ES2190091T3 - Procedimiento para la preparacion del acido (2-((8,9)-dioxo-2,6 diazabiciclo(5.2.0)-non-1(7)-en-2-2-il)-etil)fosfonico. - Google Patents

Procedimiento para la preparacion del acido (2-((8,9)-dioxo-2,6 diazabiciclo(5.2.0)-non-1(7)-en-2-2-il)-etil)fosfonico.

Info

Publication number
ES2190091T3
ES2190091T3 ES98937292T ES98937292T ES2190091T3 ES 2190091 T3 ES2190091 T3 ES 2190091T3 ES 98937292 T ES98937292 T ES 98937292T ES 98937292 T ES98937292 T ES 98937292T ES 2190091 T3 ES2190091 T3 ES 2190091T3
Authority
ES
Spain
Prior art keywords
acid
dioxo
ester
ethyl
amino
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 - Lifetime
Application number
ES98937292T
Other languages
English (en)
Inventor
Andre Alfred Asselin
William Alvin Kinney
Jean Schmid
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.)
Wyeth LLC
Original Assignee
Wyeth LLC
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 Wyeth LLC filed Critical Wyeth LLC
Application granted granted Critical
Publication of ES2190091T3 publication Critical patent/ES2190091T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/645Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having two nitrogen atoms as the only ring hetero atoms
    • 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
    • C07F9/38Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
    • C07F9/40Esters thereof
    • C07F9/4003Esters thereof the acid moiety containing a substituent or a structure which is considered as characteristic
    • C07F9/4006Esters of acyclic acids which can have further substituents on alkyl

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La invención se refiere a un procedimiento para la preparación del compuesto de fórmula (I), ácido [2-((8,9)-dioxo-2,6-diazabicilo[5.2.0]nona-1(7)-en-2-il)etil]fosfónico, antagonista de NMDA útil como anticonvulsivos y neuroprotector en situaciones en las que se produce una liberación excesiva de aminoácidos excitantes. En el procedimiento de la presente invención el 1,1-dimetiletil éster del ácido 3-aminopropilcarbámico reacciona con un dialquil vinilfosfonato para obtener el éster dialquílico del ácido N-[3-(3-butiloxicarbonil-amino)propil]-2-amino etilfosfónico (d) con rendimiento del 80%. La reacción de (d) con 3,4-dialcoxiciclobut-3-en-1,2-diona da el 1,1-dimetiletil éster del ácido [3-[[2-dialcoxifosforil)etil](2-alcoxi-3,4-dioxo-1,2-ciclobuten-1-il)amino]propil]carbámico (e) con rendimiento del 96%. La desprotección y ciclización de (e) en ácido trifluoroacético da el éster dialquílico del ácido [2-((8,9)-dioxo-2,6-diazabicilo[5.2.0]nona-1(7)-en-2-il)etil]fosfónico (c) con rendimiento del 58%. El éster dietílico del ácido fosfónico (c) se trata con bromotrimetilxilano para dar el compuesto de fórmula (I).
ES98937292T 1997-08-01 1998-07-31 Procedimiento para la preparacion del acido (2-((8,9)-dioxo-2,6 diazabiciclo(5.2.0)-non-1(7)-en-2-2-il)-etil)fosfonico. Expired - Lifetime ES2190091T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US90509197A 1997-08-01 1997-08-01

Publications (1)

Publication Number Publication Date
ES2190091T3 true ES2190091T3 (es) 2003-07-16

Family

ID=25420284

Family Applications (1)

Application Number Title Priority Date Filing Date
ES98937292T Expired - Lifetime ES2190091T3 (es) 1997-08-01 1998-07-31 Procedimiento para la preparacion del acido (2-((8,9)-dioxo-2,6 diazabiciclo(5.2.0)-non-1(7)-en-2-2-il)-etil)fosfonico.

Country Status (19)

Country Link
EP (1) EP1000072B1 (es)
JP (1) JP4383651B2 (es)
KR (1) KR100606580B1 (es)
CN (2) CN1257174C (es)
AT (1) ATE232875T1 (es)
AU (1) AU746119B2 (es)
BR (1) BR9811807A (es)
CA (1) CA2297411C (es)
DE (1) DE69811507T2 (es)
DK (1) DK1000072T3 (es)
ES (1) ES2190091T3 (es)
HK (1) HK1027814A1 (es)
HU (1) HUP0002505A3 (es)
IL (2) IL163574A (es)
NO (1) NO325420B1 (es)
NZ (1) NZ502509A (es)
RU (1) RU2205834C2 (es)
SI (1) SI1000072T1 (es)
WO (1) WO1999006417A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA78529C2 (en) 2001-10-10 2007-04-10 Wyeth Corp Derivatives of [[2-(amino-3,4-dioxo-1-cyclobutene-1-yl)amino]alkyl] acid for treating pain
WO2004092189A1 (en) 2003-04-09 2004-10-28 Wyeth Derivatives of 2-(8,9-dioxo-2,6-diazabicyclo(5.2.0)non-1(7)-en-2-yl)alkyl phosphonic acid and their use as n-methyl-d-aspartate (nmda) recetor antagonists
TW200514775A (en) 2003-10-22 2005-05-01 Wyeth Corp Methods for the preparation of {2-[(8,9)-dioxo-2,6-diaza-bicyclo[5.2.0]-non-1(7)-en-2-yl]ethyl} phosphonic acid and esters thereof
AU2010226479A1 (en) * 2009-03-19 2011-09-22 Wyeth Llc Methods for the preparation of [2-(8,9-dioxo-2,6-diazabicyclo[5.2.0]non-1(7) -en-2-yl)ethyl]phosphonic acid and precursors thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5168103A (en) * 1991-01-22 1992-12-01 American Home Products Corporation [[2-(amino-3,4-dioxo-1-cyclobuten-1-yl) amino]alkyl]-acid derivatives

Also Published As

Publication number Publication date
KR100606580B1 (ko) 2006-08-01
NO20000488L (no) 2000-01-31
JP4383651B2 (ja) 2009-12-16
IL163574A (en) 2008-06-05
BR9811807A (pt) 2000-08-15
EP1000072B1 (en) 2003-02-19
DE69811507D1 (de) 2003-03-27
DE69811507T2 (de) 2003-07-24
DK1000072T3 (da) 2003-04-22
IL134082A0 (en) 2001-04-30
HUP0002505A2 (hu) 2000-11-28
ATE232875T1 (de) 2003-03-15
NO325420B1 (no) 2008-04-21
HK1027814A1 (en) 2001-01-23
NZ502509A (en) 2002-08-28
HUP0002505A3 (en) 2002-02-28
AU8603798A (en) 1999-02-22
CA2297411C (en) 2008-12-02
AU746119B2 (en) 2002-04-18
CN1526714A (zh) 2004-09-08
CN1257174C (zh) 2006-05-24
NO20000488D0 (no) 2000-01-31
KR20010022492A (ko) 2001-03-15
SI1000072T1 (en) 2003-06-30
CN1265664A (zh) 2000-09-06
RU2205834C2 (ru) 2003-06-10
EP1000072A1 (en) 2000-05-17
WO1999006417A1 (en) 1999-02-11
IL163574A0 (en) 2005-12-18
JP2001512129A (ja) 2001-08-21
CA2297411A1 (en) 1999-02-11
CN1149218C (zh) 2004-05-12

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