KR940005589A - 6-아릴피리미딘 화합물들 및 그의 제초제적 용법 - Google Patents
6-아릴피리미딘 화합물들 및 그의 제초제적 용법 Download PDFInfo
- Publication number
- KR940005589A KR940005589A KR1019930013498A KR930013498A KR940005589A KR 940005589 A KR940005589 A KR 940005589A KR 1019930013498 A KR1019930013498 A KR 1019930013498A KR 930013498 A KR930013498 A KR 930013498A KR 940005589 A KR940005589 A KR 940005589A
- Authority
- KR
- South Korea
- Prior art keywords
- group
- alkyl
- alkenyl
- alkynyl
- halo
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title claims 14
- 230000002363 herbicidal effect Effects 0.000 title claims 4
- 239000004009 herbicide Substances 0.000 title 1
- 241000196324 Embryophyta Species 0.000 claims abstract 8
- -1 polyhaloalkenyl Chemical group 0.000 claims abstract 8
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract 6
- 125000000304 alkynyl group Chemical group 0.000 claims abstract 5
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 5
- 239000001301 oxygen Substances 0.000 claims abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 3
- 125000004414 alkyl thio group Chemical group 0.000 claims abstract 3
- 229910052717 sulfur Chemical group 0.000 claims abstract 3
- 239000011593 sulfur Chemical group 0.000 claims abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims abstract 2
- 125000001475 halogen functional group Chemical group 0.000 claims abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 2
- 239000001257 hydrogen Substances 0.000 claims abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 5
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 4
- 125000006710 (C2-C12) alkenyl group Chemical group 0.000 claims 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 3
- 125000006711 (C2-C12) alkynyl group Chemical group 0.000 claims 3
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 3
- 125000001246 bromo group Chemical group Br* 0.000 claims 3
- 125000001309 chloro group Chemical group Cl* 0.000 claims 3
- 125000001153 fluoro group Chemical group F* 0.000 claims 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 3
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 2
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 claims 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 2
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 239000001963 growth medium Substances 0.000 claims 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 1
- 125000006529 (C3-C6) alkyl group Chemical group 0.000 claims 1
- CVTNCTUVSGGMBY-UHFFFAOYSA-N 2,3-diethyl-6-phenyl-5-prop-2-ynylpyrimidin-4-one Chemical compound O=C1N(CC)C(CC)=NC(C=2C=CC=CC=2)=C1CC#C CVTNCTUVSGGMBY-UHFFFAOYSA-N 0.000 claims 1
- SIYVGGFCSAAZJJ-UHFFFAOYSA-N 2,3-dimethyl-6-phenyl-5-prop-2-ynylpyrimidin-4-one Chemical compound O=C1N(C)C(C)=NC(C=2C=CC=CC=2)=C1CC#C SIYVGGFCSAAZJJ-UHFFFAOYSA-N 0.000 claims 1
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- 125000004211 3,5-difluorophenyl group Chemical group [H]C1=C(F)C([H])=C(*)C([H])=C1F 0.000 claims 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims 1
- DRHFVLCKIHGXCT-UHFFFAOYSA-N 3-ethyl-6-phenyl-2-propan-2-yl-5-prop-2-ynylpyrimidin-4-one Chemical compound O=C1N(CC)C(C(C)C)=NC(C=2C=CC=CC=2)=C1CC#C DRHFVLCKIHGXCT-UHFFFAOYSA-N 0.000 claims 1
- PHFDIKGBVJVPFD-UHFFFAOYSA-N 3-ethyl-6-phenyl-5-prop-2-ynyl-2-(trifluoromethyl)pyrimidin-4-one Chemical compound O=C1N(CC)C(C(F)(F)F)=NC(C=2C=CC=CC=2)=C1CC#C PHFDIKGBVJVPFD-UHFFFAOYSA-N 0.000 claims 1
- 125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims 1
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 1
- 125000004434 sulfur atom Chemical group 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000001188 haloalkyl group Chemical group 0.000 abstract 2
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000006684 polyhaloalkyl group Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- 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
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/34—One oxygen atom
- C07D239/36—One oxygen atom as doubly bound oxygen atom or as unsubstituted hydroxy radical
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/74—Quinazolines; Hydrogenated quinazolines with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring
- C07D239/76—N-oxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
본 발명은 잡초들의 구제에 유용한 다음 일반식들의 일군의 6-알릴피리미딘 화합물들에 관한 것이다.
