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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 475892생성일: 2026년 10월 27일

Sulfuric Acid → 7-(4-fluorophenyl)-N2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-N4-methyl-6,7-dihydro-5H-cyclopenta(d)pyrimidine-2,4-diamine

https://huagongshe.com/reaction/475892

반응식

참여 물질

역할이름HCID투입량
반응물Sulfuric AcidHCID 1118—
반응물Sodium BicarbonateHCID 516892—
반응물2-chloro-7-(4-fluorophenyl)-N-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amineHCID 58075812—
반응물3-Methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)anilineHCID 59577818—
용매WaterHCID 962—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물7-(4-fluorophenyl)-N2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-N4-methyl-6,7-dihydro-5H-cyclopenta(d)pyrimidine-2,4-diamineHCID 58075317—

반응 조건

온도100 °C

반응 단계

To a solution of 2-chloro-7-(4-fluorophenyl)-N-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-amine (Preparation Hh) (141.2 mg, 0.508 mmol) and 3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)aniline (Preparation D) (208 mg, 1.017 mmol) in N-Methyl-2-pyrrolidinone (4067 μL) was added H2SO4 (43.4 μL, 0.813 mmol). The solution was heated to 100° C. When the reaction was complete, water and NaHCO3 were added. After extraction into CH2Cl2, the organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. Applied the residue to SG and eluted with a EtOAc/Hex gradient, which yielded 7-(4-fluorophenyl)-N2-(3-methoxy-4-(3-methyl-1H-1,2,4-triazol-1-yl)phenyl)-N4-methyl-6,7-dihydro-5H-cyclopenta[d]pyrimidine-2,4-diamine (Example 44).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637525B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-703d6d2a1ddb42ef9b8fab5727535276
출처 메모uspto-grants-2014_01