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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627574Generated: October 25, 2026

HCID 71711558, compound → (2,4-Dichloro-3-(3-fluorophenyl)-8-methylquinolin-6-yl)(4-fluorophenyl)(1-methyl-1H-imidazol-5-yl)methanol

https://huagongshe.com/reaction/627574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71711558HCID 71711558—
Reactant6-Bromo-2,4-dichloro-3-(3-fluorophenyl)-8-methylquinolineHCID 86716097—
ReactantButyllithiumHCID 178418339—
Product(2,4-Dichloro-3-(3-fluorophenyl)-8-methylquinolin-6-yl)(4-fluorophenyl)(1-methyl-1H-imidazol-5-yl)methanolHCID 86716155—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A round bottom flask was charged with 6-bromo-2,4-dichloro-3-(3-fluorophenyl)-8-methylquinoline (1.00 g, 2.60 mmol, Intermediate 50, step c) and (4-fluorophenyl)(1-methyl-1H-imidazol-5-yl)methanone (583 mg, 2.86 mmol, Intermediate 49, step b) and was evacuated and re-filled with argon (three times). THF (20 mL) was added, and the solution was cooled in a dry ice acetone bath for 2 minutes. At this point the mixture began to turn cloudy and n-BuLi (1.6 M in hexane, 2.11 mL, 3.38 mmol), was added over about 1 minute. The mixture was stirred at −78° C. for 10 minutes, then in an ice water bath for 1 hour. The reaction was quenched by addition of saturated aqueous NH4Cl, diluted with water and extracted with EtOAc (3×). The organic phase was dried (Na2SO4), filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 30-60% acetone-DCM) to afford slightly impure title compound as an off-white solid. 1H NMR (400 MHz, CHLOROFORM-d) δ 8.09 (s, 1H), 7.60 (s, 1H), 7.44-7.55 (m, 1H), 7.30-7.39 (m, 3H), 7.15-7.23 (m, 1H), 7.01-7.12 (m, 4H), 6.40 (s, 1H), 4.00 (br. s., 1H), 3.40 (s, 3H), 2.74 (s, 3H). MS m/e 510.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09309222B2
Source datasetuspto-grants-2016_04
ORD IDord-b9c96b407c334ea2886876e16b647319
Source noteuspto-grants-2016_04