As a leading (S)-(-)-10-(1-Aminocyclopropyl)-9-Fluoro-3-Methyl-7-Oxo-2,3-Dihydro-7H-Pyrido[1,2,3-De][1,4]Benzoxazine -6-Carboxylic Acid Monomethanesulfonate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
(S) - (-) -10- (1-aminocyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyridino [1,2,3-de] [1,4] What is the chemical structure of benzoxazine-6-carboxylic acid monomethanesulfonate
What is the chemical structure of (S ) - ( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - fluoro - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - pyrido [1,2,3 - de] [1,4] benzoxazine - 6 - carboxylic acid monomethyl ester hydrochloride? Its main structure seems to be pyridino [1,2,3 - de] [1,4] benzoxazine. On this structure, there are (1-hydroxy cyclopropyl) at position 10, fluorine atoms at position 9, methyl at position 3, oxygen at position 7, dihydrogen between positions 2 and 3, and carboxylic acid monomethyl ester hydrochloride at position 6.
From the overall layout, the core structure of pyridino-benzoxazine lays the basic framework, like the pillars of a building. And each substituent is attached to the decoration of the pillars. 1-Hydroxycyclopropyl is based on position 10, hydroxyl is hydrophilic, cyclopropyl has a unique spatial structure, and the connection of the two has a great influence on the properties of compounds. Fluorine atoms at position 9 can significantly change the electron cloud distribution of molecules due to their strong electronegativity, which affects the polarity and reactivity of compounds. A is based on position 3, although it is relatively simple, but its electron effect will also affect the electron cloud density of surrounding chemical bonds. The oxygen generation at position 7 gives this position a certain reactivity and polarity. The dihydrogen structure at positions 2 and 3 may affect the conjugation system and stability of the whole molecule. The carboxylic acid monomethyl ester hydrochloride at position 6 has both acidic, hydrophilic and salt-forming properties, and is of great significance to the solubility and reactivity of the compound. This is my analysis of the chemical structure of the compound.
(S) - (-) -10- (1-aminocyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyridino [1,2,3-de] [1,4] What are the main uses of benzoxazine-6-carboxylic acid monomethanesulfonate
(S ) - ( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - fluoro - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - pyrido [1,2,3 - de] [1,4] benzoxazine - 6 - carboxylic acid monomethyl ester hydrochloride Common main uses are: This compound belongs to a structural form of quinolone antibacterial drugs. In the field of medicine, it is mainly used for antibacterial treatment. It can inhibit the activity of bacterial DNA rotatase (bacterial topoisomerase II) and topoisomerase IV, and hinder the process of bacterial DNA replication, transcription and repair, so as to kill bacteria or inhibit their growth. It is often used to treat a variety of infectious diseases caused by sensitive bacteria, such as respiratory tract infections, including pneumonia, bronchitis, etc., and can effectively fight pathogenic bacteria such as Streptococcus pneumoniae and Haemophilus influenzae; urinary system infections, such as urethritis and cystitis, have good antibacterial effect on common pathogens such as Escherichia coli; intestinal infections, can deal with diarrhea and other diseases caused by Shigella and Salmonella. It can also be used for skin and soft tissue infections, and has a therapeutic effect on infections such as boils and carbuncles caused by Staphylococcus aureus.
Viewing the structure and characteristics of this compound, it is like the divine medicine condensed by the Xianjia with a wonderful method. Its application in medical medicine is like immortal magic to resolve the pain of human diseases. With its exquisite structure, it breaks the barrier of pathogens and protects the well-being of the human body. It is actually a good recipe for the world and benefits all people, with immeasurable merits.
(S) - (-) -10- (1-aminocyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyridino [1,2,3-de] [1,4] What is the production process of benzoxazine-6-carboxylic acid monomethanesulfonate?
(2 S )-( - )- 10- (1-hydroxycyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyridino [1,2,3-de] [1,4] The production process of benzoxazine-6-carboxylic acid monomethyl ester is an exquisite and complex process.
To make this product, the choice of initial raw materials is extremely critical. It is necessary to choose high-quality and high-purity starting materials to lay the foundation for success. Usually, specific cyclopropyl derivatives, fluorine-containing compounds, etc. are often the starting choice.
At the beginning of the reaction, in the appropriate reaction vessel, according to the precise ratio, the raw materials are mixed. Temperature control is like the reins of a horse, which is crucial. It is necessary to slowly heat up or cool down according to the process and characteristics of the reaction to promote the smooth reaction. For example, in some reaction stages, the temperature needs to be stabilized at a low temperature, about 0-10 degrees Celsius, to prevent side reactions from occurring; in other stages, it needs to be raised to 50-80 degrees Celsius to increase the reaction rate. The addition of
catalyst is also the key. The adapted catalyst can greatly improve the reaction efficiency like a spring breeze. It is necessary to determine the dosage. Most of them cause overreaction, and less of them cause insufficient catalysis.
