RU2547721C2 - ТИАЗОЛО [5, 4-d] ПИРИМИДИНЫ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ АГРОХИМИЧЕСКИХ СРЕДСТВ - Google Patents
ТИАЗОЛО [5, 4-d] ПИРИМИДИНЫ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ АГРОХИМИЧЕСКИХ СРЕДСТВ Download PDFInfo
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- RU2547721C2 RU2547721C2 RU2012133570/13A RU2012133570A RU2547721C2 RU 2547721 C2 RU2547721 C2 RU 2547721C2 RU 2012133570/13 A RU2012133570/13 A RU 2012133570/13A RU 2012133570 A RU2012133570 A RU 2012133570A RU 2547721 C2 RU2547721 C2 RU 2547721C2
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- Prior art keywords
- lower alkyl
- compound
- species
- phenyl
- halogen
- Prior art date
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- LICQIAOGSISXOZ-UHFFFAOYSA-N tert-butyl-[2-(4-hydroxyphenyl)ethyl]carbamic acid Chemical compound CC(C)(C)N(C(O)=O)CCC1=CC=C(O)C=C1 LICQIAOGSISXOZ-UHFFFAOYSA-N 0.000 description 1
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- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
-
- 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
- A61K31/425—Thiazoles
- A61K31/429—Thiazoles condensed with heterocyclic ring systems
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/04—Antibacterial agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (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)
- Epidemiology (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US29301410P | 2010-01-07 | 2010-01-07 | |
US61/293,014 | 2010-01-07 | ||
PCT/US2011/020351 WO2011085084A1 (en) | 2010-01-07 | 2011-01-06 | THIAZOLO[5,4-d] PYRIMIDINES AND THEIR USE AS AGROCHEMICALS |
Publications (2)
Publication Number | Publication Date |
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RU2012133570A RU2012133570A (ru) | 2014-02-20 |
RU2547721C2 true RU2547721C2 (ru) | 2015-04-10 |
Family
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2012133570/13A RU2547721C2 (ru) | 2010-01-07 | 2011-01-06 | ТИАЗОЛО [5, 4-d] ПИРИМИДИНЫ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ АГРОХИМИЧЕСКИХ СРЕДСТВ |
Country Status (18)
Cited By (2)
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RU2837648C1 (ru) * | 2020-02-11 | 2025-04-02 | Сингента Кроп Протекшн Аг | Способ контроля грибов |
US12317896B2 (en) | 2020-02-11 | 2025-06-03 | Syngenta Crop Protection Ag | Method of controlling fungi |
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NZ597050A (en) | 2009-06-29 | 2014-02-28 | Incyte Corp | Pyrimidinones as pi3k inhibitors |
US9056877B2 (en) | 2011-07-19 | 2015-06-16 | Infinity Pharmaceuticals, Inc. | Heterocyclic compounds and uses thereof |
JPWO2013031694A1 (ja) * | 2011-08-26 | 2015-03-23 | 富山化学工業株式会社 | アミン化合物またはその塩 |
ES2722524T3 (es) | 2011-09-02 | 2019-08-13 | Incyte Holdings Corp | Heterociclaminas como inhibidores de pi3k |
US9055750B2 (en) | 2012-02-03 | 2015-06-16 | Basf Se | Fungicidal pyrimidine compounds |
US9072301B2 (en) | 2012-02-03 | 2015-07-07 | Basf Se | Fungicidal pyrimidine compounds |
WO2013135672A1 (en) | 2012-03-13 | 2013-09-19 | Basf Se | Fungicidal pyrimidine compounds |
AR090548A1 (es) | 2012-04-02 | 2014-11-19 | Incyte Corp | Azaheterociclobencilaminas biciclicas como inhibidores de pi3k |
CN103668956B (zh) * | 2012-09-21 | 2015-08-12 | 上海韬鸿化工科技有限公司 | 防螨虫整理剂、织物的防螨虫整理方法及防螨虫织物 |
EP3409115A3 (en) * | 2013-03-15 | 2019-02-27 | The Regents of The University of California | Methods for identifying arthropod repellents, and compounds and compositions identified by such methods |
