WO2004111055A1 - 1.3.4-triaza-phenalene and 1,3,4,6-tetraazaphenalene derivatives - Google Patents

Abstract

Novel 1,3,4-triaza-phenalene and 1,3,4,6-tetraazaphenalene derivatives of formula (I) are disclosed. These compounds inhibit epidermal growth factor receptor ('EGFW') tyrosinc kinase. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and are useful, inter alia, in the treatment or control of cancer, in particular solid tumors. This invention also relates to pharmaceutical compositions containing such compounds and to rnethods of treating or controlling cancer, most particularly the treatment or control of breast, lung, colon and prostate tumors.

Description

IAZA- PHENALENE AND 1 , 3 , 4 , 6-TETRAAZAPHENALENE DERIVATIVES

The present invention relates to novel 1,3,4-triaza-phcnalcnc and 1,3,4,6- tclraazaphenalcnc derivatives that inhibit epidermal growth factor receptor ("EGFR") tyrosine kinase. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and arc useful, inter alia, in the treatment or control of cancer, in particular solid tumors. This invention also relates to pharmaceutical compositions containing such compounds and to methods of treating or controlling cancer, most particularly the treatment or control of breast, lung, colon and prostate tumors. Finally, this invention is also directed to novel intermediate compounds useful in the preparation of the novel phenalene derivatives herein disclosed. Receptor tyrosine kinases arc transmembrane proteins that participate in cell signal transduction. Specifically, they transmit growth factor signals from the cell surface to certain intracellular processes that control critical function such as growth, differentiation and angiogcncsis. A. A. Adjei, Drugs of the Future 2001, 26(11):1087- 1092. Many cancers are associated with aberrant signaling. In particular, deregulated signaling via tyrosine kinases plays a key role in the growth and spread of cancers. A. D. Laird and J. M. Chcrrington, Expert Opin. Invctig. Drugs, 2003, 12(l):51-64. One family of receptor tyrosine kinases is the epidermal growth factor receptor (EGFR) tyrosine kinase. These receptors have been found to be over expressed in a number of epithelial cancers and have been implicated in tumor aggressiveness.

The role of receptor tyrosine kinases (RTKs), and in particular of EGFR, in the growth and spread of cancers is well established. See, Laird and Cherrington, supra, and Adjey, supra. There is thus extensive research to develop small molecule inhibitors of RTKs, and in particular of EGFR. For reviews of compounds inhibiting EGFR and then- therapeutic use see Laird and

Cherrington, supra; Adjcy, supra; Drugs of the Future 2002, 27(4):339-345; M. R. Myers el al., Bioorganic & Medicinal Chemistry Letters, 1997, 7(4) : 421 -424; A. J. Bridges ct al., J. Med. Chem., 1996, 39:267-276; G. W. Rewcastle et al., J. Med. Chem. 1995, 38:3482- 3487.

FS/23.03.2004 The present invention relates to novel 1,3,4- triaza-plienalene and 1,3,4,6- tetraazaphenalene derivatives of the formula

wherein

Z is C or N;

R¹ and R² arc independently selected from H, lower alkyl, lower alkyl substituted with OR⁶, NR⁶R⁷, hctcrocyclc, andhclcroaryl; R³ and R⁴ arc each independently selected from H, F, Cl, and Br;

R⁵ is selected from H, OH, SH, oxo, thionc, and Ci - C₃ alkyl; and

R⁶ and R⁷ arc each independently selected from H, and lower alkyl or, alternately NR 'R⁷ together can form a ring having 3 to 7 atoms, said ring optionally including up to three additional hctcroatoms and being optionally substituted by one or more lower alkyl; or the pharmaceutically acceptable salts or esters thereof.

The dotted lines in the above formula signify that a double bond exists either between Z and the carbon atom to which R⁵ is attached or between the carbon atom and R⁵. Use of dotted lines to depict tautomeric forms is well known in the art.

These compounds inhibit epidermal growth factor receptor ("EGER") tyrosine kinase. These compounds and their pharmaceutically acceptable salts and esters have antiproliferative activity and are useful, inter alia, in the treatment or control of cancer, in particular solid tumors.

