Furan-3-boronic acid → Methyl 6-(3-fluorobenzenesulphonylmethyl)-3-(furan-3-yl)-2-methoxybenzoate
Reaction equation
C1(S(CC2C(C(OCC)=O)=C(O)C([C:23]3[CH:27]=[CH:26][O:25][CH:24]=3)=CC=2)(=O)=O)C=CC=CC=1.Br[C:29]1[C:30]([O:50][CH3:51])=[C:31]([C:36]([CH2:39][S:40]([C:43]2[CH:48]=[CH:47][CH:46]=[C:45]([F:49])[CH:44]=2)(=[O:42])=[O:41])=[CH:37][CH:38]=1)[C:32]([O:34][CH3:35])=[O:33].O1C=CC(B(O)O)=C1>>[F:49][C:45]1[CH:44]=[C:43]([S:40]([CH2:39][C:36]2[C:31]([C:32]([O:34][CH3:35])=[O:33])=[C:30]([O:50][CH3:51])[C:29]([C:23]3[CH:27]=[CH:26][O:25][CH:24]=3)=[CH:38][CH:37]=2)(=[O:42])=[O:41])[CH:48]=[CH:47][CH:46]=1Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 36, starting from methyl 3-bromo-6-(3-fluorobenzenesulphonylmethyl)-2-methoxybenzoate (Intermediate 99) and furan-3-yl boronic acid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-d866c35a793445ad8477e7829b797a4a
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
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