Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 2-Chloro-5-fluoropyrimidine | HCID 583466 | — |
| Reactant | (Octahydro-2H-pyrido[1,2-a]pyrazin-7-yl)methanol | HCID 9855588 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54484575 | HCID 54484575 | 75% |
Reaction Steps
A mixture of 2.31 g (13.6 mmol) of (7S,9aS)-7-hydroxymethyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (Preparation 2), 1.98 g (15.0 mmol) of 2-chloro-5-fluoropyrimidine (B. Baasner, E. Klauke, J. Fluorine Chem., 1989, 45, 417), 4.32 g (40.8 mmol) of sodium carbonate and 50 mL of water was heated at reflux for 16 h. The mixture was cooled to room temperature and extracted with chloroform (3×). The combined organic layers were dried (magnesium sulfate), filtered and evaporated. Purification by flash silica gel chromatography with 95:5 chloroform:methanol gave, 2.7 g (75%) of the title compound. mp (base) 111–112° C. 13C NMR (base, CDCl3): δ 26.5, 27.3, 34.2, 44.3, 49.8, 54.8, 58.8, 60.7, 68.2, 145.0, 145.3, 149.9, 153.2, 158.6. HRMS calcd for C13H19FN4O: 266.1543, found: 266.1530.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07220753B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-b973863cd2fd40f3b4cde83b8efbcc5b |
|---|
| Source note | uspto-grants-2007_05 |
|---|