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HRID 354825作成日:2026年10月26日

Dimethylformamide → 7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline

https://huagongshe.com/reaction/354825

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物2-Amino-3,4-dimethoxybenzonitrileHCID 18778990—
反応物Ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochlorideHCID 20506452—
溶媒WaterHCID 962—
生成物7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazolineHCID 12920014—

反応手順

To a stirred solution of 1.78 g. (0.01 mole) 3,4-dimethoxy-2-aminobenzonitrile in 30 ml. of N,N-dimethylformamide is added 2.88 g. (0.01 mole) ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochloride followed by 855 mg. (0.02 mole) of a 56.1% dispersion of sodium hydride in mineral oil. The reaction mixture is stirred at ambient temperature for 30 minutes, and then it is heated to ca. 100° C. and maintained at that temperature for 12 hours. The reaction mixture is cooled to ambient temperature, diluted with an excess of water, and then extracted with chloroform. The chloroform extract is washed several times with water, dried using anhydrous magnesium sulfate, and then evaporated to dryness in vacuo. This affords crude 7,8-dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazoline, which is purified further by recrystallization from aqueous ethanol.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04377581
出典データセットuspto-grants-1983_03
ORD IDord-dd3efd42fee9452f99c9a7ee85a8f6e5
出典メモuspto-grants-1983_03