Cyclohexene → 4-[1-propyl-7-(trifluoromethyl)-1H-indazol-3-yl]phenol
Reaction equation
C[O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:17]3[C:12](=[C:13]([C:18]([F:21])([F:20])[F:19])[CH:14]=[CH:15][CH:16]=3)[N:11]([CH2:22][CH2:23][CH3:24])[N:10]=2)=[CH:5][CH:4]=1.B(Br)(Br)Br.C1CCCCC=1>>[CH2:22]([N:11]1[C:12]2[C:17](=[CH:16][CH:15]=[CH:14][C:13]=2[C:18]([F:21])([F:20])[F:19])[C:9]([C:6]2[CH:5]=[CH:4][C:3]([OH:2])=[CH:8][CH:7]=2)=[N:10]1)[CH2:23][CH3:24]Participants
4
Procedure
Prepared according to Method D step C from 3-(4-methoxyphenyl)-1-propyl-7-trifluoromethyl-1H-indazole (0.058 g, 0.17 mmol), boron tribromide (0.094 mL, 1.0 mmol) and 0.3 mL of cyclohexene to give the product (0.047 g) as an off-white solid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-e886ab030565404bb64b74fc2fce23fa
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07241791B2
Reaction notes
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