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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 558592Generated: October 25, 2026

Sodium Carbonate → 8-Methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/558592

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant4-(Trifluoromethyl)phenylboronic acidHCID 2734389—
Reactant6-Bromo-8-methylimidazo(1,2-a)pyridineHCID 5260647—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product8-Methyl-6-(4-trifluoromethyl-phenyl)-imidazo[1,2-a]pyridineHCID 6700111091%

Reaction Conditions

Temperature23 °C

Reaction Steps

A mixture of 6-bromo-8-methyl-imidazo[1,2-a]pyridine (example C.20 step 1) (7.0 g, 33 mmol), commercially available 4-(trifluoromethyl)phenylboronic acid (6.929 g, 36 mmol), Pd(PPh3)4 (383 mg, 1 mol %) and 1M Na2CO3-solution (77 mL, 77 mmol) in DME (150 mL) was stirred at reflux for 1 h. Cooled to 23° C., diluted with water, extracted with EtOAc, washed the organic layer with brine, dried over MgSO4. Removal of the solvent in vacuum left a brown solid, which was purified by silica gel column chromatography with EtOAc/MeOH to give the title compound as a white solid (8.29 g, 91%). MS (ISP) 277.1 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08063048B2
Source datasetuspto-grants-2011_11
ORD IDord-4c68418817ee4a018819d6c835ca52bc
Source noteuspto-grants-2011_11