Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 22642Generated: October 26, 2026

Thiomorpholine → 4-(5-Nitro-2-pyridinyl)thiomorpholine

https://huagongshe.com/reaction/22642

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiomorpholineHCID 67164—
Reactant2-Chloro-5-nitropyridineHCID 78308—
SolventTetrahydrofuranHCID 8028—
Product4-(5-Nitro-2-pyridinyl)thiomorpholineHCID 2798452—

Reaction Steps

To a solution of 20 g (126 mmol) of 2-chloro-5-nitropyridine in 200 ml tetrahydrofuran were added dropwise 32.5 ml (315 mmol) thiomorpholine within 10 min. The reaction mixture was refluxed for additional 2 h. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved in 200 ml ethyl acetate. The organic phase was washed with 200 ml 1 N sodium bicarbonate solution, dried (magnesium sulfate) and evaporated to give 29.3 g (quantitative) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06849624B2
Source datasetuspto-grants-2005_02
ORD IDord-0a6d260271f0483bbbb1796c2958fed9
Source noteuspto-grants-2005_02