HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856501Generated: October 29, 2026
Sodium Thiosulfate → HCID 69521335, compound
https://huagongshe.com/reaction/856501
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 69523141 | HCID 69523141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69521335 | HCID 69521335 | 53.5% |
Reaction Steps
To a solution of 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[(2-methyl-3-pyridinyl)methyl]sulfanyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (0.27 g) in methylene chloride (8.1 ml) was added dropwise a solution of m-chloroperbenzoic acid (86 mg) in methylene chloride (5.4 ml) at −78° C., and the mixture was stirred for 15 minutes. To the reaction mixture was added an aqueous solution of saturated sodium thiosulfate. The mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine and dried over magnesium sulfate. The solvent was removed under reduced pressure, and the obtained residue was purified by silica gel column chromatography, and recrystallized from ethanol, to give 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[(2-methyl-3-pyridinyl)methyl]sulfinyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (Compound 251) (148 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07262185B2 |
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| Source dataset | uspto-grants-2007_08 |
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| ORD ID | ord-db854e38451847fd82bf516bd01b4616 |
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| Source note | uspto-grants-2007_08 |
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