Nitrogen-containing heterocyclic compound or salt thereof
A compound and heterocyclic technology, applied in the direction of active ingredients of heterocyclic compounds, drug combinations, organic chemistry, etc.
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Embodiment 1
[0844] (1)
[0845] [chemical formula 45]
[0846]
[0847] To a solution of 11.6 g of ethyl 4-chloro-2-(methylthio)pyrimidine-5-carboxylate in 100 mL of tetrahydrofuran, 8.4 mL of triethylamine and 5.1 mL of propylamine were added under ice-cooling, and stirred at room temperature for 30 minute. A 1.0 mol / L aqueous hydrochloric acid solution and ethyl acetate were added to the reaction mixture. The organic layer was separated, washed successively with saturated aqueous sodium bicarbonate and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure to obtain oily 2-(methylthio)-4-( Propylamino)pyrimidine-5-carboxylic acid ethyl ester (A1) 11.7g.
[0848] 1 H-NMR (CDCl 3 )δ: 8.61 (1H, s), 8.27 (1H, brs), 4.32 (2H, q, J=7.0Hz), 3.55-3.48 (2H, m), 2.53 (3H, s), 1.73-1.60 (2H , m), 1.37(3H, t, J=7.3Hz), 0.99(3H, t, J=7.6Hz).
[0849] (2)
[0850] [chemical formula 46]
[0851]
[0852] In a s...
Embodiment 2
[0884] (1)
[0885] [chemical formula 53]
[0886]
[0887] 302 mg of N-(3-aminophenyl)-2,2,2-trifluoro-N-methylacetamide, 4-(propylamino)-2-((2- (Pyridin-4-yl) ethyl) amino) pyrimidine-5-carboxylic acid (A3) 627mg, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride 545mg and 1 Add 15 mL of N,N-dimethylformamide and 766 μL of triethylamine to 377 mg of -hydroxybenzotriazole monohydrate at room temperature, seal the reaction vessel, and stir at 100°C for 40 minutes using a microwave reactor . After cooling the reaction mixture to room temperature, it was added to saturated aqueous sodium bicarbonate and ethyl acetate. The organic layer was separated, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography (eluent: 97-96% ethyl acetate / methanol) to give 4-(propylamino)-2-((2-(pyridin-4-yl )ethyl)amino)-N-(3-(2,2,2-trifluoro-N-methylacetamide)phenyl)pyri...
Embodiment 3
[0907] Compounds (1-3) to (1-12) were obtained by the same method as in Example 1(7) or Example 1(8).
[0908] Table 16
[0909]
[0910] Table 17
[0911]
[0912] Table 18
[0913]
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