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N-(2-nitrobenzoyl)pyrrole-2-carboxaldehyde → 10,11-Dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | N-(2-nitrobenzoyl)pyrrole-2-carboxaldehyde | HCID 21837074 | — |
| 触媒 | Hydrochloric Acid | HCID 313 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 10,11-Dihydro-5H-pyrrolo[2,1-c][1,4]benzodiazepin-5-one | HCID 21837076 | 82.1% |
反応手順
A mixture of 1.5 g of N-(2-nitrobenzoyl)pyrrole-2-carboxaldehyde in 50 ml of ethyl acetate, 2 drops of concentrated HCl and 0.3 g of 10% Pd/C is shaken in a Parr apparatus under hydrogen pressure for 1.75 hours. The mixture is filtered, 0.4 g of 10% Pd/C added and the mixture shaken in a Parr apparatus under hydrogen pressure for 2 hours. The reaction mixture is filtered through diatomaceous earth and the filtrate concentrated in vacuo to give 1.0 g of a yellow oil. The residue is purified on thick layer chromatography plates by elution with 4:1 ethyl acetate:hexane to give 107 mg of the desired product as an oily solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05733905 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-3085189734d041b78484ffa27fd0825c |
| 出典メモ | uspto-grants-1998_03 |