HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942486Generated: November 2, 2026
Methyl morpholine oxide → HCID 86656356, compound
https://huagongshe.com/reaction/1942486
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | HCID 67333667 | HCID 67333667 | — |
| Catalyst | HCID 178419074 | HCID 178419074 | — |
| Solvent | Acetonitrile methylene chloride | HCID 21877088 | — |
| Product | HCID 86656356 | HCID 86656356 | 69% |
Reaction Steps
Under the nitrogen atmosphere, to a solution of tert-butyl (2R,5R)-5-[{[4-{2-[(difluoroacetyl)-amino]ethyl}-2,2-dimethyl-3-oxo-7-(trifluoromethyl)-3,4-dihydro-2H-1,4-benzoxazin-6-yl]carbonyl}-(isopropyl)amino]-2-(2-hydroxyethyl)piperidine-1-carboxylate (1.1 g) in methylene chloride -acetonitrile (5 ml, 5 ml) were added N-methylmorpholine oxide (283 mg) and molecular sieve 4 Å (750 mg), and the mixture was stirred at room temperature for a while. Then, tetrapropylammonium perruthenate (56 mg) was added thereto, and the mixture was stirred at room temperature for 3 hours. Then, the insoluble materials were removed by filtration, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (the developing solvent: hexane/acetone=2/1) to give the title compound (757 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08389511B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-b43ed03412e34d74bcc7c5051ad44d20 |
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| Source note | uspto-grants-2013_03 |
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