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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544546Generated: October 30, 2026

2-Amino-5-(trifluoromethyl)benzoic acid → 1-ethyl-7-trifluoromethyl-2,3-dihydro-imidazo[2.1-b]quinazolin-5(1H)-one

https://huagongshe.com/reaction/544546

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-(trifluoromethyl)benzoic acidHCID 10465535—
Reactant1-Ethyl-2-(methylsulfanyl)-4,5-dihydro-1H-imidazoleHCID 12504492—
SolventDimethylacetamideHCID 31374—
Product1-ethyl-7-trifluoromethyl-2,3-dihydro-imidazo[2.1-b]quinazolin-5(1H)-oneHCID 20458267—

Reaction Steps

A solution of 3.6 g. of 1-ethyl-2-methylthioimidazoline, 5.0 g. of 2-amino-5-trifluoromethylbenzoic acid and 50 ml. of dimethylacetamide is refluxed for 24 hours and then the reaction mixture concentrated in vacuo. The residue is dissolved in methylene chloride, washed first with 2 N sodium hydroxide solution and then with water, dried over magnesium sulfate, filtered and chromatographed on silica gel while eluding with methylene chloride to obtain 1-ethyl-7-trifluoromethyl-2,3-dihydro-imidazo[2.1-b]quinazolin-5(1H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04451464
Source datasetuspto-grants-1984_05
ORD IDord-a7a673129f4148ee9f42d0da7402b3f3
Source noteuspto-grants-1984_05