GB1529150A - Alkyl substituted cyclic alkyltetramines - Google Patents

Alkyl substituted cyclic alkyltetramines

Info

Publication number
GB1529150A
GB1529150A GB37243/77A GB3724377A GB1529150A GB 1529150 A GB1529150 A GB 1529150A GB 37243/77 A GB37243/77 A GB 37243/77A GB 3724377 A GB3724377 A GB 3724377A GB 1529150 A GB1529150 A GB 1529150A
Authority
GB
United Kingdom
Prior art keywords
alkyl
alkyltetramines
substituted cyclic
alkyl substituted
those compounds
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
GB37243/77A
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.)
TABUSHI I
Original Assignee
TABUSHI I
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 JP5600077A external-priority patent/JPS53141175A/en
Priority claimed from JP5712477A external-priority patent/JPS53144593A/en
Priority claimed from JP5712577A external-priority patent/JPS53144592A/en
Application filed by TABUSHI I filed Critical TABUSHI I
Publication of GB1529150A publication Critical patent/GB1529150A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12C—BEER; PREPARATION OF BEER BY FERMENTATION; PREPARATION OF MALT FOR MAKING BEER; PREPARATION OF HOPS FOR MAKING BEER
    • C12C11/00—Fermentation processes for beer
    • C12C11/02—Pitching yeast
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22B—PRODUCTION AND REFINING OF METALS; PRETREATMENT OF RAW MATERIALS
    • C22B3/00—Extraction of metal compounds from ores or concentrates by wet processes
    • C22B3/20—Treatment or purification of solutions, e.g. obtained by leaching
    • C22B3/22—Treatment or purification of solutions, e.g. obtained by leaching by physical processes, e.g. by filtration, by magnetic means, or by thermal decomposition
    • C22B3/24—Treatment or purification of solutions, e.g. obtained by leaching by physical processes, e.g. by filtration, by magnetic means, or by thermal decomposition by adsorption on solid substances, e.g. by extraction with solid resins
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
    • C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
    • C07C29/147—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
    • C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00—Technologies related to metal processing
    • Y02P10/20—Recycling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Environmental & Geological Engineering (AREA)
  • General Life Sciences & Earth Sciences (AREA)
  • Geochemistry & Mineralogy (AREA)
  • Geology (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Microbiology (AREA)
  • Mycology (AREA)
  • Food Science & Technology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1529150 Alkyl substituted cyclic alkyltetramines I TABUSHI 7 Sept 1977 [17 May 1977 19 May 1977 (2)] 37243/77 Heading C2C [Also in Division C7] The invention comprises alkyl substituted cyclic alkyltetramines resulting from substitution of one or more ring hydrogens of the skeleton represented by the general formula I wherein R 1 , R 2 , R 3 and R 4 are (-CH 2 -) 2 or (-CH 2 -) 3 whereby alkyl groups containing at least 8 carbon atoms. The compounds of Formula I may be prepared by: in the first place the cyclic alkyl tetramine skeletons are synthesized by condensation-reacting those compounds having -NH 2 or -NHX (wherein X is sulphenyl, acyl or the like) at the both ends thereof and those compounds having -Cl, -Br, -I, -COOH, -COOR (wherein R is alkyl or aryl), or -SO 3 R (wherein R is alkyl or aryl) at the both ends thereof, in one step or two steps. Next, introduction of alkyl groups as substituents is carried out by reacting those compounds being subjected to the above condensation reaction or amide compounds obtained by the condensation reaction with alkyl halide and the like.
GB37243/77A 1977-05-17 1977-09-07 Alkyl substituted cyclic alkyltetramines Expired GB1529150A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP5600077A JPS53141175A (en) 1977-05-17 1977-05-17 Method of uranium separation by film method
JP5712477A JPS53144593A (en) 1977-05-19 1977-05-19 Alklycyclum
JP5712577A JPS53144592A (en) 1977-05-19 1977-05-19 122alkyll1*4*7*100tetrazacyclotridecane

Publications (1)

Publication Number Publication Date
GB1529150A true GB1529150A (en) 1978-10-18

Family

ID=27295773

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37243/77A Expired GB1529150A (en) 1977-05-17 1977-09-07 Alkyl substituted cyclic alkyltetramines

Country Status (2)

