HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856545Generated: October 30, 2026
Sodium Thiosulfate → HCID 69522943, compound
https://huagongshe.com/reaction/856545
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 69521218 | HCID 69521218 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69522943 | HCID 69522943 | 51.5% |
Reaction Steps
To a solution of 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-cyclopropylmethylimidazol-2-yl)methyl]sulfanyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (125 mg) in dichloromethane (10 ml) was added dropwise 70% solution of 3-chloroperbenzoic acid (68 mg) in dichloromethane (10 ml) at −78° C. To the mixture was added an aqueous solution of sodium thiosulfate, and the mixture was allowed to be at room temperature, 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 and purified with silica gel column chromatography (ethyl acetate→methanol:ethyl acetate=1:9), to give 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-cyclopropylmethylimidazol-2-yl)methyl]sulfinyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (65.9 mg) (Compound 348) as yellow amorphous.
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-1dea8788bb164a5190ff7b816a19d4c1 |
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| Source note | uspto-grants-2007_08 |
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