Indole → HCID 52899902, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[NH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][N:11]=1.N1C2C(=CC=CC=2)C=C1.[NH:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[C:27]([C:34]([O:36]C)=O)=[CH:26]1>>[N:11]1[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=1[NH:9][C:34]([C:27]1[C:28]2[C:33](=[CH:32][CH:31]=[CH:30][CH:29]=2)[N:25]([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=2)[CH:26]=1)=[O:36]Participants
5
Procedure
R5Br=Bromomethylbenzene; NH2A=2-aminopyridine; Indole starting material=methyl indole 3-carboxylate
Sources & evidence
- ORD record
- ord-4e4bdb01a10a4df8adb11e8ba53ece03
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Reaction notes
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