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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus pentachlorideHCID 24819—
ReactantN-(2-chlorophenyl)-5-(methylsulfonyl)picolinamideHCID 67958704—
SolventBenzeneHCID 241—
ProductN-(2-chlorophenyl)-5-(methylsulfonyl)picolinimidoyl chlorideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096587B2
Source datasetuspto-grants-2015_08
ORD IDord-445d20486157401781622a6306e127f2
Source noteuspto-grants-2015_08