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HRID 1050964作成日:2026年10月26日

Dimethylformamide → 4-(4-Methoxy-carbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/1050964

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Methyl iodideHCID 6328—
反応物Potassium CarbonateHCID 11430—
反応物4-(4-Carboxy-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 22492859—
生成物4-(4-Methoxy-carbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 118272431—

反応手順

To a solution of 4-(4-carboxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester (828 mg, 2.71 mmol) in DMF (5 ml) are added iodomethane (577 mg, 4.07 μl) and potassium carbonate (375 mg, 2.71 mmol) and the reaction mixture is stirred for 4 hours at room temperature. The reaction mixture is evaporated and the residue is treated with dichloromethane. The solids are filtered off and the filtrate is evaporated to dryness to afford 4-(4-methoxy-carbonyl-phenyl)-piperidine-1-carboxylic acid tert-butyl ester as yellow solid; HPLC/MS 2.21 min (A), [M-tBu] 264.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09388142B2
出典データセットuspto-grants-2016_07
ORD IDord-5b6c8380a4cc400898f493f1c5eab4df
出典メモuspto-grants-2016_07