The present invention also relates to pharmaceutical compositions comprising one or more compounds of the invention, or a pharmaceutically acceptable salt or ester thereof, and a pharmaceutically acceptable carrier or excipient.

The present invention further relates to a method for treating or controlling cancer, more particularly the treatment or control of a solid tumor, most particularly to the treatment or control of breast, lung and colon and prostate tumors by administering to a patient in need of such therapy a therapeutically effective amount of a compound of formula I, or a pharmaceutically acceptable salt or ester thereof.

Finally, this invention also relates to novel intermediate compounds useful in the preparation of a compound of formula I.

As used herein, the following terms shall have the following definitions.

"Alkyl" alone or in conjunction with another term, e.g. alkyl-heterocycle, denotes a straight-chain or branched saturated aliphatic hydrocarbon having 1 to 12, preferably 1 to 10, carbon atoms. Preferred alkyl groups arc "lower alkyl" groups having 1 to 6, preferably 1 to 4, carbon atoms. Typical lower alkyl groups include methyl, ethyl, propyl, isopropyl, butyl, f-butyl, 2-butyl, pentyl, hexyl and the like. As used herein, C₁-C₃ alkyl means an alkyl group having 1 to 3 carbon atoms. "Aryl" alone or in conjunction with another term means a monovalent, monocyclic or bicyclic, aromatic carbocyclic hydrocarbon radical, preferably a 6-10 mcmbcrcd aromatic aromatic ring system. Preferred aryl groups include, but are not limited to, phenyl, naphthyl, tolyl and xylyl.

"Effective amount" means an amount that is effective to prevent, alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated.

"Halogen" means fluorine, chlorine, bromine or iodine, preferably fluorine, chlorine or bromine.

"Hctcro atom" means an atom selected from N, O and S.

"Hctcroaryl" means an aromatic heterocyclic ring system containing up to two rings. Preferred hclcroaryl groups include, but arc not limited to, thicnyl, furyl, indolyl, pyrrolyl, pyridinyl, pyridine, pyrazinyl, oxazolyl, thiaxolyl, quinolinyl, pyrimidinyl, imidazole and tctrazolyl.

"Heterocycle" or "heterocyclyl" means a saturated or partially unsaturated, non- aiOinatic cyclic radical of 3 to 8 ring atoms in which from one to 4 ring atoms arc helcro atoms selected from nitrogen, oxygen, sulfur, or a combination thereof, the remaining ring atoms being C. Examples of preferred hctcrocyclcs arc pipcridinc, piperazinc, pyrrolidine, morpholine, indolinc, tclrahydropyranyl, thiomorpholino, pcntamcthylenc sulfide, and pentam ethylene sulfone.

"IC₅₀" refers to the concentration of a particular compound according to the invention required to inhibit 50% of a specific measured activity. IC»can be measured, inter alia, as is described in Example 23, infra.

"Oxo" means =O.

"Pharmaceutically acceptable ester" refers to a conventionally esterified compound of formula I having an alcohol or a carboxyl group, which esters retain the biological effectiveness and properties of the compounds of formula I and arc cleaved in vivo (in the organism) to the corresponding active alcohol or carboxylic acid. Examples of ester groups which arc cleaved (in this case hydrolyzcd) in vivo to the corresponding carboxylic acids (R⁴⁰CX=O)OH) arc lower alkyl cslcrs which may be substituted with NR⁴¹R⁴² where R⁴' and R⁴² are lower alkyl, or where NR⁴¹R⁴² taken together form a monocyclic aliphatic heterocycle, such as pyrrolidine, piperidinc, morpholine, N- mcthylpipcrazinc, etc.; and carbonate cslcrs of the formula R⁴⁰C(=O)OCHR⁴³OC(=O), where R⁴³ is hydrogen or methyl. R⁴¹Ms a compound according to the invention. It is shown in its carboxylic acid form (after being administered to a patient as an ester and being cleaved to the corresponding acid). Examples of lower alkyl esters arc the acetyl, propionyl esters, and the like.

