RU2000114825A - TRIFFORMETHYLBIPHENYLDIGALOPHENYLAZOLINES AS PESTICIDES - Google Patents
TRIFFORMETHYLBIPHENYLDIGALOPHENYLAZOLINES AS PESTICIDESInfo
- Publication number
- RU2000114825A RU2000114825A RU2000114825/04A RU2000114825A RU2000114825A RU 2000114825 A RU2000114825 A RU 2000114825A RU 2000114825/04 A RU2000114825/04 A RU 2000114825/04A RU 2000114825 A RU2000114825 A RU 2000114825A RU 2000114825 A RU2000114825 A RU 2000114825A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- compound
- salt
- tautomer
- free
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 18
- 150000003839 salts Chemical group 0.000 claims 8
- 239000000203 mixture Substances 0.000 claims 7
- 239000000463 material Substances 0.000 claims 5
- 239000011780 sodium chloride Substances 0.000 claims 5
- 230000000240 adjuvant Effects 0.000 claims 4
- 239000002671 adjuvant Substances 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 3
- 241000238876 Acari Species 0.000 claims 2
- 241001465754 Metazoa Species 0.000 claims 2
- 238000006243 chemical reaction Methods 0.000 claims 2
- 244000078703 ectoparasites Species 0.000 claims 2
- 244000079386 endoparasites Species 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- QNIHBTRLIJORED-UHFFFAOYSA-N 2,4-bis(2-methoxyphenyl)-2,4-bis(sulfanylidene)-1,3,2$l^{5},4$l^{5}-dithiadiphosphetane Chemical compound COC1=CC=CC=C1P1(=S)SP(=S)(C=2C(=CC=CC=2)OC)S1 QNIHBTRLIJORED-UHFFFAOYSA-N 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 claims 1
- CYQAYERJWZKYML-UHFFFAOYSA-N Phosphorus pentasulfide Chemical compound S1P(S2)(=S)SP3(=S)SP1(=S)SP2(=S)S3 CYQAYERJWZKYML-UHFFFAOYSA-N 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 125000002346 iodo group Chemical group I* 0.000 claims 1
- 230000000361 pesticidal Effects 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 238000000926 separation method Methods 0.000 claims 1
Claims (15)
где Х и Y независимо друг от друга обозначают фтор или хлор и Z обозначает О или S,
и при определенных условиях его возможные таутомеры, в каждом случае либо в свободной форме, либо в форме соли.1. The compound of the formula
where X and Y are independently fluorine or chlorine and Z is O or S,
and under certain conditions its possible tautomers, in each case either in free form or in salt form.
а) взаимодействие соединения формулы
где Х и Y имеют значения, указанные для формулы (I), a Q обозначает бром или йод, с соединением формулы
б) при необходимости для получения соединения формулы (I), в котором Z обозначает S, взаимодействие полученного соединения формулы (I), в котором Z обозначает O, с 2,4-бис(метоксифенил)-1,3-дитиа-2,4-дифосфетан-2,4-дисульфидом или с пентасульфидом фосфора, в каждом случае при необходимости превращение соединения формулы (I), полученного данным способом или по другим методам, или его таутомера, присутствующего в свободной форме или в форме соли, в другое соединение формулы (I) или в его таутомер, разделение смеси изомеров, полученных данным способом, и выделение требуемого изомера и/или превращение свободного соединения формулы (I), полученного данным способом, или его таутомера в соль или превращение соли, полученной данным способом из соединения формулы (I) или из его таутомера, в свободное соединение формулы (I) или в его таутомер либо в другую соль.4. A method of obtaining compounds of formula (I) and under certain conditions their tautomers, in each case in free form or in salt form, including
a) the interaction of the compounds of formula
