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HRID 1016549作成日:2026年10月25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/1016549

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MethanolHCID 887—
生成物(R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl esterHCID 5991892580%

反応手順

The solution of 3(R)-(2-Nitro-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (134 mg) and Pd-C (10%, 150 mg) in MeOH (30 ml) was stirred under H2 (1 atm) for 24 hrs. After filtration through Celite, the filtrate was concentrated to give colorless oil (96.8 mg, 80%). 1H-NMR (300 MHz, CDCl3) δ 6.80 (m, 5H), 4.10 (m, 1H), 3.78 (m, 1H), 3.39 (m, 3H), 3.15 (m, 1H), 2.95 (m, 1H), 2.08 (m, 1H), 1.80 (m, 1H), 1.60 (m 3H), 1.50 (s, 9H) ppm; LRMS (calculated for C16H21N3O2-BOC)+ 191, found (M-BOC)+ 191.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06476050B2
出典データセットuspto-grants-2002_11
ORD IDord-001da17b08b44939baa48cfa86ca7224
出典メモuspto-grants-2002_11