상기 식들에서, R2는 수소, 할로, 치환 또는 비치환 알킬, 알켄일, 알킨일, 알콕시, 알킬티오, 알콕시카르보닐알킬, 폴리할로알킬, 할로알켄일, 폴리할로알켄일, 할로알킨일, 폴리할로알킨일, 시아노, 알콕시알킬, 알콕시카르보닐, 시클로알킬, 아랄킬, 알킬아미노, 디알킬아미노, 또는 디알킬아미노카르보닐 기이고; R3는 알킬, 알켄일, 알킨일, 또는 할로알킬 기이며; R5는 알킬, 알켄일, 알켄인일 도는 알콕시알킬 기이고; R6는 치환 또는 비치환 아릴기(즉, 방향족고리)이며; X는 산소 또는 황이다. R2와 R3는 고리를 형성하도록 연결될 수 있다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (13)
- 다음 일반식의 화합물.상기 일반식에서, (a) R2는 수소, 직쇄(C1-C6)알킬, 분지쇄(C3-C8)알킬, (C2-C6)알켄일, (C2-C6)알킨일, 할로(C1-C6)알킬, 폴리할로(C1-C6)알킬, 할로(C2-C6)알켄일, 폴리할로(C2-C6)알켄일, 할로(C2-C6)알킨일, 폴리할로(C2-C6)알킨일, (C1-C4)알콕시(C1-C4)알킬, (C1-C6)알킬티오, (C1-C6)알콕시, (C1-C3)알콕시카르보닐, (C1-C3)알콕시카르보닐(C1-C4)알킬, 아르(C1-C4)알킬, 시클로(C3-C7)알킬, (C1-C3)알킬아미노, 디(C1-C3)알킬아미노, 디(C1-C3)알킬아미노카르보닐, 할로 또는 시아노 기이고; (b) R3는 (C1-C3)알킬, (C3-C6)알켄일, (C3-C6)알킨일, 할로- 또는 폴리할로-(C1-C6)알킬기이며; (c) R5는 (C1-C3)알킬, (C2-C6)알켄일, (C2-C6)알킨일, (C5-C6)일켄인일, 또는 (C1-C4)알콕시, (C1-C4)알킬기이고; (d) R6는 푸릴, 페닐, 피리딜, 또는 티에닐 기로서, 각각의 기는 브로모, 클로로, 플루오로, (C1-C12)알킬, 시클로(C3-C6)알킬, (C2-C12)알켄일, 시클로(C3-C6)알켄일, (C2-C12)알킨일, 할로(C1-C12)알킬, 폴리할로(C1-C12)알킬, 할로(C2-C12)알켄일, 폴리할로(C2-C12)알켄일, 할로(C2-C6)알켄일, 폴리할로(C2-C6)알킨일, (C1-C122)알콕시, (C1-C12)알킬티오, (C1-C12)알킬술포닐, (C1-C12)알킬술피닐, 페닐, 펜(C1-C12)알킬, 펜(C2-C12)알켄일, 펜(C1-C12)알킨일, 시아노, 할로(C1-C6)알콕시, 카르보(C1-C6)알콕시, 및 니트로 기로부터 각각 선택된 3개까지의 치환제로 임의 치환된 것이며; (e) X는 산소 또는 황이다.
- 제1항에 있어서, R2가 메틸, 에틸 n-프로필, n-부틸, n-헥실, i-프로필, i-부틸 또는 t-부틸 기; 또는 메톡시 또는 에톡시기; 또는 에톡시카르보닐기; 또는 부트-2-인일, 부트-3-인일 또는 프로프-2-인일기; 또는 플루오로, 브로모, 또는 클로로 기; 또는 트리플루오로메틸 또는 펜타플루오로에틸기; 또는 메틸티오 기; 또는 메톡시메틸기; 또는 벤질기; 또는 시클로프로필 또는 시클로부틸기; 또는 디메틸아미노 기; 또는 디메틸아미노카르보닐기; 또는 알릴기인 화합물.
- 제1항에 있어서, R3가 메틸 또는 에틸 기; 프로프-2-인일 기; 또는 알릴기; 또는 트리플루오로메틸기이 화합물.
- 제1항에 있어서, R5가 메틸 또는 에틸 기 또는 알릴 기; 또는 프로프-2-인일 또는 부트-2-인일 기; 또는 메톡시메틸 기; 또는 펜트-4-엔-2-인-1일 기인 화합물.
- 제1항에 있어서, R6가 페닐, 2-플루오로페닐, 3-플루오로페닐, 4-플루오로페닐, 3-클로로페닐, 또는 3,5-디플루오로페닐 기인 화합물.
- 제1항에 있어서, X가 산소인 화합물.
