HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 622Erstellt: 24. Oktober 2026
6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amine → HCID 57512844, Verbindung
https://huagongshe.com/de/reaction/622
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amine | HCID 53402967 | — |
| Edukt | HCID 57512921 | HCID 57512921 | — |
| Reagenz | Cesium carbonate | HCID 10796 | — |
| Katalysator | 2-(Dicyclohexylphosphino)biphenyl | HCID 2734216 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | HCID 57512844 | HCID 57512844 | 73,84% |
Reaktionsschritte
8-chloro-4-methyl-2-(5-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepine (140 mg, 0.47 mmol), 6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-amine (106 mg, 0.52 mmol), 2-(DICYCLOHEXYLPHOSPHINO)BIPHENYL (16.59 mg, 0.05 mmol), PALLADIUM(II) ACETATE (10.63 mg, 0.05 mmol) and Cs2CO3 (308 mg, 0.95 mmol) were weighed into a microwave vial, the vial was capped and DME (4 mL) was added. The vial was flushed with argon and heated to 100°C in a microwave reactor for 1 h. The reaction mixture was diluted with dichloromethane and filtered and the solvents were evaporated. The residue was purified by column chromatography on Silica using gradient elution with methanol in dichloromethane (0-6 %) to give N-(6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl)-4-methyl-2-(5-methylthiazol-2-yl)-2,3,4,5-tetrahydropyrido[3,2-f][1,4]oxazepin-8-amine (162 mg, 73.8 %).
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-771383a2857c4cf6924928bdcc9bb648 |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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