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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478121Generated: November 1, 2026

Phosphorus pentachloride → N-(2-chlorophenyl)-5-(methylsulfonyl)picolinimidoyl chloride

https://huagongshe.com/reaction/1478121

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 numberUS09403812B2
Source datasetuspto-grants-2016_08
ORD IDord-fa2cc3de9ca543f58f926a5df439cd5d
Source noteuspto-grants-2016_08