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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Bicarbonate Ion | HCID 769 | — |
| 반응물 | Trifluoroacetic acid | HCID 6422 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | N-((1R)-1-(N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methylcarbamoyl)-2-(2-naphthyl)ethyl)-N-methylcarbamic acid tert-butyl-ester | HCID 53661815 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (2R)-N-(2-(2-(methylsulfonylamino)phenyl)ethyl)-N-methyl-2-(methylamino)-3-(2-naphthyl)propionamide | HCID 10670733 | 78.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06127354 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-5561c5d250414c5bbceae74fec54aced |
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| 출처 메모 | uspto-grants-2000_10 |
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