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Fexinidazole

Fexinidazole Struktur
59729-37-2
CAS-Nr.
59729-37-2
Englisch Name:
Fexinidazole
Synonyma:
HOE-239;Fexinidazole;HOE-239;HOE239;HOE 239;Fexinidazole (HOE 239);Fexinidazole, 10 mM in DMSO;1-Methyl-2-[[4-(methylthio)phenoxy]methyl]-5-nitro-1H-imidazole;1H-Imidazole, 1-methyl-2-[[4-(methylthio)phenoxy]methyl]-5-nitro-;antitrypanosomal,nitroimidazole,sleeping,HOE239,Fexinidazole,T.brucei,sickness,orally,HOE-239,Inhibitor,inhibit,HAT,Parasite
CBNumber:
CB41178746
Summenformel:
C12H13N3O3S
Molgewicht:
279.31
MOL-Datei:
59729-37-2.mol

Fexinidazole Eigenschaften

Siedepunkt:
501 °C
Dichte
1.33±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
L?slichkeit
DMF: 20 mg/mL; DMF:PBS (pH 7.2) (1:8): 0.11 mg/mL; DMSO: 10 mg/mL; Ethanol: 0.2 mg/mL
Aggregatzustand
A crystalline solid
pka
1.82±0.25(Predicted)
Farbe
Light yellow to yellow
InChI
1S/C12H13N3O3S/c1-14-11(13-7-12(14)15(16)17)8-18-9-3-5-10(19-2)6-4-9/h3-7H,8H2,1-2H3
InChIKey
MIWWSGDADVMLTG-UHFFFAOYSA-N
SMILES
CN1C(COC2=CC=C(SC)C=C2)=NC=C1[N+]([O-])=O

Sicherheit

WGK Germany  WGK 3
Speicherklasse 11 - Combustible Solids

Fexinidazole Chemische Eigenschaften,Einsatz,Produktion Methoden

Verwenden

Fexinidazole is a medication used in the treatment of African trypanosomiasis caused by trypanosoma brucei gambiense. An antitrypanosomal agent. It also functions as a medication used against the main species that cause visceral and cutaneous new World leishmaniasis.

Synthese

The synthesis of Fexinidazole started with the methylation of nitroimidazole (2.1) using dimethyl sulphate in dioxane to give intermediate 2.2 in 82% yield. The methylated imidazole 2.2 was subsequently reacted with formaldehyde in dimethyl sulfoxide to produce the corresponding imidazolyl methanol derivative 2.3 in 62% yield. Intermediate 2.3 was reacted with dichlorosulfoxide in chloroform to give the corresponding 2-chloromethyl-1-methyl-5-nitroimidazole 2.4, which was then coupled with 4-methylmercaptophenol (2.5) in the presence of acetone and potassium carbonate to produce "wet" fexinidazole hydrochloride (2.6). The final free base of fexinidazole (2) was obtained by neutralisation with 25% aqueous ammonia solution, giving an overall yield of 65% for the entire three-step reaction.
Synthesis of Fexinidazole

Fexinidazole Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Fexinidazole Anbieter Lieferant Produzent Hersteller Vertrieb H?ndler.

Global( 103)Lieferanten
Firmenname Telefon E-Mail Land Produktkatalog Edge Rate
Hebei Chuanghai Biotechnology Co,.LTD
+86-86-13131129325 +8613131129325
sales1@chuanghaibio.com China 5225 58
Capot Chemical Co.,Ltd.
+86-(0)57185586718 +86-13336195806
sales@capot.com China 29640 60
Shandong chuangyingchemical Co., Ltd.
18853181302
sale@chuangyingchem.com CHINA 5906 58
BOC Sciences
+1-631-485-4226
inquiry@bocsci.com United States 19936 58
Alchem Pharmtech,Inc.
8485655694
sales@alchempharmtech.com United States 63687 58
Shaanxi Dideu Medichem Co. Ltd
+86-29-87569266 +86-17392581500
1015@dideu.com China 3991 58
Zhengzhou Alfa Chemical Co.,Ltd
+8618530059196
sale04@alfachem.cn China 9544 58
TargetMol Chemicals Inc.
+1-781-999-5354; +17819995354
marketing@targetmol.com United States 32466 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695
laboratory@coreychem.com China 30224 58
Wuhan Demeikai Biotechnology Co., Ltd
+8618942921723
info@dmksw.xin China 717 58

59729-37-2()Verwandte Suche:


  • 1-Methyl-2-[[4-(methylthio)phenoxy]methyl]-5-nitro-1H-imidazole
  • HOE-239
  • Fexinidazole
  • Fexinidazole (HOE 239)
  • HOE-239;HOE239;HOE 239
  • antitrypanosomal,nitroimidazole,sleeping,HOE239,Fexinidazole,T.brucei,sickness,orally,HOE-239,Inhibitor,inhibit,HAT,Parasite
  • 1H-Imidazole, 1-methyl-2-[[4-(methylthio)phenoxy]methyl]-5-nitro-
  • Fexinidazole, 10 mM in DMSO
  • 59729-37-2
  • Inhibitors
  • apis
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