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GB1380603A - Binuclear heterocyclic compounds and a process for their production - Google Patents

Binuclear heterocyclic compounds and a process for their production

Info

Publication number
GB1380603A
GB1380603A GB4930172A GB4930172A GB1380603A GB 1380603 A GB1380603 A GB 1380603A GB 4930172 A GB4930172 A GB 4930172A GB 4930172 A GB4930172 A GB 4930172A GB 1380603 A GB1380603 A GB 1380603A
Authority
GB
United Kingdom
Prior art keywords
mole
reacting
cyclic ureide
epihalogenohydrin
april
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
GB4930172A
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.)
Novartis AG
Original Assignee
Ciba Geigy AG
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
Priority claimed from CH539871A external-priority patent/CH550820A/en
Application filed by Ciba Geigy AG filed Critical Ciba Geigy AG
Priority to GB4930172A priority Critical patent/GB1380603A/en
Publication of GB1380603A publication Critical patent/GB1380603A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/72—Two oxygen atoms, e.g. hydantoin
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/22—Di-epoxy compounds
    • C08G59/26—Di-epoxy compounds heterocyclic
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
    • C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
    • C08G59/20—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the epoxy compounds used
    • C08G59/32—Epoxy compounds containing three or more epoxy groups
    • C08G59/3236—Heterocylic compounds
    • C08G59/3245—Heterocylic compounds containing only nitrogen as a heteroatom

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

1380603 Imidazolidine and hexahydro pyrimidine derivatives and their preparation CIBAGEIGY AB 6 April 1972 [14 April 1971] 49301/72 Divided out of 1380602 Heading C2C Compounds of the formula wherein X represents an unsubstituted or hydrocarbon-substituted methylene or ethylene group, and R represents hydrogen or a C 1-4 alkyl group, may be prepared by reacting 2 moles of a cycloureide of formula with 1 mole of 1,3-dichloro-propan-2-ol or epihalogenohydrin containing the radical R in the 2-position. The process may be effected in one stage or in two stages by (a) reacting 1 mole of the cyclic ureide with 1 mole of an epihalogenohydrin in the presence of alkali to give the corresponding monoglycidyl compound and reacting the latter with a further mole of cyclic ureide, or (b) reacting 1 mole of the cyclic ureide with 1 mole of epihalohydrin to form the corresponding monohalogenohydrin derivative and reacting the latter with a further mole of cyclic ureide. The radical X may represent a group such as (CH 3 ) 2 C:, (CH 3 ) 2 CH.CH:, (C 2 H 5 )(CH 3 )C:, benzylidene, or where n=4 or 5.
GB4930172A 1971-04-14 1972-04-06 Binuclear heterocyclic compounds and a process for their production Expired GB1380603A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4930172A GB1380603A (en) 1971-04-14 1972-04-06 Binuclear heterocyclic compounds and a process for their production

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH539871A CH550820A (en) 1971-04-14 1971-04-14 METHOD FOR PREPARING HETEROCYCLIC TRIGLYCIDYL COMPOUNDS.
GB4930172A GB1380603A (en) 1971-04-14 1972-04-06 Binuclear heterocyclic compounds and a process for their production

Publications (1)

Publication Number Publication Date
GB1380603A true GB1380603A (en) 1975-01-15

Family

ID=25697618

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4930172A Expired GB1380603A (en) 1971-04-14 1972-04-06 Binuclear heterocyclic compounds and a process for their production

Country Status (1)

Country Link
GB (1) GB1380603A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4100348A (en) * 1975-05-30 1978-07-11 Ciba-Geigy Corporation Triols containing hydantoin rings

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4100348A (en) * 1975-05-30 1978-07-11 Ciba-Geigy Corporation Triols containing hydantoin rings

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Legal Events

Date Code Title Description
PS Patent sealed