Indole → HCID 59513978, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[CH:4]=1.[NH2:11][C:12]1[S:13][CH:14]=[CH:15][N:16]=1.N1C2C(=CC=CC=2)C=C1.[NH:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[C:28]([C:35](OC)=[O:36])=[CH:27]1>>[S:13]1[CH:14]=[CH:15][N:16]=[C:12]1[NH:11][C:35]([C:28]1[C:29]2[C:34](=[CH:33][CH:32]=[CH:31][CH:30]=2)[N:26]([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[C:5]([O:9][CH3:10])[CH:4]=2)[CH:27]=1)=[O:36]Participants
5
Procedure
R5X=1-Bromomethyl-3-methoxy-benzene; NH2A=2-aminothiazole; Indole starting material=methyl indole 3-carboxylate
Sources & evidence
- ORD record
- ord-9126ec1c2a0a441d9c84cec2ae40a551
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812043B2
Reaction notes
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