Chlorosuccinimide → 4-(3-Chloro-6-phenylimidazo[1,2-a]pyrimidin-7-yl)benzaldehyde
Reaction equation
Br[C:2]1[N:6]2[CH:7]=[C:8]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:9]([C:11]3[CH:18]=[CH:17][C:14]([CH:15]=[O:16])=[CH:13][CH:12]=3)=[N:10][C:5]2=[N:4][CH:3]=1.C1C(=O)N([Cl:32])C(=O)C1>>[Cl:32][C:2]1[N:6]2[CH:7]=[C:8]([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[C:9]([C:11]3[CH:18]=[CH:17][C:14]([CH:15]=[O:16])=[CH:13][CH:12]=3)=[N:10][C:5]2=[N:4][CH:3]=1Participants
3
Procedure
The compound was synthesized in a manner according to 4-(3-bromo-6-phenylimidazo[1,2-a]pyrimidin-7-yl)benzaldehyde by using NCS instead of NBS.
Workup
- customThe compound was synthesized in a manner
Sources & evidence
- ORD record
- ord-233e06529b614dafbb6463d7b3fe9069
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08957064B2
Reaction notes
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