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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651049Generated: October 26, 2026

Naltrexone → (5α,6α)-17-(Cyclopropylmethyl)-4,5-epoxy-6-(methylamino)morphinan-3,14-diol

https://huagongshe.com/reaction/651049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNaltrexoneHCID 5360515—
ReactantMethylamine hydrochlorideHCID 6364545—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventMethanolHCID 887—
Product(5α,6α)-17-(Cyclopropylmethyl)-4,5-epoxy-6-(methylamino)morphinan-3,14-diolHCID 1590885879.5%

Reaction Steps

Naltrexone (1.0 g) and methylamine hydrochloride (0.99 g, 5 equivalents) were dissolved in methanol (15 ml) followed by stirring for 20 minutes at room temperature. This reaction solution was added to platinum oxide (0.05 g, 5 w %) in methanol (10 ml) activated in advance in a hydrogen atmosphere followed by hydrogenation for 4 hours at room temperature and atmospheric pressure. The catalyst was removed by Celite filtration and the solvent was distilled off. After adding saturated aqueous sodium bicarbonate (20 ml) and extracting with chloroform (20 ml×2), the extract was washed with saturated brine and dried with anhydrous sodium sulfate, and the solvent was distilled off. The resulting dark reddish-violet oily substance was dissolved in chloroform (2 ml) followed by addition of ethyl acetate (4 ml) to obtain the target compound (0.83 g, yield: 79%) by crystallization. A portion of this compound was removed and various spectra were measured in the form of a hydrochloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06277859B1
Source datasetuspto-grants-2001_08
ORD IDord-7b5115f1ba784954b95d487802d57024
Source noteuspto-grants-2001_08