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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 495788생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/495788

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium SesquicarbonateHCID 10791—
반응물Sodium BicarbonateHCID 516892—
반응물N-((1R)-2-(2-Fluorophenyl)-1-(methylcarbamoyl)ethyl)-N-methylcarbamic acid tert-butylesterHCID 54285994—
용매DichloromethaneHCID 6344—
생성물(2R)-3-(2-Fluorophenyl)-N-methyl-2-(methylamino)propionamideHCID 5411188467.7%

반응 단계

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 (1 0 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06939880B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-5cc1eb061592428d9bd49122378779eb
출처 메모uspto-grants-2005_09