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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222804Generated: October 30, 2026

m-Chloroperbenzoic acid → HCID 68650589, compound

https://huagongshe.com/reaction/2222804

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 68650254HCID 68650254—
SolventDichloromethaneHCID 6344—
ProductHCID 68650589HCID 6865058974.9%

Reaction Steps

To a solution of 8-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[[4-methyl-1-propylimidazol-5-yl]methyl]sulfanyl]phenyl]-1,2,3,4-tetrahydro-1-benzoazocine-5-carboxamide (300 mg) in dichloromethane (10 ml) was added dropwise a 70% solution of 3-chloro-perbenzoic acid (117 mg) in dichloromethane (10 ml) at −78° C. After stirring as such for 1 hour, the dry ice-acetone bath was removed, and an aqueous sodium thiosulfate solution was added with vigorous stirring. 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 aqueous saturated 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 with basic silica gel column chromatography (hexane:ethyl acetate=1:4→ethyl acetate) to give 8-[4-(2-butoxyethoxy)phenyl]-1-isobutyl-N-[4-[[[4-methyl-1-propylimidazol-5-yl]methyl]sulfinyl]phenyl]-1,2,3,4-tetrahydro-1-benzoazocine-5-carboxamide (230 mg) as a yellow amorphous material (Compound 37).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07371772B2
Source datasetuspto-grants-2008_05
ORD IDord-07b280ccb6944c02aba2ce194cfd88dd
Source noteuspto-grants-2008_05