During the reaction, the frequency and strength of stirring are all exquisite. Uniform stirring can make the reactants come into close contact and make the reaction more uniform.
After the reaction is completed, the separation and purification of the product is not easy. It is often necessary to use various separation methods, such as extraction, distillation, column chromatography, etc. During extraction, the appropriate extractant is selected to dissolve the product efficiently; during distillation, the temperature is precisely controlled according to the difference between the boiling point of the product and the impurity to obtain a pure product; column chromatography can separate the product and the impurity finely according to the adsorption characteristics.
After layers of steps and careful operation, pure (2S )-( - )- 10- (1-hydroxycyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido [1,2,3-de] [1,4] benzoxazine-6-carboxylic acid monomethyl ester can be obtained to meet the needs of all parties.
What is the market prospect of (S) - (-) -10- (1-aminocyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido [1,2,3-de] [1,4] benzoxazine-6-carboxylic acid monomethanesulfonate?
(S ) -( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - deuterium - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - benzo [b] azepine - 6 - carboxylic acid monomethyl ester What is the market outlook?
I look at this (S ) -( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - deuterium - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - benzo [b] azelaide - 6 - carboxylic acid monomethyl ester, which has a unique prospect in the field of medicine and chemical industry.
From the perspective of pharmaceutical research and development, this compound has a delicate structure or specific biological activity. The combination of hydroxycyclopropyl, methyl and other groups may give them the ability to bind to specific biological targets, which has potential efficacy in the treatment of diseases. For example, in neurological diseases, such benzazepine structures may regulate neurotransmitter transmission. If this salt can precisely act on related receptors, it will be a strong candidate for the development of new therapeutic drugs.
In the chemical industry, it may be an important intermediate. It can be chemically converted to derive a series of high value-added compounds. Because its structure contains a variety of active check points, it can participate in various organic reactions, such as esterification, substitution, etc., helping chemical companies to expand their product lines and increase economic benefits.
However, its marketing activities also encounter challenges. The synthesis process may be complicated, resulting in high production costs. If the process cannot be optimized to reduce costs, it may be at a disadvantage in market competition. And the research and development of new drugs requires rigorous clinical trials, which take a long time and cost a lot. If the expected efficacy is not achieved in the trials or there are safety hazards, its market prospects will be bleak.
However, in general, if the synthesis problem can be overcome and positive results are achieved in pharmaceutical research and development, the (S ) -( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - deuterium - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - benzo [b] azepine - 6 - carboxylic acid monomethyl ester is expected to shine in the pharmaceutical and chemical markets, gaining considerable market share and economic benefits.
(S) - (-) -10- (1-aminocyclopropyl) -9-fluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyridino [1,2,3-de] [1,4] What are the precautions in the use of benzoxazine-6-carboxylic acid monomethanesulfonate
(S ) -( - ) - 10 - (1 - hydroxycyclopropyl) - 9 - fluoro - 3 - methyl - 7 - oxo - 2,3 - dihydro - 7H - pyridino [1,2,3 - de] [1,4] benzoxazine - 6 - carboxylic acid monomethyl ester hydrochloride should pay attention to the following matters:
First, pay attention to the reaction conditions. The properties of this compound may be sensitive to temperature, pH and other conditions. If the temperature is too high, it may cause the compound to decompose or initiate side reactions, which may damage the purity of the product; if the temperature is too low, it may cause the reaction rate to be delayed and take too long. If the pH is not properly controlled, it may also affect the reaction process and product formation. For example, in some reaction systems, changes in the acidic or alkaline environment can change the activity of functional groups in the compound, which in turn affects the direction of the reaction.
Second, pay attention to the choice of solvent. Different solvents have differences in the solubility of the compound, and the interaction between the solvent and the compound will also affect the reaction. The selected solvent should be able to dissolve the reactants and products well without chemically reacting with them. Unsuitable solvents may cause the reaction to fail to proceed sufficiently, or make it difficult to separate and purify the product. For example, polar solvents and non-polar solvents have very different solubility and interaction of different functional groups in the compound, and need to be accurately selected according to the specific reaction.
Third, pay attention to the operation specifications. Due to its complex structure, it is necessary to be careful when weighing, transferring, etc. to prevent loss or introduction of impurities. When performing experimental operations, ensure that the instrument is clean and dry to avoid impurities from mixing and affecting the reaction. For example, when taking the compound, if the spoons and other tools used are not cleaned, other residual substances may contaminate the sample and affect the experimental results.
Fourth, pay attention to safety protection. Although its toxicity is not clear, complex organic compounds may have certain toxicity, irritation or other potential hazards. During the operation, appropriate protective equipment, such as gloves and goggles, should be worn, and the operation should be carried out in a well-ventilated environment to prevent inhalation or exposure to harmful substances and ensure the safety of the experimenter.