Examples of lower alkyl esters substituted with NR⁴¹R⁴² arc the dicthylaminoacclyl, 2- (4- morpholinyl)acetyl, 2- (4-methylpiperazin- l-yl)acelyl esters, and the like. Examples of carbonate esters arc acctoxy-mcthoxy-formyl and 2-(dimcfhylamino)acctoxy-mcthoxy- formyl esters. Further information concerning examples of and the use of esters for the delivery of pharmaceutical compounds is available in Design of Prodrugs. Bundgaard H ed. (Elsevier, 1985). See also, H. Ansel et. al., Pharmaceutical Dosage Forms and Drug Delivery Systems (6th Ed. 1995) at pp. 108-109; Krogsgaard-Larscn, ct. al., Textbook of Drug Design and Development (2d Ed. 1996) at pp. 152-191; H. Gao et al., Synthesis 2000, 329-351; J. Alexander ct al., J. Med. Chcm. 1988, 31, 318-322.

"Pharmaceutically acceptable salt" refers to conventional acid-addition salts or base- addition salts that retain the biological effectiveness and properties of the compounds of formula I and are formed from suitable non-toxic organic or inorganic acids or organic or inorganic bases. Sample acid-addition salts include those derived from inorganic acids such as hydrochloric acid, hydrobromic acid, hydroiodic acid, sulfuric acid, sulfamic acid, phosphoric acid and nitric acid, and lhose derived from organic acids such as p-toluene sulfonic acid, salicylic acid, methanesulfonic acid, oxalic acid, succinic acid, citric acid, malic acid, lactic acid, fumaric acid, and the like. Sample base- addition salts include those derived from ammonium, potassium, sodium and, quaternary ammonium hydroxides, such as for example, tetramethylammonium hydroxide. The chemical modification of a pharmaceutical compound (i.e. drug) into a salt is a technique well known to pharmaceutical chemists to obtain improved physical and chemical stability, hygroscopicity, flowability and solubility of compounds. See, e.g., H. Ansel ct. al., Pharmaceutical Dosage Forms and Drug Delivery Systems (6th Ed. 1995) at pp. 196 and 1456-1457.

"'Pharmaceutically acceptable,'^" such as pharmaceutically acceptable carrier, excipient, etc., means pharmacologically acceptable and substantially non-toxic to the subject to which the particular compound is administered.

"Substituted," as in alkyl substituted with, means that the substitution can occur at one or more positions and, unless otherwise indicated, that the substituents at each substitution site arc independently selected from the specified options.

"'Therapeutically effective amount" means an amount of at least one compound of Formula I, or a pharmaceutically acceptable salt or ester thereof, that significantly inhibits proliferation and/or prevents differentiation of a human tumor cell, including human tumor cell lines.

"Thionc" signifies a =S at a non-terminal carbon atom.

In one embodiment, the present invention relates to compounds of formula

I, or the pharmaceutically acceptable salts or esters thereof, wherein Z and R¹ to R⁵ arc as defined above.

In a preferred embodiment of the compounds of formula I, Z is N. In another preferred embodiment, Z is C.

In another preferred embodiment of the compounds of formula I, R¹ and R² arc independently lower alkyl, preferably methyl. In a most preferred embodiment, both R¹ and R² arc methyl. In another preferred embodiment of the compounds of formula I, R¹ and R⁴ are independently selected from H, Br, Cl, and F, most preferably H. In a most preferred embodiment, R³ and R⁴ are both H.

