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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045959Generated: October 31, 2026

tert-Butyl 3-methyl-4-nitro-1H-pyrazole-1-carboxylate → tert-Butyl 4-amino-3-methyl-1H-pyrazole-1-carboxylate

https://huagongshe.com/reaction/1045959

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-methyl-4-nitro-1H-pyrazole-1-carboxylateHCID 60027346—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-amino-3-methyl-1H-pyrazole-1-carboxylateHCID 6002740456.5%

Reaction Steps

tert-Butyl 3-methyl-4-nitropyrazole-1-carboxylate (815 mg) was dissolved in MeOH (20 ml) and hydrogenated at room temperature for 40 hours with 10% Pd/C (0.2 g, 50% wet). The catalyst was filtered off and the solvent removed in vacuo. Column chromatography on silica (4 g), eluting with 1:1 EtOAc-heptane (500 ml) gave tert-butyl 4-amino-3-methylpyrazole-1-carboxylate (400 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569298B2
Source datasetuspto-grants-2013_10
ORD IDord-9af916266417465bb3a2c821e3a5036d
Source noteuspto-grants-2013_10