Cyclohexanol → 1369901-13-2
Reaction equation
C1(O)CCCCC1.CN(C)[C:10]1[CH:11]=[C:12](CO)[CH:13]=[CH:14][CH:15]=1.[Br:19][C:20]1[C:21]([Cl:27])=[C:22]([OH:26])[CH:23]=[CH:24][CH:25]=1.CC1(C)C(C)(C)OB(C2C=NNC=2)O1>>[Br:19][C:20]1[CH:25]=[CH:24][CH:23]=[C:22]([O:26][CH:10]2[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]2)[C:21]=1[Cl:27]Participants
5
Procedure
The title compound was prepared by substituting for cyclohexanol for (3-(dimethylamino)phenyl)methanol and 3-bromo-2-chlorophenol for 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 34A.
Sources & evidence
- ORD record
- ord-e3ecb0cc28da4c0683456f0363e9d60c
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940737B2
Reaction notes
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