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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,4-Dichlorophenyl isocyanateHCID 75789—
ReactantEthyl 2-amino-5-fluorobenzoateHCID 11126923—
SolventO-XyleneHCID 7237—
Productethyl N-(2,4-dichlorophenylcarbamoyl)-5-fluoroanthranilateHCID 1943503793.6%

Reaction Conditions

Temperature90 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05539114
Source datasetuspto-grants-1996_07
ORD IDord-72acfa54c5334fcca626f2a0f7f1f62d
Source noteuspto-grants-1996_07