr): 1676, 3265 cm−1
Yield: 82%
Melting point: 145 to 146° C.
1H-NMR (400 MHz, CDCl3): δ 4.26 (2H, s), 4.53 (2H, s), 5.00 (2H, s), 6.87 (2H, d, J=9.1 Hz), 6.92 (2H, d, J=9.1 Hz), 6.96 (2H, t, J=8.1 Hz), 7.30-7.42 (7H, m), 7.66 (1H, br)
IR (KBr): 1663, 3260 cm−1
Yield: 69%
Melting point: 192 to 193° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 2.34 (3H, s), 4.16 (2H, d, J=5.9 Hz), 4.57 (2H, s), 6.74 (1H, d, J=7.7 Hz), 6.77 (1H, s), 6.86 (1H, d, J=7.7 Hz), 7.20 (1H, t, J=7.7 Hz), 7.26-7.28 (2H, m), 7.37 (1H, br), 7.62 (2H, J=8.8 Hz), 8.21 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 21.10, 42.42, 66.75, 86.75, 111.73, 115.40, 121.30, 121.98, 129.23, 137.40, 138.65, 139.02, 157.64, 167.59, 168.31
IR (KBr): 1663, 3277 cm−1
Yield: 96%
Melting point: 169 to 170° C.
1H-NMR (400 MHz, CDCl3): δ 2.33 (3H, s), 4.16 (2H, d, J=5.6 Hz), 4.57 (2H, s), 5.05 (2H, s), 6.74 (1H, d, J=7.8 Hz), 6.77 (1H, s), 6.85 (1H, d, J=7.8 Hz), 6.93 (2H, d, J=9.0 Hz), 7.20 (1H, t, J=7.8 Hz), 7.32-7.43 (8H, m), 7.91 (1H, br)
IR (KBr): 1663, 3329 cm−1
Palladium hydroxide (5 mg) was added to a methanol solution (10 mL) of 2-(4-benzyloxyphenoxy)-N-[(2,6-difluorophenylcarbamoyl)methyl]acetamide (91 mg, 0.21 mmol) in a hydrogen atmosphere, and the mixture was stirred at room temperature overnight.
After filtering the reaction mixture through celite, the solvent was evaporated to obtain N-[(2,6-difluorophenylcarbamoyl)methyl]-2-(4-hydroxyphenoxy)acetamide (72 mg) as a colorless crystalline substance.
Yield: 100%
Melting point: 197 to 198° C.
1H-NMR (400 MHz, CDCl3): δ 3.98 (2H, s), 4.41 (2H, s), 6.67 (2H, d, J=8.8 Hz), 6.81 (2H, d, J=8.8 Hz), 7.14 (2H, t, J=7.6 Hz), 7.32 (1H, t, J=7.6 Hz), 8.35 (1H, br), 9.72 (1H, br)
IR (KBr): 1680, 3261 cm−1
Palladium hydroxide (10 mg) was added to a methanol-ethanol (5:1) solution (60 mL) of N-(4-benzyloxyphenylcarbamoyl)-2-m-tolyloxyacetamide (200 mg, 0.49 mmol) in a hydrogen atmosphere, and the mixture was stirred at room temperature overnight.
After filtering the reaction mixture through celite, the solvent was evaporated to obtain N-[(4-hydroxyphenylcarbamoyl)methyl]-2-m-tolyloxyacetamide (154 mg) as a colorless crystalline substance.
Yield: 99%
Melting point: 186 to 187° C.
1H-NMR (400 MHz, DMSO-d6): δ 2.27 (3H, s), 3.90 (2H, d, J=5.4 Hz), 4.51 (2H, s), 6.68 (2H, d, J=8.4 Hz), 6.77-6.82 (3H, m), 7.17 (1H, t, J=7.7 Hz), 7.33 (2H, d, J=8.4 Hz), 8.30 (1H, br), 9.20 (1H, br), 9.71 (1H, m)
13C-NMR (100 MHz, DMSO-d6): δ 21.13, 42.26, 66.82, 111.78, 115.15, 115.45, 121.04, 122.02, 129.29, 130.43, 139.09, 153.52, 157.72, 166.69, 168.27
IR (KBr): 1663, 3339 cm−1
(1) Trifluoroacetic acid (1.0 mL, 13.6 mmol) was added to a methylene chloride (5.7 mL) solution of [(2,6-difluorophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (384 mg, 1.34 mmol) in an argon atmosphere, and the mixture was stirred at room temperature overnight.
A saturated sodium bicarbonate solution was added to the reaction mixture at 0° C. until the aqueous layer became basic.
The organic layer was extracted with methylene chloride, dried over potassium carbonate, and filtered.
The solvent was evaporated to obtain 2-amino-N-(2,6-difluorophenyl)acetamide (colorless crystals) (122 mg, yield: 49%).
(2) Diethylamine (0.17 mL, 1.22 mmol) was added to a methylene chloride (4 mL) solution of 2-amino-N-(2,6-difluorophenyl)acetamide (114 mg, 0.61 mmol) in an argon atmosphere. After the addition of benzylsulfamoyl chloride (114 mg, 0.67 mmol) at 0° C., the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=4:1 to 3:1) to obtain N-(2,6-difluorophenyl)-2-phenylmethanesulfonylaminoacetamide (colorless crystals) (113 mg, DR-1).
Yield: 54%
Melting point: 141 to 142° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 3.77 (2H, s), 4.35 (2H, s), 5.00 (1H, br), 6.94 (2H, t, J=8.2 Hz), 7.19-7.24 (1H, m), 7.37-7.43 (6H, m)
The following compounds were obtained in the same manner as in Example 5.
Yield: 70%
Melting point: 129 to 130° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 2.42 (3H, s), 3.79 (2H, s), 5.36 (1H, br), 6.93 (2H, t, J=8.2 Hz), 7.17-7.24 (1H, m), 7.32 (2H, d, J=8.2 Hz), 7.72 (1H, br), 7.76 (2H, d, J=8.2 Hz)
Yield: 38%
Melting point: 147 to 148° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 1.46 (3H, d, J=7.1 Hz), 3.52 (2H, s), 4.27 (2H, s), 4.90 (1H, br), 5.06 (1H, quint, J=7.1 Hz), 6.27 (1H, br), 7.24-7.35 (10H, m)
Yield: 59%
1H-NMR (400 MHz, CDCl3): δ 1.42 (3H, d, J=7.1 Hz), 2.40 (3H, s), 3.53 (2H, s), 5.02 (1H, quint, J=7.1 Hz), 5.25 (1H, br), 6.52 (1H, br), 7.22-7.32 (7H, m), 7.70 (2H, d, J=8.3 Hz)
Yield: 30%
Melting point: 92 to 93° C.
1H-NMR (400 MHz, CDCl3): δ 3.71 (2H, d, J=5.4 Hz), 4.30 (2H, s), 4.69 (1H, br), 5.15 (2H, s), 7.30-7.42 (10H, m)
Helv. Chim. Acta, 1996, 79, 1843-1862.
Yield: 31%
1H-NMR (400 MHz, CDCl3): δ 2.32 (3H, s), 2.41 (3H, s), 3.58 (2H, d, J=5.9 Hz), 4.35 (2H, d, J=5.6 Hz), 5.07 (1H, br), 6.42 (1H, br), 7.10 (2H, d, J=7.2 Hz), 7.12 (2H, d, J=7.2 Hz), 7.29 (2H, d, J=8.2 Hz), 7.71 (2H, d, J=8.2 Hz)
Yield: 50%
Melting point: 207 to 208° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, CDCl3): δ 2.44 (3H, s), 3.61 (2H, d, J=6.1 Hz), 4.38 (2H, d, J=6.3 Hz), 5.03 (1H, br), 6.61 (1H, br), 7.12 (2H, d, J=8.3 Hz), 7.32 (2H, d, J=8.3 Hz), 7.45 (2H, d, J=8.3 Hz), 7.73 (2H, d, J=8.3 Hz)
Yield: 64%
Melting point: 123 to 124° C.
1H-NMR (400 MHz, CDCl3): δ 2.42 (3H, s), 3.58 (2H, d, J=6.3 Hz), 4.40 (2H, d, J=5.9 Hz), 5.01 (1H, br), 6.60 (1H, br), 7.16 (1H, t, J=8.1 Hz), 7.22 (1H, dd, J=8.1, 1.5 Hz), 7.23-7.24 (1H, m), 7.30 (2H, d, J=8.2 Hz), 7.70 (2H, d, J=8.2 Hz)
Indian J. Chem. Sect. B, 2002, 41B, 2635-2641.
Yield: 52%
1H-NMR (400 MHz, CDCl3): δ 3.74 (2H, d, J=6.1 Hz), 5.22 (1H, br), 7.20 (1H, t, J=8.1 Hz), 7.26-7.30 (1H, m), 7.37 (1H, d, J=8.1 Hz), 7.54 (2H, d, J=8.5 Hz), 7.74 (1H, s), 7.84 (2H, d, J=8.5 Hz), 7.93 (1H, br)
Yield: 41%
1H-NMR (400 MHz, CDCl3): δ 3.78 (2H, d, J=6.1 Hz), 5.28 (1H, br), 7.23 (1H, t, J=8.0 Hz), 7.21-7.33 (3H, m), 7.41 (1H, d, J=8.0 Hz), 7.78 (1H, s), 7.96 (2H, dd, J=8.7, 4.8 Hz), 8.04 (1H, br)
Yield: 49%
1H-NMR (400 MHz, CDCl3): δ 3.70 (2H, d, J=6.6 Hz), 3.88 (3H, s), 5.12 (1H, br), 7.01 (2H, d, J=8.9 Hz), 7.19 (1H, t, J=8.1 Hz), 7.26-7.28 (1H, m), 7.39 (1H, d, J=8.1 Hz), 7.73 (1H, s), 7.83 (2H, d, J=8.9 Hz), 8.16 (1H, br)
Yield: 67%
1H-NMR (400 MHz, CDCl3): δ 3.70 (2H, d, J=6.6 Hz), 3.87 (3H, s), 5.14 (1H, br), 7.01 (2H, d, J=8.8 Hz), 7.29 (2H, d, J=8.9 Hz), 7.45 (2H, d, J=8.9 Hz), 7.82 (2H, d, J=8.8 Hz), 8.18 (1H, br)
Yield: 54%
1H-NMR (400 MHz, CDCl3): δ 3.74 (2H, d, J=6.3 Hz), 5.19 (1H, br), 7.22-7.32 (4H, m), 7.44 (2H, d, J=8.8 Hz), 7.92 (2H, dd, J=9.0, 4.9 Hz), 7.98 (1H, br)
Indian J. Exp. Biol., 1966, 4, 190-1.
