BG108238A - 5-халоген-6-фенил-7-флуороалкиламино-триазолопиримидни за използване като фунгициди - Google Patents

5-халоген-6-фенил-7-флуороалкиламино-триазолопиримидни за използване като фунгициди Download PDF

Info

Publication number: BG108238A
Authority: BG; Bulgaria
Prior art keywords: formula; compounds; hydrogen; halogen; alkyl
Prior art date: 2001-04-11

Application number

BG108238A

Other languages

Bulgarian (bg)

English (en)

Inventor

I Blasco Jordi Tormo

Eberhard Ammermann

Klaus-Juergen Pees

Guido Albert

Annerose Rehnig

Debra Search

Original Assignee

Basf Aktiengesellschaft

Priority date (The priority date 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 date listed.)

2001-04-11

Filing date

2003-10-07

Publication date

2005-04-30

2003-10-07 Application filed by Basf Aktiengesellschaft filed Critical Basf Aktiengesellschaft

2005-04-30 Publication of BG108238A publication Critical patent/BG108238A/bg

Links

239000000417 fungicide Substances 0.000 title description 13
239000001257 hydrogen Substances 0.000 claims abstract description 32
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 32
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 21
150000002431 hydrogen Chemical group 0.000 claims abstract description 19
239000000203 mixture Substances 0.000 claims abstract description 16
241000233866 Fungi Species 0.000 claims abstract description 14
125000000217 alkyl group Chemical group 0.000 claims abstract description 13
229910052736 halogen Inorganic materials 0.000 claims abstract description 12
238000002360 preparation method Methods 0.000 claims abstract description 10
238000000034 method Methods 0.000 claims abstract description 9
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 5
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 4
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 75
-1 nitro, hydroxyl Chemical group 0.000 claims description 45
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
125000001424 substituent group Chemical group 0.000 claims description 9
150000002367 halogens Chemical group 0.000 claims description 8
239000000463 material Substances 0.000 claims description 7
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 6
229910052731 fluorine Inorganic materials 0.000 claims description 6
239000011737 fluorine Substances 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
125000006374 C2-C10 alkenyl group Chemical group 0.000 claims description 4
125000005865 C2-C10alkynyl group Chemical group 0.000 claims description 3
229910052740 iodine Inorganic materials 0.000 claims description 3
SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 3
239000002689 soil Substances 0.000 claims description 3
125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 2
125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 2
125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 2
125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 2
125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 claims description 2
125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 2
125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 2
125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 2
206010017533 Fungal infection Diseases 0.000 claims description 2
208000031888 Mycoses Diseases 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
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125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 1
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239000007788 liquid Substances 0.000 claims 1
125000001188 haloalkyl group Chemical group 0.000 abstract description 5
125000005843 halogen group Chemical group 0.000 abstract description 4
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125000000304 alkynyl group Chemical group 0.000 abstract description 3
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125000004438 haloalkoxy group Chemical group 0.000 abstract 1
239000013543 active substance Substances 0.000 description 43
241000196324 Embryophyta Species 0.000 description 29
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 20
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238000011161 development Methods 0.000 description 8
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239000000243 solution Substances 0.000 description 8
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
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238000006243 chemical reaction Methods 0.000 description 7
238000002474 experimental method Methods 0.000 description 7
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230000000052 comparative effect Effects 0.000 description 6
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239000000741 silica gel Substances 0.000 description 6
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241000209140 Triticum Species 0.000 description 5
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125000004432 carbon atom Chemical group C* 0.000 description 5
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239000006072 paste Substances 0.000 description 5
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239000011550 stock solution Substances 0.000 description 5
125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 description 4
235000007688 Lycopersicon esculentum Nutrition 0.000 description 4
244000070406 Malus silvestris Species 0.000 description 4
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
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239000002253 acid Substances 0.000 description 4
235000021016 apples Nutrition 0.000 description 4
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239000000969 carrier Substances 0.000 description 4
235000013339 cereals Nutrition 0.000 description 4
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
239000002270 dispersing agent Substances 0.000 description 4
239000008187 granular material Substances 0.000 description 4
ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
239000000047 product Substances 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
150000003839 salts Chemical class 0.000 description 4
159000000000 sodium salts Chemical class 0.000 description 4
239000007921 spray Substances 0.000 description 4
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UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000895502 Blumeria graminis f. sp. tritici Species 0.000 description 3
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
241001330975 Magnaporthe oryzae Species 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
229920001213 Polysorbate 20 Polymers 0.000 description 3
244000061456 Solanum tuberosum Species 0.000 description 3
235000002595 Solanum tuberosum Nutrition 0.000 description 3
241000317942 Venturia <ichneumonid wasp> Species 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
239000002585 base Substances 0.000 description 3
239000000460 chlorine Substances 0.000 description 3
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125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
229910052500 inorganic mineral Inorganic materials 0.000 description 3
239000011707 mineral Substances 0.000 description 3
235000010755 mineral Nutrition 0.000 description 3
150000002790 naphthalenes Chemical class 0.000 description 3
239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 3
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LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 3
235000013311 vegetables Nutrition 0.000 description 3
239000002023 wood Substances 0.000 description 3
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RMSGQZDGSZOJMU-UHFFFAOYSA-N 1-butyl-2-phenylbenzene Chemical group CCCCC1=CC=CC=C1C1=CC=CC=C1 RMSGQZDGSZOJMU-UHFFFAOYSA-N 0.000 description 2
125000004776 1-fluoroethyl group Chemical group [H]C([H])([H])C([H])(F)* 0.000 description 2
125000004778 2,2-difluoroethyl group Chemical group [H]C([H])(*)C([H])(F)F 0.000 description 2
KBLAMUYRMZPYLS-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 KBLAMUYRMZPYLS-UHFFFAOYSA-N 0.000 description 2
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical compound CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 2
HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 description 2
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241000213004 Alternaria solani Species 0.000 description 2
239000005995 Aluminium silicate Substances 0.000 description 2
244000105624 Arachis hypogaea Species 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
235000000832 Ayote Nutrition 0.000 description 2
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
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WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
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125000000027 (C1-C10) alkoxy group Chemical group 0.000 description 1
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125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
239000012071 phase Substances 0.000 description 1
IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
229910000027 potassium carbonate Inorganic materials 0.000 description 1
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
125000006413 ring segment Chemical group 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
235000015170 shellfish Nutrition 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
229910000029 sodium carbonate Inorganic materials 0.000 description 1
241000894007 species Species 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000006467 substitution reaction Methods 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical class C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical group BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 description 1
125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
235000019871 vegetable fat Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
229910052984 zinc sulfide Inorganic materials 0.000 description 1
AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Plural Heterocyclic Compounds (AREA)

