• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention provides a process for producing an optically active homophenylalanine derivative represented by the following general formula (IV), which is economically excellent and efficient, and an intermediate thereof and a method for producing the same. The present invention is the γ-oxo-homophenylalanine represented by the following general formula (I) formed by reacting a β-benzoylacrylic acid derivative represented by the following general formula (II) with a 1-arylethylamine derivative represented by the following general formula (III). It is a manufacturing method of the homophenylalanine derivative represented by following General formula (IV) which provides a derivative | guide_body to a reduction reaction.
    公开号:KR20000064799A
    申请号:KR1019980707691
    申请日:1998-02-13
    公开日:2000-11-06
    发明作者:마사히꼬 야마다；노부오 나가시마；준조 하세가와
    申请人:후루타 다케시；가네가후치 가가쿠고교 가부시키가이샤；
    IPC主号:
    专利说明:

    γ-oxo-homophenylalanine derivative and a method for producing a homophenylalanine derivative formed by reducing the same
    Conventionally, as a manufacturing method of the said optically active homophenylalanine derivative (IV), the method of using biocatalysts, such as an enzyme, the method of using the so-called asymmetric synthesis method which does not use a biocatalyst, such as an enzyme, etc. are known.
    As a method of using the biocatalyst, for example, Japanese Unexamined Patent Publication No. Hei 1-79134 discloses a method of asymmetric decomposition of a corresponding hydantoin with a hydantoinase, and Japanese Unexamined Patent Application Publication No. 2-31694 Although methods for asymmetrically decomposing aminonitriles with nitrile degrading enzymes have been disclosed, these methods require the use of toxic hydrocyanic acid compounds during raw material synthesis.
    U.S. Patent No. 5316943 discloses a method for transaminoation of a corresponding keto acid with a transaminase and described in J. Org. Chem., Vol. 55, page 5567 (1990) discloses methods for reductively aminating corresponding keto acids with phenylalanine dehydrogenase, but these methods require the use of expensive keto acids as raw materials.
    J. Am. Chem. Soc., Vol. 112, p. 945 (1990), discloses a method for asymmetric dehydration of a corresponding ester with oxygen, Bull. Chem. Soc. Jpn., Vol. 55, p. 918 (1982) discloses asymmetric hydrolysis of the corresponding acetyl bodies with acylases. However, these methods are the racemic fractionation methods. There is a drawback that only the desired compound can be obtained, and the operation is complicated.
    As a method of using the asymmetric compound, for example, a method of reducing a compound having a chloroacetyl group to an asymmetric boron complex and then dislocation (J. Am. Chem. Soc., Vol. 114, p. 1906 (1992)), 4-phenyl- Hydrogenation of 2-aminocrotonic acid derivatives using asymmetric rhodium complexes (J. Org. Chem., Vol. 52, page 5142 (1987)), Method of reacting optically active glycine derivatives with phenylpropyl bromide (J. Am. Chem. Soc., Vol. 108, p. 1103 (1986)), etc., but these asymmetric synthesis methods require the use of expensive catalysts and difficult-to-manage organometallic compounds.
    Moreover, as a method obtained by optically dividing the optically active homophenylalanine derivative (IV), for example, a method of dividing a corresponding N-formyl body using phenethylamine (Japanese Patent Laid-Open No. 63-63646), corresponding A method of dividing a methyl ester using mandelic acid (Japanese Patent Laid-Open No. 63-145256), and a method of dividing a corresponding N-acetyl body using brucin (J. Biol. Chem., Vol. 122, 348) (1937-1938), etc., but in these methods, only half of the target compound can be theoretically obtained from the total amount of the racemic material of the raw material, and there are drawbacks such as complicated operation.
    Thus, the method until now was not necessarily a satisfactory method.
    In view of the above circumstances, an object of the present invention is to provide a method for producing the optically active homophenylalanine derivative (IV) which is economically superior and efficient, an intermediate thereof and a method for producing the same.
    Summary of the Invention
    The present invention is represented by the following general formula (I);
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, a C1-C4 alkoxyl group, a C1-C4 alkyl mercapto group, or a nitro group is shown. R represents a phenyl group, a substituted phenyl group or a naphthyl group]
    Γ-oxo-homophenylalanine derivative (hereinafter referred to as "γ-oxo-homophenylalanine derivative (I)").
    The present invention also provides the following general formula (II);
    Wherein X 1 and X 2 are the same as above.
    Β-benzoylacrylic acid derivative represented by the following (hereinafter referred to as "β-benzoylacrylic acid derivative (II)") and the following general formula (III);
    [Wherein R is the same as above]
    The 1-arylethylamine derivative (henceforth "1-arylethylamine derivative (III)") represented by this invention is related with the manufacturing method of the said (gamma) -oxo- homophenylalanine derivative (I) characterized by the above-mentioned.
    The present invention further relates to a method for producing the homophenylalanine derivative (IV), wherein the γ-oxo-homophenylalanine derivative (I) is provided in a reduction reaction.
    Detailed disclosure of the invention
    The present invention is described in detail below.
    In the present invention, a γ-oxo-homophenylalanine derivative (I), which is a novel substance which can be easily prepared by the so-called Michael addition reaction comprising the β-benzoylacrylic acid derivative (II) and the 1-arylethylamine derivative (III). ), And the homophenylalanine derivative (IV) can be easily produced by reducing the γ-oxo-homophenylalanine derivative (I) in the presence of a metal catalyst.
