KR100569771B1 - 프로테아제 억제제로서 유용한 4-히드록시-2-옥소-피란유도체의 제조 방법 - Google Patents

프로테아제 억제제로서 유용한 4-히드록시-2-옥소-피란유도체의 제조 방법 Download PDF

Info

Publication number
KR100569771B1
KR100569771B1 KR1020007002546A KR20007002546A KR100569771B1 KR 100569771 B1 KR100569771 B1 KR 100569771B1 KR 1020007002546 A KR1020007002546 A KR 1020007002546A KR 20007002546 A KR20007002546 A KR 20007002546A KR 100569771 B1 KR100569771 B1 KR 100569771B1
Authority
KR
South Korea
Prior art keywords
acid
delete delete
hydroxy
salt
group
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
KR1020007002546A
Other languages
English (en)
Korean (ko)
Other versions
KR20010023864A (ko
Inventor
제임스 알. 게이지
로버트 씨. 켈리
브래들리 디. 휴이트
Original Assignee
파마시아 앤드 업존 캄파니 엘엘씨
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 파마시아 앤드 업존 캄파니 엘엘씨 filed Critical 파마시아 앤드 업존 캄파니 엘엘씨
Publication of KR20010023864A publication Critical patent/KR20010023864A/ko
Application granted granted Critical
Publication of KR100569771B1 publication Critical patent/KR100569771B1/ko
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C205/00Compounds containing nitro groups bound to a carbon skeleton
    • C07C205/49Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
    • C07C205/56Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by carboxyl groups having nitro groups bound to carbon atoms of six-membered aromatic rings and carboxyl groups bound to acyclic carbon atoms of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/30Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with halogen containing compounds, e.g. hypohalogenation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/277Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing ether groups, groups, groups, or groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40Unsaturated compounds
    • C07C59/42Unsaturated compounds containing hydroxy or O-metal groups
    • C07C59/48Unsaturated compounds containing hydroxy or O-metal groups containing six-membered aromatic rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/32Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • AIDS & HIV (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyrane Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
KR1020007002546A 1997-09-11 1998-09-03 프로테아제 억제제로서 유용한 4-히드록시-2-옥소-피란유도체의 제조 방법 Expired - Lifetime KR100569771B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US5861897P 1997-09-11 1997-09-11
US60/058,618 1997-09-11
PCT/US1998/017993 WO1999012919A1 (en) 1997-09-11 1998-09-03 Process to produce 4-hydroxy-2-oxo-pyrane derivates useful as protease inhibitors

Publications (2)

Publication Number Publication Date
KR20010023864A KR20010023864A (ko) 2001-03-26
KR100569771B1 true KR100569771B1 (ko) 2006-04-11

Family

ID=22017924

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1020007002546A Expired - Lifetime KR100569771B1 (ko) 1997-09-11 1998-09-03 프로테아제 억제제로서 유용한 4-히드록시-2-옥소-피란유도체의 제조 방법

Country Status (20)

Country Link
US (2) US6077963A (enExample)
EP (1) EP1015441B1 (enExample)
JP (3) JP4462760B2 (enExample)
KR (1) KR100569771B1 (enExample)
CN (3) CN1284763C (enExample)
AT (1) ATE266654T1 (enExample)
CA (1) CA2300204C (enExample)
CZ (1) CZ298847B6 (enExample)
DE (1) DE69823844T2 (enExample)
DK (1) DK1015441T3 (enExample)
ES (1) ES2221199T3 (enExample)
FI (1) FI120973B (enExample)
HU (1) HU228986B1 (enExample)
NO (1) NO321835B1 (enExample)
NZ (1) NZ503338A (enExample)
PL (1) PL193240B1 (enExample)
PT (1) PT1015441E (enExample)
RU (2) RU2223958C2 (enExample)
SK (1) SK284974B6 (enExample)
WO (1) WO1999012919A1 (enExample)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1161427B1 (en) * 1999-03-18 2002-10-23 PHARMACIA & UPJOHN COMPANY Improved process for asymmetric hydrogenation
US6552204B1 (en) * 2000-02-04 2003-04-22 Roche Colorado Corporation Synthesis of 3,6-dialkyl-5,6-dihydro-4-hydroxy-pyran-2-one
DE10108470A1 (de) * 2001-02-22 2002-09-05 Boehringer Ingelheim Pharma Verfahren zur Herstellung optisch aktiver Dihydropyrone
US6500963B2 (en) 2001-02-22 2002-12-31 Boehringer Ingelheim Pharma Kg Process for preparing optically active dihydropyrones
US6987123B2 (en) 2001-07-26 2006-01-17 Cadila Healthcare Limited Heterocyclic compounds, their preparation, pharmaceutical compositions containing them and their use in medicine
AU2002344438B2 (en) 2002-02-07 2008-09-11 Sumitomo Chemical Company, Limited Process for producing (R)-3-hydroxy-3-(2-phenylethyl)hexanoic acid and its intermediate
DE10313118A1 (de) 2003-03-24 2004-10-07 Boehringer Ingelheim Pharma Gmbh & Co. Kg Enantioselektive Hydrierung von Intermediaten bei der Tipranavir-Synthese
US7512945B2 (en) * 2003-12-29 2009-03-31 Intel Corporation Method and apparatus for scheduling the processing of commands for execution by cryptographic algorithm cores in a programmable network processor
CN100448836C (zh) * 2005-06-03 2009-01-07 浙江中贝化工有限公司 一种抗艾滋病药物关键中间体的制备方法
BRPI0615016A2 (pt) * 2005-08-24 2011-05-03 Pfizer compostos inibidores de hcv polimerase, métodos para prepará-los e forma cristalina
CN103996798B (zh) * 2007-11-30 2017-09-08 株式会社半导体能源研究所 发光元件、发光装置以及电子装置
US8853393B2 (en) * 2011-07-29 2014-10-07 Anhui New Star Pharmaceutical Development Co., Ltd. Intermediate for preparing tapentadol or analogues thereof

