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Chemical Synthesis Of Duloxetine

Mescaline belongs to a family of compounds known as phenethylamines, making it quite distinct from the other major psychedelics such as LSD and psilocybin, which belong to the indole family. Many synthetic "designer" psychedelics, such as ecstasy (MDMA) and 2C-B, are phenethylamines, and are related to the chemistry of mescaline. The chemical structure of mescaline is very similar to that of the neurotransmitters dopamine and norepinephrine, thus the drug can interfere with their actions in the brain.

Chemical Synthesis of Epinephrine

This article will outline the specific disadvantages of chemical catalyst synthesis and the benefits of using biocatalysis enzymes during the manufacture of Duloxetine APIs and intermediates. It will demonstrate how cost savings and improved end products are achieved through improved API quality, updated synthesis routes, process sustainability and technical benefits.

Oxidation Chemistry of (−)-Norepinephrine in the …

The specific enzymes are tyrosine hydroxylase in the synthesis of dopa and enzyme dopamine-β-hydroxylase in the synthesis of norepinephrine.

There are probably also costs & benefits involved in synthesizing, transporting and recycling various neurotranmitters in the differing chemical mileus of the brain.

Norepinephrine is synthesized from dopamine by means of the enzyme Dopamine Beta-Hydroxylase (DBH), with oxygen, copper and Vitamin Cas co-factors.

Chemical Structure and Synthesis of Hormones

The synthesis of serotonin is similar in some ways to the synthesis of dopamine and norepinephrine.

Biocatalysis is the use of natural catalysts (e.g., enzymes), in place of chemical catalysts in synthetic processes. This enables new, sustainable routes of production for intermediates and APIs. It is an important tool for medicinal, process and polymer chemists, allowing the development of efficient and highly attractive organic synthetic processes on an industrial scale.

Epinephrine may be synthesized by the reaction of catechol (1) with chloroacetyl chloride (2), followed by the reaction with methylamine to give the ketone (4), which is reduced to the desired hydroxy compound (5). The racemic mixture may be separated using tartaric acid.

Oxidation Chemistry of (−)-Norepinephrine in the Presence of l-Cysteine
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Epinephrine synthesis is solely under the control of ..

Because of the high selectivity of biocatalysis enzymes, the number of stages used during product synthesis is reduced, which in turn decreases waste production. The biocatalysis enzymes themselves can be created from renewable sources and mostly operate in water, eliminating the need for organic solvents and hazardous chemicals. Overall, the entire manufacturing process becomes more sustainable and environmentally friendly.

How can the answer be improved?

The chemical synthesis of Duloxetine is shown in Figure 1. Initially, racemic 3-(N,N-Dimethylamino)-1-(2-thienyl)propan-1-ol is formed. The mixture then undertakes resolution to form (S)-N,N-Dimethyl-N-[3-hydroxy-3-(2-thienyl)propyl]ammonium (S)-Mandelate, which is converted to (S)-Duloxetine Hydrochloride.

Chemical Synthesis - Epinephrine - Home

Peyote is a spineless cactus with small protrusions called "buttons" that are used for psychoactive hallucinogenic purposes. Mescaline, an amphetamine, is the principal active psychedelic compound in peyote. It is a hallucinogen derived from several different cacti— the Peyote cactus that grows in the southwestern United States and Mexico, the San Pedro cactus found in Peru, or the Peruvian Torch cactus . The limited growing area of this cactus restricts drug supply severely, so it is a common practice to sell other drugs such as PCP or LSD as mescaline. Mescaline can also be produced in a laboratory by chemical synthesis. A white crystalline material, mescaline sulfate, is the pure form of mescaline and can be put in capsule form. Peyote and mescaline are listed as Schedule I hallucinogens under the Controlled Substances Act in the United States. In a rare exception, "the nondrug use of peyote in bona fide religious ceremonies of the Native American Church, and by members of the Native American Church" is legal.

Biosynthesis Within the body, epinephrine ..

Molecular cloning of cDNA and chromosomal assignment of the gene for human phenylethanolamine N‐methyltransferase, the enzyme for epinephrine biosynthesis.

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