RU2002116255A - Aminoheterocycclamide derivatives with pesticidal activity - Google Patents

Aminoheterocycclamide derivatives with pesticidal activity

Info

Publication number
RU2002116255A
RU2002116255A RU2002116255/04A RU2002116255A RU2002116255A RU 2002116255 A RU2002116255 A RU 2002116255A RU 2002116255/04 A RU2002116255/04 A RU 2002116255/04A RU 2002116255 A RU2002116255 A RU 2002116255A RU 2002116255 A RU2002116255 A RU 2002116255A
Authority
RU
Russia
Prior art keywords
formula
alkyl
substituents
compounds
compound
Prior art date
Application number
RU2002116255/04A
Other languages
Russian (ru)
Other versions
RU2259370C2 (en
Inventor
Пьер ДЮКРЕ
Жак БУВЬЕ
Урс МЮЛЛЕР
Original Assignee
Новартис Аг
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.)
Filing date
Publication date
Application filed by Новартис Аг filed Critical Новартис Аг
Publication of RU2002116255A publication Critical patent/RU2002116255A/en
Application granted granted Critical
Publication of RU2259370C2 publication Critical patent/RU2259370C2/en

Links

Claims (7)

1. Соединения формулы1. Compounds of the formula
Figure 00000001
Figure 00000001
где R1 обозначает водород, галоген, C16алкил, C16алкокси, C16галоалкил или незамещенный или замещенный 1-5 заместителями фенил, где заместители выбирают из группы, включающей C16алкил, С16галоалкил, C16алкокси, арилокси, галоген, циано и нитро, причем, если количество заместителей превышает 1, то заместители могут быть одинаковыми или различными;where R 1 is hydrogen, halogen, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkyl or unsubstituted or substituted with 1-5 phenyl substituents, where the substituents are selected from the group consisting of C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, aryloxy, halogen, cyano and nitro, moreover, if the number of substituents exceeds 1, then the substituents may be the same or different; R2 обозначает водород, C16алкил, (C16алкилен)фенил, пиридил, COOR6, CONR7R8, СОК6, аллил или СН2-О-R6;R 2 is hydrogen, C 1 -C 6 alkyl, (C 1 -C 6 alkylene) phenyl, pyridyl, COOR 6 , CONR 7 R 8 , SOK 6 , allyl or CH 2 -O-R 6 ; X1 обозначает N;X 1 is N; Х2 обозначает C(CN), С(COOR6), C(COR6), С(SOR6), C(CONR7R8) или C(NO2);X 2 is C (CN), C (COOR 6 ), C (COR 6 ), C (SOR 6 ), C (CONR 7 R 8 ) or C (NO 2 ); Х3 обозначает О или S;X 3 is O or S; Q обозначает СН или N;Q is CH or N; R3 и R4 независимо друг от друга обозначают водород, C16алкил или вместе с атомом углерода, с которым они связаны, образуют С37циклоалкильное кольцо;R 3 and R 4 are independently hydrogen, C 1 -C 6 alkyl, or together with the carbon atom to which they are attached form a C 3 -C 7 cycloalkyl ring; R5 обозначает заместитель, выбранный из группы, включающей C16алкил, C26алкенил, C26алкинил, C16галоалкил, C16алкокси, арилокси, галоген, циано, гидрокси, амино, нитро и замещенный 1-5 заместителями фенил, где заместители выбирают из группы, включающей C16алкил, С26алкеиил, C26алкинил, C16галоалкил, C16алкокси, арилокси, галоген, циано, гидрокси, амино и нитро, и если количество заместителей фенила превышает 1, то они могут быть одинаковыми или различными, причем, если m больше 1, то заместители R5 могут быть одинаковыми или различными;R 5 is a substituent selected from the group consisting of C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, aryloxy, halogen, cyano , hydroxy, amino, nitro, and phenyl substituted with 1-5 substituents, where the substituents are selected from the group consisting of C 1 -C 6 alkyl, C 2 -C 6 alkeyyl, C 2 -C 6 alkynyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, aryloxy, halogen, cyano, hydroxy, amino and nitro, and if the number of phenyl substituents exceeds 1, then they can be the same or different, and if m is greater than 1, then the substituents R 5 can be the same or different; R6 обозначает C16алкил, фенил или бензил;R 6 is C 1 -C 6 alkyl, phenyl or benzyl; R7 и R8 независимо друг от друга обозначают водород или C16алкил;R 7 and R 8 are independently hydrogen or C 1 -C 6 alkyl; m обозначает 1,2 или 3; иm is 1,2 or 3; and n обозначает 0 или 1.n is 0 or 1.
