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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2243118Generated: November 3, 2026

Triethylamine → 5-Chloro-N-{2-ethyl-1-[1-(4-methoxybenzyl)-1H-pyrazol-5-yl]butyl}thiophene-2-sulfonamide

https://huagongshe.com/reaction/2243118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant5-Chlorothiophene-2-sulfonyl chlorideHCID 2733925—
Reactant{2-ethyl-1-[1-(4-methoxybenzyl)-1H-pyrazol-5-yl]butyl}amineHCID 68593849—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product5-Chloro-N-{2-ethyl-1-[1-(4-methoxybenzyl)-1H-pyrazol-5-yl]butyl}thiophene-2-sulfonamideHCID 1125990351%

Reaction Steps

To {2-ethyl-1-[1-(4-methoxybenzyl)-1H-pyrazol-5-yl]butyl}amine (0.500 g, 1.74 mmol) in CH2Cl2 (15 mL) was added triethylamine (0.29 mL, 2.1 mmol) and 5-chlorothiophene-2-sulfonyl chloride (0.450 g, 2.09 mmol). After 2 days the reaction mixture was diluted with EtOAc (30 mL), washed with 1 N HCl (30 mL), dried (Na2SO4) and concentrated. Column chromatography (EtOAc/hexane, 3:7, then 1:1) provided 5-chloro-N-{2-ethyl-1-[1-(4-methoxybenzyl)-1H-pyrazol-5-yl]butyl}thiophene-2-sulfonamide (0.415 g, 51%) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07674813B2
Source datasetuspto-grants-2010_03
ORD IDord-45101cf8d7d0403baa2b37e3dc005f60
Source noteuspto-grants-2010_03