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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2364663생성일: 2026년 10월 25일

Sodium Bicarbonate → (R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)butanoate

https://huagongshe.com/reaction/2364663

반응식

참여 물질

역할이름HCID투입량
반응물Sodium BicarbonateHCID 516892—
반응물2,4-Dichloro-5-nitropyrimidineHCID 521266—
반응물(R)-Methyl 2-(cyclopentylamino)butanoateHCID 57358664—
용매CyclohexaneHCID 8078—
생성물(R)-Methyl 2-((2-chloro-5-nitropyrimidin-4-yl)(cyclopentyl)amino)butanoateHCID 5840544772.6%

반응 조건

온도60 °C

반응 단계

Methyl (2R)-2-(cyclopentylamino)butanoate 1k (2.50 g, 13.50 mmol) and sodium bicarbonate (4.54 g, 54 mmol) were dissolved in 100 mL of cyclohexane, stirred for 30 minutes followed by the addition of 2,4-dichloro-5-nitro-pyrimidine (2.88 g, 14.84 mmol), heated to 60° C. and stirred for another 12 hours. The reaction mixture was filtered, washed with dichloromethane (50 mL), and the filtrate was concentrated under reduced pressure, the resulting residue was recrystallized by 150 mL of the mixture solvent of ethyl acetate and n-hexane (V/V=1:4) to obtain the title compound methyl (2R)-2-[(2-chloro-5-nitro-pyrimidin-4-yl)-(1-cyclopentyl)amino]butanoate 1m (3.36 g, yield: 72.6%) as a light yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08691822B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-ab0765c4c4ee474aa0f12a5b24397d9d
출처 메모uspto-grants-2014_04