HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368108Generated: November 3, 2026
Hydrochloric Acid → HCID 178461776, compound
https://huagongshe.com/reaction/2368108
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Trimethyl borate | HCID 8470 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Hydrogen peroxide water | HCID 449047 | — |
| Reactant | HCID 86658702 | HCID 86658702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178461776 | HCID 178461776 | — |
Reaction Steps
To a solution of tert-butyl [(1S)-2-{[1-(5-bromo[1,3]oxazolo[5,4-b]pyridin-2-yl)piperidin-4-yl]oxy}-1-methylethyl]carbamate (484 mg) in THF (3 mL) was added 1.6M n-butyllithium-hexane solution (1.70 mL) at −78° C., and the mixture was stirred at the same temperature for 20 min. Trimethyl borate (0.355 mL) was added to the reaction mixture, and the mixture was allowed to warm to room temperature and stirred for 30 min. 30% Hydrogen peroxide water (3 mL) and 8M aqueous sodium hydroxide solution (1 mL) were added to the reaction mixture, and the mixture was stirred at room temperature for 30 min. The reaction mixture was neutralized with 1M hydrochloric acid, and extracted with ethyl acetate, and the extract was dried over magnesium sulfate. The solvent was evaporated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (68.1 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08703758B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-e243a8368f5e4c60bd2a2b178bce3c19 |
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| Source note | uspto-grants-2014_04 |
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