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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 354825생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/354825

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Sodium hydrideHCID 24758—
반응물2-Amino-3,4-dimethoxybenzonitrileHCID 18778990—
반응물Ethyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochlorideHCID 20506452—
용매WaterHCID 962—
생성물7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazolineHCID 12920014—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04377581
출처 데이터셋uspto-grants-1983_03
ORD IDord-dd3efd42fee9452f99c9a7ee85a8f6e5
출처 메모uspto-grants-1983_03