Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 66703932 | HCID 66703932 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66704003 | HCID 66704003 | 94% |
Reaction Steps
To a solution of N-(4-((2S)-4-((1R)-1-phenylethyl)morpholin-2-yl)phenyl)-pyridin-2-amine (0.89 g, 2.5 mmol) and ammonium formate (0.78 g, 12.5 mmol) in tetrahydrofuran (15ml)-methanol (24 ml)-water (18 ml) was added 10% palladium on carbon (wet, 200 mg) and the mixture was stirred at 95° C. for one hour. 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 concentrated under reduced pressure to yield N-(4-((2S)-Morpholin-2-yl)phenyl)pyridin-2-amine (0.60 g, 94%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08106045B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-5d99c8a7647c4a7185f9ad8b0827949d |
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| Source note | uspto-grants-2012_01 |
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