HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354610Generated: October 25, 2026
Hydrochloric Acid → HCID 178485078, compound
https://huagongshe.com/reaction/354610
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | HCID 178485061 | HCID 178485061 | — |
| Product | HCID 178485078 | HCID 178485078 | — |
Reaction Steps
About 0.6 g. of N-methyl-N'-2-([2-(dimethylaminomethyl)-4-thiazolyl]methylthio)ethyl-N"-cyanoguanidine were dissolved in 8 ml. of 1.5 N aqueous hydrochloric acid. The resulting solution was allowed to remain at ambient temperature for about four days. Volatile constituents were then removed by evaporation in vacuo. The resulting residue, comprising N-methyl-N'-2-([2-(dimethylaminomethyl)-4-thiazolyl]methylthio)ethyl-N"-aminocarbonylguanidine dihydrochloride formed in the above reaction, was dissolved in ethanol and the ethanol removed by evaporation. The residue obtained thereby was recrystallized from isopropanol. The crystalline product was collected and digested with ethyl acetate. The ethyl acetate was removed by evaporation and the product obtained was crystallized from isopropanol to yield N-methyl-N'-2-([2-(dimethylaminomethyl)-4-thiazolyl]methylthio)ethyl-N"-aminocarbonylguanidine dihydrochloride melting at 156.5°-159.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04375547 |
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| Source dataset | uspto-grants-1983_03 |
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| ORD ID | ord-0a04287a4c2f44eea41feeda0c08726f |
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| Source note | uspto-grants-1983_03 |
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