p-Chlorophenylboric acid → HCID 59691690, compound
Reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:9][C:10]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][N:20]([CH3:22])[CH3:21])=[CH:15][CH:14]=2)=[O:11])=[CH:4][CH:3]=1.[Cl:23][C:24]1[CH:29]=[CH:28][C:27](OB(O)O)=[CH:26][CH:25]=1>>[Cl:23][C:24]1[CH:29]=[CH:28][C:27]([C:2]2[CH:7]=[CH:6][C:5]([NH:8][CH2:9][C:10]([NH:12][C:13]3[CH:18]=[CH:17][C:16]([CH2:19][N:20]([CH3:22])[CH3:21])=[CH:15][CH:14]=3)=[O:11])=[CH:4][CH:3]=2)=[CH:26][CH:25]=1Participants
3
Procedure
Prepared analogously to Example 130a starting from 2-(4-bromo-phenylamino)-N-(4-dimethylaminomethyl-phenyl)-acetamide (Example 163a) and 4-chloro-phenyl-boric acid.
Workup
- customPrepared analogously to Example 130a
Sources & evidence
- ORD record
- ord-abe6a09df0fd4a52bedfb38e813c5d57
- Source dataset
- uspto-grants-2008_04