4-Chloro-2-hydroxybenzonitrile → [4-(5-Chloro-2-cyanophenoxy)-4-(2-methoxy-3-pyridinyl)butyl]carbamic acid 1,1-dimethylethyl ester
Reaction equation
[CH3:1][C:2]([O:5][C:6](=[O:21])[NH:7][CH2:8][CH2:9][CH2:10][CH:11]([OH:20])[C:12]1[C:13]([O:18][CH3:19])=[N:14][CH:15]=[CH:16][CH:17]=1)([CH3:4])[CH3:3].[Cl:22][C:23]1[CH:30]=[CH:29][C:26]([C:27]#[N:28])=[C:25](O)[CH:24]=1>>[CH3:4][C:2]([O:5][C:6](=[O:21])[NH:7][CH2:8][CH2:9][CH2:10][CH:11]([O:20][C:29]1[CH:30]=[C:23]([Cl:22])[CH:24]=[CH:25][C:26]=1[C:27]#[N:28])[C:12]1[C:13]([O:18][CH3:19])=[N:14][CH:15]=[CH:16][CH:17]=1)([CH3:1])[CH3:3]Participants
3
Procedure
The sub-title compound was prepared by the method of Example 1 step (b) using the product of step (b) above and 4-chloro-2-hydroxybenzonitrile.
Sources & evidence
- ORD record
- ord-7b24bacd93774db681516064a0623a64
- Source dataset
- uspto-grants-2004_06
- Patent number
- US06743939B2
Reaction notes
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