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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1491842Generated: October 31, 2026

Dimethyl N-cyanodithioiminocarbonate → HCID 178503902, compound

https://huagongshe.com/reaction/1491842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl N-cyanodithioiminocarbonateHCID 66289—
Reactant4-(6-Aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazoleHCID 10399768—
SolventEthanolHCID 702—
ProductHCID 178503902HCID 178503902—

Reaction Steps

A mixture of 4-(6-aminomethylpyridin-2-yl)-2-(diaminomethyleneamino)thiazole (0.50 g) and dimethyl N-cyanodithioiminocarbonate [(CH3S)2C=N--CN] (0.29 g) in ethanol (10 ml) was refluxed for one hour to give 2-(diaminomethyleneamino)-4-[6-(3-cyano-2-methylisothioureido)methylpyridin-2-yl]thiazole of a crude product. After being concentrated to dry the above product, 40 weight % methanolic methylamine (1.6 ml) and N,N-dimethylformamide (10 ml) was added and the mixture was stirred at 60° C. for 5 hours. The solvent was evaporated in vacuo and the residue was mixed with water. The resulting precipitate was collected by filtration and recrystallized from aqueous N,N-dimethylformamide to give 4-[6-(2-cyano-3-methylguanidino)methylpyridin-2-yl]-2-(diaminomethyleneamino)thiazole (0.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05371097
Source datasetuspto-grants-1994_12
ORD IDord-10e81e1de69b431eade6c5cd27878962
Source noteuspto-grants-1994_12