    In the present invention, at the time of the addition reaction, by using the optically active 1-arylethylamine derivative (III), since the -Oxo-homophenylalanine derivative is selectively produced as a diastereo, this -Oxo-homo By reducing the phenylalanine derivative, (R) -homophenylalanine derivative or (S) -homophenylalanine derivative having a very high optical purity can be prepared, respectively.
    The reaction according to the present invention is represented by the reaction scheme as follows.

    In the present invention, p-methoxy-β-benzoylacrylic acid wherein X 1 is a p-methoxy group and X 2 is a hydrogen atom in view of the availability of the homophenylalanine derivative (IV) obtained as the β-benzoylacrylic acid derivative (II). Unsubstituted β-benzoylacrylic acid wherein X 1 is a hydrogen atom and X 2 is a hydrogen atom is preferable.
    The β-benzoylacrylic acid derivative (II) includes a trans and cis.
    Such transmers include, for example, Friedel-Crafts Reactions of aromatic compounds and maleic anhydride, Volume 5, page 229 (1957), dehydration condensation of acetophenone derivatives and glyoxylic acid (JP-A 52-39020). It can synthesize | combine easily by the well-known method, such as No.).
    The sheath can be prepared by, for example, isomerizing the trans-body by light irradiation.
    Any isomers of the trans- and cis-forms can be used for the Michael addition reaction in the present invention. However, from the viewpoint of industrial use, a trans-form having a low workability is preferable.
    In this invention, as said 1-arylethylamine derivative (III), 1-phenethylamine is preferable at the cheapest point. And (S) -1-phenethylamine or (R) -1-phenethylamine can be used to obtain gamma -oxo-homophenylalanine derivative which is optically active.
    A commercially available thing may be used for the said 1-arylethylamine derivative (III), and what was refine | purified by distillation etc. may be used.
    In the present invention, the β-benzoylacrylic acid derivative (II) and the 1-arylethylamine derivative (III) are further reacted to produce γ-oxo-homophenylalanine derivative (I). The benzoyl acrylic acid derivative (II) and the said 1-arylethylamine derivative (III) can be mixed in a solvent, and the method etc. can be used. More specifically, the method of dripping 1-arylethylamine derivative (III) in the ethanol solution of (beta)-benzoyl acrylic acid derivative (II), etc. are mentioned, for example.
    In the production of γ-oxo-homophenylalanine derivative (I) by the addition reaction, when 1-phenethylamine of (S) is used, the stereoconfiguration is (αS, 1S);
    Wherein X 1 and X 2 are the same as above.
    Γ-oxo-homophenylalanine derivative represented by the following formula and the following general formula (VI), wherein the stereoconfiguration is (αR, 1S);
    [Wherein X 1 and X 2 are the same as above]
    A mixture of a γ-oxo-homophenylalanine derivative represented by 2 and two diastereomers is produced.
    In the said addition reaction, the ratio (((alpha) S, 1S): ((alpha) R, 1S)) of a diastereomer is about 51 to 99%: about 49 to 1% normally. Since the (αS, 1S) sieve has low solubility in organic solvents, depending on the solvent system, (αS, 1S) sieves can be obtained with a diastereomer ratio of 70% or more by filtering out the precipitate generated in the reaction solution. Further, by selecting the reaction conditions such as raising the reaction temperature, the (αS, 1S) sieve can also obtain selectivity of 95% or more of the diastereo selectivity.
    Also, by using 1-phenethylamine of the (R) sieve, stereoconfiguration can selectively obtain (αR, 1R) chain γ-oxo-homophenylalanine derivatives in the same ratio of (αS, 1R) at a 95% or more ratio. It may be.
    Examples of the solvent used in the addition reaction include an aqueous system; Alcohols such as methanol, ethanol, isopropanol, n-propanol, t-butyl alcohol and n-hexanol; Nitrile-based compounds such as acetonitrile and propionitrile; Ethers such as diethyl ether, dioxane and tetrahydrofuran; Amide systems such as dimethylformamide, dimethylacetamide, hexamethylphosphoramide, and N-methylpyrrolidone; Halogenated hydrocarbons such as methylene chloride and chloroform; Ketones such as acetone, methyl ethyl ketone and methyl t-butyl ketone; Sulfoxides or sulfones such as dimethyl sulfoxide and sulfolane; Esters such as ethyl acetate and methyl acetate; Aromatic hydrocarbons such as benzene, toluene and xylene; Aliphatic hydrocarbons such as hexane, pentane and cyclohexane; And mixtures thereof.
    In the above addition reaction, when a solvent having high hydrophobicity is used, the diastereomer ratio of the -Oxo-homophenylalanine derivative obtained is 70% or less, which is not preferable in terms of yield. In addition, the progress of the reaction is slightly slow in a strong hydrophilic solvent. From this point of view, a protic solvent, particularly an alcohol solvent such as ethanol, n-propanol, i-propanol, is preferable, and the use thereof results in a diastereomer ratio of 80% or more.
    In the addition reaction, the mixing ratio of the β-benzoylacrylic acid derivative (II) and the 1-arylethylamine derivative (III) is usually β-benzoylacrylic acid derivative (II): 1-arylethylamine derivative (III) = The ratio of 1-arylethylamine derivative (III) to excess of β-benzoylacrylic acid (II) is higher in the range of about 3: 1 to 1: 3, and thus, 1: 1 to 1: 1.5 is preferable.
    As for the reaction temperature in the said addition reaction, 0-80 degreeC is preferable. From a viewpoint of shortening of reaction time, More preferably, it is 30-60 degreeC.
