申请人:De Corte Bart
公开号:US20080176880A1
公开(公告)日:2008-07-24
This invention concerns the use of compounds of formula
the N-oxides, the pharmaceutically acceptable addition salts, quaternary amines and the stereochemically isomeric forms thereof, wherein -a
1
=a
2
-a
3
=a
4
- forms a phenyl, pyridinyl; pyrimidinyl, pyridazinyl or pyrazinyl with the attached vinyl group; n is 0 to 4; and where possible 5. R
1
is hydrogen, al, formyl, C
1-6
alkylcarbonyl, C
1-6
alkyl, C
1-6
alkyloxy-carbonyl, substituted C
1-6
alkyl, or substituted C
1-6
alkyloxyC
1-6
alkylcarbonyl; each R
2
independently is hydroxy, halo, optionally substituted C
1-6
alkyl, C
2-6
alkenyl or C
2-6
alkynyl, C
3-7
cycloalkyl, C
1-6
alkyloxy, C
1-6
alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C
1-6
alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)
p
R
6
, —NH—S(═O)
p
R
6
, —C(═O)R
6
, —NHC(═CO)H, —C(═O)NHNH
2
, —NHC(═O)R
6
, —C(═NH)R
6
or a 5-membered heterocyclic ring; p is 1 or 2; L is optionally substituted C
1-10
alkyl, C
2-10
alkenyl, C
2-10
alkynyl or C
3-7
cycloalkyl; or L is —X—R
3
wherein R
3
is optionally substituted phenyl, pyridinyl, pyrimidinyl, pyrazinyl or pyridazinyl; X is —NR
1
—, —NH—NH—, —N═N—, —O—, —C(═O)—, —CHOH—, —S—, —S(═O)— or —S(═O)
2
—; Q is hydrogen, C
1-6
alkyl, halo, polyhalo-C
1-6
alkyl or an optionally substituted amino group; Y represents hydroxy, halo, C
3-7
cycloalkyl, optionally substituted C
1-6
alkyl, C
2-6
alkenyl or C
2-6
alkynyl, C
1-6
alkyloxy, C
1-6
alkyloxycarbonyl, carboxyl, cyano, nitro, amino, mono- or di(C
1-6
alkyl)amino, polyhalomethyl, polyhalomethyloxy, polyhalomethylthio, —S(═O)
p
R
6
, —NH—S(═O)
p
R
6
, —C(═O)R
6
, —NHC(═O)H, —C(═O)NHNH
2
, —C(—O)R
6
, —C(═NH)R
6
or aryl; aryl is optionally substituted phenyl; Het is an optionally substituted heterocyclic radical; for the manufacture of a medicine for the treatment of subjects suffering from HIV (Human Immunodeficiency Virus) infection.
本发明涉及使用式中化合物的使用,其中N-氧化物,药学上可接受的加成盐,季铵盐及其立体化学异构体形式,其中-a1=a2-a3=a4-形成苯基,吡啶基;嘧啶基,吡嗪基或吡咯基与附加的乙烯基;n为0至4;如有可能为5。R1为氢,醇基,甲酰基,C1-6烷基羰基,C1-6烷基,C1-6烷氧基羰基,取代的C1-6烷基或取代的C1-6烷氧基C1-6烷基羰基;每个R2独立地为羟基,卤素,可选取代的C1-6烷基,C2-6烯基或C2-6炔基,C3-7环烷基,C1-6烷氧基,C1-6烷氧基羰基,羧基,氰基,硝基,氨基,单烷基或双(C1-6烷基)氨基,多卤代甲基,多卤代甲氧基,多卤代甲硫基,-S(═O)pR6,-NH-S(═O)pR6,-C(═O)R6,-NHC(═CO)H,-C(═O)NHNH2,-NHC(═O)R6,-C(═NH)R6或5-成员杂环环;p为1或2;L为可选取代的C1-10烷基,C2-10烯基,C2-10炔基或C3-7环烷基;或L为-X-R3,其中R3为可选取代的苯基,吡啶基,嘧啶基,吡咯基或吡嗪基;X为-NR1-,-NH-NH-,-N═N-,-O-,-C(═O)-,-CHOH-,-S-,-S(═O)-或-S(═O)2-;Q为氢,C1-6烷基,卤素,多卤代C1-6烷基或可选取代的氨基基团;Y代表羟基,卤素,C3-7环烷基,可选取代的C1-6烷基,C2-6烯基或C2-6炔基,C1-6烷氧基,C1-6烷氧基羰基,羧基,氰基,硝基,氨基,单烷基或双(C1-6烷基)氨基,多卤代甲基,多卤代甲氧基,多卤代甲硫基,-S(═O)pR6,-NH-S(═O)pR6,-C(═O)R6,-NHC(═O)H,-C(═O)NHNH2,-C(—O)R6,-C(═NH)R6或芳基;芳基为可选取代的苯基;Het为可选取代的杂环基团;用于制造治疗感染艾滋病毒(HIV)的患者的药物。