ChemicalBook--->CAS DataBase List--->117718-84-0

117718-84-0

117718-84-0 Structure

117718-84-0 Structure
IdentificationBack Directory
[Name]

6-bromoimidazo[1,2-a]pyrazin-8-amine
[CAS]

117718-84-0
[Synonyms]

PAB 12
2-a]pyrazin-8-aMine
8-bromoimidazo[1,2-a]pyrazin-6-amine
6-bromo-8-imidazo[1,2-a]pyrazinamine
6-bromoimidazo[1,2-a]pyrazin-8-amine
8-Amino-6-bromoimidazo[1,2-a]pyrazine
6-Bromo-8-aminoimidazo[1,2-a]pyrazine
Imidazo[1,2-a]pyrazin-8-amine,6-bromo-
[Molecular Formula]

C6H5BrN4
[MDL Number]

MFCD00874115
[MOL File]

117718-84-0.mol
[Molecular Weight]

213.03
Chemical PropertiesBack Directory
[density ]

2.098±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
[storage temp. ]

Keep in dark place,Inert atmosphere,2-8°C
[pka]

3.807±0.30(predicted)
[Appearance]

Yellow to brown Solid
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
[HS Code ]

2933998090
Questions And AnswerBack Directory
[Application]

6-bromoimidazo[1,2-a]pyrazin-8-amine are a type of synthetic building block with strong pharmacological activity among nitrogen-containing heterocyclic compounds. Heterocyclic compounds are a class of small molecule compounds with strong biological activity and are widely used in fields such as biomedicine, pesticides, and optoelectronic materials. In particular, 6-haloimidazo[1,2-A]pyrazine active small molecule compounds are a research hotspot for major pharmaceutical companies.
Spectrum DetailBack Directory
[Spectrum Detail]

6-bromoimidazo[1,2-a]pyrazin-8-amine(117718-84-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

6,8-DIBROMOIMIDAZO[1,2-A]PYRAZINE

63744-22-9

6-bromoimidazo[1,2-a]pyrazin-8-amine

117718-84-0

General procedure for the synthesis of 6-bromoimidazo[1,2-A]pyrazin-8-amine from 6,8-dibromo-imidazo[1,2-A]pyrazine: The product obtained from the preparation of Example 29 (1.80 g, 6.45 mmol) was mixed with concentrated aqueous NH4OH solution (27.0 mL) in a closed pressure vessel and reacted with stirring for 24 hrs at 90 °C. Upon completion of the reaction, the solvent was removed by evaporation and the resulting residue was purified by silica gel column chromatography with EtOAc as eluent. A white solid product (1.01 g, 73% yield) was finally obtained.LCMS analysis showed that MH+ = 213.

[References]

[1] Journal of Medicinal Chemistry, 1992, vol. 35, # 18, p. 3353 - 3358
[2] Patent: US2004/63715, 2004, A1. Location in patent: Page/Page column 27
[3] Patent: WO2004/22562, 2004, A1. Location in patent: Page 28
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