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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt6-Methoxy-5-(4-methyl-1H-imidazol-1-YL)pyridin-2-amineHCID 53402967—
EduktHCID 57512921HCID 57512921—
ReagenzCesium carbonateHCID 10796—
Katalysator2-(Dicyclohexylphosphino)biphenylHCID 2734216—
KatalysatorPalladium (II) acetateHCID 4144353—
Lösungsmittel1,2-DimethoxyethaneHCID 8071—
ProduktHCID 57512844HCID 5751284473,84%

Reaktionsbedingungen

Temperatur100 °C

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

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-771383a2857c4cf6924928bdcc9bb648
Quellennotiz750 AstraZeneca ELN dataset