KR100673344B1 - 우라실 화합물 및 그의 용도 - Google Patents
우라실 화합물 및 그의 용도 Download PDFInfo
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- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
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- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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Abstract
Description
Claims (41)
- 화학식 [I] 의 우라실 화합물:[식중, Q-R3 는 하기 화학식이 나타낸 모이어티로 구성된 군으로부터 선택되는 한개 또는 두개의 질소를 갖는 5-원 또는 6-원 복소환 고리의 R3-치환기를 나타내고:(식중, 상기 복소환 고리는 할로겐, C1-C6 알킬, C1-C6 할로알킬, C2-C6 알케닐, C2-C6 할로알케닐, C2-C6 알키닐, C2-C6 할로알키닐, C1-C6 알콕시 C1-C6 알킬, C1-C6 알콕시, C1-C6 할로알콕시, C1-C6 알콕시카르보닐 C1-C6 알콕시, C1-C6 알콕시카르보닐 C1-C6 알킬, 시아노, 히드록시, 메르캅토, 옥소 및 티옥소로 구성된 군으로부터 선택되는 1 종 이상의 치환체로 치환될 수 있다.), Y 는 산소, 황, 이미노 또는 C1-C3 알킬이미노를 나타내며, R1 은 C1-C3 알킬 또는 C1-C3 할로알킬을 나타내며, R2 는 C1-C3 알킬을 나타내고, R3 는 카르복시 C1-C6 알킬, C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알키닐옥시카르보닐 C1-C6 알킬, OR7, SR8 또는 N(R9)R10 를 나타내고, X1 은 할로겐, 시아노, 티오카르바모일 또는 니트로를 나타내고, X2 는 수소 또는 할로겐을 나타낸다. {식중, R7, R8 및 R10 은 각각 독립적으로 카르복시 C1-C6 알킬, C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알키닐옥시카르보닐 C1-C6 알킬, C3-C8 시클로알콕시카르보닐 C1-C6 알킬, C3-C8 할로시클로알콕시카르보닐 C1-C6 알킬, C3-C8 시클로알케닐옥시카르보닐 C1-C6 알킬, C3-C8 할로시클로알케닐옥시카르보닐 C1-C6 알킬, C1-C6 알콕시카르보닐 C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C8 알킬리덴아민옥시카르보닐 C1-C6 알킬, 치환될 수 있는 페녹시카르보닐 C1-C6 알킬, 치환될 수 있는 페닐 C1-C4 알콕시카르보닐 C1-C6 알킬, C1-C6 알콕시아미노카르보닐 C1-C6 알킬, (C1-C6 알콕시) (C1-C3 알킬) 아미노카르보닐 C1-C6 알킬, C1-C6 알킬아미노카르보닐 C1-C6 알킬, (C1-C6 알킬) C1-C6 알킬아미노카르보닐 C1-C6 알킬, 치환될 수 있는 페닐아미노카르보닐 C1-C6 알킬, 또는 치환될 수 있는 페닐 C1-C4 알킬아미노카르보닐 C1-C6 알킬을 나타내고, R9 은 수소 또는 C1-C6 알킬을 나타낸다. }].
