Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | HCID 25004257 | HCID 25004257 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57870047 | HCID 57870047 | 84% |
Reaction Steps
To a solution of 2-((R)-3-benzylaminopyrrolidin-1-yl)-3-methyl-6-(pyridin-4-yl)-3H-pyrimidin-4-one (1.6 g, 4.4 mmol) and ammonium formate (0.55 g, 8.9 mmol) in tatrahydrofuran (15 ml), methanol (30 ml) and water (5 ml) was added 10% palladium on charcoal (wet, 160 mg). After stirring for 4 hours at 95° C., palladium on charcoal was removed by filtration. The solvent was evaporated off under reduced pressure and the residue was partitioned between water and dichloromethane. The organic layer was dried over sodium sulfate and the solvent was evaporated under reduced pressure to afford 2-((R)-3-aminopyrrolidin-1-yl)-3-methyl-6-(pyridin-4-yl)-3H-pyrimidin-4-one (1.0 g, 84%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569294B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-991dbc59844c4e62b0a8cfd9fd27f95d |
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| Source note | uspto-grants-2013_10 |
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