PH26301A - N-phenylalkylbenzamide fungicides - Google Patents

N-phenylalkylbenzamide fungicides Download PDF

Info

Publication number: PH26301A
Authority: PH; Philippines
Prior art keywords: compound; test; composition; chloro; disease
Prior art date: 1987-10-26

Application number

PH37724A

Other languages

English (en)

Inventor

Wendell Ray Arnold

James David Davenport

Original Assignee

Lilly Co Eli

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.)

1987-10-26

Filing date

1988-10-26

Publication date

1992-04-29

1988-10-26 Application filed by Lilly Co Eli filed Critical Lilly Co Eli

1992-04-29 Publication of PH26301A publication Critical patent/PH26301A/en

Links

239000000417 fungicide Substances 0.000 title claims abstract description 21
150000001875 compounds Chemical class 0.000 claims abstract description 160
239000000203 mixture Substances 0.000 claims description 67
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230000000694 effects Effects 0.000 claims description 35
SAPGTCDSBGMXCD-UHFFFAOYSA-N (2-chlorophenyl)-(4-fluorophenyl)-pyrimidin-5-ylmethanol Chemical compound C=1N=CN=CC=1C(C=1C(=CC=CC=1)Cl)(O)C1=CC=C(F)C=C1 SAPGTCDSBGMXCD-UHFFFAOYSA-N 0.000 claims description 31
238000000034 method Methods 0.000 claims description 31
KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 25
230000000855 fungicidal effect Effects 0.000 claims description 20
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 9
239000005747 Chlorothalonil Substances 0.000 claims description 8
125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 8
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 8
CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical group ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 7
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 7
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238000010410 dusting Methods 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
OYFJQPXVCSSHAI-QFPUQLAESA-N enalapril maleate Chemical compound OC(=O)\C=C/C(O)=O.C([C@@H](C(=O)OCC)N[C@@H](C)C(=O)N1[C@@H](CCC1)C(O)=O)CC1=CC=CC=C1 OYFJQPXVCSSHAI-QFPUQLAESA-N 0.000 description 1
229940117927 ethylene oxide Drugs 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
125000001207 fluorophenyl group Chemical group 0.000 description 1
FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 1
239000003517 fume Substances 0.000 description 1
244000053095 fungal pathogen Species 0.000 description 1
239000000499 gel Substances 0.000 description 1
230000002068 genetic effect Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
208000037824 growth disorder Diseases 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
238000005984 hydrogenation reaction Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
208000006278 hypochromic anemia Diseases 0.000 description 1
239000011872 intimate mixture Substances 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
235000019357 lignosulphonate Nutrition 0.000 description 1
235000011475 lollipops Nutrition 0.000 description 1
YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 1
229920000940 maneb Polymers 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
230000010534 mechanism of action Effects 0.000 description 1
WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
230000036651 mood Effects 0.000 description 1
NWJUMMHVDMNYMJ-UHFFFAOYSA-N n-benzyl-1,1,1-trifluoromethanamine Chemical compound FC(F)(F)NCC1=CC=CC=C1 NWJUMMHVDMNYMJ-UHFFFAOYSA-N 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
229920001206 natural gum Polymers 0.000 description 1
230000017074 necrotic cell death Effects 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
231100000956 nontoxicity Toxicity 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
150000007530 organic bases Chemical class 0.000 description 1
QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 description 1
125000004344 phenylpropyl group Chemical group 0.000 description 1
150000004885 piperazines Chemical class 0.000 description 1
244000000003 plant pathogen Species 0.000 description 1
238000012809 post-inoculation Methods 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
150000003230 pyrimidines Chemical class 0.000 description 1
UKHVLWKBNNSRRR-TYYBGVCCSA-M quaternium-15 Chemical compound [Cl-].C1N(C2)CN3CN2C[N+]1(C/C=C/Cl)C3 UKHVLWKBNNSRRR-TYYBGVCCSA-M 0.000 description 1
239000002516 radical scavenger Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
239000011435 rock Substances 0.000 description 1
238000013207 serial dilution Methods 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
235000019333 sodium laurylsulphate Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000011877 solvent mixture Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
235000020354 squash Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
238000010998 test method Methods 0.000 description 1
239000012085 test solution Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 1
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
238000010792 warming Methods 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/66—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C259/00—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups
- C07C259/12—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines
- C07C259/18—Compounds containing carboxyl groups, an oxygen atom of a carboxyl group being replaced by a nitrogen atom, this nitrogen atom being further bound to an oxygen atom and not being part of nitro or nitroso groups with replacement of the other oxygen atom of the carboxyl group by nitrogen atoms, e.g. N-hydroxyamidines having carbon atoms of hydroxamidine groups bound to carbon atoms of six-membered aromatic rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Dentistry (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

