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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 335280생성일: 2026년 10월 25일

Dichloromethane → 7-(6-Chloropyridin-3-yl)-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/335280

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Cesium carbonateHCID 10796—
반응물2-Chloropyridine-5-boronic acidHCID 3845034—
반응물7-bromo-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 71283181—
촉매Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물7-(6-Chloropyridin-3-yl)-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamideHCID 86695675—

반응 단계

A mixture comprising 7-bromo-N-(5-(3,4-difluorobenzylcarbamoyl)-2-fluorophenyl)imidazo[1,2-a]pyridine-3-carboxamide (Intermediate 3A) 100 mg, 0.199 mmol), 6-chloropyridin-3-ylboronic acid (31.3 mg, 0.199 mmol) and cesium carbonate (259 mg, 0.795 mmol) in DME (631 μL)/water (31.5 μL) was purged with nitrogen and treated with PdCl2(dppf).CH2Cl2 adduct (8.11 mg, 9.93 μmol) The resulting mixture was heated using microwave radiation at 100° C. for 15 mins. The water was removed by pipette and the reaction mixture was diluted with MeOH. Purification of the mixture by chromatography on silica eluting with 0-20% 2M NH3 in MeOH/DCM afforded the title compound;

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08883819B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-ae27f1868b2a41f6aa992461d0867954
출처 메모uspto-grants-2014_11