- 제 1 항에 있어서, 식중 복소환 고리가 할로겐, C1-C6 알킬, C1-C6 할로알킬, C3-C6 알케닐, C3-C6 할로알케닐, C3-C6 알키닐, C3-C6 할로알키닐, C1-C6 알콕시 C1-C6 알킬, C1-C6 알콕시, C1-C6 할로알콕시, C1-C6 알콕시카르보닐 C1-C6 알콕시, C1-C6 알콕시카르보닐 C1-C6 알킬, 시아노, 히드록시, 메르캅토, 옥소 및 티옥소로 구성된 군으로부터 선택되는 1 종 이상의 치환체로 치환될 수 있고, R3 는 카르복시 C1-C6 알킬, C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬, C3-C6 할로알키닐옥시카르보닐 C1-C6 알킬, OR7, SR8 또는 N(R9)R10 {식중, R7 , R8 및 R10 은 각각 독립적으로 카르복시 C1-C6 알킬, C1-C6 알콕시카르보닐 C1-C4 알킬, C1-C6 할로알콕시카르보닐 C1-C4 알킬, C3-C6 알케닐옥시카르보닐 C1-C4 알킬, C3-C6 알키닐옥시카르보닐 C1-C4 알킬, 치환될 수 있는 페녹시카르보닐 C1-C4 알킬, 치환될 수 있는 페닐 C1-C4 알콕시카르보닐 C1-C4 알킬, C1-C6 알콕시아미노카르보닐 C1-C4 알킬, (C1-C6 알콕시) (C1-C3 알킬) 아미노카르보닐 C1-C4 알킬, C1-C6 알킬아미노카르보닐 C1-C4 알킬, (C1-C6 알킬) C1-C6 알킬아미노카르보닐 C1-C4 알킬, 치환될 수 있는 페닐아미노카르보닐 C1-C4 알킬, 또는 치환될 수 있는 페닐 C1-C4 알킬아미노카르보닐 C1-C4 알킬을 나타내고, R9 은 수소 또는 C1-C6 알킬을 나타낸다.} 를 나타내는, 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, 식중 Q-R3 가 나타내는 기가 하기 화학식이 나타내는 모이어티로 구성된 군으로부터 선택되는 기인 우라실 화합물:[식중, R3 는 제 1 항 또는 제 2 항에 정의된 바와 같고, Z1 또는 Z2 는 각각 독립적 으로 수소, 할로겐, C1-C6 는 알킬, C1-C6 할로알킬, C2-C6 알케닐, C2-C6 할로알케닐, C2-C6 알키닐, C2-C6 할로알키닐, C1-C6 알콕시 C1-C6 알킬, C1-C6 알콕시, C1-C6 할로알콕시, C1-C6 알콕시카르보닐 C1-C6 알콕시 또는 시아노를 나타낸다.]
- 제 1 항 또는 제 2 항에 있어서, X1 이 할로겐인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, X1 이 니트로인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, X1 이 할로겐인 염소인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, X2 가 수소 또는 불소인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, X1 이 염소 및 X2 가 불소인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R1 이 CF3 인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R2 가 메틸인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, Y 가 산소 또는 황인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, Y 가 산소인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R3 가 OR7, SR8 또는 N(R9)R10 이고, R7, R8 및 R10 은 C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬 또는 C3-C8 시클로알콕시카르보닐 C1-C6 알킬인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R3 가 OR7, SR8 또는 N(R9)R10 이고, R7, R8 및 R10 은 C1-C6 알콕시카르보닐 C1-C3 알킬, C1-C6 할로알콕시카르보닐 C1-C3 알킬 또는 C3-C8 시클로알콕시카르보닐 C1-C3 알킬인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R3 가 OR7 또는 SR8 이고, R7 및 R8 은 C1-C6 알콕시카르보닐메틸 또는 1-{(C1-C6 알콕시)카르보닐}에틸인 우라실 화합물.
- 제 1 항 또는 제 2 항에 있어서, R3 가 OR7 또는 SR8 이고, R7 및 R8 은 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 우라실 화합물.
- 활성 성분으로서 제 1 항 또는 제 2 항에 따른 우라실 화합물, 및 불활성 담체 또는 희석제를 함유하는 제초 조성물.
- 제 1 항 또는 제 2 항에 따른 우라실 화합물의 유효량을 잡초 또는 잡초가 자라고 있거나 자랄 장소에 적용하는 것을 특징으로 하는, 잡초의 억제 방법.
- 3-{2-클로로-4-플루오로-5-[3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-(에톡시카르보닐)메톡시피리딘.
- 제 23 항에 있어서, Q-R3 가 나타내는 기가 하기 화학식의 모이어티로 구성된 군으로부터 선택되는 기인 화합물:[식중, X1 은 할로겐, 시아노 또는 니트로이며, X2 는 할로겐이고, Y 는 산소 또는 황이고, R1 은 C1-C3 할로알킬이고, R3 는 OR7, SR8 또는 N(R 9)R10 이고, R7, R8 및 R10 은 C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬 또는 C3-C8 시클로알콕시카르보닐 C1-C6 알킬이고, Z1 및 Z2 는 제 3 항에서 정의된 바와 같다].
