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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856539Generated: October 29, 2026

Sodium Thiosulfate → 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[(1-ethylimidazol-2-yl)methylsulfinyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide

https://huagongshe.com/reaction/856539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-ethylimidazol-2-yl)methyl]sulfanyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamideHCID 69522269—
SolventDichloromethaneHCID 6344—
Product7-[4-(2-butoxyethoxy)phenyl]-N-[4-[(1-ethylimidazol-2-yl)methylsulfinyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamideHCID 301356553.4%

Reaction Steps

To a solution of 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-ethylimidazol-2-yl)methyl]sulfanyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (150 mg) in dichloromethane (10 ml) was added dropwise 70% solution of 3-chloroperbenzoic acid (55.3 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, 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 by silica gel column chromatography (hexane:ethyl acetate=1:1), and was recrystallized from hexane-ethyl acetate, to give 7-[4-(2-butoxyethoxy)phenyl]-N-[4-[[(1-ethylimidazol-2-yl)methyl]sulfinyl]phenyl]-1-isobutyl-2,3-dihydro-1-benzazepine-4-carboxamide (82 mg) (Compound 333) as yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262185B2
Source datasetuspto-grants-2007_08
ORD IDord-17c96b1e975d412ca4cfdb03e754b594
Source noteuspto-grants-2007_08