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1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride

CAS No.
903576-44-3
Chemical Name:
1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride
Synonyms
Pitolisant HCl;CS-2751;BF 2649;CS-1548;Ciproxidine;Ciproxidine BF2649;Pitolisant HCI salt;BF 2649 hydrochloride;Pitolisant Hcl(BF2.649;Pitolisant (Ciproxidine
CBNumber:
CB62518970
Molecular Formula:
C17H26ClNO.HCl
Molecular Weight:
332
MDL Number:
MFCD09970745
MOL File:
903576-44-3.mol
Last updated:2024-04-26 17:21:34

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride Properties

storage temp. Desiccate at RT
solubility ≥16.6 mg/mL in DMSO; ≥57.4 mg/mL in H2O; ≥94.2 mg/mL in EtOH
form solid
FDA UNII YV33CH63HI

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS08
Signal word  Warning
Hazard statements  H361fd
Precautionary statements  P201-P308+P313
NFPA 704
0
2 0

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich SML2716 Pitolisant hydrochloride ≥98% (HPLC) 903576-44-3 10MG $97.4 2024-03-01 Buy
Sigma-Aldrich SML2716 Pitolisant hydrochloride ≥98% (HPLC) 903576-44-3 50MG $395 2024-03-01 Buy
Cayman Chemical 19307 Ciproxidine ≥98% 903576-44-3 1mg $37 2024-03-01 Buy
Cayman Chemical 19307 Ciproxidine ≥98% 903576-44-3 5mg $161 2024-03-01 Buy
Cayman Chemical 19307 Ciproxidine ≥98% 903576-44-3 10mg $283 2024-03-01 Buy
Product number Packaging Price Buy
SML2716 10MG $97.4 Buy
SML2716 50MG $395 Buy
19307 1mg $37 Buy
19307 5mg $161 Buy
19307 10mg $283 Buy

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride Chemical Properties,Uses,Production

Description

Pitolisant hydrochloride, a first-in-class inverse agonist of the histamine H3 receptor, was approved in the EU for the treatment of excessive daytime sleepiness (EDS) in adults with narcolepsy with or without cataplexy. The drug, which was developed by Bioprojet and has orphan drug designation in the EU and US, enhances wakefulness by increasing histaminergic neuron activity. With once daily oral administration in the morning, patients taking pitolisant exhibited significantly reduced EDS versus placebo but not versus modafinil. Plasma levels of the drug are reduced at the end of the day such that its waking effect is minimized at night (plasma t1/2 10-12 h). Several articles have been published detailing the discovery of pitolisant.

Uses

BF 2649 Hydrochloride, is a novel histamine H3 receptor antagonist and inverse agonist.

Synthesis

The most likely scale preparation of pitolisant hydrochloride consists of only four synthetic steps starting with the mesylation of commercial 3-(4-chlorophenyl)propan-1-ol (132). Displacement of the mesylate with the sodium salt of commercial 3-(piperidin-1-yl)propan-1-ol (133) in warm DMA assembled the parent drug in 97% yield over two steps. Salt formation was affected by pH adjustment to 3-4 using HCl gas in EtOAc. Recrystallization from ethyl acetate and isopropanol provided pitolisant hydrochloride (XII) on kilogram scale in 78% overall yield across the short four-step protocol. Synthesis_903576-44-3

in vitro

bf2.649 behaved as a competitive antagonist with a ki value of 0.16 nm. bf2.649 functioned as an inverse agonist with an ec50 value of 1.5 nm and an intrinsic activity about 50% higher than that of ciproxifan. pitolisant in vitro potency was approximately 6 times lower at the rodent receptor [1].

in vivo

pitolisant hcl was an oral bioavailable agonist. in mice, after oral and i.v. administrations of pitolisant hcl, the ratio of plasma areas under the curve was 84%. bf2.649 enhanced tele-methylhistamine levels in mouse brain, an index of histaminergic neuron activity in a dose dependent manner with an ed50 value of 1.6 mg/kg p.o. the response persisted after repeated administrations for 17 days [1]. treatment with 20-, 40-, or 60-mg doses of pitolisant showed a statistically significant suppressive effect (standardized photosensitive response [spr] reduction as measured with paired t-tests) in 9/14 (64%) patients of whom 6/14 (43%) showed abolition of the response to intermittent photic stimulation (ips) [3]. bf2.649 showed significant inhibitory activity in several mouse models of schizophrenia [4].

