• 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:
    A process for preparing 1-substituted azetidin-3-ol derivatives of formula: …<CHEM>… or an acid halide thereof, in which R<1> is an aryl methyl group; and R<2> is a hydrogen atom or an alkyl, aryl or aralkyl group, which comprises… (a) reacting an epoxy halide of formula: …<CHEM>… in which Hal is a halogen atom, with a primary amine of formula:… R<1> - NH2 III… (b) cyclising the resulting addition product of formula: …<CHEM>… in an aqueous medium to form the acid halide of the compound of formula I, and… (c) when the free hydroxy compound of formula I is required, treating said acid halide with a base. …<??>The compounds are intermediates e.g. for the preparation of azetidine-3-carboxylic acid derivatives which exhibit plant growth regulant properties.
    公开号:SU1318156A3
    申请号:SU843735695
    申请日:1984-05-03
    公开日:1987-06-15
    发明作者:Фергасон Орр Александр
    申请人:Шелл Интернэшнл Рисерч Маатсхаппий Б.В. (Фирма)；
    IPC主号:
    专利说明:

    The invention relates to the production of 1-benzylazetidine-3-ol, which can be used as an intermediate in the synthesis of azetidine-3-carboxylic acid derivatives, having the properties of plant growth regulators,
     The purpose of the invention is to create a new method of producing compounds that are intermediate products in the synthesis of biologically active substances.
    Example 1, Preparation of 1-benzylazetidine-3-ol.
    A. Epichlorohydrin (46.25 g) and benzylamine (53.5 g) in cshslohexane (250 ml) are stirred together at room temperature for 24 hours. The resulting precipitate is filtered and recrystallized from toluene to obtain N-benzyl-3- amino-1-chloropropan-2-ol as a crystalline solid, so pl. 70 71 ° C, yield 55%.
    B. K-Benzyl-3-amino-1-chloropropan-2-ol (10 g) obtained in Step A is heated at reflux in water (150 ml) with stirring for 24 hours. The reaction mixture is cooled and the aqueous solution is decanted from a soluble material and alkalinized by adding sodium hydroxide. The recovered oil is extracted with dichloromethane and the resulting extracts are washed with water and dried. The solvent was then removed under reduced pressure, and the residue was purified by chromatography on silica gel using acetone as an eluent, followed by recrystallization from toluene to obtain 1-benzyl-azethidin-3-ol as crystals, mp. 64.5-65, yield 27%.
    Calculated,%: C 73.6; H 8.0- N 8.6.
    C, H, 3 N0
    Found,%: C 73.5, H 8.3; N 8.6.
    NMR (CHClI): 2.95 (m, 2H); 3.6 (m, 4H); 4.40 (m, 1H); 7.30 (m, 5H) - 3.30 (1DN, shir, OH),
    Examples 2-12. Analogously to example 1, except that the water in stage B is replaced with a mixture (1: 1 by volume) of water and an organic solvent. According to the results are given in the table.
    Organic solvent
    The output of 1-benzyl-azetidine-3ola,%
    2Toluene28
    3Tetrachloroethane27
    4n-Butanol26
    5Bromobenzene25
    6 Methanol26
    7Nitrobenzene25
    8is-propanol. 26
    9 Methyl isobutyl ketone26
    10Dioksan27
    11 Carbon tetrachloride 27
    12 Ethyl acetate25
    five
    0
    five
    0
    five
    Analogously to example 1, except that in stage B the water is replaced in turn with ethanediol, acetonitrile, methanol and butanol. - In each case, 1-benzine-azetidin-3-ol is obtained.
    The resulting compound is a useful intermediate. Thus, it can be converted by conventional methods, for example, into the corresponding 3-cyanoazetidine derivatives, azetidine-3-carboxylic acid derivatives, which have the properties of plant growth regulators, especially the properties that impart sterility to the male plant organs.
