HCID 841313, compound → 4-(4-Amino-3-nitrophenylsulfinyl)-biphenyl
Reaction equation
C1(S(C2C=CC(Cl)=C([N+:16]([O-])=O)C=2)=O)C=CC=CC=1.Cl[C:20]1[CH:25]=[CH:24][C:23]([S:26]([C:28]2[CH:33]=[CH:32][C:31]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)=[CH:30][CH:29]=2)=[O:27])=[CH:22][C:21]=1[N+:40]([O-:42])=[O:41]>>[NH2:16][C:20]1[CH:25]=[CH:24][C:23]([S:26]([C:28]2[CH:33]=[CH:32][C:31]([C:34]3[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=3)=[CH:30][CH:29]=2)=[O:27])=[CH:22][C:21]=1[N+:40]([O-:42])=[O:41]Participants
3
Procedure
The procedure described in Example 1 is followed, except that as a starting material instead of phenyl-(4-chloro-3-nitrophenyl) sulfoxide a corresponding amount of 4-(4-chloro-3-nitrophenyl-sulfinyl)-biphenyl is employed.
Sources & evidence
- ORD record
- ord-148f722f6ac64d12bf52f5782f409fa6
- Source dataset
- uspto-grants-1990_09
- Patent number
- US04956007
Reaction notes
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