ES2160589T3 - Procedimiento para la sintesis de intermedios de 4-hidroxi-5-halopirrolo(2,3-d)-pirimidinas. - Google Patents

Procedimiento para la sintesis de intermedios de 4-hidroxi-5-halopirrolo(2,3-d)-pirimidinas.

Info

Publication number
ES2160589T3
ES2160589T3 ES93304733T ES93304733T ES2160589T3 ES 2160589 T3 ES2160589 T3 ES 2160589T3 ES 93304733 T ES93304733 T ES 93304733T ES 93304733 T ES93304733 T ES 93304733T ES 2160589 T3 ES2160589 T3 ES 2160589T3
Authority
ES
Spain
Prior art keywords
halopirrolo
pyrimidins
hydroxi
intermediates
synthesis
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
ES93304733T
Other languages
English (en)
Inventor
Charles Jackson Barnett
Michael Edward Kobierski
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Application granted granted Critical
Publication of ES2160589T3 publication Critical patent/ES2160589T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • 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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Saccharide Compounds (AREA)

Abstract

LAS 4-HIDROXIPIRROLO[2,3-D]PIRIMIDINAS SE HALOGENAN REGIOESPECIFICAMENTE EN LA POSICION C-5 MEDIANTE SILILACION EN PRESENCIA DE UN SOLVENTE ORGANICO INERTE Y YODACION, BROMACION O CLORACION.
ES93304733T 1992-06-22 1993-06-17 Procedimiento para la sintesis de intermedios de 4-hidroxi-5-halopirrolo(2,3-d)-pirimidinas. Expired - Lifetime ES2160589T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US07/902,116 US5235053A (en) 1992-06-22 1992-06-22 Process for the synthesis of 4-hydroxy-5-halopyrrold[2,3-d]pyrimidine intermediates

Publications (1)

Publication Number Publication Date
ES2160589T3 true ES2160589T3 (es) 2001-11-16

Family

ID=25415324

Family Applications (1)

Application Number Title Priority Date Filing Date
ES93304733T Expired - Lifetime ES2160589T3 (es) 1992-06-22 1993-06-17 Procedimiento para la sintesis de intermedios de 4-hidroxi-5-halopirrolo(2,3-d)-pirimidinas.

Country Status (15)

Country Link
US (1) US5235053A (es)
EP (1) EP0576211B1 (es)
JP (1) JPH0656838A (es)
KR (1) KR100285891B1 (es)
AT (1) ATE204577T1 (es)
BR (1) BR9302432A (es)
CA (1) CA2098694A1 (es)
DE (1) DE69330627T2 (es)
DK (1) DK0576211T3 (es)
ES (1) ES2160589T3 (es)
HU (1) HU214019B (es)
IL (3) IL119053A (es)
MX (1) MX9303671A (es)
PT (1) PT576211E (es)
TW (1) TW226376B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL107041A (en) * 1992-09-25 2000-02-17 Lilly Co Eli Process for preparing omega(2-amino-4,7-dihydro-4-oxo-3H-pyrrolo-6-¬2,3-d¾pyrimidin-5-YL)alkarylcarboxylic acids and N-(omega-(2-amino-4,7-dihydro-4-oxo-3H-pyrrolo¬2,3-d¾pyrimidin-5-YL)alk-aroyl-4-glutamic acids
US5426187A (en) * 1993-11-30 1995-06-20 Eli Lilly And Company Process for the preparation of 4-hydroxy-5-substituted ethynylpyrrolo [2,3-d]pyrimidine intermediates
US6002004A (en) * 1995-03-28 1999-12-14 Witco Vinyl Additives Gmbh Pyrrolodiazine derivatives as stabilizers for chilorine-containing polymers
JP3711238B2 (ja) * 1997-08-05 2005-11-02 ファイザー・プロダクツ・インク 神経ペプチドY受容体アンタゴニストとしての4−アミノピロ−ル(3,2−d)ピリミジン
CN100374441C (zh) * 2003-06-06 2008-03-12 天津倍方科技发展有限公司 二氢吡咯[2,3-d]嘧啶-4-酮衍生物,其制备方法及其制药用途

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NO169490C (no) 1988-03-24 1992-07-01 Takeda Chemical Industries Ltd Analogifremgangsmaate for fremstilling av terapeutisk aktive pyrrolopyrimidinderivater
IL96531A (en) * 1989-12-11 1995-08-31 Univ Princeton History of Acid N- (Diomeric-H1-Pyrolo] D-2,3 [Pyrimidine-3-Ilacyl (-glutamic, preparation and pharmaceutical preparations containing them)
US5028608A (en) 1989-12-11 1991-07-02 The Trustees Of Princeton University N-(6-Amino-(pyrrolo(2,3-d)pyrimidin-3-ylacyl) )-glutamic acid derivatives

Also Published As

Publication number Publication date
DK0576211T3 (da) 2001-10-08
US5235053A (en) 1993-08-10
JPH0656838A (ja) 1994-03-01
IL119053A (en) 1998-12-06
IL106054A0 (en) 1993-10-20
BR9302432A (pt) 1994-01-11
TW226376B (es) 1994-07-11
IL119053A0 (en) 1996-11-14
EP0576211B1 (en) 2001-08-22
PT576211E (pt) 2001-12-28
MX9303671A (es) 1993-12-01
IL106054A (en) 1997-07-13
EP0576211A3 (en) 1994-06-15
CA2098694A1 (en) 1993-12-23
HUT65439A (en) 1994-06-28
DE69330627T2 (de) 2002-06-13
KR100285891B1 (ko) 2001-04-16
EP0576211A2 (en) 1993-12-29
KR940000461A (ko) 1994-01-03
DE69330627D1 (de) 2001-09-27
HU214019B (hu) 2000-06-28
HU9301829D0 (en) 1993-09-28
ATE204577T1 (de) 2001-09-15

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