US10077277B2 (en) * | 2014-06-11 | 2018-09-18 | Incyte Corporation | Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors |
CN105594748A (zh) * | 2014-10-15 | 2016-05-25 | 浙江新安化工集团股份有限公司 | 一种精准定向、高效的防治鳞翅目害虫的杀虫组合物及其使用方法 |
CN104391070B (zh) * | 2014-12-05 | 2016-06-08 | 山东省城市供排水水质监测中心 | 一种水中烷基汞的检测方法 |
BR122021004509B1 (pt) | 2015-02-27 | 2023-11-07 | Incyte Holdings Corporation | Sais de inibidor de pi3k e processos para seu preparo |
EP3270692A4 (en) | 2015-03-18 | 2019-02-13 | The Regents of the University of California | CHEMICALS FOR PROTECTION AGAINST BRANCHES |
WO2016183063A1 (en) | 2015-05-11 | 2016-11-17 | Incyte Corporation | Crystalline forms of a pi3k inhibitor |
CN105606755A (zh) * | 2016-01-30 | 2016-05-25 | 郭庆龙 | 一种胺苯吡唑酮残留量的gc-nci-ms测定方法 |
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WO2018190350A1 (ja) | 2017-04-10 | 2018-10-18 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
US11000038B2 (en) | 2017-04-10 | 2021-05-11 | Mitsui Chemicals Agro, Inc. | Pyridone compounds and agricultural and horticultural fungicides containing the same as active ingredients |
KR102498819B1 (ko) | 2017-04-11 | 2023-02-10 | 미쓰이가가쿠 아그로 가부시키가이샤 | 피리돈 화합물 및 그것을 유효성분으로 하는 농원예용 살균제 |
US11117863B2 (en) | 2017-06-08 | 2021-09-14 | Mitsui Chemicals Agro, Inc. | Pyridone compounds and agricultural and horticultural fungicides containing the same as active ingredients |
AU2019277560B2 (en) | 2018-06-01 | 2025-04-24 | Incyte Corporation | Dosing regimen for the treatment of PI3K related disorders |
WO2020022412A1 (ja) | 2018-07-25 | 2020-01-30 | 三井化学アグロ株式会社 | ピリドン化合物およびそれを有効成分とする農園芸用殺菌剤 |
CN112010848B (zh) * | 2020-09-29 | 2021-12-24 | 南通大学 | 含三氟甲基吡啶联芳氧基结构的1,3,4-噁二唑类化合物的制备方法和应用 |
CN116250525B (zh) * | 2023-03-08 | 2024-12-24 | 内蒙古民族大学 | 一种小型哺乳类剥制标本安全防腐剂及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5962489A (en) * | 1992-07-16 | 1999-10-05 | Basf Aktiengesellschaft | Heteroaromatic compounds and crop protection agents containing them |
RU2351132C2 (ru) * | 2001-01-31 | 2009-04-10 | Байер Кропсайенс Аг | Комбинация гербицид - антидот и способ уничтожения сорняков в посевах полезных растений |
Family Cites Families (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3309359A (en) * | 1965-10-22 | 1967-03-14 | Hoffmann La Roche | N-mono-acyl-5-fluorocytosine derivatives and process |
US3368938A (en) * | 1966-01-13 | 1968-02-13 | Hoffmann La Roche | Controlling fungi with 5-fluorocytosine |
US3868373A (en) * | 1970-01-27 | 1975-02-25 | Hoffmann La Roche | 4-Amino-5-fluoro-2-tri(lower alkyl) silyloxypyrimidines |
CH579057A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-09-07 | 1976-08-31 | Hoffmann La Roche | |
FR2530636A1 (fr) | 1982-07-23 | 1984-01-27 | Rhone Poulenc Agrochimie | Nouveaux derives de la tetrahydro-2,3,6,7 5h-thiazolo (3,2-a) pyrimidine, leur preparation et leur utilisation comme herbicides |
GR80171B (en) | 1983-08-29 | 1985-01-02 | Ciba Geigy Ag | N-(2-nitrophenyl)-4-aminopyrimidine derivatives process for the preparation thereof and use |
US4845081A (en) * | 1984-10-18 | 1989-07-04 | University Of Florida | Aminomethyl derivatives of biologically active substances, and enhanced delivery thereof across topical membranes |
DE58908159D1 (de) | 1988-03-09 | 1994-09-15 | Ciba Geigy Ag | Mittel zum Schutz von Pflanzen gegen Krankheiten. |
DE3821711A1 (de) * | 1988-06-28 | 1990-02-08 | Bayer Ag | Thiazolopyrimidin-derivate, verfahren zu ihrer herstellung und ihre verwendung als schaedlingsbekaempfungsmittel |
US5034393A (en) | 1989-07-27 | 1991-07-23 | Dowelanco | Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives |
