HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1735971Generated: October 30, 2026
Triethylamine → ethyl N-(2,4-dichlorophenylcarbamoyl)-5-fluoroanthranilate
https://huagongshe.com/reaction/1735971
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichlorophenyl isocyanate | HCID 75789 | — |
| Reactant | Ethyl 2-amino-5-fluorobenzoate | HCID 11126923 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | ethyl N-(2,4-dichlorophenylcarbamoyl)-5-fluoroanthranilate | HCID 19435037 | 93.6% |
Reaction Steps
A solution of 2,4-dichlorophenyl isocyanate (47.0 g, 0.25 mol) in xylene (130 ml) is metered at room temperature into a solution of ethyl 5-fluoroanthranilate (45.2 g, 0.25 mol) in xylene (210 ml). After addition is complete, the mixture is stirred at 90° C. for 2 hours. Triethylamine (3.5 ml, 2.55 g, 0.025 mol) is metered in. The mixture is stirred at 90° C. for a further 2 hours. After cooling, the product is filtered off with suction and washed with 3×30 ml of xylene and dried. 86.9 g of ethyl N-(2,4-dichlorophenylcarbamoyl)-5-fluoroanthranilate of melting point 219° to 223° C. (decomposition) are obtained. The cyclization product 3-(2,4-dichlorophenyl)-6-fluoro-2,4(1H,3H)-quinazolinedione cannot be detected by thin-layer chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05539114 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-72acfa54c5334fcca626f2a0f7f1f62d |
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| Source note | uspto-grants-1996_07 |
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