Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl 6-chloropyridine-3-carboxylate | HCID 254249 | — |
| Reactant | (3-methyl-5-phenyl-3H-[1,2,3]triazol-4-yl)-methanol | HCID 67498121 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67498772 | HCID 67498772 | 63% |
Reaction Steps
A solution of (3-methyl-5-phenyl-3H-[1,2,3]triazol-4-yl)-methanol (189 mg, 1.0 mmol) in THF (3 mL) was added dropwise at 0° C. to a suspension of NaH (55% in oil, 48 mg, 1.1 mmol) in THF (1.5 mL) and the reaction mixture was then stirred at room temperature for 30 min. Then a solution of methyl 6-chloronicotinate (189 mg, 1.1 mmol) in THF (3 mL) was added dropwise at 0° C. and the reaction mixture stirred at room temperature for 20 h. The mixture was then poured into water extracted with ethyl acetate and the combined organic extracts washed with brine, dried over sodium sulphate, filtered and evaporated. Purification by chromatography (silica, 0 to 100% ethyl acetate in heptane) afforded the title compound (203 mg, 63%) as an off white solid. MS: m/e=325.2 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742097B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-2f922c4d5974476189b9653e02e0c096 |
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| Source note | uspto-grants-2014_06 |
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