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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227789생성일: 2026년 10월 24일

N,N,2,2-Tetramethylpropane-1,3-diamine → N-(4-(3-(2-(3-(dimethylamino)-2,2-dimethylpropylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)4-phenylphthalazin-1-amine

https://huagongshe.com/ko/reaction/227789

반응식

참여 물질

역할이름HCID투입량
반응물N,N,2,2-Tetramethylpropane-1,3-diamineHCID 104477—
반응물HCID 66731697HCID 66731697—
용매Dimethyl SulfoxideHCID 679—
생성물N-(4-(3-(2-(3-(dimethylamino)-2,2-dimethylpropylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)4-phenylphthalazin-1-amineHCID 57756233—

반응 조건

온도70 °C

반응 단계

A resealable pressure vial was charged with N-(4-(3-(2-(methylsulfonyl)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)-4-phenylphthalazin-1-amine (100 mg, 0.180 mmol) and N1,N1,2,2-tetramethylpropane-1,3-diamine (0.12 ml, 0.73 mmol) and DMSO (1.2 ml, 0.15 M). The reaction vessel was sealed and the mixture was stirred at 70° C. for 16 hrs. The reaction was cooled to RT and diluted with 3 ml of DMSO. The solution was purified by Gilson reverse phase chromatography (10% to 90% CH3CN/H2O/0.1% TFA). The product-containing fractions were combined, basified by addition of aq. NaHCO3 and extracted with ethyl acetate. The organic portion was dried with Na2SO4, filtered, and concentrated to afford pure N-(4-(3-(2-(3-(dimethylamino)-2,2-dimethylpropylamino)pyrimidin-4-yl)pyridin-2-yloxy)phenyl)4-phenylphthalazin-1-amine as a yellow solid. MS m/z=597 [M+H]+. Calc'd for C36H36N8O: 596.72.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560551B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-92b68cb256ac4dfea4160fe52c0d1268
출처 메모uspto-grants-2009_07