ES2061398B1 - Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos. - Google Patents

Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos.

Info

Publication number
ES2061398B1
ES2061398B1 ES09300403A ES9300403A ES2061398B1 ES 2061398 B1 ES2061398 B1 ES 2061398B1 ES 09300403 A ES09300403 A ES 09300403A ES 9300403 A ES9300403 A ES 9300403A ES 2061398 B1 ES2061398 B1 ES 2061398B1
Authority
ES
Spain
Prior art keywords
thyolactone
homoscistine
homocisteine
acetyl
procedure
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 - Fee Related
Application number
ES09300403A
Other languages
English (en)
Other versions
ES2061398A1 (es
Inventor
Cano Gaspar Sanchez
Leguey Vicente Montiel
Garcia Vicente Garcia
Riera Antonio Aldaz
Marti Antonio Ginebreda
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.)
Prodesfarma SA
Original Assignee
Prodesfarma SA
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 Prodesfarma SA filed Critical Prodesfarma SA
Priority to ES09300403A priority Critical patent/ES2061398B1/es
Priority to EP94870038A priority patent/EP0618312A1/en
Priority to JP6031639A priority patent/JPH072837A/ja
Publication of ES2061398A1 publication Critical patent/ES2061398A1/es
Application granted granted Critical
Publication of ES2061398B1 publication Critical patent/ES2061398B1/es
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
    • C07D333/30—Hetero atoms other than halogen
    • C07D333/36—Nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/01—Products
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/01—Products
    • C25B3/05—Heterocyclic compounds
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/01—Products
    • C25B3/07—Oxygen containing compounds
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/01—Products
    • C25B3/09—Nitrogen containing compounds
    • C—CHEMISTRY; METALLURGY
    • C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
    • C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
    • C25B3/00—Electrolytic production of organic compounds
    • C25B3/20—Processes
    • C25B3/25—Reduction

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Electrochemistry (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)

Abstract

PROCEDIMIENTO DE OBTENCION DE N-ACETIL HOMOCISTEINA TIOLACTONA, DE FORMULA (I), A PARTIR DE DL-HOMOCISTINA POR METODOS ELECTROQUIMICOS. UNA SOLUCION ACUOSA DE DL-HOMOCISTINA Y UN ACIDO MINERAL SE SOMETE A ELECTROLISIS EN UNA CELULA ELECTROLITICA, CON SEPARACION DE CATOLITO Y ANOLITO. EL CATOLITO ESTA FORMADO POR LA MENCIONADA SOLUCION, Y EL ANOLITO ES UNA SOLUCION SALINA CUALQUIERA. LOS ELECTRODOS PUEDEN SER PLANOS, TRIDIMENSIONALES, FORMANDO LECHO COMPACTO O FLUIDIZADO. LA TENSION DE CORRIENTE ESTA COMPRENDIDA ENTRE 10 MA/CM2 Y 2 A/CM2; LA TEMPERATURA ESTA COMPRENDIDA ENTRE 0 Y 90 C. LA SOLUCION OBTENIDA EN EL CATOLITO SE CONCENTRA, SE SECA Y SE ACETILA PARA OBTENER EL COMPUESTO (I), CON UN ALTO GRADO DE PUREZA. EL COMPUESTO DE LA INVENCION PUEDE UTILIZARSE PARA LA TERAPIA DE ENFERMEDADES HEPATICAS Y COMO MUCOLITICO.
ES09300403A 1993-03-02 1993-03-02 Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos. Expired - Fee Related ES2061398B1 (es)

Priority Applications (3)

Application Number Priority Date Filing Date Title
ES09300403A ES2061398B1 (es) 1993-03-02 1993-03-02 Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos.
EP94870038A EP0618312A1 (en) 1993-03-02 1994-03-01 Process for obtaining n-acetyl homocysteine thiolactone from DL-homocystine by electrochemical methods
JP6031639A JPH072837A (ja) 1993-03-02 1994-03-01 Ｄｌ−ホモシスチンから電気化学的方法によりｎ−アセチルホモシステインチオラクトンを調製する方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
ES09300403A ES2061398B1 (es) 1993-03-02 1993-03-02 Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos.

Publications (2)

Publication Number Publication Date
ES2061398A1 ES2061398A1 (es) 1994-12-01
ES2061398B1 true ES2061398B1 (es) 1996-02-16

Family

ID=8280946

Family Applications (1)

Application Number Title Priority Date Filing Date
ES09300403A Expired - Fee Related ES2061398B1 (es) 1993-03-02 1993-03-02 Procedimiento de obtencion de n-acetil homocisteina tiolactona a partir del dl-homocistina por metodos electroquimicos.

Country Status (3)

Country Link
EP (1) EP0618312A1 (es)
JP (1) JPH072837A (es)
ES (1) ES2061398B1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU8153098A (en) * 1997-06-23 1999-01-04 Nexstar Pharmaceuticals, Inc. Homocysteine assay
CN109943860B (zh) * 2019-04-26 2019-12-31 武汉本杰明医药股份有限公司 Dl-高半胱氨酸硫内酯盐酸盐的合成方法
KR102384780B1 (ko) 2020-02-27 2022-04-11 (주) 파마젠 호모시스테인 티오락톤 또는 셀레노락톤의 제조방법
CN111909374B (zh) * 2020-07-23 2022-03-29 河北工业大学 一种具有自修复性能的锂电池粘结剂的制备方法及其应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1134683B (de) * 1961-03-16 1962-08-16 Degussa Verfahren zur Herstellung von N-Acylhomocysteinthiolacton
FR2129877B1 (es) * 1971-03-18 1974-08-02 Fuveau Sa
FR2147468A5 (en) * 1971-07-28 1973-03-09 Fuveau Sa N-acetyl homocysteine thiolactone - by demethylating methionine with hydriodic acid and acetic anhydride, then acetylating
FR2265355B1 (es) * 1974-03-28 1977-11-04 Blum Jean
IT1215238B (it) * 1985-02-22 1990-01-31 Chiesi Farma Spa Derivati di omocisteina tiolattone,loro procedimento di preparazione e formulazioni farmaceutiche
JPH0273984A (ja) * 1988-09-08 1990-03-13 Nippon Rikagaku Yakuhin Kk 遊離ホモシスティンの製造法
DE3903420A1 (de) * 1989-02-06 1990-08-09 Hoechst Ag Verfahren zur herstellung von thiophenderivaten

Also Published As

Publication number Publication date
ES2061398A1 (es) 1994-12-01
EP0618312A1 (en) 1994-10-05
JPH072837A (ja) 1995-01-06

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Legal Events

Date Code Title Description
PC2A Transfer of patent
FD1A Patent lapsed

Effective date: 20101018