3-(2-Methyl-1H-indol-5-yl)-3-phenyl-acrylic acid ethyl ester → N-Methyl-3-(2-methyl-1H-indol-5-yl)-3-phenyl-acrylamide
Reaction equation
C(O[C:4](=[O:23])[CH:5]=[C:6]([C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([CH3:22])=[CH:16]2)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)C.[NH:24]1C2C(=CC=CC=2C(C2C=CC=CC=2)=CC(NC)=O)C=[CH:25]1>>[CH3:25][NH:24][C:4](=[O:23])[CH:5]=[C:6]([C:13]1[CH:14]=[C:15]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([CH3:22])=[CH:16]2)[C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1Participants
3
Procedure
N-Methyl-3-(2-methyl-1H-indol-5-yl)-3-phenyl-acrylamide LXVIII (990 mg, 83%) was prepared from 3-(2-methyl-1H-indol-5-yl)-3-phenyl-acrylic acid ethyl ester using the procedure described for 3-(1H-indol-7-yl)-N-methyl-3-phenyl-acrylamide XVIII (see Example 4).
Sources & evidence
- ORD record
- ord-0a5727609d89424db11dae1fd707b835
- Source dataset
- uspto-grants-2010_09
- Patent number
- US07803830B2
Reaction notes
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