Spiro aryl sulfone as protein kinase inhibitor
A technology of cycloalkyl and alkyl, which is applied in the direction of medical preparations containing active ingredients, organic active ingredients, organic chemistry, etc., and can solve problems such as unsatisfactory curative effect and drug loss of effectiveness
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Embodiment 1
[0103] Compound 1: 5-ChloroN4-(2-(isopropylsulfonyl)phenyl)-N2-(2-methoxy-4-(9-methyl-3,9-diazaspiro[5.5] Undec-3-yl)phenyl)pyrimidine-2,4diamine
[0104]
Embodiment 1A
[0106] 9-Benzyl-2,4-dioxo-3,9-diazaspiro[5.5]undecane-1,5-dicarbonitrile
[0107]
[0108] Ammonium acetate (2.04 g, 26.42 mmol, 0.10 eq) was added to a solution of cyanoacetate (90 g, 796 mmol, 3.00 eq) in methanol (100 mL) at 5-8°C; then 1-benzyl Basepiperidin 4-ketone (50 grams, 0.264 moles) was added to the above reaction mixture; then, below 10°C, ammonia water (46.3 grams, 370 mmoles, 1.40 equivalents) was added to the reaction mixture, and the mixture was Stir at -5°C for 1 hour. The reaction mixture was then warmed to 20°C (room temperature) and stirred for 20 hours. LCMS showed formation of product. Water (100 mL) was added to the mixture and heated to 55°C. The pH was adjusted to 4 by adding concentrated hydrochloric acid (12M) and the temperature was kept not exceeding 70°C. Then the reaction solution was cooled to 10° C., stirred for 30 minutes and then filtered. The filter cake was washed with water and left to air dry to afford the title compound (66 g, 7...
Embodiment 1B
[0110] 1′-Benzyl-3,7-diazaspiro[bicyclo[3.3.1]nonane-9,4′-piperidine]-2,4,6,8-tetraone
[0111]
[0112] A mixture of Example 1A (1.00 g, 3.10 mmol, 1.00 eq) in sulfuric acid (88%, 4 mL) was stirred at 60° C. for 4 hours. Water (1.4 mL) was then added to the reaction solution, heated to 100°C and stirred for 1 hour. Further water (5 mL) was added to the reaction mixture, cooled to 10° C., stirred at 10° C. for 30 minutes, and then filtered. The filter cake was washed with cold water (5 mL) and dried to give the title compound (1.11 g, crude) as a white solid. 1 H NMR (400MHz, CDCl 3 ): 11.87 (s, 2H), 9.56 (br.s., 1H), 7.47 (s, 5H), 4.34 (d, J=4.4Hz, 2H), 3.75 (br.s., 1H), 3.22 ( br.s., 4H), 1.88 (br.s., 4H).
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