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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 424169생성일: 2026년 10월 25일

Methanesulfonic Acid → 2,5-Diaminobenzenesulfonamide

https://huagongshe.com/reaction/424169

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물BenzylamineHCID 7504—
반응물2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
생성물2,5-DiaminobenzenesulfonamideHCID 21888765—

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 번호US08101800B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-d3febb5eec1f41b98f780bc91e009844
출처 메모uspto-grants-2012_01