Indole → HCID 59513954, compound
Reaction equation
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][CH:4]=1.[NH2:13][C:14]1[S:15][CH:16]=[CH:17][N:18]=1.N1C2C(=CC=CC=2)C=C1.[NH:28]1[C:36]2[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=2)[C:30]([C:37](OC)=[O:38])=[CH:29]1>>[S:15]1[CH:16]=[CH:17][N:18]=[C:14]1[NH:13][C:37]([C:30]1[C:31]2[C:36](=[CH:35][CH:34]=[CH:33][CH:32]=2)[N:28]([CH2:2][C:3]2[CH:8]=[CH:7][C:6]([S:9]([CH3:12])(=[O:11])=[O:10])=[CH:5][CH:4]=2)[CH:29]=1)=[O:38]Participants
5
Procedure
R5X=1-Bromomethyl-4-methanesulfonyl-benzene, NH2A=2-aminothiazole; Indole starting material=methyl indole 3-carboxylate
Sources & evidence
- ORD record
- ord-73b3e2e09a5547c8a977cfba74f7bc6e
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148413B2
Reaction notes
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