3-(Methylsulfonyl)phenylboronic acid → HCID 136359969, compound

HRID 1617464Notes

Reaction equation

HRID 1617464 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][C:20]=2[CH3:25])[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.[CH3:26][S:27]([C:30]1[CH:31]=[C:32](B(O)O)[CH:33]=[CH:34][CH:35]=1)(=[O:29])=[O:28]>>[CH3:26][S:27]([C:30]1[CH:35]=[C:34]([C:2]2[CH:3]=[CH:4][C:5]([CH:8]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[CH3:25])[CH2:9][C:10]([C:13]3[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=3)=[N:11][OH:12])=[CH:6][CH:7]=2)[CH:33]=[CH:32][CH:31]=1)(=[O:29])=[O:28]

Participants

3

Reactant 2

HCID 27735423-(Methylsulfonyl)phenylboronic acidHCID 136359968HCID 136359968, compound

Product 1

HCID 136359969HCID 136359969, compound

Procedure

In analogy to example 22, from 3-(4-bromo-phenyl)-1-pyridin-4-yl-3-o-tolyl-propan-1-one oxime (example 31) and (3-methylsulfonylphenyl)boronic acid was prepared the title compound as a mixture of E and Z isomers (2:1) as a white foam, MS (ESI+): m/z=471.1 ([M+H]+).

Sources & evidence

ORD record
ord-8385c9908cbb47aa803cfa4919a04756
Source dataset
uspto-grants-2014_07
Patent number
US08765730B2

Reaction notes

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