돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 234449생성일: 2026년 10월 23일

5-Amino-3-methylisoxazole → N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide

https://huagongshe.com/ko/reaction/234449

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-3-methylisoxazoleHCID 84590—
반응물5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
생성물N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamideHCID 22998516—

반응 단계

N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide was prepared in the same manner as described in Example 14 from 5-bromothiophene-2-sulfonyl chloride and 5-amino-3-methyl isoxazole. Purification was achieved by extraction of the crude sulfonamide into aqueous 2N NaOH, washing of the aqueous layer with ethyl acetate and acidification, using concentrated HCl, to pH ~2. Re-extraction into ethyl acetate was followed by washing of the organic material with water, brine and drying over magnesium sulfate. After evaporation of solvents, a brownish solid remained which was sufficiently pure to use in the next step.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05594021
출처 데이터셋uspto-grants-1997_01
ORD IDord-f241abfbf55942dcb756a89925fcb51b
출처 메모uspto-grants-1997_01