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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1873746Generated: November 1, 2026

Bromobenzene → HCID 178427958, compound

https://huagongshe.com/reaction/1873746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantHCID 57619613HCID 57619613—
ReactantHCID 178418311HCID 178418311—
SolventHexaneHCID 8058—
ProductHCID 178427958HCID 17842795888.9%

Reaction Steps

161 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 51 mg of 3-amino-1,2,4-triazole 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 153 mg of 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-N-(1,2,4-triazol-3-yl)-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 29) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08304437B2
Source datasetuspto-grants-2012_11
ORD IDord-94bf12cb00fb4891a68ebf76b7d0611d
Source noteuspto-grants-2012_11