HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 178461672, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Urea | HCID 1176 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | HCID 86690259 | HCID 86690259 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178461672 | HCID 178461672 | — |
Reaction Steps
A combination of urea (0.37 g, 15.6 mmol), sodium methoxide (1.47 g, 27.2 mmol) and MeOH (50 mL) was cooled to 0° C. and then a solution of (S)-ethyl 4-oxo-1-((S)-1-phenylethyl)piperidine-3-carboxylate (9.0 g, 7.8 mmol) in THF was added. The reaction mixture was allowed to warm to rt and then warmed to 60° C. and heated for 3 h. The mixture was diluted with water and EtOAc and the organic layer was then separated, dried (Na2SO4), filtered and concentrated. The residue was purified by FCC (8-10% MeOH/CH2Cl2) to give (S)-6-(1-phenylethyl)-5,6,7,8-tetrahydropyrido[4,3-d]pyrimidine-2,4-diol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846656B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-435961ec3ded4bf1a136b35e75fa1f25 |
| Source note | uspto-grants-2014_09 |