Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 5-hydroxypyridine-3-carboxylate | HCID 354317 | — |
| Reactant | HCID 21078402 | HCID 21078402 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21078399 | HCID 21078399 | — |
Reaction Steps
3-Hydroxy-5-methoxycarbonylpyridine (1.68 g, prepared using the method described in Bull. Acad. Sci. (Chem. Div.), (1976), 598) and 2-bromobromo-N-(5-methylhex-3-yn-5-yl)-butyramide (3.06 g) were dissolved in dry N,N-dimethylformamide (30 ml) containing anhydrous potassium carbonate (2.35 g). The mixture was heated to 70° C. for 3 hours with stirring, cooled to ambient temperature, diluted with water and extracted with diethyl ether (three times). The organic extracts were combined, washed with water (three times), dried over magnesium sulphate and evaporated under reduced pressure to give a brown gum. The gum was fractionated by chromatography (silica; diethyl ether) to give the required product, 2.38 g, as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07166621B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-dc898de558ae462384208164512c2e56 |
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| Source note | uspto-grants-2007_01 |
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