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HRID 881995作成日:2026年10月26日

Ethanol → 2-Hydroxy-3-(2-methoxypropyl)-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-benzo(a)quinolizine

https://huagongshe.com/reaction/881995

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物TetrabenazineHCID 6018—
反応物Sodium borohydrideHCID 4311764—
生成物2-Hydroxy-3-(2-methoxypropyl)-1,3,4,6,7,11b-hexahydro-9,10-dimethoxy-benzo(a)quinolizineHCID 8669133480%

反応条件

温度0 °C

反応手順

Tetrabenazine (Formula 1; 9.01 mg, 0.0284 mmol) was dissolved in 1 mL of ethanol, the solution was cooled to 0° C., and then NaBH4 (3.22 mg, 0.0851 mmol) was slowly added thereto. The temperature was heated to normal temperature and then the mixture was stirred for 1 hr. The mixture was distilled under reduced pressure, water (3 mL) and CH2Cl2 (3 mL) were added thereto to extract an organic layer, and the organic layer collected was washed with a saturated K2CO3 aqueous solution. Anhydrous magnesium sulfate was used to dry the organic layer, filtration under reduced pressure and evaporation under reduced pressure were performed, and then column chromatography was used to obtain 7.30 mg (yield 80%) of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993766B2
出典データセットuspto-grants-2015_03
ORD IDord-8c235ef0ec51463b8d737cf21392154f
出典メモuspto-grants-2015_03