Unii-na83F1sjsr

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Company Name: Hangzhou ICH Biofarm Co., Ltd
Tel: +86-0571-28186870; +undefined8613073685410
Email: sales@ichemie.com
Products Intro: Product Name:Pimavanserin Tartrate
CAS:706782-28-7
Purity:98% Package:1g;|10g;|25g
Company Name: Shanghai Daken Advanced Materials Co.,Ltd
Tel: +86-371-66670886
Email: info@dakenam.com
Products Intro: Product Name:Unii-na83F1sjsr
CAS:706782-28-7
Purity:99% Package:100g ;1KG ;5KG 25KG
Company Name: Beijing Cooperate Pharmaceutical Co.,Ltd
Tel: 010-60279497
Email: sales01@cooperate-pharm.com
Products Intro: Product Name:Pimavanserin tartrate
CAS:706782-28-7
Purity:98% Package:100G;1KG;5KG;10KG;25KG;50KG;100KG
Company Name: Hangzhou FandaChem Co.,Ltd.
Tel: 008657128800458; +8615858145714
Email: fandachem@gmail.com
Products Intro: Product Name:Pimavanserin tartrate fandachem
CAS:706782-28-7
Purity:As coa Package:As request Remarks:706782-28-7
Company Name: ATK CHEMICAL COMPANY LIMITED
Tel: +undefined-21-51877795
Email: ivan@atkchemical.com
Products Intro: Product Name:Pimavanserin tartrate
CAS:706782-28-7
Purity:98% HPLC Package:5G;10G;25G;50G;100G;250G;1KG

Unii-na83F1sjsr manufacturers

  • Pimavanserin Tartrate
  • Pimavanserin Tartrate pictures
  • $0.00 / 1g
  • 2023-11-01
  • CAS:706782-28-7
  • Min. Order: 1g
  • Purity: 98%
  • Supply Ability: 100kg
  • Pimavanserin Tartrate
  • Pimavanserin Tartrate pictures
  • $0.00 / 1g
  • 2022-05-18
  • CAS:706782-28-7
  • Min. Order: 10g
  • Purity: 99.0%
  • Supply Ability: 10tons
Unii-na83F1sjsr Basic information
Product Name:Unii-na83F1sjsr
Synonyms:N-(4-Fluorophenylmethyl)-N-(1-methylpiperidin-4-yl)-N'-(4-(2-methylpropyloxy)phenylmethyl) carbamide (2R,3R)-dihydroxybutanedioate (2:1);N-(4-Fluorophenylmethyl)-N-(1-methylpiperidin-4-yl)-N'-(4-(2-methylpropyloxy)phenylmethyl)carbamide;Unii-na83F1sjsr;Pimavanserin tartrate or ACP 103;BVF-048;Pimavanserin tartrate,nuplazid;N-[(4-Fluorophenyl)methyl]-N-(1-methyl-4-piperidinyl)-N'-[[4-(2-methylpropoxy)phenyl]methyl]urea (2R,3R)-2,3-dihydroxybutanedioate (2:1);N-[(4-Fluorophenyl)methyl]-N-(1-methyl-4-piperidinyl)-N'-[[4-(2-methylpropoxy)phenyl]methyl]urea (2R,3R)-2,3-dihydroxybutanedioate
CAS:706782-28-7
MF:C29H40FN3O8
MW:577.65
EINECS:1806241-263-5
Product Categories:
Mol File:706782-28-7.mol
Unii-na83F1sjsr Structure
Unii-na83F1sjsr Chemical Properties
storage temp. Store at -20°C
solubility DMSO:70.0(Max Conc. mg/mL);69.6(Max Conc. mM)
Safety Information
HS Code 29299090
MSDS Information
Unii-na83F1sjsr Usage And Synthesis
DescriptionPimavanserin, developed by San Diego-based Acadia Pharmaceuticals, is a selective and potent serotonin 2A (5-HT2A) receptor inverse agonist. The USFDA approved this once-daily drug to treat the delusions and hallucinations associated with psychosis as a function of Parkinson’s disease. Pimavanserin has a unique mechanism of action relative to other antipsychotics, behaving as a selective inverse agonist of the serotonin 5-HT2A receptor while exhibiting 40-fold selectivity over the 5-HT2C receptor and having no significant affinity or activity with the 5-HT2B or dopamine receptors.
UsesPimavanserin tartrate is a 5-HT2A inverse agonist that reverses psychosis-like behaviours and has the potential to treat various other neuropsychiatric disorders such as schizophrenia and Parkinson’s disease.
DefinitionChEBI: A tartrate salt that is the hemitartrate salt of pimavanserin. An atypical antipsychotic that is used for treatment of hallucinations and delusions associated with Parkinson's disease.
SynthesisThree patent applications filed by Acadia described the process-scale synthetic approach to pimavanserin. The kilogram-scale synthesis began with the alkylation of commercially available 4-hydroxybenzaldehyde (123) with isobutyl bromide (124) under basic conditions. Condensation of the resultant benzaldehyde 125 with hydroxylamine furnished the corresponding oxime 126 in 63% yield from 123. Hydrogenation of 126 catalyzed by Pd/C under acidic conditions produced benzylamine 127, which was isolated as the acetate salt in 41% yield. This compound underwent sodium hydroxide workup followed by reaction with HCl gas and phosgene to deliver isocyanate 128. Nucleophilic attack of this isocyanate by benzylamine 129 (prepared from reductive amination of commercially available N-methylpiperid-4-one 130 with 4-fluorobenzylamine 131) followed by salt formation using tartaric acid in aqueous isopropyl acetate, and THF completed the synthesis of pimavanserin tartrate (XI) in 50% yield over the two-step protocol and a 10.6% overall yield from 123.

Synthesis_706782-28-7

Unii-na83F1sjsr Preparation Products And Raw materials
Tag:Unii-na83F1sjsr(706782-28-7) Related Product Information
L(+)-Ornithine hydrochloride Pimavanserin 1,3-bis(4-isobutoxybenzyl)urea Bis(4-fluorobenzyl)aMine Pimavanserin N-[(4-Fluorophenyl)methyl]-1-methyl-4-piperidinamine Pimavanserin