Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890624Generated: October 31, 2026

4-(Bromomethyl)benzophenone → HCID 11326145, compound

https://huagongshe.com/reaction/1890624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Bromomethyl)benzophenoneHCID 122951—
ReactantLithium hydroxide, monohydrateHCID 168937—
Reactant2,6-Dimethyl-8-ethyl-1-deazapurineHCID 9815374—
SolventDimethylformamideHCID 6228—
ProductHCID 11326145HCID 1132614579.3%

Reaction Steps

Commercially available 4-bromomethylbenzophenone (5.00 g, 18.2 mmol) was dissolved in DMF (100 mL), and 2-ethyl-5,7-dimethylimidazo[4,5-b]pyridine (3.82 g, 21.8 mmol) and lithium hydroxide monohydrate (0.920 g, 21.9 mmol) was added to the solution, followed by stirring at room temperature for 3 hours. After the reaction mixture was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, and washed with water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=2:1), and recrystallized from ethanol to obtain Compound 1 (5.33 g, yield 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507484B2
Source datasetuspto-grants-2013_08
ORD IDord-f1e0c04690434e9f8aff6fdc553f9469
Source noteuspto-grants-2013_08