Potassium Carbonate → N-(4-[3-Phenylpropyl]piperidinocarbonyl)-2-phenylethenesulfonamide

HRID 2163690

Reaktionsgleichung

Reaktionsgleichung von HRID 2163690
[C:1]1([CH:7]=[CH:8][S:9]([NH2:12])(=[O:11])=[O:10])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C(=O)([O-])[O-].[K+].[K+].[C:19]1([CH2:25][CH2:26][CH2:27][CH:28]2[CH2:33][CH2:32][N:31]([C:34](Cl)=[O:35])[CH2:30][CH2:29]2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1.[Na]>C(Cl)(Cl)Cl>[C:19]1([CH2:25][CH2:26][CH2:27][CH:28]2[CH2:29][CH2:30][N:31]([C:34]([NH:12][S:9]([CH:8]=[CH:7][C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)(=[O:10])=[O:11])=[O:35])[CH2:32][CH2:33]2)[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1

Komponenten

6

Versuchsvorschrift

A stirred mixture of 1.83 g. (0.01 mole) of 2-phenylethenesulfonamide, 3.45 g. (0.025 mole) of potassium carbonate and 4.0 g. (0.015 mole) of 4-(3-phenylpropyl)piperidinocarbonyl chloride, in 75 ml. of chloroform is heated under reflux for 22 hours. The solvent is then removed by evaporation in vacuo, and to the residue is added 75 ml. of 0.5N sodium hydroxide and 35 ml. of ether. The mixture is stirred for 1 hour, and then the solid which remains undissolved is removed by filtration. This affords 1.84 g. (ca. 41% yield) of the title compound as a mixture of its sodium and potassium salts.

Aufarbeitung

  1. additionA stirred mixture of 1.83 g
  2. temperatureunder reflux for 22 hours
  3. customThe solvent is then removed by evaporation in vacuo
  4. additionto the residue is added 75 ml
  5. customthe solid which remains undissolved is removed by filtration

Quellen und Nachweise

ORD-Eintrag
ord-83ccda5ff10f42358c6e6ddce6feb5fa
Quelldatensatz
uspto-grants-1979_01
Patentnummer
US04136180

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