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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant5-Carbomethoxy-3-(2,5-dimethylpyrrolyl)-1-methylpyrazoleHCID 136166810—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Productmethyl 3-amino-1-methyl-1H-pyrazole-5-carboxylateHCID 1324899381.2%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04795817
Source datasetuspto-grants-1989_01
ORD IDord-af90506af5f2495d8c5cfa54e689bbaf
Source noteuspto-grants-1989_01