Furan-3-boronic acid → Methyl 6-(2-chlorobenzenesulphonylmethyl)-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(OC)[CH:38]=[CH:37][C:36]([CH2:39][S:40]([C:43]2[CH:48]=[CH:47][CH:46]=[CH:45][C:44]=2[Cl:49])(=[O:42])=[O:41])=[C:31]([C:32]([O:34][CH3:35])=[O:33])[CH2:30]1.[O:52]1C=CC(B(O)O)=[CH:53]1>>[Cl:49][C:44]1[CH:45]=[CH:46][CH:47]=[CH:48][C:43]=1[S:40]([CH2:39][C:36]1[C:31]([C:32]([O:34][CH3:35])=[O:33])=[C:30]([O:52][CH3:53])[C:29]([C:23]2[CH:27]=[CH:26][O:25][CH:24]=2)=[CH:38][CH:37]=1)(=[O:41])=[O:42]Participants
4
Procedure
Prepared by proceeding in a similar manner to Intermediate 36, starting from methyl 3-bromo-6-(2-chlorobenzenesulphonylmethyl)-3-methoxybenzoate, (Intermediate 98) and furan-3-yl boronic acid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-45e702dacb3e4072977b07841021a77c
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
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