N-[(4-Chlorophenyl)methyl]pyridin-2-amine → HCID 54561139, compound
Reaction equation
Cl[CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH:7]([NH:10][C:11](=[O:21])[C:12]2[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=2)[CH2:6][CH2:5]1.[Cl:22][C:23]1[CH:36]=[CH:35][C:26]([CH2:27][NH:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=2)=[CH:25][CH:24]=1>>[Cl:22][C:23]1[CH:36]=[CH:35][C:26]([CH2:27][N:28]([CH2:2][CH2:3][N:4]2[CH2:9][CH2:8][CH:7]([NH:10][C:11](=[O:21])[C:12]3[CH:17]=[CH:16][C:15]([N+:18]([O-:20])=[O:19])=[CH:14][CH:13]=3)[CH2:6][CH2:5]2)[C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][N:30]=2)=[CH:25][CH:24]=1Participants
3
Procedure
The title compound is prepared in a manner similar to Example 11 using 1-(2-chloroethyl)-4-(p-nitrobenzamido)piperidine and 2-(p-chlorobenzyl)aminopyridine.
Sources & evidence
- ORD record
- ord-f503d32227bb4a97a384d74ad284a8c6
- Source dataset
- uspto-grants-1977_05
- Patent number
- US04024147
Reaction notes
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