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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221361Generated: November 1, 2026

Pyridine → HCID 11360085, compound

https://huagongshe.com/reaction/221361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-Butanesulfonyl chlorideHCID 75430—
Reactant4-(5-Piperidin-4-yl-1,2,4-oxadiazol-3-yl)pyridineHCID 2761143—
SolventDichloromethaneHCID 6344—
ProductHCID 11360085HCID 11360085—

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 butane-1-sulfonyl chloride (56 μl, 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, dried (MgSO4) and evaporated. The residue was dissolved in EtOAc (5 ml) and extracted into 2M HCl (10 ml). The aqueous phase was then basified using 2M NaOH to pH=8 and extracted with CH2Cl2 (2×10 ml). The combined organic phases were dried (MgSO4) and evaporated to afford the title compound: RT=3.29 min, m/z (ES+)=351.2 [+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207147B2
Source datasetuspto-grants-2012_06
ORD IDord-c15669dce5ff455295c3ac080391fca5
Source noteuspto-grants-2012_06