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HRID 366193作成日:2026年10月27日

Trifluoroacetic acid → (2R)-3-(2-Fluorophenyl)-N-methyl-2-(methylamino)propionamide

https://huagongshe.com/reaction/366193

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoroacetic acidHCID 6422—
反応物Sodium SesquicarbonateHCID 10791—
反応物Sodium BicarbonateHCID 516892—
反応物N-((1R)-2-(2-Fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methylcarbamic acid tert-butylesterHCID 54285994—
溶媒DichloromethaneHCID 6344—
生成物(2R)-3-(2-Fluorophenyl)-N-methyl-2-(methylamino)propionamideHCID 5411188467.7%

反応手順

N-((1R)-2-(2-Fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methylcarbamic acid tert-butylester (2.4 g; 7.73 mmol) was dissolved in methylene chloride. Trifluoroacetic acid (10 mL) was added and the reaction mixture was stirred for 30 min at room temperature. Methylene chloride (30 mL), an aqueous solution of sodium hydrogen carbonate/sodium carbonate (pH 9; 30 mL) and sodium hydrogen carbonate (solid) were added to the reaction mixture until pH 8. The organic phase was dried (magnesium sulfate) and evaporated in vacuo to afford 1.1 g of (2R)-3-(2-fluorophenyl)-N-methyl-2-(methylamino)-propionamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06127391
出典データセットuspto-grants-2000_10
ORD IDord-30ace6a7992f46a8b97ce48ee8d941c4
出典メモuspto-grants-2000_10