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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1251671생성일: 2026년 10월 25일

5-Amino-3,4-dimethylisoxazole → N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide

https://huagongshe.com/reaction/1251671

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-3,4-dimethylisoxazoleHCID 88317—
반응물1-Benzofuran-2-sulfonyl chlorideHCID 2795172—
생성물N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamideHCID 22998530—

반응 단계

N-(3,4-Dimethyl-5-isoxazolyl)benzo[b]furan-2-sulfonamide was prepared, in the same manner as described in Example 34B, from 3,4-dimethyl-5-amino isoxazole (78 mg, 0.70 mmol) and benzo[b]furan-2-sulfonyl chloride (0.46 g, 2.1 mmol). Flash chromatography (30% ethyl acetate/hexanes) provided 0.186 g of a light yellow solid, which was treated with 31 mg of NaOH in 10 ml of methanol at 25° C. for 30 minutes. Recrystallization from CHCl3/hexanes yielded a light tan solid (90 mg, 44% yield), m.p. 160.5-163° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06342610B2
출처 데이터셋uspto-grants-2002_01
ORD IDord-11e63a299b4f4e8eac8aa319e6a71da0
출처 메모uspto-grants-2002_01