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HRID 1295672作成日:2026年10月27日

Cesium carbonate → 2-Fluoro-5-methyl-4-(4-ethoxycarbonyl-piperdinyl)pyridine

https://huagongshe.com/reaction/1295672

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物1-Piperidinecarboxylic acid, ethyl esterHCID 21399—
反応物1,3-Bis(diphenylphosphino)propaneHCID 81219—
反応物2-Fluoro-4-iodo-5-methylpyridineHCID 10060052—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
生成物2-Fluoro-5-methyl-4-(4-ethoxycarbonyl-piperdinyl)pyridineHCID 69426972572.6%

反応条件

温度160 °C

反応手順

Palladium acetate (0.04 mmol, 10 mg) was stirred with 1,3-bis(diphenylphosphino)propane (18 mg, 0.04 mmol) in DMF (0.5 mL) for 10 minutes. A mixture of 2-fluoro-4-iodo-5-methyl pyridine (0.42 mmol, 100 mg), ethyl-1-piperidinecarboxylate (0.5 mmol, 0.08 mL) and cesium carbonate (275 mg, 2 equiv) in DMF (1.5 mL) was then added, stirred vigorously, and heated in the microwave to 160° C. for 10 minutes. The resulting black mixture was poured onto a silica gel column and purified by flash chromatography (ethyl acetate/hexanes gradient) to afford 61 mg of the title compound as a yellow oil (54%). Rt=6.70 minutes; MS FIA 267.1 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07244735B2
出典データセットuspto-grants-2007_07
ORD IDord-119d1622fb164ab5bd1593ce872b45b0
出典メモuspto-grants-2007_07