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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Perhydropyridazine hydroiodide | HCID 12314334 | — |
| Reactant | 4-Chloro-2-fluoro-5-nitrophenylisothiocyanate | HCID 14622954 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(4-chloro-2-fluoro-5-nitrophenylaminothiocarbonyl)perhydropyridazine | HCID 14622955 | 96% |
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
| 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-3063a2a00e5c4d53b3db28b9d051684c |
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| Source note | uspto-grants-1990_03 |
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