Hydrochloric Acid → HCID 178433315, compound
Reaction equation
C([NH:3][C:4]([NH:16][CH2:17][CH2:18][NH2:19])=[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:20]>>[ClH:20].[ClH:20].[ClH:20].[NH2:19][CH2:18][CH2:17][NH:16][C:4]([NH:5][CH2:6][CH2:7][S:8][CH2:9][C:10]1[NH:14][CH:13]=[N:12][C:11]=1[CH3:15])=[NH:3]Participants
3
Procedure
N-Cyano-N'-(2-aminoethyl)-N"-[2-((4-methyl-5-imidazolyl)methylthio)ethyl]guanidine (1.0 g) (see Example 10) for 1 N hydrochloric acid (20 ml) were refluxed together for 6 hours. Evaporation and crystallisation from methanol/isopropanol gave the title compound (0.6 g), m.p. 195°-196° C.
Workup
- customEvaporation and crystallisation from methanol/isopropanol
Sources & evidence
- ORD record
- ord-42d60a7db4a342dfb19aec8329e8b332
- Source dataset
- uspto-grants-1981_01
- Patent number
- US04247558
Reaction notes
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