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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 437715Generated: October 25, 2026

Potassium Cyanide → N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidine

https://huagongshe.com/reaction/437715

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CyanideHCID 9032—
ReactantN'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidineHCID 53844528—
SolventAcetonitrileHCID 6342—
ProductN'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidineHCID 5383985863.8%

Reaction Steps

In the manner of Example VII, 7 g of N'-(4-cyano- 3-isopropyl-5-isothiazolyl)-N,N-dimethylchloroformamidine, 3.6 g of anhydrous potassium cyanide, and a catalytic amount of 2,3,11,12-dibenzo-1,4,7,10,13,16-hexaoxacycloocta- 2,11-diene in 200 ml of dry aceto-nitrile were allowed to react for several days. After solvents were removed under reduced pressure, the residue was recrystallized from methylcyclohexane to yield 4.3 g of N'-(4-cyano-3-isopropyl-5-isothiazolyl)-N,N-dimethylcyanoformamidine, mp 78°-79°. The ir and nmr spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04032322
Source datasetuspto-grants-1977_06
ORD IDord-4c0630ff68a241df971fa7fe671df2ed
Source noteuspto-grants-1977_06