4-(Methanesulfonyl)phenylboronic acid → HCID 136166953, compound

HRID 1617453Notes

Reaction equation

HRID 1617453 reaction equation
Br[C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH2:9]/[C:10](/[C:13]2[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=2)=[N:11]\[OH:12])=[CH:4][CH:3]=1.[CH3:25][S:26]([C:29]1[CH:34]=[CH:33][C:32](B(O)O)=[CH:31][CH:30]=1)(=[O:28])=[O:27]>>[CH3:25][S:26]([C:29]1[CH:34]=[CH:33][C:32]([C:2]2[CH:7]=[CH:6][C:5]([CH:8]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[CH2:9]/[C:10](/[C:13]3[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=3)=[N:11]\[OH:12])=[CH:4][CH:3]=2)=[CH:31][CH:30]=1)(=[O:28])=[O:27]

Participants

3

Reactant 2

HCID 27343644-(Methanesulfonyl)phenylboronic acidHCID 136167080HCID 136167080, compound

Product 1

HCID 136166953HCID 136166953, compound

Procedure

In analogy to example 19, from (E)-3-(4-bromo-phenyl)-3-phenyl-1-pyridin-4-yl-propan-1-one oxime (example 5) and (4-methylsulfonylphenyl)boronic acid was prepared the title compound as a light yellow foam, MS (ESI+): m/z=457.2 ([M+H]+).

Sources & evidence

ORD record
ord-fca42d07107b4a22ba2e1b12e4a1263e
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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