PH37724A 1987-10-26 1988-10-26 N-phenylalkylbenzamide fungicides PH26301A (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US11265787A	1987-10-26	1987-10-26

Publications (1)

Publication Number	Publication Date
PH26301A true PH26301A (en)	1992-04-29

Family

ID=22345154

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
PH37724A PH26301A (en)	1987-10-26	1988-10-26	N-phenylalkylbenzamide fungicides

Country Status (18)

Country	Link
EP (1)	EP0314422B1 (de)
JP (1)	JPH01151546A (de)
KR (1)	KR890006573A (de)
CN (1)	CN1033797A (de)
AT (1)	ATE92040T1 (de)
AU (1)	AU618560B2 (de)
BR (1)	BR8805502A (de)
CA (1)	CA1301188C (de)
DE (1)	DE3882646T2 (de)
DK (1)	DK592688A (de)
ES (1)	ES2058308T3 (de)
HU (1)	HUT49847A (de)
IL (1)	IL88133A0 (de)
NZ (1)	NZ226693A (de)
PH (1)	PH26301A (de)
PT (1)	PT88846B (de)
SU (1)	SU1760983A3 (de)
ZA (1)	ZA887978B (de)

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* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW575562B (en) *	1998-02-19	2004-02-11	Agrevo Uk Ltd	Fungicides
DE19931116A1 (de) *	1999-07-06	2001-01-11	Bayer Ag	Verfahren zur Herstellung von Phenethylaminen und neue chemische Verbindungen
TW200306155A (en) *	2002-03-19	2003-11-16	Du Pont	Benzamides and advantageous compositions thereof for use as fungicides
WO2006117356A1 (en) *	2005-05-03	2006-11-09	Bayer Cropscience Sa	New heterocyclylethylbenzamide derivatives
TWI435863B (zh)	2006-03-20	2014-05-01	Nihon Nohyaku Co Ltd	Ｎ-２-（雜）芳基乙基甲醯胺衍生物及含該衍生物之蟲害防治劑
JP5339055B2 (ja) *	2006-06-13	2013-11-13	日産化学工業株式会社	水性懸濁状農薬組成物
WO2008101975A2 (en) *	2007-02-22	2008-08-28	Bayer Cropscience Sa	New n-(3-phenylpropyl)benzamide derivatives
KR101604150B1 (ko)	2008-06-26	2016-03-16	노벨파마 컴퍼니 리미티드	고막 또는 외이도 재생제
KR101856577B1 (ko)	2011-03-02	2018-05-10	고쿠리츠다이가쿠호우진 도쿄다이가쿠	내부 기생충 방제제
WO2014034751A1 (ja)	2012-08-30	2014-03-06	国立大学法人東京大学	内部寄生虫防除剤及びその使用方法
CN106963760A (zh)	2012-08-30	2017-07-21	国立大学法人东京大学	体内寄生虫防治剂在制备防治体内寄生虫的药物中的用途
CN102827022A (zh) *	2012-09-21	2012-12-19	西华大学	2-乙酰氧基-n-(4-甲氧基苯基)苯甲酰胺及其制备方法和用途
KR20150135332A (ko)	2013-03-14	2015-12-02	더 보드 오브 트러스티스 오브 더 리랜드 스탠포드 쥬니어 유니버시티	미토콘드리아 알데히드 탈수소효소-2 조절인자들 및 이들의 사용 방법
BR112016017613A2 (pt)	2014-03-05	2020-11-03	The University Of Tokyo	Agente e método de controle de endoparasita, derivado de carboxamida e seu uso

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Publication number	Priority date	Publication date	Assignee	Title
FR1581075A (de) *	1968-07-15	1969-09-12
MC1329A1 (fr) *	1979-05-17	1981-04-21	Wellcome Found	Aryloxy-et arylamino-alcane-thiocarboxamides,leur preparation et leur application en tant que matieres actives de produits pesticides
US4835181A (en) *	1987-02-18	1989-05-30	Eli Lilly And Company	Anticonvulsant agents using cyano dimethylphenyl benzamides
EP0324521A3 (de) *	1988-01-11	1991-11-27	Duphar International Research B.V	Methode zur Behandlung hämatologischer Krankheiten und dafür anzuwendende pharmazeutische Zusammensetzungen