In another preferred embodiment of the compounds of formula I, R⁵ is selected from =O, =S, H and lower alkyl, most preferably H and lower alkyl. The following compounds are preferred embodiments according to the instant invention:

8,9-Dimethoxy-3-phenyl-l//,3//-l,3,4,6-tetraaza-phenalen-2-one (Example ID); 8,9-Dimelhoxy-3-phenyl-l#3tf-l,3,4,6-telraaza-phenalene-2-thione (Example 2); 8,9-Dimcthoxy-3-phcnyl-3#-l,3,4,6-tctraaza-phcnalcnc (Example 3); 8,9-Dimcthoxy-2-mcthyl-3-phcnyl-3#-l,3,4,6-tctraaza-phcnalcnc (Example 4); 2-Ethyl-8,9-dimcthoxy- 3-phcnyl- 3//- 1,3,4,6- tctraaza-phcnalcnc (Example 5); 3-(3-Bromo-phenyl)-8,9-dimethoxy-3H-l,3A6-tetraaza-phenalene (Example 6C);

3-(3-Bromo-phenyl)-8,9-dimelhoxy-lH,3H-l,3A6-tetraaza-phenalen-2-one (Example 7);

3-(3-Bromo-phenyl)-8,9-dimethoxy-2-methyl-3H-l,3,4,6-tetraaza-phenalene (Example s);

3-(3-Bromo-phenyl)-8,9-dimemoxy-lH,3H-l,3A6-tetraaza-phenalcn-2-thionc (Example 9);

3-(3-Bromo-phenyl)-2-cthyl-8,9-dimcthoxy-3H-l,3,4,6-tetraaza-phcnalcnc (Example 10); 3-(3-Chloro-phcnyl)-8,9-dimcthoxy-ltf,3/y-l,3A6-tctraaza-phcnalcn-2-onc (Example HC);

3-(3-Chloro-phenyl)-8,9-dimeihoxy-2-methyl-3//-13A6-tetraaza-phenalene (Example 12);

3-(4-ChloiO-pheny])-8,9-dimethoxy-3H-l, 3,4,6- lelraaza-phenalene (Example 13C); 3-(4-ChloiO-phenyl)-8,9-dimelhoxy-lH ,3H- 1 ,3,4,6-tetraaza-phenalen-2-thione (Example 14);

7,8-Dimelhoxy-5-methyl-4-phenyl-4ff-l,3,4-lriaza-phenalene (Example 15G);

4-(4-Chloro-phenyl)-7,8-dimelhoxy-5-methyl-4//-l,3A-triaza-phenalene (Example 16G); 4-(3-Bromo-phenyl)-7,8-dimethoxy-5-methyl-4//-l ,3,4-triaza-phenalene (Example 17G);

4-(3-Bromo-phcnyl)-7,8-dimcthoxy-5-mcthyl-4#-l,3,4-triaza-phenalcnc (Example 18G);

4-(4-Bromo-2-fluoiO-phcnyl)-7,8-dimcthoxy-5-mcthyl-4iϊ-l,3,4-triaza-phcnalcnc (Example 19G);

7,8-Dimcthoxy-4-phcnyl-4tf-l,3,4-lriaza-phcnalcnc (Example 20B); 4-(4-Chloro-phcnyl)-7,8-dimctlioxy-4fl^r- 1,3,4- triaza-phenalcnc (Example 21B); and 4-(3-Bromo-phenyl)-7,8-dimethoxy-4i7-l,3,4-triaza-phenalene (Example 22B).

The compounds disclosed herein and covered by formula I above may exhibit tautomerism or structural isomerism. It is intended that the invention encompasses any tautomeric or structural isomeric form of these compounds, or mixtures of such forms, and is not limited to any one tautomeric or structural isomeric form depicted in the formula above.

The compounds of the present invention can be prepared by any conventional means. Suitable processes for synthesizing these compounds arc provided in the examples. Generally, compounds of formula I can be prepared according to one of the below- described synthetic routes.

Scheme 1

1 ,1 '-carbonyldiimidazole

Scheme 2

1 ,1 '-thiocarbonyldiimidazole

Scheme 3

HCOOH, Heat

Scheme 4

Scheme 5

Scheme 6

Separating a mixture of stereoisomers into the optically pure stereoisomers (when compound of formula I is chiral).

The optional separation of isomeric structures of formula I can be carried out according to known methods such as for example resolution or chiral high-pressure liquid chromatography (also known as chiral HPLC). Resolution methods arc well known, and are summarized in "Enantiomers, Racemates, and Resolutions" (Jacques, J. ct al. John Wiley and Sons, NY, 1981). Methods for chiral HPLC arc also well known, and arc summarized in "Separation of Enantiomers by Liquid Chromatographic Methods" (Pirlde, W. H. and Finn, J. in "Asymmetric Synthesis", Vol. 1, Morrison, J. D., Ed., Academic Press, Inc., NY 1983, pp. 87-124).