where X and Y have the meanings indicated for formula (I), and Q is bromo or iodo, with a compound of the formula
b) if necessary, to obtain a compound of formula (I) in which Z is S, reaction of the obtained compound of formula (I) in which Z is O with 2,4-bis (methoxyphenyl) -1,3-dithia-2, 4-diphosphetane-2,4-disulfide or with phosphorus pentasulfide, in each case, if necessary, the conversion of the compound of formula (I) obtained by this method or other methods, or its tautomer, present in free or salt form, into another compound formula (I) or its tautomer, separation of a mixture of isomers obtained by this method, and adding the desired isomer and / or converting the free compound of formula (I) obtained by this method or its tautomer into a salt or converting a salt obtained by this method from a compound of formula (I) or from its tautomer into a free compound of formula (I) or its tautomer or in another salt.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH2548/97 | 1997-11-04 | ||
CH254897 | 1997-11-04 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2000114825A true RU2000114825A (en) | 2002-05-10 |
RU2222531C2 RU2222531C2 (en) | 2004-01-27 |
Family
ID=4236276
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2000114825/04A RU2222531C2 (en) | 1997-11-04 | 1998-11-02 | Trifluoromethylbiphenylyldihalophenylazolines as pesticides |
Country Status (22)
Country | Link |
---|---|
US (1) | US6413912B2 (en) |
EP (1) | EP1030850B1 (en) |
JP (1) | JP2001521930A (en) |
KR (1) | KR100607387B1 (en) |
CN (1) | CN1140519C (en) |
AR (1) | AR017544A1 (en) |
AT (1) | ATE372989T1 (en) |
AU (1) | AU742106B2 (en) |
BR (1) | BR9813920A (en) |
CA (1) | CA2309430C (en) |
CO (1) | CO5031296A1 (en) |
CY (1) | CY1106993T1 (en) |
DE (1) | DE69838431T2 (en) |
DK (1) | DK1030850T3 (en) |
ES (1) | ES2290998T3 (en) |
NZ (1) | NZ504265A (en) |
PT (1) | PT1030850E (en) |
RU (1) | RU2222531C2 (en) |
TR (1) | TR200001235T2 (en) |
TW (1) | TW518325B (en) |
WO (1) | WO1999023081A2 (en) |
ZA (1) | ZA9810039B (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MXPA01009788A (en) * | 1999-03-26 | 2002-03-27 | Novartis Ag | Pesticidal enantiomer-pure 2,4-disubstituted oxazolines. |
TWI275589B (en) | 2000-06-22 | 2007-03-11 | Dow Agrosciences Llc | 2-(3,5-disubstituted-4-pyridyl)-4-(thienyl, thiazolyl or arylphenyl)-1,3-oxazoline compounds |
US6573286B1 (en) | 2002-06-21 | 2003-06-03 | Dow Agrosciences Llc | 2-(2,6-disubstituted phenyl)-4-aryl-5-alkyl-1,3-oxazoline compounds |
NO319624B1 (en) | 2003-09-15 | 2005-09-05 | Trouw Internat Bv | Fish feed for salmonids in fresh water and use of such feed. |
EA014881B1 (en) | 2004-03-05 | 2011-02-28 | Ниссан Кемикал Индастриз, Лтд. | Substitited alkylbenzene derivatives |
US7329302B2 (en) * | 2004-11-05 | 2008-02-12 | H. L. Blachford Ltd./Ltee | Lubricants for powdered metals and powdered metal compositions containing said lubricants |
JP5007788B2 (en) * | 2005-05-16 | 2012-08-22 | 日産化学工業株式会社 | Dihydroazole-substituted benzamide compounds and pest control agents |
JP5101508B2 (en) * | 2005-08-29 | 2012-12-19 | ノバルティス アーゲー | Use of oxazole derivatives for fish parasite control |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4977171A (en) | 1988-06-09 | 1990-12-11 | Yashima Chemical Industrial Co., Ltd. | Oxa- or thia-zoline derivative |
AU634608B2 (en) * | 1989-12-09 | 1993-02-25 | Kyoyu Agri Co., Ltd. | 2-substituted phenyl-2-oxazoline or thiazoline derivatives, process for producing the same and insectides and acaricides containing the same |
