HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 861305Erstellt: 25. Oktober 2026
Brimonidine → N-(4,5-dihydro-1H-imidazol-2-yl)-5-methylquinoxalin-6-amine
https://huagongshe.com/reaction/861305
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Brimonidine | HCID 2435 | — |
| Edukt | Tetramethyltin | HCID 11661 | — |
| Katalysator | HCID 178418476 | HCID 178418476 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-(4,5-dihydro-1H-imidazol-2-yl)-5-methylquinoxalin-6-amine | HCID 185076 | 56,8% |
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, IR and mass spectral analysis.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05714486 |
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| Quelldatensatz | uspto-grants-1998_02 |
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| ORD ID | ord-3ff78ec8ede147fb96d12875dac71a79 |
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| Quellennotiz | uspto-grants-1998_02 |
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