A kind of preparation method of cilastatin sodium crude drug
A technology of cilastatin sodium and cilastatin, which is applied in the field of medicinal chemistry, can solve the problems of taking a long time, reducing the activity of raw materials, and consuming a long time, so as to avoid the reduction of chemical activity and improve the quality and yield , to avoid the effect of excessive losses
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Embodiment 1
[0086] Embodiment 1: the preparation of cilastatin sodium of the present invention
[0087] (1) Preparation of compound cilastatin shown in formula (VI):
[0088] At 0°C, add 15g of sodium hydroxide to 100g of water, stir for 10min, then add 10g of compound (Z)-7-chloro-2((S)-2,2-dimethylcyclo Propyl formamido)-2-heptenoic acid, stirred for 10min; at -5°C, 9g of cysteine hydrochloride monohydrate was added, stirred for 10min, and the reaction started at 25°C until analyzed by HPLC, Complete the reaction when the normalized content of (Z)-7-chloro-2((S)-2,2-dimethylcyclopropylcarboxamido)-2-heptenoic acid in the resulting reaction solution is less than 5%. After cooling down to 25°C, add 300g of water to the solution, stir, and slowly add 6M hydrochloric acid solution to the solution to adjust the pH value to 1. Add the obtained solution to a Φ60*5.5m macroporous adsorption resin column HZ-820, first elute with water, and then change to acetone aqueous solution for elution...
Embodiment 2
[0091] Embodiment 2: the preparation of cilastatin sodium of the present invention
[0092] (1) Preparation of compound cilastatin shown in formula (VI):
[0093] At 10°C, add 9g of sodium hydroxide to 80g of water, stir for 10min, then add 10g of compound (Z)-7-chloro-2((S)-2,2-dimethylcyclo Propyl formamido)-2-heptenoic acid, stirred for 10min; at 10°C, 8.5g of cysteine hydrochloride monohydrate was added, stirred for 10min, and the reaction started at 35°C until it was analyzed by HPLC The reaction is completed when the normalized content of (Z)-7-chloro-2((S)-2,2-dimethylcyclopropylcarboxamido)-2-heptenoic acid in the obtained reaction solution is less than 5%; After cooling down to 30° C., 250 g of water was added to the solution, stirred, and 6M hydrochloric acid solution was slowly added to the solution to adjust the pH value to 1.5. Add the obtained solution to a Φ35*3.5m macroporous adsorption resin column HZ-818, first elute with water, and then change to metha...
Embodiment 3
[0096] Embodiment 3: the preparation of cilastatin sodium of the present invention
[0097] (1) Preparation of compound cilastatin shown in formula (VI):
[0098] At 0°C, add 11g of sodium hydroxide to 70g of water, stir for 10min, then add 10g of compound (Z)-7-chloro-2((S)-2,2-dimethylcyclo Propyl formamido)-2-heptenoic acid, stirred for 10min; at 0°C, 8.3g of cysteine hydrochloride monohydrate was added, stirred for 10min, and the reaction started at 45°C until it was analyzed by HPLC The reaction is completed when the normalized content of (Z)-7-chloro-2((S)-2,2-dimethylcyclopropylcarboxamido)-2-heptenoic acid in the obtained reaction solution is less than 5%; After cooling down to 5° C., 200 g of water was added to the solution, stirred, and 6M hydrochloric acid solution was slowly added to the solution to adjust the pH value to 2. Add the obtained solution to a Φ20*2.5m macroporous adsorption resin column HZ-816, first elute with water, and then change to methanol ...
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