4-Ethoxyphenylboronic acid → 4-(4-Ethoxy-phenyl)-1h-indole-2-carboxylic acid piperidin-4-ylamide
Reaction equation
[CH2:1]([O:3][C:4]1[CH:9]=[CH:8][C:7](B(O)O)=[CH:6][CH:5]=1)[CH3:2].[NH:13]1[CH2:18][CH2:17][CH:16]([NH:19][C:20]([C:22]2[NH:23][C:24]3[C:29]([CH:30]=2)=[C:28](C2C=CC(OC)=CC=2)[CH:27]=[CH:26][CH:25]=3)=[O:21])[CH2:15][CH2:14]1>>[NH:13]1[CH2:18][CH2:17][CH:16]([NH:19][C:20]([C:22]2[NH:23][C:24]3[C:29]([CH:30]=2)=[C:28]([C:7]2[CH:8]=[CH:9][C:4]([O:3][CH2:1][CH3:2])=[CH:5][CH:6]=2)[CH:27]=[CH:26][CH:25]=3)=[O:21])[CH2:15][CH2:14]1Participants
3
Procedure
This compound has been synthesized from 4-ethoxy-phenyl-boronic acid analogously to the method described in the synthesis of 178 (see example 141).
Sources & evidence
- ORD record
- ord-e0bef7f2b3d24c23bedbe2b5e6be2184
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07858781B2
Reaction notes
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