2. Способ получения соединений формулы I по п.1, заключающийся в том, что соединение формулы2. A method of obtaining compounds of formula I according to claim 1, which consists in the fact that the compound of the formula
Figure 00000002
Figure 00000002
которое является известным или которое можно получать аналогично соответствующим известным соединениям, и в котором R1, R2, X1 и Х2 имеют значения, указанные для формулы I, подвергают взаимодействию с соединением формулыwhich is known or which can be obtained analogously to the corresponding known compounds, and in which R 1 , R 2 , X 1 and X 2 have the meanings indicated for formula I, are reacted with a compound of the formula
Figure 00000003
Figure 00000003
которое является известным или которое можно получать аналогично соответствующим известным соединениям, и в котором Х3, R3, R4, R5, m, n и Q имеют значения, указанные для формулы I, a Z обозначает уходящую группу, необязательно в присутствии основного катализатора и необязательно полученное в результате этого процесса или каким-либо иным путем соединение формулы I или его энантиомер превращают в другое соединение формулы I или его энантиомер, смесь энантиомеров, которая может быть получена в результате этого процесса, разделяют и выделяют требуемый энантиомер.which is known or which can be prepared analogously to the corresponding known compounds, and in which X 3 , R 3 , R 4 , R 5 , m, n and Q have the meanings indicated for formula I, and Z represents a leaving group, optionally in the presence of a basic the catalyst and optionally obtained as a result of this process or in any other way, the compound of formula I or its enantiomer is converted into another compound of formula I or its enantiomer, the mixture of enantiomers that can be obtained from this process is separated and isolated uemy enantiomer.
3. Композиция для борьбы с вредителями, которая включает в качестве действующего вещества по меньшей мере одно соединение формулы I по п.1 в сочетании с носителями и/или диспергирующими агентами.3. A pest control composition that includes, as an active substance, at least one compound of formula I according to claim 1 in combination with carriers and / or dispersing agents. 4. Применение соединений формулы I по п.1 для борьбы с вредителями.4. The use of compounds of formula I according to claim 1 for pest control. 5. Способ борьбы с вредителями, заключающийся в том, что эффективным в качестве пестицида количеством по меньшей мере одного соединения формулы I по п.1 обрабатывают вредителей или их места обитания.5. A method of controlling pests, which consists in treating pests or their habitat with an effective amount of at least one compound of formula I according to claim 1 as an pesticide. 6. Применение соединения формулы I по п.1 в способе борьбы с паразитами теплокровных животных.6. The use of the compounds of formula I according to claim 1 in a method for controlling parasites of warm-blooded animals. 7. Применение соединения формулы I по п.1 для приготовления фармацевтической композиции, предназначенной для борьбы с паразитами.7. The use of the compounds of formula I according to claim 1 for the preparation of a pharmaceutical composition for controlling parasites.
RU2002116255/04A 1999-11-18 2000-11-16 Aminoheterocyclamide derivatives eliciting pesticide activity RU2259370C2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH210799 1999-11-18
CH2107/99 1999-11-18

Publications (2)

Publication Number Publication Date
RU2002116255A true RU2002116255A (en) 2003-12-20
RU2259370C2 RU2259370C2 (en) 2005-08-27

Family

ID=4226042

Family Applications (1)

Application Number Title Priority Date Filing Date
RU2002116255/04A RU2259370C2 (en) 1999-11-18 2000-11-16 Aminoheterocyclamide derivatives eliciting pesticide activity

