4,4,5,5-Tetramethyl-2-(5-methylfuran-2-yl)-1,3,2-dioxaborolane → HCID 67107560, compound
Reaction equation
[C:1]1([S:7]([CH2:10][C:11]2[CH:20]=[CH:19][C:18](Br)=[CH:17][C:12]=2[C:13]([O:15][CH3:16])=[O:14])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:22][C:23]1[O:24][C:25](B2OC(C)(C)C(C)(C)O2)=[CH:26][CH:27]=1>>[C:1]1([S:7]([CH2:10][C:11]2[CH:20]=[CH:19][C:18]([C:27]3[CH:26]=[CH:25][O:24][C:23]=3[CH3:22])=[CH:17][C:12]=2[C:13]([O:15][CH3:16])=[O:14])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
Prepared by proceeding in a similar manner to Example 36, starting from methyl 2-(benzenesulphonylmethyl)-5-bromobenzoate (Intermediate 63) and 2-methylfuran-5-boronic acid pinacol ester.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-66e54186e95e432196dd0032226795e0
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09067905B2
Reaction notes
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