HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510331Generated: October 30, 2026
Hydrochloric Acid → 2-methyl-6-nitro-2H-indazole-3-carboxylic acid
https://huagongshe.com/reaction/1510331
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate | HCID 59334978 | — |
| Reactant | Methyl 1-methyl-6-nitro-1H-indazole-3-carboxylate | HCID 59335127 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-methyl-6-nitro-2H-indazole-3-carboxylic acid | HCID 59334896 | — |
Reaction Steps
670 mg of a mixture of methyl 1-methyl-6-nitro-1H-indazole-3-carboxylate and methyl 2-methyl-6-nitro-2H-indazole-3-carboxylate (Example XX) are dissolved in 20 ml of ethanol, combined with 10 ml 1 M sodium hydroxide solution and stirred for 2 hours. Then 10 ml of 1 M hydrochloric acid are added, the mixture is diluted with water and the precipitated solid is suction filtered. Then the solid is dissolved in dichloromethane/methanol 90:10. After drying with magnesium sulphate the solvents are eliminated in vacuo and the residue is dried in vacuo. 640 mg of a mixture of 1-methyl-6-nitro-1H-indazole-3-carboxylic acid and 2-methyl-6-nitro-2H-indazole-3-carboxylic acid is obtained which is further reacted directly in Example XV (1) or in XV (2), respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211923B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-e39a75dcaacc46ea970ac2a23000d164 |
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| Source note | uspto-grants-2012_07 |
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