BR9809055A - 5,7-disubstituted 4-amino-pyrido (2,3-d) pyrimidine compounds and their use as adenosinokinase inhibitors - Google Patents

5,7-disubstituted 4-amino-pyrido (2,3-d) pyrimidine compounds and their use as adenosinokinase inhibitors

Info

Publication number
BR9809055A
BR9809055A BR9809055-0A BR9809055A BR9809055A BR 9809055 A BR9809055 A BR 9809055A BR 9809055 A BR9809055 A BR 9809055A BR 9809055 A BR9809055 A BR 9809055A
Authority
BR
Brazil
Prior art keywords
alkyl
aryl
heteroaryl
heterocyclic
compounds
Prior art date
Application number
BR9809055-0A
Other languages
Portuguese (pt)
Inventor
Shripad S Bhagwatt
Chih-Hung Lee
Marlon D Cowart
Jeffrey Mckie
Anne Laure Grillot
Original Assignee
Abbott Lab
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 Abbott Lab filed Critical Abbott Lab
Publication of BR9809055A publication Critical patent/BR9809055A/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems

Abstract

"COMPOSTOS DE 4-AMINO--PIRIDO[2,3-d]PIRIMIDINA 5,7-DISSUBSTITUìDA E SEU USO COMO INIBIDORES DE ADENOSINOCINASE" Método para inibir adenosinocinase administrando um composto que tem a fórmula (I) onde R^ 1^ e R^ 2^ são independentemente selecionados entre H, alquila inferior, alcóxi (C~ 1~-C~ 6~)-alquila (C~ 1~-C~ 6~), aril-alquila (C~ 1~-C~ 6~), -C(O)-alquila (C~ 1~-C~ 6~), -C(O)-arila, -C(O)-heterocíclico, ou podem unir-se ao nitrogênio ao qual eles estão anexados, para formar um anel de 5 a 7 membros, contendo opcionalmente 1 a 2 heteroátomos adicionais, selecionados entre O, N ou S; R^ 3^ é selecionado em grupo consistindo de alquila inferior, alquenila inferior, alquinila inferior, ciclo-alquila, arila, aril-alquila, heteroarila, grupo heterocíclico, heteroaril-alquila ou heterociclo-alquila, em que os grupos heteroarila e heterocíclico estão ligados diretamente ou indiretamente por um carbono anelar; R^ 4^ é selecionado em grupo consistindo de alquila inferior, alquenila inferior, alquinila inferior, ciclo-alquila, arila, aril-alquila, heteroarila, grupo heterocíclico, heteroaril-alquila ou heterociclo-alquila; e uma linha tracejada - - - indica que uma dupla ligação está opcionalmente presente, desde que as valências apropriadas sejam mantidas, uma composição farmacêutica que compreende uma quantidade terapeuticamente eficaz de um desses compostos acima em combinação com um excipiente de uso farmacêutico, e um método para tratar isquemia cerebral, epilepsia, nicipercepção, inflamação e sepse em um mamífero que necessite desse tratamento, que compreende administrar ao mamífero uma quantidade terapeuticamente eficaz de um composto desses, um processo para preparar esses compostos, e compostos que têm a fórmula acima na qual R^ 1^, R^ 2^, R^ 3^ e R^ 4^ são definidos separadamente."4-AMINO COMPOUNDS - PIRID [2,3-d] PYRIMIDIN 5,7-DISSUBSTITUED AND THEIR USE AS ADENOSINOCINASE INHIBITORS" Method to inhibit adenosinokinase by administering a compound that has the formula (I) where R ^ 1 ^ e R ^ 2 ^ are independently selected from H, lower alkyl, (C ~ 1 ~ -C ~ 6 ~) -alkyl (C ~ 1 ~ -C ~ 6 ~), aryl-alkyl (C ~ 1 ~ -C ~ 6 ~), -C (O) -alkyl (C ~ 1 ~ -C ~ 6 ~), -C (O) -aryl, -C (O) -heterocyclic, or they can bond with the nitrogen to which they are attached, to form a 5- to 7-membered ring, optionally containing 1 to 2 additional heteroatoms, selected from O, N or S; R ^ 3 ^ is selected from the group consisting of lower alkyl, lower alkenyl, lower alkynyl, cycloalkyl, aryl, aryl-alkyl, heteroaryl, heterocyclic group, heteroaryl-alkyl or heterocycle-alkyl, in which the heteroaryl and heterocyclic groups are linked directly or indirectly by an annular carbon; R 4 is selected from the group consisting of lower alkyl, lower alkenyl, lower alkynyl, cycloalkyl, aryl, aryl-alkyl, heteroaryl, heterocyclic, heteroaryl-alkyl or heterocyclo-alkyl; and a dotted line - - - indicates that a double bond is optionally present, provided that the appropriate valencies are maintained, a pharmaceutical composition comprising a therapeutically effective amount of one of these compounds above in combination with a pharmaceutical excipient, and a method to treat cerebral ischemia, epilepsy, niciperception, inflammation and sepsis in a mammal in need of such treatment, which comprises administering to the mammal a therapeutically effective amount of such a compound, a process for preparing those compounds, and compounds having the above formula in which R ^ 1 ^, R ^ 2 ^, R ^ 3 ^ and R ^ 4 ^ are defined separately.

