Aniline → 6-(3-Chloro-phenyl)-pyridine-2-carboxylic acid phenylamide
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:8]2[N:13]=[C:12]([C:14]([OH:16])=O)[CH:11]=[CH:10][CH:9]=2)[CH:5]=[CH:6][CH:7]=1.[NH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>>[C:18]1([NH:17][C:14]([C:12]2[CH:11]=[CH:10][CH:9]=[C:8]([C:4]3[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=3)[N:13]=2)=[O:16])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
3
Procedure
The title compound was synthesized in analogy to Example 1, using 6-(3-chlorophenyl)-2-pyridinecarboxylic acid (CAN 863704-38-5) and aniline (CAN 62-53-3) as starting materials, MS (EI) m/e: 309.1 [M+H]+.
Sources & evidence
- ORD record
- ord-aeffe5cd0cf14db1b78d83e256d44759
- Source dataset
- uspto-grants-2016_04
- Patent number
- US09321727B2
Reaction notes
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