HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 65210Generated: October 29, 2026
Dimethyl Sulfoxide → 5-[4-(4-Phenyl-1-piperazinyl)butyryl]-2-benzyloxy-salicylamide
https://huagongshe.com/reaction/65210
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 20233922 | HCID 20233922 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[4-(4-Phenyl-1-piperazinyl)butyryl]-2-benzyloxy-salicylamide | HCID 70458553 | 58% |
Reaction Steps
A mixture of 1 g of 5-(4-chlorobutyryl)-2-benzyloxy-benzamide, 1.2 g of 1-phenylpiperazine, 3.3 ml of triethylamine and 10 ml of dimethyl sulfoxide was heated at 90° C. for 15 hours while stirring. After the reaction was finished, water was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with water saturated with sodium chloride, dried over anhydrous sodium sulfate and concentrated. The thus-produced residue was crystallized from ethyl acetate-ether to obtain 1.6 g of 5-[4-(4-phenyl-1-piperazinyl)butyryl]-2-benzyloxy-salicylamide (yield: 58.0%).
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-8651dec700a0474fb4974b77b5371a3b |
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| Source note | uspto-grants-1986_09 |
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