BR9809055-0A 1997-04-16 1998-04-14 5,7-disubstituted 4-amino-pyrido (2,3-d) pyrimidine compounds and their use as adenosinokinase inhibitors BR9809055A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US83821697A 1997-04-16 1997-04-16
PCT/US1998/007207 WO1998046605A1 (en) 1997-04-16 1998-04-14 5,7-disubstituted 4-aminopyrido[2,3-d]pyrimidine compounds and their use as adenosine kinase inhibitors

Publications (1)

Publication Number Publication Date
BR9809055A true BR9809055A (en) 2000-08-08

Family

ID=25276561

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9809055-0A BR9809055A (en) 1997-04-16 1998-04-14 5,7-disubstituted 4-amino-pyrido (2,3-d) pyrimidine compounds and their use as adenosinokinase inhibitors

Country Status (18)

Country Link
EP (1) EP0989986A1 (en)
JP (1) JP2001520655A (en)
KR (1) KR20010006509A (en)
CN (1) CN1252070A (en)
AR (1) AR012436A1 (en)
AU (1) AU7108398A (en)
BG (1) BG103842A (en)
BR (1) BR9809055A (en)
CA (1) CA2286909A1 (en)
CO (1) CO4940446A1 (en)
HU (1) HUP0001434A3 (en)
IL (1) IL131618A0 (en)
NO (1) NO995036D0 (en)
PL (1) PL336304A1 (en)
SK (1) SK141799A3 (en)
TR (1) TR199902455T2 (en)
WO (1) WO1998046605A1 (en)
ZA (1) ZA983177B (en)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000023444A1 (en) * 1998-10-21 2000-04-27 Abbott Laboratories 5,7-disubstituted-4-aminopyrido[2,3-d]pyrimidine compounds
ES2249574T3 (en) 2001-02-12 2006-04-01 F. Hoffmann-La Roche Ag PIRIDO-PIRIMIDINAS 6-REPLACED.
KR20040085151A (en) 2002-01-17 2004-10-07 뉴로젠 코포레이션 Substituted quinazolin-4-ylamine analogues as modulators of capsaicin
DE10335183A1 (en) * 2003-07-30 2005-02-24 Bayer Cropscience Ag Fungicidal drug combinations
ES2336603T3 (en) * 2005-07-21 2010-04-14 F. Hoffmann-La Roche Ag PIRIDO COMPOUNDS (2,3-D) PYRIMIDINE-2,4-DIAMINE AS INHIBITORS OF PTP1B.
CA2633757A1 (en) * 2005-12-21 2007-07-05 Abbott Laboratories Anti-viral compounds
US7915411B2 (en) 2005-12-21 2011-03-29 Abbott Laboratories Anti-viral compounds
CA2672737A1 (en) 2006-12-20 2008-11-06 Abbott Laboratories Anti-viral compounds
EP3311813B1 (en) 2007-08-27 2019-08-07 Dart Neuroscience (Cayman) Ltd Therapeutic isoxazole compounds
CL2008002542A1 (en) 2007-08-31 2009-01-02 Eisai R&D Man Co Ltd Imidazolyl pyridine derived compounds linked to a heterocycle via a vinyl, modulators of amyloid-beta activity; pharmaceutical composition comprising said compounds; and its use for the treatment of diseases such as Alzheimer's, dementia, Down syndrome or amyloidosis.
DE102007061764A1 (en) * 2007-12-20 2009-06-25 Bayer Healthcare Ag Anellated cyanopyridines and their use
TW201035101A (en) * 2009-02-26 2010-10-01 Eisai R&D Man Co Ltd Nitrogen-containing fused heterocyclic compound
JP6496246B2 (en) 2012-10-05 2019-04-03 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. Indoline compounds as related to aldosterone synthase inhibitors
WO2017172368A1 (en) 2016-03-31 2017-10-05 Oncternal Therapeutics, Inc. Indoline analogs and uses thereof
CN110256420B (en) * 2019-05-07 2020-04-28 江西中医药大学 Tetrahydropyridopyrimidine derivatives, their preparation and use
CN110283171A (en) * 2019-07-17 2019-09-27 鼎泰(南京)临床医学研究有限公司 Compound of the one kind containing Pyridopyrimidine -4- amine structure, pharmaceutical composition and its application

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5324731A (en) * 1989-02-14 1994-06-28 Amira, Inc. Method of inhibiting transformation of cells in which purine metabolic enzyme activity is elevated
IL112249A (en) * 1994-01-25 2001-11-25 Warner Lambert Co Pharmaceutical compositions containing di and tricyclic pyrimidine derivatives for inhibiting tyrosine kinases of the epidermal growth factor receptor family and some new such compounds
US6143749A (en) * 1995-06-07 2000-11-07 Abbott Laboratories Heterocyclic substituted cyclopentane compounds

Also Published As

Publication number Publication date
JP2001520655A (en) 2001-10-30
AR012436A1 (en) 2000-10-18
EP0989986A1 (en) 2000-04-05
ZA983177B (en) 1999-01-22
HUP0001434A2 (en) 2000-10-28
CA2286909A1 (en) 1998-10-22
WO1998046605A1 (en) 1998-10-22
HUP0001434A3 (en) 2001-01-29
KR20010006509A (en) 2001-01-26
CO4940446A1 (en) 2000-07-24
IL131618A0 (en) 2001-01-28
BG103842A (en) 2000-06-30
SK141799A3 (en) 2000-08-14
AU7108398A (en) 1998-11-11
NO995036L (en) 1999-10-15
PL336304A1 (en) 2000-06-19
TR199902455T2 (en) 2000-01-21
NO995036D0 (en) 1999-10-15
CN1252070A (en) 2000-05-03

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Legal Events

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FA10 Dismissal: dismissal - article 33 of industrial property law
B11Y Definitive dismissal - extension of time limit for request of examination expired [chapter 11.1.1 patent gazette]