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Triethylamine → 2,3-dihydro-1H-indole-1-carboxamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | 2,2,2-Trichloroethyl chloroformate | HCID 87063 | — |
| 反応物 | (-) (2aR,4S)-6-acetyl-4-[di(cyclopropylmethyl)amino]-1,2,2a,3,4,5-hexahydrobenz[cd]indole | HCID 18654740 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 2,3-dihydro-1H-indole-1-carboxamide | HCID 771524 | 248.2% |
反応手順
To a solution of (-)(2aR,4S)-6-acetyl-4-[di -(cyclopropylmethyl)amino]-1,2,2a,3,4,5-hexahydrobenz -[cd]indole (2.5 g, 7.7 mmol) and triethylamine (1.1 ml, 8 mmol) in 90 ml CH2Cl2 was added dropwise a solution of 2,2,2-trichloroethylchloroformate (1.7 g, 8 mmol) in 10 ml CH2Cl2. The reaction mixture was stirred at room temperature for one hour and then extracted with water and 1N HCl. The organic solution was washed with a saturated NaHCO3 solution and a saturated brine solution, dried over MgSO4 and then concentrated to dryness in vacuo to give 3.1 g of the 1-carbamylindoline.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05643910 |
| 出典データセット | uspto-grants-1997_07 |
| ORD ID | ord-52ba479bc8ac473382de59cdda950d00 |
| 出典メモ | uspto-grants-1997_07 |