Réaction #215

ord-20af979b60da4f278f5b92ae2abaf8ca

Équation de réaction

CC(Nc1nc(Cl)nc(N2CCOCC2)c1F)c1ncc(F)cc1F
CC(Nc1nc(Cl)nc(N2CCO
Cc1cc(N)nn1C(=O)OC(C)(C)C
Cc1cc(N)nn1C(=O)OC(C
Cc1cc(Nc2nc(NC(C)c3ncc(F)cc3F)c(F)c(N3CCOCC3)n2)n[nH]1
Cc1cc(Nc2nc(NC(C)c3n

Solvants

Conditions de réaction

Température
110°CELSIUS

Mode opératoire

9,9-Dimethyl-4,5-bis(diphenylphosphino)xanthene (27.9 mg, 0.05 mmol), 2-chloro-N-(1-(3,5-difluoropyridin-2-yl)ethyl)-5-fluoro-6-morpholinopyrimidin-4-amine (200 mg, 0.54 mmol), tert-butyl 3-amino-5-methyl-1H-pyrazole-1-carboxylate (127 mg, 0.64 mmol) and cesium carbonate (349 mg, 1.07 mmol) were added to dioxane (8 mL). The mixture was purged with nitrogen for 15 minutes. Pd2(dba)3 (29.4 mg, 0.03 mmol) was added and the mixture heated at 110 °C for 3h. No sign of any reaction.

Source

750 AstraZeneca ELN dataset