3-(Phenylsulfonyl)-8-quinolinamine → 8-Amino-6-methyl-3-phenylsulfonylquinoline
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]2[C:9](=[C:10]([N+:12]([O-])=O)[CH:11]=1)[N:8]=[CH:7][C:6]([S:15]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)(=[O:17])=[O:16])=[CH:5]2.NC1C=CC=C2C=1N=CC(S(C1C=CC=CC=1)(=O)=O)=C2>>[NH2:12][C:10]1[CH:11]=[C:2]([CH3:1])[CH:3]=[C:4]2[C:9]=1[N:8]=[CH:7][C:6]([S:15]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)(=[O:17])=[O:16])=[CH:5]2Participants
3
Procedure
Prepared from 6-methyl-8-nitro-3-phenylsulfonylquinoline (D24) in an analogous process to that described in Description 5 (D5);
Sources & evidence
- ORD record
- ord-a8e48ad4146d463b87e899e1299e838f
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08236947B2
Reaction notes
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