HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856509Generated: October 30, 2026
Sodium Thiosulfate → HCID 69522532, compound
https://huagongshe.com/reaction/856509
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 69522938 | HCID 69522938 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69522532 | HCID 69522532 | 11.7% |
Reaction Steps
7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[2-(imidazol-1-yl)ethyl]sulfanyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (0.50 g) was dissolved in methylene chloride (15 ml), and a solution of m-chloroperbenzoic acid (0.20 g) in methylene chloride (10 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]-N-[4-[[2-(imidazol-1-yl)ethyl]sulfinyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (Compound 266) (60 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-442cb6f87f894469b3aea212d2bfaa02 |
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| Source note | uspto-grants-2007_08 |
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