ES2182486T3 - Herbicidas selectivos a base de n-aril-triazolin(tio)onas y de n-arilsulfonilamino(tio)carbonil-triazolin(tio)onas. - Google Patents
Herbicidas selectivos a base de n-aril-triazolin(tio)onas y de n-arilsulfonilamino(tio)carbonil-triazolin(tio)onas.Info
- Publication number
- ES2182486T3 ES2182486T3 ES99906118T ES99906118T ES2182486T3 ES 2182486 T3 ES2182486 T3 ES 2182486T3 ES 99906118 T ES99906118 T ES 99906118T ES 99906118 T ES99906118 T ES 99906118T ES 2182486 T3 ES2182486 T3 ES 2182486T3
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- halogen
- alkyl
- cyano
- alkoxy
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000004009 herbicide Substances 0.000 title abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 30
- 229910052736 halogen Inorganic materials 0.000 abstract 19
- 150000002367 halogens Chemical class 0.000 abstract 19
- 125000000217 alkyl group Chemical group 0.000 abstract 16
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 12
- 125000003545 alkoxy group Chemical group 0.000 abstract 11
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 8
- 125000003282 alkyl amino group Chemical group 0.000 abstract 6
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 5
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- -1 cyano, thiocarbamoyl Chemical group 0.000 abstract 5
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 4
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 4
- 125000006323 alkenyl amino group Chemical group 0.000 abstract 3
- 125000005108 alkenylthio group Chemical group 0.000 abstract 3
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 3
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 3
- 125000005109 alkynylthio group Chemical group 0.000 abstract 3
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 3
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 3
- 125000005366 cycloalkylthio group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000004429 atom Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004466 alkoxycarbonylamino group Chemical group 0.000 abstract 1
- 125000003806 alkyl carbonyl amino group Chemical group 0.000 abstract 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000004367 cycloalkylaryl group Chemical group 0.000 abstract 1
- 125000004472 dialkylaminosulfonyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
Landscapes
- 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)
Abstract
Agentes herbicidas, caracterizados porque tienen un contenido de una combinación de productos activos que abarca (a) al menos una N-aril-triazolin(tio)ona de la fórmula general (I) en la que Q1 significa oxígeno o azufre, R1 significa alquilo con 1 a 5 átomos de carbono substituido en caso dado por halógeno, R2 significa alquilo con 1 a 5 átomos de carbono substituido en caso dado por halógeno, R3 significa hidrógeno o halógeno, R4 significa ciano, tiocarbamoilo o halógeno, y R5 significa nitro, ciano, carboxi, carbamoilo, tiocarbamoilo, hidroxi, mercapto, amino, hidroxiamino, aminosulfonilo, halógeno, significa alquilo, alcoxi, alquiltio, alquilsulfinilo, alquilsulfonilo, alquilcarbonilo, alcoxicarbonilo o alquil-amino con respectivamente 1 a 6 átomos de carbono, substituidos respectivamente en caso dado por ciano, por hidroxi, por alcoxi con 1 a 4 átomos de carbono, por alquil-carbonilo con 1 a 4 átomos de carbono y/o por alcoxi-carbonilo con 1 a 4 átomos de carbono, significa alquenilo, alquinilo, alqueniloxi, o alquiniloxi con respectivamente 2 a 6 átomos de carbono, substituidos respectivamente en caso dado por ciano, por carboxi, por halógeno y/o por alcoxi-carbonilo con 1 a 4 átomos de carbono, significa alquilcarbonilamino, alcoxicarbonilamino, alquil-sulfonilamino, N,N-bis-alquilsulfonil-amino