5-Azaindole → HCID 86720658, compound
Reaction equation
[NH:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1.[Cl:10][C:11]1[CH:19]=[C:18]([C:20](=[O:22])[NH2:21])[CH:17]=[C:16]([Cl:23])[C:12]=1[C:13](O)=[O:14]>>[Cl:10][C:11]1[CH:19]=[C:18]([CH:17]=[C:16]([Cl:23])[C:12]=1[C:13]([N:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[CH:3]=[CH:2]1)=[O:14])[C:20]([NH2:21])=[O:22]Participants
3
Procedure
3,5-Dichloro-4-(1H-pyrrolo[3,2-c]pyridin-1-ylcarbonyl)benzamide was prepared using 1H-pyrrolo[3,2-c]pyridine and 2,6-dichloro-4-carbamoyl benzoic acid.
Sources & evidence
- ORD record
- ord-1b5ad23c91a8461485b2a798830fc7c5
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08980911B2
Reaction notes
Loading…