2-(Trimethylstannyl)furan → 2-Amino-1-[3-(2-furyl)-4-methylphenyl]benzimidazole
Reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[C:9](I)[CH:8]=2)[C:5]2[CH:15]=[CH:16][CH:17]=[CH:18][C:4]=2[N:3]=1.C[Sn](C)(C)[C:21]1[O:22][CH:23]=[CH:24][CH:25]=1>>[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][C:10]([CH3:13])=[C:9]([C:21]3[O:22][CH:23]=[CH:24][CH:25]=3)[CH:8]=2)[C:5]2[CH:15]=[CH:16][CH:17]=[CH:18][C:4]=2[N:3]=1Participants
3
Procedure
2-Amino-1-[3-(2-furyl)-4-methylphenyl]benzimidazole was prepared from 4-(2-amino-1-benzimidazolyl)-2-iodotoluene and 2-trimethylstannylfuran according to method C. mp 155°-157° C.
Sources & evidence
- ORD record
- ord-e1151d07b0ba4204aab2070d1e274ea3
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441969
Reaction notes
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