HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 509596Generated: October 28, 2026
Phosphorus pentachloride → N-(2-chlorophenyl)-5-(methylsulfonyl)picolinimidoyl chloride
https://huagongshe.com/reaction/509596
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | N-(2-chlorophenyl)-5-(methylsulfonyl)picolinamide | HCID 67958704 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | N-(2-chlorophenyl)-5-(methylsulfonyl)picolinimidoyl chloride | HCID 86709639 | — |
Reaction Steps
N-(2-chlorophenyl)-5-(methylsulfonyl)picolinamide 5 (1.26 g, 0.0040 mol) in anhydrous benzene (20 mL) was added to PCl5 (1.26 g, 0.0060 mol) and the mixture was heated to reflux overnight. The solvent was removed and the residue was further dried under high vacuum. Crude N-(2-chlorophenyl)-5-(methylsulfonyl)picolinimidoyl chloride 6 was obtained as a yellow solid (1.60 g). The compound 6 was dissolved into anhydrous THF (30 mL) and the reaction was cooled down to 0° C. and hydrazine hydrate (9.0 mL) was added. The reaction was kept at 0° C. for 10 min and warmed to ambient temperature in 0.5 h. The solvent was removed and the residue was purified by column chromatography (eluting with hexane and ethyl acetate 1:1) to give N′-(2-chlorophenyl)-5-(methylsulfonyl) picolinimidohydrazide 7 as a yellow solid. Yield: 1.22 g, 92.0%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09096587B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-445d20486157401781622a6306e127f2 |
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| Source note | uspto-grants-2015_08 |
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