HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(piperidine-4-carbonyl)-3-(3-pridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide → N-{1-[2-(R)-hydroxy-3-(quinolin-5-yloxy)-propyl]-piperidine-4-carbonyl}-3-(3-pyridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(piperidine-4-carbonyl)-3-(3-pridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 10208518 | — |
| Reactant | (R)-5-(Oxiran-2-ylmethoxy)quinoline | HCID 11735808 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-{1-[2-(R)-hydroxy-3-(quinolin-5-yloxy)-propyl]-piperidine-4-carbonyl}-3-(3-pyridyl)-alanine [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 59885592 | 52.5% |
Reaction Steps
N-(Piperidine-4-carbonyl)-3-(3-pyridyl)-alanine [4-phenyl- 1-(3-phenyl-propyl)-butyl]-amide (87) (261.8 mg; 0.497 mmol) is dissolved in ethanol (12 mL) at ambient temperature. (R)-5-Oxiranylmethoxy-quinoline (2) (100.0 mg; 0.497 mmol) is added, then the mixture is refluxed for 25 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 (50%→100% acetone in hexanes, then 5%→20% ethanol in acetone) affording the desired product (190 mg) as a white solid. ESMS:MH+ 728.6
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135483B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-017d43c661d54381a032be5afd9c76d4 |
| Source note | uspto-grants-2006_11 |