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HRID 514736생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/514736

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 번호US09108922B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-641c9a6b3268425bac5bb73a32221841
출처 메모uspto-grants-2015_08