Reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH:8]([CH3:10])[CH3:9])[C:3]=1[Cl:11].[C:12]1([CH:18]2[CH2:23][CH2:22][C:21](=O)[CH2:20][CH2:19]2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>>[Cl:11][C:3]1[C:4]([CH:8]([CH3:9])[CH3:10])=[N:5][CH:6]=[CH:7][C:2]=1[NH:1][C@H:21]1[CH2:20][CH2:19][C@@H:18]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH2:23][CH2:22]1Participants
3
Procedure
Was prepared analogously to Example 75 starting from 4-amino-3-chloro-2-isopropylpyridine and 4-phenylcyclohexanone. Yield: 26.6%
Sources & evidence
- ORD record
- ord-4950a24c3bb24e6eb853f7c03d0888b7
- Source dataset
- uspto-grants-1998_03
- Patent number
- US05723450
Linked notes
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