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Pentylamine → N-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pentylamine | HCID 8060 | — |
| 反応物 | 5-Benzyl-4-chloro-6-methylpyrimidin-2-amine | HCID 820238 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | N-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamine | HCID 12043763 | 89.7% |
反応手順
A mixture of 5-benzyl-4-chloro-6-methylpyrimidine-2-ylamine (500 mg, 2.14 mmol) , amylamine (1.24 ml ) and dioxane (4 ml ) was kept at 95-100° C. for 19 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with chloroform and a saturated aqueous NaHCO3 solution. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (2%MeOH/CHCl3) to give the object compound (546 mg, 89.7%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06458798B1 |
| 出典データセット | uspto-grants-2002_10 |
| ORD ID | ord-0c51ed97379a4340923c28e477daca0e |
| 出典メモ | uspto-grants-2002_10 |