o N-alquicarbonil-N-aquilsulfonil-amino con respectivamente 1 a 6 átomos de carbono en los grupos alquilo, subs-tituidos respectivamente en caso dado por halógeno, o significa N-fenilcarbonil- N-alquil-sulfonil-amino, N-piridilcarbonil-N- alquilsulfonil-amino, N-furilcarbo-nil-N- alquilsulfonil-amino o N-tienil-carbonil-N- alquilsulfonil-amino con respec-tivamente 1 a 6 átomos de carbono en los grupos alquilo, substituidos respec-tivamente en caso dado por ciano, por halógeno, por alquilo con 1 a 4 átomos de carbono, por halógenoalquilo con 1 a 4 átomos de carbono, por alcoxi con 1 a 4 átomos de carbono o por halógenoalcoxi con 1 a 4 átomos de carbono, con excepción del compuesto activo 2-(2,4-dicloro-5- metilsulfonilaminofenil)-4-difluormetil-5-metil-2,4- dihidro-3H-1,2,4-triazol-3-ona (Sulfentrtazone) (¿producto activo del grupo 1¿) y (b) al menos una N-arilsulfonilamino(tio)carbonil- triazolin(tio)ona de a fórmula general (II) en la que Q2 y Q3 significan respectivamente oxígeno o azufre, R6 significa alquilo, alquenilo, alquinilo, alcoxi, alqueniloxi, alquilamino o dialquilamino con respectivamente hasta 6 átomos de carbono, substituidos res-pectivamente en caso dado por ciano, por halógeno o por alcoxi con 1 a 4 átomos de carbono, o significa cicloalquilo, cicloalquilalquilo o cicloalquilamino con res- pectivamente 3 a 6 átomos de carbono en los grupos cicloalquilo y, en caso dado,1 a 4 átomos de carbono en la parte alquilo, substituidos respectivamente en caso dado por ciano, por halógeno o por alquilo con 1 a 4 átomos de carbono, R7 significa hidrógeno, significa halógeno, significa alquilo, alcoxi, alquiltio, alquil-amino, dialquilamino, alquenilo, alquinilo, alqueniloxi, alquiniloxi, alqueniltio, alquiniltio, alquenilamino o alquinilamino con respectivamente hasta 6 átomos de carbono substituidos respectivamente en caso dado por ciano, por halógeno o por alcoxi con 1 a 4 átomos de carbono, o significa cicloalquilo, cicloalquiloxi, ciclo-alquiltio, cicloalquilamino o cicloalquilarilo con respectivamente 3 a 6 átomos de carbono en los grupos cicloalquilo y, en caso dado, 1 a 4 átomos de carbono en la parte alquilo, substituidos respectivamente en caso dado por ciano, por halógeno o por alquilo con 1 a 4 átomos de carbono, R8 significa nitro, ciano, halógeno, fenilo, fenoxi, significa alquilo, alquilcarbonilo, alcoxi, alcoxicarbonilo, alquiltio, alquilsulfinilo, alquilsulfonilo, dialquilamino-sulfonilo, alquilamino, alquenilo, alqueniloxi, alqueniltio, alquenilamino, alqui-nilo, alquiniloxi, alquiniltio con respectivamente hasta 6 átomos de carbono, subs- tituidos respectivamente en caso dado por ciano, por halógeno o por alcoxi con 1 a 4 átomos de carbono, o significa cicloalquilo, cicloalquiloxi, cicloalquiltio, cicloalquilamino con respectivamente 3 a 6 átomos de carbono en los grupos cicloalquilo, substituidos respectivamente en caso dado por ciano, por halógeno o por alquilo con 1 a 4 átomos de carbono, y R9 significa hidrógeno, nitro, ciano, halógeno, fenilo, fenoxi, significa alquilo, alquil-carbonilo, alcoxi, alcoxicarbonilo, alquiltio, alquilsulfinilo, alquilsulfonilo, alquilamino, alquenilo, alqueniloxi, alqueniltio, alquenilamino, alquinilo, alqui-niloxi o alquiniltio con respectivamente hasta 6 átomos de carbono substituidos respectivamente en caso dado por ciano, por halógeno o por alcoxi con 1 a 4 átomos de carbono, o significa cicloalquilo, cicloalquiloxi, cicloalquiltio, cicloal-quilamino con respectivamente 3 a 6 átomos de carbono en los grupos cicloal-quilo, substituidos respectivamente en caso dado por ciano, por halógeno o por alquilo con 1 a 4 átomos de carbono, y/o una sal de un compuesto de la fórmula (II) (¿producto activo del grupo 2¿).
