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Ammonia → N-[4-(2-Furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Dimethyl Sulfide | HCID 1068 | — |
| 反応物 | 1-(Benzyloxycarbonyl)-N-[4-(2-furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide | HCID 23144107 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | N-[4-(2-Furyl)-5-morpholinothiazol-2-yl]piperidine-4-carboxamide | HCID 23144542 | 39.5% |
反応手順
Compound 43 (4.71 g, 9.50 mmol) was dissolved in dichloromethane (100 mL), and dimethyl sulfide (29.4 mL, 400 mmol) and boron trifluoride-diethyl ether complex (24.6 mL, 200 mmol) were added thereto, followed by stirring overnight at room temperature. The reaction mixture was poured into 28% aqueous ammonia, followed by extraction with chloroform. The organic layer was washed with a saturated aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate, and then the solvent was distilled away under reduced pressure to afford the entitled Compound 44 (1.36 g, 38%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07880013B2 |
| 出典データセット | uspto-grants-2011_02 |
| ORD ID | ord-60055eb3e0ed49f5b102a310b78b35f4 |
| 出典メモ | uspto-grants-2011_02 |