DK131591D0 - DESOXYRIBONUCLEOSIDTHIO AND SELEN PHOSPHONATES - Google Patents

DESOXYRIBONUCLEOSIDTHIO AND SELEN PHOSPHONATES

Info

Publication number
DK131591D0
DK131591D0 DK911315A DK131591A DK131591D0 DK 131591 D0 DK131591 D0 DK 131591D0 DK 911315 A DK911315 A DK 911315A DK 131591 A DK131591 A DK 131591A DK 131591 D0 DK131591 D0 DK 131591D0
Authority
DK
Denmark
Prior art keywords
denotes
general formula
see diagramm
given above
meanings given
Prior art date
Application number
DK911315A
Other languages
Danish (da)
Other versions
DK166585C (en
DK166585B (en
DK131591A (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 DK131591D0 publication Critical patent/DK131591D0/en
Publication of DK131591A publication Critical patent/DK131591A/en
Publication of DK166585B publication Critical patent/DK166585B/en
Application granted granted Critical
Publication of DK166585C publication Critical patent/DK166585C/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 System
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/48Phosphonous acids R—P(OH)2; Thiophosphonous acids including RHP(=O)(OH); 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

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.
DK131591A 1983-09-06 1991-07-05 DESOXYRIBONUCLEOSIDTHIO AND SELEN PHOSPHONATES DK166585C (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
DK131591D0 true DK131591D0 (en) 1991-07-05
DK131591A DK131591A (en) 1991-07-05
DK166585B DK166585B (en) 1993-06-14
DK166585C DK166585C (en) 1993-10-25

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 Before (2)

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

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) ES535627A0 (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
ATE151076T1 (en) * 1990-07-02 1997-04-15 Hoechst Ag OLIGONUCLEOTIDE ANALOGUES WITH TERMINALS 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
AU678769B2 (en) * 1992-07-27 1997-06-12 Hybridon, Inc. Oligonucleotide alkylphosphonothioates
ES2100051T3 (en) * 1993-01-08 1997-06-01 Hybridon Inc SYNTHESIS OF DIMER BLOCKS AND THEIR USE IN THE ASSEMBLY OF OLIGONUCLEOTIDES.
US6087491A (en) * 1993-01-08 2000-07-11 Hybridon, Inc. Extremely high purity oligonucleotides and methods of synthesizing them using dimer blocks
CN1121721A (en) * 1993-01-25 1996-05-01 海布里顿公司 Oligonucleotido alky phosphate and alky substituted phosphate
US6417138B1 (en) * 1994-07-26 2002-07-09 Sony Corporation Method for transcribing an image and a support for transcription and ink ribbon employed therefor
ATE245161T1 (en) * 1995-05-26 2003-08-15 Genta Inc METHOD FOR SYNTHESIS OF ORGANIC PHOSPHOROGANIC COMPOUNDS
ATE254627T1 (en) * 1996-05-03 2003-12-15 Avecia Biotechnology Inc IN SITU PRODUCTION OF NUCLEOSIDE PHOSPHORAMIDITES AND THEIR USE IN OLIGONUCLEOTIDE SYNTHESIS
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
ES8505384A1 (en) 1985-05-16
DK162895B (en) 1991-12-23
DK424784A (en) 1985-03-07
EP0136543B1 (en) 1988-11-23
DK162895C (en) 1992-05-11
DK167359B1 (en) 1993-10-18
DE3475307D1 (en) 1988-12-29
DK166585C (en) 1993-10-25
IE57904B1 (en) 1993-05-05
JPH0662662B2 (en) 1994-08-17
GR80287B (en) 1985-01-07
ATE38839T1 (en) 1988-12-15
CA1235079A (en) 1988-04-12
DK131691A (en) 1991-07-05
AU3275684A (en) 1985-03-14
DK424784D0 (en) 1984-09-05
AU1138488A (en) 1988-07-14
PT79172B (en) 1986-09-10
AU570266B2 (en) 1988-03-10
PT79172A (en) 1984-10-01
DK166585B (en) 1993-06-14
EP0136543A3 (en) 1986-07-16
DK131691D0 (en) 1991-07-05
JPH0531560B2 (en) 1993-05-12
JPS6072899A (en) 1985-04-24
ES535627A0 (en) 1985-05-16
AU601257B2 (en) 1990-09-06
IE842268L (en) 1985-03-06
EP0136543A2 (en) 1985-04-10
DE3332068A1 (en) 1985-03-21
DK131591A (en) 1991-07-05
JPH05262787A (en) 1993-10-12

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