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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217259Generated: October 25, 2026

Cyanamide → HCID 178436275, compound

https://huagongshe.com/reaction/217259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantIodo benzene diacetateHCID 12217721—
Reactant5-[1-(Methylthio)ethyl]-2-(trichloromethyl)pyridineHCID 59218620—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178436275HCID 17843627540%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 5-[1-(methylthio)ethyl]-2-(trichloromethyl)-pyridine (B) (0.55 g, 2.3 mmol) and cyanamide (0.097 g, 2.3 mmol) in THF (7 mL) cooled to 0° C. was added iodobenzene diacetate (0.75 g, 2.3 mmol) in one portion. The resulting mixture was stirred at 0° C. for 1 hr and then at room temperature for 2 hr. The solvent was removed in vacuo and the resulting mixture was purified on silica gel using 50% acetone in hexane to give 0.254 g of (1E)-methyl {1-[6-(trichloromethyl)pyridin-3-yl]ethyl}-λ4-sulfanylidenecyanamide (C) as an off-white solid in 40% yield. 1H NMR for the diastereomeric mixture (300 MHz, d6-acetone) δ 8.87 (s, 1H), 8.21-8.25 (m, 2H), 4.65-4.76 (m, 1H), 2.86-2.66 (m, 3H), 1.88-1.92 (m, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08193364B2
Source datasetuspto-grants-2012_06
ORD IDord-59f4ff569add4922bc0dcd13b8df5609
Source noteuspto-grants-2012_06