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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548573Generated: October 28, 2026

Bromobenzene → HCID 57672140, compound

https://huagongshe.com/reaction/548573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantAminopyrazineHCID 78747—
ReactantEthyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylateHCID 57619607—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 57672140HCID 5767214099.2%

Reaction Steps

211 mg of ethyl 1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 95 mg of aminopyrazine were added to 6 ml of bromobenzene, and the mixture was stirred for 3 hours under the heat-refluxing condition. The reaction mixture was cooled to room temperature, and t-butyl methyl ether was added to the mixture. The resulting solid was collected by filtration, washed with t-butyl methyl ether, and dried to obtain 258 mg of N-(2-pyrazinyl)-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 1) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943614B2
Source datasetuspto-grants-2011_05
ORD IDord-2671e7ac9d4f4aa28ae62c801dfbb121
Source noteuspto-grants-2011_05