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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370580Generated: October 30, 2026

Dimethyl N-cyanodithioiminocarbonate → HCID 178503889, compound

https://huagongshe.com/reaction/370580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl N-cyanodithioiminocarbonateHCID 66289—
ReactantHCID 13269217HCID 13269217—
SolventEthanolHCID 702—
ProductHCID 178503889HCID 17850388925.1%

Reaction Steps

A mixture of 20 g of 3-amino-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide and 8.8 g of dimethyl cyanodithioiminocarbonate in 150 ml of absolute ethanol is heated with reflux for 30 hours, then it is concentrated under reduced pressure and the crude oil thus obtained is poured on a silica column and eluted with a mixture chloroform:methanol 4:1. The fairly pure fractions are collected and the solvent is evaporated under reduced pressure. Thus, 6.5 g of 3-(3-cyano-2-methylisothioureido)-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide are obtained as an oil which is mixed with 10 ml of a 33% solution of methylamine in ethanol. The mixture thus obtained is left to stand 48 hours at room temperature, then the excess of methylamine is eliminated under reduced pressure. Thus 5 g of an oil are obtained which is submitted to a flash chromatography on silica by eluting with a mixture chloroform:ethanol 1:1. The pure fractions are collected and evaporated, the residue is crystallized twice from isopropanol. Thus, 2.5 g of 3-(2-cyano-3-methylguanidino)-N-[2-(5-dimethylaminomethylfuran-2-ylmethylthio)ethyl]benzamide are obtained; m.p. 140°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04526995
Source datasetuspto-grants-1985_07
ORD IDord-85960da6f7584fba9f5c1dc576ff1282
Source noteuspto-grants-1985_07