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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221358Generated: November 3, 2026

Pyridine → HCID 11484315, compound

https://huagongshe.com/reaction/221358

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantIsobutyl chloroformateHCID 62365—
Reactant4-(5-Piperidin-4-yl-1,2,4-oxadiazol-3-yl)pyridineHCID 2761143—
SolventDichloromethaneHCID 6344—
ProductHCID 11484315HCID 11484315—

Reaction Steps

A solution of pyridine (18 μl, 0.22 mmol) and 4-(5-piperidin-4-yl-[1,2,4]oxadiazol-3-yl)pyridine (Example 51, 50 mg, 0.22 mmol) in CH2Cl2 (4 ml) was treated with isobutylchloroformate (54 mg, 0.43 mmol). The reaction was stirred at rt for 18 h then quenched with saturated aqueous NaHCO3 (1 ml). The organic phase was separated, evaporated and the residue purified by flash chromatography (IH-EtOAc, 1:1 to 0:1) to afford the title compound: RT=3.42 min, m/z (ES+)=331.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207147B2
Source datasetuspto-grants-2012_06
ORD IDord-05bada90c5404bd48c13a8e4c03f6048
Source noteuspto-grants-2012_06