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HRID 333192作成日:2026年10月25日

Ammonium bisulfate → (alphaR)-alpha-[(1S)-2-(Dimethylamino)-1-methylethyl]-alpha-ethyl-3-methoxybenzenemethanol

https://huagongshe.com/reaction/333192

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium bisulfateHCID 24655—
反応物Talabostat mesylateHCID 11522448—
反応物(2S)-3-(Dimethylamino)-1-(3-methoxyphenyl)-2-methyl-1-propanoneHCID 25146676—
反応物HCID 178418443HCID 178418443—
溶媒TetrahydrofuranHCID 8028—
生成物(alphaR)-alpha-[(1S)-2-(Dimethylamino)-1-methylethyl]-alpha-ethyl-3-methoxybenzenemethanolHCID 994297999%

反応条件

温度5 °C

反応手順

(S)-3-(Dimethylamino)-1-(3-methoxyphenyl)-2-methylpropan-1-one (774.6 g, 3.5 mol, ee 95%) was dissolved in dry tetrahydrofuran (800 mL) in a 10 L double jacket vessel equipped with an electrical impeller stirrer, a gas transition line, Pt100 temperature measuring equipment and an oil based cooling/heating system and ethyl magnesium bromide (2 L, 2 M in THF) was added at a temperature of 15° C. within 2 hours. The reaction mixture was stirred for two hours at that temperature, cooled to 5° C. and aqueous ammonium hydrogen sulfate solution (10% by weight, 2 L) was added. The phases were separated and the organic phase was concentrated in vacuo at 40° C. until a pressure of 5 mbar was reached. (2S,3R)-1-(Dimethylamino)-3-(3-methoxyphenyl)-2-methylpentan-3-ol (871.1 g, 99%) was obtained as a colorless oil (ee 95%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08877974B2
出典データセットuspto-grants-2014_11
ORD IDord-122f5501f9b44ff88ec18d6e1c6d58b6
出典メモuspto-grants-2014_11