UA79135C2 - 4-trifluoromethylpyrazolyl-substituted pyridines and pyrimidines, herbicidal agent - Google Patents
4-trifluoromethylpyrazolyl-substituted pyridines and pyrimidines, herbicidal agent Download PDFInfo
- Publication number
- UA79135C2 UA79135C2 UAA200501767A UA2005001767A UA79135C2 UA 79135 C2 UA79135 C2 UA 79135C2 UA A200501767 A UAA200501767 A UA A200501767A UA 2005001767 A UA2005001767 A UA 2005001767A UA 79135 C2 UA79135 C2 UA 79135C2
- Authority
- UA
- Ukraine
- Prior art keywords
- alkyl
- halogen
- hydrogen
- alkoxy
- methyl
- Prior art date
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- -1 4-trifluoromethylpyrazolyl-substituted pyridines Chemical class 0.000 title claims abstract description 25
- 239000004009 herbicide Substances 0.000 title claims abstract description 18
- 150000003230 pyrimidines Chemical class 0.000 title abstract description 6
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 70
- 229910052739 hydrogen Inorganic materials 0.000 claims description 28
- 239000001257 hydrogen Substances 0.000 claims description 28
- 229910052736 halogen Inorganic materials 0.000 claims description 24
- 150000002367 halogens Chemical class 0.000 claims description 24
- 150000002431 hydrogen Chemical class 0.000 claims description 18
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 12
- 230000002363 herbicidal effect Effects 0.000 claims description 11
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 11
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 125000006530 (C4-C6) alkyl group Chemical group 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- 150000003839 salts Chemical class 0.000 claims description 6
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052717 sulfur Inorganic materials 0.000 claims description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 2
- 125000002462 isocyano group Chemical group *[N+]#[C-] 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 229920002554 vinyl polymer Polymers 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 150000003222 pyridines Chemical class 0.000 abstract description 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract description 4
- 125000003118 aryl group Chemical group 0.000 abstract description 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract description 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
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- 125000001424 substituent group Chemical group 0.000 description 11
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 10
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- 238000000227 grinding Methods 0.000 description 7
- 108090000623 proteins and genes Proteins 0.000 description 7
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- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
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- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 4
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- JFSLKQBFXHGCHW-UHFFFAOYSA-N 5-(trifluoromethyl)thiophen-3-ol Chemical compound OC1=CSC(C(F)(F)F)=C1 JFSLKQBFXHGCHW-UHFFFAOYSA-N 0.000 description 3
- 239000005995 Aluminium silicate Substances 0.000 description 3
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- 244000299507 Gossypium hirsutum Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
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- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 108091028043 Nucleic acid sequence Proteins 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
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- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 3
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- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 3
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- KDEJQUNODYXYBJ-UHFFFAOYSA-N 4-(trifluoromethyl)-1h-pyrazole Chemical compound FC(F)(F)C=1C=NNC=1 KDEJQUNODYXYBJ-UHFFFAOYSA-N 0.000 description 2
- HZKBYBNLTLVSPX-UHFFFAOYSA-N 6-[(6,6-dimethyl-5,7-dihydropyrrolo[2,1-c][1,2,4]thiadiazol-3-ylidene)amino]-7-fluoro-4-prop-2-ynyl-1,4-benzoxazin-3-one Chemical compound C#CCN1C(=O)COC(C=C2F)=C1C=C2N=C1SN=C2CC(C)(C)CN21 HZKBYBNLTLVSPX-UHFFFAOYSA-N 0.000 description 2
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- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
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- RJKCKKDSSSRYCB-UHFFFAOYSA-N tebutam Chemical compound CC(C)(C)C(=O)N(C(C)C)CC1=CC=CC=C1 RJKCKKDSSSRYCB-UHFFFAOYSA-N 0.000 description 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
