6-Azaindole → (4-Bromo-2,6-dichlorophenyl)(1H-pyrrolo[2,3-c]pyridin-3-yl)methanone
Reaction equation
[NH:1]1[C:5]2=[CH:6][N:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.[Br:10][C:11]1[CH:19]=[C:18]([Cl:20])[C:14]([C:15](Cl)=[O:16])=[C:13]([Cl:21])[CH:12]=1>>[Br:10][C:11]1[CH:12]=[C:13]([Cl:21])[C:14]([C:15]([C:3]2[C:4]3[C:5](=[CH:6][N:7]=[CH:8][CH:9]=3)[NH:1][CH:2]=2)=[O:16])=[C:18]([Cl:20])[CH:19]=1Participants
3
Procedure
(4-Bromo-2,6-dichlorophenyl)(1H-pyrrolo[2,3-c]pyridin-3-yl)methanone was prepared from 1H-Pyrrolo[2,3-c]pyridine and 4-bromo-2,6-dichloro benzoyl chloride (Compound No. 10).
Sources & evidence
- ORD record
- ord-0cef2d7aab62439cba2d64f95c71fcbd
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08980911B2
Reaction notes
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