    Using 1-benzyl azethidine-3-ol to obtain azetidine-3-carboxylic acid,
    A. 1-Bensh1azetidin-3-ol (5.0 g), prepared according to Example 1, methinsul- (} ynsh1chloride (g) and triethylamine (6 ml) in dichloromethane (40 ml) are stirred together for 18 hours. The mixture is filtered and solvent is ud
    31
    FLYING under reduced pressure. The residue is purified by chromatography on silica gel using isopropanol in dichloromethane as eluant to obtain 1-benzsh1azetydin-3-ol mesylate, yield 4.25 g,
    B. 1-Benzyl-azethidin-3-ol mesylate (1.7 g) obtained by method (a) and sodium cyanide (1.2 g) are mixed together in 1 ml of water and 20 ml of dimethylformamide with for 16 The solvent is removed under reduced pressure and the residue is purified by chromatography on a sylcagel using isopropanol in dichloromethane as eluant to give 1-benzyl-3-cyanoazetidine, yield 0.5 g,
    B. 1-Benzyl-3-cyanoazetidine (0.5 g obtained by method (b), in an unsaturated solution of barium hydroxide (10 ml), is heated at the boiling point under reflux for 30 hours. The reaction mixture is cooled, saturated with gaseous carbon dioxide and filtered. The solvent is removed from the filtrate under reduced pressure to give 1-benzyl azethidine 3-carboxylic acid with a code of 80%.
    G. 1-Benzylazidine-Z-carboxylic acid (0.5 g), obtained by method
    Compiled by I. Bocharova Editor M. Kelemesh Tehred N. Glushchenko Proofreader L. Pilipenx
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    564
    8, in methanol (15 ml), hydrogenated in the presence of 5% palladium on carbon as a catalyst at room temperature. The catalyst is filtered off and the solvent is removed from the filtrate under reduced pressure to obtain azetidine-3-carboxylic acid with a yield of 90%.
    权利要求:
    Claims (2)
    [1]
    1. A method of producing 1-benzyl-azetidin-3-ol, which is such that epichlorohydrin is reacted with benzylamine, followed by cyclization of the obtained M-benzyl-3-amino-1-chloropropan-2-ol in water or in a mixture of water and an organic solvent in a 1: 1 ratio at reflux temperature and treatment of the reaction mixture with an alkali metal hydroxide.
    [2]
    2. A method according to claim 1, characterized in that the organic solvent used is hydrocarbon, hydrogen halide, alcohol, ketone, cyclic ether, ester or electrical compounds.
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    DE934508C|1954-04-23|1955-10-27|Dehydag Gmbh|Process for the production of galvanic metal coatings|
    DE1111638B|1956-06-22|1961-07-27|Ernst Schneider Dipl Chem Dr R|Process for the preparation of trimethyleneimine compounds|
    GB1236078A|1968-07-04|1971-06-16|Beecham Group Ltd|Substituted azetidinols|
    US3649618A|1970-10-02|1972-03-14|Abbott Lab|Certain 1-aralkyl azetidines|
    US4341887A|1980-03-07|1982-07-27|Petrolite Corporation|Azetidinium salts and polymers and copolymers thereof|GB8412814D0|1984-05-18|1984-06-27|Shell Int Research|1-substituted azetidine-3-ol derivatives|
    GB8419085D0|1984-07-26|1984-08-30|Shell Int Research|Azetidine derivatives|
    GB8627493D0|1986-11-18|1986-12-17|Shell Int Research|Catalytic hydrogenolysis|
    AU759022B2|1999-02-18|2003-04-03|Kaken Pharmaceutical Co., Ltd.|Novel amide derivatives as growth hormone secretagogues|
    CN101911773B|2008-01-16|2013-12-04|阿尔卡特朗讯美国公司|Accessing networks for limited purposes|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    GB838312104A|GB8312104D0|1983-05-04|1983-05-04|Preparation of 1-substituted azetidin-3-ol derivatives|
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