YU63496A - Novel compounds, farmacutical prepartions containing them and a process for the preparation thereof - Google Patents

Novel compounds, farmacutical prepartions containing them and a process for the preparation thereof

Info

Publication number
YU63496A
YU63496A YU63496A YU63496A YU63496A YU 63496 A YU63496 A YU 63496A YU 63496 A YU63496 A YU 63496A YU 63496 A YU63496 A YU 63496A YU 63496 A YU63496 A YU 63496A
Authority
YU
Yugoslavia
Prior art keywords
hydrogen
optionally substituted
alkyl
denotes
group
Prior art date
Application number
YU63496A
Other languages
Serbo-Croatian (sh)
Inventor
Imre Bata
Sandor Batori
Judit Bence
Zsolt Bocskei
Eva Csikos
Sandor Erdo
Csaba Gonczi
Istvan Hermecz
Gergely Heja
Viktor Lakicz
Csilla Majlath
Peter Molnar
Benjamin Podanyi
Imola Ritz
Csutor Andrea Santane
Szappanos Andrea Szokene
Gyorgyne Szvoboda
Original Assignee
Chinoin, Gyogyszer Es Vegyeszeti Termekek
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 Chinoin, Gyogyszer Es Vegyeszeti Termekek filed Critical Chinoin, Gyogyszer Es Vegyeszeti Termekek
Publication of YU63496A publication Critical patent/YU63496A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/50Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with hetero atoms directly attached to ring nitrogen atoms
    • C07D241/54Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/36Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
    • C07D241/38Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
    • C07D241/40Benzopyrazines
    • C07D241/44Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring

Abstract

Pronalazak se odnosi na nove 3-amino-hinoksalin-2-on derivate opste formule I, na njihove soli, tautomerne oblike i N-okside, na farmaceutske preparate koji sadrze ova jedinjenja i na postupak za njihovo dobijanje, gde Z1 oznacava vodonik, hidroksi, C1-4 alkil, C7-9 fenilalkil, po izboru supstituisanu fenil, COOC1-4 alkil, C2-14 acil, C1-4 alkilsulfonil, trifluorometil-sulfonil, po izboru supstituisanu benzoil, i po izboru supstituisanu fenil-sulfonil grupu; Y1 oznacava vodonik ili po izboru supstituisanu amino grupu ili Y1 i Z1 grade zajedno -CO-O- grupu gde Y2 i Z2 oznacavaju zajedno valentnu vezu ili Y1 i Y2 oznacavaju zajedno valentnu vezu, i u isto vreme Z2 oznacava vodonik, hidroksi, C1-4 alkil, C7-9 fenilalkil, po izboru supstituisanu fenil, COOC1-4 alkil, C2-14 acil, C1-4 alkilsulfonil, trifluorometil-sulfonil, po izboru supstituisanu benzoil, i po izboru supstituisanu fenil-sulfonil grupu; X1 i X2 oznacavaju zajedno =O ili =S ili X1 oznacava vodonik, -NHR4 ili -WR5 grupe i u isto vreme X2 oznacava vodonik ili X2 i X3 zajedno grade valentnu vezu; X3 oznacava vodonik, C1-4 alkil, C7-9 fenilalkil, po izboru supstituisanu fenil grupu; R1 i R2 oznacavaju vodonik, halogen, C1-4 alkil, trifluorometil, cijano, merkapto ili sulfonilamido grupu; R3 oznacava vodonik ili nitro grupu; R4 oznacava vodonik ili hidroksi grupu; R5 oznacava vodonik, C1-4 alkil, C7-9 fenilalkil grupu; W oznacava kiseonik ili sumpor, uz pretpostavku, da a) ako bar jedan od supstituenata R1, R2 i R3 nije vodonik ili b) ako znacenja Z1 i Z2 su vodonik, tada R1 je 6-hloro, R3 je vodonik, R2 nije 7-hloro ili R1 je 6-metil, R3 je vodonik, R2 nije 7-metil, jedinjenja opste formule I pokazuju znacajnu aktivnost na glicin vezujuce mesto NMDA receptora i stoga se mogu koristiti kao aktivni sastojci farmaceutskih preparata.The invention relates to novel 3-amino-quinoxalin-2-one derivatives of general formula I, to their salts, tautomeric forms and N-oxides, to pharmaceutical preparations containing these compounds and to a process for their preparation, wherein Z 1 denotes hydrogen, hydroxy , C1-4 alkyl, C7-9 phenylalkyl optionally substituted phenyl, COOC1-4 alkyl, C2-14 acyl, C1-4 alkylsulfonyl, trifluoromethylsulfonyl, optionally substituted benzoyl, and optionally substituted phenylsulfonyl; Y1 denotes hydrogen or an optionally substituted amino group or Y1 and Z1 form together a -CO-O- group where Y2 and Z2 denote together a valence bond or Y1 and Y2 denote together a valence bond and at the same time Z2 denotes hydrogen, hydroxy, C1-4 alkyl, C7-9 phenylalkyl optionally substituted phenyl, COOC1-4 alkyl, C2-14 acyl, C1-4 alkylsulfonyl, trifluoromethylsulfonyl, optionally substituted benzoyl, and optionally substituted phenylsulfonyl; X1 and X2 denote together = O or = S or X1 denotes hydrogen, -NHR4 or -WR5 groups and at the same time X2 denotes hydrogen or X2 and X3 together form a valence bond; X3 denotes hydrogen, C1-4 alkyl, C7-9 phenylalkyl, optionally substituted phenyl group; R 1 and R 2 represent hydrogen, halogen, C 1-4 alkyl, trifluoromethyl, cyano, mercapto or sulfonylamido group; R3 denotes hydrogen or a nitro group; R4 denotes a hydrogen or hydroxy group; R5 denotes hydrogen, a C1-4 alkyl, a C7-9 phenylalkyl group; W denotes oxygen or sulfur, assuming that a) if at least one of the substituents R1, R2 and R3 is not hydrogen or b) if the meanings Z1 and Z2 are hydrogen, then R1 is 6-chloro, R3 is hydrogen, R2 is not 7- chloro or R1 is 6-methyl, R3 is hydrogen, R2 is not 7-methyl, the compounds of general formula I show significant activity on the glycine binding site of the NMDA receptor and can therefore be used as active ingredients in pharmaceutical preparations.

