Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | HCID 58485358 | HCID 58485358 | — |
| Product | HCID 58485336 | HCID 58485336 | — |
Reaction Steps
Hydrogen peroxide (35% in water, 0.1 mL) was added to a mixture of 2-[5-(4-{(S)-1-[(S)-6-(2-hydroxy-2-methyl-propyl)-2-oxo-6-phenyl-[1,3]oxazinan-3-yl]-ethyl}-phenyl)-pyridin-2-yl]-2-methyl-propionitrile (0.21 g; for preparation see Example 194) and K2CO3 (0.03 g) in ddimethyl sulfoxide (2 mL) at room temperature. After stirring the mixture for 3 h at room temperature, another portion of hydrogen peroxide (35% in water, 0.1 mL) and K2CO3 (0.03 g) were added. The mixture was further stirred at room temperature for 1 h and at 40° C. overnight. After cooling to room temperature, little aqueous Na2S2O3 solution was added and then the mixture was concentrated. The residue was purified by HPLC on reversed phase (methanol/water/ammonia) to furnish the title compound. Yield: 0.03 g (14% of theory); Mass spectrum (ESI+): m/z=516 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08569292B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-d31aff7e29fb4c6a9fd80131dfd348da |
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| Source note | uspto-grants-2013_10 |
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