4-Chloro-2-fluorobenzonitrile → [3-(5-Chloro-2-cyanophenoxy)pentyl]methylcarbamic acid, 1,1-dimethylethyl ester
Reaction equation
[OH:1][CH:2]([CH2:14][CH3:15])[CH2:3][CH2:4][N:5]([CH3:13])[C:6](=[O:12])[O:7][C:8]([CH3:11])([CH3:10])[CH3:9].[Cl:16][C:17]1[CH:24]=[CH:23][C:20]([C:21]#[N:22])=[C:19](F)[CH:18]=1>>[Cl:16][C:17]1[CH:18]=[CH:19][C:20]([C:21]#[N:22])=[C:23]([CH:24]=1)[O:1][CH:2]([CH2:14][CH3:15])[CH2:3][CH2:4][N:5]([CH3:13])[C:6](=[O:12])[O:7][C:8]([CH3:10])([CH3:11])[CH3:9]Participants
3
Procedure
The title compound was prepared according to the method of Example 3 step (b) but using (3-hydroxypentyl)methylcarbamic acid, 1,1-dimethylethyl ester and 4-chloro-2-fluorobenzonitrile.
Sources & evidence
- ORD record
- ord-ac6a0ebfb43741f08ae243912c5f8d6a
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06900243B2
Reaction notes
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