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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702482Generated: October 31, 2026

Hydrochloric Acid → HCID 178485068, compound

https://huagongshe.com/reaction/1702482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPhosphorus pentachlorideHCID 24819—
ReactantN-cyano-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]thioureaHCID 12918615—
ReactantHCID 178433674HCID 178433674—
SolventDichloromethaneHCID 6344—
ProductHCID 178485068HCID 1784850681.5%

Reaction Steps

To a suspension of N-cyano-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]thiourea (monohydrate, 765 mg) in CH2Cl2 (7 ml) was introduced dry HCl gas for a few minutes under ice-cooling. PCl5 (1.25 g) was added to the mixture and stirred at room temperature for 3 hrs. The reaction mixture containing N'-cyano-N-[2-(5-methylimidazol-4-ylmethylthio)ethyl]chloroformamidine was concentrated to small volume, diluted with CH2Cl2 (5 ml) and cooled to -5° C. To the mixture was added a solution of CH3NH2 in C2H5OH (40%, 15 ml) below 30° C. After stirring for 20 hrs. at room temperature, the reaction mixture was filtered and the filtrate was concentrated to small volume, diluted with CH3CN and filtered agein. The filtrate was dried up and the residue was purified with column chromatography [SiO2, CH3CN-CH3OH (4:1)], preparative thin layer chromatography [SiO 2, CH3COOC2H5 --CH3OH-- 28% NH3 (aq) (10:1:1)] and then recrystallization from CH3CN to give N"-cyano-N-methyl-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]guanidine (10.4 mg). Yield 1.5%, m.p. 136.5°-138° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381395
Source datasetuspto-grants-1983_04
ORD IDord-8dd19c4da9c64f988c05a425f1015eac
Source noteuspto-grants-1983_04