JP3339888B2 - カルボン酸エステル保護基、それらの生成法及びそれらの官能基へのカップリング - Google Patents

カルボン酸エステル保護基、それらの生成法及びそれらの官能基へのカップリング

Info

Publication number
JP3339888B2
JP3339888B2 JP26715892A JP26715892A JP3339888B2 JP 3339888 B2 JP3339888 B2 JP 3339888B2 JP 26715892 A JP26715892 A JP 26715892A JP 26715892 A JP26715892 A JP 26715892A JP 3339888 B2 JP3339888 B2 JP 3339888B2
Authority
JP
Japan
Prior art keywords
group
ester
peptide
groups
amino acids
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
JP26715892A
Other languages
English (en)
Japanese (ja)
Other versions
JPH05221941A (ja
Inventor
ホルスト・クンツ
ギユンター・ブラウム
ペーター・ブラウン
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.)
Hoechst AG
Original Assignee
Hoechst 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
Application filed by Hoechst AG filed Critical Hoechst AG
Publication of JPH05221941A publication Critical patent/JPH05221941A/ja
Application granted granted Critical
Publication of JP3339888B2 publication Critical patent/JP3339888B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/06—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents
    • C07K1/061—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups
    • C07K1/063—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length using protecting groups or activating agents using protecting groups for alpha-amino functions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/06—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton
    • C07C229/08—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one amino and one carboxyl group bound to the carbon skeleton the nitrogen atom of the amino group being further bound to hydrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C229/34—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings
    • C07C229/36—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton containing six-membered aromatic rings with at least one amino group and one carboxyl group bound to the same carbon atom of the carbon skeleton
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K1/00—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/12—General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length by hydrolysis, i.e. solvolysis in general
    • 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
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Peptides Or Proteins (AREA)
JP26715892A 1991-10-07 1992-10-06 カルボン酸エステル保護基、それらの生成法及びそれらの官能基へのカップリング Expired - Fee Related JP3339888B2 (ja)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
DE4133139 1991-10-07
DE4213706:3 1992-04-25
DE4133139:7 1992-04-25
DE4213706 1992-04-25

Publications (2)

Publication Number Publication Date
JPH05221941A JPH05221941A (ja) 1993-08-31
JP3339888B2 true JP3339888B2 (ja) 2002-10-28

Family

ID=25907995

Family Applications (1)

Application Number Title Priority Date Filing Date
JP26715892A Expired - Fee Related JP3339888B2 (ja) 1991-10-07 1992-10-06 カルボン酸エステル保護基、それらの生成法及びそれらの官能基へのカップリング

Country Status (6)

Country Link
US (2) US5439806A (OSRAM)
EP (1) EP0536671B1 (OSRAM)
JP (1) JP3339888B2 (OSRAM)
CA (1) CA2079921A1 (OSRAM)
DE (1) DE59205565D1 (OSRAM)
DK (1) DK0536671T3 (OSRAM)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1008355A1 (en) 1998-12-08 2000-06-14 Debio Recherche Pharmaceutique S.A. Method for identifying or analyzing polymer linkage sites on macromolecules using amino acid report binding
EP1555327A4 (en) * 2002-10-16 2006-08-02 Kyowa Medex Co Ltd PROCESS AND REAGENT FOR MEASURING CHOLESTEROL IN HIGH DENSITY LIPOPROTEINS
US20110230479A1 (en) * 2005-04-15 2011-09-22 Longo Frank M Neurotrophin mimetics and uses thereof
EP2594318B1 (en) * 2005-04-15 2020-06-10 University Of North Carolina At Chapel Hill Methods of facilitating cell survival using neurotrophin mimetics
US7612209B2 (en) * 2006-06-28 2009-11-03 Hoffmann-La Roche Inc. Pseudo proline dipeptides
EP2498782B1 (en) 2009-11-12 2019-01-09 Pharmatrophix Inc. Crystalline forms of neurotrophin mimetic compounds and their salts
US10273219B2 (en) 2009-11-12 2019-04-30 Pharmatrophix, Inc. Crystalline forms of neurotrophin mimetic compounds and their salts

