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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1963883생성일: 2026년 10월 26일

Sodium Carbonate → 5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-4-carbonitrile

https://huagongshe.com/reaction/1963883

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물(5-Chloro-2-fluoropyridin-4-yl)boronic acidHCID 44754822—
반응물2-Chloro-6-(3-fluorobenzylamino)isonicotinonitrileHCID 83073097—
촉매HCID 178418397HCID 178418397—
용매1,2-DimethoxyethaneHCID 8071—
용매Ethyl AcetateHCID 8857—
생성물5'-Chloro-2'-fluoro-6-(3-fluorobenzylamino)-2,4'-bipyridine-4-carbonitrileHCID 6693696747%

반응 조건

온도110 °C

반응 단계

To a degassed suspension of 2-chloro-6-(3-fluorobenzylamino) isonicotinonitrile (150 mg, 0.573 mmol) and 5-chloro-2-fluoropyridin-4-ylboronic acid (151 mg, 0.860 mmol) in DME (5 ml) was added Na2CO3 (1.433 ml, 2M, 2.87 mmol) and Pd(Ph3P)4 (66.2 mg, 0.057 mmol). The reaction mixture was capped and heated to 110° C. in an oil bath for 2 hr. The reaction mixture was diluted with EtOAc and washed with sat NaHCO3, and then sat NaCl. The organic layer was dried over Na2SO4, filtered and concentrated. The resulting residue was purified purified by column chromatography on silica gel (0-20% EtOAc/Hexane) to give 5′-chloro-2′-fluoro-6-(3-fluorobenzylamino)-2,4′-bipyridine-4-carbonitrile (95 mg, 47%). LCMS (m/z): 357.0 (MH+), retention time=1.09 min

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08415381B2
출처 데이터셋uspto-grants-2013_04
ORD IDord-9c3eddaaa67c4555af9f2a82a76fb298
출처 메모uspto-grants-2013_04