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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384755Generated: October 30, 2026

Methanol → 7-Chloro-3H-quinazolin-4-one

https://huagongshe.com/reaction/384755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Amino-4-chlorobenzoic acidHCID 66646—
ReactantAmmonium AcetateHCID 517165—
ReactantMethylorthoformateHCID 53629101—
SolventWaterHCID 962—
Product7-Chloro-3H-quinazolin-4-oneHCID 13541617592%

Reaction Steps

In a 10-mL volume stainless steel pressure-resistant vessel were placed 1.00 g (5.8 mmol) of 4-chloroanthranilic acid, 2.47 g (23.3 mmol) of methyl orthoformate, 1.80 g (23.3 mmol) of ammonium acetate, and 4.0 mL of methanol. The reaction was carried out at 120° C. for 3 hours. After the reaction was complete, the reaction mixture was cooled to room temperature, and 40 mL of water was added to the reaction mixture. The resulting aqueous mixture was stirred for 15 minutes and filtered to give 0.96 g (isolated yield: 92%) of 7-chloroquinazolin-4-one as a white crystalline product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367824B2
Source datasetuspto-grants-2013_02
ORD IDord-bbd2b8829fea4858b244db8b8e1089f0
Source noteuspto-grants-2013_02