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19802697A DE19802697A1 (de) | 1998-01-24 | 1998-01-24 | Selektive Herbizide auf Basis von N-Aryl-triazolin(thi)onen und N-Arylsulfonylamino(thio)carbonyltriazolin(thi)onen |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2182486T3 true ES2182486T3 (es) | 2003-03-01 |
Family
ID=7855586
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES99906118T Expired - Lifetime ES2182486T3 (es) | 1998-01-24 | 1999-01-12 | Herbicidas selectivos a base de n-aril-triazolin(tio)onas y de n-arilsulfonilamino(tio)carbonil-triazolin(tio)onas. |
Country Status (19)
Country | Link |
---|---|
US (1) | US6297192B1 (es) |
EP (1) | EP1049376B1 (es) |
CN (1) | CN100438763C (es) |
AT (1) | ATE226016T1 (es) |
AU (1) | AU735402B2 (es) |
CA (1) | CA2319225C (es) |
CZ (1) | CZ298793B6 (es) |
DE (2) | DE19802697A1 (es) |
DK (1) | DK1049376T3 (es) |
ES (1) | ES2182486T3 (es) |
HU (1) | HUP0100565A3 (es) |
NZ (1) | NZ505899A (es) |
PL (1) | PL196504B1 (es) |
RU (1) | RU2228032C2 (es) |
SI (1) | SI1049376T1 (es) |
SK (1) | SK285006B6 (es) |
TR (1) | TR200002114T2 (es) |
UA (1) | UA67766C2 (es) |
WO (1) | WO1999037153A1 (es) |
Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE19845407B4 (de) * | 1998-10-02 | 2012-06-28 | Arysta LifeScience North America Corp.(n.d.Ges.d.Staates Californien) | Selektive Herbizide auf Basis eines substituierten Phenylsulfonylaminocarbonyl-triazolinons |
CA2388428A1 (en) * | 1999-09-30 | 2001-04-05 | Bayer Aktiengesellschaft | Selective herbicides on the basis of n-aryl-triazoline(thi)ones |
DE10031825A1 (de) * | 2000-06-30 | 2002-01-10 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
US7893097B2 (en) * | 2008-02-02 | 2011-02-22 | Dow Pharmaceutical Sciences, Inc. | Methods and compositions for increasing solubility of azole drug compounds that are poorly soluble in water |
TWI735416B (zh) | 2014-10-06 | 2021-08-11 | 美商維泰克斯製藥公司 | 囊腫纖維化症跨膜傳導調節蛋白之調節劑 |
PL3436446T3 (pl) | 2016-03-31 | 2023-09-11 | Vertex Pharmaceuticals Incorporated | Modulatory mukowiscydozowego przezbłonowego regulatora przewodnictwa |
CN109803962B (zh) | 2016-09-30 | 2022-04-29 | 弗特克斯药品有限公司 | 囊性纤维化跨膜传导调控蛋白的调节剂、以及药物组合物 |
MA54847A (fr) | 2016-12-09 | 2021-12-08 | Vertex Pharma | Forme crystalline d'un n-(pyrazol-4-yl)sulfonyl-6-(pyrazol-1-yl)-2-(pyrrolidin-1-yl)pyridine-3-carboxamide pour traiter la mucoviscidose |
EP3634402A1 (en) | 2017-06-08 | 2020-04-15 | Vertex Pharmaceuticals Incorporated | Methods of treatment for cystic fibrosis |
WO2019018395A1 (en) | 2017-07-17 | 2019-01-24 | Vertex Pharmaceuticals Incorporated | METHODS OF TREATING CYSTIC FIBROSIS |
ES2912657T3 (es) | 2017-08-02 | 2022-05-26 | Vertex Pharma | Procesos para preparar compuestos de pirrolidina |
AU2018351533B2 (en) | 2017-10-19 | 2023-02-02 | Vertex Pharmaceuticals Incorporated | Crystalline forms and compositions of CFTR modulators |
KR20200097293A (ko) | 2017-12-08 | 2020-08-18 | 버텍스 파마슈티칼스 인코포레이티드 | 낭포성 섬유증 막횡단 전도 조절자의 조정제의 제조 방법 |
TWI810243B (zh) | 2018-02-05 | 2023-08-01 | 美商維泰克斯製藥公司 | 用於治療囊腫纖化症之醫藥組合物 |
US11414439B2 (en) | 2018-04-13 | 2022-08-16 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator, pharmaceutical compositions, methods of treatment, and process for making the modulator |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4318731A (en) | 1979-08-25 | 1982-03-09 | Nihon Nohyaku Co., Ltd. | Δ2 -1,2,4-triazolin-5-one derivatives and herbicidal usage thereof |
WO1985001637A1 (en) * | 1983-10-13 | 1985-04-25 | Fmc Corporation | Herbicidal 1-aryl-delta2-1,2,4-triazolin-5-ones |
