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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691721Generated: October 29, 2026

1,4-Dioxane hydrochloride → HCID 66906082, compound

https://huagongshe.com/reaction/1691721

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 66906065HCID 66906065—
ProductHCID 66906082HCID 66906082—

Reaction Steps

To 302 mg of the crude product of 4-({[4-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-phenylpiperidin-1-yl]carbonyl}amino)-3-chlorobenzoic acid was added 2.0 mL of a 4 M hydrogen chloride/1,4-dioxane solution, followed by stirring at room temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, and to the residue was then added isopropanol, followed by heating under reflux. The mixture was cooled to room temperature, and the precipitate was then isolated by filtration, and dried under reduced pressure to obtain 147 mg of 3-chloro-4-({[4-({[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-3-phenylpiperidin-1-yl]carbonyl}amino)benzoic acid hydrochloride as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153658B2
Source datasetuspto-grants-2012_04
ORD IDord-10de8aeb091046f28f81dc007dce7962
Source noteuspto-grants-2012_04