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What is the chemical structure of 5-Methoxy-2- [ (4-methoxy-3, 5-dimethyl-pyridin-2-yl) methylsulfinyl] -3H-benzoimidazole
This is the chemical structure analysis of 5-methoxy-2- [ (4-methoxy-3,5-dimethylpyridine-2-yl) methylsulfonyl] -3H-benzimidazole. Its structure is composed of several parts, such as the core skeleton of benzimidazole, which is a class of nitrogen-containing heterocyclic structures with unique chemical and biological activities. In the second position of the benzimidazole ring, there is a specific substituent, namely (4-methoxy-3,5-dimethylpyridine-2-yl) methylsulfonyl, which contains a pyridine ring. The pyridine ring is also a nitrogen-containing heterocyclic ring with methoxy at the fourth position and methyl at the 3rd and 5th positions. The second position of the pyridine ring is connected to the methylene sulfinyl group and then to the benzimidazole ring. In addition, the benzimidazole ring is connected to the methoxy group at the 5th position. The presence of this methoxy group will affect the physical, chemical and biological properties of the compound. In summary, the chemical structure of this compound is composed of a benzimidazole ring, a pyridine ring containing a specific substituent, connected by sulfinyl and methylene, and modified with methoxy at the 5 position of the benzimidazole ring. This complex structure endows the compound with specific chemical and biological properties.
What are the main uses of 5-Methoxy-2- [ (4-methoxy-3, 5-dimethyl-pyridin-2-yl) methylsulfinyl] -3H-benzoimidazole
5-Methoxy-2 - [ (4-methoxy-3,5-dimethyl-pyridine-2-yl) methylsulfonyl] -3H-benzimidazole is widely used in the field of medicine. The first way is to be a proton pump inhibitor. It can strongly inhibit the proton pump of gastric parietal cells, namely H
, K
-ATPase, thereby significantly reducing the secretion of gastric acid.
For peptic ulcers, such as gastric ulcers and duodenal ulcers, this medicine can help heal the ulcer surface. Because of the decrease in gastric acid secretion, the stimulation of the ulcer is also reduced, and the healing environment is better. According to the ancient saying, it is like a place for ulcers, building a protective embankment to prevent the erosion of gastric acid, so that the body can recover its essence.
The treatment of reflux esophagitis is also commonly used. The esophagus is invaded due to acid reflux, causing inflammation. This medicine inhibits stomach acid, can slow down esophageal inflammation, reduce the pain of heartburn and acid reflux in patients. If it is an invaded esophagus, apply a good medicine to relieve its pain and return to its normal state.
In addition, it is also useful in Helicobacter pylori eradication therapy. It is often combined with antibiotics to create an environment that is unfavorable to the survival of Helicobacter pylori, and to help antibiotics better exert their bactericidal effect in order to achieve the purpose of eradicating bacteria, such as working together to defend against enemies and eliminate diseases in the body.
What is the preparation method of 5-Methoxy-2- [ (4-methoxy-3, 5-dimethyl-pyridin-2-yl) methylsulfinyl] -3H-benzoimidazole
5-Methoxy-2 - [ (4-methoxy-3,5-dimethyl-pyridine-2-yl) methylsulfonyl] -3H-benzimidazole, which is a fine organic compound, The preparation method is very complicated, and the details are as follows.
First of all, the raw materials need to be prepared. 4-methoxy-3,5-dimethyl-2-chloromethylpyridine, 5-methoxy-2-mercaptobenzimidazole are all necessary. In a suitable reaction vessel, add an appropriate amount of alkaline catalyst, such as potassium carbonate. The amount of this catalyst needs to be precisely controlled, and more is too much, and less is not enough catalysis. In an organic solvent such as acetonitrile, stir evenly, control the temperature, and slowly heat up to 60-70 ° C. This temperature range is very critical, which is related to the reaction rate and product purity. During the reaction, molecules interact, chemical bonds are rearranged, and after several hours, the reaction is gradually completed.
Then, the product is initially formed, but it still contains impurities, and needs to be purified. It is appropriate to use column chromatography, select silica gel as the fixed phase, and prepare a suitable proportion of eluent, such as the mixture of petroleum ether and ethyl acetate. The ratio needs to be carefully debugged according to the characteristics of the product. Slowly inject the eluent, so that the product flows with it, and different impurities flow out one after another due to the different forces of the fixed phase, so that the pure product can be separated.