Country Status (12)

Country Link
EP (1) EP1230239A1 (en)
JP (1) JP2003514816A (en)
KR (1) KR20020058023A (en)
CN (1) CN1384832A (en)
AU (1) AU764228B2 (en)
BR (1) BR0015671A (en)
CA (1) CA2386318A1 (en)
MX (1) MXPA02005023A (en)
NZ (1) NZ518376A (en)
RU (1) RU2259370C2 (en)
WO (1) WO2001036415A1 (en)
ZA (1) ZA200203861B (en)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2010601A (en) * 1999-12-16 2001-07-03 Novartis Ag Organic compounds
US6667326B1 (en) * 2000-11-16 2003-12-23 Novartis Animal Health Us, Inc. Pesticidal aminoheterocyclamide compounds
US7196106B2 (en) 2002-11-05 2007-03-27 Merck & Co., Inc Cyanothiophene derivatives, compositions containing such compounds and methods of use
PT1585739E (en) * 2003-01-06 2011-05-13 Lilly Co Eli Substituted arylcyclopropylacetamides as glucokinase activators
JP5208411B2 (en) 2003-02-06 2013-06-12 ドムペ・ファ.ル.マ・ソチエタ・ペル・アツィオーニ 2-Aryl-acetic acid, derivatives thereof, and pharmaceutical compositions containing them
ES2791303T3 (en) * 2004-01-30 2020-11-03 Vertex Pharma ATP-binding cassette transporter modulators intermediate
JP5491871B2 (en) 2007-02-28 2014-05-14 アドビナス セラピュティックス プライベート リミテッド 2,2,2-Trisubstituted acetamide derivatives as glucokinase activators, methods and pharmaceutical applications thereof
UA115126C2 (en) * 2011-07-12 2017-09-25 ДАУ АГРОСАЙЄНСІЗ ЕлЕлСі Pesticidal compositions and processes related thereto
US8987465B2 (en) 2011-11-04 2015-03-24 Syngenta Participation Ag Pesticidal compounds
EP2878339A1 (en) 2013-12-02 2015-06-03 Siena Biotech S.p.A. SIP3 antagonists
WO2017040742A1 (en) * 2015-09-04 2017-03-09 Dow Agrosciences Llc Molecules having pesticidal utility, and intermediates, compositions, and processes, related thereto
WO2019226213A2 (en) 2018-03-08 2019-11-28 Incyte Corporation AMINOPYRAZINE DIOL COMPOUNDS AS PI3K-y INHIBITORS
WO2020010003A1 (en) 2018-07-02 2020-01-09 Incyte Corporation AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS
WO2022194841A1 (en) 2021-03-19 2022-09-22 Bayer Aktiengesellschaft Substituted 1,2,4-thiadiazoles, salts thereof and their use as herbicidally active substances
WO2022194842A1 (en) 2021-03-19 2022-09-22 Bayer Aktiengesellschaft Substituted 1,2,4-thiadiazoles, salts thereof and their use as herbicidally active substances
WO2022194843A1 (en) 2021-03-19 2022-09-22 Bayer Aktiengesellschaft Substituted 1,2,4-thiadiazoles, salts thereof and their use as herbicidally active substances
WO2023020963A1 (en) 2021-08-17 2023-02-23 Bayer Aktiengesellschaft Substituted 1,2,4-thiadiazolyl nicotinamides, salts or n-oxides thereof and their use as herbicidally active substances
WO2023020962A1 (en) 2021-08-17 2023-02-23 Bayer Aktiengesellschaft Substituted 1,2,4-thiadiazolyl nicotinamides, salts or n-oxides thereof and their use as herbicidally active substances
CN118159536A (en) 2021-08-17 2024-06-07 拜耳公司 Substituted 1,2, 4-thiadiazolyl nicotinamide, salts or N-oxides thereof and their use as herbicidal active substances
EP4238973A1 (en) 2022-03-04 2023-09-06 Bayer AG Substituted 1,2,4-thiadiazolyl isonicotinamides, salts or n-oxides thereof and their use as herbicidally active substances
EP4238972A1 (en) 2022-03-04 2023-09-06 Bayer AG Substituted 1,2,4-thiadiazolyl picolinamides, salts or n-oxides thereof and their use as herbicidally active substances

