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CNV1014802 (hydrochloride)

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CNV1014802 (hydrochloride) manufacturers

CNV1014802 (hydrochloride) Basic information
Product Name:CNV1014802 (hydrochloride)
Synonyms:CNV1014802 (hydrochloride);(2S,5R)-5-(4-((2-Fluorobenzyl)oxy)phenyl)pyrrolidine-2-carboxamide hydrochloride;(5R)-5-(4-{[(2-fluorophenyl)methyl]oxy}phenyl)-L-prolinamide hydrochloride;GSK-1014802 hydrochloride;2-Pyrrolidinecarboxamide, 5-[4-[(2-fluorophenyl)methoxy]phenyl]-, hydrochloride (1:1), (2S,5R)-;(5R)-5-(4-{[(2-fluorophenyl)methyl]oxy}phenyl)-L-prolinamide HYDROCHLRIDE;Raxatrigine HCl;Raxatrigine hydrochloride
CAS:934240-31-0
MF:C18H20ClFN2O2
MW:350.8150032
EINECS:
Product Categories:
Mol File:934240-31-0.mol
CNV1014802 (hydrochloride) Structure
CNV1014802 (hydrochloride) Chemical Properties
Melting point >206°C (dec.)
storage temp. Hygroscopic, Refrigerator, under inert atmosphere
solubility DMSO (Slightly), Methanol (Slightly, Sonicated)
form Solid
color White to Off-White
Stability:Hygroscopic
Safety Information
MSDS Information
CNV1014802 (hydrochloride) Usage And Synthesis
UsesRaxatrigine Hydrochloride is used as co-therapy for the treatment of epilepsy and related disorders.
Synthesis
GSK1014802

934240-30-9

CNV1014802 (hydrochloride)

934240-31-0

(2S,5R)-5-(4-((2-fluorobenzyl)oxy)phenyl)pyrrolidine-2-carboxamide (5.46 g, 17.37 mmol) was used as a raw material, which was dissolved in ethyl acetate (140 mL), stirred for 30 min and filtered. To the filtrate was added a dioxane solution (6.51 mL, 26.05 mmol) in 4 M HCl and the reaction was stirred at room temperature for 20 minutes, followed by cooling in an ice bath for 15 minutes. The resulting solid was collected by filtration, washed with cold ethyl acetate (2 x 20 mL) and dried under vacuum first at 35 °C overnight and then at 50 °C for 2 h to give an off-white solid product (E1, 5.87 g, 96% yield).LC-MS showed MH+ = 315 (corresponding to molecular formula C18H19FN2O2).1H NMR (d6-DMSO) data were as follows: δ 1.95-2.20 (2H, m), 2.30 (2H, m), 3.35 (1H, s), 4.30 (1H, m), 4.61 (1H, m), 5.18 (2H, s), 7.10 (2H, d, J = 9 Hz), 7.18-7.30 (2H, m), 7.40 (1H, m), 7.47 (2H, d, J = 9 Hz), 7.56 (1H, s), 7.72 (1H, s), 8.07 (1H, s), 10.60 (1H, br s).

IC 50Nav1.7
References[1] Patent: WO2016/102967, 2016, A1. Location in patent: Page/Page column 43
[2] Patent: WO2011/29762, 2011, A1. Location in patent: Page/Page column 23-24
[3] Patent: WO2007/42239, 2007, A1. Location in patent: Page/Page column 45
[4] Patent: WO2007/42239, 2007, A1. Location in patent: Page/Page column 45-46
[5] Patent: WO2007/42239, 2007, A1. Location in patent: Page/Page column 46
Tag:CNV1014802 (hydrochloride)(934240-31-0) Related Product Information
GSK1014802 Propanamide, 2-[[3-[4-[(2-fluorophenyl)methoxy]phenyl]propyl]amino]-, (2S)- (2S,4S)-4-Fluoro-1-[[4-[(3-fluorophenyl)methoxy]phenyl]methyl]-2-pyrrolidinecarboxamide CNV1014802 (hydrochloride) 2-Pyrrolidinecarboxamide, 1-[[4-[(3-fluorophenyl)methoxy]phenyl]methyl]-, (2S)- 2-Azetidinecarboxamide, 1-[[4-[(3-fluorophenyl)methoxy]phenyl]methyl]-, (2S)-