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Ammonium Acetate → 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonium Acetate | HCID 517165 | — |
| 反応物 | Sodium cyanoborohydride | HCID 5003444 | — |
| 反応物 | 1-(3-Phenylpropionyl)-4-ketopiperidine | HCID 17817612 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one | HCID 16793772 | 47% |
反応手順
To 3.2 g (13.8 mmol) of 135 in 125 mL of anhydrous methanol was added 21.3 g of ammonium acetate and 20 g of 3A molecular sieves. After stirring 30 min, 3.47 g (55.2 mmol) of sodium cyanoborohydride was added portionwise with stirring. After 3 hours, the mixture was gravity filtered, and the methanol evaporated under vacuum. The residue was partitioned between ice/HCl and ether. The acidic aqueous phase was extracted twice more with ether. The aqueous phase was made basic with ice and 50% aqueous NaOH. The mixture was extracted with CH2Cl2, dried, and evaporated under vacuum to give 1.5 g (47%) of the title amine 136. GC/MS indicated 100% purity with a molecular ion of 232.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06706740B2 |
| 出典データセット | uspto-grants-2004_03 |
| ORD ID | ord-08ae6f502bb042ebb1e5e2dd2d00758b |
| 出典メモ | uspto-grants-2004_03 |