Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethyl phosphonoacetate | HCID 13345 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 59334473 | HCID 59334473 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66720782 | HCID 66720782 | 84.3% |
Reaction Steps
Under nitrogen atmosphere, to a suspension of sodium hydride (1.42 g, 35.5 mmol) in tetrahydrofuran (35 mL) was added a solution of ethyl diethylphosphonoacetate (7.10 mL, 35.5 mmol) in tetrahydrofuran (5.0 mL) at 0° C., and the mixture was stirred for 20 min. To the reaction mixture was added a solution of 2-methyl[1,2,4]triazolo[1,5-a]pyridine-8-carbaldehyde (5.20 g, 32.3 mmol) in tetrahydrofuran (60 mL), and the mixture was warmed to room temperature over 4 hr. Water was added and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1) to give the title compound (6.30 g, yield 84%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08110585B2 |
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| Source dataset | uspto-grants-2012_02 |
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| ORD ID | ord-f6928ccaffde445ea5ff7b166cc63da8 |
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| Source note | uspto-grants-2012_02 |
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