Cesium carbonate → 3-Methoxy-N-methyl-4-((5-(pyridin-4-yl)-4-((tetrahydro-2H-pyran-4-yl)oxy)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidin-2-yl)amino)benzamide

Participants

Reaction Conditions

Reaction Steps

To a solution of 2-chloro-5-(pyridin-4-yl)-4-((tetrahydro-2H-pyran-4-yl)oxy)-7-((2-(trimethylsilyl)ethoxy)methyl)-7H-pyrrolo[2,3-d]pyrimidine (1 equiv), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (0.2 equiv), tris(dibenzylideneacetone)dipalladium(0) (0.1 equiv), 4-amino-3-methoxy-N-methylbenzamide (1.1 equiv) in 1,4-dioxane (0.1 M) was added cesium carbonate (3 equiv). The reaction mixtures were heated, with microwave irradiation, in a microwave reactor at 150° C. for 2 h. The reaction mixture was quenched with saturated aqueous sodium chloride and then washed with ethyl acetate. The organic phase was combined and washed with saturated aqueous sodium chloride. The organic layer was dried (magnesium sulfate), filtered, and concentrated. The crude was purified by silica gel column chromatography (0-90%) ethyl acetate (with 10% 1N ammonia in methanol) in hexane) to give the title compound (49.1% yield) as yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm −0.11 (s, 9 H) 0.85-0.93 (m, 2 H) 1.68-1.82 (m, 2 H) 2.06-2.18 (m, 2 H) 2.79 (d, J=4.30 Hz, 3 H) 3.51-3.66 (m, 4 H) 3.77-3.86 (m, 2 H) 3.96 (s, 3 H) 5.47-5.55 (m, 1 H) 5.56 (s, 2 H) 7.50-7.57 (m, 2 H) 7.71-7.76 (m, 2 H) 7.83 (s, 1 H) 7.92 (s, 1 H) 8.34 (q, J=4.43 Hz, 1 H) 8.52-8.60 (m, 3 H); MS (ESI) m/z 605.6 [M+1]+.

Provenance & Evidence