3-(4-Hydroxybutoxy)phenylboronic acid → HCID 178422050, compound

HRID 1425485Notes

Reaction equation

HRID 1425485 reaction equation
C(CCCC[C:8]1[CH:9]=[C:10](/[C:14](=[CH:48]\[CH:49]=[C:50]2/[C:51]([CH3:69])([CH3:68])[C:52]3[C:53](=[N:67]/2)[N:54]([CH2:59][CH2:60][CH2:61][CH2:62][S:63]([O-:66])(=[O:65])=[O:64])[CH:55]=[C:56]([Cl:58])[CH:57]=3)/[CH:15]=[CH:16]/[C:17]2[C:25]([CH3:27])([CH3:26])[C:24]3[C:23]4[CH:28]=[C:29]([S:36]([O-:39])(=[O:38])=[O:37])[CH:30]=[C:31]([S:32]([O-:35])(=[O:34])=[O:33])[C:22]=4[CH:21]=[CH:20][C:19]=3[N+:18]=2[CH2:40][CH2:41][CH2:42][CH2:43][S:44]([O-:47])(=[O:46])=[O:45])[CH:11]=[CH:12][CH:13]=1)(O)=O.[Na+:70].[Na+].[Na+].[OH:73][CH2:74][CH2:75][CH2:76][CH2:77][O:78]C1C=C(B(O)O)C=CC=1>>[Cl:58][C:56]1[CH:57]=[C:52]2[C:51]([CH3:69])([CH3:68])/[C:50](=[CH:49]\[CH:48]=[C:14](/[C:10]3[CH:11]=[CH:12][CH:13]=[C:8]([O:73][CH2:74][CH2:75][CH2:76][CH2:77][OH:78])[CH:9]=3)\[CH:15]=[CH:16]\[C:17]3[C:25]([CH3:26])([CH3:27])[C:24]4[C:23]5[CH:28]=[C:29]([S:36]([O-:39])(=[O:37])=[O:38])[CH:30]=[C:31]([S:32]([O-:35])(=[O:33])=[O:34])[C:22]=5[CH:21]=[CH:20][C:19]=4[N+:18]=3[CH2:40][CH2:41][CH2:42][CH2:43][S:44]([O-:47])(=[O:45])=[O:46])/[N:67]=[C:53]2[N:54]([CH2:59][CH2:60][CH2:61][CH2:62][S:63]([O-:66])(=[O:65])=[O:64])[CH:55]=1.[Na+:70].[Na+:70].[Na+:70]

Participants

3

Reactant 2

HCID 596235293-(4-Hydroxybutoxy)phenylboronic acidHCID 178422046HCID 178422046, compound

Product 1

HCID 178422050HCID 178422050, compound

Procedure

Compound 51 is prepared analogously to compound 28, except with 3-(4-hydroxybutoxy)phenylboronic acid as a starting material.

Sources & evidence

ORD record
ord-8727876b63a24c6eb3eff0eae170f095
Source dataset
uspto-grants-2015_01
Patent number
US08927719B2

Reaction notes

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