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Benzimidazole → 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazole
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzimidazole | HCID 5798 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 2-(4-(4-Bromobutyl)piperazin-1-yl)pyrimidine | HCID 14726843 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazole | HCID 9819148 | — |
反応手順
A mixture of 6 g (20 mmol) of 2-[4-(4-bromobutyl)-1-piperazinyl]-pyrimidine, 2.36 g (20 mmol) of benzimidazole and 4.1 g (30 mmol) of potassium carbonate in 60 ml of dimethylformamide is refluxed for 14 hours. The reaction mixture is evaporated under vacuum, chloroform is added, the mixture is washed with water, dried over sodium sulphate and evaporated under vacuum and 4.8 g of 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]-butyl}-1H-benzimidazole are obtained, which may be recrystallised from ethyl ether, with a melting point of 85°-88° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05382586 |
| 出典データセット | uspto-grants-1995_01 |
| ORD ID | ord-bb9f9015a0814603b73a671f894d6868 |
| 出典メモ | uspto-grants-1995_01 |