4-Fluorophenylboronic acid → N-(6-(4-Fluorophenyl)-1,2,3,4-tetrahydroquinolin-3-yl)benzene sulfonamide
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH2:7][CH:6]([NH:12][S:13]([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)(=[O:15])=[O:14])[CH2:5]2.[F:22][C:23]1[CH:28]=[CH:27][C:26](B(O)O)=[CH:25][CH:24]=1.C(N1C2C(=CC(C3C=CC=CC=3)=CC=2)C[C@H](NS(C2C=CC=CC=2)(=O)=O)C1)C1C=CC=CC=1>>[F:22][C:23]1[CH:28]=[CH:27][C:26]([C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[NH:8][CH2:7][CH:6]([NH:12][S:13]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)(=[O:15])=[O:14])[CH2:5]3)=[CH:25][CH:24]=1Participants
4
Reactant 3
Product 1
Procedure
Compound 113A was prepared from 87A and 4-fluorophenylboronic acid by procedures analogous to those described in 89E.
Sources & evidence
- ORD record
- ord-97be8f69114c4109a3a8038e61bc7b0e
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884113B2
Reaction notes
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