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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595164Generated: October 29, 2026

Acetic Acid → 1-(2-((3-Bromo-5-methylphenyl)amino)pyrimidin-4-yl)ethanol

https://huagongshe.com/reaction/595164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-Bromo-5-methylanilineHCID 3018526—
Reactant1-(2-Chloropyrimidin-4-yl)ethanolHCID 77231066—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product1-(2-((3-Bromo-5-methylphenyl)amino)pyrimidin-4-yl)ethanolHCID 118208763—

Reaction Steps

1-(2-Chloropyrimidin-4-yl)ethanol (5.25 g, 33.1 mmol) and 3-bromo-5-methylaniline (9.24 g, 49.7 mmol) were suspended in 1,4-dioxane (30 mL). Acetic acid (1.90 ml, 33.1 mmol) was added, and the resultant mixture was heated to 100° C. for 14 h. The reaction mixture was allowed to cool to room temperature and then was diluted with dichloromethane. The resultant solution was adsorbed on silica gel and purified by column chromatography on silica (10-100% ethyl acetate/hexanes) to afford 1-(2-((3-bromo-5-methylphenyl)amino)pyrimidin-4-yl)ethanol as a black semi-solid. MS ESI calc'd. for C13H15BrN3O [M+H]+ 308, 310. found 308, 310.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242984B2
Source datasetuspto-grants-2016_01
ORD IDord-7fef91b3bc604fe5aa3fab21dcc072f2
Source noteuspto-grants-2016_01