Diethylamine → 3-[(4'-{[(2R,5R)-2,5-dimethylpyrrolidinyl]carbonyl}[1,1'-biphenyl]-4-yl)oxy]-N,N-diethyl-1-propanamine
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[CH:17]=[CH:16][C:15]([C:18]([N:20]3[C@H:24]([CH3:25])[CH2:23][CH2:22][C@H:21]3[CH3:26])=[O:19])=[CH:14][CH:13]=2)=[CH:8][CH:7]=1.[CH2:27]([NH:29][CH2:30][CH3:31])[CH3:28]>>[CH3:26][C@@H:21]1[CH2:22][CH2:23][C@@H:24]([CH3:25])[N:20]1[C:18]([C:15]1[CH:16]=[CH:17][C:12]([C:9]2[CH:10]=[CH:11][C:6]([O:5][CH2:4][CH2:3][CH2:2][N:29]([CH2:30][CH3:31])[CH2:27][CH3:28])=[CH:7][CH:8]=2)=[CH:13][CH:14]=1)=[O:19]Participants
3
Procedure
The product from Example 4A and diethylamine were processed as described in Example 10F to provide the title compound.
Sources & evidence
- ORD record
- ord-16a38cb0df644fa5ab88b27816fb7b95
- Source dataset
- uspto-grants-2001_11
- Patent number
- US06316475B1
Reaction notes
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