Yield: 27%
1H-NMR (400 MHz, CDCl3): δ 3.83 (2H, d, J=6.1 Hz), 5.27 (1H, br), 7.02 (1H, t, J=7.9 Hz), 7.22 (2H, t, J=8.5 Hz), 7.32 (1H, t, J=7.9 Hz), 7.55 (1H, d, J=7.9 Hz), 7.94 (2H, dd, J=8.5, 5.1 Hz), 8.23 (1H, d, J=7.9 Hz), 8.37 (1H, br)
Yield: 29%
1H-NMR (400 MHz, CDCl3): δ 3.83 (2H, d, J=6.1 Hz), 5.43 (1H, br), 7.02 (1H, t, J=8.1 Hz), 7.31 (1H, t, J=8.1 Hz), 7.51 (2H, d, J=8.7 Hz), 7.54 (1H, d, J=8.1 Hz), 7.85 (2H, d, J=8.7 Hz), 8.21 (1H, d, J=8.1 Hz), 8.37 (1H, br)
(1) Trifluoroacetic acid (1.6 mL, 22.07 mmol) was added to a methylene chloride (9 mL) solution of [(3-bromophenylcarbamoyl)methyl]carbamic acid tert-butyl ester (717 mg, 2.18 mmol) in an argon atmosphere, and the mixture was stirred at room temperature overnight.
A saturated sodium bicarbonate solution was added to the reaction mixture at 0° C. until the aqueous layer became basic.
The organic layer was extracted with methylene chloride, dried over potassium carbonate, and filtered.
The solvent was evaporated to obtain 2-amino-N-(3-bromophenyl)acetamide (colorless crystals) (421 mg, yield: 84%).
(2) Triethylamine (0.17 mL, 1.22 mmol) and DMAP (41 mg, 0.33 mmol) were added to a methylene chloride (5 mL) solution of 2-amino-N-(3-bromophenyl)acetamide (80 mg, 0.33 mmol) in an argon atmosphere. After the addition of benzylsulfamoyl chloride (69 mg, 0.36 mmol) at 0° C., the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=6:1 to 4:1) to obtain N-(3-bromophenyl)-2-phenylmethanesulfonylaminoacetamide (colorless crystals) (41 mg, DR-12).
Yield: 31%
Melting point: 215 to 216° C. (recrystallization solvent: toluene)
1H-NMR (400 MHz, CDCl3): δ 3.69 (2H, d, J=6.3 Hz), 4.38 (2H, s), 4.84 (1H, br), 7.17-7.27 (3H, m), 7.35-7.45 (5H, m), 7.75 (1H, s), 7.80 (1H, br)
The following compounds were obtained in the same manner as in Example 7.
Yield: 28%
Melting point: 200 to 201° C.
1H-NMR (400 MHz, CDCl3): δ 3.69 (2H, d, J=6.3 Hz), 4.38 (2H, s), 4.84 (1H, br), 7.42-7.52 (9H, m), 7.81 (1H, br)
Yield: 45%
1H-NMR (400 MHz, CDCl3): δ 3.67 (2H, d, J=6.3 Hz), 4.36 (2H, s), 4.84 (1H, br), 7.10 (1H, d, J=7.6 Hz), 7.20-7.32 (2H, m), 7.35-7.45 (5H, m), 7.60 (1H, s), 7.81 (1H, br)
Yield: 86%
1H-NMR (400 MHz, CDCl3): δ 2.43 (3H, s), 3.70 (2H, d, J=5.9 Hz), 5.04 (2H, s), 5.19 (1H, br), 6.93 (2H, d, J=8.8 Hz), 7.34-7.43 (9H, m), 7.77 (2H, d, J=8.1 Hz), 7.93 (1H, br)
Yield: 37%
1H-NMR (400 MHz, CDCl3): δ 2.34 (3H, s), 3.63 (2H, s), 4.36 (2H, d, J=5.9 Hz), 6.25 (1H, br), 7.10 (2H, d, J=8.2 Hz), 7.14 (2H, d, J=8.2 Hz), 7.15-7.21 (3H, m), 7.87 (2H, dd, J=8.7, 5.0 Hz)
(1) Palladium hydroxide (5 mg) was added to a methanol solution (30 mL) of [N′-[2-(4-fluorophenyl)acetyl]hydrazinocarbamoylmethyl]carbamic acid butyl ester (298 mg, 0.83 mmol) in a hydrogen atmosphere, and the mixture was stirred at room temperature overnight.
After filtering the reaction mixture through celite, the solvent was evaporated to obtain 2-amino-N′-(2-(4-fluorophenyl)acetyl)acetohydrazide (colorless crystals) (233 mg, yield: 100%).
(2) Triethylamine (0.084 mL, 0.60 mmol) and DMAP (37 mg, 0.30 mmol) were added to a methylene chloride (5 mL) solution of 2-amino-N′-(2-(4-fluorophenyl)acetyl)acetohydrazide (68 mg, 0.30 mmol) in an argon atmosphere. After the addition of toluenesulfamoyl chloride (63 mg, 0.33 mmol) at 0° C., the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=2:1 to 1.5:1) to obtain N-(2-{N′-[2-(4-fluorophenyl)acetyl]hydrazino}-2-oxoethyl)-4-methylbenzenesulfonamide (colorless crystals) (82 mg, DR-19).
Yield: 71%
1H-NMR (400 MHz, CDCl3): δ 2.44 (3H, s), 3.59 (2H, s), 4.81 (2H, s), 7.05 (2H, t, J=8.7 Hz), 7.10 (1H, br), 7.10-7.26 (4H, m), 7.36 (2H, d, J=8.2 Hz), 7.72 (2H, d, J=8.2 Hz)
(1) Tetrahydrofuran (1.6 mL, 2.37 mmol) was added to a methylene chloride (2 mL) solution of the Boc compound (144 mg, 0.44 mmol) in an argon atmosphere, and the mixture was stirred at room temperature overnight.
A saturated sodium bicarbonate solution was added to the reaction mixture at 0° C. until the aqueous layer became basic. The organic layer was extracted with methylene chloride, dried over potassium carbonate, and filtered, and the solvent was evaporated to obtain an amine compound (98 mg, 98%) as a colorless crystalline substance.
(2) Triethylamine (0.12 mL, 0.86 mmol) was added to a methylene chloride (5 mL) solution of the amine compound (98 mg, 0.43 mmol) in an argon atmosphere. After the addition of the sulfonyl chloride compound (102 mg, 0.47 mmol) at 0° C., the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=8:1 to 5:1) to obtain N-(2-bromophenyl)-2-(2-tolylethanesulfonylamino)acetamide (DR-30) (colorless crystals) (75 mg, yield: 43%).
1H-NMR (400 MHz, CDCl3): δ 2.39 (3H, s), 3.92 (2H, d, J=6.1 Hz), 5.12 (1H, br), 6.74 (1H, d, J=15.2 Hz), 7.01 (1H, t, J=7.9 Hz), 7.21 (2H, d, J=8.2 Hz), 7.30 (1H, t, J=7.9 Hz), 7.38 (2H, d, J=8.2 Hz), 7.53 (1H, d, J=7.9 Hz), 7.54 (1H, d, J=15.2 Hz), 8.28 (1H, d, J=7.9 Hz), 8.53 (1H, br);
Melting point: 132 to 133° C.
The following compounds were obtained in the same manner as in Example 9.
Yield: 83%
1H-NMR (400 MHz, CDCl3): δ 2.41 (3H, s), 3.74 (2H, d, J=4.4 Hz), 4.39 (2H, d, J=5.9 Hz), 5.07 (1H, br), 6.58 (1H, br), 6.66 (1H, d, J=15.5 Hz), 7.09 (2H, d, J=8.1 Hz), 7.23 (2H, d, J=7.8 Hz), 7.36-7.38 (4H, m), 7.51 (1H, d, J=15.5 Hz)
Melting point: 200 to 201° C.
Yield: 35%
1H-NMR (500 MHz, CDCl3): δ 2.39 (3H, s), 3.79 (3H, s), 3.83 (2H, d, J=4.6 Hz), 5.14 (1H, br), 6.70 (1H, d, J=15.5 Hz), 6.85 (2H, d, J=9.2 Hz), 7.21 (2H, d, J=8.0 Hz), 7.37-7.39 (4H, m), 7.52 (1H, d, J=15.5 Hz), 7.93 (1H, br)
Melting point: 145 to 146° C.
Yield: 65%
1H-NMR (500 MHz, CDCl3): δ 2.39 (3H, s), 3.83 (2H, d, J=6.3 Hz), 5.22 (1H, br), 6.69 (1H, d, J=15.2 Hz), 7.21 (2H, d, J=8.0 Hz), 7.36 (2H, d, J=8.0 Hz), 7.39-7.43 (4H, m), 7.51 (1H, d, J=15.2 Hz), 8.19 (1H, br)
Melting point: 216 to 219° C.
