化工社化工社 化学情報印刷レポート · 研究参考用
Formic Acid → 7-Chloro-1H-benzo[d]imidazol-5-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Formic Acid | HCID 284 | — |
| 反応物 | Formamide | HCID 713 | — |
| 反応物 | 6-Chloro-2,4-dinitroaniline | HCID 19052 | — |
| 反応物 | HCID 178522168 | HCID 178522168 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Hydrochloric Acid | HCID 313 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 溶媒 | Acetic Anhydride | HCID 7918 | — |
| 生成物 | 7-Chloro-1H-benzo[d]imidazol-5-amine | HCID 178507673 | — |
反応手順
Methanolic solution of 6-chloro-2,4-dinitroaniline (2.4 g, 11 mmol) was stirred overnight with 100 mg of 10% Pd/C under H2. Reaction mixture was filtered and concentrated in vacuo to provide an oil which was dissolved in 10 ml of acetic anhydride and 10 ml of formic acid and stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo, yielding a brown oil which was characterized as 4-chloro-6-foramidylbenzimidazole in NMR analysis. The formamide was dissolved in 20 ml of HCl sat'd EtOH and stirred for 3h at 25° C. The reaction mixture was purified in column chromatography (5% MeOH/EtOAc) to provide 0.89 g (5.3 mmol, 48% overall) of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06316637B1 |
| 出典データセット | uspto-grants-2001_11 |
| ORD ID | ord-98b5b6c4ca6e4c908c7280faa5b61774 |
| 出典メモ | uspto-grants-2001_11 |