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5-Aminoimidazole-4-carboxamide hydrochloride → 4-(2-Thienyl)imidazo[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 | Sodium Acetate | HCID 517045 | — |
| 反応物 | 3-(Dimethylamino)-1-(2-thienyl)-2-propen-1-one | HCID 602399 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 4-(2-Thienyl)imidazo[1,5-a]pyrimidine-8-carboxamide | HCID 20508957 | — |
反応手順
A mixture of 0.01 mol of 3-dimethylamino-1-(2-thienyl)-2-propen-1-one (prepared as described in Example 1, Part A), 0.01 mol of 4amino-5-imidazolecarboxamide hydrochloride and 0.01 mol of anhydrous sodium acetate in 25 ml. of glacial acetic acid can be refluxed for 16 hours. The reaction mixture can be cooled and the crystalline precipitate collected by filtration and washed with water to produce 4-(2-thienyl)imidazo[1,5-a]pyrimidine-8-carboxamide.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US04374988 |
| 出典データセット | uspto-grants-1983_02 |
| ORD ID | ord-aead6c4625aa4cd5aa47356fb23eea00 |
| 出典メモ | uspto-grants-1983_02 |