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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548574Generated: October 29, 2026

Bromobenzene → HCID 57672127, compound

https://huagongshe.com/reaction/548574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant6-Amino-3-chloropyridazineHCID 21643—
ReactantHCID 57619613HCID 57619613—
SolventHexaneHCID 8058—
ProductHCID 57672127HCID 5767212786.4%

Reaction Steps

168 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 82 mg of 3-amino-6-chloropyridazine were added to 1.5 ml of bromobenzene, and the mixture was stirred for 4 hours under heat refluxing. The reaction mixture was cooled to room temperature, and n-hexane was added to the reaction mixture. The resulting solid was collected by filtration, washed with a mixture of t-butyl methyl ether and n-hexane, and dried to obtain 180 mg of N-(6-chloro-3-pyridazinyl)-5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereafter, referred to as present compound 17) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943614B2
Source datasetuspto-grants-2011_05
ORD IDord-2c24126f38af41008bd818188b126e93
Source noteuspto-grants-2011_05