Quinazoline derivatives as kinase inhibitors
Abstract
The Present invention relates to nitrogen-containing heterocyclic compounds and pharmaceutically acceptable salts thereof which have inhibitory activity on the phosphorylation of kinases, which inhibits the activity of such kinases. The invention is also related to a method of inhibiting kinases and treating disease states in a mammal by inhibiting the phosphorylation of kinases. In a particular aspect the present invention provides nitrogen-containing heterocyclic compounds and pharmaceutically acceptable salts thereof which inhibit phosphorylation of a PDGF receptor to hinder abnormal cell growth and cell wandering, and a method for preventing or treating cell-proliferative diseases such as arteriosclerosis, vascular reobstruction, cancer and glomerulosclerosis.
Claims
exact text as granted — not AI-modified1 .- 12 . (canceled)
13 . A compound selected from the group consisting of:
{4-[6-methoxy-7-(2-methoxyethoxy)quinazolin-4-yl]piperazinyl}-N-(4-naphthyloxyphenyl)carboxamide
{4-[6-methoxy-7-(2-methoxyethoxy)quinazolin-4-yl]piperazinyl}-N-(4-phenoxyphenyl)carboxamide
{4-[6-methoxy-7-(ethoxy)quinazolin-4-yl]piperazinyl}-N-(4-phenoxyphenyl)carboxamide
{4-[6-methoxy-7-(ethoxy)quinazolin-4-yl]piperazinyl}-N-(4-phenyl)carboxamide
{4-[6-methoxy-7-(ethoxy)quinazolin-4-yl]piperazinyl}-N-(4-cyanophenyl)carboxamide
{4-[6-methoxy-7-(prop-2-enylethoxy)quinazolin-4-yl]piperazinyl}-N-(4-cyanophenyl)carboxamide
{4-[6-methoxy-7-(prop-2-enylethoxy)quinazolin-4-yl]piperazinyl}-N-(4-methylethoxyphenyl)carboxamide
[4-(6-methoxy-7-prop-2-enyloxyquinazolin-4-yl)piperazinyl]-N-(4-naphthyloxyphenyl)carboxamide
N-(4-indol-4-yloxyphenyl)[4-(6-methoxy-7-prop-2-enyloxyquinazolin-4-yl)piperazinyl]carboxamide
[4-(6-methoxy-7-prop-2-enyloxyquinazolin-4-yl)piperazinyl]-N-(4-phenoxyphenyl)carboxamide
N-(4-cyanophenyl) [4-(6-methoxy-7-prop-2-ynyloxyquinazolin-4-yl)piperazinyl]carboxamide
[4-(6-methoxy-7-prop-2-ynyloxyquinazolin-4-yl)piperazinyl]-N-(4-(methylethoxy)phenyl]carboxamide
[4-(6-methoxy-7-prop-2-ynyloxyquinazolin-4-yl)piperazinyl]-N-(4-naphthyloxyphenyl)carboxamide
N-(4-indol-4-yloxyphenyl)[4-(6-methoxy-7-prop-2-ynyloxy quinazolin-4-yl)piperazinyl]carboxamide
[4-(6-methoxy-7-prop-2-ynyloxyquinazolin-4-yl)piperazinyl]-N-(4-phenoxyphenyl)carboxamide
{4-[7-(2-hydroxy-3-piperidylpropoxy)-6-methoxyquinazolin-4-yl]piperazinyl}-N-[4-(methylethoxy)phenyl]carboxamide
{4-[7-(2-fluoro-3-piperidylpropoxy)-6-methoxyquinazolin-4-yl]piperazinyl}-N-[4-(methylethoxy)phenyl]carboxamide
[4-(6-methoxy-7-{3-[(2-methylpropyl)sulfonyl]propoxy}quinazolin-4-yl)piperazinyl]-N-[4-(methylethoxy)phenyl]carboxamide
(4-{6-methoxly-7-[3-(propylsulfonyl)propoxy]quinazolin-4-yl}piperazinyl)-N-[4-(methylethoxy)phenyl]carboxamide
methyl 4-({4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}carbonylamino)benzoate
N-(4-acetylphenyl) {4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}carboxamide
N-(4-bromophenyl){4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}carboxamide
{4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}-N-[4-(trifluoromethyl)phenyl]carboxamide
{4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}-N-(4-methylphenyl)carboxamide
{4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}-N-[4-(methylsulfonyl)phenyl]carboxamide
N-(4-fluorophenyl){4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}carboxamide
4-({4-[6-methoxy-7-(3-pyrrolidinylpropoxy)quinazolin-4-yl]piperazinyl}carbonylamino)benzoic acid
and all pharmaceutically acceptable salts or hydrates thereof.