Country Link
DE (1) DE2740170C2 (en)
GB (1) GB1529150A (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4309305A (en) * 1978-07-24 1982-01-05 The United States As Represented By The United States Department Of Energy In vitro removal of actinide (IV) ions
WO1982004252A1 (en) * 1981-06-01 1982-12-09 Dale Johannes N-hydroxyethylated macrocyclic polyamines,the preparation of such amines and their use
EP0073456A1 (en) * 1981-08-24 1983-03-09 Asahi Kasei Kogyo Kabushiki Kaisha Tetraazaannulene cobalt complex compounds and method for preparation thereof
US4442305A (en) * 1981-08-24 1984-04-10 The United States Of America As Represented By The United States Department Of Energy Polycatecholamide chelating agents
US4543213A (en) * 1978-07-24 1985-09-24 The United States Of America As Represented By The United States Department Of Energy Process for preparing 2,3-dihydroxybenzoic acid amides of tetraazaalkanes and cycloalkanes
US4702998A (en) * 1985-03-30 1987-10-27 Konishiroku Photo Industry Co., Ltd. Processing solution for light-sensitive silver halide photographic material comprises metal complexes of large polyamine derivatives
FR2613718A1 (en) * 1987-04-10 1988-10-14 Centre Nat Rech Scient MONOFUNCTIONALIZED CYCLIC TETRAMINES, PROCESS FOR THEIR PREPARATION, POLYMERS AND USE THEREOF
EP0392423A2 (en) * 1989-04-11 1990-10-17 Hoechst Aktiengesellschaft Substituted 1,4-7-10-tetraazacyclotridecanes, method for their preparation and use of the same for labelling substances with radionuclides
US4983376A (en) * 1984-10-18 1991-01-08 Board Of Regents, The University Of Texas System Triazamacrocyclic NMR contrast agents and methods for their use
US5155215A (en) * 1985-11-18 1992-10-13 Access Pharmaceuticals Inc. Polychelating agents for image and spectral enhancement (and spectral shift)
US5188816A (en) * 1984-10-18 1993-02-23 Board Of Regents, The University Of Texas System Using polyazamacrocyclic compounds for intracellular measurement of metal ions using MRS
US5213788A (en) * 1988-09-29 1993-05-25 Ranney David F Physically and chemically stabilized polyatomic clusters for magnetic resonance image and spectral enhancement
US5284944A (en) * 1992-06-30 1994-02-08 Lever Brothers Company, Division Of Conopco, Inc. Improved synthesis of 1,4,7-triazacyclononane
US5310539A (en) * 1991-04-15 1994-05-10 Board Of Regents, The University Of Texas System Melanin-based agents for image enhancement
US5316757A (en) * 1984-10-18 1994-05-31 Board Of Regents, The University Of Texas System Synthesis of polyazamacrocycles with more than one type of side-chain chelating groups
US5342606A (en) * 1984-10-18 1994-08-30 Board Of Regents, The University Of Texas System Polyazamacrocyclic compounds for complexation of metal ions
US5362476A (en) * 1984-10-18 1994-11-08 Board Of Regents, The University Of Texas System Alkyl phosphonate polyazamacrocyclic cheates for MRI
US5428154A (en) * 1988-05-25 1995-06-27 The United States Of America As Represented By The Department Of Health And Human Services Complexes of functionalized tetraazacyclododecane chelates with bismuth, lead, ytriium, actinium, or lanthanide metal ions
WO1996028420A2 (en) * 1995-03-10 1996-09-19 Nycomed Salutar, Inc. Preparation of n-arylmethyl aziridine derivatives, 1,4,7,10-tetraazacyclododecane derivatives obtained therefrom and n-arylmethyl-ethanol-amine sulphonate esters as intermediates
WO1997008157A2 (en) * 1995-08-28 1997-03-06 Johnson Matthey Public Limited Company Process for preparing 1,4,8,11-tetraazacyclotetradecane

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3772785D1 (en) * 1986-01-23 1991-10-17 Squibb & Sons Inc 1-SUBSTITUTED-4,7,10-TRISCARBOXYMETHYL-1,4,7,10-TETRAAZACYCLODODECAN AND ANALOG.

