Hydrochloric Acid → HCID 178433693, compound
Reaction equation
[CH3:1][C:2]1[NH:6][CH:5]=[N:4][C:3]=1[CH2:7][S:8][CH2:9][CH2:10][NH2:11].[C:12]([O-:17])(=[S:16])[C:13]([NH2:15])=[O:14].[K+].Cl>O>[CH3:1][C:2]1[NH:6][CH:5]=[N:4][C:3]=1[CH2:7][S:8][CH2:9][CH2:10][NH:11][NH:15][C:13](=[O:14])[C:12]([OH:17])=[S:16]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(5-Methyl-4-imidazolylmethylthio)ethylamine is added to a solution of potassium thiooxamate in water. After 2 hours at room temperature the solution is acidified with hydrochloric acid to yield N-[2-(5-methyl-4-imidazolylmethylthio)ethylamino]thiooxamic acid. This is then reacted with 2-(5-methyl-4-imidazolylmethylthio)ethylamine and trilead tetroxide according to the general procedure of Example 2 to yield N,N'-bis-[2-(5-methyl-4-imidazolylmethylthio)ethyl]amidinoformic acid.
Sources & evidence
- ORD record
- ord-1210da263ee442bda39f9dacdc9baaf2
- Source dataset
- uspto-grants-1984_03
- Patent number
- US04438127
Reaction notes
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