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Triethylamine → N-[2-[4-(2-Pyrimidinyl)-1-piperazinyl]ethyl]-2-benzofurancarboxamide Dihydrochloride Hydrate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2-Benzofurancarbonyl chloride | HCID 38949 | — |
| 反応物 | 1-Piperazineethanamine, 4-(2-pyrimidinyl)- | HCID 13885358 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-[2-[4-(2-Pyrimidinyl)-1-piperazinyl]ethyl]-2-benzofurancarboxamide Dihydrochloride Hydrate | HCID 18995774 | — |
反応手順
To a stirred solution of [4-(2-pyrimidinyl)piperazinyl]ethylamine (2.0 g, 0.01 mol) in 50 mL of methylene chloride, benzofurane-2-carboxylic acid chloride (2.6 g, 0.014 mol) and triethylamine (2 g, 0.02 mol) were added. Stirring was continued at room temperature overnight. The methylene chloride solution was washed with water, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The remaining residue was subjected to preparative HPLC. The title compound was separated and converted to the dihydrochloride hydrate salt with ethanolic HCl (0.5 g), m.p. 193° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05106849 |
| 出典データセット | uspto-grants-1992_04 |
| ORD ID | ord-51aea6e7b6104bdca38c124634842102 |
| 出典メモ | uspto-grants-1992_04 |