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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256034Generated: November 1, 2026

Pyridine → HCID 19029125, compound

https://huagongshe.com/reaction/2256034

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPhenylmethyl 4-(5-ethoxy-4,5-dihydro-5-methyl-1,3,4-oxadiazol-2-yl)-1-piperidinecarboxylateHCID 19029164—
SolventTolueneHCID 1140—
ProductHCID 19029125HCID 1902912582.4%

Reaction Steps

A solution of 1-benzyloxycarbonyl-4-(5-ethoxy-5-methyl-1,3,4-oxadiazolin-2-yl)piperidine (200 mg) in toluene (5 mL) containing pyridine (0.25 mL) was heated under reflux for 20 hours. The mixture was cooled to room temperature, and the solvent was evaporated. The residue was purified by chromatography, eluting with chloroform:methanol:ammoniumhydroxide (98:2:1), to give the 1,3,4-oxadiazole derivative (0.143 g) as a clear oil; NMR (CDCl3): 7.35 (m, 5), 5.13 (s, 2), 4.16 (broad d, 2, J=12.8), 3.05 (m, 1), 2.50 (s, 3), 2.04 (m, 2), 1.83 (m, 2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654299
Source datasetuspto-grants-1997_08
ORD IDord-fe40d9c154354efb89fb98d1604bdf02
Source noteuspto-grants-1997_08