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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164710Generated: November 2, 2026

Pyridine → 9-(4-Chloro-2-fluoro-5-nitrophenyl)imino-8-thia-1,6-diazabicyclo[4.3.0]nonane-7-thione

https://huagongshe.com/reaction/1164710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantThiophosgeneHCID 10040—
ReactantN-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazineHCID 14622955—
SolventDichloromethaneHCID 6344—
Product9-(4-Chloro-2-fluoro-5-nitrophenyl)imino-8-thia-1,6-diazabicyclo[4.3.0]nonane-7-thioneHCID 1462295644.5%

Reaction Conditions

Temperature-5 °C

Reaction Steps

While maintaining a reaction temperature of -5° C., 7.75 g (0.0850 mole) of pyridine was added dropwise to a stirred solution of 9.0 g (0.028 mole) of N-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazine in 250 mL of methylene chloride. To this mixture was added dropwise 3.25 g (0.0282 mole) of thiophosgene. This mixture was stirred at -5° C. for 30 minutes, then was allowed to warm to room temperature and was stirred for approximately 18 hours. The reaction mixture was washed with an aqueous, 5% hydrochloric acid solution followed by an aqueous, saturated sodium chloride solution. The washed reaction mixture was dried over anhydrous magnesium sulfate and was filtered. The filtrate was evaporated under reduced pressure leaving a solid residue. The residue was purified by recrystallization to yield 4.5 g of 9-(4-chloro-2-fluoro-5-nitrophenyl)imino-8-thia-1,6-diazabicyclo[4.3.0]nonane-7-thione, mp 171°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04906281
Source datasetuspto-grants-1990_03
ORD IDord-72d6f713c76e42a0a26e789d3967688f
Source noteuspto-grants-1990_03