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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526827Generated: November 1, 2026

Ammonium Chloride → (2,4-Dichloro-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanol

https://huagongshe.com/reaction/526827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant1-methyl-1H-imidazole-5-carbaldehydeHCID 573592—
Reactant6-Bromo-2,4-dichloro-3-phenylquinolineHCID 86716057—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(2,4-Dichloro-3-phenylquinolin-6-yl)(1-methyl-1H-imidazol-5-yl)methanolHCID 118006175—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a cloudy mixture of 6-bromo-2,4-dichloro-3-phenylquinoline (290.5 mg, 0.823 mmol, Intermediate 1: step c) and 1-methyl-1H-imidazole-5-carbaldehyde (90.6 mg, 0.823 mmol) in THF (8 mL) under nitrogen at −78° C. was added n-BuLi (1.6 M in hexane, 0.643 mL, 1.03 mmol) dropwise. The resulting solution was stirred at −78° C. for 3 hours, then was warmed to 0° C. for 15 minutes before addition of saturated aqueous NH4Cl to quench. The mixture was diluted with water and was extracted three times with EtOAc. The organic phase was dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 0-6% MeOH-DCM) to afford the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346782B2
Source datasetuspto-grants-2016_05
ORD IDord-398e13f5c3e6453ea8f346ebcbc5804d
Source noteuspto-grants-2016_05