2-Isopropyl-5-methyl-cyclohexanecarboxylic acid (4-methoxy-2-nitrophenyl)-amide → 2-Isopropyl-5-methyl-cyclohexanecarboxylic (2-amino-4-methoxyphenyl)-amide

HRID 18487Notes

Reaction equation

HRID 18487 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([NH:9][C:10]([CH:12]2[CH2:17][CH:16]([CH3:18])[CH2:15][CH2:14][CH:13]2[CH:19]([CH3:21])[CH3:20])=[O:11])=[C:5]([N+:22]([O-])=O)[CH:4]=1>[Pd].C1COCC1.[OH-].[OH-].[Pd+2]>[NH2:22][C:5]1[CH:4]=[C:3]([O:2][CH3:1])[CH:8]=[CH:7][C:6]=1[NH:9][C:10]([CH:12]1[CH2:17][CH:16]([CH3:18])[CH2:15][CH2:14][CH:13]1[CH:19]([CH3:21])[CH3:20])=[O:11]

Participants

5

Procedure

2-Isopropyl-5-methyl-cyclohexanecarboxylic acid (4-methoxy-2-nitrophenyl)-amide (4.9 g) was dissolved in a suspension of 10% Pd—C (5 g) and THF (150 mL). The reaction mixture was hydrogenated over 20% Pd(OH)2 for 48 h with a balloon. The reaction mixture was filtered and concentrated to give the desired compound in sufficient purity to use in the next reaction without further purification.

Workup

  1. filtrationThe reaction mixture was filtered
  2. concentrationconcentrated

Sources & evidence

ORD record
ord-a860dc1234664d85860b5e65b26f0f48
Source dataset
uspto-grants-2010_06
Patent number
US07741355B2

Reaction notes

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