HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291364Generated: October 30, 2026
Potassium Hydroxide → methyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate
https://huagongshe.com/reaction/2291364
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | 5-Carbomethoxy-3-(2,5-dimethylpyrrolyl)-1-methylpyrazole | HCID 136166810 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | methyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate | HCID 13248993 | 81.2% |
Reaction Steps
A solution of potassium hydroxide (5.08 g, 90.7 mmol) in water (76 mL) and ethanol (76 mL) was added to a slurry of hydroxylamine hydrochloride (11.44 g, 169.5 mmol) in ethanol (127 mL). Then, 5-carbomethoxy-3-(2,5-dimethylpyrrolyl)-1-methylpyrazole (8.5 g, 36.6 mmol) was added and the mixture was refluxed under a nitrogen atmosphere for 65 h. The solvents were removed at reduced pressure and the residue was triturated with ether. Sodium sulfate was added and the heterogenous mixture was filtered. The filtrate was concentrated and the residue was chromatographed on Silica Woelm®TSC (300 g, ethyl acetate-hexane gradient) to give 4.61 g, 81% of 5-carbomethoxy-3-amino-1-methylpyrazole as a white solid mp 114° to 118° C.; 1H-NMR (CDCl3) σ 6.17 (s, 1H), 4.02 (s, 3H), 3.88 (s, 1H), 3.7 (br s, 2H); IR (KBr) 1719, 1551, 1263, 1102, 756 cm-1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04795817 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-af90506af5f2495d8c5cfa54e689bbaf |
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| Source note | uspto-grants-1989_01 |
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