HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → Brimonidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | 5-Bromo-6-isothiocyanatoquinoxaline | HCID 4460274 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Brimonidine | HCID 2435 | — |
Reaction Steps
The 5-bromo-6-isothiocyanato-quinoxaline (3.5 g.) is directly dissolved in benzene (400 ml) and added dropwise to a well-stirred solution of ethylene diamine (15 g.) in benzene (50 ml). During a period of about two hours, an oil separates as a lower layer. The upper benzene layer is poured off and the oil is washed with diethyl ether and then dissolved in methanol (500 ml). The methanolic solution is refluxed until hydrogen sulfide evolution ceases. The methanolic solution is concentrated in vacuo to a volume of approximately 100 ml upon which a yellow solid precipitates. The precipitate is collected by filtration and recrystallized from methanol to afford of (5-Bromo-quinoxalin-6-yl)-(4,5-dihydro-1H-imidazol-2-yl)-amine: m.p. 250-251 C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08557817B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-b70347e967344cce98a0c948f6088740 |
| Source note | uspto-grants-2013_10 |