- 다음 일반식의 화합물.상기 일반식에서, (a) R2와 R3는 2-또는 5-원자 링크부분(two to five membered link moiety)으로서 접합되며, 상기 링크 멤버들의 각각은 탄소, 산소 및 황 원자들로 구성된 군으로부터 선택된 것이고; (b) R5는 (C1-C4) 알킬, (C2-C6)알켄일, (C2-C6)알킨일, (C1-C4)알콕시(C1-C4)알킬, 또는 (C5-C6)알켄인일 기이며; (c) R6는 푸릴, 페닐, 피리딜, 또는 티에닐 기로서, 각각의 기는 브로모, 클로로, 플루오로, (C1-C12)알킬, 시클로(C3-C4)알킬, 할로(C1-C12)알켄일, 시클로(C3-C8)알켄일, (C2-C12)알킨일, 할로(C1-C12)알킬, 폴리할로(C1-C12)알콕시, (C1-C12)알킬티오, (C1-C12)알킬술포닐, (C1-C12)알킬술포닐, (C1-C12)알킬술피닐, 페닐, 펜(C1-C12)알킬, 펜(C2-C12)알켄일, 펜(C2-C12)알킨일, 시아노, 할로(C1-C6)알콕시, 카르보(C1-C6)알콕시, 및 니트로 기로부터 각각 선택된 3개까지의 치환제로 임의 치환된 것이며; (d) X는 산소 또는 황이다.
- 제7항에 있어서, (a) 상기 R2-R3링크는 -(CH2)2-5-및-SCH2CH2-로부터 선택되고; (b) R5는 프로파길이며; (c) R6는 페닐인 화합물.
- 제1항에 있어서, 2,3-디메틸-6-페닐-5-프로파길-4(3H)-피리미디논; 3-메틸-6-페닐-5-프로파길-2-프로필-4(3H)-피리디미논; 2,3-디에틸-6-페닐-5-프로파길-4(3H)-피리미디논; 3-에틸-6-페닐-5-프로파길-2-트리플루오로메틸-4(3H)-피리미디논; 및 3-에틸-2-이소프로필-6-페닐-5-프로파길-4(3H)-피리미디논으로부터 선택된 화합물.
- 청구범위 제1항의 화합물을 함유하는 제초조성물.
- 청구범위 제7항의 화합물을 함유하는 제초조성물.
- 제초 유효량의 청구범위 제1항의 화합물을 잡초 또는 잡초의 영역 또는 잡초의 생장 매체에 적용함을 특징으로 하는 잡초 구제방법.
- 제초 유효량의 청구범위 제7항의 화합물을 잡초 또는 잡초의 영역 또는 잡초의 생장 매체에 적용함을 특징으로 하는 잡초 구제방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US07/916,315 US5298481A (en) | 1992-07-17 | 1992-07-17 | 6-arylpyrimidines and herbicidal use |
US916,315 | 1992-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR940005589A true KR940005589A (ko) | 1994-03-21 |
Family
ID=25437051
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930013498A KR940005589A (ko) | 1992-07-17 | 1993-07-16 | 6-아릴피리미딘 화합물들 및 그의 제초제적 용법 |
Country Status (19)
Country | Link |
---|---|
US (2) | US5298481A (ko) |
EP (1) | EP0579425B1 (ko) |
JP (1) | JPH06100544A (ko) |
KR (1) | KR940005589A (ko) |
CN (1) | CN1081439A (ko) |
AT (1) | ATE143951T1 (ko) |
AU (1) | AU672408B2 (ko) |
BR (1) | BR9302830A (ko) |
CA (1) | CA2099923A1 (ko) |
DE (1) | DE69305265T2 (ko) |
DK (1) | DK0579425T3 (ko) |
ES (1) | ES2092768T3 (ko) |
HK (1) | HK7497A (ko) |
HU (1) | HUT65123A (ko) |
IL (1) | IL106231A0 (ko) |
MX (1) | MX9304218A (ko) |
NZ (1) | NZ248089A (ko) |
TW (1) | TW239063B (ko) |
ZA (1) | ZA935032B (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100356738B1 (ko) * | 2000-09-07 | 2002-10-18 | 주식회사 삼양제넥스 | 염기성 단백질로부터 엔도톡신을 제거하는 방법 |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5270317A (en) * | 1990-03-20 | 1993-12-14 | Elf Sanofi | N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present |
JPH0687835A (ja) * | 1992-07-17 | 1994-03-29 | Rohm & Haas Co | 除草性2−アリール−5,6−縮合環−ピリミジン |
EP0579424B1 (en) * | 1992-07-17 | 1996-10-23 | Rohm And Haas Company | 2-substituted pyrimidines and herbicidal use thereof |
US5391541A (en) * | 1993-08-11 | 1995-02-21 | Fmc Corporation | Herbicidal 3-(substituted-benzyl)-1-methyl-6-trifluoromethyluracils |
EP0724573A1 (en) * | 1993-10-20 | 1996-08-07 | PHARMACIA & UPJOHN COMPANY | Pyrimidinones as antiarthritic and anti-inflammatories |
US6410729B1 (en) | 1996-12-05 | 2002-06-25 | Amgen Inc. | Substituted pyrimidine compounds and methods of use |
US6096753A (en) * | 1996-12-05 | 2000-08-01 | Amgen Inc. | Substituted pyrimidinone and pyridone compounds and methods of use |
