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(R)-3-(2-Nitrophenylamino)piperidine-1-carboxylic acid tertbutyl ester → (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester
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 ester | HCID 59073577 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | (R)-3-(2-Aminophenylamino)piperidine-1-carboxylic acid tertbutyl ester | HCID 59918925 | 80% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06476050B2 |
| 出典データセット | uspto-grants-2002_11 |
| ORD ID | ord-001da17b08b44939baa48cfa86ca7224 |
| 出典メモ | uspto-grants-2002_11 |