2-Aminopyridine → 2-Oxo-2-(4-phenylpiperidin-1-yl)ethyl 2-(2'-chloro[1,1'-biphenyl]-4-yl)propanoate
Reaction equation
N[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[C:8](O)(=O)[C:9](O)=O.[Cl:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:21]1[CH:26]=[CH:25][C:24]([CH:27]([CH3:34])[C:28]([O:30][CH2:31][CH:32]=[O:33])=[O:29])=[CH:23][CH:22]=1>>[Cl:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[C:21]1[CH:26]=[CH:25][C:24]([CH:27]([CH3:34])[C:28]([O:30][CH2:31][C:32]([N:3]2[CH2:4][CH2:5][CH:6]([C:9]3[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=3)[CH2:7][CH2:2]2)=[O:33])=[O:29])=[CH:23][CH:22]=1Participants
3
Procedure
2-(2-aminopyridine(-2-oxoethyl 2-(2'-chloro-4-biphenylyl)propionate oxalate.
Sources & evidence
- ORD record
- ord-ebb652dcd7b1461aaf55d4e49a251802
- Source dataset
- uspto-grants-1985_04
- Patent number
- US04510142
Reaction notes
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