Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | HCID 86624089 | HCID 86624089 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86624091 | HCID 86624091 | — |
Reaction Steps
16.7 g (52 mmol) of methyl 6-(heptafluoropropyl)-2-oxo-1,2-dihydropyridine-3-carboxylate were dissolved in 160 ml of N,N-dimethylformamide, and 7.08 g (52 mmol) of N-chlorosuccinimide were added at room temperature. After 3 hours of stirring at 50° C., the reaction mixture was added to water and extracted repeatedly with ethyl acetate. The organic phase was then separated off, washed with water and dried. The resulting crude product was then purified by preparative RP-HPLC. This gave 10.1 g (54% of theory) of the product as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102623B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-57a74fb1f3c04336b0646c555a6a6a2a |
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| Source note | uspto-grants-2015_08 |
|---|