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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 130446생성일: 2026년 10월 24일

(3-Chlorophenyl)boronic acid → 3'-Chloro-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-4-biphenylsulfonamide

https://huagongshe.com/ko/reaction/130446

반응식

참여 물질

역할이름HCID투입량
반응물(3-Chlorophenyl)boronic acidHCID 2734323—
반응물Potassium tert-butoxideHCID 23665647—
반응물4-Bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamideHCID 44452776—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물3'-Chloro-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]-4-biphenylsulfonamideHCID 59007081—

반응 조건

온도100 °C

반응 단계

To a mixture of 4-bromo-N-[5-(cis-3,5-dimethyl-1-piperazinyl)-2-(methyloxy)phenyl]benzenesulfonamide (E106) (75 mg, 0.17 mmol) and (3-chlorophenyl)boronic acid (56 mg, 0.36 mmol) in DME (3 ml) was added potassium tert-butoxide (180 mg, 1.60 mmol) and tetrakis(triphenylphosphine)palladium(0) (15 mg, 0.01 mmol) in water (1 ml) and the resulting mixture stirred in a microwave (set at high absorbance) at 100° C. for 30 minutes. The resulting mixture was then evaporated in vacuo and purified using an SCX cartridge eluting with methanol followed by ammonia (2M in methanol). The appropriate fractions were combined and evaporated in vacuo and the residue purified further by mass directed autoprep HPLC to afford the title compound (E111). MS (ES+) m/e 486/488 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07381728B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-66994927e0a249ea89366cc7dc7e81b2
출처 메모uspto-grants-2008_06