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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 545285Generated: October 29, 2026

Bromobenzene → HCID 57619617, compound

https://huagongshe.com/reaction/545285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
Reactant2-AminobenzimidazoleHCID 13624—
ReactantHCID 57619613HCID 57619613—
SolventHexaneHCID 8058—
ProductHCID 57619617HCID 5761961782.5%

Reaction Steps

199 mg of ethyl 5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxylate and 98 mg of 2-amino-benzimidazole were added to 2 ml of bromobenzene, then, the mixture was stirred for 9.5 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 202 mg of N-(2-benzimidazolyl)-5-chloro-1,6-dimethyl-4-hydroxy-2-oxo-1,2-dihydropyridine-3-carboxamide (hereinafter, referred to as present compound 28) represented by the formula:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935716B2
Source datasetuspto-grants-2011_05
ORD IDord-4820a7a14c6943cf8aadd7be7a9d0fb3
Source noteuspto-grants-2011_05