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The Production Process of N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine: An Overview in Chemical Industry
In the field of pharmaceuticals, the production of new drugs is a complex and time-consuming process.
It involves various stages, including research and development, synthesis, purification, and quality control.
The process of developing a new drug can take years, and the success rate is relatively low.
One of the drugs that have been recently developed is N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine, which is commonly referred to as Y27632.
This drug is an antagonist of the G protein-coupled receptor 55 (GPR55), and it has been shown to have potential therapeutic effects on various diseases, including cancer and cardiovascular disease.
In this article, we will discuss the production process of N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine, including the chemical synthesis, purification, and quality control methods used in its production.
Chemical Synthesis of N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
The synthesis of N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine involves several steps, including the preparation of the starting materials, the condensation reactions, and the purification process.
The starting materials for the synthesis of Y27632 include 2-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-4H-pyrrole-1,2-dione, which is also known as Compound 1, and N-methylamine.
The synthesis of Compound 1 is achieved through a series of steps, including the condensation of 1- phenyl-3-propanamine and 3-methyl-2-butenoic acid, followed by acylation with teicoplanin.
The synthesis of N-methylamine involves the reduction of methyl iodide using hydrogen gas.
The condensation of N-methylamine and Compound 1 is achieved using an appropriate condensation agent, such as dicyclohexylcarbodiimide (DCC) and hydroxybenzotriazole (HOBT).
Purification of N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine
After the synthesis of Y27632, the product must be purified to remove any impurities that may have been introduced during the synthesis process.
This is important for ensuring the safety and effectiveness of the final product.
There are several methods that can be used for purifying N-Methyl-N-[(3R,4R)-4-methyl-1-(phenylmethyl)-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine, including crystallization, column chromatography, and high-performance liquid chromatography (HPLC).
Crystallization is a commonly used method for purifying small molecules like Y27632.
In this method, the