Abstract:
A solid oxidized glutathione salt is produced by heating an oxidized glutathione at 30°C or higher while the oxidized glutathione is brought into contact with an aqueous medium in the presence of a substance for providing a cation, to produce the salt of the oxidized glutathione and the cation as a solid, wherein the aqueous medium is composed of water and/or a water-soluble medium, and the cation is at least one selected from an ammonium cation, a calcium cation and a magnesium cation.
Abstract:
PROBLEM TO BE SOLVED: To find a method for efficiently and stably producing an N-alkoxycarbonyl-tert-leucine of high quality by a simple operation. SOLUTION: The N-alkoxycarbonyl-tert-leucine is produced by causing an N-alkoxycarbonylation agent in an amount of at least 0.90 molar time and at most 1.00 molar time the amount of tert-leucine to react with tert-leucine in the presence of water while controlling the pH of the solution within the range of 9-13 by using a basic reagent. COPYRIGHT: (C)2010,JPO&INPIT
Abstract:
sal de glutationa oxidada e método para produzir o mesmo um sal de glutationa oxidada sólida é produzido por aquecimento de uma glutationa oxidada a 30°c ou superior, enquanto a glutationa oxidada é coloca-da em contato com um meio aquoso na presença de uma substância para fornecimento de um cátion, para produzir o sal de glutationa oxidada e o cátion como um sólido, em que o meio aquoso é constituído por água e/ou um meio solúvel em água, e o cátion é, pelo menos, um selecionado a partir de um cátion de amônio, um cátion de cálcio e um cátion de magnésio.
Abstract:
The process for producing N -(1(S)-carboxy-3-phenylpropyl)-L-lysyl-L-proline in a simple, efficient and industrially advantageous manner, which comprises: the first step of subjecting the N -(1(S)-alkoxycarbonyl-3-phenylpropyl)-N -trifluoroacetyl-L-lysyl -L-proline (1) to alkali hydrolysis in a mixed solution composed of water and a hydrophilic organic solvent using an inorganic base in an amount of n molar equivalents (n >/= 3) per mole of the above compound (1), the second step of neutralizing the hydrolysis product using an inorganic acid in an amount of (n - 1) to n molar equivalents (n >/= 3) and removing the inorganic salt formed by causing the same to precipitate out from a solvent system suited for decreasing the solubility of the inorganic salt, and the third step of causing the compound (2) existing in the mixture after removal of the inorganic salt to crystallize out at the isoelectric point thereof and thereby recovering the compound (2) in the form of crystals while retaining the salts comprising the trifluoroacetic acid-derived organic acid salt in a state dissolved in the mother liquor.
Abstract:
The present invention provides a method capable of suppressing a decrease in optical purity due to the exposure to heat during distillation of an optically active epoxide to permit an optically active epoxide of high quality to be simply obtained on an industrial scale. In the method, an optically active epoxide is distilled in the presence of a base to suppress a decrease in optical purity.
Abstract:
The present invention provides a method capable of suppressing a decrease in optical purity due to the exposure to heat during distillation of an optically active epoxide to permit an optically active epoxide of high quality to be simply obtained on an industrial scale. In the method, an optically active epoxide is distilled in the presence of a base to suppress a decrease in optical purity.
Abstract:
The application is concerned with a process for producing a 3-hydroxytetrahydrofuran of the formula (3): by cyclizing a 4-halo-1,3-butanediol of the general formula (2): wherein X represents a halogen atom in an aqueous solution, which comprises carrying out the cyclization reaction under weakly acidic to neutral conditions. Furthermore several methods are disclosed for the isolution of highly pure 3-hydroxytetrahydrofuran.
Abstract:
The present invention relates to a process for the preparation of N2 -(1(S)-carboxy-3-phenylpropyl)-L-lysyl-L-proline in a simple, efficient and industrially advantageous manner, which comprises: the first step of subjecting the Ne2-(1(S)-alkoxycarbonyl-3-phenylpropyl)-Ne6-trifluorocetyl-L-lysyl-L-proline (1) to alkali hydrolysis in a mixed solution composed of water and a hydrophilic organic solvent using an inorganic base, the second step of neutralizing the hydrolysis product using an inorganic acid and removing the inorganic salt formed by causing the same to precipitate out from a solvent system suited for decreasing the solubility of the inorganic salt, and the third step of causing the final product existing in the mixture after removal of the inorganic salt to crystallize out at the isoelectric point thereof and thereby recovering the Ne2-(1(S)-carboxy-3-phenylpropyl)-L-lysyl-L-proline in the form of crystals while retaining the salts comprising the trifluoroacetic acid-derived organic acid salt in a state dissolved in the mother liquor.
Abstract:
An object of the present invention is to provide a process for producing a beta -amino- alpha -hydroxy acid derivative via efficient and industrially utilizable steps. The present invention provides a process for producing a beta -amino- alpha -hydroxy acid derivative represented by the general formula (2) given below which comprises hydrolyzing an alpha -amino- alpha ', alpha '-dihaloketone derivative of the general formula (1) given below in the presence of a base, followed by protecting the amino group or without protecting the same.