Yield: 65%
1H-NMR (500 MHz, CDCl3): δ 2.40 (3H, s), 3.73 (2H, d, J=6.3 Hz), 4.44 (2H, d, J=6.3 Hz), 5.01 (1H, br), 6.58 (1H, br), 6.65 (1H, d, J=15.5 Hz), 7.15-7.20 (2H, m), 7.22 (2H, d, J=8.0 Hz), 7.25-7.30 (1H, m), 7.36 (2H, d, J=8.0 Hz), 7.47 (1H, d, J=15.5 Hz);
13C-NMR (125 MHz, DMSO-d6): 21.02, 35.64 (d, J=4.8 Hz), 44.95, 118.32 (d, J=23.9 Hz), 119.99 (d, J=9.6 Hz), 125.46 (d, J=15.6 Hz), 125.64, 127.28 (d, J=3.6 Hz), 128.36, 129.54, 130.05, 130.80 (d, J=4.8 Hz), 139.20, 140.44, 159.73 (d, J=249.5 Hz), 168.53
Melting point: 161 to 162° C.
DR-35
Yield: 66%
1H-NMR (400 MHz, CDCl3): δ 2.36 (3H, s), 3.80 (2H, d, J=6.1 Hz), 5.00 (2H, s), 5.29 (1H, br), 6.68 (1H, d, J=15.4 Hz), 6.88 (2H, d, J=9.0 Hz), 7.17 (2H, d, J=7.8 Hz), 7.25-7.45 (9H, m), 7.49 (1H, d, J=15.4 Hz), 8.02 (1H, br)
13C-NMR (125 MHz, DMSO-d6): δ 20.99, 45.59, 69.33, 114.79, 120.80, 125.89, 127.64, 127.77, 128.31, 128.39, 129.51, 130.07, 131.90, 137.13, 139.05, 140.35, 154.38, 166.45
Melting point: 178 to 179° C.
(1) Concentrated hydrochloric acid (one drop) was added to an ethanol (3 mL) solution of the carboxylic acid represented by the general formula 4w (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, a saturated sodium bicarbonate solution was added to the mixture until the aqueous layer became basic, followed by extraction with methylene chloride.
The organic layer was dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain the ethyl ester compound represented by the general formula 4aw.
(2) Hydrazine monohydrate (0.05 mL, 1 mmol) was added to an ethanol (0.5 mL) solution of the ethyl ester compound represented by the general formula 4aw (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight to obtain the hydrazine compound represented by the general formula 3w.
After evaporating the solvent, a methylene chloride (5 mL) solution of the isothiocyanate compound represented by the general formula 2aw (1 mmol) was added to the mixture using a cannula, and the mixture was stirred at room temperature overnight.
The reaction mixture was filtered under suction to obtain the thiourea compound represented by the general formula 1aw.
Yield: 64%
Melting point: 232 to 233° C. (recrystallization solvent: ethanol)
1H-NMR (400 MHz, DMSO-d6): δ 3.85 (2H, s), 6.95-7.01 (3H, m), 7.38 (1H, dd, J=5.0, 1.3 Hz), 7.53 (2H, d, J=8.5 Hz), 7.64 (2H, d, J=8.5 Hz), 7.73 (1H, d, J=15.9 Hz), 11.16 (1H, br), 11.66 (1H, br), 12.57 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.90, 120.18, 125.18, 126.65, 126.67, 129.20, 129.90, 132.97, 135.26, 136.19, 143.14, 165.56, 166.26, 176.63
IR (KBr): 3211, 1684, 1655, 1630 cm−1
MS (EI): m/z 379 (M+)
Yield: 81%
Melting point: 219 to 220° C. (recrystallization solvent: hexane-acetone)
1H-NMR (400 MHz, DMSO-d6): δ 3.86 (2H, s), 6.95-6.98 (2H, m), 7.14 (1H, d, J=16.1 Hz), 7.38 (1H, dd, J=5.0, 1.3 Hz), 7.72 (1H, d, J=16.1 Hz), 7.81 (2H, s), 11.2 (1H, br), 11.9 (1H, br), 12.5 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.89, 125.18, 126.63, 126.65, 128.05, 129.00, 130.17, 134.61, 134.88, 136.16, 136.68, 164.59, 166.29, 176.44
IR (KBr): 3196, 1682, 1653, 1624 cm−1
MS (EI): m/z 447 (M+)
Yield: 60%
Melting point: 222 to 223° C. (recrystallization solvent: hexane-acetone)
1H-NMR (400 MHz, DMSO-d6) δ: 3.88 (2H, s), 6.97-7.00 (2H, m), 7.17 (1H, d, J=16.3 Hz), 7.40 (1H, dd, J=5.1, 1.5 Hz), 7.86 (1H, d, J=16.3 Hz), 7.89 (2H, d, J=8.9 Hz), 8.32 (2H, d, J=8.9 Hz), 11.20 (1H, br), 11.78 (1H, br), 12.56 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 33.89, 123.72, 124.25, 125.19, 126.66, 126.67, 129.25, 136.17, 140.38, 141.79, 148.16, 165.00, 166.28, 176.46
IR (KBr): 3244, 1682, 1655, 1522, 1342 cm−1
MS (EI): m/z 390 (M+)
Yield: 77%
Melting point: 212 to 213° C. (recrystallization solvent: ethanol)
1H-NMR (400 MHz, DMSO-d6): δ 2.33 (3H, s), 3.85 (2H, s), 6.92-6.98 (3H, m), 7.27 (2H, d, J=7.9 Hz) 7.38 (1H, dd, J=5.1, 1.0 Hz), 7.51 (2H, d, J=7.9 Hz), 7.69 (1H, d, J=15.9 Hz), 11.14 (1H, br), 11.60 (1H, br), 12.59 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 21.09, 33.92, 118.26, 125.20, 126.66, 126.69, 128.30, 129.75, 131.32, 136.22, 140.95, 144.69, 165.96, 166.26, 176.69
IR (KBr): 3227, 1684, 1661, 1630 cm−1
MS (EI): m/z 359 (M+)
Yield: 89%
Melting point: 215 to 216° C. (recrystallization solvent: acetone)
1H-NMR (400 MHz, DMSO-d6): δ 3.85 (2H, s), 6.93 (1H, d, J=15.9 Hz), 6.96-6.99 (2H, m), 7.31 (2H, t, J=8.8 Hz), 7.38 (1H, dd, J=4.9, 1.5 Hz), 7.69 (2H, dd, J=8.8, 5.6 Hz), 7.74 (1H, d, J=15.9 Hz), 11.15 (1H, br), 11.64 (1H, br), 12.58 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.93, 116.25 (d, J=22.3 Hz), 119.25, 125.23, 126.69, 126.72, 130.63 (d, J=8.3 Hz), 130.73 (d, J=3.3 Hz), 136.22, 143.42, 163.46 (d, J=248.9 Hz), 165.73, 166.31, 176.78
IR (KBr): 3186, 1680, 1651, 1628 cm−1
MS (EI): m/z 363 (M+)
Yield: 70%
Melting point: 207 to 208° C. (recrystallization solvent: methanol)
1H-NMR (600 MHz DMSO-d6) δ: 3.82 (3H, s), 3.85 (2H, s), 3.88 (3H, s), 6.62 (2H, m), 6.97 (3H, m), 7.38 (1H, dd, J=5.1, 1.5 Hz), 7.47 (1H, d, J=9.5 Hz), 7.81 (1H, d, J=15.8 Hz), 11.11 (1H, br), 11.56 (1H, br), 12.68 (1H, br)
13C-NMR (150 MHz, DMSO-d6) δ: 33.89, 55.54, 55.72, 98.45, 106.33, 115.42, 116.66, 125.15, 126.61, 126.65, 130.97, 136.22, 140.07, 159.98, 163.05, 166.19, 166.80, 176.94
IR (KBr): 3225, 1670, 1606, 1531, 1215, 1132.1 cm−1
MS (EI): m/z 405 (M+)
Yield: 81%
Melting point: 212 to 213° C. (recrystallization solvent: hexane-acetone)
1H-NMR (400 MHz, DMSO-d6): δ 3.85 (2H, s), 6.95-6.98 (2H, s), 7.06 (1H, d, J=15.9 Hz), 7.38 (1H, dd, J=4.9, 1.5 Hz), 7.67 (1H, d, J=15.9 Hz), 7.84 (2H, d, J=1.5 Hz), 7.92 (1H, d, J=1.5 Hz), 11.17 (1H, br), 11.59 (1H, br), 12.48 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 33.91, 122.77, 123.13, 125.22, 126.70, 129.69, 129.80, 134.89, 136.19, 138.31, 141.07, 165.00, 166.34, 176.59
IR (KBr): 3184, 1686, 1663, 1632 cm−1
MS (EI): m/z 501 (M+)
Yield: 50%
Melting point: 201 to 202° C. (recrystallization solvent: ethyl acetate)
1H-NMR (400 MHz, DMSO-d6): δ1.20 (6H, d, J=6.8 Hz), 2.91 (1H, sept, J=6.8 Hz), 3.85 (2H, s), 6.93-6.98 (3H, m), 7.34 (2H, d, J=8.1 Hz), 7.38 (1H, dd, J=5.0, 1.3 Hz), 7.54 (2H, d, J=8.1 Hz), 7.70 (1H, d, J=15.9 Hz), 11.14 (1H, br), 11.62 (1H, br), 12.59 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 23.56, 33.40, 33.89, 118.37, 125.18, 126.64, 126.67, 127.12, 128.40, 131.73, 136.20, 144.63, 151.64, 165.92, 166.24, 176.78
MS (EI): m/z 387 (M+)
Yield: 85%
Melting point: 231 to 232° C.
1H-NMR (400 MHz, DMSO-d6): δ 3.86 (2H, s), 6.96-6.99 (2H, m), 7.04 (1H, d, J=15.9 Hz), 7.38-7.41 (2H, m), 7.48 (2H, t, J=7.6 Hz), 7.70-7.80 (7H, m), 11.16 (1H, br), 11.66 (1H, br), 12.61 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.91, 119.26, 125.19, 126.68, 126.72, 127.30, 128.08, 128.94, 129.05, 131.31, 133.13, 136.21, 139.07, 142.26, 144.13, 165.79, 166.27, 176.74
MS (EI): m/z 421 (M+)
Yield: 59%
Melting point: 220 to 221° C. (recrystallization solvent: hexane-acetone)
1H-NMR (400 MHz, DMSO-d6): δ 3.87 (8H, s), 6.71 (2H, d, J=8.3 Hz), 6.96-6.98 (2H, m), 7.34-7.38 (3H, m), 8.06 (1H, d, J=15.9 Hz), 11.12 (1H, br), 11.67 (1H, br), 12.73 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.90, 55.92, 104.07, 110.99, 120.95, 125.18, 126.62, 126.67, 132.55, 135.32, 136.23, 159.82, 166.17, 167.53, 176.86;
IR (KBr): 3219, 1670, 1653, 1611 cm−1
MS (EI): m/z 405 (M+)
Yield: 69%
Melting point: 207 to 208° C.
