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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 330394Erstellt: 24. Oktober 2026

Triethylamine → N-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleate

https://huagongshe.com/de/reaction/330394

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt((2-Chloroethyl)sulphonyl)benzeneHCID 13646—
EduktHexahydro-1H-azepine-1-ethanamineHCID 40002—
EduktMaleic AcidHCID 444266—
LösungsmittelMethanolHCID 887—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-[2-(Phenylsulfonyl)ethyl]-1-homopiperidineethanamine maleateHCID 7036055760,7%

Reaktionsschritte

A mixture of 20.06 g (0.098 mole) of [(2-chloroethyl)sulfonyl]benzene 15.44 g (0.109 mole) of N-(2-aminoethyl)homopiperidine, and 15.0 g (0.149 mole) of triethylamine in 800 ml of acetonitrile was stirred at room temperature for 18 hr. The solvent was removed in vacuo, and the residue was partitioned between methylene chloride and water. The methylene chloride solution was dried over magnesuim sulfate, and the solvent waas removed in vacuo to give an oil. This was dissolved in methanol, and the solution was treated with a solution of 2 equivalents of maleic acid (25.52 g, 0.22 mole) in methanol. A white solid precipitated at room temperature to give 32.3 g (60.7%) of title compound as a white solid; mp 144°-146° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04895840
Quelldatensatzuspto-grants-1990_01
ORD IDord-79450b90b97243f09b921d594904fb8c
Quellennotizuspto-grants-1990_01