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    우라실계 화합물 및 이를 포함하는 제초제
    1.
    发明公开
    우라실계 화합물 및 이를 포함하는 제초제 有权
    尿素化合物和包含化合物的除草剂

    公开(公告)号：KR1020100038052A

    公开(公告)日：2010-04-12

    申请号：KR1020090090692

    申请日：2009-09-24

    Applicant: 한국화학연구원 ,  주식회사 팜한농

    Inventor： 고영관 ,  정근회 ,  류재욱 ,  우재춘 ,  구동완 ,  김대황 ,  김태준 ,  최인영 ,  김영권 ,  오태현 ,  최준혁 ,  석미영 ,  김경성 ,  정봉진

    IPC: C07D239/54 ,  A01N43/54 ,  A01N41/06

    CPC classification number: C07D239/54 ,  A01N43/54

    Abstract: PURPOSE: A herbicide containing uracil compound as an active ingredient is provided to use as a non-selective herbicide which removes broad weeds. CONSTITUTION: A uracil compound is denoted by chemical formula 1. A herbicide contains the uracil compound of chemical formula 1, agriculturally acceptable salt or mixture thereof as an active ingredient. A herbicide composition contains 0.1-99.9 weight% of uracil compound of chemical formula 1, its agriculturally acceptable salt, or mixture thereof, and 0.1-99.9 weight% of additive of surfactant, or solid or liquid diluents. The composition is formulated in a form of suspension, emulsion, liquid, dispersion liquid, or tablet.

    Abstract translation: 目的：提供含有尿嘧啶化合物作为活性成分的除草剂，用作去除宽阔杂草的非选择性除草剂。 构成：尿嘧啶化合物由化学式1表示。除草剂含有化学式1的尿嘧啶化合物，农业上可接受的盐或其混合物作为活性成分。 除草剂组合物含有0.1-99.9重量％的化学式1的尿嘧啶化合物，其农业上可接受的盐或其混合物，和0.1-99.9重量％的表面活性剂添加剂，或固体或液体稀释剂。 将组合物配制成悬浮液，乳液，液体，分散液或片剂的形式。

    제초활성을 가지는 페닐이속사졸린계 화합물 및 이의 용도
    7.
    发明授权
    제초활성을 가지는 페닐이속사졸린계 화합물 및 이의 용도 有权
    具有除草活性的苯并恶唑化合物及其用途

    公开(公告)号：KR101093102B1

    公开(公告)日：2011-12-13

    申请号：KR1020110100842

    申请日：2011-10-04

    Applicant: 한국화학연구원 ,  주목우연구소

    Inventor： 고영관 ,  연규환 ,  류재욱 ,  구동완 ,  남준호 ,  표성완 ,  황재민 ,  구석진 ,  황기환 ,  이동국 ,  전만석 ,  조남규 ,  김성헌 ,  임종수 ,  정근회

    IPC: C07D261/04 ,  A01N43/80 ,  A01P13/00

    CPC classification number: A01N43/80 ,  C07D261/04

    Abstract: PURPOSE: A phenylisoxazoline compound and a method for preparing the same are provided to ensure high herbicidal activity with safety and to improve productivity of crops. CONSTITUTION: An ortho-substituted phenylisoxazoline compounds containing 2,6-difluorobenzyloxymethyl is denoted by chemical formula 1. In chemical formula I, R1 is C1-C4 alkyl group, halogen group, or haloalkyl group; R2 is hydrogen, methyl group, or ethyl group. An herbicide contains phenylisoxazoline compounds of chemical formula 1, racemic body thereof, or mirror image isomer as an active ingredient.

