HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828521Generated: October 29, 2026
Triethyl 2-phosphonopropionate → HCID 86588145, compound
https://huagongshe.com/reaction/1828521
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethyl 2-phosphonopropionate | HCID 107155 | — |
| Reactant | HCID 22063658 | HCID 22063658 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86588145 | HCID 86588145 | 23.3% |
Reaction Steps
Under nitrogen atmosphere, triethyl 2-phosphonopropionate (155 mg, 0.65 mmol) was dissolved in tetrahydrofuran (2 ml), added with n-butyl lithium (1 M, 0.65 ml) at −78° C., and stirred at the same temperature for 20 minutes. The reaction mixture was added with a solution of 8-[2-(4-isopropyl-1,3-thiazol-2-yl)ethyl]-2-morpholino-4-oxo-4H-pyrido[1,2-a]pyrimidine-3-carbaldehyde (50 mg) dissolved in tetrahydrofuran (1 ml). The cooling bath was removed, and the reaction mixture was warmed to room temperature and stirred overnight at room temperature. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain the title compound (14 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07056917B2 |
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| Source dataset | uspto-grants-2006_06 |
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| ORD ID | ord-07196da2e29c418e9b1e28de66dce235 |
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| Source note | uspto-grants-2006_06 |
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