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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2269247Generated: October 30, 2026

(2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidine → (2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidine dihydrochloride

https://huagongshe.com/reaction/2269247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidineHCID 15549736—
ReactantHydrochloride methanolHCID 21893726—
SolventDichloromethaneHCID 6344—
Product(2S,3S)-2-Phenyl-3-(5-(2,2,2-trifluoro-1-(trifluoromethyl)ethyl)-2-methoxybenzyl)aminopiperidine dihydrochlorideHCID 8675765083%

Reaction Steps

To a solution of Compound 14 (160 mg) in CH2Cl2 (10 ml) was added an excess amount of 10% HCl-MeOH (6 ml). After the solvent was evaporated in vacuo, the residual solid was recrystallized from IPA to give Compound 15 (130 mg, 83%; three steps) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06329396B1
Source datasetuspto-grants-2001_12
ORD IDord-1f5a8a7fa10f4113816b6e2ee061c48d
Source noteuspto-grants-2001_12