ChemicalBook--->CAS DataBase List--->69214-33-1

69214-33-1

69214-33-1 Structure

69214-33-1 Structure
IdentificationBack Directory
[Name]

8-Chloro-imidazo[1,2-a]pyrazine
[CAS]

69214-33-1
[Synonyms]

8-Chloro-imidazo[1,2-a]pyrazine
Imidazo[1,2-a]pyrazine, 8-chloro-
8-chloroimidazo[1,2-a]pyrazine hydrobromide
[Molecular Formula]

C6H4ClN3
[MDL Number]

MFCD09834910
[MOL File]

69214-33-1.mol
[Molecular Weight]

153.569
Questions And AnswerBack Directory
[Uses]

8-Chloroimidazo[1,2-a]pyrazine is a useful research chemical.
Chemical PropertiesBack Directory
[density ]

1.51±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

1.50±0.30(Predicted)
[Appearance]

White to off-white Solid
[InChI]

InChI=1S/C6H4ClN3/c7-5-6-9-2-4-10(6)3-1-8-5/h1-4H
[InChIKey]

PREWHWRWNMLCNH-UHFFFAOYSA-N
[SMILES]

C12=NC=CN1C=CN=C2Cl
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H332-H335
[Precautionary statements ]

P261-P280-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

8-Chloro-imidazo[1,2-a]pyrazine(69214-33-1)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-Amino-3-chloropyrazine

6863-73-6

Bromoacetaldehyde diethyl acetal

2032-35-1

8-Chloro-imidazo[1,2-a]pyrazine

69214-33-1

GENERAL STEPS: Mix 48% aqueous hydrogen bromide solution (0.893 mL) with distilled water (9 mL) and add 2-bromo-1,1-diethoxyethane (5.98 mL, 38.5 mmol). It was heated and stirred under reflux conditions for 1 hour. After completion of the reaction, distilled water and ether were added to the reaction mixture for partitioning. The aqueous phase was extracted with ether, all organic phases were combined, dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was mixed with a solution of 3-chloropyrazin-2-amine (2.0 g, 15.4 mmol) in dimethoxyethane (22 mL) and 48% aqueous hydrogen bromide (0.3 mL) was added. It was heated and stirred under reflux conditions for 3 hours. At the end of the reaction, the solid product was collected by filtration and washed with ether to afford 8-chloroimidazo[1,2-a]pyrazine (2.07 g, 88% yield) as a black solid. Mass spectrum (ESI) m/z = 154 ([M + H]+).

[References]

[1] Patent: US2012/59162, 2012, A1. Location in patent: Page/Page column 38-39
[2] Patent: WO2010/69684, 2010, A1. Location in patent: Page/Page column 96
[3] Patent: WO2011/110545, 2011, A1. Location in patent: Page/Page column 73
[4] Patent: US2012/329792, 2012, A1. Location in patent: Page/Page column 33
[5] Patent: WO2009/12482, 2009, A2. Location in patent: Page/Page column 90
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