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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533440Generated: October 25, 2026

1-Methyl-4-nitro-3-propyl-1H-pyrazole-5-carboxamide → 4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/1533440

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-4-nitro-3-propyl-1H-pyrazole-5-carboxamideHCID 2754492—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-Amino-1-methyl-3-propyl-1H-pyrazole-5-carboxamideHCID 3338044—

Reaction Steps

A stirred suspenson of 1-methyl-4-nitro-3-propyl-1H-pyrazole-5-carboxamide (EP-A-0463756; 237.7 g, 1.12 mol) and 5% palladium on charcoal (47.5 g) in ethyl acetate (2.02 1) was hydrogenated at 344.7 kPa (50 psi) and 50° C. for 4 hours, when the uptake of hydrogen was complete. The cool reaction mixture was filtered, then the filter pad washed with ethyl acetate, the combined filtrate and washings thus furnishing an ethyl acetate solution of the title compound (EP-A-0463756) which was of sufficient purity to use directly in the next stage of the reaction sequence.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207829B1
Source datasetuspto-grants-2001_03
ORD IDord-548dcdd8288c4c94a79275848b95ca7c
Source noteuspto-grants-2001_03