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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928892Generated: October 30, 2026

Water → HCID 68649854, compound

https://huagongshe.com/reaction/1928892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethyl SulfideHCID 1068—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68649978HCID 68649978—
SolventDichloromethaneHCID 6344—
ProductHCID 68649854HCID 6864985459.8%

Reaction Steps

To a solution of 8-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[[1-propylimidazol-2-yl]methyl]sulfanyl]phenyl]-1,2,3,4-tetrahydro-1-benzoazocine-5-carboxamide (400 mg) in dichloromethane (10 ml) was added dropwise a 70% solution of 3-chloro-per-benzoic acid (217 mg) in dichloromethane (10 ml) at −78° C. After stirring as such for 1 hour, dimethyl sulfide (0.1 ml) was added. The mixture was returned to room temperature and stirred for 30 minutes, after which water was added and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate solution and saturated aqueous brine, and was dried with magnesium sulfate. The solvent was distilled off under reduced pressure, and the resulting residue was separated and purified by basic silica gel column chromatography (hexane:ethyl acetate=1:4→ethyl acetate) and recrystallized from diisopropyl ether-ethyl acetate to give 8-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[[1-propylimidazol-2-yl]methyl]sulfinyl]phenyl]-1,2,3,4-tetrahydro-1-benzoazocine-5-carboxamide (245 mg) as yellow crystals (Compound 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-f10b089aad104559b19aa4ac639d7fd5
Source noteuspto-grants-2012_05