BG108238A 2001-04-11 2003-10-07 5-халоген-6-фенил-7-флуороалкиламино-триазолопиримидни за използване като фунгициди BG108238A (bg)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP01109011		2001-04-11

Publications (1)

Publication Number	Publication Date
BG108238A true BG108238A (bg)	2005-04-30

Family

ID=8177112

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BG108238A BG108238A (bg)	2001-04-11	2003-10-07	5-халоген-6-фенил-7-флуороалкиламино-триазолопиримидни за използване като фунгициди

Country Status (27)

Country	Link
US (1)	US7105664B2 (ru)
EP (1)	EP1381609B1 (ru)
JP (1)	JP2004531527A (ru)
KR (1)	KR20030087073A (ru)
CN (1)	CN1257904C (ru)
AR (1)	AR035823A1 (ru)
AT (1)	ATE287405T1 (ru)
AU (1)	AU2002257757B2 (ru)
BG (1)	BG108238A (ru)
BR (1)	BR0208756A (ru)
CA (1)	CA2443696A1 (ru)
CZ (1)	CZ295558B6 (ru)
DE (1)	DE60202672T2 (ru)
EA (1)	EA006710B1 (ru)
EE (1)	EE200300499A (ru)
ES (1)	ES2236509T3 (ru)
HU (1)	HUP0401092A3 (ru)
IL (1)	IL158218A0 (ru)
MX (1)	MXPA03009002A (ru)
NZ (1)	NZ528745A (ru)
PL (1)	PL367107A1 (ru)
PT (1)	PT1381609E (ru)
SK (1)	SK12522003A3 (ru)
TW (1)	TWI275590B (ru)
UA (1)	UA74069C2 (ru)
WO (1)	WO2002083676A1 (ru)
ZA (1)	ZA200307888B (ru)

