PROCESS FOR MANUFACTURING 5-FORMYL-PYRIDINE-2,3-DICARBOXYLIC ACID ESTERS
    3.
    发明申请
    PROCESS FOR MANUFACTURING 5-FORMYL-PYRIDINE-2,3-DICARBOXYLIC ACID ESTERS 审中-公开
    制备5-甲基吡啶-2,3-二羧酸酯的方法

    公开(公告)号:WO2010066668A1

    公开(公告)日:2010-06-17

    申请号:PCT/EP2009/066495

    申请日:2009-12-07

    CPC classification number: C07D213/80

    Abstract: A process for manufacturing a 5-formyl-pyridine-2,3-dicarboxylic acid ester (I) wherein Z is hydrogen or halogen; Z 1 is hydrogen, halogen, cyano or nitro and R 1 , R 2 are independently C 1 -C 10 -alkyl, comprising the steps of (i) reacting a compound of formula (II), wherein the symbols are as in formula (I), with a nitrosation agent (III) R 3 -O-N=O (III) wherein R 3 is C 1 -C 8 -alkyl, in the presence of an alkali metal or alkaline earth metal alcoholates or carbonates in a polar aprotic solvent at a temperature of from -45 to 40°C, to obtain an oxime compound (IV) where Z, Z 1 , R 1 and R 2 are as in formula (I), and (ii) reacting oxime compound (IV) with an aliphatic C 1 -C 10 -aldehyde in the presence of a Lewis acid at a temperature in the range of from 0 to 100°C. The compounds of formula (I) are useful intermediates in the synthesis of herbicidal imidazolinones, like imazamox.

    Abstract translation: 制备其中Z为氢或卤素的5-甲酰基 - 吡啶-2,3-二羧酸酯(I)的方法; Z1是氢,卤素,氰基或硝基,R1,R2独立地是C1-C10-烷基,包括以下步骤:(ⅰ)使符号如式(I)所示的式(ⅱ)化合物与式 在碱金属或碱土金属醇盐或碳酸盐存在下,在极性非质子溶剂中,温度为-45〜40℃的亚硝化剂(Ⅲ)R3-ON = O(Ⅲ)其中R3为C1-C8-烷基 ℃,得到其中Z,Z 1,R 1和R 2如式(I)中的肟化合物(Ⅳ),和(ⅱ)使肟化合物(Ⅳ)与脂族C 1 -C 10 - 醛在 路易斯酸,温度范围为0-100℃。 式(I)化合物是合成除草咪唑啉酮类似咪唑氧化物的有用中间体。

    Process for manufacturing substituted 3-pyridylmethyl ammonium bromides
    6.
    发明公开
    Process for manufacturing substituted 3-pyridylmethyl ammonium bromides 审中-公开
    制备取代的3-吡啶基甲基溴化铵的方法

    公开(公告)号:EP2365965A1

    公开(公告)日:2011-09-21

    申请号:EP09755886.0

    申请日:2009-11-13

    Applicant: BASF SE

    Abstract: A process for manufacturing 5,6-disubstituted-3-pyridylmethyl ammonium bromides (I), wherein Q is a tertiary aliphatic or cyclic, saturated, partially unsaturated or aromatic amine; Z is hydrogen or halogen; Z1 is hydrogen, halogen, cyano or nitro; Y and Y1 are each independently OR1, NR1R2, or when taken together YY1 is —O—, —S— or NR3—; R1 and R2 are each independently hydrogen, C1-C4 alkyl optionally substituted with C1-C4 alkoxy or phenyl optionally substituted with one to three C1-C4 alkyl groups, C1-C4 alkoxy groups or halogen atoms, or phenyl optionally substituted with one to three C1-C4 alkyl groups, C1-C4 alkoxy groups or halogen atoms; R3 is hydrogen or C1-C4 alkyl; comprises the steps of (i) reacting a compound of formula (II), wherein the symbols have the meaning given in formula (I), with bromine in the presence of a radical initiator in a solvent mixture comprising an aqueous phase and an organic phase, where the organic phase comprises a solvent selected from 1,2-dichloroethane, chlorobenzene, 1,2-dichlorobenzene, 1,3-dichlorobenzene, 1,4-dichlorobenzene and tetrachloromethane, and where the pH-value of the aqueous phase is from 3 to

    Abstract translation: 制备5,6-二取代-3-吡啶基甲基溴化铵(I)的方法包括以下步骤:(i)使式(II)化合物反应,得到3-溴甲基-5,6-二取代的吡啶化合物( (ii)使式(III)的溴化合物与叔胺碱Q在溶剂中在约0℃至100℃的温度范围内反应。

    PROCESS FOR MANUFACTURING 5-FORMYL-PYRIDINE-2,3-DICARBOXYLIC ACID ESTERS
    8.
    发明公开
    PROCESS FOR MANUFACTURING 5-FORMYL-PYRIDINE-2,3-DICARBOXYLIC ACID ESTERS 有权
    用于生产5-甲酰基吡啶-2,3-二羧酸酯

    公开(公告)号:EP2376472A1

    公开(公告)日:2011-10-19

    申请号:EP09764528.7

    申请日:2009-12-07

    Applicant: BASF SE

    CPC classification number: C07D213/80

    Abstract: A process for manufacturing a 5-formyl-pyridine-2,3-dicarboxylic acid ester (I) wherein Z is hydrogen or halogen; Z
    1 is hydrogen, halogen, cyano or nitro and R
    1 , R
    2 are independently C
    1 -C
    10 -alkyl, comprising the steps of (i) reacting a compound of formula (II), wherein the symbols are as in formula (I), with a nitrosation agent (III) R
    3 -O-N=O (III) wherein R
    3 is C
    1 -C
    8 -alkyl, in the presence of an alkali metal or alkaline earth metal alcoholates or carbonates in a polar aprotic solvent at a temperature of from -45 to 40°C, to obtain an oxime compound (IV) where Z, Z
    1 , R
    1 and R
    2 are as in formula (I), and (ii) reacting oxime compound (IV) with an aliphatic C
    1 -C
    10 -aldehyde in the presence of a Lewis acid at a temperature in the range of from 0 to 100°C. The compounds of formula (I) are useful intermediates in the synthesis of herbicidal imidazolinones, like imazamox.

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