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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18645생성일: 2026년 10월 23일

Sulfanilamide → 4-(2-Methyl-5-m-tolyl-pyrrol-1-yl)-benzenesulfonamide

https://huagongshe.com/ko/reaction/18645

반응식

참여 물질

역할이름HCID투입량
반응물SulfanilamideHCID 5333—
반응물Methyl vinyl ketoneHCID 6570—
반응물3-MethylbenzaldehydeHCID 12105—
생성물4-(2-Methyl-5-m-tolyl-pyrrol-1-yl)-benzenesulfonamideHCID 68484259—

반응 단계

Meta-methylbenzaldehyde and but-3-en-2-one were treated according to the procedure outlined in General Procedure C followed by subjecting the resulting product to conditions outlined in General Procedure D along with p-aminosulfonyl phenylamine to obtain the titled compound. 1H NMR (CDCl3) δ ppm 2.15 (3H), 2.05 (3H), 4.90 (2H), 6.10 (1H), 6.30 (1H), 6.89-7.90 (8H); MS (ESI) m/z 327 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741364B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5c2fa4e2b03541a59abf59fc72cb1df7
출처 메모uspto-grants-2010_06