3-(Methoxycarbonyl)benzeneboronic acid → HCID 69414424, compound
Reaction equation
[CH2:1]1[N:9]2[C:4](=[N:5][S:6](=[O:16])(=[O:15])[C:7]3[CH:13]=[C:12]([OH:14])[CH:11]=[CH:10][C:8]=32)[CH2:3][CH2:2]1.[CH3:17][O:18][C:19]([C:21]1[CH:22]=[C:23](B(O)O)[CH:24]=[CH:25][CH:26]=1)=[O:20]>>[O:16]=[S:6]1(=[O:15])[C:7]2[CH:13]=[C:12]([O:14][C:25]3[CH:26]=[C:21]([CH:22]=[CH:23][CH:24]=3)[C:19]([O:18][CH3:17])=[O:20])[CH:11]=[CH:10][C:8]=2[N:9]2[CH2:1][CH2:2][CH2:3][C:4]2=[N:5]1Participants
3
Procedure
The procedure is as in Step B of Example 1, using the compound obtained in Step A of Example 1 and [3-(methoxycarbonyl)phenyl]boronic acid as starting materials.
Sources & evidence
- ORD record
- ord-3264951a2ccd4f2f8a6f9bb8245d9b0d
- Source dataset
- uspto-grants-2007_08
- Patent number
- US07253162B2
Reaction notes
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