US4702763A (en) | 1983-10-13 | 1987-10-27 | Fmc Corporation | Herbicidal 1-aryl-delta2-1,2,4-triazolin-5-ones |
AU566839B2 (en) | 1984-03-29 | 1987-10-29 | Fmc Corporation | Herbicidal 1-aryl-2-1, 2, 4-triazolin-5-ones |
GB8418424D0 (en) | 1984-07-19 | 1984-08-22 | Scras | Inhibition of platelets aggregation |
WO1986002642A1 (en) | 1984-10-31 | 1986-05-09 | Fmc Corporation | Herbicidal aryl triazolinones |
US4806145A (en) | 1984-10-31 | 1989-02-21 | Fmc Corporation | Herbicidal aryl triazolinones |
US4818276A (en) | 1984-11-20 | 1989-04-04 | Fmc Corporation | Herbicidal 1-aryl-Δ2 -1,2,4-triazolin-5-ones |
CA1281724C (en) | 1985-02-04 | 1991-03-19 | Lester L. Maravetz | Haloalkyl triazolinones |
CN85106905A (zh) | 1985-08-08 | 1987-02-04 | Fmc公司 | 含有1-芳基-δ2-1,2,4,-三唑啉-5-酮类的除草剂及其制备方法 |
US4845232A (en) | 1985-10-26 | 1989-07-04 | Nihon Nohyaku Co., Ltd. | Process for producing 1,2,4-triazolin-5-one derivatives, and intermediates therefor |
JPS6299368A (ja) | 1985-10-26 | 1987-05-08 | Nippon Nohyaku Co Ltd | Δ↑2−1,2,4−トリアゾリン−5−オン誘導体及びその製法並びにその用途 |
US5041155A (en) | 1989-04-03 | 1991-08-20 | Fmc Corporation | Herbicidal aryl triazolinones |
US4906284A (en) | 1986-03-25 | 1990-03-06 | Fmc Corporation | Herbicidal fluoropropyl compounds |
DE3934081A1 (de) | 1989-10-12 | 1991-04-18 | Bayer Ag | Sulfonylaminocarbonyltriazolinone |
DE3815765A1 (de) | 1988-05-09 | 1989-11-23 | Bayer Ag | 2-sulfonylaminocarbonyl-2,4-dihydro-3h-1,2,4- triazol-3-one einschliesslich 4,5-kondensierter, bicyclischer derivate, verfahren und neue zwischenprodukte zu ihrer herstellung und ihre verwendung als pflanzenbehandlungsmittel |
DE3936623A1 (de) | 1989-11-03 | 1991-05-08 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit ueber schwefel gebundenen substituenten |
DE3936622A1 (de) | 1989-11-03 | 1991-05-08 | Bayer Ag | Halogenierte sulfonylaminocarbonyltriazolinone |
WO1988009617A1 (en) | 1987-06-12 | 1988-12-15 | Fmc Corporation | 1-(4-chloro-2-fluoro-5-methoxyphenyl)-3-methyl-4-difluoromethyl-delta2-1,2,4-triazolin-5-one as herbicidal agent |
US5541337A (en) | 1989-04-13 | 1996-07-30 | Bayer Aktiengesellschaft | Substituted 5-alkoxy-1,2,4-triazol-3-(thi)ones |
DE4110795A1 (de) * | 1991-04-04 | 1992-10-08 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit ueber sauerstoff gebundenen substituenten |
US5300480A (en) | 1989-04-13 | 1994-04-05 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyltriazolinones having two substituents bonded via oxygen |
CA1331463C (en) | 1988-08-31 | 1994-08-16 | Kathleen Megan Poss | Herbicidal triazolinones |
DE4238125A1 (de) | 1992-11-12 | 1994-05-19 | Bayer Ag | Substituierte Triazolinone |
DE3839480A1 (de) | 1988-11-23 | 1990-05-31 | Bayer Ag | N-aryl-stickstoffheterocyclen, verfahren sowie neue zwischenprodukte zu ihrer herstellung und ihre verwendung als herbizide und pflanzenwuchsregulatoren |
US4909831A (en) | 1989-02-06 | 1990-03-20 | Fmc Corporation | Safening of crops against a triazolinone herbicide with 1,8-naphthalic anhydride |
US5035740A (en) | 1989-05-16 | 1991-07-30 | Fmc Corporation | Herbicidal compounds |
DE3937475A1 (de) * | 1989-11-10 | 1991-05-16 | Bayer Ag | Selektiv-herbizide mittel, enthaltend metribuzin in kombination mit bromoxynil |
US5534486A (en) | 1991-04-04 | 1996-07-09 | Bayer Aktiengesellschaft | Herbicidal sulphonylaminocarbonyl triazolinones having substituents bonded via oxygen |
