HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856511Generated: October 30, 2026
Sodium Thiosulfate → HCID 69522309, compound
https://huagongshe.com/reaction/856511
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 69522366 | HCID 69522366 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69522309 | HCID 69522309 | 54.9% |
Reaction Steps
7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[6-[(3-pyridinylmethyl)sulfanyl]-3-pyridinyl]-2,3-dihydro-1-benzazepine-4-carboxamide (0.32 g) was dissolved in methylene chloride (9.6 ml), and a solution of m-chloroperbenzoic acid (130 mg) in methylene chloride (6.4 ml) was added to the mixture at −78° C., and the mixture was stirred for 15 minutes. The reaction mixture was added to an aqueous solution of saturated sodium thiosulfate, and extracted with ethyl acetate. 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, to give 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[6-[(3-pyridinylmethyl)sulfinyl]-3-pyridinyl]-2,3-dihydro-1-benzazepine-4-carboxamide (Compound 270) (180 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-887a536ffa3a44d1a16673e951d27341 |
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| Source note | uspto-grants-2007_08 |
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