HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467313Generated: October 30, 2026
Hydrochloric Acid → 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acid
https://huagongshe.com/reaction/1467313
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylate | HCID 67984978 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acid | HCID 67984975 | 98.6% |
Reaction Steps
In a sealed flask was added ethyl 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylate (420 mg, 0.802 mmol), MeOH (6 ml), and sodium hydroxide (1N in water, 4 ml, 4.00 mmol). The resulting mixture was then heated for 60 min at a temperature of 80° C. with stirring. The mixture was then neutralized with HCl (2N in water), diluted with 10% isopropanol in chloroform, washed with water, dried with sodium sulfate, filtered, and concentrated to afford 3-(2-methylpyridin-4-yl)-1-trityl-1H-indazole-5-carboxylic acid (392 mg, 0.791 mmol) as a light yellow solid. The crude product was progressed to the next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999957B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-7fe3d1c8fcca471b8d6273e8759085f1 |
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| Source note | uspto-grants-2015_04 |
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