HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856530Generated: October 30, 2026
Sodium Thiosulfate → HCID 3013561, compound
https://huagongshe.com/reaction/856530
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 69522671 | HCID 69522671 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 3013561 | HCID 3013561 | 71.5% |
Reaction Steps
To a solution of 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[(thiazol-2-ylmethyl)sulfanyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (150 mg) in dichloromethane (10 ml) was added dropwise 70% solution of 3-chloroperbenzoic acid (57.6 mg) in dichloromethane (10 ml) at −78° C. After finishing the dropping, an aqueous solution of sodium thiosulfate was added to the mixture, and the mixture was allowed to be at room temperature, and stirred for 30 minutes, and extracted with ethyl acetate. The organic layer was washed with an aqueous solution of saturated sodium bicarbonate, and saturated brine, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure. The obtained residue was separated purified by silica gel column chromatography (hexane:ethyl acetate=1:3→ethyl acetate), and was recrystallized from hexane-ethyl acetate, to give 7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[(thiazol-2-ylmethyl)sulfinyl]phenyl]-2,3-dihydro-1-benzazepine-4-carboxamide (110 mg) (Compound 317) as yellow crystals.
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-864e7266757348df9e2d2dc7da5433ec |
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| Source note | uspto-grants-2007_08 |
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