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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277759Generated: October 26, 2026

Phosphorus oxychloride → 4-Chloro-6,7-dimethoxyquinazoline

https://huagongshe.com/reaction/277759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
Reactant6,7-Dimethoxy-3H-quinazolin-4-oneHCID 135495016—
Product4-Chloro-6,7-dimethoxyquinazolineHCID 2769364—

Reaction Steps

The key starting material, 4-chloro-6,7-dimethoxyquinazoline, was prepared according to published procedures (Nomoto, et al., 1990, Chem. Pharm. Bull., 38:1591-1595; Thomas, C. L., 1970, IN:Catalytic Processes and Proven Catalysts, Academic Press, New York, N.Y.) as outlined below in Scheme 1. Specifically, 4,5dimethoxy-2-nitrobenzoic acid (compound 1) was treated with thionyl chloride to form acid chloride, followed by reacting with ammonia to yield 4,5-dimethoxy-2-nitrobenzamide (compound 2). Compound 2 was reduced with sodium borohydride in the presence of catalytic amounts of copper sulphate to give 4,5-dimethoxy-2-aminobenzamide (compound 3), which was directly refluxed with formic acid to yield 6,7-dimethoxyquinazoline-4(3H)-one (compound 4). Compound 4 was refluxed with phosphorus oxytrichloride to give 4-chloro-6,7-dimethoxyquinazoline (compound 5) in good yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358962B2
Source datasetuspto-grants-2002_03
ORD IDord-9f3580f88e534facb98405d085378ddd
Source noteuspto-grants-2002_03