Allyl bromide → HCID 18785619, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][C:10]([C:12]2[NH:16][C:15]([CH3:17])=[C:14]([CH3:18])[CH:13]=2)=[O:11])=[CH:4][CH:3]=1.Br[CH2:20][CH:21]=[CH2:22]>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][CH2:9][C:10]([C:12]2[N:16]([CH2:22][CH:21]=[CH2:20])[C:15]([CH3:17])=[C:14]([CH3:18])[CH:13]=2)=[O:11])=[CH:6][CH:7]=1Participants
3
Procedure
The title compound was prepared as a pale yellow oil in 60.3% yield in a similar procedure to that described in Referential Example 97 by using. -5-[3-(4-fluorphenyl)propionyl)-2,3-dimethylpyrrole and 3-bromo-1-propene.
Sources & evidence
- ORD record
- ord-686ba6e05d92419e95d86cac070102e2
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063782
Reaction notes
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