Looking at it again, many details need to be treated carefully during the reaction process. The purity of the raw material must be high. If it contains impurities, it is easy to cause side reactions to clump and affect the quality of the product. The reaction temperature and time also need to be precisely controlled. If the temperature is too high, it may cause the product to decompose; if the time is too short, the reaction will not be fully functional. And the operating environment needs to be clean to prevent external impurities
In summary, the preparation of 5-methoxy-2- [ (4-methoxy-3,5-dimethyl-pyridine-2-yl) methylsulfonyl] -3H-benzimidazole requires expertise in raw material selection, regulation of reaction conditions and purification to obtain high-quality products.
What are the physicochemical properties of 5-Methoxy-2- [ (4-methoxy-3, 5-dimethyl-pyridin-2-yl) methylsulfinyl] -3H-benzoimidazole
5-Methoxy-2-[ (4-methoxy-3,5-dimethyl-pyridine-2-yl) methylsulfonyl] -3H-benzimidazole is an organic compound. Its physical and chemical properties are particularly important for its application in various fields.
Looking at its properties, it is mostly in the state of white to quasi-white crystalline powder under normal circumstances, which is convenient for preliminary identification and resolution. Its melting point is very critical, about 137-140 ° C. The exact value of the melting point can provide a strong basis for the determination of material purity and characteristics. < Br >
Solubility is also an important property. The compound is slightly soluble in water, but it exhibits good solubility in organic solvents such as methanol, ethanol, dichloromethane, etc. This solubility characteristic is of great significance in its preparation, separation and purification, and preparation development. For example, in the synthesis process, selecting a suitable organic solvent can effectively promote the reaction and improve the yield; in the production of the preparation, the solubility determines whether the drug can be uniformly dispersed, which in turn affects the efficacy of the drug.
In terms of stability, the compound is relatively stable in a dry environment at room temperature. However, if exposed to high temperature, high humidity or strong light environment, its structure may be affected, and changes such as degradation may occur. This suggests that appropriate protective measures need to be taken during storage and transportation to ensure its quality and activity.
From the theory of chemical properties, its molecular structure contains benzimidazole rings, pyridine rings, and functional groups such as methoxy and sulfinyl groups. The benzimidazole ring endows it with certain basicity and can react with acids to form salts. This property can be used to improve drug solubility and stability in drug development. Pyridine rings also have unique reactivity and can participate in many nucleophilic and electrophilic substitution reactions. Sulfinyl groups affect the electron cloud distribution and spatial structure of compounds, which in turn affect their chemical and biological activities. In conclusion, the physicochemical properties of 5-methoxy-2- [ (4-methoxy-3,5-dimethyl-pyridine-2-yl) methylsulfonyl] -3H-benzimidazole play an indispensable role in its synthesis, application, storage, etc. In-depth understanding of these properties can be better utilized.
5-Methoxy-2- [ (4-methoxy-3, 5-dimethyl-pyridin-2-yl) methylsulfinyl] -3H-benzoimidazole
5-Methoxy-2 - [ (4-methoxy-3,5-dimethylpyridine-2-yl) methylsulfonyl] -3H-benzimidazole, a chemical known to the world by its trade name omeprazole. Looking at its market prospects, it is like a scene of a thousand sails racing, with magnificent waves.
Since its inception, it has been a mainstay in the treatment of digestive system diseases due to its excellent acid suppression effect. Many diseases such as gastric ulcers, duodenal ulcers, reflux esophagitis, etc. rely on it to relieve symptoms and promote healing. With the acceleration of the pace of life, the number of patients with digestive system diseases is increasing day by day, just like a surging river, continuous, creating a broad market space for it.
In addition, medical technology is changing with each passing day, and this substance is also evolving. Many new preparations continue to emerge, such as enteric-coated capsules, sustained-release tablets, etc., like stars, which not only improve the convenience and compliance of patients with medication, but also inject vitality into the market.
However, the market is not calm, and the degree of competition is intense, like a galloping horse. Similar acid-suppressing drugs are on the rise one after another, each showing its ability and wanting to get a piece of the pie. In this situation, only by constantly improving the quality and expanding the application field can we be like a midstream hit and stand on the tide.
Overall, 5-methoxy-2- [ (4-methoxy-3,5-dimethylpyridine-2-yl) methylsulfonyl] -3H-benzimidazole has broad prospects, but it also needs to overcome obstacles in order to ride the waves in the market and move forward.