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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 558104생성일: 2026년 10월 25일

Pyridine → n-{4-Chloro-2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamide

https://huagongshe.com/reaction/558104

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물4-Cyano-2-fluorobenzoic acidHCID 590659—
반응물2-Amino-5-chloro-N-(5-chloropyridin-2-yl)benzamideHCID 21906418—
용매DichloromethaneHCID 6344—
용매Thionyl ChlorideHCID 24386—
생성물n-{4-Chloro-2-[n-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamideHCID 10181017111.3%

반응 단계

A solution of 2-fluoro-4-cyanobenzoic acid (1 g, 6.06 mmol) in thionyl chloride (5 ml) was refluxed for 2 hr. After concentration, the residue was dissolved in dichloromethane (5 ml). And a solution of the compound of (2-amino-5-chlorophenyl)-N-(5-chloro(2-pyridyl))carboxamide (1.2 g, 4.25 mmol) in dichloromethane (10 ml) and pyridine (1.47 ml, 18.18 mmol) were added. The mixture was stirred at r.t. overnight. The precipitate was filtered and washed with a little amount of dichloromethane to give N-{4-chloro-2-[N-(5-chloro(2-pyridyl))carbamoyl]phenyl}(2-fluoro-4-cyanophenyl)carboxamide (2.03 g, 78%). MS found for C20H11C12FN4O2 M+=429, (M+2)+=431.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08063036B2
출처 데이터셋uspto-grants-2011_11
ORD IDord-1da4aa5c9fe84f9690377bd44c7bf5b0
출처 메모uspto-grants-2011_11