2-Aminobiphenyl → N-Biphenyl-2-yl-4-methyl-benzenesulfonamide

HRID 1663254Notes

Reaction equation

HRID 1663254 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.[CH3:14][C:15]1[CH:20]=[CH:19][C:18]([S:21](Cl)(=[O:23])=[O:22])=[CH:17][CH:16]=1>>[C:3]1([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:4]=[CH:5][CH:6]=[CH:7][C:2]=1[NH:1][S:21]([C:18]1[CH:19]=[CH:20][C:15]([CH3:14])=[CH:16][CH:17]=1)(=[O:23])=[O:22]

Participants

3

Reactant 2

HCID 70152-AminobiphenylHCID 73974-Toluenesulfonyl chloride

Product 1

HCID 818647N-Biphenyl-2-yl-4-methyl-benzenesulfonamide

Procedure

The title compound was prepared from 2-aminobiphenyl (Aldrich) and 4-methyl-benzenesulfonyl chloride according to the method described in Example 1b.

Sources & evidence

ORD record
ord-d51aa15fc3a741debd34ff38e354bd13
Source dataset
uspto-grants-2011_10
Patent number
US08034827B2

Reaction notes

Loading…