HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 10586250, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 10488983 | HCID 10488983 | — |
| Product | HCID 10586250 | HCID 10586250 | — |
Reaction Steps
By reaction of 4-chloro-1-methylimidazo[1,2-a]quinoxaline (example 2) with ethanolamine according to a procedure that is similar to that followed in example 3 there is obtained 4-(2-hydroxyethylamino)-1-methyl imidazo[1,2-a]quinoxaline. m.p. (DSC)=173.4° C. (onset); IR (KBr): 3415, 3217, 1558 cm-1 ; 1H-NMR (CDCl3): δ8.0 (1H,dd), 7.7.÷7.2 (3H,m), 7.2 (1H,m), 6.6 (1H,m), 5.3 (1H,sb), 3.85 (3H,m), 2.8 (3H,s); UV (EtOH): λmax =225, 242, 271, 301, 314, 327 nm. Elementary analysis for C13H14N4 (m.w. 242.28): calcd. C 64.45, H 5.82, N 23.12%; found C 64.29, H 5.91, N 23.13%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06124287 |
| Source dataset | uspto-grants-2000_09 |
| ORD ID | ord-8600305beb3847018e56490343e4befe |
| Source note | uspto-grants-2000_09 |