4-chloro-6-methyl-pyrido[3,4-d]pyrimidine 、 3-氨基苯乙炔 在
silica 、 acetone hexanes 作用下,
以afforded 166 mg of the title product as its free-base which的产率得到(3-ethynyl-phenyl)-(6-methyl-pyrido[3,4-d]pyrimidin-4-yl)-amine hydrochloride
The invention relates to compounds of the formula
1
and to pharmaceutically acceptable salts thereof, wherein R
1
, R
2
and Z are as defined herein. The invention also relates to pharmaceutical compositions containing the compounds of formula I and to methods of using said compounds in the treatment of hyperproliferative diseases such as cancer.
Compounds represented by the following general formula:
[wherein A
g
is an optionally substituted 5- to 14-membered heterocyclic group, etc.; X
g
is —O—, —S—, etc.; Y
g
is an optionally substituted C
6-14
aryl group, an optionally substituted 5- to 14-membered heterocyclic group, etc.; and T
g1
is a group represented by the following general formula:
(wherein E
g
is a single bond or —N(R
g2
)—, R
g1
and R
g2
each independently represent a hydrogen atom, an optionally substituted C
1-6
alkyl group, etc. and Z
g
represents a C
1-8
alkyl group, a C
3-8
alicyclic hydrocarbon group, a C
6-14
aryl group, etc.)],
salts thereof or hydrates of the foregoing.
Compounds represented by the following general formula:
wherein A
g
is an optionally substituted 5- to 14-membered heterocyclic group, etc.; X
g
is —O—, —S—, etc.; Y
g
is an optionally substituted C
6-14
aryl group, an optionally substituted 5- to 14-membered heterocyclic group, etc.; and T
g1
is a group represented by the following general formula:
(wherein E
g
is a single bond or —N(R
g2
)—), R
g1
and R
g2
each independently represent a hydrogen atom, an optionally substituted C
1-6
alkyl group, etc. and Z
g
represents a C
1-8
alkyl group, a C
3-8
alicyclic hydrocarbon group, a C
6-14
aryl group, etc.), salts thereof or hydrates of the foregoing.