Converting a compound of formula I that bears a basic nitrogen into a pharmaceutically acceptable acid addition sail. The optional conversion of a compound of formula I that bears a basic nitrogen into a pharmaceutically acceptable acid addition salt can be effected by conventional means. For example, the compound can be treated with an inorganic acid such as for example hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, or with an appropriate organic acid such as acetic acid, citric acid, tartaric acid, melhanesulfonic acid, /7-toluene sulfonic acid, or the like.

Converting a compound of formula I that bears a carboxylic acid group into a pharmaceutically acceptable alkali metal salt.

The optional conversion of a compound of formulal that bears a carboxylic acid group into a pharmaceutically acceptable alkali metal salt can be effected by conventional means. For example, the compound can be treated with an inorganic base such as lithium hydroxide, sodium hydroxide, potassium hydroxide, or the like.

Converting a compound of formula 1 that bears an alcohol or a carboxylic acid group into a pharmaceutically acceptable ester.

The optional conversion of a compound of formula I that bears an alcohol or a carboxylic acid group into a pharmaceutically acceptable ester can be effected by conventional means. The conditions for the formation of the ester will depend on the stability of the other functional groups in the molecule to the reaction conditions. If the other moieties in the molecule are stable to acidic conditions, the ester may be conveniently prepared by heating in a solution of a mineral acid (c.g., sulfuric acid) in an alcohol. Alternatively, the ester may be prepared by the condensation of an alcohol with an acid anhydride or an acid halide under conditions known in the art. Other methods of preparing the ester, which may be convenient if the molecule is not stable to acidic conditions include treating the compound with an alcohol and acid in the presence of a coupling agent and in the optional presence of additional agents that may accelerate the reaction. Many such coupling agents are known to one skilled in the art of organic chemistry. Two examples arc dicyclohcxylcarbodiimidc and triphcnylphosphinc /diethyl azodicarboxylale. In the case where dicyclohexyl-carbodiimide is used as the coupling agent, the reaction is conveniently carried out by treating the acid with the alcohol, dicyclohcxylcarbodiimide, and the optional presence of a catalytic amount (0- 10 mole%) of N^-dimethylaminopyridine, in an inert solvent such as a halogen ated hydrocarbon (e.g., dichloromethane) at a temperature between about 0 degree and about room temperature, preferably at about room temperature. In the case where triphcnylphosphinc/diethyl azodicarboxylalc is used as the coupling agent, the reaction is conveniently carried out by treating the acid with the alcohol, triphenylphosphine and diethyl azodicarboxylate, in an inert solvent such as an ether (e.g., tctrahydrofuran) or an aromatic hydrocarbon (e.g., benzene) at a temperature between about 0 degrees and about room temperature, preferably at about 0 degree.

In an alternative embodiment, the present invention includes pharmaceutical compositions comprising at least one compound of formula I, or a pharmaceutically acceptable salt or ester thereof and a pharmaceutically acceptable cxcipicnt and/or carrier. These pharmaceutical compositions can be administered orally, for example in the form of tablets, coated tablets, dragees, hard or soft gelatin capsules, solutions, emulsions or suspensions. They can also be administered rectally, for example, in the form of suppositories, or parcntcrally, for example, in the form of injection solutions.

The pharmaceutical compositions of the present invention comprising compounds of formula I, and/or the salts or esters thereof, maybe manufactured in a manner that is known in the art, e.g. by means of conventional mixing, encapsulating, dissolving, granulating, emulsifying, entrapping, dragee-making, or lyophilizing processes. These pharmaceutical preparations can be formulated with therapeutically inert, inorganic or organic carriers. Lactose, corn starch or derivatives thereof, talc, stcric acid or its salts can be used as such carriers for tablets, coated tablets, dragecs and hard gelatin capsules. Suitable carriers for soft gelatin capsules include vegetable oils, waxes and fats. Depending on the nature of the active substance, no carriers arc generally required in the case of soft gelatin capsules. Suitable carriers for the manufacture of solutions and syrups are water, polyols, saccharose, invert sugar and glucose. Suitable carriers for injection are water, alcohols, polyols, glycerine, vegetable oils, phospholipids and surfactants. Suitable carriers for suppositories arc natural or hardened oils, waxes, fats and semi- liquid polyols.

