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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042009Generated: October 25, 2026

Ethylenediamine → Brimonidine

https://huagongshe.com/reaction/1042009

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant5-Bromo-6-isothiocyanatoquinoxalineHCID 4460274—
SolventBenzeneHCID 241—
ProductBrimonidineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557817B2
Source datasetuspto-grants-2013_10
ORD IDord-b70347e967344cce98a0c948f6088740
Source noteuspto-grants-2013_10