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1. 发明申请

WO2003047931A1 FEATHER DUSTER FOR VEHICLE 审中-公开
标题翻译：飞机杜宾车
公开(公告)号：WO2003047931A1
公开(公告)日：2003-06-12
申请号：PCT/KR2002/002280
申请日：2002-12-05
申请人： KWAK, Dong-Hwan , LEE, Hye-Suk , KIM, Seng-Baek
发明人： KWAK, Dong-Hwan , LEE, Hye-Suk , KIM, Seng-Baek
IPC分类号： B60S3/00
CPC分类号： A46B5/0075 , A46B5/0062 , A46B5/0083 , A46B2200/3026 , A46B2200/3046 , A47L13/38
摘要： Disclosed is a feather duster for vehicles having a feather portion to remove dust. The feather duster includes: a body that includes locking threshold on skirt of lower end thereof to install the feather portion, through hole at center of upper surface thereof, and fixing projections projecting upward around the through hole; fixer that includes fixing grooves corresponding to the fixing projections at lower surface thereof for accepting the fixing projections, and second through hole at center thereof; a locker that includes locking axis installed through the through hole of the body and the second through hole of the fixer, stop ring installed at end of the locking axis, and spring interposing between the stop ring and lower surface of the body to couple the body to the fixer with tension; and handle installed at the fixer for allowing users to use the feather duster.
摘要翻译：公开了一种具有羽毛部分以除去灰尘的车辆的羽毛除尘器。羽毛除尘器包括：主体，其在其下端的裙部上包括锁定阈值，以安装羽毛部分，其上表面中心的通孔，以及围绕通孔向上突出的固定突起; 固定器，其包括与其下表面处的固定突起相对应的固定槽，用于接收固定突起，以及其中心的第二通孔; 一个储物柜，其包括通过本体的通孔安装的锁定轴和固定器的第二通孔，安装在锁定轴端的端部的止动环，以及插入在止动环和主体的下表面之间的弹簧以将身体紧张的固定器; 并安装在固定器上，以允许用户使用羽毛除尘器。

2. 发明申请

WO1995032198A1 IMIDAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF 审中-公开
标题翻译：咪唑衍生物及其制备方法
公开(公告)号：WO1995032198A1
公开(公告)日：1995-11-30
申请号：PCT/KR1995000058
申请日：1995-05-19
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , YOO, Sung, Eun , YI, Kyu, Yang , LEE, Sang, Hee , KIM, Hye, Ryung , SUH, Jee, Hee , KIM, Nak, Jeong , KIM, Seon, Ju , CHA, Ok, Ja , SHIN, Young, Ah , SHIN, Wha, Sup , LEE, Sung, Hou , JUNG, Yi, Sook , LEE, Byung, Ho , SEO, Ho, Won , LEE, Hye, Suk
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D403/14
CPC分类号： C07D401/14
摘要： Novel imidazole derivatives of formula (I) inhibit effectively the action of angiotensin II and have a superior antihypertensive activity, wherein A is a straight, branched or cyclic C1-C6 alkyl group, or OR1 wherein R1 is a hydrogen, or a straight, baranched or cyclic C1-C6 alkyl radical; B is a halogen, CF3 or CF2CF3; X is N or N-oxide; Y is -CH2-, -CH(OR1)- wherein R1 is the same as defined above or, -C(=O)-; n is 0 or an integer of 1 to 4; Z is a halogen, -OH, -OR1, -NR1R2, -N(=O)R3R4, -C(=O)R1, -C(=O)OR1, -CH(OR1)2 or -C(=O)NR1R2, wherein R1 is the same as defined above, R2 is, independently of R1, a hydrogen, or a straight, branched or cyclic C1-C6 alkyl radical, and R3 and R4 are independendtly a straight, branched or cyclic C1-C6 alkyl radical; and D is a hydrogen, or a straight, branched or cyclic C1-C6 alkyl radical.
摘要翻译：式（I）的新型咪唑衍生物有效地抑制血管紧张素II的作用并具有优异的抗高血压活性，其中A是直链，支链或环状的C 1 -C 6烷基或OR 1，其中R 1是氢或直链，或环状C 1 -C 6烷基; B是卤素，CF 3或CF 2 CF 3; X是N或N-氧化物; Y是-CH 2 - ， - CH（OR 1） - ，其中R 1与上述相同或者是-C（= O） - ; n为0或1〜4的整数， Z是卤素，-OH，-OR1，-NR1R2，-N（= O）R3R4，-C（= O）R1，-C（= O）OR1，-CH（OR1）2或-C ）NR1R2，其中R1与上述定义相同，R2独立地为R1，氢或直链，支链或环状的C1-C6烷基，R3和R4独立地为直链，支链或环状的C1-C6 烷基; 并且D是氢或直链，支链或环状的C 1 -C 6烷基。

