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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2400564Generated: October 30, 2026

Ammonia → 5-Methyl-1-(4-methylbenzyl)-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/2400564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(4-Methylbenzyl)-5-methyl-1H-pyrazole-3-carboxylic acidHCID 2747048—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product5-Methyl-1-(4-methylbenzyl)-1H-pyrazole-3-carboxamideHCID 59504701—

Reaction Steps

To a mechanically stirred solution of 5-methyl-1-(4-methylbenzyl)-1H-pyrazole-3-carboxylic acid (Intermediate B, 500 mg, 2.17 mmol) in dichloromethane (15 mL) was added dropwise oxalylchloride (950 μL, 10.9 mmol) and one drop DMF. After stirring at rt for 1 h, all volatiles were removed in vacuo. The crude acid chloride thus obtained was re-dissolved in dioxane (10 mL) and added dropwise to aqueous ammonia (33%, 6.4 mL) at 0° C. After the addition was complete, the reaction mixture was stirred at rt for 30 minutes. A white precipitate formed which was collected by filtration and washed with water. The title compound was obtained after drying in vacuo (436 mg, 89%): 1H NMR (400 MHz, DMSO-d6) δ 7.37 (broad s, 1H), 7.14 (d, 2H, and broad s, 1H), 7.02 (d, 2H), 6.43 (s, 1H), 5.28 (s, 2H), 2.27 (s, 3H), 2.19 (s, 3H); ES-MS m/z 230 (MH)+; HPLC RT (Method E) 1.39 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796253B2
Source datasetuspto-grants-2014_08
ORD IDord-e0ec9b153a0c424ab0660989703d2969
Source noteuspto-grants-2014_08