    Abstract translation: 目的：提供苯基异恶唑啉化合物及其制备方法，以确保高度的除草活性，安全性和提高农作物的生产力。 构成：化学式1表示含有2,6-二氟苄氧基甲基的邻位取代苯基异恶唑啉化合物。化学式I中，R 1为C 1〜C 4烷基，卤素基或卤代烷基。 R2是氢，甲基或乙基。 除草剂含有化学式1的苯基异恶唑啉化合物，其外消旋体或镜像异构体作为活性成分。

    글리벤클라마이드의 제조방법
    8.
    发明授权
    글리벤클라마이드의 제조방법 失效
    글리벤클라마이드의제조방법

    公开(公告)号：KR100402055B1

    公开(公告)日：2003-10-17

    申请号：KR1020010022944

    申请日：2001-04-27

    Applicant: 한국화학연구원

    Inventor： 김대황 ,  정근회 ,  장해성 ,  고영관 ,  류재욱 ,  우재춘 ,  구동완 ,  김선옥 ,  황의형

    IPC: C07C317/32

    Abstract: PURPOSE: Provided is a method for economically synthesizing glibenclamide, with powder shape, which is used as an intermediate for synthesis of medicine useful for treatment of diabetes. CONSTITUTION: The method comprises the steps of (i) reacting N-phenethyl-5-chloro-2-methoxybenzamide with chlorosulfonic acid(ClSO3H) represented by formula 2 in the presence of thionyl chloride(SOCl2) to form p-(N-phenethyl-5-chloro-2-methoxybenzamide)sulfonylchloride represented by formula 3; (ii) reacting sulfonylchloride compound represented by formula 3 with ammonia to form p-(N-phenethyl-5-chloro-2-methoxybenzamide)sulfoneamide represented by formula 4; (iii) reacting sulfoneamide compound represented by formula with alkali metal hydroxide in the presence of alcohol solvent to form p-(N-phenethyl-5-chloro-2-methoxybenzamide)sulfone amide-metal salt represented by formula 5; and (iv) reacting the metal represented by formula 5 with cyclohexyl isocyanate or phenylcyclohexyl carbamate to form glibenclamide represented by formula 1.

    Abstract translation: 目的：提供一种经济地合成格列本脲粉末状的方法，其用作合成用于治疗糖尿病的药物的中间体。 构成：该方法包括以下步骤：（i）使N-苯乙基-5-氯-2-甲氧基苯甲酰胺与式2代表的氯磺酸（ClSO 3 H）在亚硫酰氯（SOCl 2）存在下反应形成对 - （N-苯乙基 -5-氯-2-甲氧基苯甲酰胺）磺酰氯，由式3表示; （ii）使由式3表示的磺酰氯化合物与氨反应以形成由式4表示的对 - （N-苯乙基-5-氯-2-甲氧基苯甲酰胺）磺酰胺; （ⅲ）在醇溶剂存在下使下式表示的磺酰胺化合物与碱金属氢氧化物反应，生成式5表示的对 - （N-苯乙基-5-氯-2-甲氧基苯甲酰胺）磺酰胺 - 金属盐; （iv）使由式5表示的金属与环己基异氰酸酯或苯基环己基氨基甲酸酯反应以形成由式1表示的格列本脲。

    6-클로로벤족사졸-2-온의 새로운 제조방법
    10.
    发明授权
    6-클로로벤족사졸-2-온의 새로운 제조방법 失效
    6-氯苯并恶唑-2-酮的制备方法

    公开(公告)号：KR100543345B1

    公开(公告)日：2006-01-20

    申请号：KR1020030025121

    申请日：2003-04-21

    Applicant: 한국화학연구원

    Inventor： 김대황 ,  정근회 ,  장해성 ,  고영관 ,  류재욱 ,  우재춘 ,  구동완

    IPC: C07D263/58

    Abstract: 본 발명은 다음 화학식 1로 표시되는 6-클로로벤족사졸-2-온의 새로운 제조방법에 관한 것으로서, 보다 상세하게는 다음 화학식 2로 표시되는 벤족사졸-2-온과 염소가스(Cl
    2 )를 특정 양성자성 유기용매(protic organic solvent)와 온도조건에서 반응시켜서 높은 순도와 생성 수율로 6-클로로벤족사졸-2-온을 경제적으로 제조하는 방법에 관한 것이다.

    벤족사졸-2-온, 염소가스, 6-클로로벤족사졸-2-온, 양성자성 유기용매(protic organic solvent)

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