IL40060A - Compositions for controlling plant pathogenic organisms containing s-triazole(4,3-alpha)quinoline derivatives and cetain 4,5-dohydro-s-triazolo(4,3-alpha)quinolines rtain 4,5-dihydro-s-triazolo(4,3-alpha)quinolines - Google Patents
Compositions for controlling plant pathogenic organisms containing s-triazole(4,3-alpha)quinoline derivatives and cetain 4,5-dohydro-s-triazolo(4,3-alpha)quinolines rtain 4,5-dihydro-s-triazolo(4,3-alpha)quinolinesInfo
- Publication number
- IL40060A IL40060A IL40060A IL4006072A IL40060A IL 40060 A IL40060 A IL 40060A IL 40060 A IL40060 A IL 40060A IL 4006072 A IL4006072 A IL 4006072A IL 40060 A IL40060 A IL 40060A
- Authority
- IL
- Israel
- Prior art keywords
- triazolo
- hydrogen
- formula
- dihydro
- alpha
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom 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
- C07D215/38—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
1374369 s-Triazoloquinoline derivatives ELI LILLY & CO 15 Aug 1972 [16 Aug 1971] 37989/72 Heading C2C Novel s-triazoloquinoline derivatives having the formula and known s-triazoloquinoline derivatives of the formula wherein R is hydrogen, halogen, (C 1 -C 3 ) alkyl, (C 1 -C 3 ) alkoxy, formyl, cyano, -CF 3 or substituted methyl radical of the formula -CH 2 Y wherein Y is amino, (C 1 -C 3 ) alkylamino, cyano, hydroxy, halogen or (C 1 -C 3 ) alkoxy; R<SP>2</SP> is hydrogen, (C 1 -C 5 ) alkyl, vinyl, (C 3 -C 6 ) cycloalkyl, hydroxy, (C 1 -C 3 ) alkoxy, mercapto, (C 1 -C 3 ) alkylthio, benzylthio, halogen, amino, (C 1 -C 3 ) alkylamino, di-(C 1 -C 3 ) alkylamino, carbamoyl, thiocyanato, acetamido, -CF 3 , a radical of the formula -COOR<SP>4</SP> wherein R<SP>4</SP> is Na, K or (C 1 -C 3 ) alkyl, or a substituted methyl radical of the formula -CH 2 Y<SP>1</SP> wherein Y<SP>1</SP> is amino, (C 1 -C 3 ) alkylamino, cyano, halogen, (C 1 -C 3 ) alkoxy, (C 1 -C 2 ) alkoxymethyl or halomethyl; and R<SP>3</SP> is hydrogen, (C 1 -C 3 ) alkyl, or halogen, provided that (i) not more than two R<SP>3</SP> groups represent halogen or alkyl, (ii) in the second formula, not more than three of the groups represented by R<SP>1</SP> and R<SP>2</SP> are moieties other than hydrogen, (iii) in the first formula, not more than three of R<SP>1</SP>, R<SP>2</SP> and R<SP>3</SP> represent a moiety other than hydrogen, and (iv) in both formulµ, at least one of R<SP>2</SP> and R<SP>1</SP> at the 9th position represents hydrogen; as well as the phytologically-acceptable mineral acid addition salts thereof, are useful as controllants for plant-pathogenic organisms.
[GB1374369A]
Claims (6)
1. CLAIMS 1. Compositions for controlling plant- pathogenic organisms which comprise,-- as the active agent a¾ least one compound selected from the s_-trlazolo ( ,3-a)quinoline compounds- of the formulae 20 and the phytologlcally-acceptable mineral acid addition · salts thereof, wherein each R1 independently represents hydrogen, halo, loweralkyl of C^-C-j, loweralkoxy of C-^-C^, *8.72 X R2 represents hydrogen, loweralkyl of C-^-C^, vinyl, cyclo-. alkyl of C^-Cg, hydroxy, loweralkoxy of C-^-C-,, mercapto, loweralkylthio of O^-C^, benzylthio, halo, amino (loweralkyl of amino, carbamoyl, acetamido, trifluoromethyl, a radical of the formula wherein R4 represents sodium, potassium, or loweralkyl of C^-C-j, or a radical of the .72 formula -CHp-Y' wherein Y' represents loweralkoxy of C ' of halo, subject to the limitation that no more than two groups represent halo or loweralk l as defined the foregoing definitions being subject to the further limitations (1) that in Formula X not more than three of B1 and R2 are other than hydrogen; (2) that in Formula IX 1 2 3 not more than three of R , R and R^ are other than hydrogen; and (3) that in both Formulae X and II at least one of the 2 1 R and the R substituents at the 9-position represents hydrogen.
