HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1162996Generated: October 26, 2026
Triethylamine → ethyl 6-hydroxy-4-oxo-1H-quinazoline-2-carboxylate
https://huagongshe.com/reaction/1162996
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Hydroxyanthranilic acid | HCID 164592 | — |
| Reactant | Ethyl 2-ethoxy-2-iminoacetate | HCID 10920638 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | ethyl 6-hydroxy-4-oxo-1H-quinazoline-2-carboxylate | HCID 178470314 | — |
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 (16.5 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07820818B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-3890eacfac754a66a6c81230f894be3a |
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| Source note | uspto-grants-2010_10 |
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