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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 481487Generated: October 25, 2026

(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine → (2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine dihydrochloride

https://huagongshe.com/reaction/481487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidineHCID 9799042—
ReactantHydrochloride methanolHCID 21893726—
Product(2S,3S)-3-(5-(1-Cyanocyclopropyl)-2-methoxybenzyl)amino-2-phenylpiperidine dihydrochlorideHCID 995459285%

Reaction Steps

Compound 4 (89 mg, 0.25 mmol) was treated with hydrogen chloride-methanol (5 ml). After the solvent was evaporated in vacuo, the residue (pale yellow solid) was recrystallized from ethanol-diethyl ether to give Compound 5 (91 mg, 85%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05789423
Source datasetuspto-grants-1998_08
ORD IDord-f263c02321954e629af05718b16c72d2
Source noteuspto-grants-1998_08