HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7070Generated: October 23, 2026
Pentafluorophenol → N-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamide
https://huagongshe.com/en/reaction/7070
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pentafluorophenol | HCID 13041 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | N-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamide | HCID 22019637 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[3-(N-cyclohexylcarbamoyl)phenyl]-4-hydroxy-3-methoxyphenylacetamide | HCID 22019598 | 94.7% |
Reaction Steps
A mixture of N-(3-carboxyphenyl)-4-hydroxy-3-methoxyphenylacetamide (500 mg), pentafluorophenol (305 mg), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (320 mg) and methylene chloride (10 ml) is stirred at 25° C. for 18 hours. The reaction solution is washed with water, and the solvent is evaporated under reduced pressure. To the residue are added ethyl acetate (10 ml) and cyclohexylamine (174 mg), and the mixture is heated with stirring at 60° C. for 18 hours. The solvent is evaporated and the residue is purified by silica gel column chromatography (eluent: gradient from 0% to 100% hexane/ethyl acetate) to give the desired compound (600 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07084176B2 |
|---|
| Source dataset | uspto-grants-2006_08 |
|---|
| ORD ID | ord-e923ca3883c74703a1879eb55299542a |
|---|
| Source note | uspto-grants-2006_08 |
|---|