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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 328118Generated: October 26, 2026

Dimethylformamide → 1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dione

https://huagongshe.com/reaction/328118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dioneHCID 12812377—
SolventWaterHCID 962—
Product1(m-nitrophenyl)-3-allylquinazoline-2,4(1H, 3H)-dioneHCID 1327234490.7%

Reaction Steps

To a solution of 2.8 g of 1-(m-nitrophenyl)quinazoline-2,4(1H, 3H)-dione and 30 ml of dimethylformamide was added 0.6 g of approximately 55 % sodium hydride and the solution was stirred for 30 minutes at room temperature. To this was further added 3.6 g of allyl bromide, and the mixture was reacted for 2 hours at room temperature. Then, the solvent was distilled off from the resulting mixture under reduced pressure to leave a residue, to which was added water to precipitate a crude product. This product was recrystallized from methanol to yield 2.9 g of 1(m-nitrophenyl)-3 -allylquinazoline- 2,4(1H, 3H)-dione as light brown needles, melting at 165°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04016166
Source datasetuspto-grants-1977_04
ORD IDord-c0bfb59fdce74feeaef789a5fb0ed9a2
Source noteuspto-grants-1977_04