JP3109012B2 (ja) * | 1992-06-18 | 2000-11-13 | クミアイ化学工業株式会社 | チアゾロ[5,4−d]ピリミジン誘導体及び農園芸用殺菌剤 |
US5326766A (en) * | 1992-08-19 | 1994-07-05 | Dreikorn Barry A | 4-(2-(4-(2-pyridinyloxy)phenyl)ethoxy)quinazoline and analogues thereof |
AU6478396A (en) * | 1995-07-05 | 1997-02-05 | E.I. Du Pont De Nemours And Company | Fungicidal pyrimidinones |
PL328777A1 (en) | 1996-03-11 | 1999-02-15 | Novartis Ag | Pesticides |
HRP970239B1 (en) | 1997-05-09 | 2004-04-30 | Inst Ru Er Bouekovic | Process for the preparation of sulfonyl-pyrimidine derivatives with antitumor activity |
GT199900185A (es) * | 1998-11-06 | 2001-04-18 | Novedosa pirimidin-4-enamina como fungicida. | |
US6448262B1 (en) * | 1998-11-16 | 2002-09-10 | American Cyanamid Company | Pesticidal and parasiticidal use of 2-(substituted thio) thiazolo-[4,5-b]pyridine compounds |
US7914799B2 (en) * | 2001-08-27 | 2011-03-29 | Immunitor USA, Inc. | Anti-fungal composition |
ATE363829T1 (de) * | 2001-09-10 | 2007-06-15 | Basf Ag | Pestizide und parasitizide di- und trifluorsubstituierte alkenverbindungen |
WO2005095419A1 (ja) | 2004-04-01 | 2005-10-13 | Takeda Pharmaceutial Company Limited | チアゾロピリミジン誘導体 |
EP1937691A1 (en) | 2005-10-21 | 2008-07-02 | Dow Agrosciences LLC | Thieno-pyrimidine compounds having fungicidal activity |
EP2044086A2 (en) * | 2006-06-30 | 2009-04-08 | Janssen Pharmaceutica N.V. | Thiazolopyrimidine modulators of trpv1 |
EP2562164A1 (en) | 2008-01-22 | 2013-02-27 | Dow AgroSciences LLC | 5-fluoro pyrimidine derivatives as fungicides |
CN102215691B (zh) | 2008-08-01 | 2015-02-04 | 陶氏益农公司 | 5-氟胞嘧啶作为杀真菌剂的用途 |
USRE46144E1 (en) | 2009-01-23 | 2016-09-13 | Purdue Pharmaceutical Products L.P. | Hydroxamic acid derivatives |
CN101613362B (zh) * | 2009-07-31 | 2011-11-16 | 南京工业大学 | 3-羰基-6-乙氧甲酰基-噻唑并嘧啶类化合物及其合成方法和用途 |
CN102574831B (zh) * | 2009-08-07 | 2014-12-10 | 陶氏益农公司 | N1-磺酰基-5-氟代嘧啶酮衍生物 |
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Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5962489A (en) * | 1992-07-16 | 1999-10-05 | Basf Aktiengesellschaft | Heteroaromatic compounds and crop protection agents containing them |
RU2351132C2 (ru) * | 2001-01-31 | 2009-04-10 | Байер Кропсайенс Аг | Комбинация гербицид - антидот и способ уничтожения сорняков в посевах полезных растений |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2837648C1 (ru) * | 2020-02-11 | 2025-04-02 | Сингента Кроп Протекшн Аг | Способ контроля грибов |
US12317896B2 (en) | 2020-02-11 | 2025-06-03 | Syngenta Crop Protection Ag | Method of controlling fungi |
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EP2521452A1 (en) | 2012-11-14 |
JP2013516476A (ja) | 2013-05-13 |
CO6612238A2 (es) | 2013-02-01 |
CA2786250A1 (en) | 2011-07-14 |
UA109780C2 (uk) | 2015-10-12 |
IN2012DN06323A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 2015-10-02 |
PT2521452E (pt) | 2015-02-24 |
ZA201204871B (en) | 2013-09-25 |
CL2012001851A1 (es) | 2012-12-14 |
ES2529247T3 (es) | 2015-02-18 |
RU2012133570A (ru) | 2014-02-20 |
HK1176236A1 (en) | 2013-07-26 |
CN102791135A (zh) | 2012-11-21 |
KR20120115538A (ko) | 2012-10-18 |
US8921382B2 (en) | 2014-12-30 |
CN102791135B (zh) | 2015-05-20 |
US20110166164A1 (en) | 2011-07-07 |
PL2521452T3 (pl) | 2015-05-29 |
KR101814835B1 (ko) | 2018-01-04 |
EP2521452A4 (en) | 2013-07-03 |
EP2521452B1 (en) | 2014-12-24 |
BR112012016866A2 (pt) | 2015-09-01 |
JP5781090B2 (ja) | 2015-09-16 |
MX2012007954A (es) | 2012-08-03 |
WO2011085084A1 (en) | 2011-07-14 |
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