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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348854Generated: November 1, 2026

2-Aminothiazole → HCID 22637126, compound

https://huagongshe.com/reaction/1348854

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriethylamineHCID 8471—
ReactantTriphosgeneHCID 94429—
Reactant3-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]anilineHCID 21890564—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
ProductHCID 22637126HCID 22637126132.2%

Reaction Steps

3-Chloro-4-[(6,7-dimethoxy-4-quinazolinyl)oxy]aniline (84 mg) was dissolved in chloroform (2.5 ml) and triethylamine (0.25 ml) to prepare a solution. A solution of triphosgene (38 mg) in chloroform was then added to the solution, and the mixture was stirred at room temperature for 5 min. Next, 2-aminothiazole (28 mg) was added thereto, and the mixture was further stirred at room temperature overnight. Water was added to the reaction solution, and the mixture was subjected to separatory extraction with chloroform. The organic layer was concentrated and was evaporated to dryness. Next, diethyl ether was added to the solid, and the solid was then collected by filtration. Further, the collected solid was washed with methyl alcohol to give the title compound (77.5 mg, yield 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211587B2
Source datasetuspto-grants-2007_05
ORD IDord-68722f869a2748fe9ed26d9db959b45f
Source noteuspto-grants-2007_05