Extracurricular laboratory: Synthetic route of 21778-81-4

In some applications, this compound(21778-81-4)Product Details of 21778-81-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called Amide-Amine Replacement in Indole-2-carboxamides Yields Potent Mycobactericidal Agents with Improved Water Solubility, published in 2021-05-13, which mentions a compound: 21778-81-4, mainly applied to methylamine carboxamide benzothiophene benzoselenophene preparation antimycobacterial lipophilicity, Product Details of 21778-81-4.

Indolecarboxamides are potent but poorly soluble mycobactericidal agents. Here, it was found that modifying the incipient scaffold by amide-amine substitution and replacing the indole ring with benzothiophene or benzoselenophene led to striking (10-20-fold) improvements in solubility Potent activity could be achieved without the carboxamide linker but not in the absence of the indole ring. The indolylmethylamine, N-cyclooctyl-6-trifluoromethylindol-2-ylmethylamine (MIC90Mtb 0.13μM, MBC99.9Mtb 0.63μM), exemplifies a promising member that is more soluble and equipotent to its carboxamide equivalent It is also an inhibitor of the mycolate transporter MmpL3, a property shared by the methylamines of benzothiophene and benzoselenophene.

In some applications, this compound(21778-81-4)Product Details of 21778-81-4 is unique.If you want to know more details about this compound, you can contact with the author or consult more relevant literature.

Reference:
Pyridazine – Wikipedia,
Pyridazine | C4H4N2 – PubChem