    The concentration in the addition reaction is preferably 0.1 to 20% with respect to the β-benzoylacrylic acid derivative (II). However, when the concentration is thin, the reaction rate decreases, more preferably 1 to 20%. In order to control the reaction such that the reaction proceeds rapidly at an early stage and selectively acquires a diastereomer later, for example, the reaction of β-benzoylacrylic acid derivative (II) and 1-arylethylamine derivative (III) is first performed. It is also possible to prepare by the reaction concentration control, such as 5 hours to 2% concentration, and then diluted to 1%.
    Since the addition reaction is accelerated under basic conditions, a base may be added as an additive in the reaction solution. Examples of the base include amines such as triethylamine, trimethylamine, diisopropylamine and diazabicyclooctane; Alkali metal carbonates such as sodium bicarbonate, potassium bicarbonate, sodium carbonate and potassium carbonate; Alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and lithium hydroxide; Alkaline earth metal hydroxides such as calcium hydroxide, magnesium hydroxide and barium hydroxide; Transition metal hydroxides such as iron hydroxide and zinc hydroxide; And quaternary ammonium hydroxides such as tetramethylammonium hydroxide, tetraethylammonium hydroxide, and benzyltrimethylammonium hydroxide.
    In the above addition reaction, isolation of the target product, γ-oxo-homophenylalanine derivative (I), may be carried out by filtration of the target product generated as a precipitate during the reaction, but the reaction solution is heated, concentrated and filtered. Alternatively, the residue may be further purified by column chromatography, preparative HPLC, or the like, or may be purified by recrystallization of acetonitrile-based water or the like as a solvent. Further, after the addition reaction, an acid such as hydrochloric acid or sulfuric acid can be quickly added to the reaction system to convert the target product into a corresponding hydrochloride or sulfate, and isolate.
    The following reduction operation may be carried out continuously by adding an equivalent amount of sulfuric acid or hydrochloric acid to the γ-oxo-phenylalanine derivative (I) produced by the addition reaction.
    In the present invention, the homophenylalanine derivative (IV) can be obtained by providing the γ-oxo-phenylalanine derivative (I) to the reduction reaction.
    As the reaction used in the reduction reaction, for example, a catalytic reduction reaction carried out in the presence of a metal catalyst; So-called clemencene-type reduction reactions which are reduced in an acidic solvent in the presence of metals such as zinc, zinc amalgam, mercury and tin; Reduction reaction using hydrazine; Reduction reaction using a silicon hydride compound; A reduction reaction in which the ketone is once thioketalized and then reduced to ranic nickel; A reduction reaction in which the ketone is once tosylhydrazone and then reduced to sodium borohydride; And a reduction reaction in which the ketone is once reduced to a metal hydride and then reduced in the presence of a metal catalyst.
    Among them, a catalytic reduction reaction carried out in the presence of a metal catalyst is preferable at a low cost.
    Examples of the metal catalyst used in the catalytic reduction reaction include palladium carbon, palladium hydroxide, palladium oxide, Pd-BaSO 4 , Pd-CaCO 3 , Pd-Al 2 O 3 , palladium-triphenylphosphine, Pd [P (C 6 H 5 ) 3 ] 4 , palladium catalysts, such as a chlordra catalyst and colloidal palladium; Platinum catalysts such as platinum oxide and platinum carbon; Nickel catalysts, such as a nickel nickel; Zinc catalysts, such as zinc powder, etc. are mentioned. Especially, a palladium catalyst is preferable at the point which provides a product with a high yield, and especially palladium carbon is preferable at the point of selectivity.
    In the catalytic reduction reaction, the following reducing agents can be used. Examples of the reducing agent include hydrogen; Formic acid, formate; Metal hydrides; Metals such as zinc, zinc amalgam, mercury and tin; Hydrazine; Silicon hydride compounds; Raney Nickel etc. are mentioned. Among them, hydrogen, formic acid, formate, and metal hydride are preferred because they are inexpensive.
    Examples of the formate include ammonium formate, sodium formate, triethylammonium formate, and the like.
    Examples of the metal hydride include sodium borohydride, NaB (CN) H 3 , and the like.
    The reduction reaction proceeds mildly and with good yield, for example by conducting in a polar protic solvent in the presence of an acid.
    Examples of the acid include mineral acids such as sulfuric acid, hydrochloric acid and phosphoric acid. As for the addition amount of the said acid, about 1-30 times equivalent is preferable with respect to (gamma) -oxo- homophenylalanine derivative (I). If the amount is less than 1 equivalent, the reduction reaction may not proceed sufficiently. If the amount exceeds 30 times, the post-reaction treatment becomes complicated.
    As said polar protic solvent, For example, water, alcohol, acetic acid; Although these mixtures etc. are mentioned, Alcoholic solvents, such as methanol, ethanol, n-propanol, i-propanol, are preferable at the point of operability.
    The reaction example performed using hydrogen as a reducing agent in the alcohol solvent containing a photoacid as said reduction reaction is demonstrated below.
    About 1-100% of palladium carbon is added as a catalyst with respect to (αR, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine, and hydrogen is used as a reducing agent, and it is 0-. It is 100-C, Preferably it is 5-70 degreeC, Alcohol solvents, such as ethanol, are made to react (R) -p-meth almost quantitatively by making it react with stirring conditions for several to 80 hours in presence of acids, such as said photoacid, as a solvent. Can be converted to oxy-homophenylalanine. The reaction time can also be shortened by increasing the amount of catalyst.
    In the above catalytic reduction reaction, since the asymmetry on α of the γ-oxo-homophenylalanine derivative (I) is maintained, the stereoconfiguration on α is obtained from the γ-oxo-homophenylalanine derivative whose stereoconfiguration is (αS, 1S). S) From the γ-oxo-homophenylalanine derivative whose stereoconfiguration is (αR, 1R), the homophenylalanine derivative having the stereoconfiguration above (R) can be synthesized.