2. , A composition according to Claim 1 which contains a surface active dispersing agent and an inert finely divided solid. 3· The composition of Claim 2 wherein the active agent is l^methyl-s.-triazolo(4,3-a)qulnoline. 4. The composition of Claim 2 wherein the active agent is l-chloro-s-triazolo(4,3-a)qulnoline. 5. The composition of Claim 2 wherein the active agent is 9-chloro-s-triazolo(4,3-a)qulnoline. 6. The composition of Claim 2 wherein the active agent is 9-methyl-s-trlazolo(4,3-a)qulnoline. 7. The compositon of Claim 2 wherein the active agent is 4» 5-dihydro-s-triazolo(4,3-a)qulnoline. 8. The composition of Claim 2 wherein the active agent is 4, 5-dihydro-l-methyl^s-triazolo(4»3-a)qulnoline. 40060/ 4 10. The composition of Claim 2 wherein the active agent is 4 , 5-dihydro-9-methyl-s-tria olo( , 3-a)quinoline . 11. s-Triazolo(4, 3-a)quinoline compounds of the formula and. the phytologlcall -acceptable mineral acid addition salts thereof, wherein R1 is hydrogen, halogen, or lower- alkyl, and R2 is hydrogen, lower alkyl or trifluoromethyl ; provided that (l) not more than three of R1 and R2 are othe than hydrogen, and (2) that at least one of R2 and the substituent R1 at the 9-position represent hydrogen. 12. 4, 5-Dihydro-s-triazolo(4,3-a)quinoline. 1
3. 4, 5-Dihydro-l-methyl-s-triazolo ;(4,3-a)quinoline". 1
4. 9-Chloro-4 , 5-dihydro-s-triazolo (4 , 3-a)quinoline . 1
5. 4, 5-Dihydro-9-methyl-s-triazol6'( , quinoline. 1
6. A process for controlling plant-'pathc-genic organisms which comprises applying to a locus of the organism an effective amount of a composition according tocany of Claims 1 to, 9L P md
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17231771A | 1971-08-16 | 1971-08-16 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| IL40060A0 IL40060A0 (en) | 1972-10-29 |
| IL40060A true IL40060A (en) | 1976-08-31 |
Family
ID=22627199
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IL40060A IL40060A (en) | 1971-08-16 | 1972-08-07 | Compositions for controlling plant pathogenic organisms containing s-triazole(4,3-alpha)quinoline derivatives and cetain 4,5-dohydro-s-triazolo(4,3-alpha)quinolines rtain 4,5-dihydro-s-triazolo(4,3-alpha)quinolines |
Country Status (31)
| Country | Link |
|---|---|
| JP (1) | JPS5760321B2 (en) |
| KR (1) | KR790000421B1 (en) |
| AR (2) | AR195289A1 (en) |
| AT (1) | AT324767B (en) |
| AU (1) | AU461057B2 (en) |
| BE (1) | BE787536A (en) |
| BG (3) | BG24409A3 (en) |
| CA (1) | CA997766A (en) |
| CH (2) | CH564016A5 (en) |
| CS (1) | CS190371B2 (en) |
| DD (2) | DD107462A5 (en) |
| DE (1) | DE2239892A1 (en) |
| DK (1) | DK139832B (en) |
| EG (1) | EG10668A (en) |
| ES (1) | ES405899A1 (en) |
| FR (1) | FR2149467B1 (en) |
| GB (1) | GB1374369A (en) |
| GT (1) | GT197225694A (en) |
| HU (1) | HU167272B (en) |
| IE (1) | IE36916B1 (en) |
| IL (1) | IL40060A (en) |
| IT (1) | IT962096B (en) |
| MY (1) | MY7800200A (en) |
| NL (1) | NL177173C (en) |
| PH (1) | PH10204A (en) |
| PL (1) | PL94442B1 (en) |
| RO (2) | RO79165A (en) |
| SE (2) | SE405313B (en) |
| SU (1) | SU554815A3 (en) |
| YU (1) | YU36937B (en) |
