Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545287Generated: October 29, 2026

2-Aminothiazole → HCID 57619640, compound

https://huagongshe.com/reaction/545287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantBromobenzeneHCID 7961—
ReactantHCID 57619613HCID 57619613—
SolventHexaneHCID 8058—
ProductHCID 57619640HCID 5761964075.7%

Reaction Steps

160 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 60 mg of 2-aminothiazole were added to 1.5 ml of bromobenzene, then, the mixture was stirred for 5 hours under heat refluxing condition. The reaction mixture was cooled to room temperature, then, hexane was added to this and the resultant mixture was allowed to stand still. The resulting solid was collected by filtration, and washed with a mixture of t-butyl methyl ether and n-hexane and dried to obtain 136 mg of 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-N-(2-thiazolyl)-1,2-d ihydropyridine-3-carboxamide (hereinafter, referred to as present compound 30) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935716B2
Source datasetuspto-grants-2011_05
ORD IDord-de68aa8a0b9340a9b6e7d40984a917de
Source noteuspto-grants-2011_05