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Sodium Hydroxide → N-(3-nitrophenyl)-4-(2-pyridyl)-2-pyrimidine-amine
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-Nitrophenylguanidine Nitrate | HCID 178512513 | — |
| 溶媒 | Isopropanol | HCID 3776 | — |
| 生成物 | N-(3-nitrophenyl)-4-(2-pyridyl)-2-pyrimidine-amine | HCID 10708835 | — |
反応手順
1 g (5.68 mmol)of 3-dimethylamino-1-(2-pyridyl)-2-propen-1-one [EP-A-233 461] is dissolved in 8 ml of isopropanol, and 1.38 g (5.68 mmol) of 3-nitrophenylguanidine nitrate are added. After the addition of 0.25 g (6.24 mmol) of sodium hydroxide, the yellow suspension is heated at reflux for 20 hours, then cooled to 0°, filtered and washed with 30 ml of isopropanol. The filtration residue is stirred in 15 ml of ethanol for 20 minutes, filtered and washed with a small amount of cold ethanol, yielding N-(3-nitrophenyl)-4-(2-pyridyl)-2-pyrimidine-amine; m.p. 213°-219°.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05521184 |
| 出典データセット | uspto-grants-1996_05 |
| ORD ID | ord-b845d6dc1b164499ac1a9b2ef9232286 |
| 出典メモ | uspto-grants-1996_05 |