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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 4222Erstellt: 24. Oktober 2026

Piperidine-1-propylamine → N-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]urea

https://huagongshe.com/de/reaction/4222

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPiperidine-1-propylamineHCID 19049—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktN-(2-phenylsulfonylethyl)-2-propanamineHCID 13655034—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN-(1-Methylethyl)-N-[2-(phenylsulfonyl)ethyl]-N'-[3-(1-piperidinyl)propyl]ureaHCID 2015282827,1%

Reaktionsschritte

A mixture of 5.16 g (0.0319 mole) of 1,1'-carbonyldiimidazole and 4.16 g (0.029 mole) of N-(3-aminopropyl)piperidine in 400 ml of tetrahydrofuran was stirred at room temperature for 1 hr. A solution of 6.13 g (0.027 mole) of N-[2-(phenylsulfonyl)ethyl]-2-propanamine in 50 ml of tetrahydrofuran was added, and the mixture was refluxed for 20 hr. The solvent was removed in vacuo, and the residue was dissolved in a 60/40 mixture of ether and methylene chloride, respectively. The solution was extracted with three portions of water and was dried over magnesium sulfate. The solvent was removed in vacuo to give an oil. Flash chromatography on silica gel (chloroform and methanol, gradiently eluted with methanol up to 10% methanol) gave 2.89 g (27.1%) of oil:

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04724235
Quelldatensatzuspto-grants-1988_02
ORD IDord-f9350ef6ad3d4d59a6d8bded0cf293e3
Quellennotizuspto-grants-1988_02