Reaktion #1990

ord-fab91be0255847869bf52f34533aab78

Reaktionsgleichung

O=C(C1CC1)C1CCN(Cc2ccccc2)C1
compound
O=C(C1CC1)C1CCN(Cc2ccccc2)C1
(1-benzyl-pyrroldin-3-yl)-cyclopropyl-methanone
CC(=O)[O-].[NH4+]
ammonium acetate
[BH3-]C#N.[Na+]
NaBH3CN
NC(C1CC1)C1CCN(Cc2ccccc2)C1
title compound
NC(C1CC1)C1CCN(Cc2ccccc2)C1
1-(1-benzyl-pyrroldin-3-yl)-1-cyclopropyl-methylamine

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITION1.2 g of 4 Å molecular sieves were added
  2. 2
    FiltrationThe mixture was filtered
  3. 3
    Waschenthe sieves washed with methanol
  4. 4
    Waschenthe wash
  5. 5
    Einengenconcentrated
  6. 6
    workup.DISSOLUTIONThe residue was dissolved in 100 mL of methylene chloride
  7. 7
    workup.ADDITION30 mL of 15% NaOH was added
  8. 8
    WaschenThe organic phase and a second wash of the aqueous phase
  9. 9
    Waschenwashed with water and brine
  10. 10
    Trocknendried over MgSO4
  11. 11
    SonstigeThe solvent was removed
  12. 12
    Sonstigethe residue was chromatographed on silica gel

Vorschrift

A 1 g sample of the compound from step 470b, 3.37 g of ammonium acetate and 274 mg of NaBH3CN were dissolved in 15 mL of methanol, 1.2 g of 4 Å molecular sieves were added, and the mixture was stirred at room temperature under N2 for 16 hours. The mixture was filtered, the sieves washed with methanol, the wash and filtrate combined, and concentrated. The residue was dissolved in 100 mL of methylene chloride, and 30 mL of 15% NaOH was added. The organic phase and a second wash of the aqueous phase were combined and washed with water and brine, then dried over MgSO4. The solvent was removed, and the residue was chromatographed on silica gel to give 460 mg of the title compound.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05726182uspto-grants-1998_03