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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234312생성일: 2026년 10월 27일

5-Amino-3,4-dimethylisoxazole → N-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamide

https://huagongshe.com/reaction/234312

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-3,4-dimethylisoxazoleHCID 88317—
반응물2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
용매PyridineHCID 1049—
생성물N-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamideHCID 1061532265%

반응 단계

2-Methoxycarbonylthiophene-3-sulfonyl chloride (2.50 g, 10.05 mmol) was added to a solution of 5-amino-3,4-dimethylisoxazole(0.98 g, 8.75 mmol) in dry pyridine (5.0 ml). The reaction mixture was stirred at room temperature for 16 h. Pyridine was removed under reduced pressure and the residue was partitioned between water and dichloromethane. The organic layer was washed with 1N HCl (2×50 ml) and dried over anhydrous magnesium sulfate. Evaporation of the solvents left an oily residue, which, after purification by column chromatography over silica gel (1:1 hexanes/ethyl acetate as eluent), yielded 2.20 mg (65%) of a brown solid. Further purification was achieved by recrystallization from ethyl acetate/hexanes, giving the pure product as a white solid, m.p. 113°-116° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594021
출처 데이터셋uspto-grants-1997_01
ORD IDord-a980ca657da34400a5d38a3146522957
출처 메모uspto-grants-1997_01