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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234471Generated: October 26, 2026

2-Amino-4,5-dimethoxybenzonitrile → N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamide

https://huagongshe.com/reaction/234471

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4,5-dimethoxybenzonitrileHCID 735967—
ReactantN-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamideHCID 10696210—
ProductN-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4, 5-dimethoxyphenyl)aminocarbonyl]-thiophene-3-sulfonamideHCID 9956918—

Reaction Steps

N-(4-chloro-3-methyl-5-isoxazolyl)-2-[(2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]thiophene-3-sulfonamide was prepared by the method set forth for N-(4-chloro-3-methyl-5-isoxazolyl)2-{[2-acetyl-4,5-(methylenedioxy)phenyl]aminocarbonyl}thiophene-3-sulfonamide (EXAMPLE 148) except that 2-amino-4,5-dimethoxybenzonitrile was used instead of 2'-amino-4',5'-(methylenedioxy)acetophenone. N-(4-chloro-3-methyl-5-isoxazolyl)-2-[{2-cyano-4,5-dimethoxyphenyl)aminocarbonyl]thiophene-3-sulfonamide was obtained via HPLC purification as a light brown powder (36% yield, m.p. 53°-56° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05594021
Source datasetuspto-grants-1997_01
ORD IDord-05c784d4bf2d499ca2faa00f6bef4363
Source noteuspto-grants-1997_01