3-Carboxyphenylboronic acid → HCID 178422043, compound
Reaction equation
C(C1C=CC(C2/C(=C/C=C3/N(CCCS([O-])(=O)=O)C4C(C/3(C)C)=CC(S([O-])(=O)=O)=CC=4)/CCCC=2C=CC2C(C)(C)C3C(N=2)=[N+](CCCS([O-])(=O)=O)C=CC=3)=CC=1)(O)=O.[Na+:60].[Na+].Cl[C:63]1=[C:64]([CH:90]=[CH:91][C:92]2[C:100]([CH3:102])([CH3:101])[C:99]3[C:94](=[CH:95][CH:96]=[C:97]([S:103]([O-:106])(=[O:105])=[O:104])[CH:98]=3)[N+:93]=2[CH2:107][CH2:108][CH2:109][CH2:110][S:111]([O-:114])(=[O:113])=[O:112])[CH2:65][CH2:66]/[C:67]/1=[CH:68]\[CH:69]=[C:70]1/[C:71]([CH3:89])([CH3:88])[C:72]2[C:73](=[N:87]/1)[N:74]([CH2:79][CH2:80][CH2:81][CH2:82][S:83]([O-:86])(=[O:85])=[O:84])[CH:75]=[C:76]([Cl:78])[CH:77]=2.[Na+].[Na+].B([C:120]1[CH:121]=[C:122]([CH:126]=[CH:127][CH:128]=1)[C:123]([OH:125])=[O:124])(O)O>>[C:123]([C:122]1[CH:121]=[C:120]([C:63]2=[C:64]([CH:90]=[CH:91][C:92]3[C:100]([CH3:102])([CH3:101])[C:99]4[C:94](=[CH:95][CH:96]=[C:97]([S:103]([O-:106])(=[O:105])=[O:104])[CH:98]=4)[N+:93]=3[CH2:107][CH2:108][CH2:109][CH2:110][S:111]([O-:114])(=[O:113])=[O:112])[CH2:65][CH2:66]/[C:67]/2=[CH:68]\[CH:69]=[C:70]2/[C:71]([CH3:88])([CH3:89])[C:72]3[C:73](=[N:87]/2)[N:74]([CH2:79][CH2:80][CH2:81][CH2:82][S:83]([O-:86])(=[O:85])=[O:84])[CH:75]=[C:76]([Cl:78])[CH:77]=3)[CH:128]=[CH:127][CH:126]=1)([OH:125])=[O:124].[Na+:60].[Na+:60]Participants
4
Reactant 3
Product 1
Procedure
Compound 40 is prepared analogously to compound 17 (Example 17), except with compound 39 and 3-boronobenzoic acid as starting materials.
Sources & evidence
- ORD record
- ord-460402802311404d955fdba7a953c8c8
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08927719B2
Reaction notes
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