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- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- 125000002088 tosyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])[H])S(*)(=O)=O 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 125000001425 triazolyl group Chemical group 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
-
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- C07D401/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D417/14—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 three or more hetero rings
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10234875A DE10234875A1 (de) | 2002-07-25 | 2002-07-25 | 4-Trifluormethylpyrazolyl substituierte Pyridine und Pyrimidine |
PCT/EP2003/007573 WO2004013131A2 (de) | 2002-07-25 | 2003-07-14 | 4-trifluormethylpyrazolyl substituierte pyridine und pyrimidine |
Publications (1)
Publication Number | Publication Date |
---|---|
UA79135C2 true UA79135C2 (en) | 2007-05-25 |
Family
ID=30010525
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UAA200501767A UA79135C2 (en) | 2002-07-25 | 2003-07-14 | 4-trifluoromethylpyrazolyl-substituted pyridines and pyrimidines, herbicidal agent |
Country Status (18)
Country | Link |
---|---|
US (2) | US7022650B2 (es) |
EP (1) | EP1527069A2 (es) |
JP (1) | JP2006504662A (es) |
CN (1) | CN1671702A (es) |
AR (1) | AR040668A1 (es) |
AU (1) | AU2003250942A1 (es) |
BR (1) | BR0312926A (es) |
CA (1) | CA2494593A1 (es) |
DE (1) | DE10234875A1 (es) |
HR (1) | HRP20050073A2 (es) |
MX (1) | MXPA05000953A (es) |
MY (1) | MY131916A (es) |
PL (1) | PL375390A1 (es) |
RS (1) | RS20050029A (es) |
RU (1) | RU2005105575A (es) |
TW (1) | TWI269797B (es) |
UA (1) | UA79135C2 (es) |
WO (1) | WO2004013131A2 (es) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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JP2005510464A (ja) * | 2001-09-07 | 2005-04-21 | ビーエーエスエフ アクチェンゲゼルシャフト | 4−アルキル−置換チエニルオキシピリジン類 |
DE10234875A1 (de) * | 2002-07-25 | 2004-02-05 | Bayer Cropscience Gmbh | 4-Trifluormethylpyrazolyl substituierte Pyridine und Pyrimidine |
-
2002
- 2002-07-25 DE DE10234875A patent/DE10234875A1/de not_active Withdrawn
-
2003
- 2003-07-14 CN CNA038175983A patent/CN1671702A/zh active Pending
- 2003-07-14 WO PCT/EP2003/007573 patent/WO2004013131A2/de active Application Filing
- 2003-07-14 PL PL03375390A patent/PL375390A1/xx not_active Application Discontinuation
- 2003-07-14 RS YUP-2005/0029A patent/RS20050029A/sr unknown
- 2003-07-14 AU AU2003250942A patent/AU2003250942A1/en not_active Abandoned
- 2003-07-14 RU RU2005105575/04A patent/RU2005105575A/ru not_active Application Discontinuation
- 2003-07-14 UA UAA200501767A patent/UA79135C2/uk unknown
- 2003-07-14 CA CA002494593A patent/CA2494593A1/en not_active Abandoned
- 2003-07-14 MX MXPA05000953A patent/MXPA05000953A/es not_active Application Discontinuation
- 2003-07-14 BR BR0312926-8A patent/BR0312926A/pt not_active IP Right Cessation
- 2003-07-14 JP JP2004525188A patent/JP2006504662A/ja not_active Abandoned
- 2003-07-14 EP EP03766160A patent/EP1527069A2/de not_active Withdrawn
- 2003-07-23 AR AR20030102640A patent/AR040668A1/es not_active Application Discontinuation
- 2003-07-23 TW TW092120100A patent/TWI269797B/zh not_active IP Right Cessation
- 2003-07-24 US US10/627,573 patent/US7022650B2/en not_active Expired - Fee Related
- 2003-07-24 MY MYPI20032796A patent/MY131916A/en unknown
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2005
- 2005-01-24 HR HR20050073A patent/HRP20050073A2/xx not_active Application Discontinuation
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2006
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MXPA05000953A (es) | 2005-05-16 |
PL375390A1 (en) | 2005-11-28 |
BR0312926A (pt) | 2005-07-12 |
DE10234875A1 (de) | 2004-02-05 |
WO2004013131A3 (de) | 2004-05-06 |
JP2006504662A (ja) | 2006-02-09 |
CN1671702A (zh) | 2005-09-21 |
US7022650B2 (en) | 2006-04-04 |
US20060122063A1 (en) | 2006-06-08 |
TWI269797B (en) | 2007-01-01 |
TW200403235A (en) | 2004-03-01 |
CA2494593A1 (en) | 2004-02-12 |
MY131916A (en) | 2007-09-28 |
WO2004013131A2 (de) | 2004-02-12 |
US20040072692A1 (en) | 2004-04-15 |
RS20050029A (en) | 2007-09-21 |
EP1527069A2 (de) | 2005-05-04 |
HRP20050073A2 (en) | 2006-03-31 |
RU2005105575A (ru) | 2005-10-10 |
AR040668A1 (es) | 2005-04-13 |
US7211673B2 (en) | 2007-05-01 |
AU2003250942A1 (en) | 2004-02-23 |
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