2-Isopropyl-5-methyl-cyclohexanecarboxylic acid (4-methoxy-2-nitrophenyl)-amide → 2-Isopropyl-5-methyl-cyclohexanecarboxylic (2-amino-4-methoxyphenyl)-amide
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
Reactant 1
Product 1
Reagents, catalysts & solvents 3
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
- filtrationThe reaction mixture was filtered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-a860dc1234664d85860b5e65b26f0f48
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741355B2
Reaction notes
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