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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | N2,N2-dimethyl-N1-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)glycinamide | HCID 66594605 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N2,N2-dimethyl-N1-(4-((2S)-morpholin-2-yl)phenyl)glycinamide | HCID 66594891 | 96% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08106045B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-6bff4777ed2042dbbe60bc6dffe6fccf |
|---|
| Source note | uspto-grants-2012_01 |
|---|