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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 449929생성일: 2026년 10월 24일

Diisopropylethylamine → N-(2-bromopyridin-4-yl)-2-chloro-4-cyano-6-fluorobenzamide

https://huagongshe.com/ko/reaction/449929

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4-Amino-2-bromopyridineHCID 346455—
반응물2-Chloro-4-cyano-6-fluorobenzoyl chlorideHCID 86648965—
용매AcetonitrileHCID 6342—
용매DichloromethaneHCID 6344—
생성물N-(2-bromopyridin-4-yl)-2-chloro-4-cyano-6-fluorobenzamideHCID 8664896453.4%

반응 단계

To a cooled (0° C.) solution of 4-amino-2-bromopyridine (346 mg, 2.0 mmol) and diisopropylethylamine (461 mg, 4.0 mmol) in dichloromethane (5 mL) and CH3CN (0.5 mL) was added a solution of 2-chloro-4-cyano-6-fluorobenzoyl chloride (484 mg, 2.2 mmol) in dichlormethane (5 mL) drop wise. The reaction mixture was warmed up to room temperature and stirred for 16 hours. The reaction was quenched with saturated NH4Cl (40 mL) and extracted with EtOAc (3×50 mL). The combined organic extractss were dried with Na2SO4 and concentrated under reduced pressure. The residue wars purified by silica gel column chromatography (0-50% EtOAc/hexane) to give N-(2-bromopyridin-4-yl)-2-chloro-4-cyano-6-fluorobenzamide as an off-white solid (379 mg, yield: 53%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08486950B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-c2f844975da0402cbe3c51f97dd0fb00
출처 메모uspto-grants-2013_07