- 제 23 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Q-R3 는 제 3 항에 정의된 바와 같고, Z1 및 Z2 는 수소이고, R1 은 트리플루오로메틸이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 24 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Z1 및 Z2 는 수소이고, R1 은 트리플루오로메틸이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 27 항에 있어서, Q-R3 가 나타내는 기가 하기 화학식의 모이어티로 구성된 군으로부터 선택되는 기인 화합물:[식중, X1 은 할로겐, 시아노 또는 니트로이며, X2 는 할로겐이고, Y 는 산소 또는 황이고, R3 는 OR7, SR8 또는 N(R9)R10 이고, R 7, R8 및 R10 은 C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬 또는 C3-C8 시클로알콕시카르보닐 C1-C6 알킬이고, Z1 및 Z2 는 제 3 항에서 정의된 바와 같다].
- 제 27 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Q-R3 는 제 3 항에 정의된 바와 같고, Z1 및 Z2 는 수소이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 28 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Z1 및 Z2 는 수소이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 27 항에 있어서, 하기로 구성된 군으로부터 선택되는 화합물:4-클로로-2-플루오로-5-{2-(메톡시카르보닐)메톡시-3-피리딜옥시}아닐린,4-클로로-2-플루오로-5-{2-(에톡시카르보닐)메톡시-3-피리딜옥시}아닐린,4-클로로-2-플루오로-5-[2-{1-(메톡시카르보닐)에톡시}-3-피리딜옥시]아닐린,4-클로로-2-플루오로-5-[2-{1-(에톡시카르보닐)에톡시}-3-피리딜옥시]아닐린,4-클로로-2-플루오로-5-[4-(메톡시카르보닐)메톡시-2-피리미딜옥시]아닐린,4-클로로-2-플루오로-5-[4-(에톡시카르보닐)메톡시-2-피리미딜옥시]아닐린,4-클로로-2-플루오로-5-[4-{1-(메톡시카르보닐)에톡시}-2-피리미딜옥시]아닐린, 및 4-클로로-2-플루오로-5-[4-{1-(에톡시카르보닐)에톡시}-2-피리미딜옥시]아닐린.
- 제 32 항에 있어서, Q-R3 가 나타내는 기가 하기 화학식의 모이어티로 구성된 군으로부터 선택되는 기인 화합물:[식중, X1 은 할로겐, 시아노 또는 니트로이며, X2 는 할로겐이고, Y 는 산소 또는 황이고, R3 는 OR7, SR8 또는 N(R9)R10 이고, R7, R8 및 R10 은 C1-C6 알콕시카르보닐 C1-C6 알킬, C1-C6 할로알콕시카르보닐 C1-C6 알킬, C3-C6 알케닐옥시카르보닐 C1-C6 알킬, C3-C6 알키닐옥시카르보닐 C1-C6 알킬 또는 C3-C8 시클로알콕시카르보닐 C1-C6 알킬이고, Z1 및 Z2 는 제 3 항에 정의된 바와 같다].
- 제 32 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Q-R3 는 제 3 항에 정의된 바와 같고, Z1 및 Z2 는 수소이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 33 항에 있어서, X1 은 염소이며, X2 는 불소이고, Y 는 산소이고, Z1 및 Z2 는 수소이고, R3 는 OR7 또는 SR8 이고, R7 및 R8 는 메톡시카르보닐메틸, 에톡시카르보닐메틸, 1-(메톡시카르보닐)에틸 또는 1-(에톡시카르보닐)에틸인 화합물.
- 제 32 항에 있어서, 하기로 구성된 군으로부터 선택되는 화합물:4-클로로-2-플루오로-5-{2-(메톡시카르보닐)메톡시-3-피리딜옥시}페닐 이소시아네이트,4-클로로-2-플루오로-5-{2-(에톡시카르보닐)메톡시-3-피리딜옥시}페닐 이소시아네이트,4-클로로-2-플루오로-5-[2-{1-(메톡시카르보닐)에톡시}-3-피리딜옥시]페닐 이소시아네이트,4-클로로-2-플루오로-5-[2-{1-(에톡시카르보닐)에톡시}-3-피리딜옥시]페닐 이소시아네이트,4-클로로-2-플루오로-5-[4-(메톡시카르보닐)메톡시-2-피리미딜옥시}페닐 이소시아네이트,4-클로로-2-플루오로-5-[4-(에톡시카르보닐)메톡시-2-피리미딜옥시]페닐 이소시아네이트,4-클로로-2-플루오로-5-[4-{1-(메톡시카르보닐)에톡시}-2-피리미딜옥시]페닐 이소시아네이트, 및4-클로로-2-플루오로-5-[4-{1-(에톡시카르보닐)에톡시}-2-피리미딜옥시]페닐 이소시아네이트.
