2r 1 5 Amino 2 1 Benzyloxy 2 M Thyl 2 Propanyl 6 Fluoro 1h Indol 1 Yl 3 Benzyloxy 2 Propanol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
(2R)-1-{5-Amino-2-[1-(benzyloxy)-2-méthyl-2-propanyl]-6-fluoro-1H-indol-1-yl}-3-(benzyloxy)-2-propanol
Chemical Name (2R)-1-{5-Amino-2-[1-(benzyloxy)-2-methyl-2-propanyl]-6-fluoro-1H-indol-1-yl}-3-(benzyloxy)-2-propanol
Chemical Formula C31H41FN2O4
Molecular Weight 536.67
Stereochemistry (2R)-configuration
Functional Groups Amino, indole, benzyloxy, propanol
Chemical Name (2R)-1-{5-Amino-2-[1-(benzyloxy)-2-methyl-2-propanyl]-6-fluoro-1H-indol-1-yl}-3-(benzyloxy)-2-propanol
Chemical Name (2R)-1-{5-Amino-2-[1-(benzyloxy)-2-methyl-2-propanyl]-6-fluoro-1H-indol-1-yl}-3-(benzyloxy)-2-propanol
FAQ

What is the chemical structure of (2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propanyl] -6-fluoro-1H-indol-1-yl} -3- (benzyloxy) -2-propanol?

The chemical structure of (2R) - 1 - {5 - amino - 2 - [1 - (benzyloxy) - 2 - methyl - 2 - propyl] - 6 - fluoro - 1H - indole - 1 - yl} - 3 - (benzyloxy) - 2 - propanol is the object of fine investigation in the field of organic chemistry.

In the structure of this compound, the core is an indole ring. On the 1H-indole-1-group, there is an amino group at the 5th position. This amino group has certain reactivity and can participate in many nucleophilic reactions. The [1- (benzyloxy) -2-methyl-2-propyl] group connected at the 2nd position, the benzyloxy part, the benzyl group has a certain steric resistance and electronic effect, while the oxygen atom is connected to the propyl structure, which makes the overall structure more complex. The fluorine atom at the 6th position has a great influence on the electron cloud distribution of the indole ring due to its strong electronegativity, which in turn affects the physical and chemical properties of the compound.

Furthermore, the 3 - (benzyloxy) - 2 - propanol side chain connected at 1 position, the benzyloxy group on this side chain is similar to the aforementioned benzyloxy group, and has its unique electronic and spatial effects. The presence of the hydroxyl group in the 2-propanol part endows the compound with hydrophilicity, and can participate in various reactions such as esterification and ether formation. The R configuration of its 2 position determines the spatial three-dimensional structure of the whole compound, which often plays a key role in many biological activities and chemical reactions. The complex and delicate structure of this compound has laid an important foundation for its research and application in the fields of medicinal chemistry and organic synthesis.

What are the physical properties of (2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propanyl] -6-fluoro-1H-indol-1-yl} -3- (benzyloxy) -2-propanol?

(2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propyl] -6-fluoro-1H-indole-1-yl} -3- (benzyloxy) -2-propanol, this is an organic compound. Its physical properties are quite important, related to its application in different fields.

Looking at its properties, it is mostly solid at room temperature and pressure, with a fine texture. This property may be caused by intermolecular forces and arrangements. The determination of its melting point is of great significance, because the melting point is often a key indicator for identification and purity evaluation. The melting point of the compound is determined by experiments in a specific temperature range, which is an inherent property of the compound and is affected by the molecular structure and crystal structure.

Solubility is also a key physical property. In organic solvents, such as common ethanol and dichloromethane, it exhibits a certain solubility. This is because the molecular structure of the compound contains specific functional groups, and there are interaction forces with organic solvent molecules, such as van der Waals force, hydrogen bond, etc., to promote its dissolution. However, the solubility in water is poor, and the interaction between the polarity of water molecules and the structure of the compound is weak.

Furthermore, its density is also of research value. Density reflects the mass per unit volume of a substance and is related to the closeness of the compound molecule. The density can be accurately determined by experimental means. This value has important reference significance in chemical production, pharmaceutical preparation and other fields, and is related to the setting of parameters such as substance dosage and mixing ratio.

In addition, the refractive index of the compound is also one of the physical properties. The refractive index can reflect the change of light propagation speed and direction in the substance, and is related to the molecular structure and electron cloud distribution, providing another dimension of information for substance identification and purity analysis.

What is the synthesis method of (2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propanyl] -6-fluoro-1H-indol-1-yl} -3- (benzyloxy) -2-propanol?

To prepare (2R) - 1 - {5 - amino - 2 - [1 - (benzyloxy) - 2 - methyl - 2 - propyl] - 6 - fluoro - 1H - indole - 1 - yl} - 3 - (benzyloxy) - 2 - propanol, it can be synthesized according to the following ancient method.

