ChemicalBook--->CAS DataBase List--->1224288-92-9

1224288-92-9

1224288-92-9 Structure

1224288-92-9 Structure
IdentificationBack Directory
[Name]

5-Chloropyrazolo[1,5-a]pyriMidine-3-carbonitrile
[CAS]

1224288-92-9
[Synonyms]

5-chloropyrazolo[1,5-a]pyrimidin-3-carbonitrile
5-Chloropyrazolo[1,5-a]pyriMidine-3-carbonitrile
Pyrazolo[1,5-a]pyrimidine-3-carbonitrile, 5-chloro-
[Molecular Formula]

C7H3ClN4
[MDL Number]

MFCD18073765
[MOL File]

1224288-92-9.mol
[Molecular Weight]

178.579
Chemical PropertiesBack Directory
[Melting point ]

138-142℃ (isopropanol )
[density ]

1.56±0.1 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,2-8°C
[pka]

-3.08±0.40(Predicted)
[Appearance]

Off-white to light yellow Solid
[InChI]

InChI=1S/C7H3ClN4/c8-6-1-2-12-7(11-6)5(3-9)4-10-12/h1-2,4H
[InChIKey]

OYGONYREIXSORZ-UHFFFAOYSA-N
[SMILES]

C12=C(C#N)C=NN1C=CC(Cl)=N2
Questions And AnswerBack Directory
[Uses]

5-chloropyrazole[1,5-A]pyrimidine-3-carboxynitrile can be used in organic synthesis, pharmaceutical intermediates, etc.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Spectrum DetailBack Directory
[Spectrum Detail]

5-Chloropyrazolo[1,5-a]pyriMidine-3-carbonitrile(1224288-92-9)1HNMR
Hazard InformationBack Directory
[Synthesis]

5-Oxo-4,5-dihydropyrazolo[1,5-a]pyriMidine-3-carbonitrile

1224288-95-2

5-Chloropyrazolo[1,5-a]pyriMidine-3-carbonitrile

1224288-92-9

General procedure for the synthesis of 5-chloropyrazolo[1,5-a]pyrimidine-3-carbonitrile from 5-oxo-4,5-dihydropyrazolo[1,5-a]pyrimidine-3-carbonitrile: 5-hydroxypyrazolo[1,5-a]pyrimidine-3-carbonitrile (10.00 g, 62.45 mmol) was mixed with phosphorus triclosamide (200.00 mL), heated to 150 °C, and the reaction took 4 hour. The progress of the reaction was monitored by thin layer chromatography (TLC, unfolding agent ratio petroleum ether: ethyl acetate = 1:1). Upon completion of the reaction, the excess of phosphorous trichloride was removed by distillation under reduced pressure, and the residue was dissolved in dichloromethane and concentrated again. Finally, it was purified by silica gel column chromatography (eluent was dichloromethane) to afford 5-chloropyrazolo[1,5-a]pyrimidine-3-carbonitrile (6.00 g, yield 53.80%) as a white solid.

[References]

[1] Patent: WO2017/87778, 2017, A1. Location in patent: Page/Page column 27; 28
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