Indole → HCID 58217500, compound
Reaction equation
[CH:1]1([CH2:7]Br)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[NH2:9][C:10]1[S:11][CH:12]=[CH:13][N:14]=1.N1C2C(=CC=CC=2)C=C1.[NH:24]1[C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[C:26]([C:33]([O:35]C)=O)=[CH:25]1>>[S:11]1[CH:12]=[CH:13][N:14]=[C:10]1[NH:9][C:33]([C:26]1[C:27]2[C:32](=[CH:31][CH:30]=[CH:29][CH:28]=2)[N:24]([CH2:7][CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)[CH:25]=1)=[O:35]Participants
5
Procedure
R5Br=Cyclohexylmethylbromide; NH2A=2-aminothiazole; Indole starting material=methyl indole 3-carboxylate
Sources & evidence
- ORD record
- ord-88bed95887ca4453924390ce80e7bab7
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Reaction notes
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