GB701209A - Improvements in or relating to substituted dicarboxylic acid amides - Google Patents

Improvements in or relating to substituted dicarboxylic acid amides

Info

Publication number
GB701209A
GB701209A GB1190150A GB1190150A GB701209A GB 701209 A GB701209 A GB 701209A GB 1190150 A GB1190150 A GB 1190150A GB 1190150 A GB1190150 A GB 1190150A GB 701209 A GB701209 A GB 701209A
Authority
GB
United Kingdom
Prior art keywords
bis
acid
methiodide
dimethylaminoethylamide
ethiodide
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
GB1190150A
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.)
Wellcome Foundation Ltd
Original Assignee
Wellcome Foundation 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 Wellcome Foundation Ltd filed Critical Wellcome Foundation Ltd
Priority to GB1190150A priority Critical patent/GB701209A/en
Publication of GB701209A publication Critical patent/GB701209A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/12Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
    • C07D295/125Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/13Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain

Landscapes

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

Abstract

The invention comprises compounds of the general formula <FORM:0701209/IV (b)/1> wherein m = 4 or 5 and n = 2-7, and their non-toxic salts (e.g. hydrochlorides). These compounds, which possess the property of prolonging the curarizing action of succinylcholine, may be prepared by heating b -aminoethyl-piperidine or -pyrrolidine with dimethyl or diethyl esters of the appropriate dicarboxylic acids, and, if desired, neutralizing aqueous solutions of the resulting bases with an acid. Examples describe the preparation of N:N1-bis-(b -piperidinoethyl) - succinamide, - pimelamide, - glutaramide, -adipamide and -azelä-amide, and N:N1-bis-(b -pyrrolidinoethyl)-succinamide and -adipamide. U.S.A. Specification 2,438,200 is referred to. The Provisional Specification comprises compounds of the general formulae <FORM:0701209/IV (b)/2> and <FORM:0701209/IV (b)/3> <FORM:0701209/IV (b)/4> wherein R1 and R2 represent methyl or ethyl radicals or NR1R2 represents a piperidino, pyrrolidino or morpholino radical, R3 denotes hydrogen or a methyl, ethyl or benzyl radical, -X denotes an anion derived from a non-toxic acid and n = 1-8. Additional compounds described are succinic acid bis-b -dimethylaminoethylamide and its bis methiodide, methochloride, ethiodide, ethochloride, metho- and etho-sulphates and benzochloride, malonic and sebacic acid bis-b -dimethylaminoethylamide bis methiodides, glutaric acid bis-b -dimethylaminoethylamide and its bis methiodide, adipic acid bis-b -dimethylaminoethylamide and its bis methiodide and ethiodide, suberic acid bis-b -dimethylaminoethylamide and its bis methiodide and benzochloride, azelaic acid bis-b -dimethylaminoethylamide and its bis methiosulphate and ethiodide, succinic acid bisdiethylaminoethylamide and its bis methiodide, ethiodide and benzochloride, the bis methiodides of succinic acid bis-morpholino- and -piperidino - ethylamides, glutaric acid bispynrolidinoethylamide and its bis methiodide, ethiodide and benzochloride, glutaric acid bisdiethylaminoethylamide bis methiodide, and the bis methiodides of malonic, glutaric and adipic acid bis-morpholinoethylamides.ALSO:The curarizing action of succinyl-choline is prolonged by p admixing there-with a compound of the general formula <FORM:0701209/VI/1> m = 4 or 5 and n = 2-7), and their non-toxic salts, e.g. N:N1-bis-(b -pipe-rindinoethyl)-succinamide, -pimelamide, -glutaramide, -adipamide or -azel<\>aamide, or N:N1-bis-(b -pyrrolidinoethyl)-succinamide or adipamide. U.S.A. Specification 2,438,200 is referred to. According to the Provisional Specification, the active curarizing agent may be any compound of the general formula <FORM:0701209/VI/2> (wherein R and R1 represent methyl or ethyl radicals and X the anion of a nontoxic acid), and the agent for prolonging its activity may be any compound of either of the general formulae <FORM:0701209/VI/3> (wherein R1 and R2 represent methyl or ethyl radicals or NR1R2 represents a piperidino, pyrrolidino or morpholino radical, R3 represents hydrogen or a methyl, ethyl or benzyl radical and n = 1-8).
GB1190150A 1950-05-12 1950-05-12 Improvements in or relating to substituted dicarboxylic acid amides Expired GB701209A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1190150A GB701209A (en) 1950-05-12 1950-05-12 Improvements in or relating to substituted dicarboxylic acid amides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1190150A GB701209A (en) 1950-05-12 1950-05-12 Improvements in or relating to substituted dicarboxylic acid amides

Publications (1)

Publication Number Publication Date
GB701209A true GB701209A (en) 1953-12-23

Family

ID=9994730

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1190150A Expired GB701209A (en) 1950-05-12 1950-05-12 Improvements in or relating to substituted dicarboxylic acid amides

Country Status (1)

Country Link
GB (1) GB701209A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4774075A (en) * 1980-06-06 1988-09-27 L'oreal Compositions containing bis-(quaternary ammonium) derivatives for the treatment of keratin materials and natural non-keratin materials or synthetic textile materials
FR2763954A1 (en) * 1997-05-27 1998-12-04 Commissariat Energie Atomique New delta-permethylated ornithine peptide(s)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4774075A (en) * 1980-06-06 1988-09-27 L'oreal Compositions containing bis-(quaternary ammonium) derivatives for the treatment of keratin materials and natural non-keratin materials or synthetic textile materials
US4828819A (en) * 1980-06-06 1989-05-09 L'oreal Compositions containing bis-(quaternary ammonium) derivatives for the treatment of keratin materials and natural non-keratin or synthetic textile materials
FR2763954A1 (en) * 1997-05-27 1998-12-04 Commissariat Energie Atomique New delta-permethylated ornithine peptide(s)

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