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HRID 242819作成日:2026年10月26日

(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester → (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester

https://huagongshe.com/reaction/242819

反応式

関与物質

役割名称HCID仕込み量
反応物(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 59073577—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物(R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 59918925—

反応手順

A mixture of (R)-3-(2-nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester (2.48 g, 7.72 mmol) and 10% Pd/C (250 mg) in EtOAc (50 mL) was degassed with a stream of nitrogen and stirred at RT under a hydrogen atmosphere for 20 h. The suspension was then filtered through a PTFE frit and the filtrate was concentrated in vacuo affording (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester as a clear glass (2.25 g, quantitative). LCMS: RT 2.64 min [M+H-Boc]+ 192.1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08653089B2
出典データセットuspto-grants-2014_02
ORD IDord-782192cd7b5c42ae8147566990c677f8
出典メモuspto-grants-2014_02