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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222811Generated: November 1, 2026

Sodium Thiosulfate → HCID 68649933, compound

https://huagongshe.com/reaction/2222811

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68650298HCID 68650298—
SolventDichloromethaneHCID 6344—
ProductHCID 68649933HCID 6864993380.9%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 8-[4-(2-butoxyethoxy)phenyl]-1-propyl-N-[4-[[(4-propyl-4H-1,2,4-triazol-3-yl)methyl]thio]phenyl]-1,2,3,4-tetrahydro-1-benzazocine-5-carboxamide (0.70 g) in dichloromethane (20 ml) was added dropwise a solution of 3-chloro-perbenzoic acid (70%, 0.39 g) in dichloromethane (10 ml) and the mixture was stirred at −78° C. for 1 hour. To a reaction system was added an aqueous sodium thiosulfate solution, and the mixture was stirred at room temperature for several minutes. The mixture was extracted with ethyl acetate, the organic layer was washed with aqueous sodium bicarbonate solution and saturated brine, and was dried with magnesium sulfate. The resultant was concentrated under reduced pressure, after which the residue was separated and purified with column chromatography (basic silica gel, ethyl acetate→ethanol:ethyl acetate 1:19), followed by recrystallization (ethyl acetate-diisopropyl ether) to give 8-[4-(2-butoxyethoxy)phenyl]-1-propyl-N-[4-[[(4-propyl-4H-1,2,4-triazol-3-yl)methyl]sulfinyl] phenyl]-1,2,3,4-tetrahydro-1-benzazocine-5-carboxamide (579.7 mg) as yellow crystals (Compound 51).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371772B2
Source datasetuspto-grants-2008_05
ORD IDord-4b04dfc6b8b04e0fbc66c87988327c68
Source noteuspto-grants-2008_05