Sertaconazole nitrate

Sertaconazole nitrate
  • CAS No.:99592-32-2
Other grades of this product :
Sertaconazole nitrate Basic information
Product Name:Sertaconazole nitrate
Synonyms:1-(2-((7-chlorobenzo(b)thien-3-yl)methoxy)-2-(2,4-dichlorophenyl)ethyl)-1h-i;Dermofix;FI-7056;Zalain;1-[2-[(7-Chlorobenzo[b]thiophen-3-yl)methoxy]-2-(2,4-dichlorophenyl)ethyl]-1H-imidazole;1-[β-[(7-Chlorobenzo[b]thiophene-3-yl)methoxy]-2,4-dichlorophenethyl]-1H-imidazole;Sertaconazol;(+-)-1-(2,4-Dichloro-beta-((7-chlorobenzo(b)thien-3-yl)methoxy)phenethyl)imidazole
CAS:99592-32-2
MF:C20H15Cl3N2OS
MW:437.77
EINECS:1312995-182-4
Product Categories:Aromatics;Heterocycles;Intermediates & Fine Chemicals;Pharmaceuticals;Sulfur & Selenium Compounds
Mol File:99592-32-2.mol
Sertaconazole nitrate Chemical Properties
Melting point 146-147°
Boiling point 614.1±55.0 °C(Predicted)
density 1.43±0.1 g/cm3(Predicted)
storage temp. Refrigerator
solubility DMSO (Slightly), Methanol (Slightly)
form Solid
pka6.68±0.12(Predicted)
color White to Pale Yellow
CAS DataBase Reference99592-32-2(CAS DataBase Reference)
Safety Information
MSDS Information
Sertaconazole nitrate Usage And Synthesis
DescriptionSertaconazole has been developed and launched for the treatment of dermatological fungal infections by Ferrer Internacional S. A. Mylan received FDA approval for sertaconazole nitrate cream for the treatment of athlete's foot (tinea pedis) at the end of 2003.
UsesAn imidazole antifungal agent, inhibits the synthesis of ergosterol, an essential cell wall component of fungi.
Synthesis2,4-Dichloro acetophenone 169 was brominated at low temperature to give bromide intermediate 170, which was used without isolation. To the same pot, five-fold excess of imidazole was added to give imidazolylacetophenone 171 in 71% yield from 169. Sodium borohydride was employed to reduce ketone 171 to alcohol 172 in 78% yield. Racemic alcohol 172 was resolved with (-)-DIP-chloride to give its corresponding chiral R-alcohol 173 in 80% yield. Compound 173 was then alkylated with 3-bromomethyl-7-chlorobenzo[b]thiophene (174) in dry DMF in the presence of potassium t-butoxide to give the alkylation product in 68% yield. Finally, 60% nitric acid was used to make sertaconazole mononitrate (XXI) in 89% yield.
Sertaconazole nitrate Preparation Products And Raw materials
Raw materialsSodium hydride-->Silica gel-->Thianaphthene-->Hexamethylphosphoramide

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