CH636093A5 - Mikrobizide mittel. - Google Patents

Mikrobizide mittel. Download PDF

Info

Publication number: CH636093A5
Authority: CH; Switzerland
Prior art keywords: formula; compound; halogen; hydrogen; methyl
Prior art date: 1978-01-28

Application number

CH93078A

Other languages

German (de)

English (en)

Inventor

Walter Dr Kunz

Adolf Dr Hubele

Wolfgang Dr Eckhardt

Original Assignee

Ciba Geigy Ag

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.)

1978-01-28

Filing date

1978-01-28

Publication date

1983-05-13

1978-01-28 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1978-01-28 Priority to CH93078A priority Critical patent/CH636093A5/de

1979-01-24 Priority to FR7901801A priority patent/FR2415634A1/fr

1979-01-24 Priority to NL7900565A priority patent/NL7900565A/xx

1979-01-25 Priority to DE19792902861 priority patent/DE2902861A1/de

1979-01-26 Priority to IT19650/79A priority patent/IT1109779B/it

1979-01-26 Priority to AU43699/79A priority patent/AU525223B2/en

1979-01-26 Priority to GB7902893A priority patent/GB2013201B/en

1979-01-26 Priority to AT0060279A priority patent/AT363279B/de

1979-01-26 Priority to ZA79337A priority patent/ZA79337B/xx

1979-01-26 Priority to BE0/193086A priority patent/BE873723A/fr

1979-01-26 Priority to IL56512A priority patent/IL56512A0/xx

1979-01-26 Priority to PH22127A priority patent/PH15351A/en

1979-01-27 Priority to JP865579A priority patent/JPS54109964A/ja

1983-05-13 Publication of CH636093A5 publication Critical patent/CH636093A5/de

Links

239000002855 microbicide agent Substances 0.000 title claims description 3
150000001875 compounds Chemical class 0.000 claims description 45
229910052739 hydrogen Inorganic materials 0.000 claims description 21
239000001257 hydrogen Substances 0.000 claims description 21
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 21
229910052736 halogen Inorganic materials 0.000 claims description 18
150000002367 halogens Chemical group 0.000 claims description 18
-1 2,3,6-trimethylphenyl Chemical group 0.000 claims description 17
239000000203 mixture Substances 0.000 claims description 14
239000002253 acid Substances 0.000 claims description 12
150000002431 hydrogen Chemical group 0.000 claims description 11
241000251730 Chondrichthyes Species 0.000 claims description 9
241000233866 Fungi Species 0.000 claims description 9
238000000034 method Methods 0.000 claims description 9
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
238000002360 preparation method Methods 0.000 claims description 7
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 6
229910052801 chlorine Inorganic materials 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 6
125000000350 glycoloyl group Chemical group O=C([*])C([H])([H])O[H] 0.000 claims description 6
125000004432 carbon atom Chemical group C* 0.000 claims description 5
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
125000001424 substituent group Chemical group 0.000 claims description 5
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
238000006136 alcoholysis reaction Methods 0.000 claims description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
229910052794 bromium Inorganic materials 0.000 claims description 4
239000000969 carrier Substances 0.000 claims description 4
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 4
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 3
230000010933 acylation Effects 0.000 claims description 3
238000005917 acylation reaction Methods 0.000 claims description 3
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240000008067 Cucumis sativus Species 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 2
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VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
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229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
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239000003513 alkali Substances 0.000 description 2
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235000011152 sodium sulphate Nutrition 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
SRAWNDFHGTVUNZ-UHFFFAOYSA-M sodium;3,6-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)C1=CC(CCCC)=CC2=CC(CCCC)=CC=C21 SRAWNDFHGTVUNZ-UHFFFAOYSA-M 0.000 description 1
238000009331 sowing Methods 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
230000009885 systemic effect Effects 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
125000005270 trialkylamine group Chemical group 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/26—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D307/30—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
- C07D307/32—Oxygen atoms
- C07D307/33—Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero atom

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Furan Compounds (AREA)

