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HRID 1936710作成日:2026年10月26日

1-Acetyl-7-(1-methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole → 7-(1-Methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole

https://huagongshe.com/reaction/1936710

反応式

関与物質

役割名称HCID仕込み量
反応物1-Acetyl-7-(1-methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indoleHCID 22462547—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
溶媒Sodium HydroxideHCID 14798—
生成物7-(1-Methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indoleHCID 1789895261.4%

反応手順

To a stirred suspension of 1-acetyl-7-(1-methylpiperidin-4-yl)-1,2,3,5-tetrahydropyrrolo[2,3-f]indole (D5, 0.55 g, 1.85 mmole) in ethanol (10 ml) and 10% sodium hydroxide solution (10 ml) was added sodium hydroxide pellets (0.50 g) and the resultant mixture was heated at reflux under argon for 18 hours. The mixture was cooled, diluted with water (75 ml) and extracted with dichloromethane (5×30 ml). The combined organic extracts were washed with brine, dried (MgSO4) and evaporated to dryness. The residue was triturated with diethyl ether and the solid filtered off and dried in vacuo to afford the title compound as an off-white powder (0.29 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06391891B1
出典データセットuspto-grants-2002_05
ORD IDord-5b3a5230f34840c1bdb1304e9a1eca36
出典メモuspto-grants-2002_05