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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80249Generated: October 25, 2026

Hydrogen Bromide → 5-Chloroimidazo[1,2-A]pyrazine

https://huagongshe.com/reaction/80249

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium CarbonateHCID 10340—
Reactant2-Bromo-1,1-dimethoxyethaneHCID 81672—
Reactant2-Amino-6-ChloropyrazineHCID 118458—
ReactantSodium BicarbonateHCID 516892—
CatalystWaterHCID 962—
SolventIsopropanolHCID 3776—
SolventHexaneHCID 8058—
SolventEthyl AcetateHCID 8857—
Product5-Chloroimidazo[1,2-A]pyrazineHCID 1284158825.31%

Reaction Steps

NaHCO3 (4.215 g, 50.1736 mmol) and IPA (40 mL) were added to a mixture of 2-bromo-1,1-dimethoxy-ethane (6.37 mL, 10.8066 mmol), 40% HBr (475 mL, 2.3157 mmol) and 2 drops of water previously refluxed for 1 hr. The reaction mixture was stirred for 5 mins and filtered. To the filtrate was added 6-chloro-pyrazin-2-ylamine (1 g, 7.7190 mmol) and the resulting mixture was refluxed for overnight. The reaction was monitored by TLC (50% ethylacetate in hexane). The reaction mixture was neutralized with Na2CO3 and partitioned between ethylacetate and water. The organic layer was washed with water, brine, dried over Na2SO4 and concentrated. Purification by column chromatography on silica gel (1-2% MeOH in CHCl3) afforded 300 mg of the product (25.31% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE045173E1
Source datasetuspto-grants-2014_09
ORD IDord-fe65c3a1d8c0408b94f2bf59208ad84f
Source noteuspto-grants-2014_09