HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228153Generated: October 31, 2026
Sodium Thiosulfate → HCID 18472310, compound
https://huagongshe.com/reaction/2228153
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 18472482 | HCID 18472482 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18472310 | HCID 18472310 | 65.6% |
Reaction Steps
To a solution of N-[4—(3-methoxymethoxypyridin-2-ylmethyl)phenyl]-7—(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (300 mg) in tetrahydrofuran (10 ml) was added 3-chloroperbenzoic acid (70%, 0.22 g) at 0° C., and the mixture was stirred at room temperature for 18 hours. To the mixture was added sodium thiosulfate, and the mixture was stirred for a few minutes. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated sodium bicarbonate solution and saturated sodium chloride solution, dried with magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified with column chromatography (ethanol/ethyl acetate=1:15→1:10), and recrystallized from ethanol to give N-[4—(1-oxido-3-methoxymethoxypyridin-2-ylmethyl)phenyl]-7—(4-methylphenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (Compound 173) (203 mg) as colorless 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-3c43c7bb94e14434884842beee1202aa |
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| Source note | uspto-grants-2002_07 |
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