1-Cyano-2,3-dimethylisothiourea → 1-Cyano-2-methyl-3-(2-(((5-methyl-1H-imidazol-4-yl)methyl)thio)ethyl)isothiourea
Reaction equation
[NH2:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[N:7]=[CH:8][NH:9][C:10]=1[CH3:11].[C:12]([NH:14][C:15](=NC)[S:16][CH3:17])#[N:13]>>[C:12]([NH:14][C:15](=[N:1][CH2:2][CH2:3][S:4][CH2:5][C:6]1[N:7]=[CH:8][NH:9][C:10]=1[CH3:11])[S:16][CH3:17])#[N:13]Participants
3
Procedure
Furthermore, the final compound I can be obtained by reacting 4-[(2-aminoethyl)-thiomethyl]-5-methyl imidazole with N-cyano-N',S-dimethylisothiourea or with dimethylcyanodithioimido carbonate to form N-cyano-N'-{2-[(5-methylimidazole-4-yl)-methylthio]-ethyl}-S-methylisothiourea, which reacts with methylamine, thus yielding the final compound I.
Sources & evidence
- ORD record
- ord-283a9fab509d42b290276d309c3385d8
- Source dataset
- uspto-grants-1980_04
- Patent number
- US04200761
Reaction notes
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