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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732694Generated: October 30, 2026

L-Threonine → methyl 4-[(3R,4S)-3-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]-3,5-difluorobenzoate

https://huagongshe.com/reaction/732694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-ThreonineHCID 6288—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3,4,5-trifluorobenzoateHCID 2783211—
Reactanttert-butyl [(1R)-1-(1-naphthyl)ethyl]{[(3R,4S)-4-phenylpyrrolidin-3-yl]methyl}carbamateHCID 86628525—
SolventDimethyl SulfoxideHCID 679—
SolventEthyl AcetateHCID 8857—
Productmethyl 4-[(3R,4S)-3-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]-3,5-difluorobenzoateHCID 68915177—

Reaction Conditions

Temperature110 °C

Reaction Steps

A 10 ml DMSO solution of tert-butyl [(1R)-1-(1-naphthyl)ethyl]{[(3R,4S)-4-phenylpyrrolidin-3-yl]methyl}carbamate was mixed with 1.3 g of potassium carbonate and 1.0 g of methyl 3,4,5-trifluorobenzoate and stirred overnight at 110° C. Thr reaction solution was mixed with ethyl acetate, washed with water and dried with anhydrous sodium sulfate. This was concentrated under a reduced pressure, and the thus obtained residue was purified by a silica gel column chromatography (hexane-ethyl acetate) to obtain 2.1 g of methyl 4-[(3R,4S)-3-({(tert-butoxycarbonyl)[(1R)-1-(1-naphthyl)ethyl]amino}methyl)-4-phenylpyrrolidin-1-yl]-3,5-difluorobenzoate as a colorless amorphous substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585886B2
Source datasetuspto-grants-2009_09
ORD IDord-a510ec91c6224ea39e4bb0083b0cd018
Source noteuspto-grants-2009_09