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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548278생성일: 2026년 10월 25일

Methanesulfonic Acid → 2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamide

https://huagongshe.com/reaction/548278

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물Methanesulfonyl chlorideHCID 31297—
반응물2-Amino-5-nitrobenzenesulfonamideHCID 15358386—
반응물2,5-DiaminobenzenesulfonamideHCID 21888765—
생성물2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamideHCID 24950657—

반응 단계

The 2-chloro-5-nitro-benzenesulfonamide intermediate (prepared as described in scheme 14) can be treated with a benzylic amine, such as benzylamine, to displace the chloro moiety. Hydrogenation under standard conditions in the presence of an acid (e.g., methanesulfonic acid) can be used to remove the benzylic group and to reduce the nitro group at the same time to afford the 2,5-diamino-benzenesulfonamide intermediate as a salt. Alternatively, the 2,5-diamino-benzenesulfonamide salt can be prepared by reduction of the 2-amino-5-nitro-benzenesulfonamide (prepared as described in schemes 14 and 15) under standard hydrogenation conditions in the presence of an acid (e.g., methanesulfonic acid). Subsequent reaction with methanesulfonyl chloride affords the desired 2-amino-5-methanesulfonylamino-benzenesulfonamide intermediate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939524B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-7b9ef24be76941f6b7ecc3bb9f4dc127
출처 메모uspto-grants-2011_05