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HRID 459711作成日:2026年10月26日

3-Ethoxy-2-propenoyl chloride → 1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-one

https://huagongshe.com/reaction/459711

反応式

関与物質

役割名称HCID仕込み量
反応物3-Ethoxy-2-propenoyl chlorideHCID 3014429—
反応物2,3,4,5-tetrahydro-1H-benzo[b]azepin-8-amineHCID 18444221—
溶媒DichloromethaneHCID 6344—
溶媒Sodium HydroxideHCID 14798—
生成物1,6,7,8,9,10-Hexahydro-2h-azepino[3,2-g]quinolin-2-oneHCID 9899244—

反応条件

温度50 °C

反応手順

A solution of 2,3,4,5-tetrahydro-1H-1-benzazapin-8-amine (0.6 g, 3.4 mmol) and 3-ethoxyacryloyl chloride (0.45 g, 3.4 mmol) in CH2Cl2 (50 mL) and 3N NaOH (10 mL) was stirred for 1 h at ambient temperature. The reaction was partitioned between CH2Cl2 and water. The organic layer was concentrated and the remaining brown oil was dissolved in 70% aq. H2SO4 (20 mL) and heated gently (50° C.) for 2 h. The reaction was cooled and neutralized with aq. NH4OH and partitioned between water and EtOAc. The organic layer was washed with brine, dried over MgSO4, filtered and concentrated. The residue was dissolved in DMF (1 mL) and purified on a GILSON automated system affixed with a YMC COMBIFLASH 50 mm×20 mm reverse phase column eluted 5–95% CH3CN in water at 30 mL/min over 10.5 min to provide pure desired product. HRMS m/z (M+1) calcd 215.1179; found 215.1186.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07196076B2
出典データセットuspto-grants-2007_03
ORD IDord-f67beddc9b33443db36a36f7388ba7e4
出典メモuspto-grants-2007_03