3-Fluorophenylboronic acid → 5-(3-fluorophenyl)-1H-pyrrolo[2,3-b]pyridin-2(3H)-one
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[CH2:10][C:9](=[O:11])[NH:8][C:5]2=[N:6][CH:7]=1.[F:12][C:13]1[CH:14]=[C:15](B(O)O)[CH:16]=[CH:17][CH:18]=1>>[F:12][C:13]1[CH:18]=[C:17]([C:2]2[CH:3]=[C:4]3[CH2:10][C:9](=[O:11])[NH:8][C:5]3=[N:6][CH:7]=2)[CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
The title compound was prepared in 32% yield according to the procedure described in Example 2, starting from 5-bromo-1,3-dihydro-pyrrolo[2,3-b]pyridin-2-one (prepared according to the procedure described in WO2003082868, Page 33) and 3-fluoro-phenyl boronic acid. 1H NMR is the same as the one reported in WO2003082868, page 34.
Workup
- customprepared
Sources & evidence
- ORD record
- ord-2a3ffec6f675480492649423f7849e35
- Source dataset
- uspto-grants-2009_10
- Patent number
- US07608712B2
Reaction notes
Loading…