ChemicalBook--->CAS DataBase List--->865887-02-1

865887-02-1

865887-02-1 Structure

865887-02-1 Structure
IdentificationBack Directory
[Name]

4-Methoxyindazole-3-carboxylic acid
[CAS]

865887-02-1
[Synonyms]

4-METHOXYINDAZOLE-3-CARBOXYLIC ACID
4-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID
1H-Indazole-3-carboxylic acid, 4-methoxy-
[Molecular Formula]

C9H8N2O3
[MDL Number]

MFCD07371558
[MOL File]

865887-02-1.mol
[Molecular Weight]

192.17
Chemical PropertiesBack Directory
[Boiling point ]

467.6±25.0 °C(Predicted)
[density ]

1.459±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

14.85±0.40(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]

GHS hazard pictograms
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2933998090
Hazard InformationBack Directory
[Uses]

4-Methoxy-1H-indazole-3-carboxylic Acid is used in the preparation of tricyclic compounds such as alpha-7 nicotinic acetylcholine receptor ligands for treatment of central nervous system disorders.
[Synthesis]

4-Methoxy-indoline-2,3-dione

108937-87-7

4-Methoxyindazole-3-carboxylic acid

865887-02-1

The general procedure for the synthesis of 4-methoxy-1H-indazole-3-carboxylic acid from 4-methoxyindoline-2,3-dione was as follows: 4-methoxyindoline-2,3-dione (20.7 mmol) was mixed with 1M sodium hydroxide solution (23 mL) and the reaction mixture was heated to 30-40 °C and maintained at this temperature for 30 minutes. Subsequently, the reaction mixture was cooled to 0 °C and treated with an aqueous solution (5.1 mL) of sodium nitrite (20.7 mmol) and maintained for 20 minutes. This solution was slowly added dropwise to a mixture of concentrated sulfuric acid (2.24 mL) and water (43.3 mL) that had been pre-cooled to 0-5 °C, and the reaction mixture was kept at 0-5 °C for 0.5 hours. Next, a concentrated hydrochloric acid (19.6 mL) solution of tin(II) chloride (50.5 mmol) was added drop by drop and the reaction mixture was kept at 0-5 °C for 1 hour. Upon completion of the reaction, the precipitated solid was separated by filtration and dried to afford 4-methoxy-1H-indazole-3-carboxylic acid as a yellow solid (100% yield).

[References]

[1] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 67
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