Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 66975256 | HCID 66975256 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 136340701 | HCID 136340701 | 49.7% |
Reaction Steps
Sodium hydrogen carbonate (145 mg) and hydroxylamine monohydrochloride (120 mg) were added to a solution of tert-butyl (6RS,7SR)-6-(3-cyano-2-oxopyridin-1(2H)-yl)-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (100 mg) in DMSO (4 mL), and the mixture was stirred at 80° C. overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was dissolved in THF (10 mL), diazabicycloundecene (0.032 mL) and CDI (52 mg) were added, and the mixture was heated under reflux for 1 hr. To the reaction mixture was added 1 N aqueous hydrochloric acid solution, and the mixture was extracted with ethyl acetate. The extract was washed with water and brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound (56 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08722662B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-d3ecdd8626474e619e69a0ec6e5b9898 |
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| Source note | uspto-grants-2014_05 |
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