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1-Chloroethyl chloroformate → 4-[(2S,5R)-2,5-Dimethylpiperazin-1-yl]-2-methylbenzonitrile

HRID 1445462
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1445462
C([N:8]1[C@H:13]([CH3:14])[CH2:12][N:11]([C:15]2[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[C:17]([CH3:23])[CH:16]=2)[C@@H:10]([CH3:24])[CH2:9]1)C1C=CC=CC=1.C(Cl)(=O)OC(Cl)C>ClC(Cl)C>[CH3:24][C@H:10]1[CH2:9][NH:8][C@H:13]([CH3:14])[CH2:12][N:11]1[C:15]1[CH:22]=[CH:21][C:18]([C:19]#[N:20])=[C:17]([CH3:23])[CH:16]=1
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Komponenten

4

Edukt 2

HCID 5213051-Chloroethyl chloroformateHCID 686953104-[(2S,5R)-4-benzyl-2,5-dimethylpiperazin-1-yl]-2-methylbenzonitrile

Produkt 1

HCID 686963004-[(2S,5R)-2,5-Dimethylpiperazin-1-yl]-2-methylbenzonitrileAusbeute 85,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 63651,1-DichloroethaneLösungsmittel

Versuchsvorschrift

Into 50 ml of dichloroethane was dissolved 1.81 g of 4-[(2S,5R)-4-benzyl-2,5-dimethylpiperazin-1-yl]-2-methylbenzonitrile, and then 1.62 g of 1-chloroethyl chlorocarbonate was added thereto, followed by heating under refluxing overnight. After the reaction solution was concentrated, 50 ml of methanol was added thereto, followed by heating under refluxing overnight. After the reaction solution was concentrated, water was added thereto, followed by washing with ether. The aqueous phase was made basic with a 1M sodium hydroxide aqueous solution, followed by extraction with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and then solvent was removed by evaporation to obtain 1.11 g of the title compound.

Aufarbeitung

  1. temperatureby heating
  2. temperatureunder refluxing overnight
  3. concentrationAfter the reaction solution was concentrated
  4. addition50 ml of methanol was added
  5. temperatureby heating
  6. temperatureunder refluxing overnight
  7. concentrationAfter the reaction solution was concentrated
  8. additionwater was added
  9. washby washing with ether
  10. extractionfollowed by extraction with ethyl acetate
  11. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  12. customsolvent was removed by evaporation

Quellen und Nachweise

ORD-Eintrag
ord-56224c689aa64b1a9ae698e6d5708924
Quelldatensatz
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07666873B2

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