GB1158619A - New Formimino Ethers - Google Patents

New Formimino Ethers

Info

Publication number
GB1158619A
GB1158619A GB17595/67A GB1759567A GB1158619A GB 1158619 A GB1158619 A GB 1158619A GB 17595/67 A GB17595/67 A GB 17595/67A GB 1759567 A GB1759567 A GB 1759567A GB 1158619 A GB1158619 A GB 1158619A
Authority
GB
United Kingdom
Prior art keywords
naphthyl
general formula
formimino
ethers
carbon atoms
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
GB17595/67A
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.)
Egyt Gyogyszervegyeszeti Gyar
Original Assignee
Egyt Gyogyszervegyeszeti Gyar
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 Egyt Gyogyszervegyeszeti Gyar filed Critical Egyt Gyogyszervegyeszeti Gyar
Publication of GB1158619A publication Critical patent/GB1158619A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C257/00Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
    • C07C257/04Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines without replacement of the other oxygen atom of the carboxyl group, e.g. imino-ethers
    • C07C257/06Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines without replacement of the other oxygen atom of the carboxyl group, e.g. imino-ethers having carbon atoms of imino-carboxyl groups bound to hydrogen atoms, to acyclic carbon atoms, or to carbon atoms of rings other than six-membered aromatic rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1,158,619. N-Naphthyl-formimino ethers. EGYESULT GYOGYSZER-ES TAPSZERGYAR. 17 April, 1967 [21 April, 1966], No. 17595/67. Heading C2C. Novel N-naphthyl-formimino ethers of the general formula A-N=CH-OR, wherein A is naphthyl or 1,2,3,4-tetrahydronaphthyl optionally mono- or di-substituted by substituents selected from halogen atoms, hydroxyl groups and sulphonic acid groups and R is a saturated or unsaturated, straight or branched chain alkyl group containing 1 to 16 carbon atoms, except when A is an unsubstituted α-naphthyl group when R contains 2 to 16 carbon atoms, or a cycloalkyl, di-C 1 -C 4 -alkylaminoalkyl or aralkyl group, and therapeutically acceptable acid addition salts and quaternary ammonium derivatives thereof are prepared by reaction of an amine of the general formula A-NH 2 with an orthoformate ester of the general formula CH#(OR) 3 and optional transetherification of a resulting N-naphthyl-formimino ether of the first formula above wherein R is a methyl or ethyl group with a higher alcohol of the general formula R<SP>1</SP>OH, wherein R<SP>1</SP> is an alkyl group of at least 3 carbon atoms or a cycloalkyl, di- C 1 -C 4 -alkylaminoalkyl or aralkyl group; followed optionally by conversion to a therapeutically acceptable acid addition salt or quaternary ammonium derivative of the product. Pharmaceutical compositions having anthelmintic activity comprise, as active ingredient, an N-naphthyl-formimino ether of the first general formula above or a therapeutically acceptable acid addition salt or quaternary ammonium derivative thereof, together with a pharmaceutically acceptable carrier or diluent.
GB17595/67A 1966-04-21 1967-04-17 New Formimino Ethers Expired GB1158619A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HUEE001239 1966-04-21

Publications (1)

Publication Number Publication Date
GB1158619A true GB1158619A (en) 1969-07-16

Family

ID=10995190

Family Applications (1)

Application Number Title Priority Date Filing Date
GB17595/67A Expired GB1158619A (en) 1966-04-21 1967-04-17 New Formimino Ethers

Country Status (10)

Country Link
AT (1) AT268259B (en)
BE (1) BE697217A (en)
CH (1) CH513130A (en)
CS (1) CS157030B2 (en)
DE (1) DE1618310B2 (en)
DK (1) DK124255B (en)
GB (1) GB1158619A (en)
IL (1) IL27806A (en)
NL (1) NL151359B (en)
SE (1) SE332977B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102141269B1 (en) 2013-12-18 2020-08-05 셰브론 필립스 케미컬 컴퍼니 엘피 Phosphinyl formamidine compounds, metal complexes, catalyst systems, and their use to oligomerize or polymerize olefins

Also Published As

Publication number Publication date
DK124255B (en) 1972-10-02
SE332977B (en) 1971-03-01
DE1618310B2 (en) 1974-03-21
BE697217A (en) 1967-10-02
DE1618310A1 (en) 1971-03-11
CH513130A (en) 1971-09-30
DE1618310C3 (en) 1974-11-28
CS157030B2 (en) 1974-08-23
NL6705576A (en) 1967-10-23
IL27806A (en) 1971-04-28
NL151359B (en) 1976-11-15
AT268259B (en) 1969-02-10

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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