ChemicalBook--->CAS DataBase List--->33064-36-7

33064-36-7

33064-36-7 Structure

33064-36-7 Structure
IdentificationBack Directory
[Name]

Pyrazole-3-carboxamide
[CAS]

33064-36-7
[Synonyms]

Pyrazole-3-carboxamide
1H-Pyrazole-3-carboxamide
[Molecular Formula]

C4H5N3O
[MDL Number]

MFCD11036164
[MOL File]

33064-36-7.mol
[Molecular Weight]

111.1
Chemical PropertiesBack Directory
[Melting point ]

159-160 °C
[Boiling point ]

469.6±18.0 °C(Predicted)
[density ]

1.394
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

11.76±0.10(Predicted)
[Appearance]

White to off-white Solid
Questions And AnswerBack Directory
[Uses]

Pyrazole-3-carboxamide has a wide range of biological activities and can be used in pharmaceutical and pesticide research.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P280-P301+P312-P302+P352-P305+P351+P338
[HazardClass ]

IRRITANT
Spectrum DetailBack Directory
[Spectrum Detail]

Pyrazole-3-carboxamide(33064-36-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

4-Nitropyrazole

2075-46-9

Pyrazole-3-carboxamide

33064-36-7

This Example illustrates the preparation of compound 108, 3-pyridine carboxylic acid, 5-[(4-amino-1H-pyrazol-1-yl)carbonyl]-2-methoxy-4-(2-methylpropyl)-6-(trifluoromethyl)-, methyl ester. A tetrahydrofuran (THF, 100 mL) solution of 4-nitropyrazole (22.62 g, 200 mmol) was cooled to 0 °C, followed by slow dropwise addition of a THF solution of sodium bis(trimethylmethylsilyl)amide (204.3 mmol) at 0 °C. Subsequently, a THF (100 mL) solution of compound 84 (70.75 g, 200 mmol) was added slowly dropwise at 0 °C. After the dropwise addition was completed, the reaction mixture was stirred at 25 °C for 30 min. After completion of the reaction, the mixture was poured into 5% hydrochloric acid solution and extracted with dichloromethane. The organic layer was dried with anhydrous magnesium sulfate (MgSO?) and the solvent was subsequently removed by rotary evaporator. The residue was purified by silica gel column chromatography (eluent: 5% ethyl acetate/hexane) to afford pyrazolamide (compound 101) 70.14 g in 82% yield.

[References]

[1] Patent: US5125956, 1992, A
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