Potassium Phosphate, Tribasic → HCID 66678170, Verbindung

Beteiligte Stoffe

Reaktionsbedingungen

Reaktionsschritte

To a reactor was charged, 3-Amino-6-bromo-N-(pyridin-3-yl)pyrazine-2-carboxamide (1580 g), tert-butyl (3-methoxypropyl){3-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]propyl}carbamate (2778 g) 1-butanol (23.7 L), potassium phosphate, tribasic, N-hydrate (2740 g) and water (1.58 L). The contents were stirred under nitrogen at ambient (21° C.). In a second reactor was made up a solution of 3-(di-tert-butylphosphonium)propane sulphonate (DTBPPS) (83.04 g); sodium tetrachloropalladate (45.52 g) and water (1.58 L). The catalyst/ligand solution was poured into the reaction; the reaction was inerted and heated up to 80° C. The reaction was stirred for 2 hours at 80° C. The batch was cooled to 60° C. and water (22.1 L) was added. The contents washed with water at 60° C. The organic layer and interface were filtered through perlite (500 g) made up with 1-Butanol (3.95 L). The organic liquors were recharged to the vessel and washed with water (11.1 L) at 60° C. The organic liquor was washed with 10% w/v aqueous sodium chloride (11.2 L) at 60° C. The organic liquors were heated up to 60° C. and distilled under vacuum to ˜10 relative volumes. The batch was cooled to 20° C. and left to stir for 16 hours under nitrogen. The contents were filtered and washed with 1-Butanol (4 L×2). The yellow free flowing solid was discharged and dried in vacuum oven at 40° C. overnight (tert-butyl (3-{4-[5-amino-6-(pyridin-3-ylcarbamoyl)pyrazin-2-yl]phenyl}propyl)(3-methoxypropyl)carbamate (2428 g)).

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