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6-Nitro-2-(trifluoromethyl)-1H-benzimidazole → 5-Amino-2-(trifluoromethyl)benzimidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 6-Nitro-2-(trifluoromethyl)-1H-benzimidazole | HCID 67595 | — |
| 反応物 | 2-Nitro-1H-benzimidazole | HCID 97234 | — |
| 反応物 | 4-Nitro-1,2-phenylenediamine | HCID 5111791 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Trifluoroacetic acid | HCID 6422 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | 5-Amino-2-(trifluoromethyl)benzimidazole | HCID 19345 | 80% |
反応手順
A solution of 4-nitro-1,2-phenylenediamine (3.0 g, 20 mmol) in 15 ml of trifluoroacetic acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a oily residue, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. The organic layer was dried over MgSO4 and concentrated in vacuo to provide an oil which was characterized as 2-trifluoromethyl-5-nitrobenzimidazole and subjected to the following reaction without further purification. The nitrobenzimidazole and 500 mg of 10% Pd—C were dissolved in 100 ml of MeOH and stirred for 12 h under H2. The reaction mixture was filtered and concentrated in vacuo, yielding 3.2 g (16 mmol, 80%) 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-608787df50804d9f8286080e62b98460 |
| 出典メモ | uspto-grants-2001_11 |