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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397877Generated: October 25, 2026

Ethanol → 3-(4-Chloro-phenyl)-5-(2-methyl-imidazol-1-yl-methyl)-pyridine Hydrochloride

https://huagongshe.com/reaction/397877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium CarbonateHCID 10340—
Reactant4-Chlorophenylboronic acidHCID 74299—
ReactantPotassium AcetateHCID 517044—
Reactant3-Bromo-5-(2-methyl-imidazol-1-ylmethyl)-pyridineHCID 23444965—
CatalystHCID 178419050HCID 178419050—
Solvent1,4-DioxaneHCID 31275—
Product3-(4-Chloro-phenyl)-5-(2-methyl-imidazol-1-yl-methyl)-pyridine HydrochlorideHCID 234451401,224.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 3-bromo-5-(2-methyl-imidazol-1-ylmethyl)-pyridine (120 mg, 0.48 mmol), bis(triphenylphosphine)palladium (II) choride (10 mg, 0.01 mmol) and KOAc (140 mg, 0.14 mmol) were stirred in dioxane (10 ml) for 1 h at 20° C. 4-Chlorophenyl boronic acid (78 mg, 0.05 mmol) and 2N Na2CO3 solution (1.2 ml) were then added and the mixture heated to 100° C. for 7-24 h under an argon atmosphere. After cooling, the solvent was evaporated and 2N NaOH (5 ml) and AcOEt were added. The mixture was shaken and the aqueous phase separated and further extracted with AcOEt, the combined organic extracts were washed with brine then dried over Na2SO4, filtered and evaporated. The residue was chromatographed [silica, elution with CH2Cl2/(2M NH3 in MeOH) 97:3)]. The product was dissolved in MeOH, cooled to 4° C. with stirring and treated with HC/EtOH (1.46 M 1.1 eq) for 45 min. Evaporation of the solvent and drying under high vacuum at 50° C. for 2 h afforded the title compound (98 mg, 64%) as a light brown solid. MS: m/e=284.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610723B2
Source datasetuspto-grants-2003_08
ORD IDord-221937262f914b4dbade9ef9ff46c264
Source noteuspto-grants-2003_08