4-Benzylideneaminopyridine → N-[alpha-(2-benzthiazolyl)benzyl]-4-pyridinamine
Reaction equation
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[Li].[CH:11](=[N:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:11]([NH:18][C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1Participants
3
Procedure
The title compound is prepared in a manner similar to Examples 5, 6 and 7 by reacting 2-benzthiazolyl lithium (formed by treating benzothiazole with butyl lithium) and 4-benzylideneaminopyridine.
Sources & evidence
- ORD record
- ord-135cf0490f064acda3d9adaa3dc4f58b
- Source dataset
- uspto-grants-1979_12
- Patent number
- US04180670
Reaction notes
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