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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221357Generated: October 31, 2026

Trifluoroacetic acid → 4-(5-Piperidin-4-yl-1,2,4-oxadiazol-3-yl)pyridine

https://huagongshe.com/reaction/221357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57954381HCID 57954381—
SolventDichloromethaneHCID 6344—
Product4-(5-Piperidin-4-yl-1,2,4-oxadiazol-3-yl)pyridineHCID 2761143—

Reaction Steps

Trifluoroacetic acid (20 ml) was added to a stirred solution of 4-(3-pyridin-4-yl-[1,2,4]oxadiazol-5-yl)piperidine-1-carboxylic acid tert-butyl ester (Example 2, 1.64 g, 4.96 mmol) in CH2Cl2 (35 ml). After 2.5 h at rt, the solvent was evaporated under reduced pressure. The residual solid was suspended in EtOAc (150 ml) and washed with saturated aqueous Na2CO3 (20 ml). The aqueous was separated and extracted with EtOAc (3×30 ml). The combined organic extracts were dried (MgSO4) and evaporated under reduced pressure to afford the title compound: RT=3.48 min, m/z (ES+)=231.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207147B2
Source datasetuspto-grants-2012_06
ORD IDord-19e6641f26994c159f56e6339993d2d0
Source noteuspto-grants-2012_06