A kind of atropine hapten and its synthesis method, antigen, antibody and application
A synthetic method and atropine technology, which are applied in chemical instruments and methods, material testing products, animal/human proteins, etc., to achieve the effects of low cost, convenient use, and economical speed.
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Embodiment 1
[0036] The preparation of embodiment 1 atropine hapten
Embodiment 1-1
[0037] Embodiment 1-1 a kind of synthetic method of atropine hapten, it may further comprise the steps:
[0038]
[0039] (1): Add 2.5g of nortropine alcohol, 2.8g of anhydrous potassium carbonate and 27mL of DMF (N,N-dimethylformamide) into a 100mL single-necked flask and stir evenly, then add 6-bromo-1 - 3.3 g of hexene, stirred and reacted at 80° C. for 6 h (detected on a TLC plate, color developed by potassium permanganate). After the reaction was completed, cool to room temperature, rotate the oil pump to evaporate under reduced pressure, distill off the solvent DMF, add methanol to dissolve and filter out insoluble matter. After methanol was evaporated to dryness, it was purified by column to obtain a brown viscous oil, that is, intermediate 1; the specific chemical reaction formula involved in this step is shown above.
[0040]
[0041] (2): at N 2 Under the atmosphere, 3.0 g of methyl phenylacetate, 2.2 g of ethyl formate, and 60 mL of dichloromethane were adde...
Embodiment 1-2
[0048] Embodiment 1-2 a kind of synthetic method of atropine hapten, it may further comprise the steps:
[0049] (1): Add 5.0g of nortropine alcohol, 11.2g of anhydrous potassium carbonate and 100mL of DMF (N,N-dimethylformamide) into a 250mL single-necked flask and stir evenly, then add 6-bromo-1 - 8.0 g of hexene, stirred and reacted at 80° C. for 6 h (detected on a TLC plate, color developed by potassium permanganate). After the reaction was completed, cool to room temperature, rotate the oil pump to evaporate under reduced pressure, distill off the solvent DMF, add methanol to dissolve and filter out insoluble matter. After methanol was evaporated to dryness, it was purified by column to obtain a brown viscous oil, namely Intermediate 1.
[0050] (2): at N 2 Under the atmosphere, 6.0 g of methyl phenylacetate, 8.8 g of ethyl formate, and 100 mL of dichloromethane were added into a 250 mL single-necked flask, stirred evenly, and cooled to 0°C. While stirring, 12.0 g of t...
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