Boron tribromide → HCID 66699206, compound
Reaction equation
[Cl:1][C:2]1[C:3](=[O:26])[N:4]([CH3:25])[CH:5]=[C:6]([C:8]([OH:24])([C:20]([F:23])([F:22])[F:21])[CH:9]([C:11]2[CH:16]=[CH:15][C:14]([O:17]C)=[CH:13][C:12]=2[Cl:19])[CH3:10])[CH:7]=1.B(Br)(Br)Br>>[Cl:1][C:2]1[C:3](=[O:26])[N:4]([CH3:25])[CH:5]=[C:6]([C:8]([OH:24])([C:20]([F:22])([F:23])[F:21])[CH:9]([C:11]2[CH:16]=[CH:15][C:14]([OH:17])=[CH:13][C:12]=2[Cl:19])[CH3:10])[CH:7]=1Participants
3
Procedure
In analogy to Example 147, step 5, 3-chloro-5-[2-(2-chloro-4-methoxy-phenyl)-1-hydroxy-1-trifluoromethyl-propyl]-1-methyl-1H-pyridin-2-one was reacted with BBr3 to give the title compound as an off-white solid. MS (m/e, ISP neg. ion)=393.8 [M−H+].
Sources & evidence
- ORD record
- ord-32d2bd4f4f6a4059b2233d73940f52e1
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08138189B2
Reaction notes
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