Family Cites Families (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1355668A (fr) * 1963-02-05 1964-03-20 Moteur rotatif à combustion interne perfectionné
FR1355667A (fr) * 1963-02-05 1964-03-20 Meci Materiel Elect Contr Gaine tubulaire pour électrode servant à la mesure du ph
FR2096877B1 (enExample) * 1970-07-09 1973-08-10 Hexachimie
JPH0665657B2 (ja) * 1984-11-08 1994-08-24 日本化薬株式会社 光学活性マンデル酸の製法
JPH072677B2 (ja) * 1988-02-19 1995-01-18 株式会社クラレ (±)―2―ヒドロキシ―4―フェニルブタン酸の光学分割法
JPH01221345A (ja) * 1988-02-27 1989-09-04 Ajinomoto Co Inc マンデル酸誘導体の光学分割方法
JP3084577B2 (ja) * 1991-09-27 2000-09-04 山川薬品工業株式会社 光学活性なアトロラクチン酸の製造方法および製造の中間体
JP3178086B2 (ja) * 1992-06-17 2001-06-18 山川薬品工業株式会社 光学活性α−メチルベンジルアミンの製造方法
ZA938019B (en) * 1992-11-13 1995-04-28 Upjohn Co Pyran-2-ones and 5,6-dihydropyran-2-ones useful for treating HIV and other retroviruses
PT1142887E (pt) * 1993-11-19 2004-08-31 Parke Davis & Co Derivados de 5,6-di-hidropirona como inibidores de protease e agentes antivirais
IL129871A (en) * 1994-05-06 2003-11-23 Pharmacia & Upjohn Inc Process for preparing 4-phenyl-substituted octanoyl-oxazolidin-2-one intermediates that are useful for preparing pyran-2-ones useful for treating retroviral infections
RU2074169C1 (ru) * 1995-05-10 1997-02-27 Акционерное общество открытого типа "Химпром" Способ получения этилового эфира п-нитробензойной кислоты

Also Published As

Publication number Publication date
FI20000553L (fi) 2000-03-10
EP1015441B1 (en) 2004-05-12
CN1298714C (zh) 2007-02-07
EP1015441A1 (en) 2000-07-05
PL193240B1 (pl) 2007-01-31
RU2003131081A (ru) 2005-04-10
NO20001274D0 (no) 2000-03-10
KR20010023864A (ko) 2001-03-26
HU228986B1 (en) 2013-07-29
HK1030418A1 (en) 2001-05-04
AU9296598A (en) 1999-03-29
CA2300204A1 (en) 1999-03-18
US6077963A (en) 2000-06-20
CZ2000804A3 (cs) 2000-08-16
ATE266654T1 (de) 2004-05-15
PL339138A1 (en) 2000-12-04
NO321835B1 (no) 2006-07-10
FI120973B (fi) 2010-05-31
HUP0003593A2 (hu) 2001-02-28
PT1015441E (pt) 2004-08-31
RU2263106C2 (ru) 2005-10-27
WO1999012919A1 (en) 1999-03-18
RU2223958C2 (ru) 2004-02-20
JP5016621B2 (ja) 2012-09-05
JP2001515895A (ja) 2001-09-25
SK2262000A3 (en) 2000-10-09
CZ298847B6 (cs) 2008-02-27
HUP0003593A3 (en) 2002-12-28
NZ503338A (en) 2002-03-01
JP2009138002A (ja) 2009-06-25
CA2300204C (en) 2006-12-12
DE69823844D1 (de) 2004-06-17
CN100471832C (zh) 2009-03-25
DE69823844T2 (de) 2005-04-14
US6265604B1 (en) 2001-07-24
CN1268947A (zh) 2000-10-04
ES2221199T3 (es) 2004-12-16
HK1063776A1 (en) 2005-01-14
JP4462760B2 (ja) 2010-05-12
JP5266194B2 (ja) 2013-08-21
SK284974B6 (sk) 2006-03-02
AU743496B2 (en) 2002-01-24
CN1511820A (zh) 2004-07-14
NO20001274L (no) 2000-05-10
CN1284763C (zh) 2006-11-15
HK1104027A1 (zh) 2008-01-04
JP2010090157A (ja) 2010-04-22
CN1990452A (zh) 2007-07-04
DK1015441T3 (da) 2004-07-26

