Реакция #1987

ord-a4ea40c7f75d4214b8389b24edce6e3b

Уравнение реакции

[Cl-].[NH4+]
Ammonium chloride
CCOC(=O)C1CN(Cc2ccccc2)CC1C(=O)OCC
compound
CCOC(=O)C1CN(Cc2ccccc2)CC1C(=O)OCC
N-benzyl-3,4-pyrrolidinedicarboxylic acid diethyl ester
C1CCOC1
THF
N
NH3
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1
title compound
O=C1CC2CN(Cc3ccccc3)CC2C(=O)N1
2-benzyl-4,6-dioxooctahydropyrrolo[3.4-c]pyridine

Условия реакции

Температура
-40°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added over a 10 minute period
  2. 2
    workup.STIRRINGthe reaction mixture was stirred at -33° C. for 3 hours
  3. 3
    workup.STIRRINGwith stirring
  4. 4
    Температураthe mixture was warmed to room temperature
  5. 5
    Другоеthe excess ammonia was evaporated
  6. 6
    workup.ADDITIONTo this was added 60 mL of water
  7. 7
    Экстракцияthe mixture was extracted with methylene chloride
  8. 8
    ПромывкаThe extract was washed with brine
  9. 9
    Другоеdried
  10. 10
    Концентрированиеconcentrated
  11. 11
    ДругоеThe residue was chromatographed on silica gel

Методика

A solution of 9.00 mmol of Na in liquid NH3 was prepared at -78° C. To this was added 15 mg of FeCl3, and the reaction mixture was warmed to -40° C. To this solution, stirred under N2, a cooled (-40° C.) solution of the compound (957 mg) from step 457a in THF was added over a 10 minute period, and the reaction mixture was stirred at -33° C. for 3 hours. Ammonium chloride (1.5 g) was added with stirring, then the mixture was warmed to room temperature and the excess ammonia was evaporated. To this was added 60 mL of water, and the mixture was extracted with methylene chloride. The extract was washed with brine, dried and concentrated. The residue was chromatographed on silica gel to give 425 mg of the title compound.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05726182uspto-grants-1998_03