KR950000669A - 4-아미노-2-퀴놀린온 유도체 - Google Patents
4-아미노-2-퀴놀린온 유도체 Download PDFInfo
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- KR950000669A KR950000669A KR1019930011382A KR930011382A KR950000669A KR 950000669 A KR950000669 A KR 950000669A KR 1019930011382 A KR1019930011382 A KR 1019930011382A KR 930011382 A KR930011382 A KR 930011382A KR 950000669 A KR950000669 A KR 950000669A
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- UGZHBEHGSJQMGC-UHFFFAOYSA-N 4-amino-1h-quinolin-2-one Chemical class C1=CC=C2C(N)=CC(=O)NC2=C1 UGZHBEHGSJQMGC-UHFFFAOYSA-N 0.000 title claims abstract 9
- 125000000217 alkyl group Chemical group 0.000 claims abstract 20
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 13
- 239000001257 hydrogen Substances 0.000 claims abstract 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract 13
- 125000003118 aryl group Chemical group 0.000 claims abstract 10
- 229910052736 halogen Inorganic materials 0.000 claims abstract 8
- 150000002367 halogens Chemical class 0.000 claims abstract 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 7
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 7
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract 7
- 150000002431 hydrogen Chemical class 0.000 claims abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 claims abstract 5
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims abstract 5
- -1 phenylacetyl Chemical group 0.000 claims abstract 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract 4
- 125000004104 aryloxy group Chemical group 0.000 claims abstract 4
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 4
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract 3
- 125000000623 heterocyclic group Chemical group 0.000 claims abstract 3
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims abstract 2
- 239000004009 herbicide Substances 0.000 claims abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract 2
- 239000004480 active ingredient Substances 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 2
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical class C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims 2
- KWMUSDDZNYHIBR-UHFFFAOYSA-N 3-amino-1h-quinolin-2-one Chemical class C1=CC=C2NC(=O)C(N)=CC2=C1 KWMUSDDZNYHIBR-UHFFFAOYSA-N 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 claims 1
- 230000000855 fungicidal effect Effects 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 230000002363 herbicidal effect Effects 0.000 claims 1
- 150000002460 imidazoles Chemical class 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 238000006467 substitution reaction Methods 0.000 claims 1
- 244000052616 bacterial pathogen Species 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
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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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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
- A01N43/42—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings condensed with carbocyclic rings
