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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 533402생성일: 2026년 10월 24일

3,5-Difluoropyridine → Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate

https://huagongshe.com/ko/reaction/533402

반응식

참여 물질

역할이름HCID투입량
반응물3,5-DifluoropyridineHCID 642820—
반응물Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylateHCID 86666251—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
촉매HCID 178418397HCID 178418397—
용매TetrahydrofuranHCID 8028—
생성물Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylateHCID 6777447220.8%

반응 단계

Under argon gas atmosphere, n-butyllithium (1.6 M THF solution, 0.7 mL) was added dropwise to a mixture of 3,5-difluoropyridine (123 mg) and THF (3 mL) at −78° C., followed by stirring at the same temperature for one hour. Then, zinc chloride (146 mg) was added, and stirred for an additional hour. Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylate (330 mg) and tetrakis(triphenylphosphine)palladium (206 mg) were added thereto, followed by heating under stirring in an oil bath at 60° C. for 3 hours. The reaction mixture was concentrated under reduced pressure and purified under silica gel column chromatography (hexane/ethyl acetate) to obtain methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylate (62 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08853242B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-684a031afcaa4e1b8a4c20dd142e9d36
출처 메모uspto-grants-2014_10