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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 255Erstellt: 23. Oktober 2026

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline → (R)-2-(8-(3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)acetonitrile

https://huagongshe.com/de/reaction/255

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-methoxy-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 45480181—
EduktHCID 178418223HCID 178418223—
ReagenzCesium carbonateHCID 10796—
Katalysator2-(Dicyclohexylphosphino)biphenylHCID 2734216—
KatalysatorPalladium (II) acetateHCID 4144353—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
Produkt(R)-2-(8-(3-Methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)acetonitrileHCID 498193697,81%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

3-methoxy-4-(4-methyl-1H-imidazol-1-yl)aniline (195 mg, 0.96 mmol), (R)-2-(8-chloro-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)acetonitrile (288 mg, 0.96 mmol) Palladium acetate (21.55 mg, 0.10 mmol) and Cesium carbonate (938 mg, 2.88 mmol) were added in a microwave vial. The mixture was capped and flushed with argon. 1,2-dimethoxyethane (5 mL) was added, the reaction mixture was flushed with argon and the mixture was run in a microwave for 60 minutes at 100°C. Only after two additional additions of catalyst and ligand with 3h extra runtime was the reaction complete. The reaction mixture was filtrated through Celite and washed with dichloromethane. The filtrate was concentrated and the crude product was purified by preparative chromatography 3 times yielding (R)-2-(8-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenylamino)-2-phenyl-2,3-dihydropyrido[3,2-f][1,4]oxazepin-4(5H)-yl)acetonitrile (35.0 mg, 7.81 %).

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-64de42ce56244836b512746d4c6a3fee
Quellennotiz750 AstraZeneca ELN dataset