    After completion of the catalytic reduction reaction, the homophenylalanine derivative (IV) obtained by removing the solvent after separation of the catalyst can be obtained as a high purity crystal. If necessary, it may be recrystallized using a solvent such as ethanol-aqueous system. Further, purification may be performed using ion exchange resins such as cation exchange resins, reverse phase chromatography, and the like.
    The optically active homophenylalanine derivative (IV) obtained as described above is prepared by a known method commonly used for heptide synthesis, such as an acid chloride, an NCA method, an active ester method, a mixed acid anhydride method, or a hydroxy compound. It can be easily induced with the ACE inhibitor.
    In the present invention, the gamma -oxo-homophenylalanine derivative (I) is prepared from an inexpensive β-benzoylacrylic acid derivative (II) and an optically active 1-arylethylamine derivative (III) by adjusting the Michael addition reaction and its treatment method. Diastereo can optionally be obtained in very high yields, and furthermore, the derivatives can be derived in high yield with homophenylalanine derivatives (IV) which are optically active by reduction reactions.
    Embodiment of the present invention
    The present invention will be described in more detail with reference to the following Examples, but the present invention is not limited to these Examples.
    The present invention is represented by the following general formula (IV);
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, an alkoxyl group having 1 to 4 carbon atoms, an alkyl mercapto group having 1 to 4 carbon atoms, or a nitro group;
    The present invention relates to a method for producing an optically active homophenylalanine derivative represented by γ-oxo-homophenylalanine derivative and an intermediate thereof.
    Homophenylalanyl derivatives (hereinafter referred to as "homophenylalanine derivatives (IV)") which are optically active represented by the above formula (IV) are constituted of medicines, mainly angiotensin converting enzyme inhibitors (hereinafter referred to as "ACE inhibitors"). It is a very important amino acid as a component.
    As described in JP-A-64-71934, the homophenylalanine derivative (IV) can be easily induced with the ACE inhibitor after reacting the amino group with nitrous acid to form a hydroxy compound.
    Example 1
    Synthesis of (αR, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    206 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 20 ml of ethanol and the temperature was adjusted to 40 ° C. 121 mg (1 equivalent) of (R) -1-phenethylamine was added and reacted as it is at 40 degreeC for 15 hours. The precipitated precipitate was filtered off, recrystallized with acetonitrile-water, and dried in vacuo to give 170 mg of white needles as (αR, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine. To yield (52% yield).
    TLC (silica gel); Rf = 0.55 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 160 ~ 161 ℃
    [α] 20 D = -90.2 (c = 0.051, MeOH: 1 NH 2 SO 4 = 3: 1, v / v)
    Elemental Analysis Found: C, 69.66; H, 6.53; N, 4.11
    Calculated Value: C, 69.71; H, 6. 47; N, 4.28
    Example 2
    (αR, 1R) -N- (1-Phenyl) -γ-oxo-p-methoxy-homophenylalanine and (αS, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy Synthesis of Homophenylalanine
    410 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 20 ml of ethanol and the temperature was adjusted to 20 ° C. 240 mg (1 equivalent) of (R) -1-phenethylamine was added and it was made to react as it is at 20 degreeC for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to give (αR, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine and (αS, 1R) -N- (1 as white precipitates. A mixture of -phenethyl) -γ-oxo-p-methoxy-homophenylalanine was obtained with a diastereomer ratio 6: 4. Yield 370 mg. Yield 56% as the sum of the two diastereomers. The (αS, 1R) sieve was purified by preparative HPLC.
    (αS, 1R) sieve
    TLC (silica gel); Rf = 0.55 (n-butanol: acetic acid: water = 4: 1: 1)
    Example 3
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    410 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 20 ml of ethanol and the temperature was adjusted to 40 ° C. 240 mg (1 equivalent) of (S) -1-phenethylamine was added and it was made to react at 40 degreeC for 5 hours. 20 mL of ethanol was added to the reaction solution, and the reaction was further carried out for 10 hours. The precipitated precipitate was filtered off and dried in vacuo to yield ( S, 1S) -N- (1-phenethyl)- -Oxo-p-methoxy-homophenylalanine as a white precipitate of 380 mg. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S) body) was 95/5 or more (yield 58%). Precipitated precipitate was filtered and then recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as white needle crystal.
    TLC (silica gel); Rf = 0.55 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 160 ~ 161 ℃
    [α] 20 D = +90.1 (c = 0.051, MeOH: 1 NH 2 SO 4 = 3: 1, v / v)
    Elemental Analysis Found: C, 69.76; H, 6. 35; N, 4.12
    Calculated Value: C, 69.71; H, 6. 47; N, 4.28
    Example 4
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    185 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 10 ml of ethanol and the temperature was adjusted to 40 ° C. 121 mg (1.1 equiv) of (S) -1-phenethylamine was added and reacted as it is at 40 degreeC for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as 210 mg white precipitate. Yield 71%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more.
    Example 5
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    206 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 10 ml of ethanol and the temperature was adjusted to 40 ° C. 109 mg (0.9 equivalent) of (S) -1-phenethylamine was added and reacted as it is at 40 degreeC for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as a white precipitate of 165 mg. Yield 42%. The diastereomeric ratio of the (αS, 1S) and (αR, 1S) bodies was 85/15.
