HRID2274526

反应详情

EQUATION

反应方程式

HRID 2274526 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

For reference purposes 2-((4R,6S)-6-((E)-2-(4-(4-fluorophenyl)-6-isopropyl-2-(N-methylmethylsulfonamido)pyrimidin-5-yl)vinyl)-2,2-dimethyl-1,3-dioxan-4-yl)acetate 4-methylpentan-2-yl ester was prepared from rosuvastatin methyl ester (EP 521471). Thus, rosuvastatin methyl ester (30 g, 61 mmol) was added to 200 mL of acetonitrile and 2N aqueous NaOH was added until the pH was stable at 12.5. The reaction mixture was stirred for 2 h at 20° C. Then the pH was lowered to 5.0 with 2N aqueous HCl. To the reaction mixture was added 200 mL of ethyl acetate and the organic phase was separated and washed 2 times with 100 mL of water. The ethyl acetate phase was dried over Na2SO4, filtered and evaporated to a syrup (≈30 g of rosuvastatin acid). Part of this syrup (20 g) was dissolved in toluene and heated to reflux under azeotropic water removal for 4 h. The reaction mixture was cooled to 20° C. and stirred for 18 h. The precipitated solid was filtered, washed with toluene (2×10 mL) and dried to give 16.1 g (35 mmol) of N-(4-(4-fluorophenyl)-5-((E)-2-((2S,4R)-4-hydroxy-6-oxotetrahydro-2H-pyran-2-yl)vinyl)-6-isopropylpyrimidin-2-yl)-N-methylmethanesulfonamide as a white solid. 1H NMR (300 MHz, CDCl3) δ 7.62 (dd, 2H), 7.11 (dd, 2H), 6.72 (dd, 1H), 5.48 (dd, 1H), 5.28-5.20 (m, 1H), 4.38-4.30 (m, 1H), 3.58 (s, 3H), 3.52 (s, 3H), 3.38-3.30 (m, 1H), 2.80-2.60 (m, 2H), 2.10-2.00 (m, 1H), 1.95-1.85 (m, 1H), 1.73-1.68 (m, 1H), 1.28 (d, 3H), 1.26 (d, 3H).

WORKUP

后处理

  1. additionwas added until the pH
  2. customthe organic phase was separated
  3. washwashed 2 times with 100 mL of water
  4. dry with materialThe ethyl acetate phase was dried over Na2SO4
  5. filtrationfiltered
  6. customevaporated to a syrup (≈30 g of rosuvastatin acid)
  7. dissolutionPart of this syrup (20 g) was dissolved in toluene
  8. temperatureheated
  9. temperatureto reflux under azeotropic water
  10. customremoval for 4 h
  11. temperatureThe reaction mixture was cooled to 20° C.
  12. stirringstirred for 18 h
  13. filtrationThe precipitated solid was filtered
  14. washwashed with toluene (2×10 mL)
  15. customdried