HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1978791Generated: October 30, 2026
Sodium Thiosulfate → HCID 21995960, compound
https://huagongshe.com/reaction/1978791
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 21995697 | HCID 21995697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21995960 | HCID 21995960 | 79.2% |
Reaction Steps
To a solution of 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[hydroxy(2-pyridyl)methyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (Compound 150) (230 mg) in dichloromethane (10 ml) was added at 0° C. 3-chloroperbenzoic acid (70%, 0.12 g), and the mixture was stirred at room temperature for 24 hours. To the reaction mixture was added sodium thiosulfate solution, and the mixture was stirred for a few minutes and extracted with ethyl acetate. The organic layer was washed with sodium bicarbonate solution and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was purified with column chromatography (ethanol/ethyl acetate=1:9→1:4) to give colorless crystals of 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[hydroxy(1-oxidopyridin-2-yl)methyl]phenyl]-1,1-dioxo-2,3-dihydro-1-benzothiepine-4-carboxamide (Compound 151) (187 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06235771B1 |
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| Source dataset | uspto-grants-2001_05 |
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| ORD ID | ord-330dad00243c48ac9fd9d458513e9f4d |
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| Source note | uspto-grants-2001_05 |
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