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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382821Generated: October 28, 2026

1-Acetylpiperidine-4-carbonyl chloride → 1-acetyl-N-[5-(3-furyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]piperidine-4-carboxamide

https://huagongshe.com/reaction/2382821

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Acetylpiperidine-4-carbonyl chlorideHCID 100950—
Reactant5-(Furan-3-yl)-[1,2,4]triazolo[1,5-a]pyridin-2-amineHCID 25215938—
Product1-acetyl-N-[5-(3-furyl)[1,2,4]triazolo[1,5-a]pyridin-2-yl]piperidine-4-carboxamideHCID 25213511—

Reaction Steps

The title compound was prepared following procedure and work up described for example 19, but starting from 5-(3-furyl)[1,2,4]triazolo[1,5-a]pyridin-2-amine ((A2), 50 mg; 0.25 mmol; 1.0 eq.) and 1-acetylpiperidine-4-carbonyl chloride (57 mg; 0.3 mmol; 1.2 eq.) as a white powder (41.3 mg, 46%). HPLC, Rt: 2.15 min. (purity 93.3%). LC/MS, M+(ESI): 354.4, M−(ESI): 352.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263595B2
Source datasetuspto-grants-2012_09
ORD IDord-ea5adeb5962c4fdca0a695a42008b278
Source noteuspto-grants-2012_09