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2-Nitro-1H-benzimidazole → 2-cyclopropyl-1H-benzimidazol-5-amine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Nitro-1H-benzimidazole | HCID 97234 | — |
| 反応物 | 4-Nitro-1,2-phenylenediamine | HCID 5111791 | — |
| 反応物 | 2-cyclopropyl-5-nitro-1H-1,3-benzodiazole | HCID 16227522 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 溶媒 | Cyclopropanecarboxylic acid | HCID 15655 | — |
| 生成物 | 2-cyclopropyl-1H-benzimidazol-5-amine | HCID 18379863 | 75% |
反応手順
A solution of 4-nitro-1,2-phenylenediamine (1.0 g, 6.6 mmol) in 15 ml of cyclopropanecarboxylic acid was stirred at reflux for 12 h. The reaction mixture was concentrated in vacuo to yield a oil, which was dissolved in 100 ml of EtOAc and washed with aqueous NaHCO3. Organic layer was dried over MgSO4 and concentrated in vacuo, yielding an oil which was characterized as 2-cyclopropyl-5-nitrobenzimidazole and subjected to a following reaction without further purification. The nitrobenzimidazole and 50 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 to provide 0.87 g (4.9 mmol, 75%) of the desired product.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06495583B1 |
| 出典データセット | uspto-grants-2002_12 |
| ORD ID | ord-08eaca019fa94be39a12b79f84a7b015 |
| 出典メモ | uspto-grants-2002_12 |