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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65206Generated: October 26, 2026

Dimethyl Sulfoxide → 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochloride

https://huagongshe.com/reaction/65206

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantSodium CarbonateHCID 10340—
Reactant5-(5-Chloropentanoyl)-2-methoxybenzenesulfonamideHCID 21886980—
SolventWaterHCID 962—
Product5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methoxy-benzenesulfonamide dihydrochlorideHCID 20233947123.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 2.6 g of 5-(5-chlorovaleryl)-2-methoxy-benzenesulfonamide, 1.8 g of 1-(2-methoxyphenyl)piperazine, 1 g of sodium carbonate and 20 ml of dimethyl sulfoxide was stirred at 90° C. for 3 hours. After the reaction was finished, water was added to the reaction mixture and then the mixture was extracted with ethyl acetate. The extract was washed with water saturated with sodium chloride and dried over anhydrous sodium sulfate. The solvent was distilled away and the residue was dissolved in acetone followed by adding concentrated hydrochloric acid in required amount to produce crystals. The thus-produced crystals were recrystallized from methanol to obtain 2.8 g of the titled compound (yield: 61%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04613598
Source datasetuspto-grants-1986_09
ORD IDord-851a04a25f894117b3242313f905eb84
Source noteuspto-grants-1986_09