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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250612Generated: November 3, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 54459706, compound

https://huagongshe.com/reaction/1250612

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantTriethylamineHCID 8471—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-Nitro-2,4(1H,3H)-quinazolinedioneHCID 816982—
ReactantBUT-3-EN-2-AMINE HCLHCID 18185425—
SolventWaterHCID 962—
ProductHCID 54459706HCID 54459706—

Reaction Steps

To 278 mg (1.45 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 0.71 ml of 1,3-dimethyl-2-imidazolidinone and 5.48 g (35.76 mmol) of phosphorus oxychloride, and the resulting mixture was subjected to heating under reflux for 3 hours. After phosphorus oxychloride was removed in vacuo, the mixture was dissolved in 3 ml of acetonitrile, followed by addition of 2.81 ml (20.07 mmol) of triethylamine and 281 mg (2.61 mmol) of 1-methyl-2-propenylamine hydrochloride and stirring under ice cooling for 2 hours. To the reaction solution was added water, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off to give 2-chloro-4-(1-methyl-2-propenylamino)-6-nitroquinazoline. After 1.00 ml (10.12 mmol) of n-butylamine was added thereto and then the mixture was stirred at room temperature for 3 hours, water was added to the reaction solution, followed by extraction with ethyl acetate, washing with brine and drying over anhydrous sodium sulfate. After the solvent was distilled off, the residue was purified by a silica gel column to give 73 mg (17.3%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-ae2cc88b4ba04e1c91dcbef892969cc1
Source noteuspto-grants-2002_01