HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 4-(4-Morpholinyl)imidazo[1,2-a]quinoxaline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-Chloroimidazo[1,2-a]quinoxaline | HCID 10774525 | — |
| Product | 4-(4-Morpholinyl)imidazo[1,2-a]quinoxaline | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124287 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-a464a377e304425da25c715410a7eca9 |
| Source note | uspto-grants-2000_09 |