HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 898148Generated: October 30, 2026
Methanol → methyl 1H-indazole-3-carboxylate
https://huagongshe.com/reaction/898148
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Indazole-3-carboxylic acid | HCID 78250 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 1H-indazole-3-carboxylate | HCID 657476 | — |
Reaction Steps
To indazole-3-carboxylic acid (40 g, 247 mmol) suspended in methanol (700 mL) was added concentrated H2SO4 (10 mL) slowly while stirring the mixture. The mixture was stirred and refluxed at 80° C. for 24 h. The mixture was cooled, filtered, and concentrated under reduced pressure to afford a pale yellow solid. The solid was suspended in water (700 mL), crushed to fine powder, collected by filtration, and rinsed with water (˜400 mL). The product was suspended in toluene, and evaporated to dryness under reduced pressure, affording indazole-3-carboxylic acid methyl ester as a pale yellow solid (45 g, >95% pure). (m/z): [M+H]+ calcd for C9H8N2O2 177.07; found, 177.0. 1H-NMR (CD3OD, 300 MHz): δ (ppm) 8.0 (1H, d), 7.5 (1H, d), 7.4 (1H, t), 7.2 (1H, t), 3.9 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07351704B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-310f9bcd4ebd4a0eb44d9e6778bbaa1b |
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| Source note | uspto-grants-2008_04 |
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