Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | Dimethyl[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]propanedioate | HCID 68684268 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 131728169 | HCID 131728169 | — |
Reaction Steps
A mixture of dimethyl[3-fluoro-6-(methyloxy)-1,5-naphthyridin-4-yl]propanedioate (52 g, 169 mmol), lithium chloride (14.5 g, 340 mmol) and water (3.43 ml, 190 mmol) in DMSO (1175 ml) was heated at 100° C. for 24 hours and cooled. The solution was shaken with water and ethyl acetate, separated and the organic phase washed twice with water. The total aqueous was re-extracted with ethyl acetate and this water-washed. The combined organic phase was dried and evaporated and the residue chromatographed, using a hexane/ethyl acetate gradient, to give the desired product containing about 10% of starting material (35.79 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732461B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-96383d4113704fa5824ad9656debf080 |
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| Source note | uspto-grants-2010_06 |
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