A kind of synthetic method of palbociclib
A synthetic method and compound technology, applied in the field of drug synthesis, can solve the problems of rare raw materials, cumbersome operations, and low total yield of products, and achieve the effects of mild and controllable reaction conditions, simplified reaction routes, and simple process routes
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Embodiment 1
[0040] (1) Preparation of Compound 3
[0041] Add 18.62g of compound 4, 22.03g of compound 5, and 13.33g of aluminum trichloride into a three-neck flask, add 250ml of ethanol, stir at room temperature for 4h, add 4.00g of sodium hydroxide, stir at room temperature for 3h, adjust the pH to 5 with 2M dilute hydrochloric acid , stirred for 30 minutes and then raised to 60°C, cooled to room temperature after the solid was completely dissolved, filtered under reduced pressure, and dried to obtain 29.02g of compound 3 with a yield of 84.69% and a purity of 99.92%.
[0042] (2) Preparation of compound 1
[0043] Mix 17.12g of compound 3 with 200ml of isopropanol, add 4.26g of cyclopentylamine, control the temperature at 20-60°C, heat to reflux for 4h, add 2.70g of sodium methoxide, stir for 30min, add 6.46g of compound 2 for reflux reaction for 3h, drop to normal temperature, filtered, washed with deionized water, and dried in vacuum to obtain 20.15 g of compound 1 with a yield of 8...
Embodiment 2
[0045] (1) Preparation of Compound 3
[0046] Add 20.18g of compound 4, 22.03g of compound 5, and 24.33g of ferric chloride into the three-neck flask, add 250ml of dichloromethane, stir at room temperature for 4h, add 11.22g of potassium hydroxide, stir at room temperature for 3h, adjust the pH with 2M dilute hydrochloric acid to 5, stirred for 30 minutes and then raised to 60°C, cooled to room temperature after the solid was completely dissolved, filtered under reduced pressure, and dried to obtain 28.91g of compound 3 with a yield of 84.33% and a purity of 99.87%.
[0047] (2) Preparation of compound 1
[0048] Mix 17.12g of compound 3 with 200ml of dichloromethane, add 3.83g of cyclopentylamine, control the temperature at 20-60°C, heat to reflux for 4h, add 6.81g of sodium ethylate, stir for 30min, add 6.46g of compound 2 for reflux reaction for 3h, drop to normal temperature, filtered, washed with deionized water, and dried in vacuum to obtain 18.23 g of compound 1 with a...
Embodiment 3
[0050] (1) Preparation of Compound 3
[0051] Add 19.55g of compound 4, 22.03g of compound 5, 16.36g of zinc dichloride into the three-neck flask, add 250ml of methanol, stir at room temperature for 4h, 13.8g of potassium carbonate, stir at room temperature for 3h, adjust the pH to 5 with 2M dilute hydrochloric acid, and stir After 30 minutes, it was raised to 60°C, cooled to room temperature after the solid was completely dissolved, filtered under reduced pressure, and dried to obtain 28.98 g of compound 3 with a yield of 84.56% and a purity of 99.90%.
[0052] (2) Preparation of compound 1
[0053] Mix 17.12g of compound 3 with 200ml of ethanol, add 4.26g of cyclopentylamine, control the temperature at 20-60°C, heat and reflux for 4h, add 5.40g of sodium methoxide, stir for 30min, add 6.46g of compound 2 for reflux reaction for 3h, and lower to room temperature , filtered, washed with deionized water, and dried in vacuum to obtain 20.10 g of compound 1 with a yield of 89.65...
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