Ceftriaxone sodium compound prepared by adopting supermolecular mechanism and preparation thereof
A technology of ceftriaxone sodium and its compounds, which is applied in the field of ceftriaxone sodium compounds and its preparations, and can solve the problems of poor product quality, waste of raw materials, instability between batches, etc.
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Embodiment 1
[0025] Add 50ml of water and 15ml of N,N-dimethylformamide into a jacketed reactor, then add 15.12g of crude ceftriaxone sodium into the above mixture, stir continuously until dissolved, and then adjust the pH value with sulfuric acid 5.5. After the reaction was complete, the liquid was transferred to a jacketed crystallizer, the temperature was lowered to 22°C in a water bath, an elliptical seed crystal was added, and the crystal was grown for 3 hours. Carbon tetrachloride was slowly added to the above solution and filtered. Dissolve the above filtrate in 25ml of water, add 0.2g of activated carbon, stir and absorb for 30min, and filter. Add 100ml of acetone to the filtrate, stir until it is completely precipitated, and filter. The filtrate was washed with 25ml×2 acetone, and dried under vacuum at 40°C for 3h to obtain 14.91g of ceftriaxone sodium.
[0026] X-ray powder diffraction (XRPD) was used to study and characterize the crystalline form of ceftriaxone sodium.
[00...
Embodiment 2
[0033] Add 50ml of water and 15ml of N-methylacetamide into the jacketed reactor, then add 15.04g of crude ceftriaxone sodium into the above mixture, stir continuously until dissolved, and then adjust the pH to 5.2 with hydrochloric acid. After the reaction was complete, the liquid was transferred to a jacketed crystallizer, the temperature was lowered to 25°C in a water bath, an elliptical seed crystal was added, and the crystal was grown for 3 hours. Carbon trichloride was slowly added to the above solution and filtered. Dissolve the above filtrate in 25ml of water, add 0.2g of activated carbon, stir and absorb for 30min, and filter. Add 100ml of acetone to the filtrate, stir until it is completely precipitated, and filter. Wash the filtrate with 25ml×2 acetone, and dry it under vacuum at 35°C for 4h to obtain 14.71g of ceftriaxone sodium.
Embodiment 3
[0035] Add 50ml of water and 15ml of N,N-dimethylformamide into a jacketed reactor, then add 15.10g of crude ceftriaxone sodium into the above mixture, stir continuously until dissolved, then adjust the pH value with hydrochloric acid 6.0. After the reaction was complete, the liquid was transferred to a jacketed crystallizer, cooled to 23° C. in a water bath, and needle-shaped seed crystals were added to grow the crystals for 3 hours. Carbon tetrachloride was slowly added to the above solution and filtered. Dissolve the above filtrate in 25ml of water, add 0.2g of activated carbon, stir and absorb for 30min, and filter. Add 100ml of acetone to the filtrate, stir until it is completely precipitated, and filter; wash the filtrate with 25ml of acetone x 2, and dry it under vacuum at 35°C for 4h to obtain 14.74g of ceftriaxone sodium.
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