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5399564A (en) * 1991-09-03 1995-03-21 Dowelanco N-(4-pyridyl or 4-quinolinyl) arylacetamide and 4-(aralkoxy or aralkylamino) pyridine pesticides
CA2189573A1 (en) * 1994-05-17 1995-11-23 Ronald E. Hackler N-(5-isothiazolyl)amide pesticides
DE19542372A1 (en) * 1995-11-14 1997-05-15 Bayer Ag Acylated 5-aminoisothiazoles
DE19601794A1 (en) * 1996-01-19 1997-07-24 Teves Gmbh Alfred Overload protection for steering column switch with automatic reset
DE19727162A1 (en) * 1997-06-26 1999-01-07 Bayer Ag Substituted amino heterocyclylamides
DE19736545A1 (en) * 1997-08-22 1999-02-25 Bayer Ag New acylated 5-amino-isothiazole derivatives

Similar Documents

Publication Publication Date Title
RU2002116255A (en) Aminoheterocycclamide derivatives with pesticidal activity
RU2222536C2 (en) Derivatives of pyrimidinylbenzimidazole and triazinylbenzimidazole and fungicide comprising thereof for agriculture/horticulture
RU2002117428A (en) Aminoheterocyclamides as pesticides and antiparasitic agents
RU2002116224A (en) N-heteroaryl-alpha-alkoxyminocarbosamides with pesticidal activity
RU2003122196A (en) ORGANIC COMPOUNDS
RU2221778C2 (en) N-sulfonylglycinealkynyloxyphenethylamide derivatives eliciting bactericidal activity
KR880002853A (en) Disinfectant
ATE106392T1 (en) ARYLPYRROLS AS INSECTICIDES, ACARICIDES AND NEMATICIDES AND PROCESSES FOR THEIR MANUFACTURE.
RU93049322A (en) OXADIASINE DERIVATIVES
RU99104181A (en) CARBANILIDES AS A MEANS FOR COMBATING PERSONS
RU2000124062A (en) Derivatives of 2-pyridylmethylamine, suitable as fungicides
RU2003124076A (en) PHARMACEUTICAL COMPOSITION CONTAINING DERIVATIVES OF AMINOACETONITRID AND ITS APPLICATION IN PREPARATION OF PHARMACEUTICAL COMPOSITION FOR THE PROCESSING OF ENDOPARASITAL PESTS IN ANIMALS
JP2004521097A5 (en)
RU2004114240A (en) ORGANIC COMPOUNDS
EP0269363A3 (en) Amino-alkylated hydroxy compounds and their use as fungicides
RU2004120790A (en) AMINOACETONITRIL DERIVATIVES AND THEIR APPLICATION FOR STRUGGLE AGAINST PARASITES
RU2005101203A (en) N-SULFONILAMINOACETONITRILES WITH PESTICIDAL PROPERTIES
RU2004137655A (en) N-Acylamino-acetonitrile derivatives and their use for controlling parasites
KR920006348A (en) Picoline oxide and preparation method thereof
RU2004137657A (en) ORGANIC COMPOUNDS
RU2004125858A (en) AMIDOACETONITRIL DERIVATIVES
RU97121852A (en) DERIVATIVES OF PHENILALKANAMIDES AND AGRICULTURAL AND GARDEN FUNGICIDES
JPS5419943A (en) Urea or thiourea compounds, their preparation, and agricultural and horticultural fungicides comprising them as active constituents
ATE129237T1 (en) 3,3-BIS(ALKYLTHIO>-2-PYRIDYLACRYLIC ACID DERIVATIVES AS FUNGICIDES.
RU2003134179A (en) ORGANIC COMPOUNDS