CH93078A 1978-01-28 1978-01-28 Mikrobizide mittel. CH636093A5 (de)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
CH93078A CH636093A5 (de)	1978-01-28	1978-01-28	Mikrobizide mittel.
FR7901801A FR2415634A1 (fr)	1978-01-28	1979-01-24	Nouvelles 3-(n-hydroxyacetyl-n-phenyl)-amino-tetrahydro-2-furanones utiles comme agents microbicides
NL7900565A NL7900565A (nl)	1978-01-28	1979-01-24	Microbicide middelen.
DE19792902861 DE2902861A1 (de)	1978-01-28	1979-01-25	Mikrobizide mittel
IT19650/79A IT1109779B (it)	1978-01-28	1979-01-26	Prodotti microbicidi e procedimento per la loro preparazione
AU43699/79A AU525223B2 (en)	1978-01-28	1979-01-26	Substituted n-acyl-amino-tetrahydro-2-furanones
GB7902893A GB2013201B (en)	1978-01-28	1979-01-26	Microbicidally active compounds
AT0060279A AT363279B (de)	1978-01-28	1979-01-26	Fungizides mittel
ZA79337A ZA79337B (en)	1978-01-28	1979-01-26	Microbicidal compositions
BE0/193086A BE873723A (fr)	1978-01-28	1979-01-26	Nouvelles lactones utiles comme agents microbicides
IL56512A IL56512A0 (en)	1978-01-28	1979-01-26	Anilide derivatives, their preparation and plant-microbicidal compositions containing them
PH22127A PH15351A (en)	1978-01-28	1979-01-26	Microbicidal compositions
JP865579A JPS54109964A (en)	1978-01-28	1979-01-27	Furanone compound*its manufacture and microbicide containing it as active component

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH93078A CH636093A5 (de)	1978-01-28	1978-01-28	Mikrobizide mittel.

Publications (1)

Publication Number	Publication Date
CH636093A5 true CH636093A5 (de)	1983-05-13

Family

ID=4198474

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH93078A CH636093A5 (de)	1978-01-28	1978-01-28	Mikrobizide mittel.

Country Status (13)

Country	Link
JP (1)	JPS54109964A (fr)
AT (1)	AT363279B (fr)
AU (1)	AU525223B2 (fr)
BE (1)	BE873723A (fr)
CH (1)	CH636093A5 (fr)
DE (1)	DE2902861A1 (fr)
FR (1)	FR2415634A1 (fr)
GB (1)	GB2013201B (fr)
IL (1)	IL56512A0 (fr)
IT (1)	IT1109779B (fr)
NL (1)	NL7900565A (fr)
PH (1)	PH15351A (fr)
ZA (1)	ZA79337B (fr)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2845454A1 (de) *	1977-11-01	1979-05-10	Chevron Res	3-(n-acyl-n-arylamino)- gamma -butyrolactone und - gamma -butyrothiolactone sowie fungizide mittel
DE3135239A1 (de) *	1981-09-05	1983-03-17	Basf Ag, 6700 Ludwigshafen	N-substituierte brenztraubensaeureamide, verfahren zu ihrer herstellung und diese enthaltende fungizide
GB0500895D0 (en)	2005-01-17	2005-02-23	Isis Innovation	Biocidal surface functionalisation
GB0616724D0 (en)	2006-08-23	2006-10-04	Isis Innovation	Surface adhesion using arylcarbene reactive intermediates
KR101753917B1 (ko)	2009-03-02	2017-07-04	옥스포드 어드밴스드 서패이시즈 리미티드	공유결합 3차원 네트워크를 형성할 수 있는 화학제
CN104206163A (zh) *	2014-09-24	2014-12-17	江苏农林职业技术学院	一种花生的栽培方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2417781A1 (de) *	1974-04-11	1975-10-30	Basf Ag	Glykolsaeureanilid-n-methylolaether
US4012519A (en) *	1975-02-10	1977-03-15	Chevron Research Company	Fungicidal 3-(N-acyl-N-arylamino) lactones and lactams
US3933860A (en) *	1975-02-10	1976-01-20	Chevron Research Company	3-(N-acyl-N-arylamino) lactones
US4143155A (en) *	1976-09-17	1979-03-06	Ciba-Geigy Corporation	Sulfonylglycolic anilide fungicides
US4147792A (en) *	1977-02-04	1979-04-03	Ciba-Geigy Corporation	Fungicidal compositions
DE2845454A1 (de) *	1977-11-01	1979-05-10	Chevron Res	3-(n-acyl-n-arylamino)- gamma -butyrolactone und - gamma -butyrothiolactone sowie fungizide mittel
FR2408601A1 (fr) *	1977-11-01	1979-06-08	Chevron Res	Procede d'acylation d'une aniline substituee par une lactone en l'absence d'accepteur d'acide

