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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1091390Generated: November 1, 2026

Methanol → N2,N2-dimethyl-N1-(4-((2S)-morpholin-2-yl)phenyl)glycinamide

https://huagongshe.com/reaction/1091390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium formateHCID 2723923—
ReactantN2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamideHCID 66594605—
CatalystPalladiumHCID 23938—
SolventWaterHCID 962—
ProductN2,N2-dimethyl-N1-(4-((2S)-morpholin-2-yl)phenyl)glycinamideHCID 6659489196%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of N2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamide (0.91 g, 2.5 mmol) and ammonium formate (0.79 g, 12.5 mmol) in mixture of tetrahydrofuran (20 ml), methanol (40 ml) and water (7 ml) was added 10% palladium on carbon (wet, 300 mg) and stirred at 95° C. for 3 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 to give N2,N2-dimethyl-N1-(4-((2S)-morpholin-2-yl)phenyl)glycinamide (0.63 g, 96%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129377B2
Source datasetuspto-grants-2012_03
ORD IDord-be01f6be38a748f6833c2b87f8afc5e0
Source noteuspto-grants-2012_03