Borneol derivative antibacterial agent and preparation method and application thereof
A technology of derivatives and antibacterial agents, which is applied in the field of synthetic pharmaceutical small molecules, can solve the problems of bacterial multidrug resistance, reduced curative effect, and ineffectiveness, and achieve the effects of good biocompatibility, great development potential, and strong antibacterial activity
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[0037] As mentioned above, bacterial infection has always been a concern, and antibiotics play a vital role in the treatment and control of microbial infections. This makes many conventional antibiotics less effective or ineffective against bacterial infections. In view of this, the present inventors have conducted a lot of research on antibacterial and bactericidal substances.
[0038] The inventors noticed borneol, and designed to prepare an antibacterial small molecule substance based on borneol.
[0039] Borneol, also known as borneol, has a structural formula as shown in formula (II), is a dicyclic monoterpene alcohol widely present in plants, and has a wide range of clinical and medical values, such as analgesic, antiseptic, and sedative. Borneo is almost non-toxic to the human body, and it is also a very good penetration enhancer. It has the physiological function of loosening the cell wall or increasing its permeability. It can help some drugs penetrate various physio...
Embodiment 1
[0077] In the present embodiment, the preparation flow diagram of the antibacterial small molecular substance with molecular structure as shown in formula (I) is as follows figure 1 shown.
[0078] Weigh 1.6mmol of 4-formylbenzoic acid into a reaction flask, and add 30mL of tetrahydrofuran to provide a solvent environment. Then, add 0.2mmol DMAP and 2.0mmol DCC to the solvent in sequence. After completely dissolving, add 1mmol borneol to the above system, and continue the reaction at 30°C for 24h. Suction filtration, sedimentation and purification in a large amount of petroleum ether for 2 times, and finally through column chromatography (petroleum ether: ethyl acetate = 10:1 (v / v)) and post-processing steps such as vacuum drying to obtain the target product 4-aldehyde group The pure product of bornyl benzoate (BF) has a yield of 95%. The reaction has the advantages of mild conditions and simple operation.
[0079] Adopt Fourier Transform Infrared Spectrometer (Thermo Fishe...
Embodiment 2
[0082]Weigh 1.6mmol of 4-formylbenzoic acid into a reaction flask, and add 30mL of tetrahydrofuran to provide a solvent environment. Then, add 0.2mmol DMAP and 2.0mmol DCC to the solvent in sequence. After completely dissolving, add 1mmol borneol to the above system, and continue the reaction at 25°C for 24h. Suction filtration, sedimentation and purification in a large amount of petroleum ether for 2 times, and finally through column chromatography (petroleum ether: ethyl acetate = 10:1 (v / v)) and post-processing steps such as vacuum drying to obtain the target product 4-aldehyde group The pure product of bornyl benzoate (BF) has a yield of 88%. The reaction has the advantages of mild conditions and simple operation.
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