HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65207Generated: October 29, 2026
Dimethyl Sulfoxide → 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methylthio-benzenesulfonamide
https://huagongshe.com/reaction/65207
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 70458488 | HCID 70458488 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-[5-[4-(2-Methoxyphenyl)-1-piperazinyl]valeryl]-2-methylthio-benzenesulfonamide | HCID 70458354 | 80.5% |
Reaction Steps
A mixture of 5 g of 5-(5-chlorovaleryl)-2-methylthio-benzenesulfonamide, 3.4 g of 1-(2-methoxyphenyl)piperazine, 2.0 g of sodium carbonate and 25 ml of dimethyl sulfoxide was heated at 90° C. for 6 hours while stirring. After the reaction was finished, 100 ml of water and 100 ml of ethyl acetate were added to the reaction mixture and the stirring was continued for 30 minutes to produce crystals. The thus-produced crystals was filtered off to obtain 6.0 g of the titled compound (yield: 80.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04613598 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-6115671937c641e39f7099fffa0b4332 |
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| Source note | uspto-grants-1986_09 |
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