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Sodium Hydroxide → N-(3-(1H-imidazol-1-yl)phenyl)-4-(2-pyridinyl)-2-pyrimidinamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Sodium Hydroxide | HCID 14798 | — |
| 反応物 | 3-Dimethylamino-1-(2-pyridyl)prop-2-en-1-one | HCID 566993 | — |
| 反応物 | [3-(1H-Imidazol-1-yl)phenyl]guanidine, dihydrochloride | HCID 178478791 | — |
| 溶媒 | 1-Propanol | HCID 1031 | — |
| 生成物 | N-(3-(1H-imidazol-1-yl)phenyl)-4-(2-pyridinyl)-2-pyrimidinamine | HCID 163890 | 85% |
反応手順
Thirteen and seven tenths grams of [3-(1H-imidazol-1-yl)phenyl]guanidine, dihydrochloride (2) from Example 1, 8.8 g of 3-dimethylamino-1-(2-pyridyl)-2-propen-1-one (3), 50 ml of n-propanol and 10 ml of 10N sodium hydroxide is refluxed for 18 hours. The reaction is diluted with 50 ml of n-propanol and filtered. The collected yellow solid is stirred in 300 ml of water for 0.5 hour, filtered and washed with 50 ml of n-propanol followed by 100 ml of diethyl ether. The solid is air dried overnight giving 13.4 g (85%) of the desired product, mp 210°-211° C. The overall yield following this procedure is 73%.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05064963 |
| 出典データセット | uspto-grants-1991_11 |
| ORD ID | ord-f7a7a792e05042bd8c3706df6930a809 |
| 出典メモ | uspto-grants-1991_11 |