Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397666Generated: October 29, 2026

Hydrazinecarboxaldehyde → (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidine

https://huagongshe.com/reaction/397666

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazinecarboxaldehydeHCID 12229—
Reactantethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidateHCID 57097015—
SolventTolueneHCID 1140—
Solvent1,4-DioxaneHCID 31275—
Product(2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidineHCID 17852736132.6%

Reaction Steps

Formylhydrazine (120 mg) was added to a solution of ethyl (2S)-1-[(4-fluorophenyl)sulfonyl]-2-piperidinecarboximidate (295 mg) [see Preparation 41] in toluene (5 ml) and 1,4-dioxane (5 ml). The reaction mixture was stirred at reflux for 26 hours after which time the solvent was removed under reduced pressure. The residue was diluted with ethyl acetate and washed with water. The organic layer was separated, dried over magnesium sulphate and the solvent removed under reduced pressure. The crude product was purified by column chromatography on silica gel eluting with a solvent gradient of 100:0 changing to 0:100 (in 10% increments), by volume, hexane:ethyl acetate to afford (2S)-1-[(4-fluorophenyl)sulfonyl]-2-(1H-1,2,4-triazol-3-yl)piperidine (95 mg) as an off-white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06610707B1
Source datasetuspto-grants-2003_08
ORD IDord-1c9e22cef2ba480d9c6bc29238cd09e3
Source noteuspto-grants-2003_08