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GB1499850A - Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine - Google Patents

Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine

Info

Publication number
GB1499850A
GB1499850A GB4575575A GB4575575A GB1499850A GB 1499850 A GB1499850 A GB 1499850A GB 4575575 A GB4575575 A GB 4575575A GB 4575575 A GB4575575 A GB 4575575A GB 1499850 A GB1499850 A GB 1499850A
Authority
GB
United Kingdom
Prior art keywords
trihydroxypyrimidine
aminocarbonyl
manufacture
anaphthalene
heading
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
GB4575575A
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries Ltd
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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB4575575A priority Critical patent/GB1499850A/en
Priority to IT2715676A priority patent/IT1070801B/en
Priority to DE19762641979 priority patent/DE2641979A1/en
Priority to FR7630645A priority patent/FR2330683A1/en
Priority to JP13158076A priority patent/JPS5259176A/en
Priority to CH1374676A priority patent/CH599170A5/xx
Publication of GB1499850A publication Critical patent/GB1499850A/en
Expired legal-status Critical Current

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
    • C07D239/60—Three or more oxygen or sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Pyridine Compounds (AREA)
  • Paper (AREA)

Abstract

1499850 5 - Aminocarbonyl - 2,4,6 - trihydroxypyrimidine IMPERIAL CHEMICAL INDUSTRIES Ltd 13 Aug 1976 [4 Nov 1975] 45755/75 Heading C2C 5 - Aminocarbonyl - 2,4,6 - trihydroxypyrimidine is made by heating barbituric acid with an aqueous solution of urea. The reaction medium may also include a water-miscible organic liquid (e.g. ethylene glycol or its monoethyl ether) or a surface-active agent (e.g. the sodium salt of a condensate of anaphthalene sulphonic acid and formaldehyde).
GB4575575A 1975-11-04 1975-11-04 Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine Expired GB1499850A (en)

Priority Applications (6)

Application Number Priority Date Filing Date Title
GB4575575A GB1499850A (en) 1975-11-04 1975-11-04 Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine
IT2715676A IT1070801B (en) 1975-11-04 1976-09-13 PROCESS FOR THE PREPARATION OF 5 AMINOCARBONYL 2,4,6 TRIIDOXYPYRIMIDINE
DE19762641979 DE2641979A1 (en) 1975-11-04 1976-09-17 PROCESS FOR THE PREPARATION OF 5-AMINOCARBONYL-2,4,6-TRIHYDROXYPYRIMIDINE
FR7630645A FR2330683A1 (en) 1975-11-04 1976-10-12 PROCESS FOR THE PRODUCTION OF 5-AMINOCARBONYL-2,4,6-TRIHYDROXYPYRIMIDINE
JP13158076A JPS5259176A (en) 1975-11-04 1976-11-01 Preparation method of 55 aminocarbonyll2*4*66trihydroxyy pyrimidine
CH1374676A CH599170A5 (en) 1975-11-04 1976-11-01

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4575575A GB1499850A (en) 1975-11-04 1975-11-04 Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine

Publications (1)

Publication Number Publication Date
GB1499850A true GB1499850A (en) 1978-02-01

Family

ID=10438457

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4575575A Expired GB1499850A (en) 1975-11-04 1975-11-04 Process for the manufacture of 5-aminocarbonyl-2,4,6-trihydroxypyrimidine

Country Status (6)

Country Link
JP (1) JPS5259176A (en)
CH (1) CH599170A5 (en)
DE (1) DE2641979A1 (en)
FR (1) FR2330683A1 (en)
GB (1) GB1499850A (en)
IT (1) IT1070801B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4753940A (en) * 1985-02-15 1988-06-28 Ciba-Geigy Corporation Barbituric acid derivatives

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PH24423A (en) * 1985-02-15 1990-06-25 Ciba Geigy Ag 5-(azolyloxyphenylcarbamoyl)barbituric acid derivatives as anthelmintics

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4753940A (en) * 1985-02-15 1988-06-28 Ciba-Geigy Corporation Barbituric acid derivatives

Also Published As

Publication number Publication date
FR2330683B3 (en) 1979-06-22
IT1070801B (en) 1985-04-02
CH599170A5 (en) 1978-05-12
DE2641979A1 (en) 1977-05-12
JPS5259176A (en) 1977-05-16
FR2330683A1 (en) 1977-06-03

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee