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Lurasidone hydrochloride is an atypical antipsychotic drug that is used to treat schizophrenia and bipolar disorder.
Its chemical name is 2-[4-(4-fluorophenyl)-4-oxo-butyl]-1,3-oxazepine hydrochloride, and it is commonly referred to as AGN 102400.
The synthesis of Lurasidone hydrochloride involves a number of steps, including the preparation of the starting material 4-fluoro-2-nitrobenzaldehyde, which is synthesized from 4-fluorophenol.
The aldehyde is then treated with sodium hydroxide to form the corresponding sodium salt, which is then reduced with lithium aluminum hydride to form the corresponding alcohol.
The alcohol is then treated with a halogenating agent, such as chlorine gas, to form the 4-chloro-2-nitrobenzaldehyde.
This compound is then nitrated with nitric acid to form the 4-nitro-2-nitrobenzaldehyde.
The nitrated aldehyde is then treated with a base, such as sodium hydroxide, to form the corresponding sodium nitrate.
This sodium salt is then treated with an amine, such as methylamine, to form the corresponding amide.
The amide is then treated with trimethyl orthoformate and hydrogen chloride in the presence of a metal catalyst, such as palladium on barium carbonate, to form the corresponding nitrile.
This compound is then reduced with lithium aluminum hydride to form the 2-[4-(4-fluorophenyl)-4-oxo-butyl]-1,3-oxazepine.
The final step in the synthesis of Lurasidone hydrochloride involves the treatment of the oxazepine with hydrochloric acid to form the corresponding hydrate.
The resulting Lurasidone hydrochloride is then purified and dried to remove any remaining impurities.
Lurasidone hydrochloride is a white to off-white powder that is soluble in water and other polar solvents.
It has a molecular formula of C21H21ClFN4O3 and a molecular weight of 435.
9 g/mol.
The chemical structure of Lurasidone hydrochloride is shown below:
The pharmacology of Lurasidone hydrochloride is complex and involves multiple mechanisms of action.
It is believed to act on a variety of neurotransmitter systems, including dopamine, serotonin, and glutamate receptors.
Lurasidone hydrochloride has been shown to have a high affinity for dopamine D2, D3, and D4 receptors, as well as for serotonin 5-HT2A and 5-HT7 receptors.
It has also been shown to act as a partial agonist at opioid receptors, particularly at the mu-opioid receptor.
In addition to its effects on neurotransmitter systems, Lurasidone hydrochloride has been shown to have anti-inflammatory and anti-oxidant effects, and it has been suggested that these effects may contribute to its therapeutic efficacy.
Lurasidone hydrochloride is primarily prescribed for the treatment of schizophrenia and bipolar disorder.
It has been shown to be effective in reducing the positive and negative symptoms of schizophrenia, as well as in improving cognitive function.
It is also used in the treatment of acute mania associated with bipolar disorder, and it has been shown to be effective in reducing manic symptoms and improving mood stability.
Lurasidone hydrochloride is usually administered orally, and the dosage and duration of treatment will depend on the condition being treated and the response of the patient.
It is generally recommended to start with a low dose and gradually increase the dose over time to minimize the risk of side effects.
The most common side effects of Lurasidone