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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732699Generated: October 30, 2026

1,4-Dioxane hydrochloride → 915386-24-2

https://huagongshe.com/reaction/732699

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
ReactantHCID 68916166HCID 68916166—
Product915386-24-2HCID 68913969—

Reaction Steps

A 1.05 g portion of 4-({[(3R,4S)-3-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]carbonyl}oxy)benzoic acid was dissolved in 10 ml of 4 M hydrogen chloride/1,4-dioxane solution and stirred at room temperature for 1Hour, and then the reaction solution was concentrated under a reduced pressure. In order to remove excess hydrogen chloride, the residue was dissolved in chloroform and again concentrated under a reduced pressure. By suspending the thus obtained residue in THF-toluene, 784 mg of 4-({[(3S,4S)-3-({[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]carbonyl}oxy)benzoic acid hydrochloride was obtained as a crude product. A 235 mg portion of the thus obtained crude product was suspended in THF-toluene and heated under reflux for 50 minutes, and then the resulting precipitate was collected by filtration to obtain 217 mg of 4-({[(3S,4S)-3-({[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]carbonyl}oxy)benzoic acid hydrochloride as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-2c3cf97453bf4941b504b624b97f67f8
Source noteuspto-grants-2009_09