TERT-BUTYL 5-NITRO-1H-INDOLE-1-CARBOXYLATE → tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylate

HRID 252049Notes

Reaction equation

HRID 252049 reaction equation
[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([N+:17]([O-])=O)=[CH:14][CH:15]=2)[CH:10]=[CH:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>CO.CCOC(C)=O.[OH-].[OH-].[Pd+2]>[C:1]([O:5][C:6]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([NH2:17])=[CH:14][CH:15]=2)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:2])[CH3:3]

Participants

4

Reactant 1

HCID 11680504TERT-BUTYL 5-NITRO-1H-INDOLE-1-CARBOXYLATE

Product 1

HCID 22240520tert-Butyl 5-amino-2,3-dihydro-1H-indole-1-carboxylateYield 98.5%

Reagents, catalysts & solvents 2

HCID 9942167Palladium hydroxideCatalystHCID 21584119Ethylacetate methanolSolvent

Procedure

A solution of 5-nitro-indole-1-carboxylic acid tert-butyl ester (0.50 g) and catalytic amount of Pd(OH)2 in a mixture of MeOH-EtOAc was stirred at room temperature under hydrogen for 1 h. The reaction mixture was filtered through celite and the filtrate was concentrated to provide 5-amino-2,3-dihydro-indole-1-carboxylic acid tert-butyl ester (0.44 g, 98%).

Workup

  1. filtrationThe reaction mixture was filtered through celite
  2. concentrationthe filtrate was concentrated

Sources & evidence

ORD record
ord-613fa916f9dd4d5f97dde07a190c8e64
Source dataset
uspto-grants-2011_01
Patent number
US07868002B2

Reaction notes

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