storage

Desiccate at RT

References

[1] ligneau x, perrin d, landais l, camelin jc, calmels tp, et al, bf2. 649 [1-{3-[3-(4-chlorophenyl)propoxy]propyl}piperidine, hydrochloride], a nonimidazole inverse agonist/antagonist at the human histamine h3 receptor: preclinical pharmacology. j pharmacol exp ther.2007 jan;320(1):365-75.
[2] t a esbenshade, k e browman, r s bitner, m strakhova, m d cowart, j d brioni the histamine h3 receptor: an attractive target for the treatment of cognitive disorders. br j pharmacol. 2008 jul; 154(6): 1166–1181.
[3] kasteleijn-nolst trenité d, parain d, genton p, masnou p, schwartz jc, hirsch e. efficacy of the histamine 3 receptor (h3r) antagonist pitolisant (formerly known as tiprolisant; bf2.649) in epilepsy: dose-dependent effects in the human photosensitivity model. epilepsy behav.2013 jul;28(1):66-70.
[4] ligneau x, landais l, perrin d, piriou j, uguen m, denis e, robert p, parmentier r, anaclet c, lin js, burban a, arrang jm,schwartz jc. brain histamine and schizophrenia: potential therapeutic applications of h3-receptor inverse agonists studied with bf2.649. biochem pharmacol. 2007 apr 15;73(8):1215-24. a

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 98)Suppliers
Supplier Tel Email Country ProdList Advantage
Henan Fengda Chemical Co., Ltd
+86-371-86557731 +86-13613820652 info@fdachem.com China 16801 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21689 55
ATK CHEMICAL COMPANY LIMITED
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BOC Sciences
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Chongqing Chemdad Co., Ltd
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Zhejiang J&C Biological Technology Co.,Limited
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ChemExpress
+86-021-58950125 info@chemexpress.com China 555 58
InvivoChem
+1-708-310-1919 +1-13798911105 sales@invivochem.cn United States 6393 58

View Lastest Price from 1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride pictures 2024-04-27 1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride
903576-44-3
US $10.00-3.00 / KG 1KG 99% g-kg-tons, free sample is available Henan Fengda Chemical Co., Ltd
Pitolisant hydrochloride pictures 2024-03-20 Pitolisant hydrochloride
903576-44-3
US $10.00 / g 1g 98%+HPLC 5KG Wuhan Topule Biopharmaceutical Co., Ltd
1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride pictures 2019-07-06 1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride
903576-44-3
US $2.00 / kg 1kg 99% 100kg Career Henan Chemical Co

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride Spectrum

903576-44-3(1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride)Related Search:

1-[3-[3-(4-Chlorophenyl)propoxy]propyl]-piperidinehydrochloride BF 2649 Ciproxidine Pitolisant (hydrochloride) 1-[3-[3-(4-Chlorophenyl)propoxy]propyl]piperidine monohydrochloride Piperidine, 1-[3-[3-(4-chlorophenyl)propoxy]propyl]-, hydrochloride BF 2649 hydrochloride Ciproxidine BF2649 PITOLISANT;CIPROXIDINE BF2649 Pitolisant hydrochloride (Ciproxidine CS-2751 CS-1548 Pitolisant Hcl(BF2.649 CIPROXIDINE;BF 2649;BF2649;BF-2649 Pitolisant HCI salt 1-[3-[3-(4-Chlorophenyl)propoxy]propyl]piperidine HCl PITOLISANT HYDROCHLORIDE;BF 2649;BF2649;BF-2649 Pitolisant (Ciproxidine Pitolisant HCl Pitolisant hydrochloride,BF-2649,inhibit,BF2649,Inhibitor,Histamine Receptor,Pitolisant 903576-44-3 C17H26ClNOHCl Inhibitor