Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | (Octahydro-1H-pyrido[1,2-A]pyrazin-7-YL)methanol | HCID 12985539 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | HCID 19963216 | HCID 19963216 | 42% |
Reaction Steps
A mixture of 1.0 g (5.9 mmol) of (7RS,9aSR)-7-hydroxymethyl-2,3,4,6,7,8,9,9a-octahydro-1H-pyrido[1,2-a]pyrazine (U.S. Pat. No. 5,326,874); 4.6 g (29 mmol) of 2-bromopyridine, 1.5 g (14 mmol) of sodium carbonate and 50 mL of isoamyl alcohol were refluxed for 18 h. The mixture was cooled to room temperature, filtered, and concentrated in vacuo. The residue was dissolved in ethyl acetate and washed with saturated sodium carbonate. The organic layer was dried (magnesium sulfate), filtered and evaporated, and the crude product was purified by flash chromatography on silica gel eluting first with chloroform followed by 95:5 chloroform:methanol to give 0.61 g (42%) of the title compound. 13C NMR (base, CDCl3): δ26.8, 29.0, 39.0, 45.1, 50.7, 54.8, 58.7, 60.8, 66.0, 107.1, 113.3, 137.5, 147.9, 159.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06231833B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-e96f85fb8cdf40dda905c8fb2be19d0c |
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| Source note | uspto-grants-2001_05 |
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