    Examples 6-19
    (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine and (αR, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy Synthesis of Homophenylalanine
    20 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 2 ml of the solvent shown in Table 1, and the temperature was adjusted to 40 ° C. 13 mg (1.1 equivalent) of (S) -1-phenethylamine was added and reacted as it was at 40 degreeC for 15 hours. The whole reaction solution was added to 18 ml of acetonitrile aqueous solution (acetonitrile: pH 2.5 buffer = 8: 2 v / v), analyzed by HPLC, and the yield and diastereomer ratio shown in Table 1 were (αS, 1S)-. N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine and (αR, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine were obtained.
    The yield in Table 1 shows the sum of two diastereomers.
    menstruumYield (%)(αS, 1S) sieve: (αR, 1S) sieve ratio Example 6Hexane4553: 47 Example 7toluene9056: 43 Example 8chloroform8060: 40 Example 9Ethyl acetate9059: 41 Example 10Tetrahydrofuran9055: 45 Example 112-propanol8687: 13 Example 121-propanol8792: 8 Example 13Acetone4062: 38 Example 14ethanol9070: 30 Example 15Methanol7167: 33 Example 16DMF7080: 20 Example 17Acetonitrile9070: 30 Example 18Ethanol / Water (1/1)6791: 9 Example 19Acetonitrile / water (1/1)6068: 32
    Example 20
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    206 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 20 ml of ethanol and the temperature was adjusted to 50 ° C. 135 mg (1.1 equivalent) of (S) -1-phenethylamine was added and reacted as it was at 50 degreeC for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as 255 mg of white precipitate. Yield 78%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more.
    Example 21
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    500 mg of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 10 ml of ethanol and the temperature was adjusted to 50 ° C. 323 mg (1.1 equivalent) of (S) -1-phenethylamine was added and reacted as it was at 50 ° C for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as a white precipitate of 650 mg. Yield 83%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more.
    Example 22
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine
    1.0 g of trans-p-methoxy-β-benzoylacrylic acid was dissolved in 10 ml of ethanol and the temperature was adjusted to 50 ° C. 646 mg (1.1 equivalent) of (S) -1-phenethylamine was added and reacted as it is at 50 degreeC for 15 hours. Precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine as 1.27 g of white precipitate. Yield 80%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more.
    Example 23
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-homophenylalanine
    176 mg of trans-β-benzoylacrylic acid was dissolved in 20 ml of ethanol and the temperature was adjusted to 50 ° C. 121 mg (1 equivalent) of (S) -1-phenethylamine was added and reacted as it is at 50 degreeC for 15 hours. The precipitated precipitate was filtered off and dried in vacuo to give 240 mg of white precipitate as (αS, 1S) -N- (1-phenethyl) -γ-oxo-homophenylalanine and (αR, 1S) -N- (1-pe A mixture of netyl) -γ-oxo-homophenylalanine was obtained with a diastereomer ratio of about 90:10. Yield 81%. Recrystallization with acetonitrile-water afforded ( S, 1S) -N- (1-phenethyl)- -Oxo-homophenylalanine as a white plate crystal.
    TLC (silica gel); Rf = 0.50 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting point 178-179 ℃ (decomposition)
    [a] 20 D = +80.9 (c = 0.047, MeOH: 1 NH 2 SO 4 = 3: 1, v / v)
    Elemental Analysis Found: C, 72.84; H, 6.53; N, 4.80
    Calc .: C, 72.71; H, 6. 44; N, 4.71
    Example 24
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-chloro-homophenylalanine
    210 mg of trans-p-chloro-β-benzoylacrylic acid was dissolved in 5 ml of ethanol and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to yield ( S, 1S) -N- (1-phenethyl)- -Oxo-p-chloro-homophenylalanine as a white precipitate of 280 mg. Yield 85%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 99/1 or more. The precipitated precipitate was filtered off and recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-chloro-homophenylalanine as a white needle crystal.
    TLC (silica gel); Rf = 0.65 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting point 172-174 캜
    [α] 20 D = +24.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 65.01; H, 5.53; N, 4.32
    Calc .: C, 65.16; H, 5. 47; N, 4.22
    Example 25
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methyl-homophenylalanine
    190 mg of trans-p-methyl-β-benzoylacrylic acid was dissolved in 5 ml of ethanol and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to give (aS, 1S) -N- (1-phenethyl) -γ-oxo-p-methyl-homophenylalanine as a white precipitate of 299 mg. Yield 95%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 97/3 or more. Precipitated precipitate was filtered and then recrystallized with acetonitrile-water to obtain ( S, 1S) -N- (1-phenethyl)- -Oxo-p-methyl-homophenylalanine as white needle crystal.
    TLC (silica gel); Rf = 0.60 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 205-207 ° C
    [α] 20 D = +33.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 73.21; H, 6.94; N, 4.49
    Calc .: C, 73.29; H, 6. 80; N, 4.50
    Example 26
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-nitro-homophenylalanine
    221 mg of trans-p-nitro-β-benzoylacrylic acid was dissolved in 5 ml of ethanol and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-nitro-homophenylalanine as a yellow precipitate of 290 mg. Yield 85%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more. The precipitated precipitate was filtered off and recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-nitro-homophenylalanine as a yellow needle.
    TLC (silica gel); Rf = 0.60 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 152-154 ℃
    [α] 20 D = +23.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 63.28; H, 5. 36; N, 8.06
    Calculated Value: C, 63.15; H, 5. 30; N, 8.18
    Example 27
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-fluoro-homophenylalanine
    194 mg of trans-p-fluoro-β-benzoylacrylic acid was dissolved in 3 ml of methanol, and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to afford 190 mg of white precipitate as (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-fluoro-homophenylalanine. Yield 70%. The diastereomeric ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 90/10 or more. Precipitated precipitate was filtered and then recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-fluoro-homophenylalanine as white needle crystal.
