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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606008Generated: October 30, 2026

Toluene → HCID 24856033, compound

https://huagongshe.com/reaction/606008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantSodium CarbonateHCID 10340—
Reactant6-bromo-2-(4-methylphenyl)imidazo[1,2-a]pyridineHCID 1412838—
Reactant[3-(Hydroxymethyl)phenyl]boronic acidHCID 2734662—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductHCID 24856033HCID 2485603345.7%

Reaction Steps

Under a stream of nitrogen, 200 mg of 6-bromo-2-p-tolylimidazo[1,2-a]pyridine, 160 mg of 3-(hydroxymethyl)phenylboronic acid and 24 mg of tetrakis(triphenylphosphine)palladium are placed in a microwave tube containing 2 ml of toluene degassed beforehand under a stream of nitrogen, 2 ml of acetonitrile and 2 ml of a 2M solution of sodium carbonate. The tube is placed in a microwave apparatus and irradiated at 150° C. for 15 min. The organic phase is separated and dried and the filtrate is concentrated under reduced pressure. The residue obtained is taken up with 6 ml of dichloromethane. The precipitate is recovered by filtration, washed with dichloromethane and dried in a desiccator under reduced pressure. 100 mg of compound are obtained. Mp=171-173° C. 1H NMR (DMSO-d6, δ in ppm): 2.32 (s, 3H); 4.57 (d, J=5.6 Hz, 2H); 5.23 (t, J=5.7 Hz, 1H); from 7.19 to 7.67 (m, 8H); 7.84 (d, J=8 Hz, 2H); 8.32 (s, 1H); 8.82 (m, 1H). M+H=315.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915284B2
Source datasetuspto-grants-2011_03
ORD IDord-01b63b4a7dbc458aaf8360f5ba84c9d8
Source noteuspto-grants-2011_03