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公开(公告)号:SI1556387T1
公开(公告)日:2007-08-31
申请号:SI200330818
申请日:2003-10-17
Applicant: SERVIER LAB
Inventor: COUDERT GERARD , LEPIFRE FRANCK , CAIGNARD DANIEL-HENRI , RENARD PIERRE , HICKMAN JOHN , PIERRE ALAIN , KRAUS-BERTHIER LAURENCE
IPC: C07D498/00 , A61K31/00 , A61P35/00 , C07D265/00 , C07D497/04 , C07D497/14
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22.
公开(公告)号:UA80046C2
公开(公告)日:2007-08-10
申请号:UAA200511454
申请日:2004-05-04
Applicant: SERVIER LAB
Inventor: GRANDORGE EMMANUEL , FRANCOTTE PIERRE , BOVERY STEPHANE , DE TUILLOT PASCAL , PIROTTE BERNARD , LIEUSTAGE PIERRE , DANOBER LAURENCE , RENARD PIERRE , KENIARD DANIEL-HENRY
IPC: A61P25/18 , C07D513/04
Abstract: Compounds of the formula (I): , (I) wherein: A, is thienyl, furyl, pyrolyl, oxathiol, thiazole, isothiazole, oxazole or imidazole group, is ordinary or double bound, R1 is hydrogen atom, linear or branched (C1-C6)alkyl group, optionally substituted with one or more halogen atoms,or (C1-C6)alkoxy-(C1-C6)alkyl group, R2 is hydrogen atom linear or branched (C1-C6)alkyl group, optionally substituted with one or more halogen atoms, R3 is hydrogen atom or group, selected from linear or branched (C1-C6)alkyl, CONHR' and SO2NHR', wherein R' is linear or branched (C1-C6)alkyl group, enantiomers or diastereomers thereof as well as additive salts thereof with pharmaceutically accepted acid or base. Medicinal agents.
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23.
公开(公告)号:EA008446B1
公开(公告)日:2007-06-29
申请号:EA200500717
申请日:2003-11-04
Applicant: SERVIER LAB
Inventor: RAULT SYLVAIN , LANCELOT JEAN-CHARLES , KOPP MARINA , CAIGNARD DANIEL-HENRI , PFEIFFER BRUNO , RENARD PIERRE , BIZOT-ESPIARD JEAN-GUY
IPC: C07D471/04 , A61K31/44 , A61P3/04 , A61P3/06 , A61P3/10 , A61P9/10 , C07D221/00 , C07D235/00
Abstract: Соединенияформулы (I)вкоторой Rпредставляетсобойатомводорода, атомгалогенаилиалкильную, полигалоалкильную, циано, нитро, гидроксикарбонильную, алкоксикарбонильную, аминокарбонильную, алкиламинокарбонильнуюилидиалкиламинокарбонильнуюгруппу,Rпредставляетсобойатомводорода, алкильнуюгруппу, необязательнозамещеннуюарильнуюгруппу, необязательнозамещеннуюгетероарильнуюгруппу, илигруппу R -С(Х)-, вкоторойRпредставляетсобойалкильнуюгруппу, алкоксигруппу, аминогруппу, алкиламиногруппу, диалкиламиногруппу, необязательнозамещеннуюарильнуюгруппуилинеобязательнозамещеннуюгетероарильнуюгруппу,X представляетсобойатомкислорода, атомсеры, илигруппу NR, вкоторой Rпредставляетсобойатомводородаилиалкильнуюгруппу,Rпредставляетсобойатомводородаилиалкильнуюгруппу,n представляетсобойцелоечислоот 1 до 6 включительно.Изображениеобозначаетилиихэнантиомеры, диастереоизомеры, атакжеихсолиприсоединенияс фармацевтическиприемлемойкислотойилиоснованием. Лекарственныесредства.
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24.
公开(公告)号:UA79448C2
公开(公告)日:2007-06-25
申请号:UA20040907252
申请日:2003-02-04
Applicant: SERVIER LAB
Inventor: DASSONVILLE ALEXANDRA , BRETECHE ANNE , DUFLOS MURIEL , LE BAUT GUILLAUME , PFEIFFER BRUNO , RENARD PIERRE , LEVENS NIGEL , HUSSON-ROBERT BERNADETTE
IPC: A61K31/122 , A61K31/222 , A61K31/4402 , A61P3/10 , C07C45/00 , C07C45/28 , C07C46/00 , C07C46/10 , C07C50/00 , C07C50/28 , C07C50/30 , C07D213/50
Abstract: The invention concerns a compound of formula (I), wherein: R1 and R2, identical or different, represent each a hydrogen atom or an acyl or alkyl group; Ar represents an aryl or heteroaryl group; A represents a group selected from formula (II); R4 represents a hydrogen atom or an alkyl group; R5 represents a hydrogen atom or a group selected among alkyl, aryl and heteroaryl; R3 represents an aryl, heteroaryl, dicyclopropylmethyl or benzhydryl group, or A-R3 represents an optionally substituted naphthyl group, excluding 2,5-dihydioxy-3-(4-methoxyphenyl)-6-(2-phenylethenyl)-1,4-benzoquinone, 2,5-dihydroxy-3-(4-methoxyphenyl)-6-(2-naphthyl)-1,4-benzoquinone, and 2,5-dihydroxy-3 (2-naphthyl)-6-phenyl-1,4-benzoquinone. The inventive compound is useful for preparing medicines.
