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HRID 533402作成日:2026年10月25日

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

https://huagongshe.com/reaction/533402

反応式

関与物質

役割名称HCID仕込み量
反応物3,5-DifluoropyridineHCID 642820—
反応物Methyl 4-chloro-1-{[(trifluoromethyl)sulfonyl]oxy}isoquinoline-7-carboxylateHCID 86666251—
反応物ButyllithiumHCID 178418339—
触媒ZincchlorideHCID 3007855—
触媒HCID 178418397HCID 178418397—
溶媒TetrahydrofuranHCID 8028—
生成物Methyl 4-chloro-1-(3,5-difluoropyridin-4-yl)isoquinoline-7-carboxylateHCID 6777447220.8%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08853242B2
出典データセットuspto-grants-2014_10
ORD IDord-684a031afcaa4e1b8a4c20dd142e9d36
出典メモuspto-grants-2014_10