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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701972Generated: October 30, 2026

Phosgene → HCID 20504611, compound

https://huagongshe.com/reaction/1701972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantSodium HydroxideHCID 14798—
ReactantSodiumHCID 5360545—
Reactant4-(2-Aminoethyl)-N-(cyclohexylcarbamoyl)benzene-1-sulfonamideHCID 12795527—
Reactant4-Methylpiperidin-2-oneHCID 14146878—
ReactantHCID 54018391HCID 54018391—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
ProductHCID 20504611HCID 20504611—

Reaction Steps

1.6 g of N-(4-[2-amino-ethyl]-benzenesulfonyl)-N'-cyclohexyl urea and 0.2 g of sodium hydroxide are dissolved in 10 ml of water and 50 ml of acetone. With agitation and ice cooling, a solution of 0.85 g of 4-methyl-2-oxo-piperidine-1-carboxylic acid chloride (prepared by reaction of the sodium compound of 4-methyl-2-oxo-piperidine with phosgene) in 20 ml of acetone is added dropwise to this solution, and agitation is continued for 2 hours at room temperature. Subsequently, the acetone is evaporated under reduced pressure, the batch is acidified, suction-filtered, the product is reprecipitated from dilute ammonia and recrystallized from dilute acetone. The N-(4-[2-(4-methyl-2-oxo-piperidine-1-carboxamido)-ethyl]-benzenesulfonyl)-N'-cyclohexyl urea obtained has a melting point of 177°-178° C. and is identical with the product obtained according to Example 8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04379785
Source datasetuspto-grants-1983_04
ORD IDord-fedf82b360404700adffd8eb0cb6c93b
Source noteuspto-grants-1983_04