Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908595Generated: October 25, 2026

Cyanamide → (1-[6-[Pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-lambda4-sulfanylidenecyanamide

https://huagongshe.com/reaction/1908595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanamideHCID 9864—
ReactantIodo benzene diacetateHCID 12217721—
Reactant5-(1-Methylthioethyl)-2-pentafluoroethylpyridineHCID 59218602—
SolventTetrahydrofuranHCID 8028—
Product(1-[6-[Pentafluoroethyl]pyridin-3-yl]ethyl)(methyl)-lambda4-sulfanylidenecyanamideHCID 5921861685.7%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of the 5-(1-methylthioethyl)-2-pentafluoro-ethylpyridine (A) (0.16 g, 0.6 mmol) and cyanamide (0.025 g, 0.6 mmol) in THF (3 mL) cooled to 0° C. was added iodobenzene diacetate (0.19 g, 0.6 mmol) in one portion and the resulting mixture was stirred at 0° C. for 2 h and then at room temperature overnight. The solvent was removed in vacuo and the resulting mixture was suspended in brine-saturated NaHCO3 (9:1), which was then extracted with CH2Cl2-EtOAc (1:1, v/v) two times. The combined organic layer was dried over Na2SO4, filtered, concentrated, and dried to give 0.16 g of (1-{6-[pentafluoroethyl]pyridin-3-yl}ethyl)(methyl)-λ4-sulfanylidenecyanamide (B) as a brownish oil in 85% yield. LC-MS: mass calcd for C11H10F5N3S [M]+ 311.28. Found [M−1]+ 309.84

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598214B2
Source datasetuspto-grants-2013_12
ORD IDord-8020fc61ab444fdf932ecf9488f79e7e
Source noteuspto-grants-2013_12