Similar Documents

Publication Publication Date Title
JP5266194B2 (ja) プロテアーゼインヒビターとして有用な4−ヒドロキシ−2−オキソ−ピラン誘導体の製法
US4719048A (en) Crysene compound
EP0641306A1 (en) Carbocyclic and heterocyclic hiv protease inhibitors
AU743496C (en) Process to produce 4-hydroxy-2-oxo-pyrane derivates useful as protease inhibitors
MXPA00002411A (en) Process to produce 4-hydroxy-2-oxo-pyrane derivates useful as protease inhibitors
KR101033290B1 (ko) 다이아이소프로필((1-(하이드록시메틸)-사이클로프로필)옥시)메틸포스포네이트의 새로운 제조 방법
US4829090A (en) Chrysene derivatives
US4810727A (en) Chrysene compound
HK1104027B (en) Compounds useful to produce a protease inhibitor
EP1100799B1 (fr) Preparation de derives de la camptothecine et de la nothapodytine
FR2801589A1 (fr) Derives de 2-arylquinoleine, leur preparation et leur application en therapeutique
HK1030418B (en) Process to produce 4-hydroxy-2-oxo-pyrane derivates useful as protease inhibitors
HK1063776B (en) Compounds usefull to produce a protease inhibitors
FR2696174A1 (fr) Nouveaux dérivés chroméniques à chaîne triénique diméthylée, leur procédé de préparation et les compositions pharmaceutiques les renfermant.
JPS6411022B2 (enExample)

Legal Events

Date Code Title Description
PA0105 International application

Patent event date: 20000310

Patent event code: PA01051R01D

Comment text: International Patent Application

PG1501 Laying open of application
A201 Request for examination
PA0201 Request for examination

Patent event code: PA02012R01D

Patent event date: 20030819

Comment text: Request for Examination of Application

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20050628

Patent event code: PE09021S01D

E902 Notification of reason for refusal
PE0902 Notice of grounds for rejection

Comment text: Notification of reason for refusal

Patent event date: 20051012

Patent event code: PE09021S01D

E701 Decision to grant or registration of patent right
PE0701 Decision of registration

Patent event code: PE07011S01D

Comment text: Decision to Grant Registration

Patent event date: 20060315

GRNT Written decision to grant
PR0701 Registration of establishment

Comment text: Registration of Establishment

Patent event date: 20060404

Patent event code: PR07011E01D

PR1002 Payment of registration fee

Payment date: 20060405

End annual number: 3

Start annual number: 1

PG1601 Publication of registration
PR1001 Payment of annual fee

Payment date: 20090331

Start annual number: 4

End annual number: 4

PR1001 Payment of annual fee

Payment date: 20100331

Start annual number: 5

End annual number: 5

PR1001 Payment of annual fee

Payment date: 20110330

Start annual number: 6

End annual number: 6

FPAY Annual fee payment

Payment date: 20120329

Year of fee payment: 7

PR1001 Payment of annual fee

Payment date: 20120329

Start annual number: 7

End annual number: 7

FPAY Annual fee payment

Payment date: 20130329

Year of fee payment: 8

PR1001 Payment of annual fee

Payment date: 20130329

Start annual number: 8

End annual number: 8

FPAY Annual fee payment

Payment date: 20160330

Year of fee payment: 11

PR1001 Payment of annual fee

Payment date: 20160330

Start annual number: 11

End annual number: 11

FPAY Annual fee payment

Payment date: 20170330

Year of fee payment: 12

PR1001 Payment of annual fee

Payment date: 20170330

Start annual number: 12

End annual number: 12

FPAY Annual fee payment

Payment date: 20180329

Year of fee payment: 13

PR1001 Payment of annual fee

Payment date: 20180329

Start annual number: 13

End annual number: 13

EXPY Expiration of term
PC1801 Expiration of term

Termination date: 20190303

Termination category: Expiration of duration