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HRID 263417作成日:2026年10月25日

Triethylamine → 2,3-dihydro-1H-indole-1-carboxamide

https://huagongshe.com/reaction/263417

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2,2,2-Trichloroethyl chloroformateHCID 87063—
反応物(-) (2aR,4S)-6-acetyl-4-[di(cyclopropylmethyl)amino]-1,2,2a,3,4,5-hexahydrobenz[cd]indoleHCID 18654740—
溶媒DichloromethaneHCID 6344—
生成物2,3-dihydro-1H-indole-1-carboxamideHCID 771524248.2%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US05643910
出典データセットuspto-grants-1997_07
ORD IDord-52ba479bc8ac473382de59cdda950d00
出典メモuspto-grants-1997_07