4-Aminobenzoic Acid → 4-(2-(4-Aminophenyl)-1H-benzo[d]imidazol-6-yl)benzene-1,2-diamine
Reaction equation
[C:1]1([C:9]2[CH:14]=[CH:13][C:12]([NH2:15])=[C:11]([NH2:16])[CH:10]=2)[CH:6]=[CH:5][C:4]([NH2:7])=[C:3]([NH2:8])[CH:2]=1.[NH2:17][C:18]1[CH:26]=[CH:25][C:21]([C:22](O)=O)=[CH:20][CH:19]=1>>[NH2:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]2[NH:16][C:11]3[CH:10]=[C:9]([C:1]4[CH:2]=[C:3]([NH2:8])[C:4]([NH2:7])=[CH:5][CH:6]=4)[CH:14]=[CH:13][C:12]=3[N:15]=2)=[CH:20][CH:19]=1Participants
3
Procedure
Prepared by Method 1, using a 1:1 ratio of biphenyl-3,3′,4,4′-tetraamine to 4-aminobenzoic acid and a reaction time of 2 h.
Workup
- customPrepared by Method 1
- customa reaction time of 2 h.
Sources & evidence
- ORD record
- ord-e71913baa87142ef970f49cbc53c9c3f
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975416B2
Reaction notes
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