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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2241145생성일: 2026년 10월 25일

3-Chlorobenzenesulphonyl chloride → 4-[4-Chloro-3-(3-chloro-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl ester

https://huagongshe.com/reaction/2241145

반응식

참여 물질

역할이름HCID투입량
반응물3-Chlorobenzenesulphonyl chlorideHCID 17909—
반응물Ethyl 4-[(4-chloro-3-nitrobenzoyl)amino]benzoateHCID 711250—
생성물4-[4-Chloro-3-(3-chloro-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl esterHCID 67549757—

반응 단계

4-[4-Chloro-3-(3-chloro-benzenesulfonylamino)-benzoylamino]-benzoic acid, MS (ISP): m/e=463.1 (M+H+), was prepared in analogy to example 1, steps A to D. Step A was performed using 4-chloro-3-nitro-benzoyl chloride and yielded 4-(4-chloro-3-nitro-benzoylamino)-benzoic acid ethyl ester. This was reduced to 4-(4-Chloro-3-nitro-benzoylamino)-benzoic acid ethyl ester in step B. This was coupled with 3-chloro-benzenesulfonyl chloride in step C, yielding 4-[4-chloro-3-(3-chloro-benzenesulfonylamino)-benzoylamino]-benzoic acid ethyl ester, which was hydrolyzed in step D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07723538B2
출처 데이터셋uspto-grants-2010_05
ORD IDord-ba9ea59c8bdb44959eee2006ec0655c8
출처 메모uspto-grants-2010_05