申请人:Mciver Edward Giles
公开号:US20100317646A1
公开(公告)日:2010-12-16
A compound of formula I, or a pharmaceutically acceptable salt or ester thereof,
wherein R
1
is selected from: aryl; heteroaryl; —NHR
3
; fused aryl-C
4-7
-heterocycloalkyl; —CONR
4
R
5
; —NHCOR
6
; —C
3-7
-cycloalkyl; —O—C
3-7
-cycloalkyl; —NR
3
R
6
; and optionally substituted —C
1-6
alkyl; wherein said aryl, heteroaryl, fused aryl-C
4-7
-heterocycloalkyl and C
4-7
-heterocycloalkyl are each optionally substituted;
R
2
is selected from hydrogen, aryl, C
1-6
-alkyl, C
2-6
-alkenyl, C
3-7
-cycloalkyl, heteroaryl, C
4-7
heterocycloalkyl and halogen, wherein said C
1-6
-alkyl, C
2-6
-alkenyl, aryl, heteroaryl and C
4-7
-heterocycloalkyl are each optionally substituted;
R
3
is selected from aryl, heteroaryl, C
4-7
-heterocycloalkyl, C
3-7
-cycloalkyl, fused aryl-C
4-7
-heterocycloalkyl and C
1-6
-alkyl, each of which is optionally substituted;
R
4
and R
5
are each independently hydrogen, or optionally substituted C
3-7
-cycloalkyl, aryl, heteroaryl, C
1-6
-alkyl or C
3-6
-heterocycloalkyl; or R
4
and R
5
together with the N to which they are attached form a C
3-6
-heterocycloalkyl ring;
each R
6
is independently selected from C
1-6
-alkyl, C
3-7
cycloalkyl, C
4-7
-heterocycloalkyl, aryl and heteroaryl, each of which is optionally substituted
each R
7
is selected from hydrogen, optionally substituted C
1-6
-alkyl and C
3-7
-cycloalkyl;
each of R
8
and R
9
is independently hydrogen or optionally substituted C
1-6
-alkyl; or
R
8
and R
9
together with the N to which they are attached form a C
4-6
-heterocycloalkyl;
each R
10
is selected from C
3-7
-cycloalkyl and optionally substituted C
1-6
-alkyl;
each R
11
is independently selected from C
1-6
-alkyl, C
3-7
-cycloalkyl, C
1-6
alkyl-C
3-7
-cycloalkyl, C
4-7
-heterocycloalkyl, aryl and heteroaryl, each of which is optionally substituted;
A is selected from halogen, —NR
4
SO
2
R
5
, —CN, —OR
6
, —NR
4
R
5
, —NR
7
R
11
, hydroxyl, —CF
3
, —CONR
4
R
5
, —NR
4
COR
5
, —NR
7
(CO)NR
4
R
5
, —NO
2
, —CO
2
H, —CO
2
R
6
, —SO
2
R
6
, —SO
2
NR
4
R
5
, —NR
4
COR
5
, —NR
4
COOR
5
, C
1-6
-alkyl and —COR
6
.
Further aspects relate to pharmaceutical compositions, therapeutic uses and process for preparing compounds of formula I.
化合物I的公式,或其药学上可接受的盐或
酯,其中R1选自:芳基;杂环芳基;—NHR3;融合的芳基-C4-7-杂
环烷基;—CONR4R5;—NHCOR6;—C3-7-
环烷基;—O—C3-7-
环烷基;—NR3R6;和可选择取代的—C1-6烷基;其中所述的芳基,杂环芳基,融合的芳基-C4-7-杂
环烷基和C4-7-杂
环烷基均可选择取代;R2选自
氢,芳基,C1-6-烷基,C2-6-
烯基,C3-7-
环烷基,杂环芳基,C4-7-杂
环烷基和卤素,其中所述的C1-6-烷基,C2-6-
烯基,芳基,杂环芳基和C4-7-杂
环烷基均可选择取代;R3选自芳基,杂环芳基,C4-7-杂
环烷基,C3-7-
环烷基,融合的芳基-C4-7-杂
环烷基和C1-6-烷基,每种均可选择取代;R4和R5各自独立地选自
氢,或可选择取代的C3-7-
环烷基,芳基,杂环芳基,C1-6-烷基或C3-6-杂
环烷基;或R4和R5与它们连接的N一起形成C3-6-杂
环烷基环;每个R6各自独立地选自C1-6-烷基,C3-7-
环烷基,C4-7-杂
环烷基,芳基和杂环芳基,每种均可选择取代;每个R7选自
氢,可选择取代的C1-6-烷基和C3-7-
环烷基;每个R8和R9各自独立地选自
氢或可选择取代的C1-6-烷基;或R8和R9与它们连接的N一起形成C4-6-杂
环烷基;每个R10选自C3-7-
环烷基和可选择取代的C1-6-烷基;每个R11各自独立地选自C1-6-烷基,C3-7-
环烷基,C1-6-烷基-C3-7-
环烷基,C4-7-杂
环烷基,芳基和杂环芳基,每种均可选择取代;A选自卤素,—NR4SO2R5,—CN,—OR6,—NR4R5,—NR7R11,羟基,—
CF3,—CONR4R5,—NR4COR5,—NR7(CO)NR4R5,—
NO2,—CO2H,—CO2R6,—SO2R6,—SO2NR4R5,—NR4COR5,—NR4COOR5,C1-6-烷基和—COR6。进一步方面涉及公式I化合物的制药组合物,治疗用途和制备过程。