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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926601Generated: October 31, 2026

5-bromo-1,2-dimethyl-1H-imidazole → HCID 118006150, compound

https://huagongshe.com/reaction/926601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-bromo-1,2-dimethyl-1H-imidazoleHCID 7204879—
Reactant(4-Chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(2,6-dimethylpyridin-3-yl)methanolHCID 86715629—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 118006150HCID 118006150—

Reaction Steps

A solution of n-BuLi (2.5 M in hexanes, 0.82 mL, 2.05 mmol) was added dropwise by syringe to a solution of 5-bromo-1,2-dimethyl-1H-imidazole (361.1 mg, 2.063 mmol) in dry THF (20 mL) in a dry ice-acetone bath. After 1-2 minutes, a solution of (4-chloro-2-methoxy-3-(4-(trifluoromethyl)benzyl)quinolin-6-yl)(2,6-dimethylpyridin-3-yl)methanone (0.500 g, 1.03 mmol, Intermediate 12: step f) in dry THF (5 mL) was added dropwise. The reaction was stirred for 1.5 hours, then was removed from the cold bath and allowed to warm to room temperature. The reaction was quenched with saturated aqueous ammonium chloride. The mixture was partitioned between water and dichloromethane. The separated aqueous phase was further extracted with dichloromethane. The organic phase was dried (Na2SO4), filtered, and concentrated. The crude product was purified by flash column chromatography (silica gel, 0-3% MeOH-DCM) to provide the title compound. 1H NMR (400 MHz, CDCl3) δ 8.15 (d, J=2.2 Hz, 1H), 7.72 (d, J=8.7 Hz, 1H), 7.53-7.48 (m, 2H), 7.42-7.36 (m, 3H), 7.11 (d, J=8.0 Hz, 1H), 6.91 (d, J=8.0 Hz, 1H), 5.99 (s, 1H), 4.33 (s, 2H), 4.06 (s, 3H), 3.36 (s, 3H), 2.52 (s, 3H), 2.40 (s, 3H), 2.31 (s, 3H); MS m/e 581.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09284308B2
Source datasetuspto-grants-2016_03
ORD IDord-6cdb84fb14034323af3c93af2525076b
Source noteuspto-grants-2016_03