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HRID 71754作成日:2026年10月27日

Methyl chloroformate → 2-(3-Methoxycarbonylamino-2-oxo-piperidin-1-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/71754

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl chloroformateHCID 6586—
反応物4-MethylmorpholineHCID 7972—
反応物2-(3-Amino-2-oxo-piperidin-1-yl)-propionic acid ethyl esterHCID 64237918—
溶媒DichloromethaneHCID 6344—
生成物2-(3-Methoxycarbonylamino-2-oxo-piperidin-1-yl)-propionic acid ethyl esterHCID 6662016475%

反応手順

Methyl chloroformate (192 μL, 2.5 mmol) was added to a solution of 2-(3-amino-2-oxo-piperidin-1-yl)-propionic acid ethyl ester (353 mg, 1.6 mmol) and 4-methylmorpholine (907 μL, 8.24 mmol) in dichloromethane (10 mL). After 15 minutes the mixture was diluted with dichloromethane (20 mL) and washed with water (10 mL), and aqueous hydrogen chloride (0.5 N, 10 mL). The organic phase was dried over sodium sulfate and filtered. The solvent was removed under reduced pressure to provide 2-(3-methoxycarbonylamino-2-oxo-piperidin-1-yl)-propionic acid ethyl ester (332 mg, 1.2 mmol, 75%). C12H20N2O5 calculated 272.1 observed [M+1]+ 273.0; rt=1.82 min.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822430B2
出典データセットuspto-grants-2014_09
ORD IDord-028737be47904862ac2e9db153c841f3
出典メモuspto-grants-2014_09