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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443215Generated: October 28, 2026

Phosphorus pentachloride → 2-Methylquinazolin-5-amine

https://huagongshe.com/reaction/1443215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 136342146HCID 136342146—
CatalystPalladiumHCID 23938—
SolventPhosphorus oxychlorideHCID 24813—
Product2-Methylquinazolin-5-amineHCID 179850585.4%

Reaction Steps

12.7 g (62 mmol) of 2-methyl-5-nitro-3H-quinazolin-4-one (M. T. Bogert, V. J. Chambers J. Org Chem. 1905, 649-658) and 37.5 g of phosphorus pentachloride are refluxed in 75 ml of phosphoryl chloride over 20 hours. After cooling, it is poured into saturated NaHCO3 solution and extracted with ethyl acetate. The organic phase is dried, and the solvent is removed. 14 g of 4-chloro-2-methyl-5-nitroquinazoline, of which 4.5 g (20.2 mmol) in 225 ml of ethyl acetate and 22.5 ml of triethylamine are dissolved, is obtained. 2 g of palladium on carbon is added, and it is stirred while being cooled with ice for 4 hours under a hydrogen atmosphere at normal pressure. Catalyst is removed from the solution by means of filtration through Celite, whereby it is rewashed with 200 ml of ethanol and concentrated by evaporation. After chromatography on silica gel with ethyl acetate-ethanol (0-10%), 530 mg of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659297B2
Source datasetuspto-grants-2010_02
ORD IDord-f3958abb3e6f455db09c1b214b028f9f
Source noteuspto-grants-2010_02