4-Fluorophenylboronic acid → HCID 11656385, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]2[CH2:10][N:9]([C:11]([C:13]3[CH:18]=[C:17]([S:19]([CH3:22])(=[O:21])=[O:20])[CH:16]=[CH:15][C:14]=3[O:23][C@@H:24]([CH3:29])[C:25]([F:28])([F:27])[F:26])=[O:12])[CH2:8][C:5]2=[N:6][CH:7]=1.[F:30][C:31]1[CH:36]=[CH:35][C:34](B(O)O)=[CH:33][CH:32]=1>>[F:30][C:31]1[CH:36]=[CH:35][C:34]([C:2]2[CH:3]=[C:4]3[CH2:10][N:9]([C:11]([C:13]4[CH:18]=[C:17]([S:19]([CH3:22])(=[O:20])=[O:21])[CH:16]=[CH:15][C:14]=4[O:23][C@@H:24]([CH3:29])[C:25]([F:28])([F:26])[F:27])=[O:12])[CH2:8][C:5]3=[N:6][CH:7]=2)=[CH:33][CH:32]=1Participants
3
Procedure
Prepared in analogy to Example 321 from (3-Bromo-5,7-dihydro-pyrrolo[3,4-b]pyridin-6-yl)-[5-methanesulfonyl-2-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-phenyl]-methanone (example 22) and 4-fluorophenyl boronic acid. White solid. MS (m/e): 509.2 [M+H]+, 100%).
Sources & evidence
- ORD record
- ord-45db73c4960f456cbf68d0ee3bca17c1
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07557114B2
Reaction notes
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