2-(Tributylstannyl)pyrazine → HCID 67484199, compound
Reaction equation
Br[C:2]1[CH:3]=[C:4]([N:8]2[C:12]3[CH:13]=[CH:14][C:15]([CH2:17][N:18]4[C:26](=[O:27])[C:25]5[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=5)[C:19]4=[O:28])=[CH:16][C:11]=3[N:10]=[CH:9]2)[CH:5]=[CH:6][CH:7]=1.C([Sn](CCCC)(CCCC)[C:34]1[CH:39]=[N:38][CH:37]=[CH:36][N:35]=1)CCC>>[N:35]1[CH:36]=[CH:37][N:38]=[CH:39][C:34]=1[C:2]1[CH:3]=[C:4]([N:8]2[C:12]3[CH:13]=[CH:14][C:15]([CH2:17][N:18]4[C:19](=[O:28])[C:20]5[C:25](=[CH:24][CH:23]=[CH:22][CH:21]=5)[C:26]4=[O:27])=[CH:16][C:11]=3[N:10]=[CH:9]2)[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
This was prepared analogously from 2-[1-(3-bromo phenyl)-1H-benzimidazole-5-yl methyl]-isoindole-1,3-dione and 2-tri butylstannylpyrazine.
Sources & evidence
- ORD record
- ord-c89dbd0708a248df92a3606a21c69f80
- Source dataset
- uspto-grants-2010_12
- Patent number
- US07851490B2
Reaction notes
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