Water → HCID 20139720, compound

HRID 1252329Notes

Reaction equation

HRID 1252329 reaction equation
[OH-].[Na+].[CH2:3]([C:6]1[CH:7]=[C:8]2[C:14](=[O:15])[N:13]([C:16]([CH:21]([CH3:23])[CH3:22])([CH3:20])[C:17]([NH2:19])=[O:18])[C:12](=O)[C:9]2=[N:10][CH:11]=1)[CH2:4][CH3:5].O>C1(C)C=CC=CC=1>[CH:21]([C:16]1([CH3:20])[N:13]2[C:14](=[O:15])[C:8]3[C:9](=[N:10][CH:11]=[C:6]([CH2:3][CH2:4][CH3:5])[CH:7]=3)[C:12]2=[N:19][C:17]1=[O:18])([CH3:23])[CH3:22]

Participants

5

Procedure

With the simultaneous addition of 0.5 g of powdered sodium hydroxide, a solution of α-[3-n-propyl-6H-pyrrolo[3,4-b]pyridine-5,7-dione-6-yl]-α-isopropyl-α-methyl-acetamide (m.p.: 82° C.) in 100 ml of toluene is heated under reflux for 2 hours in a water separator. After the reaction solution has cooled, it is filtered through silica gel and the filtrate is washed with ethyl acetate and then concentrated by evaporation. The residue is recrystallised from ethyl acetate/petroleum ether, affording 13.1 g of the title compound which melts at 116° C.

Workup

  1. temperatureAfter the reaction solution has cooled
  2. filtrationit is filtered through silica gel
  3. washthe filtrate is washed with ethyl acetate
  4. concentrationconcentrated by evaporation
  5. customThe residue is recrystallised from ethyl acetate/petroleum ether

Sources & evidence

ORD record
ord-83d5c0794eba442c8f9aeb6bdb712243
Source dataset
uspto-grants-1988_05
Patent number
US04743296

Reaction notes

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