Pyrimidine derivative with ALK inhibitory activity, synthesis method and applications thereof
A pyrimidine derivative and a technology for inhibiting activity are applied in the field of structure and preparation of pyrimidine derivatives, which can solve the problems of drug resistance, patient resistance and the like, and achieve the effects of easy operation and simple preparation process.
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Embodiment 1
[0037] Example 1: 5-chloro-2-(4-(5-isopropoxy-4-((5-isopropylpyrazin-2-yl)amino)-2-methylphenyl)piperidine- 1-yl)-N-(2-(isopropylsulfonyl)phenyl)pyrimidin-4-amine
[0038]
[0039] Step 1: tert-butyl 4-(5-isopropoxy-4-((5-isopropylpyrazin-2-yl)amine)-2-methylphenyl)piperidine-1-carboxylate preparation of
[0040]Add tert-butyl 4-(4-amino-5-isopropoxy-2-methylphenyl)piperidine-1-carboxylate (220mg, 0.60mmol), 2-chloro- 5-isopropylpyrazine (110μL, 0.60mmol), 10mL of dioxane, add 4,5-bisdiphenylphosphine-9,9-dimethylxanthene (34.7mg, 0.06mmol), acetic acid Palladium (6.8mg, 0.03mmol), sodium tert-butoxide (172.8mg, 1.80mmol), stirred, filled with argon and evacuated, heated to 120°C in an oil bath. React for 10 h, wash with water, extract three times with ethyl acetate, combine the organic phases, dry over anhydrous magnesium sulfate, filter and concentrate in vacuo. The crude material was purified by silica gel chromatography (petroleum ether: ethyl acetate = 20:1, 8:1) t...
Embodiment 2
[0048] Example 2: 5-chloro-2-(4-((5-isopropylpyrazin-2-yl)amino)piperidin-1-yl)-N-(2-(isopropylsulfonyl)benzene base) pyrimidin-4-amine
[0049]
[0050] Step 1: Preparation of tert-butyl 4-((5-isopropylpyrazin-2-yl)amino)piperidine-1-carboxylate
[0051] Add tert-butyl 4-aminopiperidine-1-carboxylate (150mg, 0.75mmol), 2-chloro-5-isopropylpyrazine (150μL, 0.75mmol) and 10mL toluene successively in a 50mL reaction flask, and add 4,5-bisdiphenylphosphine-9,9-dimethylxanthene (43.5mg, 0.075mmol), palladium acetate (10mg, 0.045mmol), sodium tert-butoxide (216mg, 2.25mmol), stirring, Fill with argon to evacuate, and heat the oil bath to 120°C. Reacted for 4.5 hours, washed with water, extracted three times with ethyl acetate, combined organic phases, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The crude material was purified by silica gel chromatography (petroleum ether:ethyl acetate=50:1, 20:1, 8:1, 4:1) to obtain a light yellow solid with a ...
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