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25.
公开(公告)号:PT998471E
公开(公告)日:2007-06-05
申请号:PT98925703
申请日:1998-05-14
Applicant: SERVIER LAB
Inventor: RENARD PIERRE , VIAUD MARIE-CLAUDE , GUILLAUMET GERALD , GUARDIOLA-LEMAITRE BEATRICE , CHARTON ISABELLE , MAMAI AHMED , BENNEJEAN CAROLINE , DAUBOS PHILIPPE
IPC: C07D311/58 , A61K31/335 , A61K31/35 , A61K31/352 , A61K31/353 , A61K31/357 , A61K31/38 , A61K31/382 , A61K31/385 , A61K31/39 , A61P3/04 , A61P3/10 , A61P9/06 , A61P9/12 , A61P15/00 , A61P25/00 , A61P25/04 , A61P25/16 , A61P25/18 , A61P25/20 , A61P25/22 , A61P25/28 , A61P35/00 , A61P43/00 , C07D311/60 , C07D311/80 , C07D311/92 , C07D319/20 , C07D327/06 , C07D335/06 , C07D339/08 , C07D493/04
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公开(公告)号:NZ539195A
公开(公告)日:2007-05-31
申请号:NZ53919503
申请日:2003-10-17
Applicant: SERVIER LAB
Inventor: COUDERT GERARD , AYERBE NATHALIE , LEPIFRE FRANCK , ROUTIER SYLVAIN , CAIGNARD DANIEL-HENRI , RENARD PIERRE , HICKMAN JOHN , PEIRRE ALAIN , LEONCE STEPHANE
IPC: A61P35/00 , C07D471/14 , C07D487/04 , C07D491/14 , C07D491/147 , C07D491/22 , C07D498/14 , C07D498/22 , A61K31/5365
Abstract: Disclosed are compounds of formula (I) wherein: A, together with the carbon atoms to which it is bonded represents a group of formula (a) or (b) with substituents as defined in the specification; Y represents an oxygen atom or a methylene group; R2 represents H and R3 represents H, alkyl, aryl, aryl-alkyl and SO2CF3, or R2 and R3 form a bond; R1 represents a group selected from hydrogen or optionally substituted alkyl, aryl, aryl-alkyl or alkylene; Z1 and Z2 each represent a hydrogen atom or Z1 and Z2 together with the carbon atoms carrying them, form a phenyl group. Also disclosed are methods of forming the above compounds and their use in the treatment of tumours.
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公开(公告)号:ES2271653T3
公开(公告)日:2007-04-16
申请号:ES03767889
申请日:2003-11-04
Applicant: SERVIER LAB
Inventor: RAULT SYLVAIN , LANCELOT JEAN-CHARLES , KOPP MARINA , CAIGNARD DANIEL-HENRI , PFEIFFER BRUNO , RENARD PIERRE
IPC: C07D471/04 , A61K31/44 , A61P3/04 , A61P3/06 , A61P3/10 , A61P9/10 , C07D221/00 , C07D235/00
Abstract: Compuestos de **fórmula**, en la cual: R1 representa un átomo de hidrógeno, halógeno, un grupo alquilo, polihaloalquilo, ciano, nitro, hidroxicarbonilo, alcoxicarbonilo, aminocarbonilo, alquilaminocarbonilo o dialquilaminocarbonilo, R2 representa un átomo de hidrógeno, un grupo alquilo, arilo eventualmente sustituido, heteroarilo eventualmente sustituido o un grupo R20¿C(X)¿
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公开(公告)号:AT358677T
公开(公告)日:2007-04-15
申请号:AT03809362
申请日:2003-10-17
Applicant: SERVIER LAB
Inventor: COUDERT GERARD , LEPIFRE FRANCK , CAIGNARD DANIEL-HENRI , RENARD PIERRE , HICKMAN JOHN , PIERRE ALAIN , KRAUS-BERTHIER LAURENCE
IPC: A61P35/00 , C07D497/04 , C07D497/14 , C07D498/04 , A61K31/535 , C07D498/14 , C07D265/38
Abstract: Benzo(e)(1,4)oxazino(3,2-g)isoindole derivatives (I), and their enantiomers, diastereoisomers, N-oxides and addition salts with acids and bases are new. Benzo(e)(1,4)oxazino(3,2-g)isoindole derivatives of formula (I), and their enantiomers, diastereoisomers, N-oxides and addition salts with acids and bases are new W1 = atoms that complete phenyl or pyridyl; Z = hydrogen, halo, 1-6C alkyl or alkoxy (both optionally substituted by aryl), aryl, aryloxy or hydroxy; R1 = hydrogen, 1-6C alkyl, optionally substituted by aryl, aryl, COR5 or 1-6C alkylene, substituted by one or more of halo, cyano, OR6, NR6R7, COOR6, COR6 or CONHR6; R2 = hydrogen or -CH2CH2OR8; R3 and R4 = hydrogen, 1-6C alkyl, optionally substituted by aryl, or aryl, or together they complete a 5 or 6-membered, monocyclic heterocycle, optionally including an additional oxygen or nitrogen; n = 1-6; R5 = hydrogen, 1-6C alkyl or alkoxy, hydroxy, aryl, aryl(1-6C)alkyl or aryloxy; R6 and R7 = hydrogen, 1-6C alkyl, aryl(1-6C)alkyl or aryl, or together they complete a heterocycle as above; R8 = hydrogen, 1-6C alkyl, aryl, aryl(1-6C)alkyl, S(O)tR6 or -T1-R9; t = 0-2; T1 = 1-6C alkylene; R9 = halo, cyano, OR6, NR6R7, CHO, COOR6 or CONR6R7; and aryl = phenyl, naphthyl, di- or tetra-hydronaphthyl, indenyl or indanyl, all optionally substituted by one or more of halo, 1-6C (trihalo)alkyl or alkoxy, hydroxy or amino, optionally substituted by 1 or 2 1-6C alkyl. Independent claims are also included for the following:0041658 (1) methods for the preparation of (I); and (2) intermediates of formulae (X), (XI) and (XIV). Boc = tert-butoxycarbonyl; and Pg = Boc or phenoxycarbonyl.
