Benzamidine → HCID 178454583, compound

HRID 2295338Notes

Reaction equation

HRID 2295338 reaction equation
[CH:1]([NH2:3])=[NH:2].C(N)(=[NH:6])C.C(N)(=N)C1C=CC=CC=1.C(N=[C:25]1[CH2:32][CH2:31]CCN[C:26]1=[O:27])C1C=CC=CC=1.C(NC(=NCC1C=CC=CC=1)C1C=CC=CC=1)C.C(NC(=NCC1C=CC=CC=1)C)(C)(C)C.C(NNC(=NCC1C=CC=CC=1)C)CCC>>[C:26]([NH:2][C:1]([NH2:6])=[NH:3])(=[O:27])[CH2:25][CH2:32][CH3:31]

Participants

8

Reactant 7

HCID 2332BenzamidineHCID 67171AcetamidineHCID 68047FormamidineHCID 19763484HCID 19763484, compoundHCID 20455774HCID 20455774, compoundHCID 21693434HCID 21693434, compoundHCID 131713356HCID 131713356, compound

Product 1

HCID 178454583HCID 178454583, compound

Procedure

The following compounds are also suitable amidines for salt formation: formamidine, acetamidine, caproylamidine, benzamidine, benzylimino-caprolactam, n- and t-butyl-iminocaprolactam, N-ethyl-N'-benzyl-benzamidine, N-t-butyl-N'-benzyl-acetamidine and N-n-butylamino-N'-benzyl-acetamidine.

Sources & evidence

ORD record
ord-539e7ec4a8c84a8c893fc48c805800e2
Source dataset
uspto-grants-1984_01
Patent number
US04424313

Reaction notes

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