Trimethylsilyl iodide → 5-(3-Aminomethyl-cyclohexyl)-3-methyl-5h-2-oxa-1,5,6-triaza-cyclopenta[a]naphthalen-4-one hydroiodide

HRID 1823269Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1823269
C(OC(=O)[NH:10][CH2:11][CH:12]1[CH2:17][CH2:16][CH2:15][CH:14]([N:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][N:26]=3)[C:21]3=[N:28][O:29][C:30]([CH3:31])=[C:20]3[C:19]2=[O:32])[CH2:13]1)C1C=CC=CC=1.[I:34][Si](C)(C)C>ClCCl>[IH:34].[NH2:10][CH2:11][CH:12]1[CH2:17][CH2:16][CH2:15][CH:14]([N:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][N:26]=3)[C:21]3=[N:28][O:29][C:30]([CH3:31])=[C:20]3[C:19]2=[O:32])[CH2:13]1

Komponenten

4

Versuchsvorschrift

Dissolve [3-(3-methyl-4-oxo-5H-2-oxa-1,5,6-triaza-cyclopenta-[a]naphthalen-5yl)-cyclohexylmethyl]-carbamic acid benzyl ester (0.52 g, 0.0012 mol) in dry dichloromethane and cool in an ice bath under nitrogen. Add iodotrimethylsilane (0.50 mL, 0.0035 mol) and stir overnight while warming to ambient temperature. Quench the mixture with methanol (approx. 5 mL) and concentrate in vacuo. Take up the resulting residue in minimal dichloromethane and add diethyl ether. Concentrate and titrate from dichloromethane/diethyl ether to give a dark solid. Decant the solvent and dry the solid in vacuo to give a near quantitative yield of the crude amine salt as a dark solid. Use directly without purification. MS(ES): (M+1)+ 313.2, 314.2 m/z.

Aufarbeitung

  1. temperaturecool in an ice bath under nitrogen
  2. customQuench the mixture with methanol (approx. 5 mL)
  3. concentrationconcentrate in vacuo
  4. additionadd diethyl ether
  5. concentrationConcentrate
  6. customtitrate from dichloromethane/diethyl ether to give a dark solid
  7. customDecant the solvent
  8. customdry the solid in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-fa42a99d8571436ea144b04400a2c31e
Quelldatensatz
uspto-grants-2006_05
Patentnummer
US07037921B2

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