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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1623767Generated: October 30, 2026

Methanol → HCID 51357512, compound

https://huagongshe.com/reaction/1623767

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant(1-Bromoethyl)benzeneHCID 11454—
ReactantPotassium HydroxideHCID 14797—
ReactantPotassiumHCID 5462222—
ReactantHCID 24285249HCID 24285249—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 51357512HCID 51357512—

Reaction Steps

The compound 5-bromo-2-hydroxy-N-3-pyridinylbenzamide (may be prepared as described in Description 35; 300 mg, 1.02 mmol) was added to a solution of potassium hydroxide (57.4 mg, 1.02 mmol) in methanol (2 ml, 49.4 mmol). The mixture was then stirred at room temperature for 15 min and the solvent was removed in vacuo. To the potassium salt was added DMF (10 ml) and (1-bromoethyl)benzene (189 mg, 1.023 mmol), The reaction mixture was then heated under reflux for 2 h. The mixture was cooled, diluted with water (20 ml) and the precipitate was collected, and finally crystallized from ethyl acetate to yield the title compound. 63 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778939B2
Source datasetuspto-grants-2014_07
ORD IDord-38a8cf9f64744a70adea8a733c8a9124
Source noteuspto-grants-2014_07