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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091389Generated: November 1, 2026

Dimethylamine, hydrochloride → N2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamide

https://huagongshe.com/reaction/1091389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantPotassium CarbonateHCID 11430—
Reactant2-chloro-N-{4-[(2S)-4-((1R)-1-phenylethyl)morpholin-2-yl]phenyl}acetamideHCID 66594640—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductN2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamideHCID 66594605125.2%

Reaction Steps

A solution of 2-chloro-N-((2S)-4-(((1R)-1-phenylethyl)morpholin-2-yl)phenyl)acetamide (0.9 g, 2.5 mmol), potassium carbonate (1.72 g, 12.5 mmol), and dimethylamine hydrochloride (1.00 g, 12.5 mmol) in tetrahydrofuran (40 ml) and acetonitrile (80 ml) was stirred at 95° C. for 10 hours. After filtration, the solvent was removed in vacuo and the residue was partitioned between water and dichloromethane. The organic layer was dried over anhydrous sodium sulfate and the solvent was evaporated under reduced pressure give N2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamide (1.15 g, quant.) as an yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129377B2
Source datasetuspto-grants-2012_03
ORD IDord-cc072b96b8d24a49b85b0541b753cfde
Source noteuspto-grants-2012_03