The pharmaceutical preparations can also contain preserving agents, solubilizing agents, stabilizing agents, wetting agents, emulsifying agents, sweetening agents, coloring agents, flavoring agents, salts for varying the osmotic pressure, buffers, coating agents or antioxidants. They can also contain other therapeutically valuable substances, including additional active ingredients other than those of formula I.

As mentioned above, the compounds of the present invention, including the compounds of formula I, are useful in the treatment or control of cell proliferative disorders, including chemoprevention of cancer. Chemoprevention is defined as inhibiting the development of invasive cancer by either blocking the initiating mutagenic event or by blocking the progression of prc-malignant cells that have already suffered an insult or inhibiting tumor relapse. These compounds and formulations containing said compounds are particularly useful in the treatment or control of solid tumors, such as, for example, breast, colon, lung and prostate tumors.

A therapeutically effective amount of a compound in accordance with this invention means an amount of compound that is effective to prevent, alleviate or ameliorate symptoms of disease or prolong the survival of the subject being treated. Determination of a therapeutically effective amount is within the skill in the art.

The therapeutically effective amount or dosage of a compound according to this invention can vary within wide limits and may be determined in a manner known in the art. Such dosage will be adjusted to the individual requirements in each particular case including the specific compound(s) being administered, the route of administration, the condition being treated, as well as the patient being treated. In general, in the case of oral or parenteral administration to adult humans weighing approximately 70 Kg, a daily dosage of about 10 mg to about 10,000 mg, preferably from about 200 mg to about 1,000 mg, should be appropriate, although the upper limit may be exceeded when indicated. The daily dosage can be administered as a single dose or in divided doses, or for parenteral administration, it may be given as continuous infusion.

Combinations The compounds of this invention maybe used in combination (administered in combination or sequentially) with known anti-cancer treatments such as radiation therapy or with cytostatic or cytotoxic agents, such as for example, but not limited to, DNA interactive agents, such as cisplatin or doxorubicin; topoisomcrasc II inhibitors such as etoposide: topoisomerase I inhibitors such as CPT- 1 1 or topotecan; tubulin interacting agents, such as paclitaxcl, docctaxcl or cpothiloncs; hormonal agents such as tamoxifen; thymidilate synthase inhibitors, such as 5-fluorouracil; and anti-metabolites such as methotrexate. Compounds of formula I may also be useful in combination with modulators of p53 transaclivation.

If formulated as a fixed dose, the above-described combination products include the compounds of this invention within the dosage range described above and the other pharmaceutically active agent or treatment within its approved dose range. Compounds of formula I may also be administered sequentially with known anticancer or cytotoxic agents when concomitant administration or a combination is inappropriate. This invention is not limited in the sequence of administration: compounds of formula I may be administered cither prior to or after administration of the known anticancer or cytotoxic agent.

Intermediates

In another embodiment, the present invention also relates to novel intermediates useful in the preparation of compounds of formula I. These novel intermediates include the following compounds:

(5- Allyl-6,7-dimcthoxy-quinazolin-4-yl)-phcnyl-aminc (Example 15E);

5-Iodomethyl-7,8-dimcthoxy-4-phcnyl-5,6-dihydiO-4H-l,3,4-lriaza-plicnalcnc (Example 15F); 5-Ally!-4-(4-chloro-phenylamino)-7-mclhoxy-quinazolin-6-ol (Example 16D); (5-Allyl-6,7-dimcthoxy-quinazolin-4-yl)-(4-chloro-phcnyl)-aminc (Example 16E);

