تفاعل #472

ord-f01bb0709ba64daa9f491765ab642ed8

معادلة التفاعل

Fc1cc(F)cc(Br)c1
Fc1cc(F)cc(Br)c1
COC(=O)c1cc(C2CCCN2)c2oc(N3CCOCC3)cc(=O)c2c1
COC(=O)c1cc(C2CCCN2)
COC(=O)c1cc(C2CCCN2c2cc(F)cc(F)c2)c2oc(N3CCOCC3)cc(=O)c2c1
COC(=O)c1cc(C2CCCN2c
المردود 58.1%

المذيبات

ظروف التفاعل

درجة الحرارة
80°CELSIUS

الإجراء التجريبي

Pd complexe (33.2 mg, 0.04 mmol) was added to a stirred mixture of methyl 2-morpholino-4-oxo-8-(pyrrolidin-2-yl)-4H-chromene-6-carboxylate (270 mg, 0.75 mmol), 1-bromo-3,5-difluorobenzene (0.095 ml, 0.83 mmol) and cesium carbonate (368 mg, 1.13 mmol) dissolved in 1,4-dioxane (5 ml). The resulting suspension was degased with argon and then stirred at 80 °C. After 18 hours, lcms showed incomplete reaction: 5% more reactants were added and heating was continued at 100 °C for 5 additionnal hours. Lcms showed ~ complete reaction after 23 hours. The reaction mixture was allowed to cool to room temperature, filtered and concentrated. The crude product was purified by flash chromatography on silica gel eluting with 0 to 6% methanol in ethyl acetate. The solvent was evaporated to dryness to afford methyl 8-(1-(3,5-difluorophenyl)pyrrolidin-2-yl)-2-morpholino-4-oxo-4H-chromene-6-carboxylate (206 mg, 58.1 %) as a clear yellow foam. LCMS and NMR are OK

المصدر

750 AstraZeneca ELN dataset