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公开(公告)号:AT356814T
公开(公告)日:2007-04-15
申请号:AT98925703
申请日:1998-05-14
Applicant: SERVIER LAB
Inventor: GUILLAUMET GERALD , VIAUD MARIE-CLAUDE , MAMAI AHMED , CHARTON ISABELLE , RENARD PIERRE , BENNEJEAN CAROLINE , GUARDIOLA BEATRICE , DAUBOS PHILIPPE
IPC: A61K31/352 , A61K31/353 , A61K31/357 , A61K31/382 , A61K31/385 , A61K31/39 , A61P3/04 , A61P3/10 , A61P9/06 , A61P9/12 , A61P15/00 , A61P25/00 , A61P25/04 , A61P25/16 , A61P25/18 , A61P25/20 , A61P25/22 , A61P25/28 , A61P35/00 , A61P43/00 , C07D311/58 , C07D311/60 , C07D311/80 , C07D311/92 , C07D319/20 , C07D327/06 , C07D335/06 , C07D339/08 , C07D493/04 , A61K31/35
Abstract: The invention relates to compounds of formula (I):wherein:R1, R2 and R3 are as defined in the description,X is as defined in the description,Y represents an oxygen atom, a sulphur atom, a C(H)q group, SO or SO2,n is equal to from 0 to 5,A represents a NR5R6 group,and medicinal products containing the same which are useful in treating or in preventing melatoninergic disorders.
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公开(公告)号:DE60307875T2
公开(公告)日:2007-04-12
申请号:DE60307875
申请日:2003-11-04
Applicant: SERVIER LAB
Inventor: RAULT SYLVAIN , LANCELOT JEAN-CHARLES , KOPP MARINA , CAIGNARD DANIEL-HENRI , PFEIFFER BRUNO , RENARD PIERRE , BIZOT-ESPIARD JEAN-GUY
IPC: C07D471/04 , A61K31/44 , A61P3/04 , A61P3/06 , A61P3/10 , A61P9/10 , C07D221/00 , C07D235/00
Abstract: Imidazopyridine derivatives (I) are new. Imidazopyridine derivatives of formula (I), their enantiomers, diastereoisomers, and their salts with acids and bases are new. R1 = H, halogen, alkyl, polyhaloalkyl, CN, NO2, hydroxycarbonyl, alkoxycarbonyl, aminocarbonyl, or dialkylaminocarbonyl; R2 = H, alkyl, aryl (optionally substituted), heteroaryl (optionally substituted) or a group of formula R20-C(X)-; R20 = alkyl, alkoxy, amino, alkylamino, dialkylamino, aryl (optionally substituted), or heteroaryl (optionally substituted); X = O, S, or NR21; R21, R3 = H or alkyl; n = 1-6; and N = pyrido ring with the N atom in the 1, 2, 3, or 4 positions. Alkyl and alkoxy groups have 1-6 C atoms, aryl is phenyl or naphthyl, polyhaloalkyl groups having 1-3 C atoms and 1-7 halogen atoms, heteroaryl groups may be mono or bicyclic of 5 - 11 ring atoms, at least one ring being aromatic, and having 2 or 3 heteroatoms (O, N, S) and may be substituted by 1-3 alkyl groups. Optional substituents on aryl groups may be 1 or 2 substituents selected from halogens, alkyl, alkoxy, polyhaloalkyl, hydroxy, CN, NO2, amino, alkylamino, dialkylamino, carboxyl, amido, and -COO-alkyl groups, and heteroaryl groups having a non-aromatic ring may be further substituted on this non-aromatic ring by oxo.
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