    TLC (silica gel); Rf = 0.65 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 175-177 ℃
    [α] 20 D = +26.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 68.65; H, 5.67; N, 4.29
    Calc .: C, 68.56; H, 5.75; N, 4.44
    Example 28
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-phenyl-homophenylalanine
    252 mg of trans-p-phenyl-β-benzoylacrylic acid was dissolved in 5 ml of methanol, and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to yield (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-phenyl-homophenylalanine as 320 mg of white precipitate. Yield 87%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more. Precipitated precipitate was filtered and then recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-phenyl-homophenylalanine as white needle crystal.
    TLC (silica gel); Rf = 0.80 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 183 ~ 185 ℃
    [α] 20 D = +42.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 77.24; H, 6. 11; N, 3.91
    Calc .: C, 77.19; H, 6. 21; N, 3.75
    Example 29
    Synthesis of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p, m-dimethoxy-homophenylalanine
    236 mg of trans-p, m-dimethoxy-β-benzoylacrylic acid was dissolved in 5 ml of methanol, and the temperature was adjusted to 60 ° C. 144 mg (1.2 equivalent) of (S) -1-phenethylamine was added and reacted for 60 hours as it was at 60 degreeC. The precipitated precipitate was filtered off and dried in vacuo to yield ( S, 1S) -N- (1-phenethyl)- -Oxo-p, m-dimethoxy-homophenylalanine as a white precipitate of 286 mg. Yield 80%. The diastereomer ratio (((alpha) S, 1S) body / ((alpha) R, 1S body) was 95/5 or more. The precipitated precipitate was filtered off and recrystallized with acetonitrile-water to obtain (αS, 1S) -N- (1-phenethyl) -γ-oxo-p, m-dimethoxy-homophenylalanine as a white needle crystal.
    TLC (silica gel); Rf = 0.70 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting Point 171-173 ° C
    [a] 20 b = +34.0 (c = 0.10, CH 3 CN: TFA = 99: 1, v / v)
    Elemental Analysis Found: C, 67.08; H, 6. 66; N, 3.83
    Calculated Value: C, 67.11; H, 6. 49; N, 3.92
    Example 30
    Synthesis of (R) -p-methoxy-homophenylalanine
    10 ml of 0.5 ml sulfuric acid was added to 10 ml of ethanol, and 327 mg of (αR, 1R) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine was added to dissolve it. 50 mg of 10% palladium carbon was added to the mixed solution, and hydrogen was added at 20 ° C. and atmospheric pressure while stirring. After the reaction, the catalyst was suction filtered and the white solid obtained by distilling the solvent was fractionated using reverse phase HPLC to obtain 105 mg of (R) -p-methoxy-homophenylalanine. Yield 50%.
    TLC (silica gel); Rf = 0.37 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting point 234 ℃
    [a] 20 D = -30.6 (c = 0.1, 5 M HCl)
    The data above is Bull. Chem. Soc. Jpn., Vol. 55, p. 918 (1982), was completely consistent with (R) -p-methoxy-homophenylalanine synthesized using the method.
    Example 31
    Synthesis of (S) -p-methoxy-homophenylalanine
    10 ml of 0.5 ml sulfuric acid is added to 10 ml of ethanol, and 163 mg of (αS, 1S) -N- (1-phenethyl) -γ-oxo-p-methoxy-homophenylalanine is added thereto and dissolved. 40 mg of 10% palladium carbon was added to the mixed solution and hydrogen was added at 50 ° C. and 5 atmospheres while stirring. After the reaction, the catalyst was suction filtered, the solvent was distilled off, and then recrystallized from ethanol-water to obtain 84 mg of (S) -p-methoxy-homophenylalanine as white cube crystals. Yield 80%.
    TLC (silica gel); Rf = 0.37 (n-butanol: acetic acid: water = 4: 1: 1)
    Melting point 234 ℃
    [α] 20 D = +30.8 (c = 0.1, 5 M HCl)
    The data above is Bull. Chem. Soc. Jpn., Vol. 55, p. 918 (1982), was completely consistent with (S) -p-methoxy-homophenylalanine synthesized using the method.
    Example 32
    Synthesis of (S) -homophenylalanine
    10 ml of 0.5 sulfuric acid is added to 10 ml of ethanol, and 298 mg of ( S, 1S) -N- (1-phenethyl)- -Oxo-homophenylalanine is added to this solution and dissolved in 30 ml of this mixture. MG 10% palladium carbon was added and hydrogen was added at 20 degreeC and 5 atmospheres, stirring. After the reaction, the catalyst was suction filtered, the solvent was distilled off, and then recrystallized from ethanol-water to obtain 125 mg of (S) -homophenylalanine as white cubic crystals. Yield 70%.
    TLC (silica gel); Rf = 0.34 (n-butanol: acetic acid: water = 4: 1: 1)
    Optical rotation is described by J. Org. Chem., Vol. 55, p. 5567 (1990) was converted to methyl esters and then measured.
    [α] 20 D = +44.5 (c = 1.0, 1 M HCl)
    The above data are available from J. Biol. And (S) -homophenylalanine prepared by the method described in Chem., Vol. 122, p. 348 (1937-1938).
    Since the γ-oxo-homophenylalanine derivative of the present invention is as described above, the optically active homophenylalanine derivative (IV) can be obtained by an economically superior and efficient production method.
