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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 3450생성일: 2026년 10월 23일

Dimethylformamide dimethyl acetal → N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino)propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N,N-dimethylformamidine

https://huagongshe.com/ko/reaction/3450

반응식

참여 물질

역할이름HCID투입량
반응물Dimethylformamide dimethyl acetalHCID 78373—
반응물6-(2,6-dichlorophenyl)-2-N-[3-(diethylamino)propyl]pyrido[2,3-d]pyrimidine-2,7-diamineHCID 5328114—
용매DimethylformamideHCID 6228—
생성물N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino)propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N,N-dimethylformamidineHCID 532817468%

반응 단계

To a suspension of 210 mg (1 mmol) of 7-amino-6-(2,6-dichlorophenyl)-2-[3-(diethylamino) propylamino]-pyrido[2,3-d]pyrimidine from Example 20 in 0.8 mL of DMF was added 0.8 mL of DMF dimethyl acetal. The mixture was stirred at room temperature for 5.5 hours, then concentrated in vacuo. The residual oil was distributed between dichloromethane and water. The organic phase was dried over magnesium sulfate, then concentrated to a glass that was crystallized from acetonitrile to give 160 mg (68%) of N'-[6-(2,6-dichlorophenyl)-2-{3-(diethylamino) propylamino}-pyrido[2,3-d]pyrimidin-7-yl]-N, N-dimethylformamidine, mp 100°-104° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05733913
출처 데이터셋uspto-grants-1998_03
ORD IDord-3b18944e08c244489c0c882a36845a09
출처 메모uspto-grants-1998_03