Reaktion #1989

ord-88b5cc36e3014d199d30d93dc27d1375

Reaktionsgleichung

[Al+3].[H-].[H-].[H-].[H-].[Li+]
LAH
O=C1CC2CNCC2C(=O)N1Cc1ccccc1
compound
O=C1CC2CNCC2C(=O)N1Cc1ccccc1
5-benzyl-4,6-dioxooctahydropyrrolo[3.4-c]pyridine
c1ccc(CN2CCC3CNCC3C2)cc1
title compound
Ausbeute 81.4%
c1ccc(CN2CCC3CNCC3C2)cc1
5-benzyl-octahydropyrrolo[3.4-c]pyridine
Ausbeute 81.4%

Reaktionsbedingungen

Temperatur
10°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe mixture was stirred under N2 for 1.5 hours
  2. 2
    SonstigeThe reaction was quenched by the sequential dropwise addition of 0.3 mL water, 0.3 mL of 15% NaOH and 0.6 mL of water
  3. 3
    workup.STIRRINGthe mixture was stirred for 1 hour
  4. 4
    Filtrationfiltered
  5. 5
    SonstigeThe filtrate was dried
  6. 6
    Einengenconcentrated

Vorschrift

A suspension of 266 mg of LAH in 10 mL of ether was stirred at 10° C. under N2. To this suspension was added 540 mg of the compound from step 457d dissolved in 10 mL of methylene chloride. The mixture was stirred under N2 for 1.5 hours. The reaction was quenched by the sequential dropwise addition of 0.3 mL water, 0.3 mL of 15% NaOH and 0.6 mL of water, then the mixture was stirred for 1 hour and filtered. The filtrate was dried and concentrated to give 389 mg of the title compound.

Quelle

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