Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | HCID 59654182 | HCID 59654182 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59654181 | HCID 59654181 | 90.4% |
Reaction Steps
A mixture of 20.0 g (62.4 mmol) of the product from Step 2 (12) and 9.2 g (93.6 mmol) of potassium acetate in 200 mL DMF was stirred at 40° C. under nitrogen for three hours. The reaction mixture was allowed to cool to ambient temperature and the addition of excess water to the reaction solution caused the product to precipitate out of solution. The product was filtered, washed with water (3×), and drying under reduced pressure at 40° C. overnight yielded 19.4 g (56.4 mmol, 90%) of (3-iodo-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)methyl acetate (13) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07504405B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-2a3d0f6d29274e9ea7dca831a61f173c |
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| Source note | uspto-grants-2009_03 |
|---|