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US6255309B1 (en) *	1999-03-19	2001-07-03	American Cyanomid Co.	Fungicidal trifluoromethylalkylamino-triazolopyrimidines
DE10124208A1 (de) *	2001-05-18	2002-11-21	Bayer Ag	Verwendung von Triazolopyrimidin-Derivaten als Mikrobizide
UA80304C2 (en) *	2002-11-07	2007-09-10	Basf Ag	Substituted 6-(2-halogenphenyl)triazolopyrimidines
CA2504192A1 (en) *	2002-11-07	2004-05-21	Basf Aktiengesellschaft	5-alkyl-7-aminotriazolopyrimidines, methods and intermediary products necessary for the production thereof, agents containing said compounds and the use thereof for fighting against harmful mushrooms
OA12957A (en) *	2002-11-15	2006-10-13	Basf Ag	Fungicidal mixtures.
GB0230020D0 (en) *	2002-12-23	2003-01-29	Syngenta Ltd	Fungicides
GB0230018D0 (en) *	2002-12-23	2003-01-29	Syngenta Ltd	Fungicides
EP1611135A1 (de) *	2003-03-31	2006-01-04	Basf Aktiengesellschaft	7-alkenylamino-triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bek mpfung von schadpilzen sowie sie enthaltende mittel
CN100355754C (zh) *	2003-04-02	2007-12-19	巴斯福股份公司	7－炔基氨基三唑并嘧啶、其制备方法及其在防治有害真菌中的用途以及包含所述化合物的制剂
ES2279452T3 (es)	2003-09-24	2007-08-16	Wyeth Holdings Corporation	6-((sustituido)fenil)triazolopirimidinas como agentes antineoplasicos.
CN100486580C (zh)	2003-09-24	2009-05-13	惠氏控股公司	作为抗癌剂的6-芳基-7-卤基-咪唑并[1,2-a]嘧啶
US7419982B2 (en)	2003-09-24	2008-09-02	Wyeth Holdings Corporation	Crystalline forms of 5-chloro-6-{2,6-difluoro-4-[3-(methylamino)propoxy]phenyl}-N-[(1S)-2,2,2-trifluoro-1-methylethyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine salts
JP2008501754A (ja) *	2004-06-09	2008-01-24	ビーエーエスエフ　アクチェンゲゼルシャフト	トリアゾロピリミジン化合物および有害菌類を防除するためのその使用
BRPI0512249A (pt) *	2004-06-22	2008-02-19	Basf Ag	compostos, processos para a preparação dos mesmos, e para o combate de fungos nocivos fitopatogênicos, agente fungicida, e, semente
EP1920654A1 (en)	2006-09-13	2008-05-14	Syngeta Participations AG	Novel pyridopyrazine N-oxides
EP1952691A3 (en) *	2007-01-31	2008-09-17	Basf Se	Method for improving plant health by application of a triazolopyrimidine derivative

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3130633A1 (de)	1981-08-01	1983-02-17	Basf Ag, 6700 Ludwigshafen	7-amino-azolo(1,5-a)pyrimidine und diese enthaltende fungizide
TW224044B (ru)	1991-12-30	1994-05-21	Shell Internat Res Schappej B V
TWI252231B (en)	1997-04-14	2006-04-01	American Cyanamid Co	Fungicidal trifluorophenyl-triazolopyrimidines
TW460476B (en) *	1997-04-14	2001-10-21	American Cyanamid Co	Fungicidal trifluoromethylalkylamino-triazolopyrimidines
GEP20053688B (en) *	2000-06-30	2005-12-12	Wyeth Corp	Substituted-Triazolopyrimidines as Anticancer Agents

2002
- 2002-04-06 PL PL02367107A patent/PL367107A1/xx not_active Application Discontinuation
- 2002-04-06 EP EP02727533A patent/EP1381609B1/en not_active Expired - Lifetime
- 2002-04-06 MX MXPA03009002A patent/MXPA03009002A/es active IP Right Grant
- 2002-04-06 KR KR10-2003-7013281A patent/KR20030087073A/ko not_active Abandoned
- 2002-04-06 HU HU0401092A patent/HUP0401092A3/hu unknown
- 2002-04-06 EA EA200301105A patent/EA006710B1/ru not_active IP Right Cessation
- 2002-04-06 CZ CZ20032721A patent/CZ295558B6/cs not_active IP Right Cessation
- 2002-04-06 IL IL15821802A patent/IL158218A0/xx unknown
- 2002-04-06 AT AT02727533T patent/ATE287405T1/de not_active IP Right Cessation
- 2002-04-06 JP JP2002581431A patent/JP2004531527A/ja not_active Withdrawn
- 2002-04-06 NZ NZ528745A patent/NZ528745A/en unknown
- 2002-04-06 PT PT02727533T patent/PT1381609E/pt unknown
- 2002-04-06 DE DE60202672T patent/DE60202672T2/de not_active Expired - Fee Related
- 2002-04-06 SK SK1252-2003A patent/SK12522003A3/sk unknown
- 2002-04-06 CA CA002443696A patent/CA2443696A1/en not_active Abandoned
- 2002-04-06 CN CNB028080807A patent/CN1257904C/zh not_active Expired - Fee Related
- 2002-04-06 WO PCT/EP2002/003829 patent/WO2002083676A1/en not_active Ceased
- 2002-04-06 AU AU2002257757A patent/AU2002257757B2/en not_active Ceased
- 2002-04-06 BR BR0208756-1A patent/BR0208756A/pt not_active IP Right Cessation
- 2002-04-06 ES ES02727533T patent/ES2236509T3/es not_active Expired - Lifetime
- 2002-04-06 EE EEP200300499A patent/EE200300499A/xx unknown
- 2002-04-06 US US10/474,460 patent/US7105664B2/en not_active Expired - Fee Related
- 2002-04-11 AR ARP020101339A patent/AR035823A1/es not_active Application Discontinuation
- 2002-04-11 TW TW091107358A patent/TWI275590B/zh not_active IP Right Cessation
- 2002-06-04 UA UA20031110122A patent/UA74069C2/uk unknown
2003
- 2003-10-07 BG BG108238A patent/BG108238A/bg unknown
- 2003-10-09 ZA ZA200307888A patent/ZA200307888B/en unknown

