4-Bromophenacyl bromide → 2,3-Dimethyl-7-(p-bromophenacyl)pyrrolo[2,3-b]pyridine, hydrobromide
Reaction equation
[CH3:1][C:2]1[NH:10][C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]=1[CH3:11].[Br:12][C:13]1[CH:22]=[CH:21][C:16]([C:17](=[O:20])[CH2:18]Br)=[CH:15][CH:14]=1>>[BrH:12].[CH3:1][C:2]1[N:10]=[C:5]2[N:6]([CH2:18][C:17]([C:16]3[CH:21]=[CH:22][C:13]([Br:12])=[CH:14][CH:15]=3)=[O:20])[CH:7]=[CH:8][CH:9]=[C:4]2[C:3]=1[CH3:11]Participants
3
Procedure
This compound was prepared by reacting 2,3-dimethylpyrrolo [2,3-b]pyridine with p-bromophenacyl bromide following the procedure in example 8.
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-5d4c422353cc4f678cadcc80b54fffe5
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05439917
Reaction notes
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