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ChemicalBook--->CAS DataBase List--->1094070-46-8

1094070-46-8

1094070-46-8 Structure

1094070-46-8 Structure
IdentificationBack Directory
[Name]

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
[CAS]

1094070-46-8
[Synonyms]

6-Methyl-8-(Methylthio)iMidazo[1,2-a]pyrazine
Imidazo[1,2-a]pyrazine, 6-methyl-8-(methylthio)-
6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine
[Molecular Formula]

C8H9N3S
[MDL Number]

MFCD17215754
[MOL File]

1094070-46-8.mol
[Molecular Weight]

179.24
Chemical PropertiesBack Directory
[density ]

1.30±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

3.47±0.30(Predicted)
[Appearance]

Off-white to yellow Solid
Safety DataBack Directory
[HS Code ]

2933998090
Hazard InformationBack Directory
[Synthesis]

6-BroMo-3-iodo-8-Methylsulfanyl-iMidazo[1,2-a]pyrazine

936360-80-4

Trimethylboroxine

823-96-1

6-Methyl-8-methylsulfanyl-imidazo[1,2-a]pyrazine

1094070-46-8

Part C: 6-bromo-3-iodo-8-(methylthio)imidazo[1,2-A]pyrazine (45.6 g), tetrakis(triphenylphosphine)palladium (10.8 g), potassium carbonate (77.4 g), and trimethylcyclotriboroxane (46.9 g) from Part A were suspended in N,N-dimethylformamide (410 mL), and the reaction was heated at 105 °C under nitrogen protection overnight. After completion of the reaction, the reaction was cooled to room temperature, the reaction mixture was diluted with ethyl acetate (1 L), washed sequentially with saturated saline (2×500 mL), the organic phase was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The crude product was purified by silica gel column chromatography to afford 6-methyl-8-(methylthio)-imidazo[1,2-a]pyrazine as a light yellow solid (21.4 g, 64% yield).

[References]

[1] Patent: WO2009/97233, 2009, A1. Location in patent: Page/Page column 40; 41
[2] Patent: WO2008/156614, 2008, A2. Location in patent: Page/Page column 72; 73
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