Process for preparing 11-methylene-18-methyl-estr-4-en-3, 17-dione, useful as intermediate compound for the synthesis of molecules having pharmacological activity

摘要

There is described a process for the industrial synthesis of 11-methylene-18-methyl-estr-4-en-3,17-dione, a compound having the structure formula (I) depicted below: (Formula I) (I) useful as intermediate compound in the synthesis of the progestin compounds Desogestrel and Etonogestrel.;

主权项

1. A method for the selective reduction of the carbonyl group in position 17 of 18-methyl-estr-5-en-3,11,17-trione 3,3′-acetal (IV) to form 17-hydroxy-18-methyl-estr-5-en-3,11-dione 3,3′-acetal (V) wherein R1 and R2 can be either separate alkyl radicals C1-C3 equal to each other, or they can form a unique bidentate alkyl radical C2-C4, and the symbol indicates that the —OH group may have configuration α or β, said reduction carried out using a metal hydride in the presence of cerium trichloride, operating at a temperature comprised between −10 and 40° C. during a time comprised between 30 minutes and 3 hours, in a solvent consisting of a mixture between at least an alcohol selected among methanol, ethanol, isopropanol and cyclohexanol, and at least a second solvent selected among ethyl ether, isopropyl ether, tetrahydrofuran, methyltetrahydrofuran, chloroform and methylene chloride.