Potassium Sodium Tartrate → Methyl 5-amino-1-methyl-1h-indole-2-carboxylate

HRID 1444327Notes

Reaction equation

HRID 1444327 reaction equation
[CH3:1][O:2][C:3]([C:5]1[N:6]([CH3:17])[C:7]2[C:12]([CH:13]=1)=[CH:11][C:10]([N+:14]([O-])=O)=[CH:9][CH:8]=2)=[O:4].O.O.Cl[Sn]Cl.[C@H](O)(C([O-])=O)[C@@H](O)C([O-])=O.[Na+].[K+].C([O-])(O)=O.[Na+]>CN(C=O)C>[CH3:1][O:2][C:3]([C:5]1[N:6]([CH3:17])[C:7]2[C:12]([CH:13]=1)=[CH:11][C:10]([NH2:14])=[CH:9][CH:8]=2)=[O:4]

Participants

6

Conditions

Temperature
60 °C

Procedure

1-Methyl-5-nitro-1H-indole-2-carboxylic acid methyl ester (70 mg, 0.3 mmol) was dissolved in DMF (5 ml) and SnCl2.2H2O (339 mg, 1.5 mmol) was added as a solid. The resulting solution was stirred at 60° C. for 4 h. After cooling to room temperature, a pre-mixed aqueous solution of saturated Rochelle's salt (3 ml) and saturated NaHCO3 (3 ml) was added to the reaction mixture and the aqueous layer was extracted with EtOAc (3×6 ml). The organic layer was washed with H2O (3 ml), 1:1 NaHCO3: Rochelle's salt solution (3 ml), dried (MgSO4), filtered and the solvent was removed in vacuo to give the title compound.

Workup

  1. temperatureAfter cooling to room temperature
  2. extractionthe aqueous layer was extracted with EtOAc (3×6 ml)
  3. washThe organic layer was washed with H2O (3 ml), 1:1 NaHCO3
  4. dry with materialRochelle's salt solution (3 ml), dried (MgSO4)
  5. filtrationfiltered
  6. customthe solvent was removed in vacuo

Sources & evidence

ORD record
ord-3be87f541b2c417a9b8da67af375a0d6
Source dataset
uspto-grants-2010_02
Patent number
US07662839B2

Reaction notes

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