Réaction #845

ord-8b2355aecdcf48e08035fb224a453205

Équation de réaction

O=S(=O)(Oc1ccc(Cl)c2cccnc12)C(F)(F)F
O=S(=O)(Oc1ccc(Cl)c2
CC(C)(C)OC(=O)N1CCNCC1
CC(C)(C)OC(=O)N1CCNC
CC(C)(C)OC(=O)N1CCN(c2ccc(Cl)c3cccnc23)CC1
CC(C)(C)OC(=O)N1CCN(
Rendement 24.3%

Solvants

Conditions de réaction

Température
75°CELSIUS

Mode opératoire

A mixture of 5-chloroquinolin-8-yl trifluoromethanesulfonate (1.8 g, 5.78 mmol), Cesium carbonate (2.63 g, 8.09 mmol), rac-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl (0.180 g, 0.29 mmol), tert- Butyl 1-piperazinecarboxylate (1.291 g, 6.93 mmol) and Palladium(II) acetate (0.065 g, 0.29 mmol) in THF (30 mL) under a nitrogen atmosphere was stirred at 75 °C for 6h. The solution was cooled to rt and diluted with ether. The mixtture was filtered through celite and the solvent was evaporated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with a gradient of 25-50% EtOAc in heptane, to afford tert-butyl 4-(5-chloroquinolin-8-yl)piperazine-1-carboxylate (0.489 g, 24.34 %) as an oil. 1H NMR (400 MHz, CHLOROFORM- _d_ ) d ppm 1.51 (s, 9 H), 3.28 - 3.37 (m, 4 H), 3.72 - 3.82 (m, 4 H), 7.06 (d, _J_ =7.81 Hz, 1 H), 7.48 - 7.57 (m, 2 H), 8.57 (dd, _J_ =8.59, 1.95 Hz, 1 H), 8.94 (dd, _J_ =4.10, 1.76 Hz, 1 H); MS m/z 348.31 [M+H]+ (ESI).

Source

750 AstraZeneca ELN dataset