US20070129282A1 (en) * | 1998-11-24 | 2007-06-07 | Ahlem Clarence N | Pharmaceutical treatments and compositions |
US6513603B2 (en) * | 2001-03-29 | 2003-02-04 | Planet Air Turf Products, Llc | Soil aeration tine |
WO2006041968A1 (en) * | 2004-10-06 | 2006-04-20 | Nps Pharmaceuticals, Inc. | Reversed pyrimidinone compounds as calcilytics |
EP2844258B1 (en) * | 2012-05-02 | 2019-09-11 | The Regents Of The University Of Michigan | Methods and compositions for treating bacterial infection |
US9814719B2 (en) | 2012-05-02 | 2017-11-14 | Curators Of The University Of Missouri | Methods and compositions for treating bacterial infection |
US10441588B2 (en) | 2012-05-02 | 2019-10-15 | Curators Of The University Of Missouri | Methods and compositions for treating bacterial infection |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1003802A (en) * | 1963-06-04 | 1965-09-08 | Searle & Co | Pyrimidinone derivatives |
US3214430A (en) * | 1963-06-04 | 1965-10-26 | Kurt J Rorig | 3, 5-dialkylated-2-amino-6-aryl-4(3h)-pyrimidinones |
IT1153066B (it) * | 1982-11-18 | 1987-01-14 | Mentedison S P A | Derivati del pirimidin-4-one ad attivita' erbicida |
US4725600A (en) * | 1984-07-13 | 1988-02-16 | Fujisawa Pharmaceutical Co., Ltd. | Pyrimidine compounds having activity as a cardiotonic anti-hypertensive cerebrovascular vasodilator and anti-platelet aggregation agent |
EP0579424B1 (en) * | 1992-07-17 | 1996-10-23 | Rohm And Haas Company | 2-substituted pyrimidines and herbicidal use thereof |
-
1992
- 1992-07-17 US US07/916,315 patent/US5298481A/en not_active Expired - Fee Related
-
1993
- 1993-06-30 JP JP5162543A patent/JPH06100544A/ja not_active Withdrawn
- 1993-07-02 DE DE69305265T patent/DE69305265T2/de not_active Expired - Fee Related
- 1993-07-02 ES ES93305208T patent/ES2092768T3/es not_active Expired - Lifetime
- 1993-07-02 DK DK93305208.6T patent/DK0579425T3/da active
- 1993-07-02 EP EP93305208A patent/EP0579425B1/en not_active Expired - Lifetime
- 1993-07-02 AT AT93305208T patent/ATE143951T1/de not_active IP Right Cessation
- 1993-07-05 IL IL106231A patent/IL106231A0/xx unknown
- 1993-07-06 AU AU41752/93A patent/AU672408B2/en not_active Ceased
- 1993-07-06 CA CA002099923A patent/CA2099923A1/en not_active Abandoned
- 1993-07-06 NZ NZ248089A patent/NZ248089A/en unknown
- 1993-07-12 BR BR9302830A patent/BR9302830A/pt not_active Application Discontinuation
- 1993-07-13 ZA ZA935032A patent/ZA935032B/xx unknown
- 1993-07-13 MX MX9304218A patent/MX9304218A/es unknown
- 1993-07-16 HU HU9302054A patent/HUT65123A/hu unknown
- 1993-07-16 KR KR1019930013498A patent/KR940005589A/ko not_active Application Discontinuation
- 1993-07-17 CN CN93108543A patent/CN1081439A/zh active Pending
- 1993-08-31 TW TW082107051A patent/TW239063B/zh active
-
1994
- 1994-03-04 US US08/206,490 patent/US5397767A/en not_active Expired - Fee Related
-
1997
- 1997-01-16 HK HK7497A patent/HK7497A/xx not_active IP Right Cessation
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100356738B1 (ko) * | 2000-09-07 | 2002-10-18 | 주식회사 삼양제넥스 | 염기성 단백질로부터 엔도톡신을 제거하는 방법 |
