4-chloro-5-iodo-7-propan-2-ylpyrrolo[2,3-d]pyrimidine

This is the naming of an organic compound, following the modern organic chemistry naming rules, and its chemical structure can be inferred. "4-chloro-5-iodo-7-propan-2-ylpyrrolo [2,3-d] pyrimidine", where "pyrrolo [2,3-d] pyrimidine" is the parent nucleus structure, namely pyrrolido [2,3-d] pyrimidine. This parent nucleus is formed by fusing a pyrrole ring with a pyrimidine ring, and the two share some atoms to form a specific fused ring system.
"4-chloro" indicates that there is a chlorine atom attached at the position of the parent nucleus structure number 4. " 5-Iodo "means that an iodine atom is connected at the position numbered 5. And" 7-propan-2-yl "means that there is an isopropyl (propan-2-yl, or -CH (CH) ²) attached at the position numbered 7. Isopropyl is a group formed by the removal of a terminal hydrogen atom of propane, which is attached to the parent nucleus as methylene (-CH -).
In summary, the chemical structure of this compound is: pyrrolido [2,3-d] pyrimidine as the parent nucleus, with chlorine atoms at the 4th position, iodine atoms at the 5th position, and isopropyl at the 7th position. In this way, the chemical structure of "4-chloro-5-iodo-7-propan-2-ylpyrrolo [2,3-d] pyrimidine" is outlined.

4-Chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine, which has a wide range of uses, is a key intermediate for the synthesis of specific drugs in the field of medicinal chemistry. It can be skillfully introduced into specific groups through fine chemical synthesis, and then targeted drugs for specific diseases can be created. For example, in the development of anti-tumor drugs, with its unique chemical structure, it may be able to precisely act on specific targets of tumor cells to achieve the purpose of high-efficiency tumor suppression.
In the field of materials science, it also has potential applications. Due to its stable structure and unique electronic properties, it may be used to prepare new organic optoelectronic materials. Such materials may exhibit excellent properties in the fields of organic Light Emitting Diodes (OLEDs), solar cells, etc., such as improving luminous efficiency and enhancing photoelectric conversion capabilities.
Furthermore, in the field of pesticide chemistry, it cannot be ignored. Using it as a starting material, new and efficient pesticides may be developed. With its special structure and biological activity, it can effectively control specific pests or pathogens, and is environmentally friendly, contributing to the sustainable development of agriculture. It is an important organic compound with multiple uses, emerging in many scientific fields, and its future application prospects are limitless.

To prepare 4-chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine, the method is as follows:
First take a suitable starting material, such as a pyrrolido pyrimidine derivative with a corresponding structure. This starting material needs to contain a modifiable check point to introduce chlorine, iodine and isopropyl.
When introducing chlorine atoms, chlorination reagents can be selected, such as chlorine-containing active compounds. Under suitable reaction conditions, such as in a specific solvent, control the temperature and reaction time, so that the chlorine atom replaces the hydrogen atom at the target position. The ratio of chlorinated reagents to the substrate also needs to be precisely adjusted. If the ratio is not correct, the reaction may be incomplete or too many by-products may be generated.
To introduce iodine atoms, an iodine substitution reaction can be used. Select a suitable iodine source, cooperate with an appropriate catalyst and reaction environment. The iodine substitution reaction conditions are very critical, and conditions that are too strong or too weak affect the reaction effect. Or inert gas protection is required to prevent iodine from being over-oxidized and causing the reaction to deviate from the expected path.
As for the introduction of isopropyl, reagents containing isopropyl can be used through nucleophilic substitution or other suitable reaction mechanisms. Such reactions often require suitable bases or catalysts to promote the reaction. The polarity and solubility of the solvent have a great impact on the reaction process, so careful selection is required.
After each step of the reaction, the product needs to be carefully separated and purified. Commonly used methods include column chromatography, recrystallization, etc. By these operations, unreacted raw materials, by-products and impurities are removed to improve the purity of the product. After multiple steps of reaction, separation and purification, 4-chloro-5-iodine-7-isopropyl pyrrolido [2,3-d] pyrimidine is finally obtained. The whole reaction process requires precise control of various parameters and attention to the details of the reaction to achieve satisfactory synthetic results.

4-Chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine, this is an organic compound. It has many physical properties.
Looking at its appearance, it is often in the form of a solid powder that is off-white to light yellow. This state is easy to store and use, and is easy to handle in most chemical operations.
When talking about the melting point, it is usually in a specific temperature range. The melting point is a material characteristic, and the melting point of the compound can help to identify and determine the purity. When heated, it melts from a solid state to a liquid state at a certain temperature. This temperature range varies slightly depending on the purity and measurement conditions.
In terms of solubility, it has a certain solubility in organic solvents such as dichloromethane and N, N-dimethylformamide (DMF). In dichloromethane, it can be well dispersed and dissolved due to the adaptation of the forces between the two molecules. In water, the solubility is very small, because its structure contains more hydrophobic groups, and the interaction force with water is weak.
The density of this compound is also an important physical property. Although the exact value varies depending on the precise measurement conditions, the relative density can reflect its sedimentation or floating characteristics in the mixture, which is of guiding significance for the separation and purification process.
In addition, its stability is good under conventional conditions. However, when exposed to strong oxidizing agents, strong acids or bases, chemical reactions may occur and cause structural changes. When storing, it should be placed in a dry and cool place to avoid contact with these substances. Light may also affect it, so it should be stored away from light.
The physical properties of 4-chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine are crucial in chemical synthesis, drug development and other fields, providing a basis for related research and applications.

4-Chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine, a chemical substance, has a multi-faceted picture when looking at its market prospects.
From the field of pharmaceutical research and development, the prospect is quite promising. Many medical researchers have invested a lot of effort in compounds containing pyrrolido pyrimidine structure, because it shows great potential in the creation of anti-tumor, antiviral and other drugs. This compound contains chlorine, iodine and isopropyl groups, which may endow it with unique biological activities and pharmacokinetic properties. For example, the introduction of chlorine and iodine atoms can change the electron cloud distribution of molecules and enhance their interaction with biological targets; the presence of isopropyl groups may affect the lipid solubility and spatial structure of molecules, which is conducive to the passage of drugs through cell membranes and improve bioavailability. Therefore, if the mechanism of action with specific biological targets can be accurately discovered in follow-up studies, it is expected to develop new specific drugs, which may occupy a place in the pharmaceutical market.
There are also potential opportunities in the field of materials science. With the in-depth research of organic optoelectronic materials, organic compounds with special structures and electronic properties have attracted much attention. The conjugated structure of 4-chloro-5-iodine-7-isopropylpyrrolido [2,3-d] pyrimidine may make it have certain photoelectric properties. After rational molecular design and modification, it may be applied to organic Light Emitting Diode (OLED), organic solar cells and other fields. For example, by adjusting the substituent, optimizing the molecular energy level, improving the charge transport and luminous efficiency of the material, thus injecting new vitality into the material market.
However, its market expansion also faces challenges. Synthesis of this compound may be difficult, complicated, and expensive, which hinders large-scale production and marketing activities. And in terms of new application development, a lot of time and resources need to be invested in research and verification, and there are many links such as regulatory approval. Only by working closely with researchers and industry to break through synthesis bottlenecks, reduce costs, and accelerate application research and development can this compound shine in the market and win broad development space.