1H-NMR (400 MHz, DMSO-d6): δ 3.85 (2H, s), 6.96-6.98 (2H, m), 7.20 (1H, d, J=16.0 Hz), 7.36-7.40 (3H, m), 7.60 (1H, d, J=16.0 Hz), 11.17 (1H, br), 11.87 (1H, br), 12.57 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.90, 101.73 (td, J=26.9, 2.5 Hz), 108.66 (td, J=15.3, 5.0 Hz), 124.64 (td, J=8.4, 3.0 Hz), 125.19, 126.65, 126.68, 129.11, 136.19, 161.35 (dt, J=254.7, 7.9 Hz), 161.42 (dt, J=254.7, 8.1 Hz), 165.39, 166.27, 176.44
IR (KBr): 3190, 1684, 1653, 1624 cm−1
MS (EI): m/z 399 (M+)
Yield: 89%
Melting point: 212 to 213° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.62 (2H, s), 6.93 (1H, d, J=15.7 Hz), 7.25-7.32 (7H, m), 7.69 (2H, dd, J=8.8, 5.6 Hz), 7.73 (1H, d, J=15.7 Hz), 11.10 (1H, s), 11.62 (1H, s), 12.56 (1H, s)
13C-NMR (100 MHz, DMSO-d6) δ: 39.57, 116.20 (d, J=21.5 Hz), 119.25, 126.61, 128.25, 129.20, 130.57 (d, J=9.1 Hz), 130.71 (d, J=3.3 Hz), 135.26, 143.33, 163.41 (d, J=248.9 Hz), 165.66, 167.29, 176.77
MS (EI): m/z 357 (M+)
Yield: 83%
Melting point: 224 to 225° C.
1H-NMR (400 MHz, DMSO-d6): δ 3.86 (2H, s), 6.95-6.99 (2H, m), 7.11 (1H, d, J=15.9 Hz), 7.38 (1H, dd, J=4.9, 1.5 Hz), 7.76-7.83 (5H, m), 11.17 (1H, br), 11.72 (1H, br), 12.53 (1H, br)
13C-NMR (100 MHz, DMSO-d6): δ 33.93, 122.34, 124.00 (q, J=272.4 Hz), 125.22, 126.02 (q, J=4.1 Hz), 126.70, 127.83, 128.86, 130.24 (q, J=32.0 Hz), 136.19, 138.03 (q, J=1.7 Hz), 142.66, 165.28, 166.34, 176.62
IR (KBr): 1636, 1661, 1684, 3196 cm−1
MS (EI): m/z 413 (M+)
Yield: 75%
Melting point: 210 to 211° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.62 (2H, s), 7.19 (1H, d, J=16.1 Hz), 7.23-7.40 (7H, m), 7.59 (1H, d, J=16.1 Hz), 11.13 (1H, br), 11.86 (1H, br), 12.53 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 39.54, 101.72 (td, J=27.3, 3.3 Hz), 108.64 (td, J=16.1, 4.1 Hz), 124.67, 126.60, 128.25, 129.07, 129.18, 135.25, 160.01 (dd, J=12.8, 9.9 Hz), 162.63 (dd, J=12.8, 9.9 Hz), 165.35, 167.28, 176.47
MS (EI): m/z 393 (M+)
Yield: 70%
Melting point: 192 to 193° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.62 (2H, s), 7.06 (1H, d, J=15.9 Hz), 7.23-7.32 (5H, m), 7.66 (1H, d, J=15.9 Hz), 7.84 (2H, s), 7.92 (1H, s), 11.13 (1H, br), 11.57 (1H, br), 12.47 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 39.59, 122.79, 123.12, 126.66, 128.30, 129.24, 129.80, 134.88, 135.26, 138.32, 141.06, 164.99, 167.42, 176.69
MS (EI): m/z 495 (M+)
Yield: 85%
Melting point: 217 to 218° C.
1H-NMR (400 MHz, DMSO-d6) δ: 6.98 (1H, d, J=15.7 Hz), 7.21 (1H, t, J=4.5 Hz), 7.32 (2H, t, J=8.7 Hz), 7.69-7.72 (2H, m), 7.77 (1H, d, J=15.7 Hz), 7.87 (1H, d, J=4.5 Hz), 7.90 (1H, d, J=4.5 Hz), 11.10 (1H, br), 11.67 (1H, br), 12.14 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 116.24 (d, J=22.3 Hz), 119.41, 128.21, 129.60, 130.63 (d, J=9.1 Hz), 130.76 (d, J=3.3 Hz), 132.00, 136.63, 143.47, 159.48, 163.45 (d, J=248.9 Hz), 165.44, 177.93
MS (EI): m/z 349 (M+)
Yield: 73%
Melting point: 211 to 212° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.62 (2H, s), 3.89 (6H, s), 6.71 (2H, d, J=8.3 Hz), 7.25-7.39 (7H, m), 8.05 (1H, d, J=15.9 Hz), 11.07 (1H, s), 11.65 (1H, s), 12.70 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 39.59, 55.94, 104.09, 111.02, 121.00, 126.63, 128.29, 129.21, 132.57, 135.19, 135.31, 159.84, 167.26, 167.53, 177.00
MS (EI): m/z 399 (M+)
Yield: 26%
Melting point: 209 to 210° C.
1H-NMR (400 MHz, DMSO-d6): δ 3.88 (6H, s), 6.72 (2H, d, J=8.5 Hz), 7.21 (1H, t, J=5.1 Hz), 7.37-7.42 (2H, m), 7.84-7.90 (2H, m), 8.09 (1H, d, J=15.9 Hz), 11.07 (1H, br), 11.68 (1H, br), 12.14 (1H, br)
MS (EI): m/z 391 (M+)
Yield: 59%
Melting point: 217 to 218° C.
1H-NMR (400 MHz, DMSO-d6) δ: 7.11 (1H, d, J=15.6 Hz), 7.21 (1H, t, J=4.3 Hz), 7.70 (1H, d, J=15.6 Hz), 7.86-7.93 (5H, m), 11.11 (1H, br), 11.62 (1H, br), 12.06 (1H, br);
13C-NMR (100 MHz, DMSO-d6) δ: 122.90, 123.11, 128.20, 129.62, 129.80, 132.022, 134.88, 136.59, 138.33, 141.16, 159.51, 164.73, 181.07
MS (EI): m/z 487 (M+)
Yield: 28%
Melting point: 195 to 196° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.61 (2H, s), 7.06 (1H, d, J=16.0 Hz), 7.11-7.35 (4H, m), 7.66 (1H, d, J=16.0 Hz), 7.84 (2H, s), 7.92 (1H, s), 11.11 (1H, br), 11.56 (1H, br), 12.44 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 30.88, 115.05 (d, J=21.5 Hz), 122.79, 123.16 (d, J=2.5 Hz), 128.35, 129.28, 129.78, 129.86, 131.11, 134.98 (d, J=8.3 Hz), 139.75 (d, J=282.9 Hz), 151.38, 176.13, 180.47
MS (EI): m/z 515 (M+)
Yield: 44%
Melting point: 224 to 225° C.
1H-NMR (400 MHz, DMSO-d6) δ: 7.11 (1H, d, J=15.7 Hz), 7.52 (2H, t, J=7.4 Hz), 7.60 (1H, t, J=7.4 Hz), 7.71 (1H, d, J=15.7 Hz), 7.87 (2H, s), 7.90 (2H, d, J=7.4 Hz), 7.93 (1H, s), 11.10 (1H, br), 11.63 (1H, br), 12.18 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 122.89, 123.12, 127.65, 128.51, 129.80, 132.02, 132.10, 134.88, 138.33, 141.13, 164.56, 164.83, 180.46
Yield: 76%
Melting point: 203 to 204° C.
1H-NMR (400 MHz, DMSO-d6) δ: 2.28 (3H, s), 3.57 (2H, s), 7.04-7.20 (5H, m), 7.66 (1H, d, J=15.9 Hz), 7.84 (2H, s), 7.91 (1H, s), 11.10 (1H, br), 11.55 (1H, br), 12.48 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 20.97, 122.78, 123.12, 126.29, 127.26, 128.18, 129.79, 129.84, 134.88, 135.11, 137.31, 138.31, 141.04, 164.97, 167.40, 176.58
Yield: 69%
Melting point: 202 to 203° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.58 (2H, s), 3.74 (3H, s), 6.81 (1H, d, J=7.9 Hz), 6.89 (1H, d, J=7.9 Hz), 6.92 (1H, s), 7.06 (1H, d, J=16.0 Hz), 7.21 (1H, t, J=7.9 Hz), 7.67 (1H, d, J=16.0 Hz), 7.83-7.84 (2H, m), 7.92 (1H, s), 11.10 (1H, br), 11.56 (1H, br), 12.45 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 39.63, 54.98, 112.17, 114.82, 121.48, 122.78, 123.11, 129.27, 129.78, 134.87, 136.69, 138.30, 141.02, 159.16, 164.95, 167.23, 176.72
Yield: 23%
Melting point: 213 to 214° C.
