Cyclohexene → HCID 136358460, compound
Reaction equation
C[O:2][C:3]1[CH:8]=[C:7]([O:9]C)[CH:6]=[CH:5][C:4]=1[C:11]1[C:19]2[C:14](=[C:15]([F:20])[CH:16]=[CH:17][CH:18]=2)[N:13]([CH:21]([CH3:23])[CH3:22])[N:12]=1.B(Br)(Br)Br.C1CCCCC=1>>[F:20][C:15]1[CH:16]=[CH:17][CH:18]=[C:19]2[C:14]=1[N:13]([CH:21]([CH3:23])[CH3:22])[N:12]=[C:11]2[C:4]1[CH:5]=[CH:6][C:7]([OH:9])=[CH:8][C:3]=1[OH:2]Participants
4
Procedure
Prepared according to Method D step C from 3-(2,4-dimethoxyphenyl)-7-fluoro-1-isopropyl-1H-indazole (0.213 g, 0.68 mmol), boron tribromide (0.513 mL, 5.0 mmol) and 1.0 mL of cyclohexene to give the product (0.160 g) as a white solid.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-2ec1aca9bcc0480ebd26f5dbe3227e9b
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07241791B2
Reaction notes
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