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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372927Generated: October 26, 2026

Water → 6-Bromo-8-(4-p-tolyl-imidazol-1-yl)-imidazo[1,2-a]pyrazine

https://huagongshe.com/reaction/1372927

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant6,8-Dibromoimidazo[1,2-a]pyrazineHCID 15025843—
ReactantHCID 178423883HCID 178423883—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
Product6-Bromo-8-(4-p-tolyl-imidazol-1-yl)-imidazo[1,2-a]pyrazineHCID 2107288684.5%

Reaction Steps

Sodium hydride (NaH) (144 milligrams (mg) of a 60% dispersion in mineral oil) is added to a solution of 4-p-tolyl-1H-imidazole (571 mg) in N,N,-dimethylformamide (DMF) (10 ml) and the mixture is stirred at room temperature (rt) for 0.5 hr. A solution of 6,8-dibromoimidazo[1,2-a]pyrazine (3) (1.0 g) in DMF (10 ml) is added. The mixture is stirred at room temperature (rt) for 16 hr. Water (50 ml) is added and the mixture is extracted with ethyl acetate (3×70 ml); extracts are washed with water (2×50 ml) and brine (1×50 ml), dried over magnesium sulfate (MgSO4), and evaporated in vacuo to give a waxy solid. The solid is slurried with a little diethyl ether and filtered to give 6-Bromo-8-(4-p-tolyl-imidazol-1-yl)-imidazo[1,2-a]pyrazine (4) (1.08 g) as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160885B2
Source datasetuspto-grants-2007_01
ORD IDord-dfd4e2d547584077899f362d469a5d8e
Source noteuspto-grants-2007_01