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5-Aminoimidazole-4-carboxamide hydrochloride → 4-Phenylimidazo[1,5-a]pyrimidine-8-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Aminoimidazole-4-carboxamide hydrochloride | HCID 66146 | — |
| 反応物 | 3-(Dimethylamino)-1-phenyl-2-propen-1-one | HCID 353460 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Phenylimidazo[1,5-a]pyrimidine-8-carboxamide | HCID 14677470 | 43.9% |
反応手順
A stirred mixture of 11.0 g of 4-amino-5-imidazolecarboxamide hydrochloride and 15.0 g of 3-dimethylaminoacrylophenone (prepared as described in Example 1) in 120 ml of glacial acetic acid was heated at reflux for 4 hours. The solvent was evaporated in vacuo to give a dark oil which was dissolved in dichloromethane, then treated by stirring with saturated sodium bicarbonate. The organic solvent was evaporated and the remaining mixture was filtered and the solid was washed with water, dried, and then was recrystallized from ethanol to give 7.08 g of the desired product as a yellow solid, mp 226°-228° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04888345 |
| 出典データセット | uspto-grants-1989_12 |
| ORD ID | ord-816a2f8c0a064c0a9685c614ac62d7c6 |
| 出典メモ | uspto-grants-1989_12 |