돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239846생성일: 2026년 10월 24일

Dichloromethane → 4'-Methoxy-biphenyl-4-sulfonic acid (2-benzoyl-4-chloro-phenyl)-amide

https://huagongshe.com/ko/reaction/239846

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Cesium carbonateHCID 10796—
반응물(4-Methoxyphenyl)boronic acidHCID 201262—
반응물N-(2-benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamideHCID 10028837—
용매1,2-DimethoxyethaneHCID 8071—
용매TriethylamineHCID 8471—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물4'-Methoxy-biphenyl-4-sulfonic acid (2-benzoyl-4-chloro-phenyl)-amideHCID 11294528—

반응 조건

온도55 °C

반응 단계

To a magnetically stirred mixture of N-(2-Benzoyl-4-chloro-phenyl)-4-iodo-benzenesulfonamide (497 mg, 1.0 mmol), [1,1′ Bis(diphenylphosphino)-ferrocene]dichloropalladium(II) complex with dichloromethane (1:1) (30 mg, 0.037 mmol) and dry cesium carbonate (511 mg, 1.57 mmol) in NMP (3 mL), was added DME (3 mL) and dry triethylamine (3 mL) under dry nitrogen. To this stirred mixture was added (4-methoxyphenyl)boronic acid (202 mg) and the mixture was stirred at 55° C. overnight. The reaction was worked up by addition to crushed ice and extracted with ethyl acetate (3×75 mL), and the organic layer was dried (MgSC4), filtered and concentrated. The crude product was chromatographed on silica gel using 10-30% EtOAc/Hexane. 1H NMR (CDCl3) δ 9.64 (br s, 1H, NH), 7.75 (dm, 1H), 7.75 (dm, 2H, J=8.8 Hz), 7.48 (m, 3H), 7.56 (dm, 2H, J=8.4 Hz), 7.51 (m), 7.32 (d 1H, J=2.2 Hz), 7.26 (d, 1H, J=7 Hz), 7.09 (d, 2H, J=8.4 Hz), 3.65 (s, 3H). MS: m/z 478.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08642808B2
출처 데이터셋uspto-grants-2014_02
ORD IDord-592736e1a81240459e7130027c172419
출처 메모uspto-grants-2014_02