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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 430458Erstellt: 25. Oktober 2026

Brimonidine → N-(4,5-dihydro-1H-imidazol-2-yl)-5-methylquinoxalin-6-amine

https://huagongshe.com/reaction/430458

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBrimonidineHCID 2435—
EduktTetramethyltinHCID 11661—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-(4,5-dihydro-1H-imidazol-2-yl)-5-methylquinoxalin-6-amineHCID 18507656,8%

Reaktionsbedingungen

Temperatur145 °C

Reaktionsschritte

A sealable reaction tube was charged with 5-bromo-6-(2-imidazolin-2-ylamino) quinoxaline (104 mg., 0.36 mmol) (prepared as noted above), tetramethyl tin (214 mg., 1.2 mmol) and (Ph3P)2PdCl2 (10 mg) and dry dimethylformamide (2 ml) in a reaction tube. The reaction mixture was purged with dry nitrogen gas. The tube was sealed and heated to 145° C. for 6 hours. The reaction mixture was cooled to room temperature and the solvent removed in vacuo. The dark brown residue was chromatographed (SiO2; 5/1 CHCl3/CH3OH saturated with NH3 (g)) to yield 46.5 mg (53%) of the title compound as a light yellow solid. An analytical sample was prepared by recrystallization from CHCl3/CH3OH and had a melting point of 183-186° C. The title compound was characterized by 1H and 13CNMR and mass spectral analysis.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06323204B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-5f2d7b429c9d42b5925b4ddc21175946
Quellennotizuspto-grants-2001_11