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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47884Generated: October 26, 2026

5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide → 4-amino-5-ethyl-1-(2-methoxyethyl)-1H-Pyrazole-3-carboxamide

https://huagongshe.com/reaction/47884

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamideHCID 11218717—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-amino-5-ethyl-1-(2-methoxyethyl)-1H-Pyrazole-3-carboxamideHCID 11264312—

Reaction Steps

A mixture of 5-ethyl-1-(2-methoxyethyl)-4-nitro-1H-pyrazole-3-carboxamide (20 g, 82.6 mMol) and 5%Pd/C (1 g) in methanol (200 mL) was pressurised at 50 psi/25° C. in a sealed vessel and stirred for 15 hours. At the end of the reaction the mixture was filtered through arbocel and the filter cake was washed with methanol. The methanolic solution was distilled at atmospheric pressure and replaced with ethyl acetate to a final volume of 100 mL. The cooled mixture was granulated at ambient temperature for 2 h filtered and washed with ethyl acetate (20 mL) to afford 4-amino-5-ethyl-1-(2-methoxyethyl)-1H-pyrazole-3-carboxamide as a white crystalline solid, 15 g, 88%. m.p.=131° C. Found: C, 50.75; H, 7.62; N, 26.38. C9H16N4O2 requires C, 50.94; H, 7.55; N, 26.42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699991B2
Source datasetuspto-grants-2004_03
ORD IDord-e67bc94a9a574addb96b61d708c3dd29
Source noteuspto-grants-2004_03