Pyrimidine and triazole containing LSD1 inhibitor and preparation method and application thereof
A technology of triazole and inhibitor, applied in the field of medicinal chemistry
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Embodiment 1
[0080] Example 1 compound 2b, R 1 = Preparation of Propyl
[0081] Barbituric acid (3g, 1eq) and triethylamine (2.9ml, 1eq) were added to 30ml of methanol, under reflux, bromopropane (1.8ml, 1eq) was slowly added dropwise, and reflux was continued for 1 hour after the addition , cooled, and suction filtered to obtain 3.7g of pink solid compound 2b with a yield of 97%.
Embodiment 2
[0082] Example 2 Compound 3b, R 1 = Preparation of Propyl
[0083] Under ice bath, carefully dissolve 3ml of fuming nitric acid in 6ml of acetic acid, then add 2.9g of compound 2b in batches, after the addition, continue to stir for 2 hours, then add the reaction solution to 18ml of ice water, filter with suction, After washing with water, a dark red powder compound 3b was obtained with a yield of 77.5%.
Embodiment 3
[0084] Example 3 Compound 4b, R 1 = Preparation of Propyl
[0085] Compound 3b (12.4g, 1eq) was dissolved in 50ml of phosphorus oxychloride, and DMA (12ml, 1.8eq) was slowly added dropwise, then heated to reflux, and reacted for 5 hours. Cool to room temperature, hydrolyze, then extract with EA, wash with water, and then wash with saturated sodium carbonate solution, and dry the organic phase to obtain 13 g of crude brown compound 4b with a yield of 90.2%.
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