| ZA (1) | ZA725365B (en) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1102524B (en) * | 1977-03-29 | 1985-10-07 | Capsugel Ag | CONTAINMENT CAPSULE FOR VISCOUS MATERIALS IN PARTICULAR A LIQUID PHARMACEUTICAL PREPARATION AND PROCEDURE FOR ITS PRODUCTION |
| JPS61186648U (en) * | 1984-12-29 | 1986-11-20 | ||
| AT393764B (en) * | 1986-09-02 | 1991-12-10 | System Elektrotechnik Gotthold | JUMPER CABLES |
| JPS63166228U (en) * | 1987-04-21 | 1988-10-28 | ||
| JP2007506788A (en) * | 2003-09-26 | 2007-03-22 | ライジェル ファーマシューティカルズ， インコーポレイテッド | HCV infection inhibitors and uses thereof |
| WO2005121138A2 (en) * | 2004-06-03 | 2005-12-22 | Rigel Pharmaceuticals, Inc. | Heterotricyclic compounds for use as hcv inhibitors |
| WO2007087250A2 (en) * | 2006-01-23 | 2007-08-02 | Amira Pharmaceuticals, Inc. | Tricyclic inhibitors of 5-lipoxygenase |
-
0
- BE BE787536D patent/BE787536A/en not_active IP Right Cessation
-
1971
- 1971-08-16 ES ES405899A patent/ES405899A1/en not_active Expired
-
1972
- 1972-08-04 ZA ZA725365A patent/ZA725365B/en unknown
- 1972-08-07 IL IL40060A patent/IL40060A/en unknown
- 1972-08-09 AU AU45397/72A patent/AU461057B2/en not_active Expired
- 1972-08-09 YU YU2043/72A patent/YU36937B/en unknown
- 1972-08-10 NL NLAANVRAGE7210957,A patent/NL177173C/en not_active IP Right Cessation
- 1972-08-10 CA CA149,119A patent/CA997766A/en not_active Expired
- 1972-08-12 IT IT52168/72A patent/IT962096B/en active
- 1972-08-14 DE DE2239892A patent/DE2239892A1/en not_active Withdrawn
- 1972-08-14 GT GT197225694A patent/GT197225694A/en unknown
- 1972-08-14 KR KR7201228A patent/KR790000421B1/en active
- 1972-08-14 PL PL1972157263A patent/PL94442B1/en unknown
- 1972-08-14 IE IE1125/72A patent/IE36916B1/en unknown
- 1972-08-15 SE SE7210551A patent/SE405313B/en unknown
- 1972-08-15 EG EG335/72A patent/EG10668A/en active
- 1972-08-15 DK DK402572AA patent/DK139832B/en not_active IP Right Cessation
- 1972-08-15 CH CH411774A patent/CH564016A5/xx not_active IP Right Cessation
- 1972-08-15 CH CH1209772A patent/CH552942A/en not_active IP Right Cessation
- 1972-08-15 CS CS725667A patent/CS190371B2/en unknown
- 1972-08-15 GB GB3798972A patent/GB1374369A/en not_active Expired
- 1972-08-15 HU HU72EI427A patent/HU167272B/hu unknown
- 1972-08-16 DD DD173662*A patent/DD107462A5/xx unknown
- 1972-08-16 DD DD165089A patent/DD104176A5/xx unknown
- 1972-08-16 PH PH13806A patent/PH10204A/en unknown
- 1972-08-16 JP JP47082060A patent/JPS5760321B2/ja not_active Expired
- 1972-08-16 RO RO7282499A patent/RO79165A/en unknown
- 1972-08-16 BG BG024104D patent/BG24409A3/en unknown
- 1972-08-16 AR AR243610A patent/AR195289A1/en active
- 1972-08-16 BG BG024103A patent/BG20354A3/en unknown
- 1972-08-16 FR FR7229270A patent/FR2149467B1/fr not_active Expired
- 1972-08-16 RO RO197271972A patent/RO63409A/en unknown
- 1972-08-16 AT AT704672A patent/AT324767B/en not_active IP Right Cessation
- 1972-08-16 BG BG21209A patent/BG19623A1/xx unknown
-
1973
- 1973-03-15 SU SU1895868A patent/SU554815A3/en active
- 1973-05-04 AR AR247862A patent/AR215825A1/en active
-
1975
- 1975-06-27 SE SE7507384A patent/SE422059B/en not_active IP Right Cessation
-
1978
- 1978-12-30 MY MY200/78A patent/MY7800200A/en unknown
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