GB889706A - Fungicidal composition - Google Patents
Fungicidal compositionInfo
- Publication number
- GB889706A GB889706A GB2485360A GB2485360A GB889706A GB 889706 A GB889706 A GB 889706A GB 2485360 A GB2485360 A GB 2485360A GB 2485360 A GB2485360 A GB 2485360A GB 889706 A GB889706 A GB 889706A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- alkyl radical
- radical
- thioimidazoline
- aminoimidazoline
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- -1 alkyl radical Chemical group 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 239000004480 active ingredient Substances 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 150000002431 hydrogen Chemical group 0.000 abstract 2
- 150000003254 radicals Chemical class 0.000 abstract 2
- WSLZAQBZPMMTIA-UHFFFAOYSA-N 2-(4-anilinophenyl)-4,5-dihydroimidazol-1-amine Chemical compound NN1CCN=C1C(C=C1)=CC=C1NC1=CC=CC=C1 WSLZAQBZPMMTIA-UHFFFAOYSA-N 0.000 abstract 1
- DISXFZWKRTZTRI-UHFFFAOYSA-N 4,5-dihydro-1h-imidazol-2-amine Chemical compound NC1=NCCN1 DISXFZWKRTZTRI-UHFFFAOYSA-N 0.000 abstract 1
- FRQGDZPERKMXNA-UHFFFAOYSA-N 4-n-(4,5-dihydro-1h-imidazol-2-yl)-1-n-phenylbenzene-1,4-diamine Chemical compound N1CCN=C1NC(C=C1)=CC=C1NC1=CC=CC=C1 FRQGDZPERKMXNA-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 abstract 1
- AHYLTZYDNWZRCP-UHFFFAOYSA-N N,N-dibutyl-4,5-dihydro-1H-imidazol-2-amine Chemical compound C(CCC)N(C=1NCCN1)CCCC AHYLTZYDNWZRCP-UHFFFAOYSA-N 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical group [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- GTPHHSDNEHXLJQ-UHFFFAOYSA-N n-(4-methylphenyl)-4,5-dihydro-1h-imidazol-2-amine Chemical compound C1=CC(C)=CC=C1N=C1NCCN1 GTPHHSDNEHXLJQ-UHFFFAOYSA-N 0.000 abstract 1
- YXQYDPYBZVVAGA-UHFFFAOYSA-N n-cyclohexyl-4,5-dihydro-1h-imidazol-2-amine Chemical compound N1CCN=C1NC1CCCCC1 YXQYDPYBZVVAGA-UHFFFAOYSA-N 0.000 abstract 1
- JCOPITWIWLFFPC-UHFFFAOYSA-N n-phenyl-4,5-dihydro-1h-imidazol-2-amine Chemical compound N1CCN=C1NC1=CC=CC=C1 JCOPITWIWLFFPC-UHFFFAOYSA-N 0.000 abstract 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, 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
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/46—Nitrogen atoms not forming part of a nitro radical with only hydrogen atoms attached to said nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/04—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D233/28—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, 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
- C07D233/44—Nitrogen atoms not forming part of a nitro radical
- C07D233/50—Nitrogen atoms not forming part of a nitro radical with carbocyclic radicals directly attached to said nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention comprises 2-p-anilinophenyl-aminoimidazoline This and other compounds of the general formula <FORM:0889706/IV (b)/1> wherein R1 is selected from the group consisting of aromatic and cycloaliphatic radicals and R2 is hydrogen, and R1 is an alkyl radical having one to four carbon atoms when R2 is the same alkyl radical as R1, and R3 is a member selected from the group consisting of hydrogen and methyl, are prepared by reacting a 2-alkyl-thioimidazoline or salt thereof, e.g. 2-n-butyl-thioimidazoline hydrobromide with an amine, e.g. p-aminodiphenylamine. U.S.A. Specification 1,912,849 is referred to.ALSO:A fungicidal composition comprises as active ingredient a 2-aminoimidazoline having the general formula <FORM:0889706/VI/1> wherein R1 is an aromatic or a cycloaliphatic radical when R2 is hydrogen, and R1 is an alkyl radical having 1 to 4 carbon atoms when R2 is the same alkyl radical as R1, and R3 is hydrogen or a methyl radical, together with a surface acting wetting agent or powdered solid carrier. Specified active ingredients are 2-p-anilinophenylaminoimidazoline, 2 - cyclohexylaminoimidazoline, 2 - di - n - butylaminoimidazoline, 2 - anilinoimidazoline and 2 - p - tolylaminoimidazoline. U.S.A. Specification 1,912,849 is referred to.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2485360A GB889706A (en) | 1960-07-16 | 1960-07-16 | Fungicidal composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2485360A GB889706A (en) | 1960-07-16 | 1960-07-16 | Fungicidal composition |
| CH1022260A CH407645A (en) | 1960-09-09 | 1960-09-09 | Fungicidal composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB889706A true GB889706A (en) | 1962-02-21 |
Family
ID=25706144
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2485360A Expired GB889706A (en) | 1960-07-16 | 1960-07-16 | Fungicidal composition |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB889706A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0017484A1 (en) * | 1979-04-03 | 1980-10-15 | Fujisawa Pharmaceutical Co., Ltd. | 2-Imidazoline derivatives, process for the preparation thereof and the pharmaceutical composition of the same |
| DE3518604A1 (en) | 1984-05-23 | 1985-11-28 | Egyt Gyógyszervegyészeti Gyár, Budapest | METHOD FOR THE PRODUCTION OF 2- (PHENYLIMINO) -IMIDAZOLIDINE DERIVATIVES |
| USRE35224E (en) * | 1987-01-13 | 1996-04-30 | The Board Of Trustees Of The Leland Stanford Junior University | Histamine derivatives as immune modulators |
| US5556872A (en) * | 1992-01-27 | 1996-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Histamine derivatives useful as immunomodulators |
-
1960
- 1960-07-16 GB GB2485360A patent/GB889706A/en not_active Expired
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0017484A1 (en) * | 1979-04-03 | 1980-10-15 | Fujisawa Pharmaceutical Co., Ltd. | 2-Imidazoline derivatives, process for the preparation thereof and the pharmaceutical composition of the same |
| DE3518604A1 (en) | 1984-05-23 | 1985-11-28 | Egyt Gyógyszervegyészeti Gyár, Budapest | METHOD FOR THE PRODUCTION OF 2- (PHENYLIMINO) -IMIDAZOLIDINE DERIVATIVES |
| USRE35224E (en) * | 1987-01-13 | 1996-04-30 | The Board Of Trustees Of The Leland Stanford Junior University | Histamine derivatives as immune modulators |
| US5556872A (en) * | 1992-01-27 | 1996-09-17 | The Board Of Trustees Of The Leland Stanford Junior University | Histamine derivatives useful as immunomodulators |
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