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
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- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/38—Nitrogen atoms
- C07D215/42—Nitrogen atoms attached in position 4
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- C07D221/04—Ortho- or peri-condensed ring systems
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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Abstract
본 발명은 농원예용 살균, 살충 및 제초제로 유용한 다음 일반식(Ⅰ)로 표시되는 신규한 4-아미노-2-퀴놀린온 유도체에 관한 것이다.
상기식중에서, R1,R2,R3,R4는 각각 적어도 하나는 수소 이외의 것을 치환된 것으로써, 수소, 아릴 또는, 아릴옥시기, C1-C10의 아르알킬 또는 알킬기, C1-C10의 알콕시기, C1-C6의 할로알킬기, 할로겐, 니트로기, 시아노기를 나타내며, 여기서, 아릴기는 페닐기 또는 치환페닐기를, 아릴옥시기는 페녹시 또는 치환페녹시기를, 알킬기는 벤질 또는 치환벤질 및 C1-C6의 직쇄 또는 측쇄의 알킬기를, 알콕시기는 C1-C5의 직쇄 또는 측쇄의 알콕시기를 할로알킬기는 할로겐이 치환된 C1-C3의 직쇄 또는 측쇄의 할로알킬기를 나타내고, R5는 C1-C6의 알킬, 아르알킬 또는 아릴을 나타내며, 여기서 알킬기는 C1-C4의 직쇄, 측쇄 또는 사이크릭의 알킬기를, 아릴기는 페닐기 또는 치환된 페닐기를 나타내고, R6은 수소 또는 C1-C5의 포화 또는 불포화된 직쇄 또는 측쇄의 알킬기를 나타내며, R7은
또는 -CH2CN을 나타내며, 여기서, R8,R9,R10,R11,R12,R13,R14,R15,R16은 수소, 할로겐, C1-C6의 알킬, 아릴, 알콕시알킬, 치환 또는 비치환된 페닐아세틸 또는 (R19)3Si를 나타내며, R17,R18은 수소 또는 C1-C5의 직쇄 또는 측쇄의 알킬기를 나타내며, R19는 C1-C5의 직쇄 또는 측쇄읠 알킬기를 나타내며, X는 O, (TR20)2또는 -T-(CH2)r-T-, Y는 O,S 또는 -SO-, Z는 헤테로고리, T는 O 또는 S, R20은 C1-C3의 알킬기, m,n,p,q,r은 1 내지 4의 정수를 각각 나타낸다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (10)
- 다음 일반식(Ⅰ)로 표시되는 4-아미노-2-퀴놀린온 유도체상기식중에서, R1,R2,R3,R4는 각각 적어도 하나는 수소 이외의 것으로 치환된 것으로써, 수소, 아릴 또는, 아릴옥시기, C1-C10의 아르알킬 또는 알킬기, C1-C10의 알콕시기, C1-C6의 할로알킬기, 할로겐, 니트로기, 시아노기를 나타내며, 여기서, 아릴기는 페닐기 또는 치환페닐기를, 아릴옥시기는 페녹시 또는 치환페녹시기를, 알킬기는 벤질 또는 치환벤질 및 C1-C6의 직쇄 또는 측쇄의 알킬기를, 알콕시기는 C1-C5의 직쇄 또는 측쇄의 알콕시기를, 할로알킬기는 할로겐이 치환된 C1-C3의 직쇄 또는 측쇄의 할로알킬기를 나타내고, R5는 C1-C6의 알킬, 아르알킬 또는 아릴을 나타내며, 여기서 알킬기는 C1-C4의 직쇄, 측쇄 또는 사이크릭의 알킬기를, 아릴기는 페닐기 또는 치환된 페닐기를 나타내고, R6은 수소 또는 C1-C5의 포화 또는 불포화된 직쇄 또는 측쇄의 알킬기를 나타내며, R7은또는, CH2CN을 나타내며, 여기서, R8,R9,R10,R11,R12,R13,R14,R15,R16은 수소, 할로겐, C1-C5의 알킬, 아릴, 알콕시알킬, 치환 또는 비치환된 페닐아세틸 또는 (R19)3Si를 나타내며, R17,R18은 수소 또는 C1-C5의 직쇄 또는 측쇄의 알킬기를 나타내며, R19는 C1-C5의 직쇄 또는 측쇄의 알킬기를 나타내며, X는 O, (TR20)2또는 -T-(CH2)r-T-, Y는 O,S 또는 -SO-, Z는 헤테로고리, T는 O 또는 S, R20은 C1-C3의 알킬기, m,n,p,q,r은 1 내지 4의 정수를 각각 나타낸다.
- 제 1 항에 있어서, 상기 R1,R2,R3,R4는 수소, 할로겐, 페닐기 또는 치환된 페닐기, 페녹시 또는 치환된 페녹시기, 벤질 또는 치환된 벤질기, C1-C6의 직쇄 또는 측의 알킬기, C1-C5의 직쇄 또는 측쇄의 알콕시기, 할로겐이 치환된 C1-C3의 직쇄 또는 측쇄의 할로알킬기인 것을 특징으로 하는 4-아미노-2-퀴놀린온 유도체.
- 제 1 항에 있어서, 상기 R5는 C1-C4의 직쇄, 측쇄 또는 사이클릭의 알킬기, 페닐 또는 치환된 페닐기, 벤질 또는 치환된 벤질기인 것을 특징으로 하는 4-아미노-2-퀴놀린온 유도체.
- 제 1 항에 있어서, 상기 R6은 수소 또는 C1-C3의 알킬, C1-C3의 알켄, C1-C3의 알킨기인 것을 특징으로 하는 4-아미노-2-퀴놀린온 유도체.
- 제 1 항에 있어서, R8,R9,R10,R11,R12,R13,R14,R15,R16은 수소, 할로겐, C1-C4의 직쇄 또는 측쇄의 알킬기, 치환 또는 비치환된 페닐기, C1-C3의 직쇄 또는 측쇄의 알콕시알킬기, 치환 또는 비치환된 페닐 아세틸기, (R19)3Si를 나타내며, R17,R18은 수소 또는 C1-C3의 직쇄 또는 측쇄의 알킬기를 나타내며, R19는 C1-C5의 직쇄 또는 측쇄의 알킬기임을 특징으로 하는 4-아미노-2-퀴놀린온 유도체.
- 제 1 항에 있어서, Z는 헤테로고리라 함은 치환 또는 비치환된 이미다졸을 특징으로 하는 4-아미노-2-퀴놀린온 유도체.
- 다음 일반식(Ⅱ)로 표시되는 4-알킬설폭시-2-퀴놀린온 유도체와 다음 일반식(Ⅲ)의 아민화합물을 불활성용매 중에서 반응시켜서 됨을 특징으로 하는 다음 일반식(Ⅰ)로 표시되는 4-아미노-2-퀴놀린온 유도체의 제조방법.상기식들 중에서, R1,R2,R3,R4,R5,R6및 R7은 각각 상기 정의된 바와 같으며, R21은 C1-C3의 알킬기를 나타낸다.