YU63496A 1995-11-30 1996-11-28 Novel compounds, farmacutical prepartions containing them and a process for the preparation thereof YU63496A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
HU9503422A HUT76302A (en) 1995-11-30 1995-11-30 Quinoxaline derivatives, pharmaceutical compositions containing them and process for producing them

Publications (1)

Publication Number Publication Date
YU63496A true YU63496A (en) 1999-03-04

Family

ID=10987414

Family Applications (1)

Application Number Title Priority Date Filing Date
YU63496A YU63496A (en) 1995-11-30 1996-11-28 Novel compounds, farmacutical prepartions containing them and a process for the preparation thereof

Country Status (6)

Country Link
AU (1) AU7705396A (en)
HR (1) HRP960564A2 (en)
HU (1) HUT76302A (en)
WO (1) WO1997019934A1 (en)
YU (1) YU63496A (en)
ZA (1) ZA9610002B (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1304404A (en) * 1998-06-01 2001-07-18 盐野义制药株式会社 Cyanoiminoquinoxaline derivatives
EP1140936B1 (en) 1999-01-11 2004-03-17 Agouron Pharmaceuticals, Inc. Tricyclic inhibitors of poly(adp-ribose) polymerases
US6927214B1 (en) * 1999-01-15 2005-08-09 Novo Nordisk A/S Non-peptide GLP-1 agonists
ECSP003637A (en) 1999-08-31 2002-03-25 Agouron Pharma TRICYCLE POLY INHIBITORS (ADP-RIBOSA) POLYMERASES
US7365209B2 (en) 2003-02-11 2008-04-29 Pharmacopeia, Inc. Nitrogen heterocycle biaryls for osteoporosis and other diseases

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3446809A (en) * 1966-01-19 1969-05-27 Eastman Kodak Co Process for the preparation of 2-amino-3-hydroxyquinoxalines
EP0030795A3 (en) * 1979-12-06 1981-09-09 Imperial Chemical Industries Plc Quinoxaline derivatives, processes therefor, pharmaceutical compositions, and benzene derivatives
US5597922A (en) * 1994-07-29 1997-01-28 State Of Oregon, Acting By And Through The Oregon State Board Of Higher Education, Acting For And On Behalf Of The Oregon Health Sciences University And The University Of Oregon Glycine receptor antagonist pharmacophore

Also Published As

Publication number Publication date
HU9503422D0 (en) 1996-01-29
HUT76302A (en) 1997-07-28
AU7705396A (en) 1997-06-19
ZA9610002B (en) 1997-06-13
WO1997019934A1 (en) 1997-06-05
HRP960564A2 (en) 1998-02-28

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