HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 43602Generated: October 31, 2026
Ethyl bromopyruvate → Ethyl cis(+/-)-2-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-1,3-oxazole-4-carboxylate
https://huagongshe.com/reaction/43602
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromopyruvate | HCID 66144 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | cis(+/-)-Benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate | HCID 131730860 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl cis(+/-)-2-(4-{[(benzyloxy)carbonyl]amino}-3-methoxypiperidin-1-yl)-1,3-oxazole-4-carboxylate | HCID 86648578 | 79.4% |
Reaction Steps
Ethyl bromopyruvate (2.93 g, 15 mmol) and sodium bicarbonate (2.10 g, 25 mmol) were added to a solution of cis(±)-benzyl (1-carbamoyl-3-methoxypiperidin-4-yl)carbamate obtained in Example (103b) (1.4 g, 4.56 mmol) in THF (30 mL), and the mixture was stirred at 70° C. for three hours. The insoluble matter was filtered off, followed by dilution with ethyl acetate. This was washed with water and brine, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (elution solvent: ethyl acetate/hexane=1/4, 1/2, 1/1, 2/1, 4/1) to obtain 1.46 g of the title compound as a colorless solid (79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08536197B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-687e6edebfb24cd7a5a56c4e57b6035d |
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| Source note | uspto-grants-2013_09 |
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