A kind of amantadine artificial hapten, artificial antigen and its preparation method and application
An artificial hapten, amantadine technology, applied in the preparation of carboxylic acid amides, chemical instruments and methods, preparation of organic compounds, etc. Good sex, improve immune characteristics, good specificity
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Embodiment 1
[0055] This implementation of a preparation method of amantadine artificial antigen (the reaction process is as figure 1 ), including the following steps:
[0056] (1) Preparation of artificial haptens:
[0057] ① Weigh 200mg amantadine (1.322mmol) and 198mg succinic anhydride (1.980mmol) in a 100ml single-necked round bottom flask, add 10ml pyridine, add a stir bar, heat the oil bath to 100°C and stir reflux for 16 hours; react After the end, the solvent was evaporated under reduced pressure. The residue was dissolved in 15ml double-distilled water. The aqueous solution was extracted with 3×15ml dichloromethane. The organic phases were combined and washed with 15ml double-distilled water. The organic phase was dried over anhydrous magnesium sulfate, filtered, and transferred. After drying, 252 mg of colorless oily product A is obtained;
[0058] The colorless oily product A was subjected to TLC detection, and the chromatographic solution was an aqueous ethanol solution with a conce...
Embodiment 2
[0075] This implementation of a preparation method of amantadine artificial antigen (the reaction process is as figure 1 ), including the following steps:
[0076] (1) Preparation of artificial haptens:
[0077] ①Weigh 200mg amantadine (1.322mmol) and 145.6mg succinic anhydride (1.455mmol) in a 100ml single-necked round bottom flask, add 10ml pyridine, add a stir bar, heat the oil bath to 105°C and stir reflux for 17 hours; After the reaction, the solvent was evaporated under reduced pressure. The residue was dissolved in 15ml of double-distilled water. The aqueous solution was extracted with 3×15ml of dichloromethane. The organic phases were combined and washed with 15ml of double-distilled water. The organic phase was dried over anhydrous magnesium sulfate and filtered. After drying, 251.5mg of colorless oily product A is obtained;
[0078] The colorless oily product A was subjected to TLC detection, and the chromatographic solution was an aqueous ethanol solution with a concentra...
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