ChemicalBook--->CAS DataBase List--->54384-74-6

54384-74-6

54384-74-6 Structure

54384-74-6 Structure
IdentificationBack Directory
[Name]

1H-Pyrazole-3-carboxamide,1,5-dimethyl-(9CI)
[CAS]

54384-74-6
[Synonyms]

1,5-DiMethylpyrazole-3-carboxaMide
1,5-Dimethyl-1H-pyrazole-3-carboxamide
1H-Pyrazole-3-carboxamide, 1,5-dimethyl-
1H-Pyrazole-3-carboxamide,1,5-dimethyl-(9CI)
1,5-Dimethyl-1H-pyrazole-3-carboxylic acid amide
[Molecular Formula]

C6H9N3O
[MDL Number]

MFCD05664820
[MOL File]

54384-74-6.mol
[Molecular Weight]

139.16
Chemical PropertiesBack Directory
[Boiling point ]

288.7±28.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

15.85±0.50(Predicted)
Safety DataBack Directory
[Risk Statements ]

36/37/38
[Safety Statements ]

26-37/39
[HS Code ]

29339900
Hazard InformationBack Directory
[Chemical Properties]

White crystals
[Synthesis]

1,5-DIMETHYL-1H-PYRAZOLE-3-CARBOXYLIC ACID

5744-59-2

1H-Pyrazole-3-carboxamide,1,5-dimethyl-(9CI)

54384-74-6

General procedure for the synthesis of 1,5-dimethyl-1H-pyrazole-3-carboxamide from 1,5-dimethyl-1H-pyrazole-3-carboxylic acid: 1,5-dimethyl-1H-pyrazole-3-carboxylic acid (10 g, 71.43 mmol) was mixed with sulfinyl chloride (SOCl2, 25.5 g, 214.29 mmol), and the reaction was carried out at reflux for 2 hours. After completion of the reaction, the mixture was concentrated under vacuum. Subsequently, 200 mL of ammonia (NH3-H2O) was slowly added dropwise to the residue at 0 °C and the reaction was carried out under stirring. At the end of the reaction, the solid product was collected by filtration to afford 8 g (81% yield) of 1,5-dimethyl-1H-pyrazole-3-carboxamide as a white solid.

[References]

[1] Patent: WO2009/139834, 2009, A1. Location in patent: Page/Page column 128-129
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