m-(Dimethylamino)benzyl alcohol → HCID 86681314, compound
Reaction equation
CN(C)[C:3]1[CH:4]=[C:5]([CH2:9]O)[CH:6]=[CH:7][CH:8]=1.[Br:12][C:13]1[C:14]([CH3:20])=[C:15]([OH:19])[CH:16]=[CH:17][CH:18]=1.[CH3:21]C1(C)C(C)(C)OB(C2C=NNC=2)O1>>[Br:12][C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH:3]2[CH2:8][CH2:7][CH2:6][C:5]([CH3:9])([CH3:21])[CH2:4]2)[C:14]=1[CH3:20]Participants
4
Procedure
The title compound was prepared by substituting 3,3-dimethylcyclohexanol for (3-(dimethylamino)phenyl)methanol and 3-bromo-2-methylphenol for 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole in EXAMPLE 34A.
Sources & evidence
- ORD record
- ord-dada172e2ddf4fac8f6b2a6797310fe1
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08940737B2
Reaction notes
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