GB968666A - Herbicidal compositions containing 3-substituted uracils - Google Patents
Herbicidal compositions containing 3-substituted uracilsInfo
- Publication number
- GB968666A GB968666A GB1742064A GB1742064A GB968666A GB 968666 A GB968666 A GB 968666A GB 1742064 A GB1742064 A GB 1742064A GB 1742064 A GB1742064 A GB 1742064A GB 968666 A GB968666 A GB 968666A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- substituted
- give
- methyl
- hydrogen
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/56—One oxygen atom and one sulfur atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Compounds of the isomeric formulae: <FORM:0968666/C1/1> or <FORM:0968666/C1/2> where R1 is a covalent organic radical of molecular weight 15-250 which is C1-10 alkyl, substituted C1-3 alkyl, phenyl which may be substituted, C7-8 aralkyl, C7-12 substituted aralkyl, C3-6 alkenyl, propynyl, butynyl, C5-8 cycloalkyl or C5-8 cycloalkenyl; R2 is hydrogen, halogen, C1-4 alkyl, C1-3 alkoxy, NO2, C2-4 alkoxymethyl, hydroxymethyl, hydroxyethyl, allyl, thiocyanato, cyano, halogenomethyl or methylthiomethyl; R3 is hydrogen, C1-5 alkyl, methoxy or ethoxy; or R2 and R3 together make up (CH2)n, where n is 3, 4 or 5; and R4 is a covalent radical of molecular weight up to 250 which is C1-3 alkyl, hydroxymethyl, hydroxyethyl, carboxyethyl, substituted carbamyl, substituted thiocarbamyl, diethylphosphoryl, a chloromethylthio group, phenylthio, halogenophenylthio, nitrophenylthio, dinitrophenylthio, tolylthio or acyl; and X is oxygen or sulphur; with the proviso that if R2 is hydrogen and R4 is methyl, then R1 is C5-8 cycloalkyl or cycloalkenyl (such compounds bring herbicides (see Division A5) are prepared by methods involving introduction of the R4 group; methods used in examples are the use of ketone to give acetyl, dialkyl sulphates or sulphonates to give alkyl, acid chlorides to give acyl, diethylphosphorochloridate to give diethylphosphoro, propiolactone to give carboxyethyl, substituted carbamyl and thiocarbamyl chloride to give substituted carbamyl and thiocarbamyl, sulphenyl chlorides to give sulphenyl, formaldehyde to give hydroxymethyl, isocyanates and isothiocyanates to give substituted carbamyl and thiocarbamyl, and alkyl halides to give alkyl groups as R4. Novel compounds. 5-Chloro-3-cyclohexyl-1, 6-dimethyluracil is claimed as novel, as well as those compounds of the formula given in which (i) R1 is C5-8 cycloalkyl or cycloalkenyl, or a group -CR5R6R7 in which R5 is hydrogen or methyl, R6 is methyl or ethyl, and R7 is C1-5 alkyl; R2 is chlorine or bromine, X is oxygen or sulphur, R3 is methyl, and R4 is as defined above (but not methyl); and (ii) R1 is C1-10 alkyl, substituted C1-3 alkyl, phenyl which may be substituted, C7-8 aralkyl, C7-12 substituted aralkyl, C3-6 alkenyl, propynyl, butynyl, C5-8 cycloalkyl or cycloalkenyl, or cyano; R2 is halogen, R3 is methyl, and R4 is acyl. Specifications 492,742, 968,662, 968,663, 968,664 and 968,665 also are referred to.ALSO:The invention comprises herbicidal compositions comprising a compound of the isomeric formul <FORM:0968666/A5-A6/1> or <FORM:0968666/A5-A6/2> where R1 is a covalent organic radical of molecular weight 15-250 which is C1-10 alkyl, substituted C1-3 alkyl, phenyl which may be substituted, C7-8 aralkyl, C7-12 substituted aralkyl, C3-6 alkenyl, propynyl, butynyl, C5-8 cycloalkyl, C5-8 cycloalkenyl or cyano; R2 is hydrogen, halogen, C1-4 alkyl, C1-3 alkoxy, C2-4 alkoxymethyl, hydroxymethyl, hydroxyethyl, allyl, thiocyanato, cyano, halogenomethyl or methylthiomethyl; R3 is hydrogen, chlorine, C1-5 alkyl, methoxy or ethoxy, or R2 and R3 