4-(3-Boronophenyl)butanoic acid → HCID 178422053, compound

HRID 1425483Notes

Reaction equation

HRID 1425483 reaction equation
C(C1C=C(/[C:10](/[CH:37]=[CH:38]/[CH:39]=[C:40]2\[C:41]([CH3:59])([CH3:58])[C:42]3[C:43](=[N:57]\2)[N:44]([CH2:49][CH2:50][CH2:51][CH2:52][S:53]([O-:56])(=[O:55])=[O:54])[CH:45]=[C:46]([Cl:48])[CH:47]=3)=[CH:11]\[CH:12]=[CH:13]\[C:14]2[C:22]([CH3:24])([CH3:23])[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([S:25]([O-:28])(=[O:27])=[O:26])[CH:20]=3)[N+:15]=2[CH2:29][CH2:30][CH2:31][CH2:32][S:33]([O-:36])(=[O:35])=[O:34])C=CC=1)(O)=O.[Na+:60].[Na+].B([C:65]1[CH:66]=[C:67]([CH2:71][CH2:72][CH2:73][C:74]([OH:76])=[O:75])[CH:68]=[CH:69][CH:70]=1)(O)O>>[C:74]([CH2:73][CH2:72][CH2:71][C:67]1[CH:66]=[C:65](/[C:10](/[CH:37]=[CH:38]/[CH:39]=[C:40]2\[C:41]([CH3:59])([CH3:58])[C:42]3[C:43](=[N:57]\2)[N:44]([CH2:49][CH2:50][CH2:51][CH2:52][S:53]([O-:56])(=[O:55])=[O:54])[CH:45]=[C:46]([Cl:48])[CH:47]=3)=[CH:11]\[CH:12]=[CH:13]\[C:14]2[C:22]([CH3:24])([CH3:23])[C:21]3[C:16](=[CH:17][CH:18]=[C:19]([S:25]([O-:28])(=[O:26])=[O:27])[CH:20]=3)[N+:15]=2[CH2:29][CH2:30][CH2:31][CH2:32][S:33]([O-:36])(=[O:34])=[O:35])[CH:70]=[CH:69][CH:68]=1)([OH:76])=[O:75].[Na+:60].[Na+:60]

Participants

3

Reactant 2

HCID 596235194-(3-Boronophenyl)butanoic acidHCID 178422054HCID 178422054, compound

Product 1

HCID 178422053HCID 178422053, compound

Procedure

Compound 44 is prepared analogously to compound 43, except with 4-(3-boronophenyl)butanoic acid as a starting material.

Sources & evidence

ORD record
ord-70cde1a4a43542ba8026597784586c37
Source dataset
uspto-grants-2015_01
Patent number
US08927719B2

Reaction notes

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