HCID 27187797, compound → HCID 86674595, compound
Reaction equation
C([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH:11](Br)[CH3:12])=[CH:7][CH:6]=1)(=O)C.[CH3:14][C:15]1[NH:16][C:17]2[C:22]([C:23]=1[CH3:24])=[CH:21][C:20]([C:25]([O:27][CH2:28][CH:29]=[CH2:30])=[O:26])=[CH:19][CH:18]=2>>[OH:4][C:5]1[CH:6]=[CH:7][C:8]([CH:11]([N:16]2[C:17]3[C:22](=[CH:21][C:20]([C:25]([O:27][CH2:28][CH:29]=[CH2:30])=[O:26])=[CH:19][CH:18]=3)[C:23]([CH3:24])=[C:15]2[CH3:14])[CH3:12])=[CH:9][CH:10]=1Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Step 2, Example 1, using 4-(1-bromoethyl)phenyl acetate and allyl 2,3-dimethyl-1H-indole-5-carboxylate.
Sources & evidence
- ORD record
- ord-b8e15b53432048b68c9a20f15fb2b539
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051265B2
Reaction notes
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