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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250597Generated: November 3, 2026

1,1-Dimethylhydrazine → HCID 18326472, compound

https://huagongshe.com/reaction/1250597

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,1-DimethylhydrazineHCID 5976—
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6-Nitro-2,4(1H,3H)-quinazolinedioneHCID 816982—
SolventWaterHCID 962—
ProductHCID 18326472HCID 18326472—

Reaction Steps

To 300 mg (1.45 mmol) of 6-nitroquinazoline-2,4(1H,3H)-dione were added 1 ml of 1,3-dimethyl-2-imidazolidinone and 1.23 g (8.05 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 520 mg (8.69 mmol) of N,N-dimethylhydrazine and stirring under ice cooling for 30 minutes. 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-(2,2-dimethylhydrazino)-6-nitroquinazoline. After 2.00 ml (26.65 mmol) of allylamine 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 (17.5%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06339089B2
Source datasetuspto-grants-2002_01
ORD IDord-784c7475af9548e391af77f290d69c49
Source noteuspto-grants-2002_01