ChemicalBook--->CAS DataBase List--->57489-70-0

57489-70-0

57489-70-0 Structure

57489-70-0 Structure
IdentificationBack Directory
[Name]

Pyrazolo[1,5-a]pyrimidine-5,7(4H,6H)-dione
[CAS]

57489-70-0
[Synonyms]

Pyrazolo[1,5-a]pyrimidine-5,7-ol
pyrazolo[1,5-a]pyrimidine-5,7-diol
7-hydroxy-1h-pyrazolo[1,5-a]pyrimidin-5-one
7-Hydroxypyrazolo[1,5-a]pyrimidin-5(4H)-one
5-Hydroxy-4H-pyrazolo[1,5-a]pyrimidin-7-one
7-Hydroxy-4H-pyrazolo[1,5-a]pyrimidin-5-one
Pyrazolo[1,5-a]pyrimidin-5(4H)-one, 7-hydroxy-
[EINECS(EC#)]

604-604-1
[Molecular Formula]

C6H5N3O2
[MDL Number]

MFCD02091625
[MOL File]

57489-70-0.mol
[Molecular Weight]

151.12
Chemical PropertiesBack Directory
[Melting point ]

239-240 °C (decomp)
[Boiling point ]

290.6±40.0 °C(Predicted)
[density ]

1.74±0.1 g/cm3(Predicted)
[storage temp. ]

2-8°C
[pka]

4.50±1.00(Predicted)
[Appearance]

Off-white to light yellow Solid
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]

Pyrazolo[1,5-a]pyrimidine-5,7(4H,6H)-dione(57489-70-0)1HNMR
Hazard InformationBack Directory
[Synthesis]

3-Aminopyrazole

1820-80-0

Diethyl malonate

105-53-3

Pyrazolo[1,5-a]pyrimidine-5,7(4H,6H)-dione

57489-70-0

Step A - Synthesis of pyrazolo[1,5-a]pyrimidine-5,7-diol (Int-9a): to 1H-pyrazol-3-amine (12.3 g, 148.0 mmol) in 50 mL of deionized water was added diethyl malonate (25.0 mL, 164.7 mmol), followed by the addition of an ethanolic solution of 21 wt% NaOEt (110 mL. 294.6 mmol) and additional ethanol (50 mL). The reaction mixture was heated at 80 °C for 16 h under argon protection. After completion of the reaction, it was cooled to room temperature. The reaction mixture was concentrated to near dryness under reduced pressure and 500 mL of water was added. Dissolution of the solid was promoted by vigorous stirring and the pH was subsequently adjusted to ~2 with hydrochloric acid, at which point a precipitate was generated. The precipitate was collected by vacuum filtration and dried to give pyrazolo[1,5-a]pyrimidine-5,7-diol (Int-9a) as a brown solid (17.13 g, 113.4 mmol, 77% yield).

[References]

[1] Patent: WO2011/2887, 2011, A1. Location in patent: Page/Page column 86
[2] Patent: WO2012/27234, 2012, A1. Location in patent: Page/Page column 39; 40
[3] Patent: US2011/294781, 2011, A1. Location in patent: Page/Page column 20
[4] Patent: WO2012/27240, 2012, A1. Location in patent: Page/Page column 47
[5] Patent: WO2012/47569, 2012, A1. Location in patent: Page/Page column 41
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