Method for preparing micro vesicle based on myristic acid and imidazole derivative non-covalent complex
A technology of myristic acid and imidazole compounds is applied in the field of preparing microvesicles based on non-covalent complexes of myristic acid and imidazole derivatives, which can solve the problem of poor stability of ordered aggregates of microvesicles, and preparation of instruments and equipment. It has the advantages of convenient industrial production and promotion, low cost, and easy operation.
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Embodiment 1
[0029] A method for preparing microvesicles based on a non-covalent complex of myristic acid and imidazole derivatives in this embodiment, comprises the following steps in sequence:
[0030] (1) Preparation of non-covalent complexes of myristic acid and N-methylimidazole
[0031] Weigh 14.02g of myristic acid, dissolve it in an appropriate amount of absolute ethanol, place it in an ice-water bath, stir and protect it under nitrogen, slowly add 8.21g of N-methylimidazole compound dropwise to a 500mL round bottom flask, and keep stirring , under the condition of nitrogen protection, slowly add the ethanol solution of myristic acid dropwise, and stir the reaction for 24 hours under nitrogen atmosphere; -Methylimidazole non-covalent compound crude product;
[0032] (2) Recrystallization and purification of non-covalent complexes of myristic acid and N-methylimidazole
[0033] Dissolve the crude myristic acid and N-methylimidazole complex in an appropriate amount of acetone under...
Embodiment 2
[0037] (1) Preparation of non-covalent complexes of myristic acid and 4-methylimidazole
[0038] Weigh 19.06g of myristic acid, dissolve it in an appropriate amount of absolute ethanol, place it in an ice-water bath, stir, and protect it under nitrogen; slowly add 10.25g of 4-methylimidazole compound dropwise to a 500mL round bottom flask, and keep stirring, Under the condition of nitrogen protection, the ethanol solution of myristic acid was slowly added dropwise, and the reaction was stirred for 18 hours under nitrogen atmosphere; Methylimidazole non-covalent complex crude product;
[0039] (2) Recrystallization and purification of non-covalent complexes of myristic acid and 4-methylimidazole
[0040] The obtained myristic acid and 4-methylimidazole non-covalent complex crude product was dissolved in an appropriate amount of acetone under heating conditions, and then 300ml of organic solvent acetonitrile was added, and the solution mixture was placed at room temperature for...
Embodiment 3
[0044] (1) Preparation of non-covalent complexes of myristic acid and 5-chloro-1-methylimidazole
[0045] Weigh 15.20g of myristic acid, dissolve it in an appropriate amount of absolute ethanol, place it in an ice-water bath, stir and protect it under nitrogen, and slowly add 16.22g of 5-chloro-1-methylimidazole compound dropwise into a 500mL round bottom flask , under the conditions of keeping stirring and nitrogen protection, slowly drop the ethanol solution of myristic acid, and stir and react under nitrogen atmosphere for 36 hours; Myristic acid and 5-chloro-1-methylimidazole non-covalent complex crude product;
[0046] (2) Recrystallization and purification of non-covalent complexes of myristic acid and 5-chloro-1-methylimidazole
[0047] Dissolve the crude myristic acid and 5-chloro-1-methylimidazole non-covalent complex in an appropriate amount of acetone under heating, then add 100ml of acetonitrile, cool slowly, and let stand for 2 hours, the solution precipitates T...
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