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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856574Generated: October 29, 2026

Sodium Thiosulfate → HCID 69522774, compound

https://huagongshe.com/reaction/856574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 69522500HCID 69522500—
SolventDichloromethaneHCID 6344—
ProductHCID 69522774HCID 6952277457.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of [5-[[[4-[[[7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-2,3-dihydro-1H-1-benzazepin-4-yl]carbonyl]amino]phenyl]thio]methyl]-1H-imidazol-1-yl]ethyl acetate (200 mg) in dichloromethane (10 ml) was added a solution of 3-chloroperbenzoic acid (70%, 0.11 g) in dichloromethane (10 ml) at −78° C. The mixture was stirred for 1 hour at −78° C., an aqueous solution of sodium thiosulfate was added to the mixture, and the mixture was stirred at room temperature for 10 minutes. The mixture was extracted with ethyl acetate, and the organic layer was washed with an aqueous solution of sodium bicarbonate and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was separated and purified by column chromatography (basic silica get, ethyl acetate:hexane 4:1→9:1), to give [5-[[[4-[[[7-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-2,3-dihydro-1H-1-benzazepin-4-yl]carbonyl]amino]phenyl]sulfinyl]methyl]-1H-imidazol-1-yl]ethyl acetate (Preparation of Compound 427) (117.6 mg) as yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262185B2
Source datasetuspto-grants-2007_08
ORD IDord-e6cba90822314c2b98a70dbdbbc886cb
Source noteuspto-grants-2007_08