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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164709Generated: November 1, 2026

Triethylamine → N-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazine

https://huagongshe.com/reaction/1164709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPerhydropyridazine hydroiodideHCID 12314334—
Reactant4-Chloro-2-fluoro-5-nitrophenylisothiocyanateHCID 14622954—
SolventDichloromethaneHCID 6344—
ProductN-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazineHCID 1462295596%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred, cold (-5° C.) solution of 8.56 g (0.0400 mole) of perhydropyridazine hydroiodide in 150 mL of methylene chloride was added dropwise 12.2 g (0.120 mole) of triethylamine. This mixture was stirred for approximately 30 minutes. A solution of 8.0 g (0.034 mole) of 4-chloro-2-fluoro-5-nitrophenylisothiocyanate in methylene chloride was added dropwise to the reaction mixture while maintaining a reaction temperature of -20° C. After complete addition, the reaction mixture was allowed to warm to room temperature and was stirred for two days. The solvent was removed from the mixture by evaporation under reduced pressure leaving a residue. The residue was subjected to column chromatography on silica gel, eluting with ethyl acetate:n-heptane (50:50), to yield 10.4 g of N-[(4-chloro-2-fluoro-5-nitrophenyl)aminothiocarbonyl]perhydropyridazine as a solid, mp 118°-120° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906281
Source datasetuspto-grants-1990_03
ORD IDord-3063a2a00e5c4d53b3db28b9d051684c
Source noteuspto-grants-1990_03