Tert Butyl 2 Amino 6 7 Dihydro 1 3 Thiazolo 5 4 C Pyridine 5 4h Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

tert-butyl 2-amino-6,7-dihydro[1,3]thiazolo[5,4-c]pyridine-5(4H)-carboxylate

    Specifications

    HS Code

    247156

    Chemical Formula C12H19N3O2S
    Molecular Weight 269.36
    Physical State Solid (usually)
    Appearance Off - white to pale yellow solid
    Melting Point Typically in a specific range (needs experimental determination)
    Solubility Soluble in some organic solvents like DMSO, less soluble in water
    Pka Relevant acidic or basic functional groups have specific pKa values (experimental determination required)
    Logp Indicates lipophilicity (value needs experimental or computational determination)
    Stability Stable under normal storage conditions, but may react with strong oxidizing or reducing agents

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    General Information
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    Frequently Asked Questions

    As a leading tert-butyl 2-amino-6,7-dihydro[1,3]thiazolo[5,4-c]pyridine-5(4H)-carboxylate supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemical structure of tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate
    "Tert-butyl" is tert-butyl, which is a branched alkyl group containing four carbons. It is trident-shaped and has a stable structure. In 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate "," 2-amino "indicates that the amino group is attached to the second position of the main ring;" 6,7-dihydro "indicates that the 6th and 7th positions of the main ring are dihydrogen structures;" [1,3] thiazolo [5,4-c] pyridine "means that the main ring is composed of thiazolopyridine, and its fusing method follows this rule;" 5 (4H) -carboxylate "means that the 5th position is connected with carboxyl derivatives, and the 4th position is a specific form of hydrogen atoms. Overall, the main structure of this compound is thiazolopyridine ring, with amino group at the 2nd position, dihydro at the 6th and 7th positions, and tert-butyl ester group derived from carboxyl group at the 5th position. Its structure is complex and delicate, and each group is related to each other. It may have unique properties and uses in the fields of organic synthesis and medicinal chemistry.
    What are the main uses of tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate
    Tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylic acid ester, this compound has a wide range of uses. In the field of medicinal chemistry, it is often used as a key intermediate to create new drugs. Drug developers are expected to develop new drugs with specific pharmacological activities for the treatment of various diseases through subtle modifications and modifications to the structure of this compound. For example, in the development of anti-tumor drugs, the structure of the compound can be adjusted to enhance its targeting and inhibitory effect on tumor cells.
    In the field of organic synthesis, it is also an extremely important building block. Due to its special structure, it can participate in a variety of organic reactions, such as nucleophilic substitution, cyclization reactions, etc., which help to synthesize a series of organic compounds with complex structures and unique functions, providing rich materials and multiple paths for the development of organic synthetic chemistry.
    In the field of materials science, if it is introduced into a specific material system, it may endow materials with novel properties. For example, integrating it into polymer materials may change the electrical and optical properties of materials, and then be applied to optoelectronic devices, sensors and other fields. From this perspective, tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylic acid esters occupy a key position in many scientific research and application fields, showing broad application prospects.
    What is the synthesis method of tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate
    To prepare tert - butyl 2 - amino - 6,7 - dihydro [1,3] thiazolo [5,4 - c] pyridine - 5 (4H) -carboxylate, the following ancient methods can be used.
    First take appropriate starting materials, with nitrogen-containing heterocyclic compounds and sulfur-containing compounds as groups. Pyridine derivatives with suitable substituents are often selected, and they reserve reaction check points at specific positions for subsequent construction of thiazole rings.
    At the beginning of the reaction, a suitable reaction environment needs to be created. Organic solvents are often used as a medium, such as dichloromethane, N, N-dimethylformamide, etc. These solvents can well dissolve the raw materials and promote the contact and collision of the reaction molecules.
    Next, a condensing agent or catalyst is introduced. For example, suitable acid catalysts, such as p-toluenesulfonic acid, can be selected, which can speed up the reaction process and promote intermolecular dehydration and condensation. During the reaction, temperature is also a key factor. Generally, it needs to be controlled in a moderate range, usually between room temperature and tens of degrees Celsius. If the temperature is too high, or side reactions occur frequently, the product is impure; if the temperature is too low, the reaction rate will be slow and take a long time. < Br >
    In the process of constructing thiazole rings, the raw material molecules are gradually formed into rings through a series of reactions such as nucleophilic substitution and cyclization. During this period, close attention should be paid to the reaction process, which can be monitored by thin layer chromatography (TLC) and other means. When the raw material point almost disappears and the product point is significant, it can be regarded as the reaction is basically completed.
    After the reaction is completed, it needs to go through a post-treatment process. It is often extracted with an organic solvent to separate the product from the reaction system, and then washed with water and dried to remove impurities. After that, purified tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate was obtained by column chromatography, recrystallization and other purification methods. The whole process requires fine operation, pay attention to the conditions of each link to control, in order to obtain the ideal product.
    What are the physical properties of tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate
    "Tiangong Kaiwu" is a scientific and technological masterpiece written by Song Yingxing in the Ming Dynasty, with a simple and concise style of writing. However, it is not easy to describe the physical properties of this compound (tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylic acid ester) in detail in classical Chinese, and today we try to do it in the style of quaint classical Chinese:
    This tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylic acid ester, looking at its shape, under normal conditions, or a crystalline body, bright and bright, or in a powder state, fine and uniform. Its color may be close to plain white, like the purity of frost and snow, or slightly yellowish, like the light halo of the early morning sun.
    As for its quality, it feels smooth to the touch, like the cocoon silk of young silkworms, delicate but not rough. Smell it, the smell is light but slightly pungent, not pungent, but also has a unique smell, which is different from all ordinary things.
    When it comes to melting, it melts when heated, just like spring ice when warm, gradually melting and fading. The number of its melting points is measured according to today's method. When it is in a specific field, this is its inherent nature and cannot be easily changed by foreign objects. < Br >
    And its solubility, in alcohols, slightly soluble, like dust into soup, gradually dispersed; in water, it is insoluble, like oil floating on water, distinct. This is all determined by the structure of its molecules and the properties of its groups, which cannot be strong by human beings.
    Its density is relatively ordinary, or slightly heavier or lighter, and it can only be accurately measured by a device. However, although the slight difference is also a sign of its physical properties, it is impossible to ignore those who use this thing.
    What is the market outlook for tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate
    The name of the compound today is "tert-butyl 2-amino-6,7-dihydro [1,3] thiazolo [5,4-c] pyridine-5 (4H) -carboxylate", and its market prospects are worth exploring. This compound may have unique potential in the field of pharmaceutical research and development. Looking at the development trend of medicine in recent years, there is a growing demand for novel and highly effective pharmacological molecules. The unique structure of this compound may be able to combine with specific biological targets, and it may emerge in the treatment of diseases, such as in the frontier fields of anti-tumor and anti-virus, with potential applications.
    In the field of materials science, it may also have extraordinary performance. Nowadays, materials research pursues substances with excellent performance and special functions. The chemical properties of this compound may make it a key raw material for the preparation of special functional materials, such as optoelectronic materials, polymer materials and other fields, or it may endow materials with different properties and open up new material applications.
    However, its market prospects are not smooth. The process of synthesizing this compound may be complex, and cost control is a major challenge. And the market competition is fierce, and compounds of the same type or similar functions are also competing. To make it stand out in the market, it is necessary to continue to make efforts at the research and development end to optimize the synthesis process, reduce costs and improve quality. At the same time, by deeply exploring its performance and application, and expanding market channels, we can gain a foothold in the competitive market and create a broad market prospect.