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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Thiophosgene | HCID 10040 | — |
| Reactant | N-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazine | HCID 14622955 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 9-(4-Chloro-2-fluoro-5-nitrophenyl)imino-8-thia-1,6-diazabicyclo[4.3.0]nonane-7-thione | HCID 14622956 | 44.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04906281 |
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| Source dataset | uspto-grants-1990_03 |
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| ORD ID | ord-72d6f713c76e42a0a26e789d3967688f |
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| Source note | uspto-grants-1990_03 |
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