HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392405Generated: November 3, 2026
m-Chloroperbenzoic acid → HCID 69312791, compound
https://huagongshe.com/reaction/1392405
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 86601115 | HCID 86601115 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 69312791 | HCID 69312791 | 74.8% |
Reaction Steps
To the solution of 4-[N-[1-[N-(benzofuran-2-ylcarbonyl)amino]cyclohexanecarbonyl]amino]-1-(2-formylphenyl)piperidin-3-ol (1.38 g, 2.8 mmol) obtained in Step 1 of Example 61 in 50 ml of chloroform, was added 486 mg of m-chloroperbenzoic acid (5.6 mmol). The reaction mixture was stirred for about 2 hours at room temperature. The resulting organic layer was washed with the solutions of sulfurous acid and sodium bicarbonate, dried on sodium sulfate. The resulting ester residue was dissolved in 100 ml of methanol and was added a drop of concentrated hydrochloride thereto. The reaction mixture was stirred for about 1 hour, was added sodium bicarbonate (0.5 g) thereto. The reaction mixture was concentrated. The resulting residue was purified with column chromatography to give 1.0 g of the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07342027B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-4236a3b3d7cd4a4891ebd29278c8dc5a |
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| Source note | uspto-grants-2008_03 |
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