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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873747Generated: November 3, 2026

2-Aminothiazole → HCID 57619640, compound

https://huagongshe.com/reaction/1873747

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-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 30) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304437B2
Source datasetuspto-grants-2012_11
ORD IDord-1e8cb8135283402bae2971f746c5ffdd
Source noteuspto-grants-2012_11