1H-NMR (400 MHz, DMSO-d6) δ: 2.57 (2H, t, J=7.8 Hz), 2.87 (2H, t, J=7.8 Hz), 7.06 (1H, d, J=16.0 Hz), 7.18-7.28 (5H, m), 7.67 (1H, d, J=16.0 Hz), 7.84 (2H, d, J=1.5 Hz), 7.92 (1H, t, J=1.5 Hz), 10.98 (1H, br), 11.54 (1H, br), 12.47 (1H, br)
13C-NMR (100 MHz; DMSO-d6) δ: 30.57, 34.46, 122.80, 123.10, 125.99, 128.22, 128.30, 129.76, 132.25, 138.30, 140.80, 154.67, 168.68, 176.29, 180.24
MS (EI): m/z 511 (M+)
(1) Concentrated hydrochloric acid (one drop) was added to an ethanol (3 mL) solution of the carboxylic acid represented by the general formula 5w (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, a saturated sodium bicarbonate solution was added to the mixture until the aqueous layer became basic, followed by extraction with methylene chloride.
The organic layer was dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain the ethyl ester compound represented by the general formula 5aw.
(2) Hydrazine monohydrate (0.05 mL, 1 mmol) was added to an ethanol (0.5 mL) solution of the ethyl ester compound represented by the general formula 4aw (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight to obtain the hydrazine compound represented by the general formula 3aw.
After evaporating the solvent, a methylene chloride (5 mL) solution of the isothiocyanate compound represented by the general formula 2bw (1 mmol) was added to the mixture using a cannula, and the mixture was stirred at room temperature overnight.
The reaction mixture was filtered under suction to obtain the thiourea compound represented by the general formula 1bw.
Yield: 63%
Melting point: 161 to 162° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.74 (2H, s), 3.81 (2H, s), 6.93-6.95 (2H, m), 7.24-7.37 (6H, m), 11.06 (1H, br), 11.73 (1H, br), 12.30 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 33.94, 42.11, 125.24, 126.70, 126.74, 127.08, 128.32, 128.51, 129.41, 134.30, 166.39, 167.43, 176.90
MS (EI): m/z 333 (M+)
Yield: 55%
Melting point: 182 to 183° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.57 (2H, s), 3.74 (2H, s), 7.11 (2H, t, J=8.7H), 7.20-7.40 (7H, m), 10.10 (1H, br), 11.02 (1H, br), 11.73 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 38.64, 42.07, 114.85 (d, J=21.5 Hz), 126.51, 127.01, 128.23, 128.45, 129.04, 129.37, 131.06 (d, J=8.3 Hz), 131.43 (d, J=2.5 Hz), 135.01 (d, J=286.9 Hz), 167.33, 172.57, 177.11
Yield: 24%
Melting point: 149 to 150° C.
1H-NMR (400 MHz, DMSO-d6) δ: 2.26 (3H, s), 3.53 (2H, s), 3.74 (2H, s), 7.09-7.29 (9H, m), 11.01 (1H, br), 11.72 (1H, br), 12.28 (1H, br)
Yield: 34%
Yield: 88%
Melting point: 174 to 175° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.67 (2H, s), 3.74 (2H, s), 7.07 (2H, t, J=7.4 Hz), 7.22-7.40 (6H, m), 11.07 (1H, br), 11.73 (1H, br), 12.23 (1H, br)
Yield: 4%
Melting point: 178 to 179° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.74 (2H, s), 4.03 (2H, s), 7.03-7.12 (3H, m), 7.23-7.34 (5H, m), 11.02 (1H, br), 11.74 (1H, br), 12.18 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 26.73, 42.06, 110.77 (d, J=20.7 Hz), 111.26 (d, J=25.6 Hz), 127.00, 128.44, 129.35, 134.29, 159.86 (d, J=8.3 Hz), 162.31 (d, J=6.3 Hz), 165.60, 172.53, 177.32
Yield: 41%
Melting point: 88 to 90° C.
1H-NMR (400 MHz, DMSO-d6) δ: 2.52 (2H, m), 2.83 (2H, m), 3.74 (2H, s), 7.16-7.30 (10H, m), 10.80 (1H, br), 11.70 (1H, br), 12.28 (1H, br)
MS (EI): m/z 341 (M+)
Yield: 35%
Melting point: 178 to 179° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.57 (2H, s), 3.74 (2H, s), 7.12-7.32 (8H, m), 11.03 (1H, br), 11.72 (1H, br), 12.28 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 38.60, 41.08, 115.03 (t, J=20.3 Hz), 128.22, 129.15, 130.38 (d, J=2.5 Hz), 131.01 (d, J=7.9 Hz), 131.32 (d, J=7.9 Hz), 161.32 (d, J=242.3 Hz), 167.24, 172.38, 176.98
MS (EI): m/z 363 (M+)
Yield: 59%
Melting point: 186 to 187° C.
1H-NMR (400 MHz, DMSO-d6) δ: 3.57 (2H, s), 3.88 (2H, s), 7.08-7.14 (4H, m), 7.30-7.40 (3H, m), 11.03 (1H, br), 11.86 (1H, br), 12.09 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 29.27, 30.70, 38.62, 111.34 (dd, J=5.8, 19.0 Hz), 114.95 (d, J=20.7 Hz), 129.83 (t, J=10.3 Hz), 131.03 (d, J=8.3 Hz), 131.40 (d, J=3.3 Hz), 159.81 (t, J=10.3 Hz), 162.25 (t, J=8.3 Hz), 167.31, 170.28, 176.85
MS (EI): m/z 381 (M+)
(1) Concentrated hydrochloric acid (one drop) was added to an ethanol (3 mL) solution of the carboxylic acid represented by the general formula 4w (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight.
After evaporating the solvent, a saturated sodium bicarbonate solution was added to the mixture until the aqueous layer became basic, followed by extraction with methylene chloride.
The organic layer was dried over sodium sulfate, and filtered, and the solvent was evaporated to obtain the ethyl ester compound represented by the general formula 4aw.
(2) Hydrazine monohydrate (0.05 mL, 1 mmol) was added to an ethanol (0.5 mL) solution of the ethyl ester compound represented by the general formula 4aw (1 mmol) in an argon atmosphere, and the mixture was refluxed with heating overnight to obtain the hydrazine compound represented by the general formula 3w.
After evaporating the solvent, a methylene chloride (5 mL) solution of the isothiocyanate compound represented by the general formula 2cw (1 mmol) was added to the mixture using a cannula, and the mixture was stirred at room temperature overnight. The reaction mixture was filtered under suction to obtain the thiourea compound represented by the general formula 1cw.
Yield: 62%
Melting point: 132 to 133° C.
1H-NMR (400 MHz, DMSO-d6) δ: 0.93-1.92 (5H, m), 2.27 (2H, d, J=6.8 Hz), 3.58 (2H, s), 7.13 (2H, t, J=8.8 Hz), 7.30-7.40 (2H, m), 11.04 (1H, br), 11.46 (1H, br), 12.42 (1H, br)
13C-NMR (100 MHz, DMSO-d6) δ: 24.48, 25.66, 32.24, 34.55, 38.60, 42.93, 114.96 (d, J=21.5 Hz), 131.04 (d, J=8.3 Hz), 131.43 (d, J=2.5 Hz), 163.90 (d, J=282.9 Hz), 167.33, 174.15, 176.75 MS (EI): m/z 351 (M+)
Yield: 28%
1H-NMR (500 MHz, DMSO-d6) δ: 3.57 (2H, s), 3.98 (2H, s), 6.96-7.00 (2H, m), 7.12 (2H, t, J=8.7 Hz), 7.33 (2H, dd, J=8.7, 5.7 Hz), 7.41 (1H, dd, J=3.8, 2.6 Hz), 11.03 (1H, br), 11.74 (1H, br), 12.18 (1H, br)
Yield: 42%
1H-NMR (500 MHz, DMSO-d6) δ: 2.72 (2H, t, J=7.5 Hz), 2.83 (2H, t, J=7.5 Hz), 3.58 (2H, s), 7.13 (2H, t, J=9.0 Hz), 7.17 (1H, td, J=7.4, 1.7 Hz), 7.21 (2H, dd, J=7.4, 1.7 Hz), 7.27 (2H, td, J=7.4, 1.7 Hz), 7.34 (2H, dd, J=9.0, 5.6 Hz), 11.02 (1H, br), 11.52 (1H, br), 12.33 (1H, br)
Phenyl isocyanate (0.051 mL, 0.47 mmol) was added to 5 mL of a methylene chloride solution of N-(2-aminoethyl)-4-methylbenzenesulfonamide (100 mg, 0.47 mmol), and the mixture was stirred at room temperature overnight.
After evaporating the solvent, the residue was purified by silica gel column chromatography (15 g, hexane:acetone=10:1 to 1:1) to obtain 4-methyl-N-[2-(3-phenylureido)ethyl]benzenesulfonamide (colorless crystals) (89 mg, 57%).
1H-NMR (400 MHz, CDCl3): δ 2.38 (3H, s), 3.06 (2H, t, J=5.4 Hz), 3.34 (2H, t, J=5.4 Hz), 5.17 (1H, br), 5.40 (1H, br), 6.51 (1H, br), 7.07 (1H, t, J=7.0 Hz), 7.24-7.31 (6H, m), 7.72 (2H, d, J=8.1 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.92, 38.82, 42.82, 117.65, 121.05, 126.55, 128.62, 129.63, 137.30, 140.40, 142.64, 155.15
IR (KBr): 1161, 1325, 1593, 1645, 3302 cm−1
MS (EI): m/z 333 (M+)
Melting point: 154 to 155° C. (recrystallization solvent: toluene)
The following compounds were obtained in the same manner as in Example 14.
