ZA200601795B - Pesticides - Google Patents

Pesticides Download PDF

Info

Publication number: ZA200601795B
Authority: ZA; South Africa
Prior art keywords: alkyl; group; substituted; compound; alkoxy
Prior art date: 2003-09-04

Application number

ZA200601795A

Other languages

English (en)

Inventor

Chou David Teh-Wei

Knauf Werner

Doeller Uwe

Seeger Karl

Original Assignee

Bayer Cropscience Sa

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.)

2003-09-04

Filing date

2006-03-02

Publication date

2007-05-30

2006-03-02 Application filed by Bayer Cropscience Sa filed Critical Bayer Cropscience Sa

2007-05-30 Publication of ZA200601795B publication Critical patent/ZA200601795B/en

Links

239000000575 pesticide Substances 0.000 title description 10
150000003254 radicals Chemical class 0.000 claims description 49
229910052736 halogen Inorganic materials 0.000 claims description 43
150000002367 halogens Chemical class 0.000 claims description 42
150000001875 compounds Chemical class 0.000 claims description 32
150000003839 salts Chemical class 0.000 claims description 18
-1 heteroaromatic rad ical Chemical class 0.000 claims description 16
125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims description 16
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 14
238000000034 method Methods 0.000 claims description 9
241000607479 Yersinia pestis Species 0.000 claims description 8
239000000203 mixture Substances 0.000 claims description 8
229910052791 calcium Inorganic materials 0.000 claims description 7
229910052731 fluorine Inorganic materials 0.000 claims description 7
229910052801 chlorine Inorganic materials 0.000 claims description 6
229910014585 C2-Ce Inorganic materials 0.000 claims description 5
125000005842 heteroatom Chemical group 0.000 claims description 5
229910052757 nitrogen Inorganic materials 0.000 claims description 5
229910052717 sulfur Inorganic materials 0.000 claims description 5
125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 5
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
125000006414 CCl Chemical group ClC* 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
229910052784 alkaline earth metal Inorganic materials 0.000 claims description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 4
239000001257 hydrogen Substances 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 3
230000000361 pesticidal effect Effects 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
125000006413 ring segment Chemical group 0.000 claims description 3
239000003513 alkali Substances 0.000 claims description 2
229920006395 saturated elastomer Polymers 0.000 claims description 2
UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 claims 1
230000002730 additional effect Effects 0.000 claims 1
239000002585 base Substances 0.000 claims 1
239000003085 diluting agent Substances 0.000 claims 1
239000003814 drug Substances 0.000 claims 1
239000004094 surface-active agent Substances 0.000 claims 1
239000011575 calcium Substances 0.000 description 38
125000000217 alkyl group Chemical group 0.000 description 8
241001465754 Metazoa Species 0.000 description 6
125000004432 carbon atom Chemical group C* 0.000 description 5
125000003545 alkoxy group Chemical group 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
244000000013 helminth Species 0.000 description 3
241000239223 Arachnida Species 0.000 description 2
241000238421 Arthropoda Species 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
125000000304 alkynyl group Chemical group 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
125000000753 cycloalkyl group Chemical group 0.000 description 2
125000005843 halogen group Chemical group 0.000 description 2
125000004435 hydrogen atom Chemical group [H]* 0.000 description 2
229910052740 iodine Inorganic materials 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
244000045947 parasite Species 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
239000000126 substance Substances 0.000 description 2
125000006583 (C1-C3) haloalkyl group Chemical group 0.000 description 1
125000006274 (C1-C3)alkoxy group Chemical group 0.000 description 1
125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
125000006650 (C2-C4) alkynyl group Chemical group 0.000 description 1
125000004961 1-arylpyrazolyl group Chemical group 0.000 description 1
125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
125000006022 2-methyl-2-propenyl group Chemical group 0.000 description 1
IIVWHGMLFGNMOW-UHFFFAOYSA-N 2-methylpropane Chemical compound C[C](C)C IIVWHGMLFGNMOW-UHFFFAOYSA-N 0.000 description 1
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 description 1
125000000474 3-butynyl group Chemical group [H]C#CC([H])([H])C([H])([H])* 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
241000282472 Canis lupus familiaris Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
201000003075 Crimean-Congo hemorrhagic fever Diseases 0.000 description 1
RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
241000244206 Nematoda Species 0.000 description 1
229910019142 PO4 Inorganic materials 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000013543 active substance Substances 0.000 description 1
125000003342 alkenyl group Chemical group 0.000 description 1
125000004414 alkyl thio group Chemical group 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
150000001450 anions Chemical class 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
229910002091 carbon monoxide Inorganic materials 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000011109 contamination Methods 0.000 description 1
239000002895 emetic Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000009472 formulation Methods 0.000 description 1
125000002541 furyl group Chemical group 0.000 description 1
125000004438 haloalkoxy group Chemical group 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000003840 hydrochlorides Chemical class 0.000 description 1
125000002883 imidazolyl group Chemical group 0.000 description 1
239000011630 iodine Substances 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000000842 isoxazolyl group Chemical group 0.000 description 1
229910052744 lithium Inorganic materials 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 1
TYOAREPKJWFWPT-UHFFFAOYSA-N methylsulfanium;chloride Chemical class [Cl-].[SH2+]C TYOAREPKJWFWPT-UHFFFAOYSA-N 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
125000006682 monohaloalkyl group Chemical group 0.000 description 1
125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
125000002971 oxazolyl group Chemical group 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
125000003373 pyrazinyl group Chemical group 0.000 description 1
125000003226 pyrazolyl group Chemical group 0.000 description 1
125000002098 pyridazinyl group Chemical group 0.000 description 1
125000004076 pyridyl group Chemical group 0.000 description 1
125000000714 pyrimidinyl group Chemical group 0.000 description 1
125000000168 pyrrolyl group Chemical group 0.000 description 1
125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
125000001113 thiadiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
230000001988 toxicity Effects 0.000 description 1
231100000419 toxicity Toxicity 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
ZBZJXHCVGLJWFG-UHFFFAOYSA-N trichloromethyl(.) Chemical compound Cl[C](Cl)Cl ZBZJXHCVGLJWFG-UHFFFAOYSA-N 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1

