FIELD: medicine, pharmaceutics.
SUBSTANCE: present invention refers to a method of producing biphosphonic acids and their pharmaceutically acceptable salts applied in medicine. In the offered method, the compounds of general formula I or their pharmaceutically acceptable salts where R1 represents alkyl, arylalkyl, an aromatic or heteroaromatic group, are produced by a reaction of carboxylic acid of formula II or its salts, formula II in which R1 has said values, with phosphorous acid and phosphorous trichloride in an aprotonic polar solvent selected from N,N'-dimethylethylene urea (DMEU), N,N'-dimethylpropylene urea (DMPU), 1-methyl-2-pyrrolidone (NMP) or their mixtures.
EFFECT: new method of producing biologically active compounds is implemented.
14 cl, 4 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF RECOVERY OF SPENT METHANESULFONIC AND PHOSPHOROUS ACIDS, AND DRY MIXTURE THEREOF | 1995 |
|
RU2152950C1 |
METHOD FOR SYNTHESIS OF PHOSPHONOALKYLIMINODIACETIC ACID | 2010 |
|
RU2553683C2 |
CYCLIC PHOSPHORUS-CONTAINING COMPOUNDS AND METHOD OF CONTINUOUS SYNTHESIS OF γ-AMINO-1-HYDROXYALKYLIDENE-1,1- -BISPHOSPHONIC ACIDS | 1994 |
|
RU2154647C2 |
METHOD FOR PREPARING N-PHOSPHONOMETHYLGLYCINE AND INTERMEDIATE SUBSTANCE FOR ITS PREPARING | 2000 |
|
RU2260010C2 |
METHOD FOR SYNTHESIS OF AMINOALKYLENE PHOSPHONIC ACID | 2013 |
|
RU2694047C2 |
METHOD OF PRODUCING CONCENTRATED PHOSPHOROUS ACID | 2009 |
|
RU2525424C2 |
PROCESS FOR PREPARATION OF IOPAMIDOL | 2014 |
|
RU2657238C2 |
METHOD OF OBTAINING DIALKYLPHOSPHITES | 2010 |
|
RU2528053C2 |
METHODS FOR SYNTHESIS OF 3-(4-(2,4-DIFLUOROBENZYLOXY)-3-BROMO-6-METHYL-2-OXOPYRIDIN-1 (2H)-YL)-N-4-DIMETHYLBENZAMIDE | 2007 |
|
RU2411236C1 |
METHOD FOR SYNTHESIS OF AMINOPOLYALKYLENE PHOSPHONIC ACID COMPOUNDS | 2005 |
|
RU2402558C2 |
Authors
Dates
2011-07-27—Published
2007-11-06—Filed