ChemicalBook--->CAS DataBase List--->77112-53-9

77112-53-9

77112-53-9 Structure

77112-53-9 Structure
IdentificationBack Directory
[Name]

IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLIC ACID
[CAS]

77112-53-9
[Synonyms]

IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLIC ACID
[Molecular Formula]

C7H5N3O2
[MDL Number]

MFCD08460077
[MOL File]

77112-53-9.mol
[Molecular Weight]

163.13
Chemical PropertiesBack Directory
[Melting point ]

280 °C (decomp)
[density ]

1.58±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

-2.07±0.41(Predicted)
[Appearance]

Off-white to light brown Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLIC ACID(77112-53-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

ETHYL IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLATE

77112-52-8

IMIDAZO[1,2-A]PYRAZINE-2-CARBOXYLIC ACID

77112-53-9

Lithium chloride monohydrate (6.50 g, 0.156 mol) was added to ethyl imidazo[1,2-a]pyrazine-2-carboxylate (9.73 g, 0.05 mol) in a mixed ethanol/water (400 mL/100 mL) solvent and the reaction was stirred at room temperature for 8 hours. After completion of the reaction, the solvent was removed by distillation under reduced pressure. The pH of the reaction mixture was adjusted to 3-4 with aqueous 1 N hydrochloric acid under cooling in an ice bath and a solid was precipitated. The precipitate was collected by filtration and washed sequentially with acetone and dichloromethane. The filter cake was dried at 50 °C and the residual solvent was removed under reduced pressure to afford imidazo[1,2-a]pyrazine-2-carboxylic acid (7.69 g, 9.4 mmol) in pink solid powder form in 93.7% yield.

[References]

[1] Patent: CN103965194, 2016, B. Location in patent: Paragraph 0214-0216
[2] Journal of Medicinal Chemistry, 1984, vol. 27, # 2, p. 206 - 212
[3] Farmaco, Edizione Scientifica, 1981, vol. 36, # 1, p. 61 - 80
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