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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466725Generated: October 30, 2026

Methyl iodide → 7-Ethyl-2-propylimidazo[4,5-b]pyridine

https://huagongshe.com/reaction/466725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant7-Methyl-2-propyl-1H-imidazo[4,5-b]pyridineHCID 15020852—
ReactantHCID 178418306HCID 178418306—
SolventTetrahydrofuranHCID 8028—
Product7-Ethyl-2-propylimidazo[4,5-b]pyridineHCID 19012227—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyllithium (0.978 mL, 1.7M/pentane) was added to a cooled (-78° C.) THF (5 mL) solution of 7-methyl-2-propylimidazo[4,5-b]pyridine (97 mg, 0.554 mmol). After 2 hour the reaction was warmed to 0° C. for 1 minute then cooled back to -78° C. MeI (0.172 mL) was added, the mixture was stirred at -78° C. for 1 hour then warmed to 0° C. for 1 minute and then quenched (NH4OH). Extractive workup and purification (SiO2, 2% MeOH/ EtOAc) gave 85 mg of 7-ethyl-2-propylimidazo[4,5-b]pyridine which was converted to the title compound as outlined in Example 7, Part B.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05157026
Source datasetuspto-grants-1992_10
ORD IDord-984931110f754bd09971162d3a2d91c4
Source noteuspto-grants-1992_10