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Pyridine → Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Pyridine | HCID 1049 | — |
| 反応物 | Ammonium Bicarbonate | HCID 14013 | — |
| 反応物 | Di-tert-butyl dicarbonate | HCID 90495 | — |
| 反応物 | 1-((Tert-butoxy)carbonyl)-4,4-difluoropiperidine-2-carboxylic acid | HCID 10106900 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 生成物 | Tert-butyl 2-carbamoyl-4,4-difluoropiperidine-1-carboxylate | HCID 67286514 | — |
反応手順
To a solution of 1-tert-butoxycarbonyl-4,4-difluoro-piperidine-2-carboxylic acid, 13f, (1.67 g, 6.30 mmol) in 1,4-dioxane (12 mL) was added pyridine (0.35 mL, 4.33 mmol), followed by di-tert-butyl dicarbonate (1.78 g, 8.17 mmol) and ammonium bicarbonate (0.63 g, 7.86 mmol). The reaction mixture was stirred at room temperature overnight. The solvent was removed under reduced pressure and the residue was taken up in EtOAc. The organic phase was washed with water, aqueous saturated KHSO4 solution, brine, dried over Na2SO4, filtered and evaporated to dryness. The crude residue was used without further purification.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08829007B2 |
| 出典データセット | uspto-grants-2014_09 |
| ORD ID | ord-e7fe087c2d5d46bab2cfd714b40831b4 |
| 出典メモ | uspto-grants-2014_09 |