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DK424784D0 - PROCEDURE FOR PREPARING NUCLEOSIDAL COOL, ARAL COOL AND ARYLPHOSPHONITES AND PHOSPHONATES - Google Patents

PROCEDURE FOR PREPARING NUCLEOSIDAL COOL, ARAL COOL AND ARYLPHOSPHONITES AND PHOSPHONATES

Info

Publication number
DK424784D0
DK424784D0 DK424784A DK424784A DK424784D0 DK 424784 D0 DK424784 D0 DK 424784D0 DK 424784 A DK424784 A DK 424784A DK 424784 A DK424784 A DK 424784A DK 424784 D0 DK424784 D0 DK 424784D0
Authority
DK
Denmark
Prior art keywords
denotes
general formula
see diagramm
given above
meanings given
Prior art date
Application number
DK424784A
Other languages
Danish (da)
Other versions
DK162895C (en
DK162895B (en
DK424784A (en
Inventor
Joachim Engels
Alfred Jaeger
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 DK424784D0 publication Critical patent/DK424784D0/en
Publication of DK424784A publication Critical patent/DK424784A/en
Publication of DK162895B publication Critical patent/DK162895B/en
Application granted granted Critical
Publication of DK162895C publication Critical patent/DK162895C/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H19/00Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof
    • C07H19/02Compounds containing a hetero ring sharing one ring hetero atom with a saccharide radical; Nucleosides; Mononucleotides; Anhydro-derivatives thereof sharing nitrogen
    • C07H19/04Heterocyclic radicals containing only nitrogen atoms as ring hetero atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/48Phosphonous acids [RP(OH)2] including [RHP(=O)(OH)]; Thiophosphonous acids including [RP(SH)2], [RHP(=S)(SH)]; Derivatives thereof
    • C07F9/4883Amides or esteramides thereof, e.g. RP(NR'2)2 or RP(XR')(NR''2) (X = O, S)
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H21/00Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Biotechnology (AREA)
  • Engineering & Computer Science (AREA)
  • Saccharide Compounds (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Silicon Polymers (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

1. Claims for the contracting states : BE, CH, LI, DE, FR, GB, IT, LU, NL, SE A process for the preparation of deoxyribonucleoside phosphonates of the general formula I see diagramm : EP0136543,P14,F1 in which T denotes a protecting group for a primary hydroxyl group, B denotes a nucleoside base radical in which any exoamino group present is protected, G denotes a protecting group for a secondary hydroxyl group, Z denotes oxygen, sulfur or selenium and R denotes alkyl having up to 8 C atoms, cyclohexyl, benzyl, or phenyl which is optionally substituted by fluorine, chlorine, bromine, lower alkyl, lower alkoxy or trifluoromethyl, characterized in that a difunctional phosphonylating reagent of the general formula II see diagramm : EP0136543,P14,F2 in which X denotes chlorine or Y and Y denotes a group of the formula see diagramm : EP0136543,P14,F3 R**1 and R**2 representing identical or different alkyl or cycloalkyl radicals having up to 8 C atoms, or phenyl radicals, or R**1 and R**2 , together with the nitrogen, representing a saturated or unsaturated heterocyclic ring which can contain further hetero atoms, being reacted with a nucleoside of the general formula III see diagramm : EP0136543,P14,F4 in which T and B have the meanings given above, the resulting compound of the general formula IV see diagramm : EP0136543,P14,F5 being reacted with a compound of the general formula V see diagramm : EP0136543,P15,F1 in which B and G have the meanings given above, and the resulting compounds of the general formula VI see diagramm : EP0136543,P15,F2 in which T, R, B and G have the meanings given above, being oxidatively converted to compound of the general formula I. 1. Claims for the contracting state AT A process for the preparation of deoxyribonucleoside phosphonates of the general formula I see diagramm : EP0136543,P15,F3 in which T denotes a protecting group for a primary hydroxyl group, B denotes a nucleoside base radical in which any exoamino group present is protected, G denotes a protecting group for a secondary hydroxyl group, Z denotes oxygen, sulfur or selenium and R denotes alkyl having up to 8 C atoms, cyclohexyl, benzyl, or phenyl which is optionally substituted by fluorine, chlorine, bromine, lower alkyl, lower alkoxy or trifluoromethyl, characterized in that a difunctional phosphonylating reagent of the general formula II see diagramm : EP0136543,P16,F1 in which X denotes chlorine or Y and Y denotes a group of the formula see diagramm : EP0136543,P16,F2 R**1 and R**2 representing identical or different alkyl or cycloalkyl radicals having up to 8 C atoms, or phenyl radicals, or R**1 and R**2 , together with the nitrogen, representing a saturated or unsaturated heterocyclic ring which can contain further hetero atoms, being reacted with a nucleoside of the general formula III see diagramm : EP0136543,P16,F3 in which T and B have the meanings given above, the resulting compound of the general formula IV see diagramm : EP0136543,P16,F4 being reacted with a compound of the general formula V see diagramm : EP0136543,P16,F5 in which B and G have the meanings given above, and the resulting compounds of the general formula VI see diagramm : EP0136543,P17,F1 in which T, R, B and G have the meanings given above, being oxidatively converted to compound of the general formula I.
DK424784A 1983-09-06 1984-09-05 METHOD OF PREPARING DESOXYRIBONUCLEOSIDE PHOSPHONATES DK162895C (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19833332068 DE3332068A1 (en) 1983-09-06 1983-09-06 METHOD FOR PRODUCING NUCLEOSIDALKYL, ARALKYL AND ARYLPHOSPHONITES AND PHOSPHONATES
DE3332068 1983-09-06

Publications (4)

