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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719934Generated: October 31, 2026

Diethyl (ethoxymethylene)malonate → Diethyl[(6-nitro-4-quinazolinylamino)methylene]propanedioate

https://huagongshe.com/reaction/1719934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (ethoxymethylene)malonateHCID 6871—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Nitroquinazolin-4-amineHCID 13060454—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
ProductDiethyl[(6-nitro-4-quinazolinylamino)methylene]propanedioateHCID 1306048560.1%

Reaction Conditions

Temperature5 °C

Reaction Steps

A mixture of 4-amino-6-nitroquinazoline (57.0 g) and diethyl ethoxymethylenepropanedioate (130 g) in anhydrous N,N-dimethylformamide (570 ml) was cooled at 5° C. To the reaction mixture was added sodium hydride (65.5% in mineral oil) (13.2 g) in the course of 30 minutes and the mixture was stirred for 1 hour and 40 minutes under ice-cooling. After ammonium chloride (47.2 g) was added to the reaction mixture and stirred for 20 minutes, ice-water (1 liter) was added to the resultant mixture with stirring and allowed to stand to give crystals, which were separated by filtration, washed with water and dried overnight at ambient temperature. The resultant crude crystals were dissolved in chloroform (1.5 liters) under heating. Insoluble materials were filtered off and the filtrate was concentrated under reduced pressure to give crystals, which were dissolved in methanol (300 ml) under heating and allowed to stand at ambient temperature. The resultant crystals were separated by filtration, washed with methanol and dried under reduced pressure to give yellowish crystalline diethyl [(6-nitro-4-quinazolinylamino)methylene]propanedioate (64.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04543356
Source datasetuspto-grants-1985_09
ORD IDord-73ac776ff16a4320be69d78bd74fb819
Source noteuspto-grants-1985_09