HCID 459925, compound → HCID 459949, compound
Reaction equation
N1([C:6]2[CH:33]=[CH:32][C:9]3[N:10]=[C:11]([C:13]4[NH:14][C:15]([C:18]5[NH:19][C:20]6[CH:26]=[C:25](N7CCN=C7)[CH:24]=[CH:23][C:21]=6[N:22]=5)=[CH:16][CH:17]=4)[NH:12][C:8]=3[CH:7]=2)CCN=C1.[N:34]1(C2C=CC3N=C(C4C=CC=C(C5NC6C=C(N7CCN=C7)C=CC=6N=5)N=4)NC=3C=2)CC[N:36]=[CH:35]1.CN1C([C:74]2[NH:75]C3C=C(C(=N)N)C=CC=3[N:78]=2)=CC=C1C1NC2C=C(C(=N)N)C=CC=2N=1.CN1C(C2NC3C=C(C4NC=CN=4)C=CC=3N=2)=CC=C1C1NC2C=C(C3NC=CN=3)C=CC=2N=1.CN1C(C2NC3C=C(C4NCCCN=4)C=CC=3N=2)=CC=C1C1NC2C=C(C3NCCCN=3)C=CC=2N=1.C(C1C=CC2N=C(C(C3C=CC=C(C(C4NC5C=C(C(=N)N)C=CC=5N=4)=O)N=3)=O)NC=2C=1)(=N)N.N1CCCN=C1C1C=CC2N=C(C3C=CC=C(C4NC5C=C(C6NCCCN=6)C=CC=5N=4)N=3)NC=2C=1.C(C1C=CC2N=C(C3OC(C4NC5C=C(C(=N)N)C=CC=5N=4)=CC=3)NC=2C=1)(=N)N.N1(C2C=CC3N=C(C4OC(C5NC6C=C(N7CCN=C7)C=CC=6N=5)=CC=4)NC=3C=2)CCN=C1>>[C:35]([C:6]1[CH:33]=[CH:32][C:9]2[N:10]=[C:11]([C:13]3[NH:14][C:15]([C:18]4[NH:19][C:20]5[CH:26]=[C:25]([C:74](=[NH:75])[NH2:78])[CH:24]=[CH:23][C:21]=5[N:22]=4)=[CH:16][CH:17]=3)[NH:12][C:8]=2[CH:7]=1)(=[NH:34])[NH2:36]Participants
10
Reactant 9
Product 1
Procedure
2,5-bis-[5-(2-imidazolinyl)-2-benzimidazolyl]pyrrole; 2,6-bis[5-(2-imidazolinyl)-2-benzimidazolyl]pyridine; 1-methyl-2,5-bis(5-amidino-2-benzimidazolyl)pyrrole; 1-methyl-2,5-bis[5-(2-imidazolyl)-2-benzimidazolyl]pyrrole; 1-methyl-2,5-bis[5-(1,4,5,6-tetrahydro-2-pyrimidinyl)-2-benzimidazolyl]pyrrole; 2,6-bis(5-amidino-2-benzimidazoyl)pyridine; 2,6-bis[5-(1,4,5,6-tetrahydro-2-pyrimidinyl)-2-benzimidazolyl]pyridine; 2,5-bis(5-amidino-2-benzimidazolyl)furan; 2,5-bis[5-(2-imidazolinyl)-2-benzimidazolyl]furan; 2,5-bis(5-N-isopropylamidino-2-benzimidazolyl)furan; and physiologically acceptable salts thereof.
Sources & evidence
- ORD record
- ord-554f8f10f6cb4fb7ba1b71e27a16d87e
- Source dataset
- uspto-grants-1999_08
- Patent number
- US05939440
Reaction notes
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