    权利要求:
    Claims (23)
    [1" claim-type="Currently amended] The following general formula (I);
    [Formula I]
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, a C1-C4 alkoxyl group, a C1-C4 alkyl mercapto group, or a nitro group is shown. R represents a phenyl group, a substituted phenyl group or a naphthyl group] Γ-oxo-homophenylalanine derivative characterized by the above.
    [2" claim-type="Currently amended] The gamma -oxo-homophenylalanine derivative according to claim 1, wherein X 1 is a p-methoxy group and X 2 is a hydrogen atom.
    [3" claim-type="Currently amended] The gamma -oxo-homophenylalanine derivative according to claim 1, wherein X 1 is a hydrogen atom and X 2 is a hydrogen atom.
    [4" claim-type="Currently amended] The gamma -oxo-homophenylalanine derivative according to claim 1, 2 or 3, wherein R is a phenyl group.
    [5" claim-type="Currently amended] The γ-oxo-homophenylalanine derivative according to claim 1, 2, 3 or 4, wherein the stereoconfiguration is (αR, 1R).
    [6" claim-type="Currently amended] The γ-oxo-homophenylalanine derivative according to claim 1, 2, 3 or 4, wherein the stereoconfiguration is (αS, 1S).
    [7" claim-type="Currently amended] The gamma-oxo-homophenylalanine derivative having the stereoconfiguration (αR, 1R) and the gamma-oxo-homophenylalanine according to claim 1, 2, 3 or 4, wherein the stereoconfiguration is (αS, 1R). Γ-oxo-homophenylalanine derivative which is a mixture of derivatives.
    [8" claim-type="Currently amended] The gamma-oxo-homophenylalanine derivative having the stereoconfiguration (αS, 1S) and the gamma-oxo-homophenylalanine according to claim 1, 2, 3 or 4, wherein the stereoconfiguration is (αR, 1S). Γ-oxo-homophenylalanine derivative which is a mixture of derivatives.
    [9" claim-type="Currently amended] The following general formula (II);
    [Formula II]
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, an alkoxyl group having 1 to 4 carbon atoms, an alkyl mercapto group having 1 to 4 carbon atoms, or a nitro group;
    Β-benzoylacrylic acid derivatives represented by the following formulas (III);
    [Formula III]
    [Wherein R represents a phenyl group, a substituted phenyl group or a naphthyl group] 1-arylethylamine derivative represented by the following formula (I) characterized by reacting;
    [Formula I]
    Wherein X 1 , X 2 and R are the same as above.
    Method for producing γ-oxo-homophenylalanine derivative represented by.
    [10" claim-type="Currently amended] The method for producing a γ-oxo-homophenylalanine derivative according to claim 9, wherein the β-benzoylacrylic acid derivative wherein X 1 is a p-methoxy group and X 2 is a hydrogen atom.
    [11" claim-type="Currently amended] The method for producing a γ-oxo-homophenylalanine derivative according to claim 9, wherein the β-benzoylacrylic acid derivative wherein X 1 is a hydrogen atom and X 2 is a hydrogen atom.
    [12" claim-type="Currently amended] The method for producing γ-oxo-homophenylalanine derivative according to claim 9, 10 or 11, wherein the 1-arylethylamine derivative is 1-phenethylamine.
    [13" claim-type="Currently amended] 13. The process according to claim 12, wherein 1-phenethylamine is a (S) sieve or (R) chain γ-oxo-homophenylalanine derivative.
    [14" claim-type="Currently amended] The method for producing γ-oxo-homophenylalanine derivatives according to claim 9, 10, 11, 12, or 13, wherein the reaction solvent is an alcohol solvent.
    [15" claim-type="Currently amended] The following general formula (I);
    [Formula I]
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, a C1-C4 alkoxyl group, a C1-C4 alkyl mercapto group, or a nitro group is shown. R represents a phenyl group, a substituted phenyl group or a naphthyl group] The following formula (IV) characterized by providing a γ-oxo-homophenylalanine derivative represented by the reduction reaction;
    [Formula IV]
    [Wherein X 1 and X 2 are the same as above] Method for producing a homophenylalanine derivative represented by.
    [16" claim-type="Currently amended] The method for producing a homophenylalanine derivative according to claim 15, wherein a γ-oxo-homophenylalanine derivative having a stereoconfiguration (αR, 1R) is used, and a homophenylalanine derivative having a stereoconfiguration over α is (R).
    [17" claim-type="Currently amended] The method for producing a homophenylalanine derivative according to claim 15, wherein a γ-oxo-homophenylalanine derivative having a stereoconfiguration (αS, 1S) is used and a homophenylalanine derivative having a stereoconfiguration above α is (S).
    [18" claim-type="Currently amended] 18. The process for producing homophenylalanine derivatives according to claim 15, 16 or 17, wherein the reduction reaction is carried out in the presence of a metal catalyst.
    [19" claim-type="Currently amended] The method for producing a homophenylalanine derivative according to claim 15, 16, 17 or 18, wherein hydrogen is used as the reducing agent.
    [20" claim-type="Currently amended] The method for producing a homophenylalanine derivative according to claim 15, 16, 17 or 18, wherein formic acid is used as a reducing agent.
    [21" claim-type="Currently amended] The method for producing a homophenylalanine derivative according to claim 18, 19 or 20, wherein the metal catalyst is a palladium catalyst.
    [22" claim-type="Currently amended] 22. The preparation of homophenylalanine derivatives according to claim 15, 16, 17, 18, 19, 20 or 21, wherein the reduction reaction is carried out in an alcoholic solvent containing a photoacid. Way.
