HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-5-(Oxiran-2-ylmethoxy)quinoline → HCID 59885598, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-5-(Oxiran-2-ylmethoxy)quinoline | HCID 11735808 | — |
| Reactant | 1-[(N-methyl)-2-aminoacetyl]-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide | HCID 18727460 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 59885598 | HCID 59885598 | — |
Reaction Steps
1-[(N-methyl)-2-aminoacetyl]-piperidine-4-carboxylic acid [4-phenyl-1-(3-phenyl-propyl)-butyl]-amide (63) (223.5 mg; 0.497 mmol]) is dissolved in ethanol (10 mL) at ambient temperature. (R)-5-Oxiranylmethoxy-quinoline (2) (100.0 mg; 0.497 mmol) is added, then the mixture is refluxed for 17.5 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 (110 mg) as a white solid. ESMS:MH+ 651.6.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07135483B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-6176a78dfbf440e6bb32f28a97d399ae |
| Source note | uspto-grants-2006_11 |