Also Published As
Publication number | Publication date |
---|---|
NZ248089A (en) | 1996-01-26 |
BR9302830A (pt) | 1994-02-16 |
DE69305265T2 (de) | 1997-05-07 |
HU9302054D0 (en) | 1993-11-29 |
DK0579425T3 (da) | 1996-11-18 |
EP0579425A1 (en) | 1994-01-19 |
TW239063B (ko) | 1995-01-21 |
AU4175293A (en) | 1994-01-20 |
HK7497A (en) | 1997-01-24 |
AU672408B2 (en) | 1996-10-03 |
ES2092768T3 (es) | 1996-12-01 |
US5397767A (en) | 1995-03-14 |
JPH06100544A (ja) | 1994-04-12 |
ZA935032B (en) | 1994-01-17 |
ATE143951T1 (de) | 1996-10-15 |
DE69305265D1 (de) | 1996-11-14 |
IL106231A0 (en) | 1993-11-15 |
EP0579425B1 (en) | 1996-10-09 |
US5298481A (en) | 1994-03-29 |
HUT65123A (en) | 1994-04-28 |
CN1081439A (zh) | 1994-02-02 |
MX9304218A (es) | 1994-02-28 |
CA2099923A1 (en) | 1994-01-18 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
KR940005589A (ko) | 6-아릴피리미딘 화합물들 및 그의 제초제적 용법 | |
KR940005588A (ko) | 2-아릴피리미딘류 및 이의 제초성 용도 | |
KR950702541A (ko) | 살충제 피리미딘 화합물(pesticidal pyrimidine compounds) | |
MA30024B1 (fr) | 5-arylisoxazolines pour lutter contre des parasites invertebres | |
JP2004521924A5 (ko) | ||
KR910016701A (ko) | 제초성 카르복사미드 유도체, 이의 제조 및 제초제로서의 이용 | |
MD960225A (ro) | Compuşi noi cu activitate erbicidă, acaricidă şi insecticidă | |
HUP0401478A2 (hu) | Fungicid hatású pirazolil-karboxanilid-származékok | |
TW200738696A (en) | Isoxazolines for controlling invertebrate pests | |
DE59508688D1 (de) | 2-[1',2',4'-triazol-3'yloxymethylen]-anilide und ihre verwendung als schädlingsbekämpfungsmittel | |
RU2002122407A (ru) | Пирролкарбоксамиды и пирролтиоамиды в качестве фунгицидов | |
KR970705545A (ko) | 복소환 유도체 및 의약(heterocyclic derivative and medicine) | |
TNSN08259A1 (en) | 5-aryl isoxazolines for controlling invertebrate pests | |
DE69509452D1 (de) | Tetrazolinon-Herbizide | |
HUP9802995A2 (hu) | Szubsztituált szulfonil-amino-(tio)karbonil-származékok, intermedierjeik, a vegyületeket hatóanyagként tartalmazó herbicid készítmények, valamint eljárás a vegyületek, és készítmények előállítására és alkalmazására | |
KR880013917A (ko) | 새로운 피리디닐피리미딘유도체, 그 제조법 및 그것을 유효성분으로 하는 살균제 | |
EP1357124A4 (en) | HETEROCYCLIC COMPOUNDS AND COMPOSITIONS IMPROVING CEREBRAL FUNCTIONS CONTAINING THESE AS ACTIVE INGREDIENTS | |
KR880009011A (ko) | 1-아미노메틸-3-아릴-4-시아노-피롤 | |
KR910016699A (ko) | 헤테로사이클릭아세토니트릴 및 그의 살균성 용도 | |
KR950032170A (ko) | 2-아릴피리미딘, 그 제조방법, 이를 함유한 조성물 및 이를 제초제로 사용하는 방법 | |
DE69110749D1 (de) | Barbitursäurederivate mit insektizider Wirkung. | |
HUP9802373A2 (hu) | Herbicid hatású szubsztituált benzo-tiazolok | |
KR940002231A (ko) | 2-아릴-5,6-고리접합 피리미딘 화합물들 및 그의 제초제적 용법 | |
KR960014107A (ko) | 피리미디닐 아크릴산 유도체 | |
HUT59560A (en) | Insecticide and acaricide composition containing heterocyclic active component and process for producing intermediates for the active components |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19930716 |
|
PC1203 | Withdrawal of no request for examination | ||
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |