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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354887생성일: 2026년 10월 24일

Water → methyl 4-oxo-10-(3-cyclopentylpropionamido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate

https://huagongshe.com/ko/reaction/354887

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Dimethyl methoxymethylenemalonateHCID 90770—
반응물4-Amino-6-(3-cyclopentylpropionamido)quinazolineHCID 13060465—
용매DimethylformamideHCID 6228—
생성물methyl 4-oxo-10-(3-cyclopentylpropionamido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylateHCID 1306055822.1%

반응 조건

온도100 °C

반응 단계

A mixture of 4-amino-6-(3-cyclopentylpropionamido)quinazoline (7.05 g) and dimethyl methoxymethylenepropanedioate (6.48 g) in N,N-dimethylformamide (28 ml) was stirred at 100° C. for 1 hour and 10 minutes. After cooling to ambient temperature, water was added to the reaction mixture. The resulting solid was separated by filtration, washed with water, and dried. The crude crystals were dissolved in a mixture of chloroform and methanol, treated with activated charcoal, and evaporated under reduced pressure until crystallization began. After cooling, the resulting solid was collected, washed with methanol and with dichloromethane, and dried. There was obtained crystalline methyl 4-oxo-10-(3-cyclopentylpropionamido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate (2.16 g). The filtrate was evaporated under reduced pressure to give a residue which was chromatographed on silica gel with 1% methanoldichloromethane. The first fractions contained methyl 4-oxo-10-(3-cyclopentylpropionamido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylate (1.9 g). The second fractions contained dimethyl [[6-(3-cyclopentylpropionamido)-4-quinazolinylamino]methylene]propanedioate (5.16 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377580
출처 데이터셋uspto-grants-1983_03
ORD IDord-ba116ebc72ef4018bfa5906de955ee09
출처 메모uspto-grants-1983_03