GB1257259A - - Google Patents

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Publication number
GB1257259A
GB1257259A GB1257259DA GB1257259A GB 1257259 A GB1257259 A GB 1257259A GB 1257259D A GB1257259D A GB 1257259DA GB 1257259 A GB1257259 A GB 1257259A
Authority
GB
United Kingdom
Prior art keywords
carbon atoms
radical containing
radical
substituted
alkyl
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
Application number
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.)
Filing date
Publication date
Application filed filed Critical
Publication of GB1257259A publication Critical patent/GB1257259A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/60Three or more oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic 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
    • C07D239/28Heterocyclic 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
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1,257,259. Uracils. E.I. DU PONT DE NEMOURS & CO. 13 May, 1969 [13 May, 1968], No. 24452/69. Heading C2C. [Also in Division A5] 1-Substituted uracils of the formula R 1 represents an alkyl radical containing 1 to 10 carbon atoms, a substituted alkyl radical containing 1 to 10 carbon atoms, wherein the or each substituent is a bromine, chlorine, hydroxy, alkoxy, alkoxycarbonyl or cyano radical; a substituted or unsubstituted carbocyclic or heterocyclic aromatic radical containing 5 to 16 carbon atoms; an aralkyl radical containing 5 to 13 carbon atoms; a substituted aralkyl radical containing 5 to 13 carbon atoms, wherein the or each substituent is a chlorine, nitro, alkyl or alkoxy radical; an alkenyl radical containing 3 to 8 carbon atoms; an alkynyl radical containing 3 to 8 carbon atoms; a cycloalkyl radical containing 3 to 12 carbon atoms; a substituted cycloalkyl radical containing 3 to 12 carbon atoms, wherein the or each substituent is a bromine, chlorine, methoxy, or alkyl radical; a cycloalkenyl radical containing 4 to 12 carbon atoms; a substituted cycloalkenyl radical containing 4 to 12 carbon atoms, wherein the or each substituent is a bromine, chlorine, methoxy, or alkyl radical; a cycloalkyl alkyl radical containing 4 to 13 carbon atoms; a substituted cycloalkyl alkyl radical containing 4 to 14 carbon atoms; wherein the or each substituent is. a. bromine, chlorine, methoxy, or C 1-4 alkyl radical; a cycloalkenyl, alkyl radical containing 5 to 13 carbon atoms; a substituted cycloalkenyl alkyl radical containing 5 to 14 carbon atoms, wherein the or each substituent is a bromine, chlorine, methoxy or C 1-4 alkyl radical; R 2 represents a hydrogen or a halogen atom or a methyl, ethyl, methoxy, ethoxy,. nitro, alkoxymethyl of 2 to 4 carbon atoms, hydroxyalkyl of 1 to 4 carbon atoms, mercapto -methyl, methylthio, ethylthio, methylmercaptomethyl, bromomethyl, chloromethyl or fluoromethyl radical; R 3 represents a hydrogen or an alkyl radical containing 1 to 3 carbon atoms.; or R 2 and R 3 together represent a divalent radical of the formula (CH 2 )q, wherein q is. 3, 4 or 5; R 4 represents an alkyl. radical containing: 1 to 10 carbon atoms; a. substituted alkyl radical containing 1 to 10 carbon atoms, wherein the or each substituent is a chlorine, bromine, fluorine or alkoxy radical of 1 to 4 carbon atoms; a phenyl radical; a chlorophenyl radical; a benzyl radical; an aryl radical containing 4 to 10 carbon atoms; an alkenyl radical containing 3 or 4 carbon atoms; or a cycloalkyl radical containing 4 to 8 carbon atoms; and X represents an oxygen or sulphur atom.; or the reaction product of a said uracil with a Lewis acid or base are prepared either by (1) reacting with sodium methoxide in the presence of an organic solvent a uracil of formula and (2) reacting the product of step (1) with an excess of R 4 X-CO-Cl or replacing sodium methoxide in the first process by sodium hydride. Amongst numerous. examples the compounds 1 methoxycarbonyl - 3 -sec -butyl-5- bromo - 6 - methyluracil, 1 - (2 - fluoroethoxycarbonyl) - 3 - propargyl - 5 - fluoro - 6 - methyluracil and 1-phenoxycarbonyl-3-cyclopropyl- 5,6-dimethyluracil are prepared. The 1 -substituted uracils of the invention have herbicidal activity and numerous examples of herbicidal compositions are given in the Specification.
GB1257259D 1968-05-13 1969-05-13 Expired GB1257259A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US72879568A 1968-05-13 1968-05-13

Publications (1)

Publication Number Publication Date
GB1257259A true GB1257259A (en) 1971-12-15

Family

ID=24928307

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1257259D Expired GB1257259A (en) 1968-05-13 1969-05-13

Country Status (6)

Country Link
JP (1) JPS4831898B1 (en)
DE (1) DE1924232A1 (en)
FR (1) FR2008386A1 (en)
GB (1) GB1257259A (en)
IL (1) IL32113A (en)
OA (1) OA03321A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4618364A (en) * 1983-07-11 1986-10-21 Roussel Uclaf 3-(2-tetrahydropyranyl)-1,2,3,4,5,6,7-hexahydro-1-p-tolyloxycarbonyl-5H-cyclopentapyrimidine-2,4-dione and herbicidal compositions and methods using it
US5017211A (en) * 1987-09-23 1991-05-21 Ciba-Geigy Corporation Heterocyclic compounds

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1283665B (en) * 1966-02-03 1968-11-21 Interelectric Ag Card for congratulatory and visitation purposes and process for their manufacture
JPS5633918U (en) * 1979-08-21 1981-04-02
DK167280B1 (en) * 1985-03-20 1993-10-04 Ciba Geigy Ag 3-ARYLURACIL DERIVATIVES, PROCEDURES FOR PREPARING THEREOF, WEED POLLUTANTS CONTAINING THESE DERIVATIVES AND THE USE OF THE DERIVATIVES FOR THE WEED PREVENTION
DK366887A (en) * 1986-07-31 1988-05-13 Hoffmann La Roche pyrimidine
AU630980B2 (en) * 1989-06-29 1992-11-12 Syngenta Participations Ag Heterocyclic compounds

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4618364A (en) * 1983-07-11 1986-10-21 Roussel Uclaf 3-(2-tetrahydropyranyl)-1,2,3,4,5,6,7-hexahydro-1-p-tolyloxycarbonyl-5H-cyclopentapyrimidine-2,4-dione and herbicidal compositions and methods using it
US5017211A (en) * 1987-09-23 1991-05-21 Ciba-Geigy Corporation Heterocyclic compounds

Also Published As

Publication number Publication date
FR2008386A1 (en) 1970-01-23
IL32113A (en) 1973-10-25
IL32113A0 (en) 1969-06-25
OA03321A (en) 1970-12-15
DE1924232A1 (en) 1969-11-27
JPS4831898B1 (en) 1973-10-02

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Legal Events

Date Code Title Description
PS Patent sealed [section 19, patents act 1949]
PCNP Patent ceased through non-payment of renewal fee