GB1010743A - Uracil derivatives - Google Patents

Uracil derivatives

Info

Publication number
GB1010743A
GB1010743A GB29040/65A GB2904065A GB1010743A GB 1010743 A GB1010743 A GB 1010743A GB 29040/65 A GB29040/65 A GB 29040/65A GB 2904065 A GB2904065 A GB 2904065A GB 1010743 A GB1010743 A GB 1010743A
Authority
GB
United Kingdom
Prior art keywords
alkyl
acid
halogenated
substituted
halogen
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
GB29040/65A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
EIDP Inc
Original Assignee
EI Du Pont de Nemours and Co
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 by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co
Publication of GB1010743A publication Critical patent/GB1010743A/en
Expired legal-status Critical Current

Links

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
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals

Abstract

The invention comprises uracil derivatives of the general formula <FORM:1010743/C2/1> wherein R1 has a molecular weight of 15 to 250 and is a substituted or unsubstituted alkyl, cycloalkyl, cycloalkyl alkyl, cycloalkenyl alkyl, alkenyl, cycloalkenyl, alkynyl, aralkyl or aryl radical in which any substituents are flourine, bromine or chlorine atoms or nitro, cyano, mercapto, hydroxy, alkyl or alkoxy radicals; R2 has a molecular weight of up to 250 and is a hydrogen or halogen atom, a nitro, thiocyano or alkylthio radical or a substituted or unsubstituted alkyl, alkoxy or alkenyl radical, in which any substituents are flourine, bromine or chlorine atoms or cyano, mercapto or hydroxy radicals; R3 has a molecular weight of up to 200 and is a hydrogen, chlorine or bromine atom or an alkyl, haloalkyl or alkoxy radical; or R2 and R3 together form a divalent alkylene bridge of formula (CH2)n, where n is 3, 4 or 5; R4 is a hydrogen atom or a C1 to C5 alkyl group; X is oxygen or sulphur; and A is boron trifluoride or an acid having an ionization constant in water at 25 DEG C. greater than 2 x 10-5 and is a halogenated C2 to C5 aliphatic acid, a halogenated benzoic acid, a halogenated phenylacetic acid, a halogenated phenoxy acetic acid, an organic sulphonic acid, an organic phosphonic acid or an inorganic phosphoric acid. Preferred acids are those of the formula <FORM:1010743/C2/2> W is halogen; Y is halogen, alkyl or haloalkyl and Z is halogen or alkyl, and RSO3H, wherein R is an aliphatic or a substituted or unsubstituted aryl radical. The compounds of the invention may be prepared by mixing, suitably at room temperature, a substituted uracil of the formula <FORM:1010743/C2/3> with an appropriate acid in an inert diluent, preferably a liquid aromatic or halogenated aromatic hydrocarbon which is liquid between 20 DEG and 30 DEG C. The addition compounds are precipitated from the reaction mixture or may be precipitated by the addition of excess non-solvent liquid paraffin or separated by vacuum evaporation at low temperatures, preferably below 50 DEG C. Said addition compounds have herbicidal activity. Specifications 968,661, 968,662, 968,663, 968,664, 968,665 and 968,666 also are referred to.
GB29040/65A 1960-12-27 1961-12-21 Uracil derivatives Expired GB1010743A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7834160A 1960-12-27 1960-12-27

Publications (1)

Publication Number Publication Date
GB1010743A true GB1010743A (en) 1965-11-24

Family

ID=22143423

Family Applications (2)

Application Number Title Priority Date Filing Date
GB29040/65A Expired GB1010743A (en) 1960-12-27 1961-12-21 Uracil derivatives
GB45847/61A Expired GB1010742A (en) 1960-12-27 1961-12-21 Herbicidal compositions containing uracil derivatives

Family Applications After (1)

Application Number Title Priority Date Filing Date
GB45847/61A Expired GB1010742A (en) 1960-12-27 1961-12-21 Herbicidal compositions containing uracil derivatives

Country Status (9)

Country Link
BE (1) BE611920A (en)
BR (1) BR6135253D0 (en)
CH (1) CH399063A (en)
DE (1) DE1299927C2 (en)
ES (1) ES273141A1 (en)
GB (2) GB1010743A (en)
MY (2) MY6700031A (en)
NL (1) NL272286A (en)
OA (1) OA01108A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2247021A (en) * 1990-08-09 1992-02-19 Sandoz Ltd Mono-, bi- or tri-carbocyclic phosphinic or phosphonic acid compounds
WO2011161424A1 (en) 2010-06-25 2011-12-29 Cambridge Display Technology Limited Organic light-emitting device and method
DE112011102125T5 (en) 2010-06-25 2013-04-25 Cambridge Display Technology Ltd. Organic light-emitting material, device and method

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL254838A (en) * 1959-08-14 1900-01-01

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2247021A (en) * 1990-08-09 1992-02-19 Sandoz Ltd Mono-, bi- or tri-carbocyclic phosphinic or phosphonic acid compounds
GB2247021B (en) * 1990-08-09 1994-11-09 Sandoz Ltd Mono-,bi- or tri-carbocyclic phosphinic or phosphonic acid compounds
WO2011161424A1 (en) 2010-06-25 2011-12-29 Cambridge Display Technology Limited Organic light-emitting device and method
WO2011161417A1 (en) 2010-06-25 2011-12-29 Cambridge Display Technology Limited Organic light-emitting material device and method
WO2011161425A1 (en) 2010-06-25 2011-12-29 Cambridge Display Technonogy Limited Organic light-emitting device and method
WO2011161416A2 (en) 2010-06-25 2011-12-29 Cambridge Display Technology Limited Organic light-emitting composition, device and method
DE112011102125T5 (en) 2010-06-25 2013-04-25 Cambridge Display Technology Ltd. Organic light-emitting material, device and method
DE112011102126T5 (en) 2010-06-25 2013-05-08 Cambridge Display Technology Limited Organic light-emitting composition, device and method
DE112011102127T5 (en) 2010-06-25 2013-05-29 Cambridge Display Technology Ltd. Organic light-emitting device and method

Also Published As

Publication number Publication date
MY6700031A (en) 1967-12-31
CH399063A (en) 1966-03-31
DE1299927B (en) 1969-07-24
OA01108A (en) 1968-08-07
MY6700030A (en) 1967-12-31
NL272286A (en)
GB1010742A (en) 1965-11-24
DE1299927C2 (en) 1973-04-19
BE611920A (en)
ES273141A1 (en) 1962-04-16
BR6135253D0 (en) 1973-05-10

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