HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 5-(4-Fluorophenyl)-3-(2-piperidinyl)pyridine fumarate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Fumaric Acid | HCID 444972 | — |
| Reactant | 5-(4-Fluorophenyl)-3-(2-piperidinyl)pyridine | HCID 19694295 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(4-Fluorophenyl)-3-(2-piperidinyl)pyridine fumarate | HCID 19694294 | 70% |
Reaction Steps
The above described pyridine derivative was converted into invention compound of Formula I by the addition of one equivalent of fumaric acid to a methanol (15 mL) solution of the free amine at 25° C. After 30 minutes the solvent was removed in vacuo and the residue pumped under high vacuum. Trituration with diethyl ether resulted in the formation of 5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine fumarate (70%) as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05723477 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-78d0ff9eaef04c19a3803165f28b1df6 |
| Source note | uspto-grants-1998_03 |