Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Bromobutyronitrile | HCID 21412 | — |
| Reactant | HCID 22678496 | HCID 22678496 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22678378 | HCID 22678378 | 60.2% |
Reaction Steps
200 mg of 1-[(2-methoxy-3-pyridyl)methyl]-4-[2-(2-oxo-1,2-dihydro-3-pyridinyl)ethyl]piperidine obtained in Example 47,95 mg of γ-bromobutyronitrile and 169 mg of potassium carbonate were suspended in 5 ml of N,N-dimethylformamide, and the mixture was stirred at 60° C. for 4 hours. Ethyl acetate was added thereto, the resulting salt was filtered off, and the solvent was evaporated. The crude product was purified by NH form silica gel column chromatography (ethyl acetate:hexane=1:4), to give 77 mg of the title compound as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06784192B2 |
|---|
| Source dataset | uspto-grants-2004_08 |
|---|
| ORD ID | ord-8eb386faa9a84e7ba2148939bbf2cdb9 |
|---|
| Source note | uspto-grants-2004_08 |
|---|