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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12143생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/12143

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 C20H11Cl2FN4O2 M+=429, (M+2)+=431.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07727982B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-78423b0ee2724e0eb24f94e6674e11e0
출처 메모uspto-grants-2010_06