9-Methyl-3,9-diazabicyclo(4.2.1)nonan-4-one → 9-Methyl-3,9-diazabicyclo[4.2.1]nonane

HRID 1986012

Reaktionsgleichung

Reaktionsgleichung von HRID 1986012
[H-].[H-].[H-].[H-].[Li+].[Al+3].[CH3:7][N:8]1[CH:14]2[CH2:15][CH2:16][CH:9]1[CH2:10][NH:11][C:12](=O)[CH2:13]2>C1COCC1>[CH3:7][N:8]1[CH:14]2[CH2:15][CH2:16][CH:9]1[CH2:10][NH:11][CH2:12][CH2:13]2

Komponenten

4

Edukt 2

HCID 5574669-Methyl-3,9-diazabicyclo(4.2.1)nonan-4-oneHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 139737309-Methyl-3,9-diazabicyclo[4.2.1]nonane

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Neat LAH (0.5 g, 13.17 mmol) was added in small portions to a stirred solution of 9-methyl-3,9-diazabicyclo[4.2.1]nonan-4-one (1.0 g, 6.48 mmol) in THF (40 ml) and the mixture was heated at reflux under nitrogen for 3-4 h. Reaction mixture was cooled in ace bath and quenched by consecutive addition of water (0.5 ml), 15% NaOH (1.5 ml) and water (0.5 ml) and then stirred for 30 min. Precipitated sodium aluminate was filtered off and the filtrate was dried over MgSO4, filtered and evaporated to dryness to afford 9-methyl-3,9-diazabicyclo[4.2.1]nonane as a light yellow oil. 1H NMR (400 MHz, CHLOROFORM-D) δ ppm 1.08-1.67 (m, 4H) 1.74-1.92 (m, 1H) 2.01-2.31 (m, 2H) 2.41-2.46 (m, 3H) 2.66 (dd, J=13.09, 2.01 Hz, 1H) 2.77-3.00 (m,2H) 3.07-3.36 (m, 2H) 3.50-4.06 (m, 1H).

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureat reflux under nitrogen for 3-4 h
  3. customReaction mixture
  4. temperaturewas cooled in ace bath
  5. customquenched by consecutive addition of water (0.5 ml), 15% NaOH (1.5 ml) and water (0.5 ml)
  6. filtrationPrecipitated sodium aluminate was filtered off
  7. dry with materialthe filtrate was dried over MgSO4
  8. filtrationfiltered
  9. customevaporated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-ef9ca1c21b2a42caabcb3d2d96412e3b
Quelldatensatz
uspto-grants-2009_06
Patentnummer
US07547690B2

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