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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283871Generated: October 27, 2026

Ammonium Chloride → 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/2283871

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantOxalyl chlorideHCID 65578—
Reactant5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylic acidHCID 66958370—
CatalystDichloromethaneHCID 6344—
SolventDimethylformamideHCID 6228—
Product5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxamideHCID 66959024—

Reaction Steps

Oxalyl chloride (7.8 mL, 90.0 mmol) was added slowly via syringe to a solution of 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxylic acid (10.5 g, 30.0 mmol) in 100 mL of dichloromethane containing one drop of DMF. After 2 hours of stirring, saturated ammonium chloride (100 mL) was added to the reaction mixture and the reaction was maintained for 1 hour. The reaction mixture was concentrated under reduced pressure, diluted with dichloromethane and washed with water. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered, and concentrated to afford 10.4 g of 5-(3-benzenesulfonylpropyl)-1-butyl-1H-pyrazole-3-carboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145410B2
Source datasetuspto-grants-2015_09
ORD IDord-914715f322224a65a5361c6ef4cfb7c3
Source noteuspto-grants-2015_09