HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Ethylpiperidine → HCID 18472556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Ethylpiperidine | HCID 13007 | — |
| Reactant | N-[4-(chloromethyl)phenyl]-7-phenyl-3,4-dihydronaphthalene-2-carboxamide | HCID 10809385 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18472556 | HCID 18472556 | — |
Reaction Steps
In DMF (3 ml) was dissolved N-[4—(chloromethyl)- phenyl]-7-phenyl-3,4-dihydronaphthalene-2-carboxamide (140 mg), and to the mixture was added 1-ethylpiperidine (154 μl). The mixture was stirred at room temperature for 14 hours and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-methanol to give 1-ethyl-1-[4—(7-phenyl-3,4-dihydro-naphthalene-2-carboxamido)benzyl]piperidinium chloride (Compound 24) (125 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413947B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-4b36ca4cc8dc4048b160d911f8c986de |
| Source note | uspto-grants-2002_07 |