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HRID 354887作成日:2026年10月26日

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

https://huagongshe.com/reaction/354887

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Dimethyl methoxymethylenemalonateHCID 90770—
反応物4-Amino-6-(3-cyclopentylpropionamido)quinazolineHCID 13060465—
溶媒DimethylformamideHCID 6228—
生成物methyl 4-oxo-10-(3-cyclopentylpropionamido)-4H-pyrimido[1,2-C]quinazoline-3-carboxylateHCID 1306055822.1%

反応条件

温度100 °C

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04377580
出典データセットuspto-grants-1983_03
ORD IDord-ba116ebc72ef4018bfa5906de955ee09
出典メモuspto-grants-1983_03