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5-Aminopyridine-2-carbonitrile → HCID 178510044、化合物
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 5-Aminopyridine-2-carbonitrile | HCID 3871395 | — |
| 反応物 | 3-Morpholinobenzaldehyde | HCID 7164584 | — |
| 触媒 | p-Toluenesulfonic acid | HCID 6101 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 178510044 | HCID 178510044 | 99.9% |
反応手順
The mixture solution of 5-amino-pyridine-2-carbonitrile (9.3 g, 78.4 mmol), 3-morpholin-4-yl-benzaldehyde (15.0 g, 78.4 mmol) and p-toluenesulfonic acid (271.8 mg, 1.4 mmol) in toluene (150 mL) was heated to reflux for 12 h. Then the reaction mixture was cooled to room temperature. The solvent was removed in vacuo and the residue was washed with ether to afford 5-{[1-(3-morpholin-4-yl-phenyl)-meth-(E)-ylidene]-amino}-pyridine-2-carbonitrile (22.9 g, quant.) as a light yellow solid: MS (ESI) M+1=293.0.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08809369B2 |
| 出典データセット | uspto-grants-2014_08 |
| ORD ID | ord-c9d7d888639e442fab511ab3e82ecc93 |
| 出典メモ | uspto-grants-2014_08 |