Réaction #85187

ord-ea74635d251246288375df08850a102c

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

416 mg (1.00 mmol) of tert-butyl [5-chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]acetate in the presence of 0.95 ml (0.95 mmol, 1.2 eq.) of bis(trimethylsilyl)lithium amide (1M in THF) and 326 mg (1.58 mmol, 2.0 eq.) of isobutyl trifluoromethanesulphonate were reacted according to General Method 7B. Yield: 139 mg (purity 85%, 34% of theory)

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US09434690B2uspto-grants-2016_09