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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045956Generated: November 1, 2026

Dimethylamine → N,N,1-trimethyl-4-nitropyrazole-3-carboxamide

https://huagongshe.com/reaction/1045956

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant1-Methyl-4-nitro-1H-pyrazole-3-carboxylic acidHCID 535976—
SolventTetrahydrofuranHCID 8028—
ProductN,N,1-trimethyl-4-nitropyrazole-3-carboxamideHCID 67076071—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 1-methyl-4-nitropyrazole-3-carboxylic acid (2.0 g) in THF (30 ml) was charged carbonyl-1,1′-diimidazole (1.9 g) over 1 hour at room temperature. The reaction was stirred overnight before cooling to 0° C. A solution of dimethylamine in THF (12 ml of a 2M solution) was added and the reaction stirred for 1 hour. The THF layer was separated and concentrated in vacuo. The crude product was purified by column chromatography on silica (30 g), eluting with 100% EtOAc (300 ml) to give N,N,1-trimethyl-4-nitropyrazole-3-carboxamide, 1235 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569298B2
Source datasetuspto-grants-2013_10
ORD IDord-fb9d8a624452451ca28cbe45e4ee5e15
Source noteuspto-grants-2013_10