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE352831C (de) * 1920-08-14 1922-05-05 Aeg Drehzahlregler fuer elektrisch angetriebene Ringspinnmaschinen
US4179337A (en) * 1973-07-20 1979-12-18 Davis Frank F Non-immunogenic polypeptides
DE2360794C2 (de) * 1973-12-06 1984-12-06 Hoechst Ag, 6230 Frankfurt Verfahren zur Herstellung von Peptiden
DE2801238C2 (de) * 1977-01-27 1986-06-05 (Zaidanhojin) Sagami Chemical Research Center, Tokio/Tokyo Verfahren zur Herstellung von Salzen aus L,L-Dipeptiden und Phenylalaninestern
JPS54119260A (en) * 1978-03-08 1979-09-17 Canon Inc Luminous flux diverging apparatus using prisms
ZA801929B (en) * 1979-04-06 1981-11-25 Forenede Bryggerier As A process for enzymatic production of peptides
JPS5645196A (en) * 1979-09-19 1981-04-24 Shionogi & Co Ltd Enzymatic synthesis of beta-lactam antibacterial agent
EP0102230B1 (en) * 1982-08-24 1987-04-29 Teijin Limited Novel 6-nitroprostaglandin derivatives, process for production thereof, and use thereof
EP0145956A1 (de) * 1983-11-16 1985-06-26 Ciba-Geigy Ag Neue Amid-Verbindungen
US5159102A (en) * 1984-03-05 1992-10-27 Teijin Limited 7-thiaprostaglandins E, and process for producing same
EP0215949B1 (en) * 1985-01-29 1990-07-04 Teijin Limited Process for preparing 16-substituted prostaglandin e's
US4668628A (en) * 1985-04-01 1987-05-26 Stauffer Chemical Company Resolution of racemic mixtures of aliphatic acid esters
DE3528631A1 (de) * 1985-08-09 1987-02-12 Basf Ag Substituierte n-acyl-(alpha)-aminosaeureester, ihre verwendung als bioregulatoren insbesondere zur senkung des endogenen ethylenspiegels in pflanzen
GB8600245D0 (en) * 1986-01-07 1986-02-12 Shell Int Research Preparation of 2-arylpropionic acids
DE3743824C2 (de) * 1987-12-23 1997-03-06 Hoechst Ag Verfahren zur enzymatischen Racematspaltung von racemischen Alkoholen mit/in Vinylestern durch Umesterung
US5108916A (en) * 1989-06-05 1992-04-28 Rhone-Poulenc Rorer, S.A. Process for stereoselectively hydrolyzing, transesterifying or esterifying with immobilized isozyme of lipase from candida rugosa
US5169780A (en) * 1989-06-22 1992-12-08 Celgene Corporation Enantiomeric enrichment and stereoselective synthesis of chiral amines
US5089392A (en) * 1990-03-30 1992-02-18 The United States Of America As Represented By Of The Department Of Health And Human Services Fluorogenic substrates for measurement of lysosomal enzyme activities within intact cells
CA2074688A1 (en) * 1991-08-08 1993-02-09 Matthew T. Scholz Catalysts and casting article, method, and composition

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
"Ａｃｔａ．Ｐｏｌ．Ｐｈａｒｍ．，"Ｖｏｌ．４２，Ｎｏ．４，ｐａｇｅｓ ４０８−４０９（
"ＣＨＥＭＩＳＣＨＥ ＢＥＲＩＣＨＴＥ，’Ｖｏｌ．１０７，Ｎｏ．４，ｐａｇｅｓ １３４４−１

Also Published As

Publication number Publication date
EP0536671A2 (de) 1993-04-14
US5639859A (en) 1997-06-17
EP0536671A3 (OSRAM) 1994-04-27
DK0536671T3 (da) 1996-08-12
DE59205565D1 (de) 1996-04-11
JPH05221941A (ja) 1993-08-31
CA2079921A1 (en) 1993-04-08
US5439806A (en) 1995-08-08
EP0536671B1 (de) 1996-03-06

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