Identification | Back 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 Properties | Back 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) |
Hazard Information | Back 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]
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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