ZA200006007B - Method for preparing sodium-hydrogen exchanger type 1 inhibitor. - Google Patents

Method for preparing sodium-hydrogen exchanger type 1 inhibitor.

Info

Publication number
ZA200006007B
ZA200006007B ZA200006007A ZA200006007A ZA200006007B ZA 200006007 B ZA200006007 B ZA 200006007B ZA 200006007 A ZA200006007 A ZA 200006007A ZA 200006007 A ZA200006007 A ZA 200006007A ZA 200006007 B ZA200006007 B ZA 200006007B
Authority
ZA
South Africa
Prior art keywords
inhibitor
exchanger type
preparing sodium
hydrogen exchanger
hydrogen
Prior art date
Application number
ZA200006007A
Other languages
English (en)
Inventor
Norma Jacqueline Tom
Original Assignee
Pfizer Prod Inc
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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of ZA200006007B publication Critical patent/ZA200006007B/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C279/00—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups
    • C07C279/04—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton
    • C07C279/10—Derivatives of guanidine, i.e. compounds containing the group, the singly-bound nitrogen atoms not being part of nitro or nitroso groups having nitrogen atoms of guanidine groups bound to acyclic carbon atoms of a carbon skeleton being further substituted by doubly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Cardiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
ZA200006007A 1999-10-29 2000-10-26 Method for preparing sodium-hydrogen exchanger type 1 inhibitor. ZA200006007B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US16237799P 1999-10-29 1999-10-29

Publications (1)

Publication Number Publication Date
ZA200006007B true ZA200006007B (en) 2002-04-26

Family

ID=22585372

Family Applications (1)

Application Number Title Priority Date Filing Date
ZA200006007A ZA200006007B (en) 1999-10-29 2000-10-26 Method for preparing sodium-hydrogen exchanger type 1 inhibitor.

Country Status (19)

Country Link
US (1) US6441176B1 (cs)
EP (1) EP1101763A3 (cs)
JP (1) JP3342475B2 (cs)
KR (2) KR100449595B1 (cs)
CN (1) CN1146557C (cs)
AR (1) AR029188A1 (cs)
AU (1) AU779106B2 (cs)
BR (1) BR0005122A (cs)
CA (1) CA2324640A1 (cs)
CZ (1) CZ20004018A3 (cs)
HU (1) HUP0004187A2 (cs)
ID (1) ID27904A (cs)
IL (1) IL139198A0 (cs)
PL (1) PL343542A1 (cs)
RU (1) RU2190605C2 (cs)
TR (1) TR200003143A2 (cs)
TW (1) TWI221152B (cs)
YU (1) YU62900A (cs)
ZA (1) ZA200006007B (cs)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6852733B2 (en) 2000-04-28 2005-02-08 Pfizer Inc. Sodium-hydrogen exchanger type 1 inhibitor
WO2002060892A1 (en) * 2001-01-31 2002-08-08 Pfizer Products Inc. Ethanolates of sodium-hydrogen exchanger type-1 inhibitor
CA2469305A1 (en) * 2001-12-19 2003-06-26 Frank Robert Busch Methods for preparing sodium-hydrogen exchanger type-1 inhibitors

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028381A (en) * 1975-05-05 1977-06-07 Ciba-Geigy Corporation Pyrazolobenzazepines
DE4226649A1 (de) * 1992-08-12 1994-02-17 Bayer Ag Neue isobutylsubstituierte Methansulfonyl-chinolylmethoxyphenyl-cycloalkylessigsäureaminole
RU2009129C1 (ru) * 1991-12-16 1994-03-15 Центр по химии лекарственных средств Арилгидразоны 5,6,7,8-тетрагидрохинолиндионы-2,5, обладающие кардиотонической активностью
US6184380B1 (en) * 1999-01-25 2001-02-06 Pfizer Inc. Process for preparing naphthyridones and intermediates
KR100449600B1 (ko) 1998-02-27 2004-09-21 화이자 프로덕츠 인크. 허혈 치료용 ｎ-[(치환된 5원 디아자 이불포화 고리)카르보닐] 구아니딘 유도체
UA72002C2 (en) 1999-10-29 2005-01-17 Pfizer Prod Inc Inhibitors crystals of sodium-hydrogen exchange of 1 type, a method for the preparation thereof (variants), a pharmaceuticalcomposition based thereon and a method for the reduction of tissue damage

Also Published As

Publication number Publication date
AU6133300A (en) 2001-05-03
IL139198A0 (en) 2001-11-25
CZ20004018A3 (cs) 2002-04-17
HU0004187D0 (cs) 2001-01-29
AU779106B2 (en) 2005-01-06
CN1146557C (zh) 2004-04-21
PL343542A1 (en) 2001-05-07
YU62900A (sh) 2003-08-29
TR200003143A2 (tr) 2001-05-21
EP1101763A2 (en) 2001-05-23
KR100449595B1 (ko) 2004-09-21
TWI221152B (en) 2004-09-21
HK1036057A1 (en) 2003-07-10
ID27904A (id) 2001-05-03
BR0005122A (pt) 2001-06-19
AR029188A1 (es) 2003-06-18
KR100443851B1 (ko) 2004-08-11
EP1101763A3 (en) 2002-04-24
RU2190605C2 (ru) 2002-10-10
CN1295070A (zh) 2001-05-16
CA2324640A1 (en) 2001-04-29
KR20010060211A (ko) 2001-07-06
US6441176B1 (en) 2002-08-27
JP2001158784A (ja) 2001-06-12
KR20030061767A (ko) 2003-07-22
JP3342475B2 (ja) 2002-11-11
HUP0004187A2 (hu) 2002-11-28

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