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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984221Generated: November 2, 2026

Triethylamine → ethyl 6-hydroxy-4-oxo-1H-quinazoline-2-carboxylate

https://huagongshe.com/reaction/1984221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Hydroxyanthranilic acidHCID 164592—
ReactantEthyl 2-ethoxy-2-iminoacetateHCID 10920638—
SolventEthanolHCID 702—
Productethyl 6-hydroxy-4-oxo-1H-quinazoline-2-carboxylateHCID 178470314—

Reaction Conditions

Temperature60 °C

Reaction Steps

2-amino-5-hydroxy-benzoic acid (15 mmol) are suspended in ethanol (water free, 600 ml) and heated up to 60° C. and stirred. Then triethylamine (30 mmol) is added and a clear solution is formed. Ethoxy-imino-acetic acid ethyl ester (1 6.5 mmol) is added at 60° C. and after 15 minutes another portion of triethylamine (15 mmol) is added and the mixture stirred for another 30 minutes. The mixture is cooled down to RT and left at RT without stirring over night. The solid material formed was filtered off, washed with ethanol/ether and dried (vacuum). A pale brown powder with mp. 258-260° C. (decomposition) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544688B2
Source datasetuspto-grants-2009_06
ORD IDord-f53824bb380a4d7f8e5c14aa625b1d2e
Source noteuspto-grants-2009_06