Cesium carbonate → tert-Butyl 5-[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo-[4,5-b]pyridin-5-yl]-3,3a,4,6a-tetrahydrocyclopenta[c]pyrrole-2(1H)-carboxylate

Participants

Reaction Conditions

Reaction Steps

tert-Butyl 5-{[(trifluoromethyl)sulfonyl]oxy}-3,3a,4,6a-tetrahydrocyclopenta-[c]pyrrole-2(1H)-carboxylate (8-2, 2 g, 5.5 mmol, 1.0 equiv), bis(pinocolato)diboron (1.5 g, 6.1 mmol, 1.1 equiv), potassium acetate (1.6 g, 16.8 mmol, 3.0 equiv) and PdCl2(dppf) (0.288 g, 0.392 mmol, 0.07 equiv) were added to anhydrous 1,4-dioxane (7 mL) and heated to 60° C. After 18 h, the reaction contents were cooled to RT, followed by the subsequent addition of water (1.4 mL), 5-chloro-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]-pyridin-2-one (1-4, 1.4 g, 5.5 mmol, 1.0 equiv), Cs2CO3 (3.6 g, 11.1 mmol, 2.00 equiv) and Bis(tri-tert-butylphosphine)palladium(0) (0.372 g, 0.728 mmol, 0.13 equiv). The resulting mixture was heated to 60° C. for 4.5 h. Following this duration, LCMS showed consumption of starting material. The contents were then cooled to room temperature, diluted with ethyl acetate (50 mL), filtered through Celite and rinsed with ethyl acetate (3×50 mL) and water (1×30 mL). The filtrate layers were separated and the combined organics were washed with saturated NaHCO3 (100 mL). The combined aqueous layers were then back-extracted with ethyl acetate (2×50 mL). The combined organics were dried over Na2SO4, filtered and concentrated in vacuo to give a dark red oil. Purification by normal-phase chromatography (0-50% EtOAc:Hex) afforded 8-3 as an off-white solid. MS m/z (M+H): calculated=427.55; observed=427.2.

Provenance & Evidence