Yield: 88%
1H-NMR (400 MHz, CDCl3): δ 2.40 (3H, s), 3.07 (2H, t, J=4.8 Hz), 3.35 (2H, t, J=4.8 Hz), 5.12 (1H, br), 5.33 (1H, br), 6.45 (1H, br), 6.97 (2H, t, J=8.2 Hz), 7.24-7.29 (4H, m), 7.72 (2H, d, J=7.8 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.92, 38.88, 42.81, 115.07 (d, J=21.6 Hz), 119.27 (d, J=8.4 Hz), 126.56, 129.64, 136.78 (d, J=2.4 Hz), 137.33, 142.65, 155.22, 156.91 (d, J=237.5 Hz)
IR (KBr): 1165, 1323, 1508, 1645, 3314 cm−1
MS (EI): m/z 351 (M+)
Melting point: 161 to 162° C. (recrystallization solvent: toluene)
Yield: 62%
1H-NMR (400 MHz, CDCl3): δ 2.40 (3H, s), 3.07 (2H, t, J=4.9 Hz), 3.37 (2H, t, J=4.9 Hz), 5.52 (2H, m), 7.01 (1H, br), 7.10 (1H, dd, J=8.7, 2.4 Hz), 7.22-7.27 (1H, m), 7.28 (2H, d, J=8.1 Hz), 7.48 (1H, d, J=2.4 Hz), 7.71 (2H, d, J=8.1 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.89, 38.90, 42.56, 117.68, 118.66, 122.24, 126.54, 129.61, 130.37, 130.90, 137.30, 140.65, 142.61, 154.76
IR (KBr): 1157, 1319, 1541, 1674, 3393 cm−1
MS (EI): m/z 401 (M+)
Melting point: 154 to 155° C.
Yield: 89%
1H-NMR (400 MHz, CDCl3): δ 2.39 (3H, s), 3.10 (2H, t, J=5.6 Hz), 3.37 (2H, t, J=5.6 Hz), 3.85 (3H, s), 5.10 (1H, br), 5.33 (1H, br), 6.80 (1H, br), 6.86 (1H, dd, J=7.8, 1.6 Hz), 6.94 (1H, td, J=7.8, 1.6 Hz), 7.01 (1H, td, J=7.8, 1.6 Hz), 7.25-7.27 (2H, m), 7.74 (2H, d, J=8.3 Hz), 7.92 (1H, dd, J=7.8, 1.6 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.92, 38.86, 42.94, 55.61, 110.53, 118.04, 120.45, 121.04, 126.58, 129.38, 129.63, 137.34, 142.65, 147.34, 155.22
IR (KBr): 1155, 1321, 1572, 1647, 3277 cm−1
MS (EI): m/z 363 (M+)
Melting point: 184 to 185° C.
Yield: 73%
1H-NMR (400 MHz, CDCl3): δ 2.41 (3H, s), 3.20 (2H, t, J=5.5 Hz), 3.78 (2H, t, J=5.5 Hz), 3.88 (3H, s), 6.49 (1H, br), 6.99-7.03 (2H, m), 7.26-7.30 (5H, m), 7.59 (1H, br), 7.71 (2H, d, J=8.3 Hz)
13C-NMR (125 MHz, CDCl3): δ 21.43, 42.43, 44.48, 55.74, 111.97, 121.10, 124.93, 125.40, 126.95, 127.80, 129.71, 136.40, 143.50, 152.46, 180.92
MS (EI): m/z 379 (M+)
Yield: 97%
1H-NMR (400 MHz, CDCl3): δ 2.38 (3H, s), 3.04 (2H, t, J=5.1 Hz), 3.33 (2H, t, J=5.1 Hz), 3.74 (3H, s), 6.58 (1H, d, J=7.8 Hz), 6.78 (1H, d, J=7.8 Hz), 6.99 (1H, s), 7.05 (1H, br), 7.13 (1H, t, J=7.8 Hz), 7.20-7.30 (2H, m), 7.72 (2H, d, J=8.3 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.92, 38.83, 42.82, 54.82, 103.47, 106.47, 110.04, 126.56, 129.37, 129.65, 137.32, 141.66, 142.66, 155.10, 159.65
IR (KBr): 1163, 1329, 1560, 1655, 3350 cm−1
MS (EI): m/z 363 (M+)
Melting point: 136 to 137° C.
Yield: 40%
1H-NMR (400 MHz, CDCl3): δ 1.45 (3H, t, J=7.1 Hz), 2.39 (3H, s), 3.11 (2H, t, J=5.4 Hz), 3.38 (2H, t, J=5.4 Hz), 4.09 (2H, q, J=7.1 Hz), 6.88 (1H, d, J=7.1 Hz), 6.93 (1H, t, J=7.1 Hz), 7.00 (1H, t, J=7.1 Hz), 7.26-7.31 (2H, m), 7.51 (1H, br), 7.74 (2H, d, J=8.1 Hz), 7.88 (1H, d, J=7.1 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 14.68, 20.92, 38.86, 42.89, 63.81, 111.56, 118.04, 120.36, 121.00, 126.56, 129.55, 129.63, 137.30, 142.64, 146.39, 155.12
MS (EI): m/z 377 (M+)
Melting point: 129 to 130° C.
Yield: 90%
1H-NMR (400 MHz, CDCl3): δ 2.39 (3H, s), 3.11 (2H, t, J=4.8 Hz), 3.37 (2H, t, J=4.8 Hz), 5.11 (1H, br), 5.33 (1H, br), 6.73 (1H, br), 7.18-7.32 (4H, m), 7.72 (2H, d, J=7.8 Hz), 8.08 (1H, d, J=8.8 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.91, 38.92, 42.62, 121.55, 121.78, 125.17, 126.56, 127.44, 128.36, 129.61, 135.89, 137.28, 142.63, 154.61
MS (EI): m/z 401 (M+)
Melting point: 161 to 162° C. (recrystallization solvent: toluene)
Yield: 53%
1H-NMR (400 MHz, CDCl3): δ 2.26 (3H, s), 2.37 (3H, s), 3.03 (2H, t, J=5.0 Hz), 3.32 (2H, t, J=5.0 Hz), 6.84 (1H, d, J=7.6 Hz), 7.02 (1H, d, J=7.6 Hz), 7.07 (1H, br), 7.12 (1H, t, J=7.6 Hz), 7.24-7.30 (5H, m), 7.71 (2H, d, J=8.1 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.96, 21.26, 38.81, 42.86, 114.89, 118.25, 121.84, 126.57, 128.47, 129.62, 137.33, 137.71, 140.30, 142.67, 155.18
Melting point: 114 to 115° C. (recrystallization solvent: toluene)
Yield: 80%
1H-NMR (400 MHz, CDCl3): δ 2.26 (3H, s), 2.40 (3H, s), 3.14 (2H, t, J=4.8 Hz), 3.73 (2H, t, J=4.8 Hz), 4.14 (1H, br), 6.16 (1H, br), 7.13-7.26 (5H, m), 7.27 (2H, d, J=7.8 Hz), 7.68 (2H, d, J=7.8 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 17.68, 21.03, 40.03, 41.71, 126.34, 126.49, 127.71, 129.67, 129.69, 130.69, 134.73, 136.72, 137.33, 142.67, 181.13
Melting point: 131 to 132° C.
Yield: 83%
1H-NMR (400 MHz, CDCl3): δ 2.29 (3H, s), 2.39 (3H, s), 3.19 (2H, t, J=5.1 Hz), 3.75 (2H, t, J=5.1 Hz), 3.82 (3H, s), 6.86 (1H, d, J=7.3 Hz), 7.00-7.15 (2H, m), 7.20-7.26 (3H, m), 7.27 (2H, d, J=8.1 Hz), 7.70 (2H, d, J=8.1 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.27, 20.96, 41.71, 43.32, 55.60, 111.53, 126.26, 126.41, 126.57, 126.80, 128.78, 129.69, 137.33, 142.67, 149.99, 180.59
Melting point: 130 to 131° C.
Yield: 99%
1H-NMR (400 MHz, CDCl3): δ 2.40 (3H, s), 3.18 (2H, t, J=5.1 Hz), 3.79 (2H, t, J=5.1 Hz), 6.63 (1H, br), 7.20-7.27 (3H, m), 7.28 (2H, d, J=7.6 Hz), 7.34 (1H, t, J=7.4 Hz), 7.40-7.52 (2H, m), 7.70 (2H, d, J=7.6 Hz)
13C-NMR (125 MHz, CDCl3): δ 21.45, 42.28, 44.65, 126.91, 127.59, 127.90, 128.05, 129.71, 129.73, 130.34, 133.54, 136.14, 143.69, 181.16
Yield: 70%
1H-NMR (400 MHz, CDCl3): δ 3.07 (2H, t, J=5.1 Hz), 3.38 (2H, t, J=5.1 Hz), 3.84 (3H, s), 6.90 (3H, m), 7.12 (1H, dd, J=9.0, 1.2 Hz), 7.20-7.30 (2H, m), 7.37 (1H, br), 7.51 (1H, d, J=1.2 Hz), 7.77 (2H, d, J=8.3 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 38.89, 42.55, 55.60, 114.36, 117.71, 118.63, 122.22, 128.70, 130.38, 130.92, 131.83, 140.68, 154.80, 162.13
Melting point: 150 to 151° C.
Yield: 45%
1H-NMR (400 MHz, CDCl3): δ 3.12 (2H, t, J=5.6 Hz), 3.40 (2H, t, J=5.6 Hz), 7.00 (1H, br), 7.14 (1H, dd, J=8.8, 2.6 Hz), 7.31 (1H, d, J=8.8 Hz), 7.35 (1H, br), 7.42 (1H, br), 7.53 (1H, d, J=2.6 Hz), 7.65 (2H, d, J=8.7 Hz), 7.72 (2H, d, J=8.7 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 42.51, 54.90, 117.69, 118.66, 122.24, 126.21, 128.53, 130.41, 130.90, 132.29, 139.53, 140.62, 154.75
MS (EI): m/z 465 (M+)
Melting point: 129 to 130° C.
Yield: 14%
1H-NMR (400 MHz, CDCl3): δ 3.08 (2H, t, J=5.1 Hz), 3.37 (2H, t, J=5.1 Hz), 5.43 (1H, br), 5.73 (1H, br), 6.94 (1H, br), 7.10 (1H, dd, J=8.4, 2.3 Hz), 7.21-7.27 (1H, m), 7.46 (2H, d, J=8.5 Hz), 7.49 (1H, d, J=2.3 Hz), 7.77 (2H, d, J=8.5 Hz)
13C-NMR (125 MHz, Acetone-d6): δ 40.25, 44.30, 118.62, 120.07, 129.90, 129.53, 130.07, 131.14, 132.43, 138.77, 140.52, 141.51, 155.94
Melting point: 139 to 140° C.
