Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1703387Generated: October 25, 2026

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

https://huagongshe.com/reaction/1703387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-3,4-dimethoxybenzonitrileHCID 18778990—
ReactantEthyl 4-(2-furoyl)piperazin-1-ylformimidate hydrochlorideHCID 20506452—
SolventWaterHCID 962—
Product7,8-Dimethoxy-4-amino-2-[4-(2-furoyl)piperazin-1-yl]quinazolineHCID 12920014—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04351940
Source datasetuspto-grants-1982_09
ORD IDord-662e012e42b440e49cc52795ac9bde36
Source noteuspto-grants-1982_09