GB1115786A - Uracil compounds and their use as herbicides - Google Patents
Uracil compounds and their use as herbicidesInfo
- Publication number
- GB1115786A GB1115786A GB51052/65A GB5105265A GB1115786A GB 1115786 A GB1115786 A GB 1115786A GB 51052/65 A GB51052/65 A GB 51052/65A GB 5105265 A GB5105265 A GB 5105265A GB 1115786 A GB1115786 A GB 1115786A
- Authority
- GB
- United Kingdom
- Prior art keywords
- uracils
- salts
- group
- substituted
- 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
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- 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
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H19/00—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
- C07H19/02—Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
- C07H19/04—Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
- C07H19/06—Pyrimidine radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Biotechnology (AREA)
- Genetics & Genomics (AREA)
- Molecular Biology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The invention comprises uracils of the formula <FORM:1115786/C2/1> where AN- is a cycloimino group containing 2-14 carbon atoms and at most 3 hetero atoms, X is oxygen or sulphur, R1 is hydrogen, chlorine, fluorine, bromine, iodine or a nitro, C1- 4 alkyl, C1- 4 alkoxy, hydroxymethyl or C2- 5 alkoxymethyl group, R2 is a C1- 3 alkyl group and R3 is hydrogen or a C1- 3 alkyl group or R1 and R2 together form a radical -(CH\2)n-, where n is 3, 4 or 5, and the salts and complexes of such uracils. The uracils are prepared by condensing an appropriately substituted urea with an a -substituted-b -keto ester, treating the resulting ureido compound with a base, followed by acidification to separate the uracil. If a b -keto-ester unsubstituted in the a -position is used, the resulting uracil can be converted to the required 5-substituted compound using conventional chlorination, bromination, iodination, nitration, formylation and alkylation processes. The 4-thiouracils can be made by treating the corresponding di-oxo compounds with phosphorus penta-sulphide. The salts and complexes may be those formed with inorganic or organic bases or acids and phenols. A large number of compounds are specified including those in which the cycloimino group is a hexahydro-1-azepinyl, morpholino, piperidino, 1-pyrrolidinyl, 10-phenothiazinyl, dihydro-1,3,5-dithiazin-5-yl, 1-aziridinyl, 1,2,3,6 -tetrahydro - 1 - pyridyl, 1 - piperazinyl, 9 - carbosolyl, 4 - pyrazolin - 1 - yl, tetrahydro - 1,4 - thiazin - 4 - yl, dihydro - 1,3,5dioxazin - 5 - yl, 1,2,3,4 - tetrahydro - 2 - isoquinolinyl, 3 - azabicyclo(3.2.2)nonan - 3 - yl, 1 - benzimidazolyl and 4 - pipecolin - 1 - yl group. The uracils are used as herbicides (see Division A5).ALSO:Herbicidal compositions comprise uracils of the formula <FORM:1115786/A5-A6/1> where A \s6 N is a cycloimino group containing 2-14 carbon atoms and at most 3 - hetero atoms, X is oxygen or sulphur, R1 is hydrogen, chlorine, bromine, fluorine or iodine or a nitro, C1-4 alkyl, C1-4 alkoxy, hydroxymethyl or C2-5 alkoxymethyl group, R2 is a C1-3 alkyl group and R3 is hydrogen or a C1-3 alkyl group, or R1 and R2 together represent - (CH2)n - where n is 3,4 or 5 and salts and complexes of such uracils. In addition to the usual diluents and additives the compositions may include other herbicidal compounds. A large number of known herbicides are specified and include substituted ureas, substituted triazines, phenols, carboxylic acids and salts, esters, amides, hydrasides and nitriles thereof, thiolcarbamates, inorganic salts, mixed inorganic/organic salts, amines, quarternary ammonium compounds, other substituted uracils and chlorinated ketones. Examples 262-273 relate to the preparation and application of the uracil composi. tions.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US41662364A | 1964-12-07 | 1964-12-07 | |
US690077A US3397050A (en) | 1964-12-07 | 1967-12-13 | Herbicidal method |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1115786A true GB1115786A (en) | 1968-05-29 |
Family
ID=27023425
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB51052/65A Expired GB1115786A (en) | 1964-12-07 | 1965-12-01 | Uracil compounds and their use as herbicides |
Country Status (5)
Country | Link |
---|---|
US (1) | US3397050A (en) |
CH (1) | CH480013A (en) |
DE (1) | DE1567038A1 (en) |
FR (1) | FR1461796A (en) |
GB (1) | GB1115786A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3516986A (en) * | 1966-11-15 | 1970-06-23 | United States Borax Chem | Esters of 2-(omega-alkyleneiminouramido) benzoic acid |
US6376426B1 (en) | 1999-04-23 | 2002-04-23 | Basf Aktiengesellschaft | Herbicidal 3-(heterocycl-1-yl)-uracils |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2969364A (en) * | 1957-12-26 | 1961-01-24 | Upjohn Co | Derivatives of 5-amino uracil |
US3002975A (en) * | 1958-08-25 | 1961-10-03 | Diamond Alkali Co | Process for the preparation of 1,3-dihalo-uracils |
US3235357A (en) * | 1959-08-14 | 1966-02-15 | Du Pont | Method for the control of undesirable vegetation |
-
1965
- 1965-09-01 CH CH1221965A patent/CH480013A/en not_active IP Right Cessation
- 1965-12-01 GB GB51052/65A patent/GB1115786A/en not_active Expired
- 1965-12-06 FR FR41041A patent/FR1461796A/en not_active Expired
- 1965-12-07 DE DE19651567038 patent/DE1567038A1/en active Pending
-
1967
- 1967-12-13 US US690077A patent/US3397050A/en not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
DE1567038A1 (en) | 1970-06-25 |
FR1461796A (en) | 1966-12-09 |
CH480013A (en) | 1969-10-31 |
US3397050A (en) | 1968-08-13 |
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