Method of purifying plavastatin
A purification method and pravastatin technology, applied in the field of salt separation or purification, can solve the problems of purity retention, reduction of pravastatin yield, unrecorded purity of pravastatin, etc.
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Embodiment 1
[0160] Example 1 Extraction from culture concentrate with n-butyl acetate
[0161] (1a) Concentration of culture solution
[0162] After adjusting 10 L of the pravastatin culture solution after transformation culture to pH 12 with sodium hydroxide, it was heated to 50° C. and stirred for 30 minutes. After the culture solution was cooled to room temperature, 500 g of Celite 545 (trademark) (manufactured by CELITE CORPORATION) was added as a filter aid and filtered. 3 L of water was added to the separated bacterial cells, suspended again, and then filtered. The obtained two concentrates were combined to obtain 10 L of culture concentrate.
[0163] (1b) Extraction with n-butyl acetate
[0164] After adjusting the resulting culture concentrate to pH 5.7 with 25% sulfuric acid, 5 L of n-butyl acetate was added and stirred to extract pravastatin. The separated aqueous layer was adjusted to pH 5.7 with 75% sulfuric acid, then 5 L of n-butyl acetate was added, and stirred for ext...
Embodiment 2
[0165] Example 2 Extraction from culture concentrate with n-propyl acetate
[0166] N-propyl acetate was used to replace n-butyl acetate, and the same treatment as in Example 1 was carried out to obtain an aqueous sodium salt solution of pravastatin. As determined by HPLC (condition A), the purity of pravastatin sodium was 85% or above. As can be seen from the results of this example, high-purity pravastatin sodium can be obtained by using n-propyl acetate.
Embodiment 3
[0167] Example 3 Decomposition of impurities with phosphoric acid
[0168] Add 350 ml of ethanol to the aqueous solution obtained in Example 1 [compound (I) / pravastatin sodium measured by HPLC (condition A) is 9.3%], adjust it to pH 3.0 with phosphoric acid, then stir at 50° C. for 10 minutes . Compound (I) / pravastatin sodium determined by HPLC (condition A) was 0.9%. From the results of this example, it was found that compound (I) can be significantly removed by using phosphoric acid.
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