together make up (CH2)n where n is 3, 4 or 5; R4 is a covalent radical of molecular weight up to 250 which is C1-3 alkyl, hydroxymethyl, hydroxyethyl, carboxyethyl, substituted carbamyl, substituted thiocarbamyl, diethylphosphoryl, a chloromethylthio group, phenylthio, halogenophenylthio, nitrophenylthio, dinitrophenylthio, tolylthio or acyl; and X is oxygen or sulphur, with the proviso that if R2 is hydrogen and R4 is methyl, then R1 is C5-8 cycloalkyl or cycloalkenyl (see Division C2); associated with a compatible diluent which is (i) at least in part an oil (see below); (ii) at least in part a solid; (iii) at least in part a liquid other than an oil (e.g. water) and a surface-active agent; or (iv) a surface-active agent (which may also be present in (i) and (ii)). The invention also comprises a method of controlling the growth of weeds at a locus by applying to the locus a herbicidally effective quantity of at least one uracil as defined above, if desired in the form of a composition as defined. An oil is defined as a liquid immiscible with water and soluble in ether, and which boils at not below 125 DEG C. Specified diluents and additives are those referred to in the parent Specification. The compositions may also contain one of the 3-substituted uracils disclosed in Specifications 968,662, 968,663, 968,664 and 968,665. Specification 492,742 also is referred to.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1742064A GB968666A (en) | 1960-08-15 | 1960-08-15 | Herbicidal compositions containing 3-substituted uracils |
MY6500107A MY6500107A (en) | 1960-08-15 | 1965-12-31 | Herbicidal compositions containing 3- substituted uracils |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1742064A GB968666A (en) | 1960-08-15 | 1960-08-15 | Herbicidal compositions containing 3-substituted uracils |
Publications (1)
Publication Number | Publication Date |
---|---|
GB968666A true GB968666A (en) | 1964-09-02 |
Family
ID=10094896
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1742064A Expired GB968666A (en) | 1960-08-15 | 1960-08-15 | Herbicidal compositions containing 3-substituted uracils |
Country Status (2)
Country | Link |
---|---|
GB (1) | GB968666A (en) |
MY (1) | MY6500107A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4859229A (en) * | 1986-07-31 | 1989-08-22 | Hoffmann-La Roche Inc. | 3-Aryluracils having an ether (thio) carbomyloxy or sulphomyloxy substituent on the aromatic moiety |
US5017211A (en) * | 1987-09-23 | 1991-05-21 | Ciba-Geigy Corporation | Heterocyclic compounds |
US5183492A (en) * | 1989-06-29 | 1993-02-02 | Ciba-Geigy Corporation | Herbicidal 3-aryluracils |
US9428465B2 (en) | 2012-05-28 | 2016-08-30 | Fondazione Istituto Italiano Di Technologia | Acid ceramidase inhibitors and their use as medicaments |
-
1960
- 1960-08-15 GB GB1742064A patent/GB968666A/en not_active Expired
-
1965
- 1965-12-31 MY MY6500107A patent/MY6500107A/en unknown
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4859229A (en) * | 1986-07-31 | 1989-08-22 | Hoffmann-La Roche Inc. | 3-Aryluracils having an ether (thio) carbomyloxy or sulphomyloxy substituent on the aromatic moiety |
US5017211A (en) * | 1987-09-23 | 1991-05-21 | Ciba-Geigy Corporation | Heterocyclic compounds |
US5183492A (en) * | 1989-06-29 | 1993-02-02 | Ciba-Geigy Corporation | Herbicidal 3-aryluracils |
US9428465B2 (en) | 2012-05-28 | 2016-08-30 | Fondazione Istituto Italiano Di Technologia | Acid ceramidase inhibitors and their use as medicaments |
Also Published As
Publication number | Publication date |
---|---|
MY6500107A (en) | 1965-12-31 |
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