HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 5-Fluoro-3-phenyl-1-(piperidin-1-ylmethyl)-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 5-Fluoro-3-Phenyl-1H-Indazole | HCID 13143709 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Fluoro-3-phenyl-1-(piperidin-1-ylmethyl)-1H-indazole | HCID 21494198 | 61.5% |
Reaction Steps
3-Phenyl-5-fluoroindazole (2.12 g), paraformaldehyde (0.33 g), piperidine (1 g) and 1N aqueous sodium hydroxide solution (1 ml) were added to ethanol (30 ml) followed by heating under reflux for 3 hours. The reaction mixture was concentrated under reduced pressure and the residue was dissolved in benzene, washed with water, dried over sodium sulfate and concentrated under reduced pressure to obtain 1.9 g of 1-piperidinomethyl-3-phenyl-5-fluoroindazole having a melting point between 82°-84° C after recrystallization from methanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03994890 |
| Source dataset | uspto-grants-1976_11 |
| ORD ID | ord-a53ca93a68814163bd1a9cb457d535b6 |
| Source note | uspto-grants-1976_11 |