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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1730950Generated: November 1, 2026

Formaldehyde → 5-Fluoro-3-phenyl-1-(piperidin-1-ylmethyl)-1H-indazole

https://huagongshe.com/reaction/1730950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPiperidineHCID 8082—
ReactantSodium HydroxideHCID 14798—
Reactant5-Fluoro-3-Phenyl-1H-IndazoleHCID 13143709—
SolventEthanolHCID 702—
Product5-Fluoro-3-phenyl-1-(piperidin-1-ylmethyl)-1H-indazoleHCID 2149419861.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03994890
Source datasetuspto-grants-1976_11
ORD IDord-a53ca93a68814163bd1a9cb457d535b6
Source noteuspto-grants-1976_11