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Potassium Carbonate → 3-(R,S)-(1-carbamoyl-1,1-diphenylmetyl)-1-[3-(4-methoxyphenyl)propyl]piperidine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 1-(3-Bromopropyl)-4-methoxybenzene | HCID 12776996 | — |
| 反応物 | 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine | HCID 13633748 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(R,S)-(1-carbamoyl-1,1-diphenylmetyl)-1-[3-(4-methoxyphenyl)propyl]piperidine | HCID 21224099 | — |
反応手順
A mixture containing 3-(R,S)-(1-carbamoyl-1,1-diphenylmethyl)piperidine (0.26 g), 1-bromo-3-(4-methoxyphenyl)propane (0.23 g), anhydrous potassium carbonate (0.3 g) and acetonitrile (10 ml) was heated under reflux for 16 hours. The mixture was partitioned between dichloromethane (30 ml) and 10% aqueous sodium carbonate (30 ml), the layers separated, and the aqueous layer extracted with dichloromethane (2×30 ml). The dichloromethane extracts were combined, dried (MgSO4) and concentrated in vacuo to give a solid which was recrystallised from ethanol to give the title compound, yield 0.19 g, m.p. 180°-182° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05422358 |
| 出典データセット | uspto-grants-1995_06 |
| ORD ID | ord-2c0f66410bbd4d81851ffca9017a268d |
| 出典メモ | uspto-grants-1995_06 |