PROCESS FOR PREPARING SUBSTITUTED ISATOIC ACID ANHYDRIDE COMPOUNDS AND DERIVATIVES THEREOF
    1.
    发明申请
    PROCESS FOR PREPARING SUBSTITUTED ISATOIC ACID ANHYDRIDE COMPOUNDS AND DERIVATIVES THEREOF 审中-公开
    制备取代的酸式无水物化合物及其衍生物的方法

    公开(公告)号:US20160229820A1

    公开(公告)日:2016-08-11

    申请号:US15029907

    申请日:2014-10-06

    Applicant: BASF SE

    Abstract: The present invention relates to a process for preparing substituted isatoic acid anhydride compounds of the formula (I) in which R1 is Cl, Br, I, or CN; and R2 is CH3, Cl, Br; using anthranilic acid derivative compounds of formula (III) and/or carbamate compounds of formula (II) wherein R1 and R2 are as defined above; RAr is CH3, Cl, NO2 and n is 0, 1, 2, 3, 4 or 5; The present invention relates also to the compounds of formula (II) and to processes comprising further preceding and/or subsequent reaction steps, leading to anthranilamide pesticides or to precursors for them.

    Abstract translation: 本发明涉及制备式(I)的取代的缩醛酸酐化合物的方法,其中R 1是Cl,Br,I或CN; 并且R 2是CH 3,Cl,Br; 使用式(III)的邻氨基苯甲酸衍生物化合物和/或式(II)的氨基甲酸酯化合物,其中R 1和R 2如上所定义; RAr为CH 3,Cl,NO 2,n为0,1,2,3,4或5; 本发明还涉及式(II)化合物和包括进一步的前述和/或后续反应步骤,导致邻氨基苯甲酰胺农药或其前体的方法。

    Process for Manufacturing 4-Propargylated Amino-Benzoxazinones
    2.
    发明申请
    Process for Manufacturing 4-Propargylated Amino-Benzoxazinones 有权
    制备4-炔丙基化氨基苯并嗪酮的方法

    公开(公告)号:US20160137615A1

    公开(公告)日:2016-05-19

    申请号:US14899755

    申请日:2014-06-17

    Applicant: BASF SE

    CPC classification number: C07D265/36 C07C17/16 C07D413/04 C07C21/22

    Abstract: The present invention relates to a process for manufacturing 4-propargylated amino-benzoxazinones of formula (I), comprising the following steps: step a) preparing propargyl chloride by reacting propargyl alcohol with thionyl chloride optionally in the presence of a catalyst; and step b) reacting the propargyl chloride prepared in step (a) with a NH-benzoxazinone of formula (II); wherein the variables are defined according to the description.

    Abstract translation: 本发明涉及制备式(I)的4-炔丙基化苯并恶嗪酮的方法,包括以下步骤:步骤a)任选地在催化剂存在下,通过炔丙醇与亚硫酰氯反应制备炔丙基氯; 和步骤b)使步骤(a)中制备的炔丙基氯与式(II)的NH-苯并嗪酮反应; 其中根据描述定义变量。

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