HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701973Generated: October 26, 2026
Thionyl Chloride → N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl urea
https://huagongshe.com/reaction/1701973
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | N-Butyl-N'-hydroxyurea | HCID 79761 | — |
| Reactant | 4-[2-(4-Methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfinic acid | HCID 20504599 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl urea | HCID 20504612 | — |
Reaction Steps
0.6 g of 4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfinic acid (crude product m.p. 113°-115° C., prepared by reaction of 4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfochloride with sodium sulfite) and 0.3 g of N-hydroxy-N'-butyl urea are dissolved in 50 ml of dioxan. 0.4 g of thionyl chloride in 10 ml of dioxan is added dropwise to this solution, and the batch is heated for 2 hours at 60° C. Subsequently, the solvent is evaporated under reduced pressure, water is added dropwise to the residue, the oily substance is separated and reprecipitated from ammonia. The N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl urea obtained has a melting point of 155°-157° C., and, with the substance obtained according to Example 8, shows no depression.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04379785 |
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| Source dataset | uspto-grants-1983_04 |
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| ORD ID | ord-a859a06453f64f2aaadcec60d2475987 |
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| Source note | uspto-grants-1983_04 |
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