Reaction equation
[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]([O:13][CH3:14])=[O:12])[C:4]([CH:15]=O)=[CH:3]1.C[C:18]1[NH:19]C2C(C=1C=O)=CC=CC=2>>[CH3:1][N:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[C:11]([O:13][CH3:14])=[O:12])[C:4]([CH2:15][NH:19][CH3:18])=[CH:3]1Participants
3
Procedure
According to the procedure of Preparation 12, except substituting 1-methyl-7-methoxycarbonyl-1H-indole 3-carboxaldehyde for the 2-methylindole-3-carboxaldehyde, the title compound (1.7 g, 92%) was obtained as an oil: MS (ES) m/e 233.2 (M+H)+.
Workup
- customAccording to the procedure of Preparation 12
Sources & evidence
- ORD record
- ord-ef4a20eef7314d66a3e37f69970bbd2f
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741339B2
Linked notes
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