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Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate → 1,1-Dimethylethyl N-[1-(2-aminoethyl)-4-piperidinyl]carbamate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzyl 2-[4-(tert-butoxycarbonylamino)piperidin-1-yl]ethylcarbamate | HCID 22989976 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | 1,1-Dimethylethyl N-[1-(2-aminoethyl)-4-piperidinyl]carbamate | HCID 23562647 | 101.8% |
反応手順
A solution of 1,1-dimethylethyl {1-[2-({[(phenylmethyl)oxy]carbonyl}amino)ethyl]-4-piperidinyl}carbamate (8.2 g, 21.8 mmol) in ethanol (500 ml) was hydrogenated overnight over 10% palladium on charcoal (50% dispersion with water, 4.0 g). The mixture was filtered, evaporated, and azeotroped with chloroform to afford the title intermediate (5.4 g, 100%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08071592B2 |
| 出典データセット | uspto-grants-2011_12 |
| ORD ID | ord-7c39fd70e4614128b5e93581d7484dd1 |
| 出典メモ | uspto-grants-2011_12 |