HCID 18785654, compound → HCID 18785653, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([C:13]1[NH:17][C:16]([CH3:18])=[C:15]([CH3:19])[CH:14]=1)=[O:12].[CH3:20][CH:21]1[CH2:23][CH:22]1[CH2:24]Br>>[F:1][C:2]1[CH:7]=[C:6]([F:8])[CH:5]=[CH:4][C:3]=1[CH2:9][CH2:10][C:11]([C:13]1[N:17]([CH2:20][CH:21]2[CH2:23][CH:22]2[CH3:24])[C:16]([CH3:18])=[C:15]([CH3:19])[CH:14]=1)=[O:12]Participants
3
Procedure
The title compound was prepared as a yellow oil in 80.2% yield in a similar procedure to that described in Referential Example 97 by using 5-[3-(2,4-difluorophenyl)propionyl]-2,3-dimethylpyrrole and 2-methylcyclopropylmethyl bromide.
Sources & evidence
- ORD record
- ord-d302945bed984dc8939cee0ce2b883bb
- Source dataset
- uspto-grants-2000_05
- Patent number
- US06063782
Reaction notes
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