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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1742425Generated: October 28, 2026

Sodium hydride → 3-(3-Bromo-6,7-dihydro-5H-[1]pyrindin-7-yl)-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine

https://huagongshe.com/reaction/1742425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantSodium BromideHCID 253881—
Reactant3-bromo-7-chloro-6,7-dihydro-5H-cyclopenta[b]pyridineHCID 67843076—
ReactantHCID 178437439HCID 178437439—
Solvent1,4-DioxaneHCID 31275—
Product3-(3-Bromo-6,7-dihydro-5H-[1]pyrindin-7-yl)-2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridineHCID 6784307213.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of NaH, 60% in oil, (163 mg) in 3 mL of 1,4-dioxane was added 2-ethyl-5,7-dimethyl-3H-imidazo[4,5-b]pyridine (1.1 gm) at room temperature and stirred for 30 minutes. Then 3-bromo-7-chloro-6,7-dihydro-5H-[1]pyrindine (500 mg, 2.15 mM) in 2 mL of 1,4-dioxane and anhydrous NaBr (442 mg) were added to the solution and the reaction was heated to 100° C. for 24 hours. The reaction was then cooled to room temperature, concentrated to dryness, and extracted into ethyl acetate from water. The organic layers were dried over MgSO4, filtered, and evaporated to dryness. The residue was purified by chromatography on silica gel to yield 110 mg of product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05338740
Source datasetuspto-grants-1994_08
ORD IDord-0ba5798fcf0c4766be13fff8fba00fe5
Source noteuspto-grants-1994_08