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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantN-Butyl-N'-hydroxyureaHCID 79761—
Reactant4-[2-(4-Methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfinic acidHCID 20504599—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-butyl ureaHCID 20504612—

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379785
Source datasetuspto-grants-1983_04
ORD IDord-a859a06453f64f2aaadcec60d2475987
Source noteuspto-grants-1983_04