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Isopropyl iodide → HCID 68820414, Verbindung

HRID 734333
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 734333
C(=O)([O-])[O-].[K+].[K+].[CH2:7]([O:14][C:15]([N:17]1[CH2:22][CH2:21][NH:20][C@@H:19]([CH3:23])[CH2:18]1)=[O:16])[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH:24](I)([CH3:26])[CH3:25]>CC#N.CCOC(C)=O>[CH:24]([N:20]1[CH2:21][CH2:22][N:17]([C:15]([O:14][CH2:7][C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)=[O:16])[CH2:18][CH:19]1[CH3:23])([CH3:26])[CH3:25]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 6362Isopropyl iodideHCID 11430Potassium CarbonateHCID 7578289(S)-Benzyl 3-methylpiperazine-1-carboxylate

Produkt 1

HCID 68820414HCID 68820414, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 6342AcetonitrileLösungsmittelHCID 8857
Ethyl Acetate
Lösungsmittel

Versuchsvorschrift

Potassium carbonate (11.2 g) was added to a solution of (S)-1-benzyloxycarbonyl-3-methylpiperazine (D19)(10.18 g) in CH3CN (60 ml), followed by isopropyl iodide (11.3 ml) and the mixture was heated at reflux overnight. The reaction mixture was then allowed to cool to rt and the inorganics were filtered off. The filtrate was evaporated to give an oil which was taken up in EtOAc (100 ml) and washed with water (2×50 ml). The EtOAc layer was dried (MgSO4) and concentrated to give the title compound (D26) as an oil (8 g). LCMS electrospray (+ve) 277 (MH+).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux overnight
  3. filtrationthe inorganics were filtered off
  4. customThe filtrate was evaporated
  5. customto give an oil which
  6. washwashed with water (2×50 ml)
  7. dry with materialThe EtOAc layer was dried (MgSO4)
  8. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-a111fd71d6fc4db98f41f74e32b3a395
Quelldatensatz
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07592347B2

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