FIELD: organic chemistry and technology. SUBSTANCE: invention relates to a method of synthesis of L-isomers of derivatives of propargyl ammonium chloride of the general formula (I): where Y - hydrogen or fluorine atom. Method involves decomposition of D-tartrate-L-isomer of amine of the general formula (II): where Y is indicated above and an interaction of obtained L-isomer of amine of the general formula (II) in the presence of the base with halogenide of the general formula (V): X- where X - halogen atom followed by interaction of obtained L-isomer of the general formula (III): with hydrogen chloride in an organic solvent. During this reaction amine base is released from D-tartrate-L-isomer of amine of the general formula (II) in an aqueous suspension using ammonium hydroxide or alkaline metal salt and/or ammonium salt and its interaction with 1-1.5 mole equivalent of halogenide of the general formula (V) at 0-50 C in buffer system, pH = 8-12. After separation of an aqueous layer a mixture containing L-isomers of amines of the general formula (II) and (III) in an organic solvent is extracted with water and a mixture of ammonium hydroxide and water and/or with phosphate salt an aqueous solution, pH = 5.5-7.5. Then L-isomer of amine of the general formula (II) or its salts is dissolved in an aqueous layer and separated its from L-isomer of amine of the general formula (III) and converted then to L-isomer of amine of the general formula (III) after distillation to L-isomer of salt of the general formula (I). EFFECT: production of pure racemic forms of product. 2 cl, 13 ex
Title | Year | Author | Number |
---|---|---|---|
METHOD OF SYNTHESIS OF QUINOLINECARBOXYLIC ACID DERIVATIVES | 1988 |
|
RU2014331C1 |
DERIVATIVES OF 3,6-SUBSTITUTED-1,2,4,5-TETRAZINE, METHODS OF THEIR SYNTHESIS, LARVICIDE AND OVICIDE-ACTIVE COMPOSITION, METHOD OF ITS PREPARING AND METHOD OF DECREASE OF AMOUNT OF MITE LARVAE AND EGGS | 1994 |
|
RU2142949C1 |
METHOD OF SYNTHESIS OF QUINOLINE CARBOXYLIC ACID DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS | 1988 |
|
RU2049783C1 |
METHOD OF SYNTHESIS OF QUINOLINE CARBOXYLIC ACID OR ITS PHARMACEUTICALLY ACCEPTABLE SALTS AND COMPOUNDS | 1990 |
|
RU2044734C1 |
PROCESS FOR PREPARING PHENYLGUANIDINE DERIVATIVES AND SULFONIC ACID DERIVATIVES AS INTERMEDIATES IN SYNTHESIS OF PHENYLGUANIDINE DERIVATIVES | 1991 |
|
RU2015963C1 |
METHOD OF PRODUCING N-/2-(4-FLUOROPHENYL)-1-METHYL/ETHYL-N-METHYL-N-PROPYNYLAMINE AS RACEMATE OR ITS L-ISOMER OR ITS SALTS | 0 |
|
SU1549477A3 |
LYOTROPIC LIQUID CRYSTALLINE COMPOSITION | 1990 |
|
RU2045564C1 |
METHOD OF SYNTHESIS OF 13,14-DIHYDRO-15(R)-17-PHENYL-18,19,20-TRINOR-PGF2α ESTER | 1993 |
|
RU2099325C1 |
ANTIMICROBIAL COMPOSITION | 1991 |
|
RU2030913C1 |
METHOD OF SYNTHESIS OF DERIVATIVES OF O-(2-HYDROXY-3-PIPERIDINO-1-PROPYL)-NICOTINIC ACID AMIDEOXIME AND THEIR SALTS (VARIANTS), O-(2-HYDROXY-3-PIPERIDINO-1-PROPYL)-NICOTINIC ACID AMIDEOXIME PURE CRYSTALLINE BASE | 1990 |
|
RU2074854C1 |
Authors
Dates
1999-05-20—Published
1994-12-09—Filed