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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189988Generated: November 1, 2026

Pyridine → HCID 59527751, compound

https://huagongshe.com/reaction/2189988

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium ChlorideHCID 5234—
ReactantTriphosgeneHCID 94429—
ReactantHCID 86646238HCID 86646238—
SolventDichloromethaneHCID 6344—
ProductHCID 59527751HCID 5952775199.9%

Reaction Steps

To a solution of triphosgene (172 mg, 0.6 mmol) in dichloromethane (6 mL) at 0° C. under an argon atmosphere was added a solution of pyridine (106 μL, 1.32 mmol) in dichloromethane (3 mL) and a solution of 4-phenyl-piperidine-4-carboxylic acid [(S)-1-(4-fluoro-phenyl)-ethyl]-amide (195 mg, 0.6 mmol) in dichloromethane (6 ml). After stirring at room temperature for 12 h the reaction mixture was poured into ice water, the aqueous layer was saturated with NaCl, then extracted 6 times with dichloromethane, the combined organic layers were dried over Na2SO4 and the solvents were evaporated. The residue was purified by flash chromatography over a 10 g silica gel column with n-heptane and ethyl acetate to yield 233 mg 4-[(S)-1-(4-fluoro-phenyl)-ethylcarbamoyl]-4-phenyl-piperidine-1-carbonyl chloride. MS ISN (m/e): 387.4 [(M−H)−].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324250B2
Source datasetuspto-grants-2012_12
ORD IDord-fb6d736062ca440280eba4ee022c9d6f
Source noteuspto-grants-2012_12