({[(5R,6R)-6-{[(2R)-2-Amino-2-Phenylacetyl]Amino}-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Hept-2-Yl]Carbonyl}Oxy)Methyl (2S,5R)-3,3-Dimethyl-7-Oxo-4-Thia-1-Azabicyclo[3.2.0]Heptane-2-Carboxylate 4,4-Dioxide 4-Methylbenzenesulfonate (1:1)

({[ (5R, 6R) -6- {[ (2R) -2-hydroxy-2-benzylacetamido] hydroxy} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} hydroxy) methyl + (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid + 4,4-dioxide + 4-methylbenzylphenylacetate + (1:1) What is the chemical structure?
Looking at this chemical structure, it is necessary to clarify what each part refers to. First, (5R, 6R) -6- {[ (2R) -2 -hydroxy-2-benzylacetamido] hydroxy} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclic [3.2.0] heptyl-2-yl] amino} hydroxy) methyl, which is a complex organic group with a specific chiral configuration, double ring structure and many substituents. ( 2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclic [3.2.0] heptane-2-carboxylic acid is also chiral and is a dicyclic thio-azo structure containing carboxyl groups. 4,4-Dioxide refers to the part modified by two oxygen atoms at a specific location. 4-Methylbenzylphenylacetate is obtained from the ester of methyl benzyl and phenylacetic acid.
However, according to the given information, the chemical structure in the (1:1) ratio is difficult to outline exactly. More information on reaction conditions, connection methods, etc. is required. If there are clues about the reaction mechanism and synthesis route, it is expected to accurately analyze its chemical structure. It may be necessary to use spectroscopic analysis, X-ray crystal diffraction and other experimental methods to clarify its exact space and connection relationship.

({[ (5R, 6R) -6- {[ (2R) -2-hydroxy-2-benzylacetamido] hydroxy} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} carbonyl) methyl + (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid + 4,4-dioxide + 4-methylbenzenesulfonate (1:1) What are the uses?
Looking at the combination of this compound, it is really delicate and complex. In the context of "Tiangong Kaiwu", everything is used to its full potential, and so should this compound.
First, it may be used in the field of medicine. Many special groups in its structure, such as hydroxyl, carbonyl, azabicyclo, etc., may have unique pharmacological activities. Or it can play a therapeutic role for specific diseases, such as inflammation, infection, etc. Because these groups can interact with targets in organisms, regulate physiological processes, and achieve therapeutic purposes.
Second, in the field of organic synthetic chemistry, this compound may be an important intermediate. Its complex structure can be chemically modified to introduce other functional groups to build more complex and diverse organic molecules. This is of great significance in the research and development of new materials and the optimization of drug lead compounds.
Third, in the chemical industry, or because of its special chemical properties, it is used for the synthesis of some special materials. Such as materials with special stability, solubility or reactivity, can meet specific industrial needs.
Fourth, at the level of scientific research exploration, or as a research model, to help researchers deeply understand the structure and activity relationship of organic molecules. Through the study of its reactivity and structure-activity relationship, it provides theoretical support and practical experience for the design and development of more compounds.

({[ (5R, 6R) -6- {[ (2R) -2-amino-2-benzylalanine] amino} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} carbonyl) methyl + (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid + 4,4-dioxide + 4-methylbenzenesulfonate + (1:1) What are the physical properties? This question is quite complicated, let me elaborate.
This compound has a complex structure and is composed of many parts. Its physical properties are affected by each group. From the perspective of group characteristics, it contains polar groups such as amino and carboxyl groups, so it has a certain polarity. Polarity makes it soluble in polar solvents such as water and alcohols.
And alkyl moieties, such as dimethyl, add hydrophobicity to the molecule. This means that in non-polar solvents such as alkanes, there may also be some solubility.
The bilicyclic structure gives the molecule a specific rigid and spatial configuration, which affects the intermolecular forces. The rigid structure may make the melting point relatively high, which requires more energy to destroy the lattice.
Furthermore, the presence of benzenesulfonate groups also plays a role in the overall properties. The benzene ring increases the molecular conjugate system, affecting the molecular color, absorption spectrum, etc. The sulfonate part affects the solubility and reactivity.
Overall, the (1:1) compound has certain polarity and hydrophobicity, a high melting point or higher, and has different solubility characteristics in different solvents. Due to the conjugate system and specific groups, it may have unique physical properties such as optical and reactivity.

To prepare ({[ (5R, 6R) -6- {[ (2R) -2-amino-2-benzylacetamido] amino} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} oxo) methyl (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4-methylbenzyl oxide (1:1), according to the method of "Tiangongkai", the ancient method is as follows:
First, all kinds of raw materials need to be prepared, the key raw materials are [ (5R, 6R) -6- {[ (2R) -2-amino-2-benzylacetamido] amino} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} oxo) methyl-related compounds, (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4,4-dioxide, 4-methylbenzyl ester, etc., and the purity and quality of the raw materials need to be ensured.
Then, in a clean vessel, the above raw materials are placed in sequence according to a specific ratio. During this period, the accuracy of the ratio is crucial, and the difference is very small, so it needs to be measured carefully.
Next, control the reaction conditions, such as temperature, pressure and reaction time. The temperature should be maintained within a certain constant range. If it is too high, the After the reaction is completed, suitable separation and purification methods are used to remove impurities and obtain pure products. Or use filtration to separate solid impurities; or use distillation to purify liquid products.
Thus, after many steps, careful operation, or can be obtained ({[ (5R, 6R) -6- {[ (2R) -2-amino-2-benzylacetamido] amino} -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptyl-2-yl] amino} oxo) methyl (2S, 5R) -3,3-dimethyl-7-oxo-4-thio-1-azabicyclo [3.2.0] heptane-2-carboxylic acid 4,4-methylbenzyl oxide (1:1).

This is a description of the reaction of complex organic compounds, involving many professional chemical structures and reaction details. The key points to be noted in the ancient classical language are as follows:
From the perspective of this organic reaction, it is a complex process involving a variety of compounds. Among them, each compound interacts according to its specific spatial configuration (such as\ ((5R, 6R )\)、\(( 2R )\)、\(( 2S, 5R) \), etc.).
First pay attention to the stereochemical configuration of each reactant. Because it has a key impact on the reaction process and product generation. Configuration differences can lead to divergent reaction paths and different products. If the configuration of the reaction initiator is precisely controlled, the basis for the expected product is obtained.
Furthermore, various functional groups are involved in the reaction, such as amino, methoxy, carbonyl, heterocyclic, etc. Each functional group has unique chemical activities and affects each other. The sequence of reactivity and interaction mechanism should be carefully observed to prevent side reactions from breeding. For example, some active functional groups react under specific conditions or take the lead, changing the overall reaction direction.
The reaction conditions cannot be ignored. Factors such as temperature, pressure, and catalyst all affect the reaction rate and equilibrium. Appropriate temperature can accelerate the reaction, but too high or too low can cause side reactions or cause reaction stagnation. The choice and dosage of catalysts have a profound impact on reaction selectivity and efficiency, and must be precisely regulated.
Product separation and purification are also important. Due to the complex reaction, or generate a variety of by-products. Appropriate separation methods, such as distillation, extraction, chromatography, etc., need to be selected to obtain high-purity target products.
In short, for such complex organic reactions, detailed attention should be paid to the reactant configuration, functional group activity, reaction conditions and product treatment, and careful operation can be used to achieve the expected reaction effect and obtain pure target products.