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
Participants
| Role | Name | HCID | Charge |
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| Reactant | [(3,4,5-Trimethoxyphenoxy)methyl]oxirane | HCID 5743635 | — |
| Reactant | Piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 12020260 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-[2-Hydroxy-3-(3,4,5-trimethoxyphenyl)-propyl]-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 86585544 | 121% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07476680B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-b47e09edb5c340f985082418b963fd06 |
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| Source note | uspto-grants-2009_01 |
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