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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454127Generated: November 4, 2026

[(3,4,5-Trimethoxyphenoxy)methyl]oxirane → 1-[2-Hydroxy-3-(3,4,5-trimethoxyphenyl)-propyl]-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide

https://huagongshe.com/reaction/1454127

Reaction equation

Participants

RoleNameHCIDCharge
Reactant[(3,4,5-Trimethoxyphenoxy)methyl]oxiraneHCID 5743635—
ReactantPiperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 12020260—
SolventIsopropanolHCID 3776—
Product1-[2-Hydroxy-3-(3,4,5-trimethoxyphenyl)-propyl]-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amideHCID 86585544121%

Reaction Conditions

Temperature70 °C

Reaction Steps

Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (4) (150.7 mg; 0.4 mmol) is dissolved in isopropanol (10 mL) at ambient temperature. (+/−)-2-(3,4,5-Trimethoxy-phenoxymethyl)-oxirane(95.2 mg; 0.4 mmol) is added, then the mixture is heated to 70° C. and maintained for 18 hours. After cooling to ambient temperature, the solution is concentrated in vacuo at 40° C. The residue is purified via silica gel chromatography with gradient elution (10%→100% acetone in hexanes) affording the desired product (145.9 mg) as an oil. ESMS: MH+ 619.4 (base).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476680B2
Source datasetuspto-grants-2009_01
ORD IDord-b47e09edb5c340f985082418b963fd06
Source noteuspto-grants-2009_01