14 . A pharmaceutical composition comprising an effective amount of a compound according to claim 13 , or a pharmaceutically acceptable salt or hydrate thereof, and a pharmaceutically acceptable diluent or carrier.
15 . A method of inhibiting phosphorylation of PDGF receptor in a patient comprising the step of administering a compound of claim 13 and all pharmaceutically acceptable salts and hydrates thereof to the patient.
16 . A method of inhibiting phosphorylation of PDGF receptor in a patient comprising the step of administering a compound of the formula:
wherein
R 1 is a member selected from the group consisting of:
CN, —X, —CX 3 , —R 5 , —CO 2 R 5 , —C(O)R 5 , —SO 2 R 5 , —O—C 1-8 alkyl that is straight or branched chained, —O-phenyl, —O-naphthyl, —O-indolyl and —O-isoquinolinyl
X is halogen;
R 5 is hydrogen or a C 1-8 alkyl that is straight or branched chained;
R 2 is —O—CH 3 ;
R 4 is a member selected from the group consisting of:
—O—CH 2 —CH═CH 2 , —O(CH 2 ), —SO 2 —R 5 and —O—CH 2 —CH(R 6 )CH 2 —R 3 ;
R 6 is —OH, —X, or a C 1-8 alkyl that is straight or branched chained;
n is 2 or 3;
R 3 is a member selected from the group consisting of:
—OH, —O—CH 3 , —O—CH 2 —CH 3 , —NH 2 , —N(—CH 3 ) 2 , —NH(—CH 2 -phenyl), —NH(-phenyl), —CN
and all pharmaceutically acceptable salts and hydrates thereof to the patient.
17 . The method of claim 16 , wherein R 1 is a member selected from the group consisting of CN, —O-methyl, —O-ethyl, —O-propyl, —O-isopropyl, —O-butyl, —O-t-butyl, —O— isoamyl, 1-naphthyloxy, 2-naphthyloxy, 4-indolyloxy, 5-indolyloxy, 5-isoquinolyloxy, and all pharmaceutically acceptable salts and hydrates of such compounds.
18 . The method of claim 16 wherein the compound has the formula I(a) or formula I(b) as follows:
wherein
R 1 is a member selected from the group consisting of CN, —O-methyl, —O-ethyl, —O-propyl, —O— isopropyl, —O-butyl, —O-t-butyl, —O-isoamyl, 1-naphthyloxy, 2-naphthyloxy, 4-indolyloxy, 5-indolyloxy, 5-isoquinolyloxy,
and all pharmaceutically acceptable salts and hydrates thereof.
19 . The method of claim 16 wherein the compound has formula I(c) or formula I(d) as follows:
wherein
R 1 is a member selected from the group consisting of CN, —O-methyl, —O-ethyl, —O-propyl, —O— isopropyl, —O-butyl, —O-t-butyl, —O-isoamyl, 1-naphthyloxy, 2-naphthyloxy, 4-indolyloxy, 5-indolyloxy, 5-isoquinolyloxy,
and all pharmaceutically acceptable salts and hydrates of such compounds.
20 . The method of claim 16 wherein the compound has formula I(e) or formula I(f) as follows:
wherein
R 1 is a member selected from the group consisting of CN, —O-methyl, —O-ethyl, —O-propyl, —O— isopropyl, —O-butyl, —O-t-butyl, —O-isoamyl, 1-naphthyloxy, 2-naphthyloxy, 4-indolyloxy, 5-indolyloxy, 5-isoquinolyloxy,
and all pharmaceutically acceptable salts and hydrates of such compounds.Join the waitlist — get patent alerts
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