N-[2,6-bis(1-Methylethyl)phenyl]-2-[(1,1-dimethyl-2-phenylethyl)amino]acetamide → 2-[Acetyl[[4-(dimethylamino)phenyl]methyl]amino]-N-[2,6-bis(1-methylethyl)phenyl]acetamide
Reaction equation
[CH3:1][CH:2]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]([CH3:12])[CH3:11])[C:5]=1[NH:13][C:14](=[O:27])[CH2:15][NH:16][CH2:17][C:18]1[CH:23]=[CH:22][C:21]([N:24]([CH3:26])[CH3:25])=[CH:20][CH:19]=1)[CH3:3].CC(C1C=CC=C(C(C)C)C=1N[C:41](=[O:54])[CH2:42]NC(C)(C)CC1C=CC=CC=1)C>>[C:41]([N:16]([CH2:17][C:18]1[CH:23]=[CH:22][C:21]([N:24]([CH3:25])[CH3:26])=[CH:20][CH:19]=1)[CH2:15][C:14]([NH:13][C:5]1[C:6]([CH:10]([CH3:11])[CH3:12])=[CH:7][CH:8]=[CH:9][C:4]=1[CH:2]([CH3:1])[CH3:3])=[O:27])(=[O:54])[CH3:42]Participants
3
Reactant 2
Product 1
Procedure
When in the procedure of Example 79 an appropriate amount of the product from Example 73 was substituted for the product of Example 5 the title compound was obtained. Total yield, 0.41 g (73%).
Sources & evidence
- ORD record
- ord-b923193acba640bf86c74b459e0f7375
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05153226
Reaction notes
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