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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 459967생성일: 2026년 10월 24일

N,N-Diethyl-1,4-butanediamine → 1-Cyclopentyl-7-(4-diethylamino-butylamino)-3-(2,6-difluoro-3,5-dimethoxy-phenyl)-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one

https://huagongshe.com/ko/reaction/459967

반응식

참여 물질

역할이름HCID투입량
반응물N,N-Diethyl-1,4-butanediamineHCID 117976—
반응물1-Cyclopentyl-3-(2,6-difluoro-3,5-dimethoxyphenyl)-7-(methylsulfinyl)-3,4-dihydropyrimido[4,5-d]pyrimidin-2(1H)-oneHCID 18444844—
용매1,4-DioxaneHCID 31275—
생성물1-Cyclopentyl-7-(4-diethylamino-butylamino)-3-(2,6-difluoro-3,5-dimethoxy-phenyl)-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-oneHCID 1036978286%

반응 단계

In a 1-L round bottom flask, 8.00 g (17.78 mmol) of 1-cyclopentyl-3-(2,6-difluoro-3,5-dimethoxy-phenyl)-7-methylsulfinyl-3,4-dihydro-1H-pyrimido[4,5-d]pyrimidin-2-one in 260 mL of dioxane was treated with 5.10 g (35.36 mmol) of 4-diethylamino-butylamine and heated at reflux for 10 hours under nitrogen atmosphere. The dioxane was evaporated in vacuo. The crude product was purified using medium-pressure chromatography eluting with a gradient of 9:0.5:0.25 to 9:1:0.5 ethyl acetate/methanol/triethylamine to give 8.14 g (86%) of the title compound as a pure partially crystalline solid. A 50 mg portion of the solid was recrystallized with 25% ethanol in hexanes to give 35 mg of title compound as pure crystalline solid: mp 132° C.–133° C. MS (APCI) (m+1)/z 533.3.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07196090B2
출처 데이터셋uspto-grants-2007_03
ORD IDord-4dc2d2c12f8c4774992c7decd3d83954
출처 메모uspto-grants-2007_03