4-Chlorophenylboronic acid → HCID 22337843, compound
Reaction equation
Br[C:2]1[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]2[CH:17]=[CH:16][CH:15]=[C:14]3[C:9]=2[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:25])([F:24])[F:23])(=[O:21])=[O:20])=[CH:13]3)=[CH:4][CH:3]=1.[Cl:28][C:29]1[CH:34]=[CH:33][C:32](B(O)O)=[CH:31][CH:30]=1>>[Cl:28][C:29]1[CH:34]=[CH:33][C:32]([C:2]2[CH:27]=[CH:26][C:5]([CH2:6][O:7][C:8]3[CH:17]=[CH:16][CH:15]=[C:14]4[C:9]=3[CH:10]=[CH:11][C:12]([NH:18][S:19]([C:22]([F:24])([F:23])[F:25])(=[O:21])=[O:20])=[CH:13]4)=[CH:4][CH:3]=2)=[CH:31][CH:30]=1Participants
3
Procedure
The title compound was prepared from the product of Example 1 and 4-chlorophenyl boronic acid according to the procedure of Example 2, m.p. 131-133.
Sources & evidence
- ORD record
- ord-d049788a878d4e65a65789fce684b77a
- Source dataset
- uspto-grants-2005_08
- Patent number
- US06933322B2
Reaction notes
Loading…