2-[4-Benzyloxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid methyl ester → 2-[4-Hydroxy-3-(2-m-tolyl-ethoxy)-benzoylamino]-indane-2-carboxylic acid methyl ester

HRID 521520Notes

Reaction equation

HRID 521520 reaction equation
[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:40])[C:16]2[CH:21]=[CH:20][C:19]([O:22]CC3C=CC=CC=3)=[C:18]([O:30][CH2:31][CH2:32][C:33]3[CH:34]=[C:35]([CH3:39])[CH:36]=[CH:37][CH:38]=3)[CH:17]=2)[CH2:13][C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[CH2:6]1)=[O:4].[H][H]>CC(=O)OCC.[Pd]>[CH3:1][O:2][C:3]([C:5]1([NH:14][C:15](=[O:40])[C:16]2[CH:21]=[CH:20][C:19]([OH:22])=[C:18]([O:30][CH2:31][CH2:32][C:33]3[CH:34]=[C:35]([CH3:39])[CH:36]=[CH:37][CH:38]=3)[CH:17]=2)[CH2:6][C:7]2[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=2)[CH2:13]1)=[O:4]

Participants

5

Procedure

The compound of step 3 of example 253 (800 mg, 1.49 mmol) was dissolved in EA (15 ml) and hydrogenated in the presence of palladium (10%) on charcoal (200 mg) at a hydrogen pressure of 5 bar and room temperature for 6 h. The mixture was filtered over silica gel and evaporated to dryness. The residue was purified by RP HPLC (water/ACN gradient) to yield 300 mg of the title compound.

Workup

  1. filtrationThe mixture was filtered over silica gel
  2. customevaporated to dryness
  3. customThe residue was purified by RP HPLC (water/ACN gradient)

Sources & evidence

ORD record
ord-e6688b5012c145caac4d7fb327f7c208
Source dataset
uspto-grants-2016_05
Patent number
US09328071B2

Reaction notes

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