1978
- 1978-01-28 CH CH93078A patent/CH636093A5/de not_active IP Right Cessation
1979
- 1979-01-24 FR FR7901801A patent/FR2415634A1/fr active Granted
- 1979-01-24 NL NL7900565A patent/NL7900565A/xx not_active Application Discontinuation
- 1979-01-25 DE DE19792902861 patent/DE2902861A1/de not_active Ceased
- 1979-01-26 IL IL56512A patent/IL56512A0/xx unknown
- 1979-01-26 BE BE0/193086A patent/BE873723A/fr not_active IP Right Cessation
- 1979-01-26 AU AU43699/79A patent/AU525223B2/en not_active Ceased
- 1979-01-26 ZA ZA79337A patent/ZA79337B/xx unknown
- 1979-01-26 PH PH22127A patent/PH15351A/en unknown
- 1979-01-26 IT IT19650/79A patent/IT1109779B/it active
- 1979-01-26 AT AT0060279A patent/AT363279B/de active
- 1979-01-26 GB GB7902893A patent/GB2013201B/en not_active Expired
- 1979-01-27 JP JP865579A patent/JPS54109964A/ja active Pending

Also Published As

Publication number	Publication date
IL56512A0 (en)	1979-03-12
GB2013201A (en)	1979-08-08
GB2013201B (en)	1982-08-11
NL7900565A (nl)	1979-07-31
IT1109779B (it)	1985-12-23
AU4369979A (en)	1979-08-02
ZA79337B (en)	1980-02-27
FR2415634A1 (fr)	1979-08-24
AU525223B2 (en)	1982-10-28
FR2415634B1 (fr)	1983-02-18
BE873723A (fr)	1979-07-26
ATA60279A (de)	1980-12-15
JPS54109964A (en)	1979-08-29
DE2902861A1 (de)	1979-08-02
AT363279B (de)	1981-07-27
PH15351A (en)	1982-12-02
IT7919650A0 (it)	1979-01-26

Publication	Publication Date	Title
DE2804299A1 (de)	1978-08-10	Fungizide mittel
DE2643477C2 (fr)	1991-01-31
DE2513730C2 (de)	1987-02-12	N-(1'-Methoxycarbonyl-äthyl)-N-halogenacetyl-2-halogenaniline, Verfahren zu deren Herstellung und diese Verbindungen enthaltende fungizide Mittel
DE2741437C2 (fr)	1987-11-05
DE2813335C2 (de)	1987-04-09	N-acylierte N-Alkylaniline, Verfahren zu ihrer Herstellung sowie mikrobizide Mittel enthaltend diese als Wirkstoffe
DE2902832C2 (fr)	1989-07-13
CH623458A5 (fr)	1981-06-15
CH636093A5 (de)	1983-05-13	Mikrobizide mittel.
DE2919825C2 (fr)	1988-09-01
CH627343A5 (en)	1982-01-15	Microbicide
DE2643445C2 (de)	1987-01-29	N-Acylierte N-Phenyl-alaninthiomethylester, Verfahren zu deren Herstellung und diese enthaltende Mittel
CH635819A5 (de)	1983-04-29	Alkoxy-alkoxy-acetyl acylalanine, deren herstellung und verwendung als pflanzenfungizide.
CH633942A5 (en)	1983-01-14	Microbicidal composition, process for the preparation of the active substance, and its use for controlling phytopathogenic fungi
DE2513788C3 (de)	1978-02-09	Substituierte Furan-2-carbonsäureanilide und Verfahren zu deren Herstellung sowie diese Verbindungen enthaltende fungizide Mittel
DE2643404C2 (de)	1987-04-09	N-Acylierte N-Phenyl-alaninthioalkylester, Verfahren zu deren Herstellung und diese Verbindungen enthaltende Mittel
CH617320A5 (en)	1980-05-30	Microbicidal composition.
DE2917893A1 (de)	1980-11-13	N-(alkoxy- bzw. alkoxycarbonalalkyl)- n-hydroxyacetyl- bzw. propionyl-anilin- derivate als pflanzenfungizide
CH618842A5 (en)	1980-08-29	Pesticides
CH631602A5 (en)	1982-08-31	Microbicides
CH633677A5 (en)	1982-12-31	Microbicidal composition, process for the preparation of the active compound and its use for the control of phytopathogenic fungi
CH607888A5 (en)	1978-12-15	Microbicides
CH614102A5 (en)	1979-11-15	Pesticides
CH630610A5 (en)	1982-06-30	Microbicide
CH625784A5 (en)	1981-10-15	Microbicides
CH630351A5 (en)	1982-06-15	Microbicide

Legal Events

Date	Code	Title	Description
1989-09-29	PL	Patent ceased
2024-10-31	PL	Patent ceased