Methyl 3-(bromomethyl)benzoate → HCID 86674599, compound
Reaction equation
Br[CH2:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[C:6]([O:8][CH3:9])=[O:7].[CH3:13][C:14]1[NH:15][C:16]2[C:21]([C:22]=1[CH3:23])=[CH:20][C:19]([C:24]([O:26][CH2:27][CH:28]=[CH2:29])=[O:25])=[CH:18][CH:17]=2>>[CH3:9][O:8][C:6]([C:5]1[CH:4]=[C:3]([CH:12]=[CH:11][CH:10]=1)[CH2:2][N:15]1[C:16]2[C:21](=[CH:20][C:19]([C:24]([O:26][CH2:27][CH:28]=[CH2:29])=[O:25])=[CH:18][CH:17]=2)[C:22]([CH3:23])=[C:14]1[CH3:13])=[O:7]Participants
3
Procedure
The title compound was prepared following the same general protocol as described in Step 2, Example 1, using methyl 3-(bromomethyl)benzoate and allyl 2,3-dimethyl-1H-indole-5-carboxylate.
Sources & evidence
- ORD record
- ord-5f1075e3bb7f4b468d7b560981a1b1ac
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051265B2
Reaction notes
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