Hydrochloric Acid → HCID 178485117, compound
Reaction equation
[C:1]([NH:3][C:4]([NH:16]C)=[N:5][CH2:6][CH2:7][S:8][CH2:9][C:10]1[NH:14][CH:13]=[N:12][C:11]=1[CH3:15])#N.[ClH:18]>>[ClH:18].[ClH:18].[CH3:1][NH:3][C:4]([NH2:16])=[N:5][CH2:6][CH2:7][S:8][CH2:9][C:10]1[NH:14][CH:13]=[N:12][C:11]=1[CH3:15]Participants
3
Procedure
A solution of N-cyano-N'-methyl-N"-[2-((4-methyl-5-imidazolyl)-methylthio)ethyl]guanidine (2.0 g.) in hydrochloric acid (25 ml.) was heated on the steam bath for 2 hours. Concentration followed by recrystallisation of the product from ethanol-ether afforded N-methyl-N"-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]guanidine dihydrochloride (1.44 g.) m.p. 204°-206°.
Workup
- concentrationConcentration
- customfollowed by recrystallisation of the product from ethanol-ether
Sources & evidence
- ORD record
- ord-f57a61dc65bf499fb2a6e1048999863f
- Source dataset
- uspto-grants-1978_12
- Patent number
- US04129657
Reaction notes
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