3. 发明申请

WO1995034564A1 PIRYDYL IMIDAZOLE DERIVATIVES AND PROCESSES FOR THE PREPARATION THEREOF 审中-公开
标题翻译：吡啶基咪唑衍生物及其制备方法
公开(公告)号：WO1995034564A1
公开(公告)日：1995-12-21
申请号：PCT/KR1995000075
申请日：1995-06-07
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , YOO, Sung, Eun , YI, Kyu, Yang , LEE, Sang, Hee , KIM, Hye, Ryung , SUH, Jee, Hee , KIM, Nak, Jeong , KIM, Seon, Ju , CHA, Ok, Ja , SHIN, Young, Ah , SHIN, Wha, Sup , LEE, Sung, Hou , JUNG, Yi, Sook , LEE, Byung, Ho , SEO, Ho, Won , LEE, Hye, Suk
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D471/04
CPC分类号： C07D471/04
摘要： Novel pyridyl imidazole derivatives of formula (I) inhibit effectively the action of angiotensin II and have a superior antihypertensive activity, wherein A is a straight, branched or cyclic C1-C6 alkyl or alkenyl group, OR (wherein R is a hydrogen, or a straight, branched or cyclic C1-C6 alkyl or alkenyl radical), or NR R (wherein R and R are independently a hydrogen, or a straight, branched or cyclic C1-C6 alkyl radical); B is a group of formula (II); D is a hydrogen; a halogen; a straight, branched or cyclic C1-C6 alkyl, C2-C6 alkenyl or C2-C6 alkynyl group which is optionally substituted with OH, a C1-C4 alkoxy radical, CO2R , COR , CON(R )2 or N(R )2, wherein R is the same as defined above; tetrazol-5-yl; a perfluoro-C1-C4 alkyl group; or N(R )2, OR , CO2R or CON(R )2, wherein R is the same as defined above; E is a hydrogen; a halogen; a straight or branched C1-C6 alkyl, C2-C6 alkenyl or C2-C6 alkynyl group which is optionally substituted with OH, a C1-C4 alkoxy radical, CO2R , COR , CON(R )2 or N(R )2, wherein R is the same as defined above; a perfluoro-C1-C4 alkyl group; NO2; or N(R )2 or OR , wherein R is the same as defined above; and n is 0 or an integer of 1 to 4.
摘要翻译：式（I）的新型吡啶基咪唑衍生物有效地抑制血管紧张素II的作用并具有优异的抗高血压活性，其中A是直链，支链或环状的C 1 -C 6烷基或链烯基，OR 1（其中R 1，是氢或直链，支链或环状的C 1 -C 6烷基或链烯基）或NR 2 R 3（其中R 2和R 3独立地是氢或直链，支链或环状C 1 -C 6烷基）; B是式（II）的一组; D是氢; 卤素任选被OH，C 1 -C 4烷氧基，CO 2 R 1，COR 1，CON（R 1）取代的直链，支链或环状C 1 -C 6烷基，C 2 -C 6烯基或C 2 -C 6炔基 >）2或N（R 1）2，其中R 1与上述定义相同; 四唑-5-基; 全氟-C 1 -C 4烷基; 或N（R 1）2，OR 1，CO 2 R 1或CON（R 1）2，其中R 1与上述定义相同; E是氢; 卤素任选被OH，C 1 -C 4烷氧基，CO 2 R 1，COR 1，CON（R 1）烷基取代的直链或支链C 1 -C 6烷基，C 2 -C 6烯基或C 2 -C 6炔基， 2或N（R 1）2，其中R 1与上述定义相同; 全氟-C 1 -C 4烷基; NO2; 或N（R 1）2或OR 1，其中R 1与上述定义相同; n为0或1〜4的整数。

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