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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732571Generated: October 31, 2026

Dimethyl N-cyanodithioiminocarbonate → HCID 20303949, compound

https://huagongshe.com/reaction/1732571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl N-cyanodithioiminocarbonateHCID 66289—
Reactant2-(2-Aminoethylthiomethyl)-6-(dimethylaminomethyl)benzofuranHCID 20303964—
SolventAcetonitrileHCID 6342—
ProductHCID 20303949HCID 20303949—

Reaction Steps

A solution of 2-(2-aminoethylthiomethyl)-6-(dimethylaminomethyl)benzofuran (12.0 g, 0.0454 mole) and dimethyl cyanodithioimidocarbonate (7.0 g., 0.048 mole) in acetonitrile (48 ml.) is allowed to stand 2 hours at room temperature. The solvent is evaporated at reduced pressure and the viscous oily residue is chromatographed on a column of 250 g. of silica gel. Elution with 8% methanol in chloroform removes the product. There is obtained 14.6 g. (89%) of N-cyano-N'-[2-(6-dimethylaminomethyl-2-(benzofuranylmethylthio)ethyl]-S-methylisothiourea as a yellow oil which gradually crystallizes, m.p. 98°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04238487
Source datasetuspto-grants-1980_12
ORD IDord-b11b07b9a3a34b868ccc4f6c41942912
Source noteuspto-grants-1980_12