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Acetic Acid → 4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetic Acid | HCID 176 | — |
| 反応物 | 3,4-Diaminopyridine | HCID 5918 | — |
| 反応物 | 1-Benzyl-4-piperidone | HCID 19220 | — |
| 溶媒 | 1,1-Dichloroethane | HCID 6365 | — |
| 生成物 | 4-Amino-3-[(1-benzylpiperidin-4-yl)amino)pyridine | HCID 22293245 | 98.2% |
反応手順
A mixture of 3,4-diaminopyridine (1.1 g, 10.1 mmol), 1-benzyl-4-piperidone (3.2 g, 16.9 mmol) sodium triacetoxyborohydride (4.0 g, 18.9 mmol), and acetic acid (10.7 mL) in dichloroethane (10 mL) was stirred for about 6 days at room temperature. The reaction was concentrated to near dryness, and partitioned between chloroform (5×50 mL) and 1N sodium hydroxide (50 mL). The organic phase was dried over magnesium sulfate and concentrated to give the title compound (2.8 g). MS 283 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07534784B2 |
| 出典データセット | uspto-grants-2009_05 |
| ORD ID | ord-3cbb4d5e31834e968563ad65ff2e0ed9 |
| 出典メモ | uspto-grants-2009_05 |