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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| 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 | Water | HCID 962 | — |
| 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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129377B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-be01f6be38a748f6833c2b87f8afc5e0 |
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| Source note | uspto-grants-2012_03 |
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