1H-Pyrazolo[3,4-b]pyridin-3(2H)-one

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1H-Pyrazolo[3,4-b]pyridin-3(2H)-one Basic information
Product Name:1H-Pyrazolo[3,4-b]pyridin-3(2H)-one
Synonyms:1H-Pyrazolo[3,4-b]pyridin-3(2H)-one;1,2-dihydropyrazolo[3,4-b]pyridin-3-one;1,2-Dihydro-3H-pyrazolo[3,4-b]pyridin-3-one;3-Hydroxy-1H-pyrazolo[3,4-b]pyridine;1H-Pyrazolo[3,4-b]pyridin-3(2H);1H,2H-pyrazolo[3,4-b]pyridin-3-one;3H-Pyrazolo[3,4-b]pyridin-3-one, 1,2-dihydro-;1H,2H,3H-pyrazolo[3,4-b]pyridin-3-one
CAS:2942-43-0
MF:C6H5N3O
MW:135.12
EINECS:
Product Categories:
Mol File:2942-43-0.mol
1H-Pyrazolo[3,4-b]pyridin-3(2H)-one Structure
1H-Pyrazolo[3,4-b]pyridin-3(2H)-one Chemical Properties
Melting point 234-236°
density 1.62±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka8.93±0.20(Predicted)
AppearanceYellow to brown Solid
Safety Information
HazardClass IRRITANT
MSDS Information
1H-Pyrazolo[3,4-b]pyridin-3(2H)-one Usage And Synthesis
Synthesis
Ethyl 2-chloronicotinate

1452-94-4

1H-Pyrazolo[3,4-b]pyridin-3(2H)-one

2942-43-0

General procedure for the synthesis of 1H-pyrazolo[3,4-b]pyridin-3(2H)-one from ethyl 2-chloropyridine-3-carboxylate: a mixed solution of 5 g (26.94 mmol) of ethyl 2-chloropyridine-3-carboxylate and 4.76 g (80.82 mmol) of 85% hydrazine hydrate in 10 ml of ethanol was heated and refluxed for 6 hours. After completion of the reaction, the reaction mixture was concentrated. The product 3.5 g was obtained in 96% yield and the [M+H]+ peak was detected as 135.9 by mass spectrometry.

References[1] Patent: WO2005/73199, 2005, A1. Location in patent: Page/Page column 31
[2] Patent: US2005/197348, 2005, A1. Location in patent: Page/Page column 10
1H-Pyrazolo[3,4-b]pyridin-3(2H)-one Preparation Products And Raw materials
Raw materialsEthyl 2-chloronicotinate-->HYDRAZINE-->Ethanol
Tag:1H-Pyrazolo[3,4-b]pyridin-3(2H)-one(2942-43-0) Related Product Information
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