HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236310Generated: October 28, 2026
m-Chloroperbenzoic acid → HCID 59301373, compound
https://huagongshe.com/reaction/2236310
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 59301300 | HCID 59301300 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59301373 | HCID 59301373 | — |
Reaction Steps
2-Phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid (6-thiomorpholin-4-yl-pyridin-3-yl)-amide (30 mg, 0.07 mmol) was dissolved in 3 mL of methylene chloride, and cooled down to −78° C. One equivalent of 3-chloroperoxybenzoic acid (12 mg, 0.07 mmol) was added. The reaction mixture was warmed up to room temperature and stirred for 2 hours. The reaction mixture was concentrated under reduced pressure, and then purified by flash chromatography (Merck silica gel 60, 230-400 mesh, 0-20% methanol in methylene chloride for 25 min) to gave 2-phenyl-5-trifluoromethyl-oxazole-4-carboxylic acid [6-(1-oxo-1λ4-thiomorpholin-4-yl)-pyridin-3-yl]-amide as an off-white solid. LCMS calcd for C20H17F3N4O3S (m/e) 450, obsd 451 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07714126B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-223e326471024a72b2cf2671b0fa2a6c |
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| Source note | uspto-grants-2010_05 |
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