- 제 1 항에 있어서, 하기로 구성된 군으로부터 선택되는 화합물:3-{2-클로로-4-플루오로-5-[3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-(메톡시카르보닐)메톡시피리딘,3-{2-클로로-4-플루오로-5-[3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-(에톡시카르보닐)메톡시피리딘,3-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-{1-(메톡시카르보닐)에톡시}피리딘,3-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-{1-(에톡시카르보닐)에톡시}피리딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-(메톡시카르보닐)메톡시피리미딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-(에톡시카르보닐)메톡시피리미딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-{1-(메톡시카르보닐)에톡시}피리미딘, 및2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-{1-(에톡시카르보닐)에톡시}피리미딘.
- 제 23 항에 있어서, 하기로 구성된 군으로부터 선택되는 화합물:3-{2-클로로-4-플루오로-5-[3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-(메톡시카르보닐)메톡시피리딘,3-{2-클로로-4-플루오로-5-[3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-(에톡시카르보닐)메톡시피리딘,3-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-{1-(메톡시카르보닐)에톡시}피리딘,3-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-2-{1-(에톡시카르보닐)에톡시}피리딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-(메톡시카르보닐)메톡시피리미딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-(에톡시카르보닐)메톡시피리미딘,2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-{1-(메톡시카르보닐)에톡시}피리미딘, 및2-{2-클로로-4-플루오로-5-{3-메틸-2,6-디옥소-4-(트리플루오로메틸)-1,2,3,6-테트라히드로피리미딘-1-일]페녹시}-4-{1-(에톡시카르보닐)에톡시}피리미딘.
- 제 39 항에 있어서, 하기로 구성된 군으로부터 선택되는 화합물:2-(메톡시카르보닐)메톡시-3-히드록시피리딘,2-(에톡시카르보닐)메톡시-3-히드록시피리딘,2-{1-(메톡시카르보닐)에톡시}-3-히드록시피리딘, 및2-{1-(에톡시카르보닐)에톡시}-3-히드록시피리딘.
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- 2001-02-02 ES ES01102178T patent/ES2226990T3/es not_active Expired - Lifetime
- 2001-02-02 DE DE60105859T patent/DE60105859T2/de not_active Expired - Lifetime
- 2001-02-02 AR ARP010100504A patent/AR027938A1/es active IP Right Grant
-
2009
- 2009-04-27 JP JP2009107533A patent/JP2009209147A/ja active Pending
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2010
- 2010-11-02 AR ARP100104049A patent/AR078875A2/es unknown
Also Published As
Publication number | Publication date |
---|---|
EP1122244A1 (en) | 2001-08-08 |
CA2334399A1 (en) | 2001-08-04 |
ES2226990T3 (es) | 2005-04-01 |
JP4356247B2 (ja) | 2009-11-04 |
AU1676001A (en) | 2001-08-16 |
BR0100318B1 (pt) | 2012-11-27 |
CN1204137C (zh) | 2005-06-01 |
BR0100318A (pt) | 2001-10-09 |
MXPA01001317A (es) | 2002-08-30 |
JP2002155061A (ja) | 2002-05-28 |
IL141034A0 (en) | 2002-02-10 |
IL167954A (en) | 2007-10-31 |
AR027938A1 (es) | 2003-04-16 |
CN1636981A (zh) | 2005-07-13 |
EP1122244B1 (en) | 2004-09-29 |
KR20010083158A (ko) | 2001-08-31 |
AU779561B2 (en) | 2005-01-27 |
CN1316426A (zh) | 2001-10-10 |
ATE277910T1 (de) | 2004-10-15 |
CA2334399C (en) | 2010-08-10 |
DK1122244T3 (da) | 2004-10-25 |
DE60105859T2 (de) | 2006-02-02 |
JP2009209147A (ja) | 2009-09-17 |
DE60105859D1 (de) | 2004-11-04 |
IL167955A (en) | 2007-10-31 |
AR078875A2 (es) | 2011-12-07 |
PT1122244E (pt) | 2004-12-31 |
IL167957A (en) | 2009-07-20 |
CN1328261C (zh) | 2007-07-25 |
IL167956A (en) | 2009-02-11 |
IL167958A (en) | 2010-11-30 |
US6537948B1 (en) | 2003-03-25 |
TR200402577T4 (tr) | 2004-12-21 |
CA2646796A1 (en) | 2001-08-04 |
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