Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | HCID 66732492 | HCID 66732492 | — |
| Product | HCID 66732609 | HCID 66732609 | 77% |
Reaction Steps
(2S,4R)-Methyl 2-(2,6-difluorobenzyl)-4-(3-oxo-2,3-dihydroisoxazol-5-yl)piperidine-1-carboxylate (344 mg, 0.98 mmol) (from example 127, step 3) was dissolved in hydrogen bromide (33% in acetic acid, 8 mL, 45.68 mmol) and the mixture stirred at room temperature for 24 h. The solvent was evaporated and the residue purified by preparative HPLC (Instrument: FractionLynx III, Mobilphase: gradient 5-95% MeCN in 0.2% NH3, pH 10, Column: Xbridge Prep C18 5 μm OBD 19*150 mm) to yield 5-((2S,4R)-2-(2,6-difluorobenzyl)piperidin-4-yl)isoxazol-3(2H)-one (222 mg, 77%). 1H NMR (600 MHz, cd3od) δ 1.47 (q, 1H), 1.68 (dq, 1H), 1.96-2.07 (m, 2H), 2.79-3.02 (m, 4H), 3.18-3.25 (m, 1H), 3.27-3.34 (m, 1H), 5.49 (s, 1H), 6.95-7.01 (m, 2H), 7.28-7.36 (m, 1H). HRMS Calculated for [C15H16F2N2O2+H]+: 295.1258. Found: 295.1240
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08415378B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-c68abd743a87453186789a9349a98ea0 |
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| Source note | uspto-grants-2013_04 |
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