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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 80249Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/80249

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
EduktSodium CarbonateHCID 10340—
Edukt2-Bromo-1,1-dimethoxyethaneHCID 81672—
Edukt2-Amino-6-ChloropyrazineHCID 118458—
EduktSodium BicarbonateHCID 516892—
KatalysatorWaterHCID 962—
LösungsmittelIsopropanolHCID 3776—
LösungsmittelHexaneHCID 8058—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-Chloroimidazo[1,2-A]pyrazineHCID 1284158825,31%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUSRE045173E1
Quelldatensatzuspto-grants-2014_09
ORD IDord-fe65c3a1d8c0408b94f2bf59208ad84f
Quellennotizuspto-grants-2014_09