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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1767144Generated: November 2, 2026

2-Amino-4-chlorobenzoic acid → 7-Chloro-3H-quinazolin-4-one

https://huagongshe.com/reaction/1767144

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-chlorobenzoic acidHCID 66646—
ReactantAmmonia methanolHCID 21705897—
ReactantMethylorthoformateHCID 53629101—
Product7-Chloro-3H-quinazolin-4-oneHCID 13541617599%

Reaction Steps

In a 2-mL volume stainless steel pressure-resistant vessel were placed 330 mg (1.9 mmol) of 4-chloroanthranilic acid, 403 mg (3.8 mmol) of methyl orthoformate, and 1.2 mL (8.4 mmol) of 15 wt. % ammonia methanol solution. The reaction was carried out at 120° C. for 2 hours. After the reaction was complete, the reaction mixture was cooled to room temperature and analyzed (according to absolute quantitative analysis) by high performance liquid chromatography. There was produced 343 mg (reaction yield: 99%) of 7-chloroquinazolin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07232903B2
Source datasetuspto-grants-2007_06
ORD IDord-e7903440e9bf485cb03d196a4f6cfdb7
Source noteuspto-grants-2007_06