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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234322생성일: 2026년 10월 26일

Ethyl Acetate → N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]thiophene-2-sulfonamide

https://huagongshe.com/reaction/234322

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물5-Amino-3,4-dimethylisoxazoleHCID 88317—
반응물1-Benzothiophene-2-sulfonyl chlorideHCID 2776333—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매PyridineHCID 1049—
생성물N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]thiophene-2-sulfonamideHCID 2344548260%

반응 단계

3,4-Dimethyl-5-amino-isoxazole (0.224 g, 2.0 mmol) and 50 mg of DMAP were stirred in 5 ml of pyridine at 25° C. The benzo[b]thiophene-2-sulfonyl chloride (0.16 g, 2.6 mmol) was added and the dark brown-yellow reaction mixture was stirred for 18 h at ambient temperature, poured into 100 ml of ethyl acetate and washed with 2% HCl (3×50 ml). The organic phase was dried with MgSO4, filtered and concentrated to collect 0.61 g of a brown oil/solid. The brown oil/solid was subjected to flash chromatography (30% ethyl acetate/hexanes) to provide 0.37 g of a light brown solid. This was stirred in 10 ml of methanol and 0.5 g of NaOH. The methanolic solution was heated for reflux for 1 h, then cooled to 25° C. and the methanol was removed in vacuo. The resulting residue was acidified to pH 1 with 2% HCl (100 ml) and extracted with ethyl acetate (2×50 ml) The organic phase was dried with MgSO4, filtered and concentrated to collect 0.225 g of a yellow-orange solid. This was recrystallized from CHCl3 /hexanes to produce a light tan-yellow solid (0.194 g, 31% yield), m.p. 157°-160° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594021
출처 데이터셋uspto-grants-1997_01
ORD IDord-8b2ab3543fee4037aba028ebd4df5eff
출처 메모uspto-grants-1997_01