Methanol → N-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamide

HRID 375408Notes

Reaction equation

HRID 375408 reaction equation
[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[NH:10][C:11]([C:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][C:20]=2[O:22]CC2C=CC=CC=2)[NH:15][CH:14]=1)=[O:12].CO.[H][H]>[Pd].C(O)C>[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[NH:10][C:11]([C:13]1[C:21]2[C:16](=[CH:17][CH:18]=[CH:19][C:20]=2[OH:22])[NH:15][CH:14]=1)=[O:12]

Participants

6

Reactant 3

HCID 887MethanolHCID 15337623HCID 15337623, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 15337630N-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamide

Reagents, catalysts & solvents 2

HCID 23938PalladiumCatalystHCID 702EthanolSolvent

Procedure

N-(2-Fluoro-4-methoxyphenyl)-4-benzyloxy-1H-indole-3-carboxamide (1.34 g, 3.4 mmol), prepared using the method above, was slurried with 10% Palladium on Carbon (134 mg) in ethanol (35 mL) in a Parr bottle and placed under a Hydrogen atmosphere (50 psi) for 5 h. Methanol (5 ml) was added and the mixture returned to the Hydrogen atmosphere for an additional 18 h. The solution was filtered through Celite, concentrated in vacuo, and the residue purified by flash chromatography to afford N-(2-fluoro-4-methoxyphenyl)-4-hydroxy-1H-indole-3-carboxamide (Compound 2) as a beige solid; mp 259°-261° C. (d).

Workup

  1. customfor 5 h
  2. filtrationThe solution was filtered through Celite
  3. concentrationconcentrated in vacuo
  4. customthe residue purified by flash chromatography

Sources & evidence

ORD record
ord-c92d1f6d36c94a2ebc22d78ed08dd669
Source dataset
uspto-grants-1996_01
Patent number
US05484944

Reaction notes

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