Also Published As

Publication number	Publication date
AR035823A1 (es)	2004-07-14
EA200301105A1 (ru)	2004-02-26
NZ528745A (en)	2005-03-24
US20040127509A1 (en)	2004-07-01
AU2002257757B2 (en)	2008-05-08
SK12522003A3 (sk)	2004-05-04
ATE287405T1 (de)	2005-02-15
WO2002083676A1 (en)	2002-10-24
US7105664B2 (en)	2006-09-12
JP2004531527A (ja)	2004-10-14
ES2236509T3 (es)	2005-07-16
TWI275590B (en)	2007-03-11
MXPA03009002A (es)	2004-02-12
BR0208756A (pt)	2004-05-11
CN1501936A (zh)	2004-06-02
EP1381609A1 (en)	2004-01-21
HUP0401092A3 (en)	2005-10-28
IL158218A0 (en)	2004-05-12
CN1257904C (zh)	2006-05-31
EP1381609B1 (en)	2005-01-19
PT1381609E (pt)	2005-05-31
DE60202672T2 (de)	2005-06-16
PL367107A1 (en)	2005-02-21
CZ20032721A3 (cs)	2004-01-14
DE60202672D1 (de)	2005-02-24
KR20030087073A (ko)	2003-11-12
EA006710B1 (ru)	2006-02-24
CZ295558B6 (cs)	2005-08-17
ZA200307888B (en)	2004-10-11
CA2443696A1 (en)	2002-10-24
EE200300499A (et)	2003-12-15
HUP0401092A2 (hu)	2004-09-28
UA74069C2 (en)	2005-10-17

Publication	Publication Date	Title
KR100529978B1 (ko)	2005-11-22	플루오로피라졸-비페닐아미드 살균제
BG108238A (bg)	2005-04-30	5-халоген-6-фенил-7-флуороалкиламино-триазолопиримидни за използване като фунгициди
AU2002257757A1 (en)	2003-04-10	5-Halogen-6-phenyl-7-fluoralkylamino-triazolopyrimidines as fungicides
EP1381610B1 (en)	2004-08-25	6-(2-chloro-6-fluoro-phenyl)-triazolopyrimidines
JP2002517413A (ja)	2002-06-18	殺菌剤としての２−（ｎ−フェニルアミノ）ピリジンの使用法、及び新規な２−（ｎ−フェニルアミノ）ピリミジン
JP2005504744A (ja)	2005-02-17	殺菌薬としての置換された６−（２−トリル）−トリアゾロピリミジン
JP2005504743A (ja)	2005-02-17	殺菌薬としての置換された６−（２−メトキシ−フェニル）−トリアゾロピリミジン
US20040162428A1 (en)	2004-08-19	6-(2,6-difluorophenyl)-triazolopyrimidines as fungicides
US6255352B1 (en)	2001-07-03	Method for combating harmful fungi
JP2004503475A (ja)	2004-02-05	フェネチルアクリルアミド類の使用、新規なフェネチルアクリルアミド類、それらの調製、およびそれらを含む組成物
DE60104087T2 (de)	2004-10-28	Fungizide 5-Alkylamino-6-phenyl-7-halogen-Triazolopyrimidine
US6482984B2 (en)	2002-11-19	Iminooxy-substituted benzyl phenyl ethers, processes and intermediates for their preparation, compositions comprising them, and their use for controlling harmful fungi
EP1295877A1 (de)	2003-03-26	Xanthonderivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung von Schadpilzen sowie sie enthaltende Mittel
JPH10513458A (ja)	1998-12-22	殺菌剤組成物
JP2003206252A (ja)	2003-07-22	ベンズヒドリル誘導体
HU200600B (en)	1990-07-28	Fungicides comprising pyridine-n-oxides and process for producing the active ingredients