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HRID 38313作成日:2026年10月23日

Ethanol → Tetrabenazine

https://huagongshe.com/ja/reaction/38313

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物WaterHCID 962—
反応物3,4-Dihydro-6,7-dimethoxyisoquinolineHCID 30058—
反応物(2-Acetyl-4-methylpentyl)trimethylammonium IodideHCID 86641883—
溶媒DichloromethaneHCID 6344—
生成物TetrabenazineHCID 601837.1%

反応手順

(2-Acetyl-4-methyl-pentyl)-trimethyl-ammonium iodide (800 mg, 2.55 mmol, 1.00 equiv) was added to a solution of 6,7-dimethoxy-3,4-dihydroisoquinoline (100 mg, 2.62 mmol, 1.00 equiv) and ethanol (10 mL). The resulting solution was heated at reflux for about 5 hours, and then water (20 mL) was added. Following standard extractive workup with dichloromethane (3×50 mL), the crude residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether (1:4)) to afford the title compound as a white solid (300 mg, yield=36%). 1H NMR (300 MHz, CDCl3), δ 6.63 (s, 1H), 6.55 (s, 1H), 3.89 (s, 3H), 3.83 (s, 3H), 3.55 (s, 1H), 3.22-3.28 (m, 1H), 2.94-3.14 (m, 4H), 2.31-2.65 (m, 4H), 1.73-1.81 (t, 1H, J=11.4), 1.33-1.39 (m, 1H), 0.996-1.067 (t, 1H, J=10.5), 0.79-0.85 (m, 6H) LC-MS: m/z=318 (MH)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524733B2
出典データセットuspto-grants-2013_09
ORD IDord-78995b4d748446c0aab3b3f8242e9a83
出典メモuspto-grants-2013_09