Classifications

- 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
- C07D401/02—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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
- 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
- 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
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/02—Antiprotozoals, e.g. for leishmaniasis, trichomoniasis, toxoplasmosis
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Veterinary Medicine (AREA)
General Health & Medical Sciences (AREA)
Medicinal Chemistry (AREA)
Pharmacology & Pharmacy (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Tropical Medicine & Parasitology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Epidemiology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)

ZA200601795A 2003-09-04 2006-03-02 Pesticides ZA200601795B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
EP03019619		2003-09-04

Publications (1)

Publication Number	Publication Date
ZA200601795B true ZA200601795B (en)	2007-05-30

Family

ID=34259146

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200601795A ZA200601795B (en)	2003-09-04	2006-03-02	Pesticides

Country Status (16)

Country	Link
US (1)	US20070072850A1 (fr)
EP (1)	EP1663985B1 (fr)
JP (1)	JP4982764B2 (fr)
KR (1)	KR20060096991A (fr)
CN (1)	CN100537545C (fr)
AR (1)	AR045562A1 (fr)
AT (1)	ATE444955T1 (fr)
AU (1)	AU2004270341B9 (fr)
BR (1)	BRPI0414081A (fr)
CA (1)	CA2536637C (fr)
DE (1)	DE602004023525D1 (fr)
ES (1)	ES2332274T3 (fr)
MX (1)	MXPA06002380A (fr)
NZ (1)	NZ545657A (fr)
WO (1)	WO2005023775A1 (fr)
ZA (1)	ZA200601795B (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
IL163790A0 (en) *	2002-03-05	2005-12-18	Bayer Cropscience Sa	5-Substituted-alkylaminopyrazole derivatives as pesticides
JP2008540351A (ja) *	2005-05-07	2008-11-20	メリアルリミテッド	５−アルキルチオアルキルアミノ−１−フェニル−ピラゾールを製造する方法
CA2867750C (fr) *	2012-03-28	2020-07-14	Lanxess Deutschland Gmbh	Compositions stables constituees de thiabendazole et de fongicides iodes
TWI579274B (zh) *	2012-04-20	2017-04-21	龍馬躍公司	製備１－芳基－５－烷基吡唑化合物的改良方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4005213A (en) *	1968-12-21	1977-01-25	Schering Aktiengesellschaft	2,5-Substituted-1,3,4-thiadiazoles as fungicides
US5629335A (en) *	1995-04-07	1997-05-13	Rhone-Poulenc Inc.	Pesticidal 1-arylpyrazole-3-carboximidothioic acid esters
DE19650197A1 (de) *	1996-12-04	1998-06-10	Bayer Ag	3-Thiocarbamoylpyrazol-Derivate
US6350771B1 (en) *	1996-12-24	2002-02-26	Rhone-Poulenc, Inc.	Pesticidal 1-arylpyrazoles
DE19824487A1 (de) *	1998-06-02	1999-12-09	Bayer Ag	Substituierte 3-Thiocarbamoylpyrazole
DE19853560A1 (de) *	1998-11-20	2000-05-25	Bayer Ag	Verfahren zur Herstellung von 5-Amino-3-(thio)carbamoylpyrazolen
AR021608A1 (es) *	1998-12-11	2002-07-31	Merial Ltd	Represion de artropodos en animales
WO2002003798A1 (fr) *	2000-07-12	2002-01-17	Ocapco, Llc	Pesticide avermectine comprenant un surfactant organosilicié

