Triethylamine → HCID 67494748, compound

Participants

Reaction Steps

Compound, tert-butyl 7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-yl(piperidin-4-ylmethyl)carbamate (1 equiv) was stirred in a mixture of methyl isocyanate (1.1 equiv), and triethylamine (1.5 equiv) in dichloromethane at 0° C. until the reaction was deemed complete by TLC, HPLC, or LC-MS analysis. The reaction mixture was poured into saturated aqueous ammonium chloride, and then extracted twice with dichloromethane. The combined organics were dried over sodium sulfate, filtered, concentrated, and purified on silica gel to give the desired product. This material (1 equiv) and NBS (1.05 equiv) in acetonitrile was stirred at room temperature until the reaction was deemed complete by HPLC, LC-MS, or TLC analysis. The reaction mixture was concentrated, re-dissolved in dichloromethane, washed with saturated aqueous sodium thiosulfate, dried over sodium sulfate, filtered, concentrated, and purified on silica gel. The resulting material was stirred with the palladium catalysts (0.2 equiv each) and stannane (1.5 equiv) in dioxane at 160° C. until the reaction was deemed complete by HPLC, LC-MS, or TLC analysis. The reaction was allowed to cool to room temperature, diluted with ethyl acetate, washed with brine, dried over sodium sulfate, filtered, concentrated, and purified in silica gel. The resulting material was stirred in TFA and water at room temperature until the reaction was deemed complete by HPLC, LC-MS, or TLC analysis. The mixture was concentrated, purified by prep-HPLC, and freeze-dried to afford compound 4-((7-amino-6-cyano-3-(6-fluoroquinolin-3-yl)pyrazolo[1,5-a]pyrimidin-5-ylamino)methyl)-N-methylpiperidine-1-carboxamide.

Provenance & Evidence