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4-Carbamoyl-1-(3-methoxyphenyl)pyridinium chloride → 1-(3-Methoxyphenyl)piperidine-4-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 4-Carbamoyl-1-(3-methoxyphenyl)pyridinium chloride | HCID 10611695 | — |
| 反応物 | HCID 178418361 | HCID 178418361 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 1-(3-Methoxyphenyl)piperidine-4-carboxamide | HCID 10609747 | 82.6% |
反応手順
A suspension of 4-carbamoyl-1-(3-methoxyphenyl)-pyridinium chloride (26 g) in methanol (300 ml) was hydrogenated at ambient temperature and pressure in the presence of 10% palladium-on-carbon catalyst (2.0 g) until hydrogen uptake ceased (~2 days) The mixture was filtered, excess triethylamine added and the solvent removed in vacuo to give a pink solid. This was partitioned between water and chloroform. The organic phase was dried and the solvent removed in vacuo to give 1-(3-methoxyphenyl)piperidine-4-carboxamide as a pink solid (19 g), m.p. 153°-156° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05767116 |
| 出典データセット | uspto-grants-1998_06 |
| ORD ID | ord-77d34deed1904da48785faccfa985f19 |
| 出典メモ | uspto-grants-1998_06 |