2019
DOI: 10.1177/1747519819873643
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An improved process for the preparation of pimavanserin tartrate

Abstract: A practical synthetic route to pimavanserin tartrate, in which the target compound was obtained with 99.84% purity and in 46% total yield via a 5-step synthesis starting from 4-hydroxybenzaldehyde and (4-fluorophenyl)methanamine, is reported. The main advantages of the route include inexpensive starting materials, mild reaction conditions and an acceptable overall yield.

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Cited by 3 publications
(1 citation statement)
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“…1 When it synthesized Pimavanserin has been administered as its tartrate salt. 2 PMT is not a dopamine receptor antagonistbutis having inverse agonist on 5-HT2A [3][4][5][6][7] subtype receptor for the treatment of psychosis in Parkinson"s disease (PD) and used in the treatment of schizophrenia. It"s also having significant effect on insomnia, it"s selective serotonin 5-HT2A receptor inverse agonist, to the slow wave sleep.…”
Section: Introductionmentioning
confidence: 99%
“…1 When it synthesized Pimavanserin has been administered as its tartrate salt. 2 PMT is not a dopamine receptor antagonistbutis having inverse agonist on 5-HT2A [3][4][5][6][7] subtype receptor for the treatment of psychosis in Parkinson"s disease (PD) and used in the treatment of schizophrenia. It"s also having significant effect on insomnia, it"s selective serotonin 5-HT2A receptor inverse agonist, to the slow wave sleep.…”
Section: Introductionmentioning
confidence: 99%