Alteconazole Usage And Synthesis

Originator

Alteconazole,Onbio Inc.

Manufacturing Process

63.6 g of potassium t-butylate in 300 ml of dry methanol were introduced into a solution of 229 g of 2,4-dichlorobenzyltriphenylphosphonium chloride in 800 ml of dry methanol at 10°C, and 77.2 g of 4-chloroacetophenone were added after half an hour. The reaction solution was refluxed for 3 hours, the precipitated salt was filtered off at room temperature, the filtrate was evaporated down under reduced pressure, the residue was digested with petroleum ether at from 50°C to 70°C to free it from triphenylphosphine oxide, and the solution was evaporated down under reduced pressure.
The residue was taken up in 1 liter of carbon tetrachloride, and the solution was refluxed with 81.7 g of N-bromosuccinimide and 4 g of 2,2'- azoisobutyrodinitrile. After the reaction was complete, the succinimide was filtered off, the filtrate was evaporated down under reduced pressure and the residue was recrystallized from methanol. 73.4 g (38.8%) of Z-1-(2,4- dichlorophenyl)-2-(4-chlorophenyl)-3-bromoprop-1-ene of melting point 128°C was obtained.
58.9 g of Z-1-(2,4-dichlorophenyl)-2-(4-chlorophenyl)-3-bromoprop-1-ene were refluxed with 52.3 g of 3-choroperoxybenzoic acid in 590 ml of chloroform. After the reaction was complete, the chloroform phase was washed acid-free with aqueous sodium bicarbonate solution and water, dried over sodium sulfate and evaporated down under reduced pressure, and the residue was recrystallized from methanol to give two crystalline fractions: 41.3 g (70.2%) of 2-bromomethyl-2-(4-chlorophenyl)-3-(2,4-dichlorophenyl) oxirane (isomer A) of melting point 98-99°C, and, 12 g (20.4%) of 2- bromomethyl-2-(4-chlorophenyl)-3-(2,4-dichlorophenyl)oxirane (isomer B) of melting point 93-95°C.
20.9 g of 1,2,4-triazole and 4.4 g of sodium hydride (50% strength dispersion in mineral oil) were dispersed in 150 mL of N,N-dimethylformamide, and a solution of 39.2 g of 2-bromomethyl-2-(4-chlorophenyl)-3-(2,4- dichlorophenyl)oxirane (isomer A) and 16.6 g of potassium iodide in 150 ml of N,N-dimethylformamide was added at room temperature. After 8 hours, the reaction solution was worked up, and the product was recrystallized from diisopropyl ether. 31 g (81.9%) of 2-(1,2,4-triazol-1-ylmethyl)-2-(4- chlorophenyl)-3-(2,4-dichlorophenyl)oxirane (isomer A) - alteconazole was obtained. MP: 119°C.

Therapeutic Function

Antifungal

Alteconazole(93479-96-0)Related Product Information

• (R)-Styrene oxide
• (R)-1-(4-CHLOROPHENYL)-1-PROPANOL
• TRANS-STILBENE OXIDE
• 1H-1,2,4-Triazole-1-propanol(9CI)
• Alteconazole
• 2,4-DICHLOROPHENETHYL ALCOHOL
• 1-(4-Chlorophenyl)-2-methyl-2-propanol
• DL-TRANS-4-CHLOROSTILBENEOXIDE
• (2-Chlorophenyl)oxirane
• 2-(4-CHLOROPHENYL)OXIRANE
• (1S,2S)-(-)-1-PHENYLPROPYLENE OXIDE
• 2-(4-CHLOROPHENYL)-2-METHYLOXIRANE
• (S)-3-CHLOROSTYRENE OXIDE
• 2,4-DICHLORO-ALPHA-METHYLBENZYL ALCOHOL
• 2-METHYL-2,3-DIPHENYL-OXIRANE
• 2-PHENYLPROPYLENE OXIDE