HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228159Generated: October 30, 2026
m-Chloroperbenzoic acid → HCID 18472669, compound
https://huagongshe.com/reaction/2228159
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 18472627 | HCID 18472627 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18472669 | HCID 18472669 | 73.7% |
Reaction Steps
To a solution of N-[4—(2-pyridylmethyl)phenyl]-6—(4-methylphenyl)-2H-1-benzopyran-3-carboxamide (250 mg) in tetrahydrofuran (10 ml) was added 3-chloroperbenzoic acid (70%, 0.21 g) at 0° C., and the mixture was stirred at room temperature for 14 hours. To the reaction mixture was added sodiumithiosulfate solution, and the mixture was stirred for a few minutes. The mixture was extracted with ethyl acetate. The organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried with magnesium sulfate and concentrated. The residue was separated and purified with column chromatography (ethanol/ethyl acetate=1:3) concentrated to give crystals, which were recrystallized from chloroform-ethanol to give N-[4—(1-oxidopyridin-2-ylmethyl)phenyl]-6—(4-methylphenyl)-2H-1-benzopyran-3-carboxamide (Compound 200) (191 mg) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06413947B1 |
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| Source dataset | uspto-grants-2002_07 |
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| ORD ID | ord-1257269c8c4e47e69a230b8a482c3296 |
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| Source note | uspto-grants-2002_07 |
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