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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1448304Generated: November 1, 2026

Water → HCID 12298161, compound

https://huagongshe.com/reaction/1448304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantHexamethylphosphoramideHCID 12679—
ReactantSodium hydrideHCID 24758—
Reactant4-Piperidinecarboxylic acid, 4-[(4-fluorophenyl)amino]-1-(phenylmethyl)-HCID 12298141—
ProductHCID 12298161HCID 12298161—

Reaction Steps

70 Parts of 4-[(4-fluorophenyl)amino]-1-(phenylmethyl)-4-piperidinecarboxylic acid are dissolved in 450 parts of dry hexamethylphosphoric triamide at 120° C. This solution is cooled to room temperature and 6 parts of sodium hydride dispersion 78% are added portionwise at a temperature below 30° C. After stirring for 1.50 hours at room temperature, there are added dropwise 32.5 parts of iodomethane at a temperature below 15° C. Upon completion, stirring is continued for 28 hours at room temperature. The reaction mixture is poured onto 800 parts of water and the product is extracted with methylbenzene. The extract is washed successively with water, a 10% sodium hydroxide solution and again twice with water, dried, filtered and evaporated. The residue is purified by column-chromatography over silica gel using a mixture of trichloromethane and 5% of methanol as eluent. The pure fractions are collected and the eluent is evaporated. The oily residue is converted into the ethanedioate salt in 2-propanol. The salt is filtered off and crystallized from 2-propanol, yielding methyl 4-[(4-fluorophenyl)amino]-1-(phenylmethyl)-4-piperidinecarboxylate ethanedioate; mp. 168.6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04179569
Source datasetuspto-grants-1979_12
ORD IDord-c2713b7c7ac74e6894d0d2831cb45033
Source noteuspto-grants-1979_12