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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379837Generated: October 31, 2026

Dimethyl N-cyanodithioiminocarbonate → HCID 178503905, compound

https://huagongshe.com/reaction/2379837

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl N-cyanodithioiminocarbonateHCID 66289—
ReactantHCID 18953880HCID 18953880—
SolventEthanolHCID 702—
ProductHCID 178503905HCID 178503905—

Reaction Steps

A mixture of 4-(2-aminomethylthiazol-5-yl)-2-(diaminomethyleneamino)thiazole (0.45 g) and dimethyl N-cyanodithioiminocarbonate [(CH3S)2C=N-CN] (0.26 g) in ethanol (10 ml) was refluxed for 5 hours with stirring to give 4-[2-(3-cyano-2-methylisothioureido)methylthiazol-5-yl]-2-(diaminomethyleneamino)thiazole as a crude product. After cooling to ambient temperature, 40% aqueous methylamine by weight (1.4 ml) was added to the suspension and the mixture was stirred for 12 hours at ambient temperature. The solvent was evaporated in vacuo and the residue was mixed with water (5 ml) and ethyl acetate (5 ml). The resulting precipitate was collected and recrystallized from aqueous N,N-dimethylformamide to give 4-[2-(2-cyano-3-methylguanidino)methylthiazol-5-yl]-2-(diaminomethyleneamino)thiazole (0.35 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364871
Source datasetuspto-grants-1994_11
ORD IDord-f271e47e273d4859b6a0784a994b8588
Source noteuspto-grants-1994_11