HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2043350Erstellt: 26. Oktober 2026
1H-Imidazole-4-carbaldehyde → (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-(3H-imidazol-4-ylmethyl)-amine
https://huagongshe.com/reaction/2043350
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| Edukt | Sodium cyanoborohydride | HCID 5003444 | — |
| Edukt | (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine | HCID 86620293 | — |
| Katalysator | Zincchloride | HCID 3007855 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | (3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-(3H-imidazol-4-ylmethyl)-amine | HCID 59728099 | 94% |
Reaktionsschritte
(3-Benzyloxy-phenyl)-(6-bromo-pyridin-2-ylmethyl)-amine (0.10 g, 0.27 mmol) was dissolved in methanol (2 ml). Then 4-formylimidazole (0.13 g, 1.35 mmol), zinc chloride (0.15 g, 1.08 mmol) and sodium cyanoborohydride (0.05 g, 0.81 mmol) were added and the reaction mixture was allowed to stir at 40° C. overnight. After cooling, the reaction mixture was poured onto ammoniumchloride/ice and extracted with ethyl acetate (2 times 50 ml). The organic layer was dried over magnesium sulfate and evaporated. The residue was purified using flash chromatography (SiO2; eluent: methanol/dichloromethane=1:9) to yield an off-white gum (0.11 g, 94%); MS (ISP): 451.1 ([81Br M+H]+), 449.1 ([79Br M+H]+).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08586617B2 |
|---|
| Quelldatensatz | uspto-grants-2013_11 |
|---|
| ORD ID | ord-8ed97e996e29403eb9a6aa0b5145949f |
|---|
| Quellennotiz | uspto-grants-2013_11 |
|---|