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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436102Generated: November 1, 2026

(S)-1-[(S)-1-(2,6-difluoropyridin-3-yl)ethylamino]propan-2-ol (+)-di-p-toluoyl-D-tartrate → (S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-6-methylmorpholine-2,3-dione

https://huagongshe.com/reaction/1436102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-1-[(S)-1-(2,6-difluoropyridin-3-yl)ethylamino]propan-2-ol (+)-di-p-toluoyl-D-tartrateHCID 131727771—
SolventSodium HydroxideHCID 14798—
Product(S)-4-[(S)-1-(2,6-difluoropyridin-3-yl)ethyl]-6-methylmorpholine-2,3-dioneHCID 68717775115.4%

Reaction Conditions

Temperature145 °C

Reaction Steps

(S)-1-[(S)-1-(2,6-difluoropyridin-3-yl)ethylamino]propan-2-ol (+)-di-p-toluoyl-D-tartrate (199 g) was dissolved in 5 N aqueous sodium hydroxide (450 mL), water (1,000 mL), and 50% toluene-THF (2,000 mL), and the organic layer was separated. The aqueous layer was washed with 50% toluene-THF (800 mL) three times. The organic layers were combined and concentrated under reduced pressure. Then, diethyl oxalate (200 mL) was added to the residue, and the reaction solution was heated and stirred at 140 to 150° C. Three hours later, the reaction solution was diluted with toluene (500 mL) and then ice-cooled while stirring. The precipitated crystals were collected by filtration, washed with toluene and diethyl ether, and then air-dried to obtain 103 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07618960B2
Source datasetuspto-grants-2009_11
ORD IDord-fc8ef3e4efd84f7c967ca5c8bac5d7c4
Source noteuspto-grants-2009_11