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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424444Generated: October 30, 2026

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

https://huagongshe.com/reaction/424444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantN2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamideHCID 66594605—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
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 tetrahydrofuran (20 ml), methanol (40 ml) and water (7 ml) was added 10% palladium on carbon (wet, 300 mg) and the mixture was 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%) a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106045B2
Source datasetuspto-grants-2012_01
ORD IDord-6bff4777ed2042dbbe60bc6dffe6fccf
Source noteuspto-grants-2012_01