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Sibutramine → (-)-Sibutramine

HRID 2183829
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2183829
[CH3:1][CH:2]([CH2:4][CH:5]([N:17]([CH3:19])[CH3:18])[C:6]1([C:10]2[CH:11]=[CH:12][C:13]([Cl:16])=[CH:14][CH:15]=2)[CH2:9][CH2:8][CH2:7]1)[CH3:3]>C(OCC)(=O)C>[CH3:3][CH:2]([CH2:4][C@H:5]([N:17]([CH3:18])[CH3:19])[C:6]1([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)[CH2:7][CH2:8][CH2:9]1)[CH3:1]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 1

HCID 5210Sibutramine

Produkt 1

HCID 937011(-)-Sibutramine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8857Ethyl AcetateLösungsmittel3×

Versuchsvorschrift

12.3 g of racemic sibutramine was dissolved in 85 ml of ethyl acetate, L-DBTA dissolved in 85 ml of ethyl acetate was added thereto. The reaction mixture was heated under reflux, cooled to room temperature and then filtered to obtain crystals (ee: about 85%). And then, the crystals were suspended in 220 ml of ethyl acetate, and heated under reflux to obtain solids. The solids were recrystallized from 450 ml of isopropyl alcohol to obtain L-DBTA salt of (−)-sibutramine (ee: ≧99.3%). The L-DBTA salt of (−)-sibutramine was neutralized with saturated sodium bicarbonate, and then extracted with chloroform to obtain (−)-sibutramine free base.

Aufarbeitung

addition
was added
  • temperatureThe reaction mixture was heated
  • temperatureunder reflux
  • filtrationfiltered
  • customto obtain crystals (ee: about 85%)
  • temperatureheated
  • temperatureunder reflux
  • customto obtain solids
  • customThe solids were recrystallized from 450 ml of isopropyl alcohol
  • Quellen und Nachweise

    ORD-Eintrag
    ord-41e3c7a37d08478284aa5be43ed05d98
    Quelldatensatz
    uspto-grants-2005_05
    DOI
    10.6084/m9.figshare.5104873.v1
    Patentnummer
    US06900245B2

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