ChemicalBook--->CAS DataBase List--->77894-69-0

77894-69-0

77894-69-0 Structure

77894-69-0 Structure
IdentificationBack Directory
[Name]

1-Methyl-1H-indazol-4-ylamine
[CAS]

77894-69-0
[Synonyms]

1-methylindazol-4-amine
4-AMino-1-Methylindazole
1-Methyl-1H-indazol-4-amine
1H-Indazol-4-aMine,1-Methyl-
1-Methyl-1H-indazole-4-amine
1-Methyl-4-aMino-1h-indazole
1-Methyl-1H-indazol-4-ylamine
[Molecular Formula]

C8H9N3
[MDL Number]

MFCD09870041
[MOL File]

77894-69-0.mol
[Molecular Weight]

147.18
Chemical PropertiesBack Directory
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[color ]

Light yellow to brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

1-Methyl-1H-indazol-4-ylamine(77894-69-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

1-Methyl-4-nitro-1H-indazole

26120-43-4

1-Methyl-1H-indazol-4-ylamine

77894-69-0

General procedure for the synthesis of 1-methyl-1H-indazol-4-amine from 1-methyl-4-nitro-1H-indazole: A catalytic amount of 10% palladium carbon was added to a solution of 1-methyl-4-nitro-1H-indazole (0.97 g, 5.5 mmol) in ethanol (50 ml). The resulting mixture was stirred under hydrogen atmosphere for 2 hours. Upon completion of the reaction, the catalyst was removed by filtration followed by evaporation of the solvent. The product was dried by azeotropy with toluene to give 1-methyl-1H-indazol-4-amine as a light brown solid (0.78 g, 96% yield). Mass spectrum (electrospray positive ion mode) m/z: 148 ([M+H]+).

[References]

[1] Patent: WO2004/46133, 2004, A1. Location in patent: Page 28
[2] Patent: WO2005/28445, 2005, A2. Location in patent: Page/Page column 36
[3] Heterocycles, 2006, vol. 68, # 12, p. 2595 - 2605
[4] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 14, p. 4740 - 4749
[5] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 17, p. 6025 - 6035
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