4-(4-Chloro-phcnyl)-5-iodomcΛyl-7,8-dimcthoxy-5,6-dihydro-4H-l,3,4-triaza- phenalene (Example 16F);

5-AUyl-4-(3-biOmo-phcnylamino)-7-mclhoxy-quinazolin-6-ol (Example 17D); (5-Allyl-6,7-dimethoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-aminc (Example 17E);

4-(3-Bromo-phcnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6-dihydro-4H- 1,3,4- triaza- phcnalcnc (Example 17F);

5-Allyl-4-(3-chloro-4-flu()ro-phcnylamino)-7-mcthoxy-quinazoUn-6-ol (Example 18D); (5-Allyl-6,7-dimethoxy-quinazolin-4-yl)-(3-chloro-4-fluoro-phenyl)-amine (Example 18E);

4-(3-Chloro-4-fluoro-phenyl)-5-iodomcthyl-7,8-dimethoxy-5,6-dihydro-4H- 1,3,4- triaza-phcnalcne (Example 18F); 5-AUyl-4-(4-bromo-2-fluoro-phcnylamino)-7-methoxy-quinazolin-6-ol (Example 19D);

(5-Allyl-6,7-dimethoxy-quin azolin -4- yl)-(4-bromo-2-fluoiO-phenyl)-aminc (Example 19E);

4-(4-Bromo-2-lluoro-phcnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6-dihydro-4H- 1,3,4- triaza-phenalene (Example 19F); 7,8-Dimclhoxy-4-phcnyl-5,6- dih ydro-4H-l , 3,4- triaza-phcnalcn-5-ol (Example 20A);

7,8-Dimcthoxy-4-phcnyl-5_I6-dihydro-4H-l,3,4-triaza-phcnalcn-5-ol (Example 21A); and

7,8-Dimclhoxy-4-(3-bromo-phcnyl)-5,6-dihydiO-4H-l,3,4-lriaza-phcnalcn-5-ol (Example 22A).

Examples

The following examples illustrate preferred methods for synthesizing and using the compounds and formulations of the present invention. These examples and preparations are illustrative and are not intended to be limiting. It should be understood that there may be other embodiments that fall within the spirit and scope of the invention as defined by the claims appended hereto.

Abbreviations Used in the Examples: DMF jV,./V-dimcthylformamidc TLC thin layer chromatography

DBU 1 ,8-diazabicyclo|5.4.0]undec-7-ene

Example 1 8,9-Dimclhoxy-3-phcnyl- lf/,3f/-l,3,4,6-lctraaza-phcnalcn-2-onc

Ci₇H₁₄N₄O₃ MW 322.33 Step A 6,7-Dimethoxy-5-nitro-3iϊ-quinazolin-4-one

C₁₀H₁₉N₃O₅ MW 251.20

6,7-Dimethoxy-5-nitro-3//-quina7.olin -4-one was prepared as a pale yellow solid according to the procedure of Chao, Qi; Deng, Lynn; Shili, Hsienchcng; Lconi, Lorenzo M.; Gcnini, Davidc; Carson, Dennis A.; Cotlarn, Howard B.; J. Med. Ch em, 1999, 42, 3860-3873. i B: (6,7-Dimethoxy-5-nitro-quinazolin -4-yl)-phenyl-amine

Ci₆H₁₄N₄O₄ MW 326.31 To a solution of 6,7-dimctlioxy-5-nitro-3//-quinazolin-4-onc (1.0 g, 3.98 mmol)

(from Example 1, Step A, supra) in SOCfe (20 mL) (Aldrich) were added a few drops of DMF. The reaction mixture was then healed with stirring at 90 ⁰C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (30 mL), then aniline (0.36 mL, 3.98 mmol) (Aldrich) was added. The reaction mixture was heated at 110⁰C for 3 hours. The reaction mixture was concentrated under reduced pressure and the residue was purified by chromatography using EtOAc / CH₂Cl₂ / NEt₃ (1:1:0.05) as eluent to give the desired (6,7-dimethoxy-5- nitro-quinazolin-4-yl)-plienyl-aminc as a yellow solid. (Yield 0.9 g, 70%).

