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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 366138생성일: 2026년 10월 26일

Bicarbonate Ion → (2R)-N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methyl-2-(methylamino)-3-(2-naphthyl)propionamide

https://huagongshe.com/reaction/366138

반응식

참여 물질

역할이름HCID투입량
반응물Bicarbonate IonHCID 769—
반응물Trifluoroacetic acidHCID 6422—
반응물Sodium BicarbonateHCID 516892—
반응물N-((1R)-1-(N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamoyl)-2-(2-naphthyl)ethyl)-N-methylcarbamic acid tert-butyl-esterHCID 53661815—
용매DichloromethaneHCID 6344—
생성물(2R)-N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methyl-2-(methylamino)-3-(2-naphthyl)propionamideHCID 1067073378.4%

반응 조건

온도0 °C

반응 단계

At 0° C., trifluoroacetic acid (1.5 ml) was added to a solution of N-((1R)-1-(N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamoyl)-2-(2-naphthyl)ethyl)-N-methylcarbamic acid tert-butyl-ester (245 mg, 0.45 mmol) in dichloromethane (1.5 ml). The reaction mixture was stirred for 1.75 h at 0° C. Dichloromethane (5 ml) and a saturated aqueous solution of sodium hydrogen carbonate (6 ml) were added successively. Solid soidum hydrogen carbonate was added until pH 7 was obtained. The phases were separated. The aqueous phase was extracted with dichloromethane (3×50 ml). The combined organic layers were dried over magnesium sulfate. The solvent was removed in vacuo. The crude product was purified by flash chromatography on silica (30 g), using dichloromethane/methanol/25% aqueous ammonia (100:10:1) as eluent, to give 155 mg of (2R)-N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methyl-2-(methylamino)-3-(2-naphthyl)propionamide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06127354
출처 데이터셋uspto-grants-2000_10
ORD IDord-5561c5d250414c5bbceae74fec54aced
출처 메모uspto-grants-2000_10