Yield: 67%
1H-NMR (400 MHz, CDCl3): δ 3.11 (2H, t, J=5.3 Hz), 3.19 (2H, t, J=5.3 Hz), 6.67 (1H, br), 6.98 (1H, br), 7.13 (1H, dd, J=8.6, 2.2 Hz), 7.18 (2H, t, J=8.7 Hz), 7.30 (1H, d, J=8.6 Hz), 7.40 (1H, br), 7.52 (1H, d, J=2.2 Hz), 7.86 (2H, dd, J=8.7, 5.0 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 38.97, 42.55, 116.34 (d, J=19.2 Hz), 117.71, 118.71, 122.29, 129.50 (d, J=9.6 Hz), 130.38, 130.92, 136.60 (d, J=3.6 Hz), 140.61, 154.80, 164.11 (d, J=249.5 Hz)
Melting point: 153 to 154° C.
Yield: 76%
1H-NMR (400 MHz, CDCl3): δ 2.41 (3H, s), 3.12 (2H, t, J=5.3 Hz), 3.41 (2H, t, J=5.3 Hz), 6.79 (1H, br), 7.00 (1H, br), 7.23 (1H, br), 7.29 (2H, d, J=8.1 Hz), 7.33 (1H, dd, J=8.8, 2.3 Hz), 7.46 (1H, d, J=2.3 Hz), 7.74 (2H, d, J=8.1 Hz), 8.02 (1H, d, J=8.8 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 21.11, 38.89, 42.78, 112.75, 122.06, 126.71, 126.72, 129.77, 130.46, 131.14, 136.41, 137.48, 142.82, 154.72
Melting point: 164 to 165° C.
Yield: 86%
1H-NMR (500 MHz, CDCl3): δ 1.68 (2H, quint, J=5.4 Hz), 2.40 (3H, s), 2.99 (2H, t, J=5.4 Hz), 3.36 (2H, t, J=5.4 Hz), 5.30 (1H, br), 5.42 (1H, br), 6.91 (1H, br), 7.15 (1H, dd, J=8.7, 2.5 Hz), 7.24-7.28 (2H, m), 7.30 (1H, d, J=8.7 Hz), 7.55 (1H, d, J=2.5 Hz), 7.72 (2H, d, J=8.6 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.96, 29.73, 38.97, 40.34, 117.64, 118.71, 122.14, 126.49, 129.54, 130.31, 130.92, 137.48, 140.76, 142.59, 154.88
Melting point: 157 to 158° C.
Yield: 80%
1H-NMR (500 MHz, CDCl3): δ 1.70 (2H, quint, J=6.0 Hz), 3.00 (2H, t, J=6.0 Hz), 3.39 (2H, t, J=6.0 Hz), 4.95 (1H, br), 5.55 (1H, br), 6.40 (1H, br), 7.13 (1H, dd, J=9.0, 2.5 Hz), 7.35 (1H, d, J=9.0 Hz), 7.54 (1H, d, J=2.5 Hz), 7.60 (2H, d, J=8.6 Hz), 7.71 (2H, d, J=8.6 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 29.73, 36.52, 40.34, 117.64, 118.71, 122.22, 126.18, 128.55, 130.38, 130.92, 132.29, 139.69, 140.76, 154.88
Melting point: 163 to 164° C.
Yield: 82%
1H-NMR (500 MHz, CDCl3): δ 1.70 (2H, quint, J=6.0 Hz), 2.99 (2H, t, J=6.0 Hz), 3.37 (2H, t, J=6.0 Hz), 6.80 (1H, br), 6.92 (1H, br), 7.13 (1H, dd, J=8.6, 2.9 Hz), 7.15 (2H, t, J=8.5 Hz), 7.24-7.30 (1H, m), 7.33 (1H, d, J=8.6 Hz), 7.53 (1H, d, J=2.9 Hz), 7.85 (2H, dd, J=8.5, 4.8 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 29.73, 36.60, 40.34, 116.34 (d, J=19.2 Hz), 117.71, 118.63, 122.14, 129.43 (d, J=9.6 Hz), 130.38, 130.92, 136.79 (d, J=2.8 Hz), 140.76, 154.88, 164.03 (d, J=249.5 Hz)
Melting point: 120 to 121° C.
Yield: 64%
1H-NMR (500 MHz, CDCl3): δ 1.70 (2H, quint, J=6.0 Hz), 2.98 (2H, t, J=6.0 Hz), 3.38 (2H, t, J=6.0 Hz), 3.84 (3H, s), 6.80 (1H, br), 6.90 (1H, br), 6.91 (2H, d, J=8.6 Hz), 7.16 (1H, dd, J=8.6, 2.3 Hz), 7.32 (1H, d, J=8.6 Hz), 7.42 (1H, br), 7.56 (1H, d, J=2.3 Hz), 7.76 (2H, d, J=8.6 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 29.21, 36.08, 39.74, 55.00, 113.76, 117.12, 118.11, 121.62, 128.10, 129.86, 130.39, 131.46, 140.24, 154.35, 161.53
Melting point: 124 to 125° C.
The following compound was obtained in the same manner as in Example 14, except that a specific compound (1-isothiocyanato-3-methoxypropane) was used instead of phenyl isocyanate.
Yield: 99%
1H-NMR (400 MHz, CDCl3): δ 1.85 (2H, quint, J=5.2 Hz), 2.40 (3H, s), 3.15 (2H, t, J=4.5 Hz), 3.33 (3H, s), 3.45-3.55 (4H, m), 3.69 (2H, t, J=4.5 Hz), 7.29 (2H, d, J=8.2 Hz), 7.72 (2H, d, J=8.2 Hz)
13C-NMR (125 MHz, CDCl3): δ 21.45, 28.55, 42.66, 43.96, 53.73, 58.61, 70.59, 126.91, 129.73, 136.21, 143.54, 181.69
The following compounds were obtained in the same manner as in Example 14, except that toluenesulfonyl isocyanate was used instead of phenyl isocyanate.
Yield: 80%
1H-NMR (400 MHz, CDCl3): δ 2.43 (3H, s), 2.44 (3H, s), 3.04 (2H, t, J=5.7 Hz), 3.33 (2H, t, J=5.7 Hz), 5.08 (1H, br), 6.70 (1H, br), 7.30 (2H, d, J=8.3 Hz), 7.35 (2H, d, J=8.5 Hz), 7.71 (2H, d, J=8.3 Hz), 7.82 (2H, d, J=8.5 Hz), 7.94 (1H, br)
13C-NMR (125 MHz, DMSO-d6): δ 20.96, 21.02, 38.91, 42.08, 126.51, 127.21, 129.43, 129.67, 137.22, 137.35, 142.71, 143.61, 151.41
IR (KBr): 1155, 1327, 1522, 1692, 3328 cm−1
Melting point: 163 to 164° C.
Yield: 14%
1H-NMR (400 MHz, CDCl3): δ 2.41 (3H, s), 2.62 (3H, s), 3.00 (2H, t, J=5.8 Hz), 3.31 (2H, t, J=5.8 Hz), 5.30 (1H, br), 6.62 (1H, br), 7.28 (2H, d, J=8.1 Hz), 7.32 (1H, d, J=7.6 Hz), 7.36 (1H, t, J=7.6 Hz), 7.51 (1H, t, J=7.6 Hz), 7.69 (2H, d, J=8.1 Hz), 8.01 (1H, d, J=7.6 Hz), 8.60 (1H, br)
13C-NMR (125 MHz, CDCl3): δ 14.11, 21.51, 39.84, 42.81, 126.44, 127.01, 129.72, 129.83, 132.73, 133.67, 136.38, 137.38, 137.44, 143.64, 152.44
Melting point: 134 to 135° C.
The following compounds were obtained in the same manner as in Example 14, except that an aminophenyl compound was used instead of the alkylamino compound.
Yield: 75%
1H-NMR (500 MHz, CDCl3): δ 2.40 (3H, s), 6.68 (1H, dd, J=7.8, 1.2 Hz), 6.92 (1H, td, J=7.8, 1.2 Hz), 7.06 (1H, br), 7.10 (1H, br), 7.18 (1H, dd, J=9.0, 2.5 Hz), 7.20-7.27 (3H, m), 7.30 (1H, d, J=9.0 Hz), 7.57 (1H, br), 7.58 (1H, d, J=2.5 Hz), 7.64 (2H, d, J=8.6 Hz), 7.79 (1H, dd, J=7.8, 1.2 Hz)
13C-NMR (100 MHz, DMSO-d6): δ 21.00, 118.14, 119.16, 121.27, 122.41, 123.10, 125.35, 127.20, 127.32, 127.61, 129.52, 130.63, 131.11, 136.26, 136.46, 140.08, 143.30, 152.18
Melting point: 204 to 205° C.
Yield: 99%
1H-NMR (500 MHz, CDCl3): δ 2.41 (3H, s), 6.38 (1H, br), 6.80 (1H, br), 6.92-7.16 (3H, m), 7.19 (1H, td, J=7.8, 1.3 Hz), 7.23-7.35 (4H, m), 7.48 (1H, td, J=7.8, 1.3 Hz), 7.76 (2H, d, J=8.0 Hz), 7.87 (1H, dd, J=7.8, 1.3 Hz), 8.30 (1H, br)
13C-NMR (125 MHz, DMSO-d6): δ 20.96, 115.04, 115.27 (d, J=19.2 Hz), 121.00, 121.99, 123.36, 125.12, 127.21 (d, J=9.6 Hz), 127.56, 129.54, 136.03, 136.41, 136.91 (d, J=3.0 Hz), 143.28, 152.74, 157.36 (d, J=239.9 Hz)
Melting point: 180 to 181° C.
