HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 10704538, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 4-Chloroimidazo[1,2-a]quinoxaline | HCID 10774525 | — |
| Product | HCID 10704538 | HCID 10704538 | — |
Reaction Steps
By reaction of 4-chloroimidazo[1,2-a]quinoxaline (example 1) with ethanolamine according to a procedure that is similar to that followed in example 3 there is obtained 4-(2-hydroxyethylamino)imidazo[1,2-a]quinoxaline. m.p. (DSC)=150.8° C. (onset); IR (KBr): 3312, 1598, 1564 cm-1 ; 1H-NMR (CDCl3 /CD3OD): δ8.2 (1H,s), 8.1÷7.55 (2H,m), 7.55 (1H,s), 7.4÷7.2 (2H,m), 3.8 (4H,s); UV (EtOH): λmax =227, 285, 297, 317, 330 nm. Elementary analysis for C12H12N4 (m.w. 228.25): calcd. C 63.14, H 5.30, N 24.55%; found C 63.16, H 5.40, N 24.99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124287 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-4ef934b2f563474abc23db6f0cb4b681 |
| Source note | uspto-grants-2000_09 |