    [23" claim-type="Currently amended] The following general formula (II);
    [Formula II]
    [Wherein, X 1 and X 2 are the same or different, and are a hydrogen atom, an alkyl group of 1 to 7 carbon atoms, an aryl group of 6 to 10 carbon atoms, an aralkyl group of 7 to 10 carbon atoms, a hydroxyl group, a halogen atom, a cyano group, and a trifluoro A methyl group, an alkoxyl group having 1 to 4 carbon atoms, an alkyl mercapto group having 1 to 4 carbon atoms, or a nitro group;
    Β-benzoylacrylic acid derivatives represented by the following formulas (III);
    [Formula III]
    [Wherein R represents a phenyl group, a substituted phenyl group or a naphthyl group] The following general formula (I) formed by reacting a 1-arylethylamine derivative represented by the following;
    [Formula I]
    Wherein X 1 , X 2 and R are the same as above.
    The following formula (IV) characterized by providing a γ-oxo-homophenylalanine derivative represented by the reduction reaction;
    [Formula IV]
    Wherein X 1 and X 2 are the same as above.
    Method for producing a homophenylalanine derivative represented by.
    类似技术:
    公开号 | 公开日 | 专利标题
    KR100572687B1|2006-04-24|Process for the preparation of optically pure 4-hydroxy-2-oxo-1-pyrrolidineacetamide
    US6392073B1|2002-05-21|Intermediates and processes for the preparation of optically active octanoic acid derivatives
    KR100906947B1|2009-07-09|Processes for the preparation of glutamic acid compounds and intermediates thereof and novel intermediates used in the processes
    US5475138A|1995-12-12|Method preparing amino acid-derived diaminopropanols
    KR100882765B1|2009-02-09|Process for preparing 3-acylaminobenzofuran-2-carboxylic acid derivative
    US4686296A|1987-08-11|Process for producing oxiracetam
    JP2009235096A|2009-10-15|Modified pictet-spengler reaction and product produced therefrom
    US4716235A|1987-12-29|Process for preparing N-[1|-ethoxycarbonyl-3-phenylpropyl]-L-alanyl-L-proline
    HU9802504A2|1999-02-01|Method of making |-3-|-5-methylhexanoic acid and it's intermediates
    US5380934A|1995-01-10|Process for producing alanylgutamine
    EP1801093B1|2009-03-18|Process for the Preparation of enantiomer-enriched 2-Alkoxy-3-Phenyl-Propionic Acid
    US20050027119A1|2005-02-03|Process for producing benzoxazine derivative and production intermediate thereof
    WO2010009630A1|2010-01-28|A process for preparing r-beta-amino phenylbutyric acid derivatives
    EP0994854B1|2002-09-18|Method for preparing a substituted perhydroisoindole
    US20110257401A1|2011-10-20|Process for producing optically active carboxylic acid
    JP2009120611A|2009-06-04|Improved method for producing enantiomerically-pure azetidine-2-carboxylic acid
    SK128494A3|1995-05-10|Method of production of indanylamine compounds
    CA2516465A1|2004-09-10|Chemical process for the preparation of intermediates to obtain n-formyl hydroxylamine compounds
    US7326805B2|2008-02-05|Method for the synthesis of 4-hydroxyisoleucine and the derivatives thereof
    EP0206993A1|1986-12-30|Sulphonic-acid esters
    US6087530A|2000-07-11|Process for preparing β-amino-α-hydroxy acid derivatives
    JPH05201882A|1993-08-10|Reductive amine conversion method of amino acid or amino acid derivative
    WO2003051852A1|2003-06-26|Intermediate and process for producing optically active compound from the intermediate
    JP2003261522A|2003-09-19|Method for producing optically active phenylalanine derivative
    KR100734069B1|2007-06-29|Process for the preparation of N5-ethylglutamine
    同族专利:
    公开号 | 公开日
    US5981794A|1999-11-09|
    WO1998035934A1|1998-08-20|
    EP0902011A4|2002-03-20|
    CN1139571C|2004-02-25|
    AT240937T|2003-06-15|
    CN1217710A|1999-05-26|
    IL126554A|2001-01-11|
    DE69814771T2|2004-03-18|
    CN1321636A|2001-11-14|
    EP0902011A1|1999-03-17|
    JPH10287632A|1998-10-27|
    EP0902011B1|2003-05-21|
    ES2200309T3|2004-03-01|
    KR100538420B1|2006-02-28|
    JP3847934B2|2006-11-22|
    DE69814771D1|2003-06-26|
    IL126554D0|1999-08-17|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    1997-02-14|Priority to JP97-047399
    1997-02-14|Priority to JP4739997
    1997-12-18|Priority to JP97-365161
    1997-12-18|Priority to JP36516197A
    1998-02-13|Application filed by 후루타 다케시, 가네가후치 가가쿠고교 가부시키가이샤
    1998-02-13|Priority to PCT/JP1998/000580
    2000-11-06|Publication of KR20000064799A
    2006-02-28|Application granted
    2006-02-28|Publication of KR100538420B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP97-047399|1997-02-14|
    JP4739997|1997-02-14|
    JP97-365161|1997-12-18|
    JP36516197A|JP3847934B2|1997-02-14|1997-12-18|γ-oxo-homophenylalanine derivative and method for producing homophenylalanine derivative obtained by reducing the same|
    PCT/JP1998/000580|WO1998035934A1|1997-02-14|1998-02-13|η-OXO-HOMOPHENYLALANINE DERIVATIVES AND PROCESS FOR PRODUCING HOMOPHENYLALANINE DERIVATIVES BY REDUCING THE SAME|
    [返回顶部]