4-Iodoaniline → 1-(2-Amino-1-benzimidazolyl)-4-iodobenzene
Reaction equation
[I:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[CH:4][CH:3]=1.[NH2:9][C:10]1N(C2C=CC=C(I)C=2)[C:13]2[CH:22]=[CH:23][CH:24]=[CH:25][C:12]=2[N:11]=1>>[NH2:9][C:10]1[N:6]([C:5]2[CH:7]=[CH:8][C:2]([I:1])=[CH:3][CH:4]=2)[C:13]2[CH:22]=[CH:23][CH:24]=[CH:25][C:12]=2[N:11]=1Participants
3
Procedure
1-(2-Amino-1-benzimidazolyl)-4-iodobenzene (mp 212°-214° C. ) was prepared from 4-iodoaniline via 4-iodo-2'-nitrodiphenylamine (mp 174°-175° C.) and 4-iodo-2'-aminodiphenylamine (mp 127°-128° C.), in analogy with the sequence used in the preparation of 1-(2-amino-1-benzimidazolyl)-3-iodobenzene.
Sources & evidence
- ORD record
- ord-4672dfb4a28f432baa5544e935121665
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441969
Reaction notes
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