4-Chloro-2-hydroxybenzonitrile → HCID 131724957, compound
Reaction equation
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([C:6]#[N:7])=[C:4]([OH:10])[CH:3]=1.O[CH:12]([CH2:24][CH:25]([CH3:27])[CH3:26])[CH2:13][CH2:14][N:15]([CH3:23])[C:16](=[O:22])[O:17][C:18]([CH3:21])([CH3:20])[CH3:19]>>[CH3:21][C:18]([O:17][C:16](=[O:22])[N:15]([CH2:14][CH2:13][CH:12]([O:10][C:4]1[CH:3]=[C:2]([Cl:1])[CH:9]=[CH:8][C:5]=1[C:6]#[N:7])[CH2:24][CH:25]([CH3:26])[CH3:27])[CH3:23])([CH3:19])[CH3:20]Participants
3
Procedure
The title compound was prepared according to the method of Example 2 step (b) but using 4-chloro-2-hydroxybenzonitrile and (3-hydroxy-5-methylhexyl)methylcarbamic acid, 1,1-dimethylethyl ester.
Sources & evidence
- ORD record
- ord-827794918c4a42dc8185462d39ba331b
- Source dataset
- uspto-grants-2005_05
- Patent number
- US06900243B2
Reaction notes
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