1988
- 1988-10-24 KR KR1019880013849A patent/KR890006573A/ko not_active Withdrawn
- 1988-10-24 IL IL88133A patent/IL88133A0/xx unknown
- 1988-10-25 BR BR8805502A patent/BR8805502A/pt not_active Application Discontinuation
- 1988-10-25 EP EP88309998A patent/EP0314422B1/de not_active Expired - Lifetime
- 1988-10-25 DK DK592688A patent/DK592688A/da not_active Application Discontinuation
- 1988-10-25 AU AU24314/88A patent/AU618560B2/en not_active Ceased
- 1988-10-25 DE DE88309998T patent/DE3882646T2/de not_active Expired - Fee Related
- 1988-10-25 ZA ZA887978A patent/ZA887978B/xx unknown
- 1988-10-25 AT AT88309998T patent/ATE92040T1/de not_active IP Right Cessation
- 1988-10-25 PT PT88846A patent/PT88846B/pt not_active IP Right Cessation
- 1988-10-25 ES ES88309998T patent/ES2058308T3/es not_active Expired - Lifetime
- 1988-10-25 CA CA000581224A patent/CA1301188C/en not_active Expired - Lifetime
- 1988-10-25 NZ NZ226693A patent/NZ226693A/en unknown
- 1988-10-25 HU HU885583A patent/HUT49847A/hu unknown
- 1988-10-25 SU SU884356787A patent/SU1760983A3/ru active
- 1988-10-26 JP JP63270615A patent/JPH01151546A/ja active Pending
- 1988-10-26 PH PH37724A patent/PH26301A/en unknown
- 1988-10-26 CN CN88107356A patent/CN1033797A/zh active Pending

Also Published As

Publication number	Publication date
IL88133A0 (en)	1989-06-30
ES2058308T3 (es)	1994-11-01
AU618560B2 (en)	1992-01-02
BR8805502A (pt)	1989-07-04
NZ226693A (en)	1990-12-21
JPH01151546A (ja)	1989-06-14
CN1033797A (zh)	1989-07-12
PT88846B (pt)	1993-01-29
CA1301188C (en)	1992-05-19
EP0314422B1 (de)	1993-07-28
EP0314422A2 (de)	1989-05-03
ATE92040T1 (de)	1993-08-15
AU2431488A (en)	1989-04-27
HUT49847A (en)	1989-11-28
DE3882646D1 (de)	1993-09-02
KR890006573A (ko)	1989-06-14
EP0314422A3 (de)	1991-02-06
SU1760983A3 (ru)	1992-09-07
DK592688A (da)	1989-04-27
DK592688D0 (da)	1988-10-25
DE3882646T2 (de)	1994-04-28
ZA887978B (en)	1989-08-30

Publication	Publication Date	Title
KR0129754B1 (ko)	1998-04-09	퀴나졸린 유도체
JP3242140B2 (ja)	2001-12-25	ジヒドロピリダジノン類および／またはピリダジノン類と殺菌剤との組み合わせ組成物
HK21394A (en)	1994-03-18	Pesticide
PH26301A (en)	1992-04-29	N-phenylalkylbenzamide fungicides
US4957533A (en)	1990-09-18	N-phenylalkylbenzamide fungicides
DE2734365A1 (de)	1978-02-09	Heterocyclische verbindungen, verfahren zu ihrer herstellung und diese verbindungen enthaltende fungizide zusammensetzungen
US4113465A (en)	1978-09-12	Herbicidal formulations
US4250179A (en)	1981-02-10	Metal complex imidazole fungicides, and methods of controlling fungi with them
JPH058161B2 (de)	1993-02-01
AU596436B2 (en)	1990-05-03	Novel fungicidal compositions
US5041154A (en)	1991-08-20	Benzoxazine compounds useful as herbicides
JP2832482B2 (ja)	1998-12-09	殺虫殺菌剤組成物
US4906650A (en)	1990-03-06	N-sulphenylated 2-amino-4-chloro-thiazole-sulphonamides, their use, process for their preparation, and the intermediates 2,4-dichlorothiazole-sulphonyl chloride and 2-amino-4-chloro-thiazole-sulphonamides
AU619934B2 (en)	1992-02-06	Substituted guanidine and amidine compounds, their production and fungicidal use
CS195717B2 (en)	1980-02-29	Herbicide and method of producing the same
US4879314A (en)	1989-11-07	Dihaloformaldoxime
WO2021053136A1 (en)	2021-03-25	Method for controlling fungus
US4767446A (en)	1988-08-30	Trifluoromethanesulfonanilides, and their production and use
US3352750A (en)	1967-11-14	Alkyl-substituted-benzoquinone-4-oximinyl nu-alkyl carbamates and use as fungicides
JP2901667B2 (ja)	1999-06-07	農園芸用殺菌剤組成物
AU616223B2 (en)	1991-10-24	2-cyano-2-aryl-1-(azole-1-yl)- ethane derivatives
US4767443A (en)	1988-08-30	Antifungal and antibacterial diazine derivatives compositions, intermediates, and method of use therefor
JPS63150204A (ja)	1988-06-22	農業用の殺虫殺菌組成物
US4228178A (en)	1980-10-14	Combating fungi with novel N-sulphenylated carbamoyl compounds
JPH04178363A (ja)	1992-06-25	尿素誘導体及びそれを含有する有害生物防除剤