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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2218695생성일: 2026년 10월 27일

3-Methylsulfonylaminophenylboronic acid → N-[3-(2,8-Dimethoxy-10,11-dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/2218695

반응식

참여 물질

역할이름HCID투입량
반응물3-Methylsulfonylaminophenylboronic acidHCID 2773535—
반응물5-bromomethylene-2,8-dimethoxy-10,11-dihydro-5H-dibenzo[a,d]cyclohepteneHCID 68936313—
생성물N-[3-(2,8-Dimethoxy-10,11-dihydro-dibenzo[a,d]cyclohepten-5-ylidenemethyl)-phenyl]-methanesulfonamideHCID 5977006139%

반응 단계

Following procedures essentially as described in Example 219, below, and using 3-methanesulfonamidophenyl boronic acid (473 mg, 2.2 mmol) with 5-bromomethylene-2,8-dimethoxy-10,11-dihydro-5H-dibenzo[a,d]cycloheptene (690 mg, 2 mmol) to give 1.3 g crude product. Purify the crude product using column chromatography eluting with 10% EtOAc/hexane to 30% EtOAc/hexane to give 340 mg (39%) product as a pale yellow solid, mp 109.6° C. MS (ES) 436 (M+1), 434 (M−1). HPLC shows 91% purity at t=3.11 min.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07411072B2
출처 데이터셋uspto-grants-2008_08
ORD IDord-1c675aa87dda4f2bb07ea253b4c898a0
출처 메모uspto-grants-2008_08