Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | O-Methylhydroxylamine hydrochloride | HCID 521874 | — |
| Reactant | HCID 86672000 | HCID 86672000 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86671999 | HCID 86671999 | 42% |
Reaction Steps
A mixture of (E)-3-(1′-(4-fluorobenzyl)-4-oxospiro[chroman-2,3′-piperidine]-6-yl)-N-hydroxyacrylamide hydrochloride (80 mg, 0.179 mmol) and O-methylhydroxylamine hydrochloride (32.6 mg, 0.390 mmol) in ethanol (2 ml) and pyridine (0.031 ml, 0.390 mmol) was heated at 80° C. for 2 h. The solvent was removed in vacuo and the crude product was purified by preparative LC-MS to give the title compound (33.04 mg) as its trifluoroacetate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08980877B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-5353c4df5f224206936d9c2a4d08dc50 |
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| Source note | uspto-grants-2015_03 |
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