Water → 4-Pyridin-3-yl-1,3-dihydroindol-2-one

HRID 1826722Notes

Reaction equation

HRID 1826722 reaction equation
[Br-].[Br-].[Br-].[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[NH+]1C=CC=CC=1.[N:22]1[CH:27]=[CH:26][CH:25]=[C:24]([C:28]2[CH:36]=[CH:35][CH:34]=[C:33]3[C:29]=2[CH:30]=[CH:31][NH:32]3)[CH:23]=1.[OH2:37]>CC(O)(C)C.C(O)C.C(O)(=O)C.[Zn]>[N:22]1[CH:27]=[CH:26][CH:25]=[C:24]([C:28]2[CH:36]=[CH:35][CH:34]=[C:33]3[C:29]=2[CH2:30][C:31](=[O:37])[NH:32]3)[CH:23]=1

Participants

8

Procedure

Pyridinium tribromide (90% (Aldrich), 5.5 g, 15.3 mmol) was added portion-wise over 10 minutes to a suspension of 4-pyridin-3-yl-1H-indole (1 g, 5.1 mmol) in 2-methyl-2-propanol (30 mL), ethanol (20 mL) and acetic acid (10 mL). The mixture was stirred at room temperature for 2 hours and then acetic acid (50 mL) was added. After stirring for an additional hour, water (0.5 mL) and zinc dust (3.3 g, 51 mmol) were added and stirring was continued for another hour. Residual zinc dust was filtered and washed with methanol. The filtrate was concentrated and the syrupy residue was stirred in water (100 mL) overnight. The solid which formed was filtered, washed with water to remove zinc and pyridine salts and dried under high vacuum to give 1.1 g (100%) of 4-pyridin-3-yl-1,3-dihydro-indol-2-one.

Workup

  1. stirringAfter stirring for an additional hour
  2. stirringstirring
  3. waitwas continued for another hour
  4. filtrationResidual zinc dust was filtered
  5. washwashed with methanol
  6. concentrationThe filtrate was concentrated
  7. stirringthe syrupy residue was stirred in water (100 mL) overnight
  8. customThe solid which formed
  9. filtrationwas filtered
  10. washwashed with water
  11. customto remove zinc and pyridine salts
  12. customdried under high vacuum

Sources & evidence

ORD record
ord-ac610527f2c6430d83a2756ff0ff66f9
Source dataset
uspto-grants-2006_05
Patent number
US07053086B2

Reaction notes

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