Publication Number Publication Date
DK424784D0 true DK424784D0 (en) 1984-09-05
DK424784A DK424784A (en) 1985-03-07
DK162895B DK162895B (en) 1991-12-23
DK162895C DK162895C (en) 1992-05-11

Family

ID=6208339

Family Applications (3)

Application Number Title Priority Date Filing Date
DK424784A DK162895C (en) 1983-09-06 1984-09-05 METHOD OF PREPARING DESOXYRIBONUCLEOSIDE PHOSPHONATES
DK131691A DK167359B1 (en) 1983-09-06 1991-07-05 NUCLEOSID PHOSPHONITES
DK131591A DK166585C (en) 1983-09-06 1991-07-05 DESOXYRIBONUCLEOSIDTHIO AND SELEN PHOSPHONATES

Family Applications After (2)

Application Number Title Priority Date Filing Date
DK131691A DK167359B1 (en) 1983-09-06 1991-07-05 NUCLEOSID PHOSPHONITES
DK131591A DK166585C (en) 1983-09-06 1991-07-05 DESOXYRIBONUCLEOSIDTHIO AND SELEN PHOSPHONATES

Country Status (11)

Country Link
EP (1) EP0136543B1 (en)
JP (2) JPS6072899A (en)
AT (1) ATE38839T1 (en)
AU (2) AU570266B2 (en)
CA (1) CA1235079A (en)
DE (2) DE3332068A1 (en)
DK (3) DK162895C (en)
ES (1) ES8505384A1 (en)
GR (1) GR80287B (en)
IE (1) IE57904B1 (en)
PT (1) PT79172B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4959463A (en) * 1985-10-15 1990-09-25 Genentech, Inc. Intermediates
DE3916871A1 (en) * 1989-05-24 1990-11-29 Boehringer Mannheim Gmbh MODIFIED PHOSPHORAMIDITE PROCESS FOR THE PREPARATION OF MODIFIED NUCLEIC ACIDS
DE59108644D1 (en) * 1990-07-02 1997-05-07 Hoechst Ag Oligonucleotide analogs with terminal 3'-3 'or. 5'-5 'internucleotide linkages
US5512668A (en) * 1991-03-06 1996-04-30 Polish Academy Of Sciences Solid phase oligonucleotide synthesis using phospholane intermediates
CA2140542A1 (en) * 1992-07-27 1994-02-03 Abeysingle Padmapriya Oligonucleotide alkylphosphonothioates
US6087491A (en) * 1993-01-08 2000-07-11 Hybridon, Inc. Extremely high purity oligonucleotides and methods of synthesizing them using dimer blocks
KR960700262A (en) * 1993-01-08 1996-01-19 다알렌 반스톤 SYNTHESIS OF DIMMER BLOCKS AND THEIR USE IN ASSEMBLING OLIGONUCLEOTIDES
CN1121721A (en) * 1993-01-25 1996-05-01 海布里顿公司 Oligonucleotido alky phosphate and alky substituted phosphate
KR100378965B1 (en) * 1994-07-26 2003-08-21 소니 가부시끼 가이샤 Image transfer method and transfer object and ink ribbon used in this
AU707369B2 (en) * 1995-05-26 1999-07-08 Genta Incorporated Compositions and methods for the synthesis of organophosphorus derivatives
AU2739797A (en) * 1996-05-03 1997-11-26 Hybridon, Inc. (in situ) preparation of nucleoside phosphoramidites and their use in synthesis of oligonucleotides
DE102004049339A1 (en) * 2004-10-08 2006-04-13 Basf Ag Process for the purification of phosphorus-containing chelate ligands
DE102007038930B4 (en) * 2007-08-13 2013-12-05 Universität Leipzig New chemical compound and its use in medicine, in particular for use in tumor therapy

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL62834A0 (en) * 1980-05-14 1981-07-31 Ens Bio Logicals Inc Polynucleotide synthesis
US4415732A (en) * 1981-03-27 1983-11-15 University Patents, Inc. Phosphoramidite compounds and processes
EP0090789A1 (en) * 1982-03-26 1983-10-05 Monsanto Company Chemical DNA synthesis
DE3239888A1 (en) * 1982-10-28 1984-05-03 Hubert Prof. Dr. 2000 Hamburg Köster METHOD FOR PRODUCING OLIGONUCLEOSIDE PHOSPHONATES

Also Published As

Publication number Publication date
IE842268L (en) 1985-03-06
PT79172A (en) 1984-10-01
DK131591D0 (en) 1991-07-05
GR80287B (en) 1985-01-07
AU601257B2 (en) 1990-09-06
JPS6072899A (en) 1985-04-24
DK162895C (en) 1992-05-11
DK167359B1 (en) 1993-10-18
EP0136543B1 (en) 1988-11-23
JPH0662662B2 (en) 1994-08-17
ATE38839T1 (en) 1988-12-15
DE3475307D1 (en) 1988-12-29
AU3275684A (en) 1985-03-14
DK166585B (en) 1993-06-14
DK166585C (en) 1993-10-25
AU1138488A (en) 1988-07-14
DK131691A (en) 1991-07-05
ES535627A0 (en) 1985-05-16
EP0136543A2 (en) 1985-04-10
JPH05262787A (en) 1993-10-12
DK131591A (en) 1991-07-05
JPH0531560B2 (en) 1993-05-12
DE3332068A1 (en) 1985-03-21
DK131691D0 (en) 1991-07-05
CA1235079A (en) 1988-04-12
IE57904B1 (en) 1993-05-05
EP0136543A3 (en) 1986-07-16
DK162895B (en) 1991-12-23
DK424784A (en) 1985-03-07
AU570266B2 (en) 1988-03-10
ES8505384A1 (en) 1985-05-16
PT79172B (en) 1986-09-10

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