1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid

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1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid Basic information
Application
Product Name:1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid
Synonyms:1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid;1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid ISO 9001:2015 REACH
CAS:932702-11-9
MF:C7H5N3O2
MW:163.13
EINECS:
Product Categories:Heterocycle-Pyridine series
Mol File:932702-11-9.mol
1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid Structure
1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid Chemical Properties
Boiling point 501.7±30.0 °C(Predicted)
density 1.617
storage temp. 2-8°C
pka1.54±0.30(Predicted)
AppearanceOff-white to yellow Solid
Safety Information
HS Code 2933998090
MSDS Information
1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid Usage And Synthesis
Application1H-pyrazolo[4,3-C]pyridine-3-carboxylic acid is an intermediate in organic synthesis and pharmaceutical research and development, and can be used in laboratory organic synthesis and chemical and pharmaceutical synthesis processes.
Synthesis
1H-Pyrazolo[4,3-c]pyridine-3-carboxamide, N,N-bis(1-methylethyl)-

932702-12-0

1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid

932702-11-9

1H-Pyrazolo[4,3-c]pyridine-3-carboxamide, N-(1-methylethyl)-

936923-48-7

The general procedure for the synthesis of 1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid and compound (CAS: 936923-48-7) using compound (CAS: 932702-12-0) as starting material was as follows: in a microwave reaction vessel, N,N-diisopropyl-1H-pyrazolo[4,3-c]pyridine-3-carboxamide (0.800 g. 0.00325 mol) was mixed with 10 M aqueous hydrogen chloride solution (3.00 mL). The mixture was heated at 120 °C for 10 min. Heating at high absorbance settings is required to avoid pressure buildup. After completion of the reaction, the reaction mixture was diluted with water and neutralized with 3 N sodium hydroxide solution. The resulting white precipitate was collected and analyzed and found to be a mixture of 1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid (47%) and monoisopropylamide (25%). The mixture could be used in subsequent steps without further purification.

References[1] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 69
[2] Patent: WO2007/56582, 2007, A1. Location in patent: Page/Page column 76
1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid Preparation Products And Raw materials
Raw materials1H-Pyrazolo[4,3-c]pyridine-3-carboxamide, N,N-bis(1-methylethyl)-
Tag:1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid(932702-11-9) Related Product Information
Pyraclostrobin Pyrazole 1H-pyrazolo[4,3-c]pyridine-3-carboxylic acid 1H-Pyrazolo[4,3-c]pyridine-3-carboxylic acid, 6-chloro-, methyl ester Methyl 1H-pyrazolo[4,3-c]pyridine-3-carboxylate ethyl 1H-pyrazolo[4,3-c]pyridine-3-carboxylate