JP3209576B2 (en) | 1992-06-12 | 2001-09-17 | 八洲化学工業株式会社 | Acaricide |
TW259693B (en) | 1993-08-04 | 1995-10-11 | Du Pont | |
DE4401098A1 (en) | 1994-01-17 | 1995-07-20 | Bayer Ag | Diphenyloxazoline derivatives |
JP3279818B2 (en) * | 1994-06-09 | 2002-04-30 | 八洲化学工業株式会社 | Insecticide and acaricide |
TW440429B (en) * | 1994-08-12 | 2001-06-16 | Bayer Ag | Substituted biphenyloxazolines |
ES2179886T3 (en) | 1994-10-06 | 2003-02-01 | Bayer Ag | SUBSTITUTED BIFENYLOXAZOLINS. |
DE19523388A1 (en) * | 1994-10-06 | 1996-04-11 | Bayer Ag | Substituted biphenyloxazolines |
DE4444111A1 (en) | 1994-12-12 | 1996-06-13 | Bayer Ag | Substituted m-biphenyloxazoline derivatives |
BR9510149A (en) | 1995-01-20 | 1998-06-02 | Du Pont | Compound arthropodicidal composition and method for arthropod control |
DE19515296A1 (en) | 1995-04-26 | 1996-10-31 | Bayer Ag | Use of oxazoline derivs. |
DE19515297A1 (en) * | 1995-04-26 | 1996-10-31 | Bayer Ag | Use of 2-(2,6-di:fluorophenyl)-4-(4-(4-tri:fluoromethoxy-phenyl)-phenyl)-2- oxazoline |
DE19520936A1 (en) | 1995-06-08 | 1996-12-12 | Bayer Ag | Ectoparasiticides means |
JPH0959115A (en) | 1995-08-25 | 1997-03-04 | Yashima Chem Ind Co Ltd | Insecticidal/acaricidal composition having excellent light stability |
WO1997013773A1 (en) | 1995-10-12 | 1997-04-17 | E.I. Du Pont De Nemours And Company | Arthropodicidal oxazolines and thiazolines |
TR199800871T2 (en) | 1995-11-17 | 1998-08-21 | Bayer Aktiengesellschaft | Biphenyl ether-oxazolinler. |
DE19548419A1 (en) * | 1995-12-22 | 1997-06-26 | Bayer Ag | Substituted thiazolines |
TW424089B (en) * | 1996-01-16 | 2001-03-01 | Du Pont | Oxazoline arthropodicides |
DE19717228A1 (en) * | 1997-04-24 | 1998-10-29 | Bayer Ag | Substituted oxazoline derivatives |
-
1998
- 1998-10-27 CO CO98062837A patent/CO5031296A1/en unknown
- 1998-11-02 PT PT98961117T patent/PT1030850E/en unknown
- 1998-11-02 KR KR1020007004823A patent/KR100607387B1/en not_active IP Right Cessation
- 1998-11-02 BR BR9813920-7A patent/BR9813920A/en not_active Application Discontinuation
- 1998-11-02 RU RU2000114825/04A patent/RU2222531C2/en not_active IP Right Cessation
- 1998-11-02 WO PCT/EP1998/006915 patent/WO1999023081A2/en active IP Right Grant
- 1998-11-02 JP JP2000518956A patent/JP2001521930A/en active Pending
- 1998-11-02 AU AU16653/99A patent/AU742106B2/en not_active Ceased
- 1998-11-02 CN CNB98811271XA patent/CN1140519C/en not_active Expired - Fee Related
- 1998-11-02 AR ARP980105506A patent/AR017544A1/en active IP Right Grant
- 1998-11-02 AT AT98961117T patent/ATE372989T1/en not_active IP Right Cessation
- 1998-11-02 DK DK98961117T patent/DK1030850T3/en active
- 1998-11-02 NZ NZ504265A patent/NZ504265A/en unknown
- 1998-11-02 EP EP98961117A patent/EP1030850B1/en not_active Expired - Lifetime
- 1998-11-02 ES ES98961117T patent/ES2290998T3/en not_active Expired - Lifetime
- 1998-11-02 CA CA002309430A patent/CA2309430C/en not_active Expired - Fee Related
- 1998-11-02 TR TR2000/01235T patent/TR200001235T2/en unknown
- 1998-11-02 US US09/530,638 patent/US6413912B2/en not_active Expired - Fee Related
- 1998-11-02 DE DE69838431T patent/DE69838431T2/en not_active Expired - Lifetime
- 1998-11-03 ZA ZA9810039A patent/ZA9810039B/en unknown
- 1998-11-04 TW TW087118321A patent/TW518325B/en not_active IP Right Cessation
-
2007
- 2007-11-08 CY CY20071101444T patent/CY1106993T1/en unknown
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