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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108474Generated: 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/1108474

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 suspension of 1-methyl-4-nitro-3-n-propylpyrazole-5-carboxamide (EP-A-0463756; 237.7 g, 1.12 mol) and 5% palladium on charcoal (47.5 g) in ethyl acetate (2.02 l) 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 (see Preparation 4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06066735
Source datasetuspto-grants-2000_05
ORD IDord-3f30ade9fc4640979157a74da85fe7b7
Source noteuspto-grants-2000_05