Reaction equation
[C:1]1([C:7]2[O:11][C:10]([C:12]([OH:14])=O)=[CH:9][CH:8]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:15][O:16][C:17]([C:19]1[N:20]([CH3:29])[C:21]2[C:26]([CH:27]=1)=[CH:25][C:24]([NH2:28])=[CH:23][CH:22]=2)=[O:18]>>[CH3:15][O:16][C:17]([C:19]1[N:20]([CH3:29])[C:21]2[C:26]([CH:27]=1)=[CH:25][C:24]([NH:28][C:12]([C:10]1[O:11][C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[CH:8][CH:9]=1)=[O:14])=[CH:23][CH:22]=2)=[O:18]Participants
3
Procedure
Carboxylic acid (56) (23 mg, 0.12 mmol) was coupled to 5-amino-1-methyl-1H-indole-2-carboxylic acid methyl ester (25 mg, 0.12 mmol) using Method D to give the title compound.
Sources & evidence
- ORD record
- ord-a3e52e3090b84f458e4b1b200a7334e7
- Source dataset
- uspto-grants-2010_02
- Patent number
- US07662839B2
Linked notes
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