CA2090807A1 (en) * | 1992-03-10 | 1993-09-11 | Shigeo Murai | Substituted pyridinesulfonamide compound or its salt, process for preparing the same, and herbicide containing the same |
DE4303376A1 (de) | 1993-02-05 | 1994-08-11 | Bayer Ag | Substituierte Triazolinone |
DE4303676A1 (de) * | 1993-02-09 | 1994-08-11 | Bayer Ag | 1-Aryltriazolin(thi)one |
US6077813A (en) | 1994-05-04 | 2000-06-20 | Bayer Aktiengesellschaft | Substituted aromatic thiocarboxylic acid amides and their use as herbicides |
DE4435547A1 (de) | 1994-10-05 | 1996-04-11 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit über Sauerstoff und Schwefel gebundenen Substituenten |
DE19508119A1 (de) | 1995-03-08 | 1996-09-12 | Bayer Ag | Sulfonylaminocarbonyltriazolinone mit Halogenalkylthio-Substituenten |
DE19508118A1 (de) | 1995-03-08 | 1996-09-12 | Bayer Ag | Sulfonylaminocarbonyltriazoline mit Halogenalkoxy-Substituenten |
DE19525162A1 (de) | 1995-07-11 | 1997-01-16 | Bayer Ag | Sulfonylamino(thio)carbonylverbindungen |
DE19638887A1 (de) * | 1996-09-23 | 1998-03-26 | Bayer Ag | Selektive Herbizide auf Basis von Arylsulfonylaminocarbonyltriazolinonen |
-
1998
- 1998-01-24 DE DE19802697A patent/DE19802697A1/de not_active Withdrawn
-
1999
- 1999-01-12 AU AU26165/99A patent/AU735402B2/en not_active Ceased
- 1999-01-12 SI SI9930180T patent/SI1049376T1/xx unknown
- 1999-01-12 NZ NZ505899A patent/NZ505899A/en unknown
- 1999-01-12 AT AT99906118T patent/ATE226016T1/de active
- 1999-01-12 ES ES99906118T patent/ES2182486T3/es not_active Expired - Lifetime
- 1999-01-12 PL PL341903A patent/PL196504B1/pl not_active IP Right Cessation
- 1999-01-12 TR TR2000/02114T patent/TR200002114T2/xx unknown
- 1999-01-12 DE DE59903090T patent/DE59903090D1/de not_active Expired - Lifetime
- 1999-01-12 CZ CZ20002715A patent/CZ298793B6/cs not_active IP Right Cessation
- 1999-01-12 RU RU2000122362/04A patent/RU2228032C2/ru not_active IP Right Cessation
- 1999-01-12 DK DK99906118T patent/DK1049376T3/da active
- 1999-01-12 WO PCT/EP1999/000130 patent/WO1999037153A1/de active IP Right Grant
- 1999-01-12 EP EP99906118A patent/EP1049376B1/de not_active Expired - Lifetime
- 1999-01-12 US US09/600,576 patent/US6297192B1/en not_active Expired - Fee Related
- 1999-01-12 CN CNB998023418A patent/CN100438763C/zh not_active Expired - Fee Related
- 1999-01-12 HU HU0100565A patent/HUP0100565A3/hu unknown
- 1999-01-12 CA CA002319225A patent/CA2319225C/en not_active Expired - Fee Related
- 1999-01-12 SK SK1100-2000A patent/SK285006B6/sk not_active IP Right Cessation
- 1999-12-01 UA UA2000084985A patent/UA67766C2/uk unknown
Also Published As
Publication number | Publication date |
---|---|
PL341903A1 (en) | 2001-05-07 |
CN100438763C (zh) | 2008-12-03 |
EP1049376A1 (de) | 2000-11-08 |
TR200002114T2 (tr) | 2000-12-21 |
RU2228032C2 (ru) | 2004-05-10 |
PL196504B1 (pl) | 2008-01-31 |
CA2319225C (en) | 2008-08-26 |
CN1288353A (zh) | 2001-03-21 |
SK285006B6 (sk) | 2006-04-06 |
DE19802697A1 (de) | 1999-07-29 |
AU735402B2 (en) | 2001-07-05 |
US6297192B1 (en) | 2001-10-02 |
AU2616599A (en) | 1999-08-09 |
DK1049376T3 (da) | 2003-02-17 |
HUP0100565A3 (en) | 2002-12-28 |
EP1049376B1 (de) | 2002-10-16 |
ATE226016T1 (de) | 2002-11-15 |
SK11002000A3 (sk) | 2001-03-12 |
CA2319225A1 (en) | 1999-07-29 |
UA67766C2 (uk) | 2004-07-15 |
SI1049376T1 (en) | 2003-06-30 |
NZ505899A (en) | 2002-06-28 |
CZ20002715A3 (cs) | 2000-11-15 |
HUP0100565A2 (hu) | 2001-06-28 |
WO1999037153A1 (de) | 1999-07-29 |
DE59903090D1 (de) | 2002-11-21 |
CZ298793B6 (cs) | 2008-01-30 |
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