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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545273Generated: October 29, 2026

Bromobenzene → HCID 57619628, compound

https://huagongshe.com/reaction/545273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant1,3,4-Thiadiazol-2-amineHCID 19909—
ReactantHCID 57619613HCID 57619613—
SolventHexaneHCID 8058—
ProductHCID 57619628HCID 5761962881%

Reaction Steps

197 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 76 mg of 2-amino-1,3,4-thiadiazole were added to 2 ml of bromobenzene, then, the mixture was stirred for 5 hours under heat refluxing condition. The reaction mixture was cooled to room temperature, then, to the reaction mixture was added n-hexane. The resulting solid was collected by filtration, and washed with a mixture of t-butyl methyl ether and n-hexane and dried to obtain 183 mg of N-(1,3,4-thiadiazol-2-yl)-5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 14) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935716B2
Source datasetuspto-grants-2011_05
ORD IDord-16c806c23d324dc99689ab0281dd14da
Source noteuspto-grants-2011_05