2004
- 2004-08-21 CN CNB2004800255503A patent/CN100537545C/zh not_active Expired - Fee Related
- 2004-08-21 ES ES04764358T patent/ES2332274T3/es not_active Expired - Lifetime
- 2004-08-21 US US10/570,136 patent/US20070072850A1/en not_active Abandoned
- 2004-08-21 KR KR1020067004574A patent/KR20060096991A/ko not_active Ceased
- 2004-08-21 AT AT04764358T patent/ATE444955T1/de not_active IP Right Cessation
- 2004-08-21 JP JP2006525066A patent/JP4982764B2/ja not_active Expired - Fee Related
- 2004-08-21 WO PCT/EP2004/009376 patent/WO2005023775A1/fr not_active Ceased
- 2004-08-21 NZ NZ545657A patent/NZ545657A/en not_active IP Right Cessation
- 2004-08-21 MX MXPA06002380A patent/MXPA06002380A/es active IP Right Grant
- 2004-08-21 EP EP04764358A patent/EP1663985B1/fr not_active Expired - Lifetime
- 2004-08-21 DE DE602004023525T patent/DE602004023525D1/de not_active Expired - Lifetime
- 2004-08-21 BR BRPI0414081-8A patent/BRPI0414081A/pt not_active Application Discontinuation
- 2004-08-21 CA CA2536637A patent/CA2536637C/fr not_active Expired - Fee Related
- 2004-08-21 AU AU2004270341A patent/AU2004270341B9/en not_active Ceased
- 2004-09-02 AR ARP040103146A patent/AR045562A1/es active IP Right Grant
2006
- 2006-03-02 ZA ZA200601795A patent/ZA200601795B/en unknown

Also Published As

Publication number	Publication date
JP4982764B2 (ja)	2012-07-25
CA2536637C (fr)	2011-12-06
HK1099746A1 (zh)	2007-08-24
EP1663985A1 (fr)	2006-06-07
BRPI0414081A (pt)	2006-10-24
AU2004270341B2 (en)	2011-04-28
DE602004023525D1 (de)	2009-11-19
WO2005023775A1 (fr)	2005-03-17
AU2004270341A1 (en)	2005-03-17
ES2332274T3 (es)	2010-02-01
CA2536637A1 (fr)	2005-03-17
AR045562A1 (es)	2005-11-02
AU2004270341B9 (en)	2011-06-30
KR20060096991A (ko)	2006-09-13
US20070072850A1 (en)	2007-03-29
JP2007504184A (ja)	2007-03-01
CN1845903A (zh)	2006-10-11
CN100537545C (zh)	2009-09-09
ATE444955T1 (de)	2009-10-15
EP1663985B1 (fr)	2009-10-07
MXPA06002380A (es)	2006-06-20
NZ545657A (en)	2010-01-29

Publication	Publication Date	Title
NZ585701A (en)	2012-09-28	Benzopyrazine derivatives as prolyl hydroxylase inhibitors
DE69526815T2 (de)	2002-11-14	Verfahren zur Sulfinylierung von heterocyclischen Verbindungen
PL162219B1 (pl)	1993-09-30	Sposób wytwarzania nowych pochodnych kwasu propenowego PL PL PL PL PL PL
ZA200503743B (en)	2006-11-29	Pesticidal 5-(acylamino) pyrazole derivatives
ATE402697T1 (de)	2008-08-15	1,3,5-trisubstituierte 4,5-dihydro-1h-pyrazol- derivative mit cb1-antagonistischer aktivität
KR930022947A (ko)	1993-12-18	제초조성물, 그의 제조방법 및 제초제로서의 사용
KR960701018A (ko)	1996-02-24	제초성의 헤테로사이클릭-치환된 피리딘(Herbicidal heterocyclic-substituted pyridines)
RU2004129579A (ru)	2005-04-20	Производные 5-замещенных алкиламинопиразолов в качестве пестицидов
JPS6233171A (ja)	1987-02-13	１−ヘテロアリ−ル−４−アリ−ル−ピラゾ−ル誘導体、その製法及び利用
KR930703302A (ko)	1993-11-29	피페리딘 유도체
ATE268752T1 (de)	2004-06-15	Aralkyl-1,2-diaminen mit calcimimetischer wirkung und verfahren zu ihrer herstellung
GB1588750A (en)	1981-04-29	Triazole derivatives and their use as fungicides
KR910021381A (ko)	1991-12-20	4-3급 부틸이미다졸 유도체, 및 이의 제조방법 및 용도
EP0001663B1 (fr)	1982-05-12	2-Arylamino-hexahydropyrimidines et- imidazolidines, leurs sels et complexes, leur méthode de préparation et compositions fongicides les contenant
ATE331721T1 (de)	2006-07-15	Kupfer-carben-komplexe und ihre verwendung
SU701537A3 (ru)	1979-11-30	Способ получени нитрилов тиазол2-коричной кислоты
JP2017509703A5 (fr)	2018-04-05
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