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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133402생성일: 2026년 10월 23일

4-Bromobenzenesulfonamide → 2-Phenylbenzene-1-sulfonamide

https://huagongshe.com/ko/reaction/133402

반응식

참여 물질

역할이름HCID투입량
반응물4-BromobenzenesulfonamideHCID 69696—
촉매PalladiumHCID 23938—
생성물2-Phenylbenzene-1-sulfonamideHCID 12371520—

반응 단계

In Scheme 1 the compounds of the invention, 1, are prepared in 4 steps. Sulfonylation of valine methyl ester with 4-bromo-benzenesulfonyl chloride was carried out in the presence of Hunig base to give sulfonamide Intermediate 1. This 4-bromo-benzenesulfonamide was furthered coupled with boronate ester using Palladium catalyst under Suzuki coupling condition to provide biphenyl sulfonamide Intermediate 2. Biphenyl sulfonamide Intermediate 2 was then alkylated with various alkylating reagents to provide biphenyl sulfonamide ester (Intermediate 3). Hydrolysis of Intermediate 3 was carried out using bases such as NaOH, or LiOH to form the final product 1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390833B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-68ca173bd40c4077ab21cedd0d8e35de
출처 메모uspto-grants-2008_06