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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702473Generated: October 30, 2026

Triethylamine → HCID 178485068, compound

https://huagongshe.com/reaction/1702473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(((2-Aminoethyl)thio)methyl)-5-methylimidazoleHCID 665568—
ReactantN-cyano-N'-methylchloroformamidineHCID 12918610—
SolventMethanolHCID 887—
ProductHCID 178485068HCID 17848506822.4%

Reaction Steps

To a stirred solution of 2-(5-methylimidazol-4-ylmethylthio)ethylamine (1.0 g) and triethylamine (0.71 g) in methanol (20 ml) was added N-cyano-N'-methylchloroformamidine (0.82 g) and stirred for 7.5 hrs. at 50°-55° C. After evaporation, the residue was subjected to chromatography on SiO2 [eluant: CHCl3 -MeOH (10:1)]. The resulting crude product was added to water (3 ml) and extracted repeatedly with ethyl acetate. Ethyl acetate extracts were dried over anhydrous MgSO4 and concentrated under a reduced pressure to small volume. The resulting crystals were collected by filtration and washed with ethyl acetate to give N"-cyano-N-methyl-N'-[2-(5-methylimidazol-4-ylmethylthio)ethyl]guanidine (0.33 g). Yield 22.4%, m.p. 134°-137° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381395
Source datasetuspto-grants-1983_04
ORD IDord-ab700c3708cf4166b010fdbf2e849a44
Source noteuspto-grants-1983_04