Yield: 97%
1H-NMR (400 MHz, CDCl3): δ 6.69 (1H, dd, J=8.1, 1.5 Hz), 6.96 (1H, td, J=8.1, 1.5 Hz), 7.06 (1H, br), 7.10 (1H, br), 7.20 (1H, dd, J=8.7, 2.4 Hz), 7.21-7.25 (1H, m), 7.32 (1H, d, J=8.7 Hz), 7.42 (1H, br), 7.55-7.58 (4H, m), 7.59 (1H, d, J=2.4 Hz), 7.72 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 118.17, 119.21, 121.48, 122.61, 123.15, 124.98, 126.93, 127.47, 127.89, 129.14, 130.61, 131.12, 132.20, 136.49, 138.36, 139.98, 152.13
Melting point: 211 to 212° C.
Yield: 83%
1H-NMR (400 MHz, CDCl3): δ 6.68 (1H, dd, J=7.6, 1.5 Hz), 6.94 (1H, td, J=7.6, 1.5 Hz), 7.15 (1H, dd, J=8.8, 2.4 Hz), 7.20 (1H, td, J=7.6, 1.5 Hz), 7.22-7.27 (2H, m), 7.29 (1H, d, J=8.8 Hz), 7.41 (2H, d, J=8.8 Hz), 7.48 (1H, br), 7.55 (1H, d, J=2.4 Hz), 7.65-7.69 (3H, m)
13C-NMR (125 MHz, DMSO-d6): δ 118.17, 119.21, 121.48, 122.60, 123.15, 125.00, 127.48, 127.89, 129.07, 129.27, 130.60, 131.12, 136.50, 137.93, 139.98, 140.06, 152.15
Melting point: 199 to 200° C.
Yield: 96%
1H-NMR (400 MHz, CDCl3): δ 6.61 (1H, dd, J=8.1, 1.5 Hz), 6.92 (1H, td, J=8.1, 1.5 Hz), 7.00 (1H, br), 7.13 (2H, t, J=8.5 Hz), 7.18-7.25 (3H, m), 7.31 (1H, d, J=8.5 Hz), 7.52 (1H, br), 7.60 (1H, d, J=2.4 Hz), 7.74 (2H, dd, J=8.5, 7.0 Hz), 7.78 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 116.31 (d, J=22.8 Hz), 118.16, 119.20, 121.35, 122.51, 123.16, 125.08, 127.46, 127.85, 130.25 (d, J=9.6 Hz), 130.62, 131.12, 135.36, 136.57, 140.01, 152.18, 164.43 (d, J=251.9 Hz)
Melting point: 203 to 204° C.
Yield: 85%
1H-NMR (400 MHz, CDCl3): δ 2.34 (3H, s), 6.70 (1H, br), 6.83 (1H, dd, J=8.1, 1.5 Hz), 6.95 (1H, td, J=8.1, 1.5 Hz), 7.12-7.22 (5H, m), 7.25-7.34 (5H, m), 7.58 (2H, d, J=8.3 Hz), 7.66 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.99, 115.89, 117.90, 118.15, 120.94, 121.84, 121.91, 125.07, 127.18, 128.81, 129.51, 136.43, 139.82, 140.87, 143.27, 152.46
Melting point: 83 to 84° C.
Yield: 93%
1H-NMR (400 MHz, CDCl3): δ 3.80 (3H, s), 6.66 (1H, dd, J=8.1, 1.5 Hz), 6.86 (2H, d, J=8.9 Hz), 6.88 (1H, td, J=8.1, 1.5 Hz), 7.13 (1H, dd, J=8.5, 2.4 Hz), 7.18 (1H, td, J=8.1, 1.5 Hz), 7.23-7.25 (2H, m), 7.29 (1H, br), 7.54 (1H, d, J=2.4 Hz), 7.61 (1H, br), 7.66 (2H, d, J=8.9 Hz), 7.76 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 55.57, 114.18, 118.15, 119.16, 121.14, 122.38, 123.09, 125.48, 127.38, 127.54, 129.37, 130.62, 130.64, 131.09, 136.46, 140.06, 152.18, 162.51
Melting point: 129 to 130° C.
Yield: 59%
1H-NMR (400 MHz, CDCl3): δ 2.33 (3H, s), 3.77 (3H, s) 6.63 (1H, dd, J=8.1, 1.5 Hz), 6.77-6.82 (3H, m), 6.84 (1H, dd, J=8.2, 1.9 Hz), 6.94 (1H, td, J=8.1, 1.5 Hz), 7.02 (1H, t, J=1.9 Hz), 7.11-7.20 (4H, m), 7.33 (1H, br), 7.58 (2H, d, J=8.5 Hz), 7.72 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 21.00, 54.88, 103.87, 107.32, 110.46, 115.89, 116.80, 121.94, 125.10, 127.20, 127.55, 129.51, 129.58, 136.43, 136.92, 141.08, 143.28, 152.40, 159.70
Melting point: 84 to 85° C.
Yield: 68%
1H-NMR (400 MHz, CDCl3): δ 2.29 (3H, s), 3.83 (3H, s), 6.86 (1H, dd, J=8.1, 1.5 Hz), 6.93-7.00 (5H, m), 7.13-7.23 (5H, m), 7.56 (1H, dd, J=8.1, 1.5 Hz), 7.57 (2H, d, J=8.3 Hz), 7.99 (1H, dd, J=8.1, 1.7 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.96, 55.73, 110.81, 119.21, 120.46, 121.84, 122.11, 122.39, 126.13, 126.64, 126.95, 127.03, 128.53, 129.47, 135.86, 136.85, 143.13, 148.18, 152.77
Melting point: 105 to 106° C.
Yield: 96%
1H-NMR (400 MHz, CDCl3): δ 6.90 (1H, br), 7.01 (1H, dd, J=8.1, 1.5 Hz), 7.08 (1H, td, J=8.1, 1.5 Hz), 7.19 (1H, br), 7.20-7.26 (3H, m), 7.35 (1H, d, J=2.4 Hz), 7.51 (2H, d, J=8.8 Hz), 7.55 (2H, d, J=8.8 Hz), 7.57 (1H, dd, J=8.1, 1.5 Hz), 8.06 (1H, d, J=9.0 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 122.14, 122.92, 123.28, 123.40, 125.78, 126.45, 126.81, 127.19, 127.52, 127.60, 128.62, 129.01, 132.17, 135.20, 135.98, 138.74, 152.34
Melting point: 209 to 210° C.
Yield: 95%
1H-NMR (400 MHz, CDCl3): δ 6.92 (1H, dd, J=8.1, 1.5 Hz), 6.93 (1H, br), 7.02-7.08 (3H, m), 7.14 (1H, br), 7.21-7.25 (2H, m), 7.32 (1H, br), 7.34 (1H, d, J=2.2 Hz), 7.63 (1H, dd, J=8.1, 1.5 Hz), 7.72 (2H, dd, J=8.8, 4.9 Hz), 8.07 (1H, d, J=9.0 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 116.27 (d, J=22.8 Hz), 122.07, 122.85, 123.31, 123.46, 125.91, 126.51, 127.21, 127.52, 127.56, 128.64, 130.12 (d, J=9.6 Hz), 135.23, 135.77 (d, J=2.4 Hz), 136.07, 152.42, 164.39 (d, J=250.7 Hz)
Melting point: 201 to 202° C.
Yield: 75%
1H-NMR (400 MHz, CDCl3): δ 6.94 (1H, br), 6.99 (1H, dd, J=8.1, 1.5 Hz), 7.07 (1H, td, J=8.1, 1.5 Hz), 7.20-7.30 (4H, m), 7.34 (1H, d, J=2.4 Hz), 7.35 (2H, d, J=8.8 Hz), 7.58 (1H, dd, J=8.1, 1.5 Hz), 7.63 (2H, d, J=8.8 Hz), 8.06 (1H, d, J=9.0 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 122.17, 122.92, 123.27, 123.41, 125.83, 126.47, 127.21, 127.50, 127.58, 128.60, 128.93, 129.22, 135.20, 135.96, 137.82, 138.33, 152.36
Melting point: 201 to 202° C.
Yield: 74%
1H-NMR (400 MHz, CDCl3): δ 2.34 (3H, s), 3.49 (1H, br), 6.79 (1H, d, J=15.9 Hz), 7.03 (1H, td, J=8.1, 1.5 Hz), 7.10-7.30 (8H, m), 7.36 (1H, d, J=15.9 Hz), 7.43 (1H, br), 7.53 (1H, d, J=2.4 Hz), 7.60 (1H, br), 7.72 (1H, dd, J=8.1, 1.5 Hz)
13C-NMR (125 MHz, DMSO-d6): δ 20.98, 118.13, 119.18, 121.42, 122.76, 123.08, 124.75, 125.57, 127.67, 128.43, 128.88, 129.45, 129.65, 130.51, 131.02, 136.29, 139.98, 140.64, 140.99, 152.20
Melting point: 182 to 183° C.
The non-peptidic amide derivatives according to the invention have serine racemase inhibitory activity, and may be used as a drug for preventing/treating pathological conditions due to excessive activation of NMDAR or neurodegenerative diseases. The non-peptidic amide derivatives may also be used as a reagent for analyzing the functions of serine racemase in the nervous system.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2012-015233 | Jan 2012 | JP | national |
| 2012-037977 | Feb 2012 | JP | national |
| 2012-049955 | Mar 2012 | JP | national |
| 2012-135591 | Jun 2012 | JP | national |
This application is the U.S. National Phase application pursuant to 35 U.S.C. §371 of PCT International Patent Application No. PCT/JP2013/051385, filed Jan. 24, 2013, which claims priority to Japanese Patent Application No. 2012-015233, filed Jan. 27, 2012, Japanese Patent Application No. 2012-037977, filed Feb. 23, 2012, Japanese Patent Application No. 2012-049955, filed Mar. 7, 2012, and Japanese Patent Application No. 2012-135591, filed Jun. 15, 2012. The contents of these applications are incorporated herein by reference in their entirety.
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP2013/051385 | 1/24/2013 | WO | 00 | 7/28/2014 |
