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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383860Generated: October 25, 2026

Triethylamine → 1-(3-Methyl-1,2,4-thiadiazol-5-yl)piperidin-4-one

https://huagongshe.com/reaction/383860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Piperidone hydrochlorideHCID 3084851—
Reactant5-Chloro-3-methyl-1,2,4-thiadiazoleHCID 12919159—
SolventEthanolHCID 702—
Product1-(3-Methyl-1,2,4-thiadiazol-5-yl)piperidin-4-oneHCID 592585108.6%

Reaction Steps

To a mixture of piperidin-4-one HCl salt (4.08 g, 30 mmol) and Et3N (20 mL, 78.6 mmol) in EtOH (50 mL) was added 5-chloro-3-methyl-1,2,4-thiadiazole (4.05 g, 30 mmol). The mixture was heated to reflux for 1.5 hours and then concentrated to dryness. The residue was dissolved in EtOAc. The solution was washed with water (30 mL×3) and brine (30 mL), dried over Na2SO4, and concentrated to dryness. The residue was recrystalled from ether to give 1-(3-methyl-1,2,4-thiadiazol-5-yl)piperidin-4-one (510 mg, 8.6%). 1H-NMR (300 MHz, CDCl3) δ 3.86 (t, J=6.3 Hz, 4H), 2.62 (t, J=6.3, Hz, 4H), 2.44 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367691B2
Source datasetuspto-grants-2013_02
ORD IDord-18d533abb515450a9f8b6b2dce905825
Source noteuspto-grants-2013_02