- 다음 일반식(Ⅰ)로 표시되는 4-아미노-2-퀴놀린온 유도체를 유효성분으로 함유하는 살균제.상기식에서, R1,R2,R3,R4,R5,R6및 R7은 각각 상기 정의된 바와 같다.
- 다음 일반식(Ⅰ)로 표시되는 2-퀴놀린온 유도체를 유효성분으로 함유하는 살충제.R1,R2,R3,R4,R5,R6및 R7은 각각 상기 정의된 바와 같다.
- 다음 일반식(Ⅰ)로 표시되는 2-퀴놀린온 유도체를 유효성분으로 함유하는 제초제.R1,R2,R3,R4,R5,R6및 R7은 각각 상기 정의된 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (9)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019930011382A KR0124946B1 (ko) | 1993-06-22 | 1993-06-22 | 4-아미노-2-퀴놀린온 유도체 |
NZ267515A NZ267515A (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives and biocidal compositions |
EP94918605A EP0707569A1 (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives |
PCT/KR1994/000079 WO1995000488A1 (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives |
AU69848/94A AU693451B2 (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives |
JP7502665A JPH08506355A (ja) | 1993-06-22 | 1994-06-21 | 4−アミノ−2−キノリノン誘導体 |
US08/564,238 US5707931A (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives |
BR9406906A BR9406906A (pt) | 1993-06-22 | 1994-06-21 | Derivados de 4-amino-2 quinolinona |
CA002165318A CA2165318C (en) | 1993-06-22 | 1994-06-21 | 4-amino-2-quinolinone derivatives |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019930011382A KR0124946B1 (ko) | 1993-06-22 | 1993-06-22 | 4-아미노-2-퀴놀린온 유도체 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR950000669A true KR950000669A (ko) | 1995-01-03 |
KR0124946B1 KR0124946B1 (ko) | 1997-12-08 |
Family
ID=19357792
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930011382A KR0124946B1 (ko) | 1993-06-22 | 1993-06-22 | 4-아미노-2-퀴놀린온 유도체 |
Country Status (9)
Country | Link |
---|---|
US (1) | US5707931A (ko) |
EP (1) | EP0707569A1 (ko) |
JP (1) | JPH08506355A (ko) |
KR (1) | KR0124946B1 (ko) |
AU (1) | AU693451B2 (ko) |
BR (1) | BR9406906A (ko) |
CA (1) | CA2165318C (ko) |
NZ (1) | NZ267515A (ko) |
WO (1) | WO1995000488A1 (ko) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011057942A1 (en) * | 2009-11-12 | 2011-05-19 | Basf Se | Insecticidal methods using pyridine compounds |
WO2012150550A1 (en) * | 2011-05-04 | 2012-11-08 | Basf Se | Novel pesticidal amino pyranone compounds |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1307336A (en) * | 1970-07-20 | 1973-02-21 | Shell Int Research | Herbicides |
BR9003627A (pt) * | 1990-07-26 | 1992-02-18 | Luiz Carlos Oliveira Da Cunha | Processo de obtencao de borracha termoplastica |
-
1993
- 1993-06-22 KR KR1019930011382A patent/KR0124946B1/ko not_active IP Right Cessation
-
1994
- 1994-06-21 AU AU69848/94A patent/AU693451B2/en not_active Ceased
- 1994-06-21 US US08/564,238 patent/US5707931A/en not_active Expired - Fee Related
- 1994-06-21 EP EP94918605A patent/EP0707569A1/en not_active Withdrawn
- 1994-06-21 NZ NZ267515A patent/NZ267515A/en unknown
- 1994-06-21 JP JP7502665A patent/JPH08506355A/ja active Pending
- 1994-06-21 CA CA002165318A patent/CA2165318C/en not_active Expired - Fee Related
- 1994-06-21 BR BR9406906A patent/BR9406906A/pt not_active Application Discontinuation
- 1994-06-21 WO PCT/KR1994/000079 patent/WO1995000488A1/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
KR0124946B1 (ko) | 1997-12-08 |
AU693451B2 (en) | 1998-07-02 |
NZ267515A (en) | 1997-11-24 |
CA2165318A1 (en) | 1995-01-05 |
WO1995000488A1 (en) | 1995-01-05 |
CA2165318C (en) | 1999-08-31 |
EP0707569A1 (en) | 1996-04-24 |
AU6984894A (en) | 1995-01-17 |
JPH08506355A (ja) | 1996-07-09 |
US5707931A (en) | 1998-01-13 |
BR9406906A (pt) | 1996-04-02 |
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