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4309305A (en) * 1978-07-24 1982-01-05 The United States As Represented By The United States Department Of Energy In vitro removal of actinide (IV) ions
US4543213A (en) * 1978-07-24 1985-09-24 The United States Of America As Represented By The United States Department Of Energy Process for preparing 2,3-dihydroxybenzoic acid amides of tetraazaalkanes and cycloalkanes
WO1982004252A1 (en) * 1981-06-01 1982-12-09 Dale Johannes N-hydroxyethylated macrocyclic polyamines,the preparation of such amines and their use
EP0073456A1 (en) * 1981-08-24 1983-03-09 Asahi Kasei Kogyo Kabushiki Kaisha Tetraazaannulene cobalt complex compounds and method for preparation thereof
US4442305A (en) * 1981-08-24 1984-04-10 The United States Of America As Represented By The United States Department Of Energy Polycatecholamide chelating agents
US5362476A (en) * 1984-10-18 1994-11-08 Board Of Regents, The University Of Texas System Alkyl phosphonate polyazamacrocyclic cheates for MRI
US5188816A (en) * 1984-10-18 1993-02-23 Board Of Regents, The University Of Texas System Using polyazamacrocyclic compounds for intracellular measurement of metal ions using MRS
US5428155A (en) * 1984-10-18 1995-06-27 Board Of Regents, The University Of Texas System Synthesis of polyazamacrocycles with more than one type of side-chain chelating groups
US4983376A (en) * 1984-10-18 1991-01-08 Board Of Regents, The University Of Texas System Triazamacrocyclic NMR contrast agents and methods for their use
US5342606A (en) * 1984-10-18 1994-08-30 Board Of Regents, The University Of Texas System Polyazamacrocyclic compounds for complexation of metal ions
US5316757A (en) * 1984-10-18 1994-05-31 Board Of Regents, The University Of Texas System Synthesis of polyazamacrocycles with more than one type of side-chain chelating groups
US4702998A (en) * 1985-03-30 1987-10-27 Konishiroku Photo Industry Co., Ltd. Processing solution for light-sensitive silver halide photographic material comprises metal complexes of large polyamine derivatives
US5155215A (en) * 1985-11-18 1992-10-13 Access Pharmaceuticals Inc. Polychelating agents for image and spectral enhancement (and spectral shift)
EP0287436A1 (en) * 1987-04-10 1988-10-19 Centre National De La Recherche Scientifique Monofunctionalized cyclic tetramines, process for their preparation, their polymers and use of these polymers
FR2613718A1 (en) * 1987-04-10 1988-10-14 Centre Nat Rech Scient MONOFUNCTIONALIZED CYCLIC TETRAMINES, PROCESS FOR THEIR PREPARATION, POLYMERS AND USE THEREOF
US5428154A (en) * 1988-05-25 1995-06-27 The United States Of America As Represented By The Department Of Health And Human Services Complexes of functionalized tetraazacyclododecane chelates with bismuth, lead, ytriium, actinium, or lanthanide metal ions
US5213788A (en) * 1988-09-29 1993-05-25 Ranney David F Physically and chemically stabilized polyatomic clusters for magnetic resonance image and spectral enhancement
EP0392423A3 (en) * 1989-04-11 1991-05-22 Hoechst Aktiengesellschaft Substituted 1,4-7-10-tetraazacyclotridecanes, method for their preparation and use of the same for labelling substances with radionuclides
EP0392423A2 (en) * 1989-04-11 1990-10-17 Hoechst Aktiengesellschaft Substituted 1,4-7-10-tetraazacyclotridecanes, method for their preparation and use of the same for labelling substances with radionuclides
US5310539A (en) * 1991-04-15 1994-05-10 Board Of Regents, The University Of Texas System Melanin-based agents for image enhancement
US5284944A (en) * 1992-06-30 1994-02-08 Lever Brothers Company, Division Of Conopco, Inc. Improved synthesis of 1,4,7-triazacyclononane
WO1996028420A3 (en) * 1995-03-10 1996-12-12 Nycomed Salutar Inc Preparation of n-arylmethyl aziridine derivatives, 1,4,7,10-tetraazacyclododecane derivatives obtained therefrom and n-arylmethyl-ethanol-amine sulphonate esters as intermediates
WO1996028420A2 (en) * 1995-03-10 1996-09-19 Nycomed Salutar, Inc. Preparation of n-arylmethyl aziridine derivatives, 1,4,7,10-tetraazacyclododecane derivatives obtained therefrom and n-arylmethyl-ethanol-amine sulphonate esters as intermediates
US6048979A (en) * 1995-03-10 2000-04-11 Nycomed Salutar, Inc. Preparation of N-arylmethyl aziridine derivatives, 1,4,7,10-tetraazacyclododecane derivatives obtained therefrom and N-arylmethyl-ethanol-amine sulphonate esters as intermediates
US6288224B1 (en) 1995-03-10 2001-09-11 Nycomed Salutar, Inc. Preparation of n-arylmethyl aziridine derivatives, 1,4,7,10-tetraazacyclododecane derivatives obtained therefrom and n-arylethyl-ethanolamine sulphonate esters as intermediates
WO1997008157A2 (en) * 1995-08-28 1997-03-06 Johnson Matthey Public Limited Company Process for preparing 1,4,8,11-tetraazacyclotetradecane
WO1997008157A3 (en) * 1995-08-28 1997-03-27 Johnson Matthey Plc Process for preparing 1,4,8,11-tetraazacyclotetradecane

Also Published As

Publication number Publication date
DE2740170C2 (en) 1982-02-04
DE2740170A1 (en) 1978-11-23

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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