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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1602223생성일: 2026년 10월 26일

Ethyl Acetate → 3-benzylamino-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine

https://huagongshe.com/reaction/1602223

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Benzenamine, 3-chloro-, hydrochloride (1:1)HCID 67336—
반응물Sodium BicarbonateHCID 516892—
반응물N'-(3-benzylamino-4-cyano-1H-pyrazol-5-yl)-N,N-dimethylformamidineHCID 53832654—
용매MethanolHCID 887—
생성물3-benzylamino-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidineHCID 5327835—

반응 조건

온도50 °C

반응 단계

With the exclusion of moisture, 79.2 g (295 mmol) of N'-(3-benzylamino-4-cyano-1H-pyrazol-5-yl)-N,N-dimethylformamidine are suspended in 700 ml of methanol; 60.6 g (369 mmol) of 3-chloro-aniline hydrochloride are added and the reaction mixture is boiled under reflux for 22 hours. The resulting yellow reaction solution is cooled to ≈50° C. and poured onto 2 liters of ice-water, 200 ml of saturated NaHCO3 solution and 1 liter of ethyl acetate. The aqueous phase is separated off and extracted twice with ethyl acetate. The organic phases are washed twice with water, saturated NaHCO3 solution, water and brine, dried (Na2SO4) and concentrated by evaporation to a residual volume of ≈1.5 liters. Inoculation and dilution with 300 ml of diethyl ether yield crystalline 3-benzylamino-4-(3-chloro-phenylamino)-1H-pyrazolo[3,4-d]pyrimidine; m.p. 214-217° C.; TLC: Rf =0.29 (ethyl acetate:hexane=1:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05981533
출처 데이터셋uspto-grants-1999_11
ORD IDord-e23e397384e44c0baf234b0b8c923f72
출처 메모uspto-grants-1999_11