HCID 27187797, compound → HCID 86674591, compound
Reaction equation
Br[CH:2]([C:4]1[CH:5]=[C:6]([CH:14]=[CH:15][CH:16]=1)[O:7][C@@H:8]([CH3:13])[C:9]([O:11][CH3:12])=[O:10])[CH3:3].[CH3:17][C:18]1[NH:19][C:20]2[C:25]([C:26]=1[CH3:27])=[CH:24][C:23]([C:28]([O:30][CH2:31][CH:32]=[CH2:33])=[O:29])=[CH:22][CH:21]=2>>[CH3:12][O:11][C:9](=[O:10])[C@@H:8]([O:7][C:6]1[CH:5]=[C:4]([CH:2]([N:19]2[C:20]3[C:25](=[CH:24][C:23]([C:28]([O:30][CH2:31][CH:32]=[CH2:33])=[O:29])=[CH:22][CH:21]=3)[C:26]([CH3:27])=[C:18]2[CH3:17])[CH3:3])[CH:16]=[CH:15][CH:14]=1)[CH3:13]Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Step 2, Example 1, using (2S)-methyl 2-(3-(1-bromoethyl)phenoxy)propanoate and allyl 2,3-dimethyl-1H-indole-5-carboxylate.
Sources & evidence
- ORD record
- ord-308b394eae834ada805996d8a25e516b
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051265B2
Reaction notes
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