First, use an appropriate starting material to find the indole-containing structure, and introduce the amino group at its 5 position. In this step, a suitable amination reagent may be selected under delicate reaction conditions, or through nucleophilic substitution, reductive amination and other paths, so that the amino group can properly occupy the place.

Furthermore, access the [1- (benzyloxy) -2-methyl-2-propyl] fragment at the 2 positions of the indole. The introduction of this fragment, or first take benzyl alcohol, treat it with a suitable base, make it into an alkoxide, and then react with the halogenated 2-methyl-2-halopropane derivative to obtain 1 - (benzyloxy) - 2 - methyl-2 - propyl halide. The halide is then reacted with the indole derivative under base catalysis, so that the fragment is connected to the indole 2 position.

As for the construction of the 3 - (benzyloxy) - 2 - propanol moiety, 3 - halo - 1 - (benzyloxy) - 2 - propanol can be prepared first, and then the indole derivative can be prepared under appropriate conditions or in an inert solvent, assisted by a metal catalyst, through a nucleophilic substitution reaction to connect the two. < Br >
Or you can build an indole skeleton first, gradually introduce each substituent, and then construct the 3- (benzyloxy) -2 -propanol part. During the reaction, the temperature, pH, reaction time and other conditions need to be strictly controlled, and after each step, when the purification method is used to remove its impurities, the product is gradually purified, and finally the target compound is obtained.

What are the application fields of (2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propanyl] -6-fluoro-1H-indol-1-yl} -3- (benzyloxy) -2-propanol?

(2R) - 1 - {5 - amino - 2 - [1 - (benzyloxy) - 2 - methyl - 2 - propyl] - 6 - fluoro - 1H - indole - 1 - yl} - 3 - (benzyloxy) - 2 - propanol, this compound has a wide application field.

In the field of pharmaceutical research and development, or has potential medicinal value. Its unique chemical structure, or can interact with specific biological targets, after in-depth research and experiments, or can be developed as a drug for the treatment of specific diseases. For example, in the development of anti-tumor drugs, such compounds containing indole structures often exhibit inhibitory activity on the growth and proliferation of tumor cells. Or in the exploration of drugs for the treatment of neurological diseases, because of their structural similarity to neurotransmitters or receptors, or their ability to modulate neurotransmission, it holds promise for the treatment of neurological diseases such as Alzheimer's disease and Parkinson's disease.

In the field of organic synthesis chemistry, it is also an important intermediate. With its diverse functional groups, it can participate in many organic reactions to construct more complex organic molecular structures. Chemists can use this compound to synthesize a series of organic compounds with different properties and uses through halogenation, esterification, amidation and other reactions, expand the types and functions of organic compounds, and provide a variety of raw materials for materials science, fragrance chemistry and other related fields.

In the field of materials science, or due to unique chemical properties and structures, it can be used to prepare special functional materials. For example, as a component of photoelectric materials, it is given specific optical and electrical properties to materials, and is applied to organic Light Emitting Diode (OLED), solar cells and other optoelectronic devices to improve their performance and efficiency.

What is the market outlook for (2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propanyl] -6-fluoro-1H-indol-1-yl} -3- (benzyloxy) -2-propanol?

(2R) -1- {5-Amino-2- [1- (benzyloxy) -2-methyl-2-propyl] -6-fluoro-1H-indole-1-yl} -3- (benzyloxy) -2-propanol, the market prospect of this product is related to various factors, allow me to describe it for you.

Looking at its structure, it contains unique indole groups and benzyloxy groups and other functional groups. In the field of pharmaceutical research and development, such structures often have potential. Indole compounds, many of which are biologically active, can act on specific targets in the human body, such as certain receptors or enzymes. This compound may be developed into a new type of drug to fight specific diseases based on its structural characteristics. If it is successfully developed, the market prospect is broad, which can benefit patients and bring rich benefits to pharmaceutical companies.

In the chemical industry, due to its complex structure and special functional groups, it can be used as a key intermediate in organic synthesis. It can be converted into a variety of functional materials or fine chemicals through a series of reactions. For example, it can be used to prepare high-performance polymer additives to improve material properties, which also expands its market application space.

However, its market prospects also pose challenges. Synthesis of this compound may require complex steps and special raw materials, and the cost may be high. If the cost is difficult to control, it may be at a disadvantage in market competition. And the research and development of new drugs takes a long time and requires huge investment. From compounds to marketed drugs, multiple rounds of trials are required, and the success rate is limited.

To sum up, (2R) -1- {5-amino-2- [1- (benzyloxy) -2-methyl-2-propyl] -6-fluoro-1H-indole-1-yl} -3- (benzyloxy) -2-propanol Although it has potential, it also needs to overcome cost and research and development problems in order to shine in the market.