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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1954714Generated: November 4, 2026

Morpholine → 4-(4-Morpholinyl)imidazo[1,2-a]quinoxaline

https://huagongshe.com/reaction/1954714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant4-Chloroimidazo[1,2-a]quinoxalineHCID 10774525—
Product4-(4-Morpholinyl)imidazo[1,2-a]quinoxalineHCID 4133357—

Reaction Steps

By reaction of 4-chloroimidazo[1,2-a]quinoxaline (example 1) with morpholine, according to a procedure that is similar to that followed in example 3, there is obtained 4-(4-morpholinyl)imidazo[1,2-a]quinoxaline. m.p. (DSC)=142.8° C. (onset); IR (KBr): 3016, 2962, 1517 cm-1 ; 1H-NMR (CDCl3): δ8.0 (1H,s), 7.8÷7.5 (3H,m), 7.5÷7.2 (2H,m), 4.4 (4H,t), 3.9 (4H,t); UV (EtOH): λmax =230, 248, 292, 304, 330 nm. Elementary analysis for C14H13N4O (m.w. 254.29): calcd. C 66.13, H 5.55, N 22.03%; found C 65.43, H 5.47, N 22.25%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06124287
Source datasetuspto-grants-2000_09
ORD IDord-a464a377e304425da25c715410a7eca9
Source noteuspto-grants-2000_09