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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918836Generated: November 1, 2026

methyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylate → methyl 3-amino-1-methyl-1H-pyrazole-5-carboxylate

https://huagongshe.com/reaction/1918836

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylateHCID 18916504—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Productmethyl 3-amino-1-methyl-1H-pyrazole-5-carboxylateHCID 13248993100%

Reaction Steps

In a 250 mL Parr hydrogenation flask was placed methyl 1-methyl-3-nitro-1H-pyrazole-5-carboxylate, (530 mg, 2.9 mmol) dissolved in ethyl acetate (15 mL) and ethanol (15 mL), to which was added 10% Pd/C (Degussa type) (100 mg). The mixture was placed on the Parr apparatus and pressurized with hydrogen to 50 PSI and shaken for 2.5 hrs. The reaction was filtered through a pad of celite which was washed with ethyl acetate. The solvent was removed under vacuum to give 119a as a white solid (450 mg, 2.9 mmol, quantitative yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618107B2
Source datasetuspto-grants-2013_12
ORD IDord-2e6840a07b754b02bda836f48042426f
Source noteuspto-grants-2013_12