ChemicalBook--->CAS DataBase List--->28036-31-9

28036-31-9

28036-31-9 Structure

28036-31-9 Structure
IdentificationBack Directory
[Name]

2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE
[CAS]

28036-31-9
[Synonyms]

2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE
3-Amino-2-methylimidazo[1,2-a]pyridine
Imidazo[1,2-a]pyridin-3-amine, 2-methyl-
[Molecular Formula]

C8H9N3
[MDL Number]

MFCD09800571
[MOL File]

28036-31-9.mol
[Molecular Weight]

147.18
Chemical PropertiesBack Directory
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

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

crystalline solid
[pka]

9.08±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P280-P305+P351+P338
[HS Code ]

2933599590
Spectrum DetailBack Directory
[Spectrum Detail]

2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE(28036-31-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

2-METHYL-3-NITROIMIDAZO[1,2-A]PYRIDINE

34165-09-8

2-METHYLIMIDAZO[1,2-A]PYRIDIN-3-AMINE

28036-31-9

General procedure: Preparation of Example 14 2-Methyl-3-nitroimidazo[1,2-a]pyridine (330.0 mg, 1.86 mmol) was dissolved in 8 mL of ethanol. 10% palladium-carbon catalyst (20 mg, 0.2 mmol) was added to the solution under argon protection. The reaction mixture was stirred under hydrogen atmosphere for 18 hours. Upon completion of the reaction, the catalyst was removed by filtration through a diatomaceous earth pad and the filtrate was concentrated under reduced pressure to afford 2-methylimidazo[1,2-a]pyridin-3-amine (260 mg, 1.76 mmol, 95% yield) as a brown solid.LRMS (m/z): 148 (M + 1)+.

[References]

[1] Patent: EP2848615, 2015, A1. Location in patent: Paragraph 0100
[2] Chemical and Pharmaceutical Bulletin, 2001, vol. 49, # 12, p. 1631 - 1635
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