Step C: 6,7-Dimethoxv-iV4-phenyl-quinazoline-4,5-diamine

Ci₆Hi₆N₄O₂ MW 296.33

K) To a solution of (6,7-dimethoxy-5-nitro-quinazolin-4-yl)-phenyl-aminc ( 1.0 g,

3.14 mmol) (from Example 1, Step B, supra), NH₄Cl (1.7 g, 31.4 mmol) in MeOH, H₂O and CHCl₃ (40 mL, 2:1:1) was added Zn powder (2.0 g, 31.4 mmol) (Aldrich). The reaction mixture was stirred at room temperature for 1 hour. The mixture was then filtered, the filtrate was concentrated and then extracted with chloroform (100 mL). The

15 organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ (1:1) as clucnt to give the desired 6,7- dimclhoxy-iV4-phcnyl-quinazolinc-4,5-diaminc as a yellow gum. (Yield 0.5 g, 54%).

Ste_D D: 8,9-Dimethoxv-3-phenγl-lff,3ff-l,3.4,6-tetraaza-phenalen-2-one

C₁₇Hi₄N₄O₃ MW 322.33

To a solution of 6,7-dirnclhoxy-W4-phcnyl-quinazolinc-4,5-diaminc (0.2 g, 0.68 25 mmol) (from Example 1 , Step C, supra) in 1 ,2-dichloroelhane (50 mL) was added 1,1 '- carbonyldiimidazolc (0.55 g, 3.4 mmol) (Aldrich). The reaction mixture was heated with stirring at 90 ⁰C for 4 hours. The solvent was evaporated and the residue was purified by chromatography using ElOAc / CH₂Cl₂ / El₃N (1 :1 :0.04) as eluent to give the desired 8,9- dimethoxy-3-phenyl-l.H^r,3.H^r-l,3,4,6-tetraaza-phenalen-2-oneas a yellow solid. (Yield 0.13 g, 59%).

Example 2 8,9-Dimethoxy-3-phcnyl-lH,3H-l,3,4,6-tetxaaza-phcnalcnc-2-thionc

CnHi₄N₄O₂S MW 338.39 To a solution of 6,7-dimetlioxy-iV4-phenyl-quinazoline-4,5-diamine (80 mg, 0.27 mmol) (from Example 1, Step, C supra) in 1,2-dichlorocthanc (30 mL) was added 1,1'- thiocarbonyldiimidazolc (0.58 g, 3.24 mmol) (Fluka). The reaction mixture was heated with stirring at 80⁰C for 4 hours. The solvent was evaporated and the residue was purified by chromatography using HOAc / CH₂Cl₂ / Et.JST (1:1:0.04) as clucnt to give the desired 8,9-dimcthoxy-3-phcnyl-l/7,377-l,3,4,6-lctraaza-phenalcnc-2-thionc _{as a} g,._ay solid. (Yield 50 mg (55%).

Example 3 8,9-Dimethoxy-3-phenyl-3//-l,3,4,6-tetraaza-phenalene

C₁₇H₁₄N₄O₂ MW 306.32

A solution of 6,7-dimethoxy-Λ'4-phenyl-quinuzoline-4,5-diamine (80 mg, 0.27 mmol) (from Example 1, Step C, supra) in formic acid (5 mL) was heated at 110⁰C for 2 hours. Aqueous NaOH solution was then added to the reaction mixture to a pH 10 - 12. The solution was diluted with chloroform (50 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography usingEtOAc / Et₃N (1:0.04) as clucnt to give the desired 8,9-dimcthoxy-3-phcnyl-3.ff- 1,3,4,6-tetraaza-phenalene as a white solid. ("Meld 45 mg, 54%).

Example 4 8,9-Dimethoxy-2-melhy]-3-phenyl-3//-l,3,4,6-tetraaza-phenalene

A solution of β^-dimcthoxy-M-phenyl-quinazolinc-^S-diaminc (60 mg, 0.20 mmol) (from Example 1, Step C, supra) in acetic anhydride (2 mL) was healed at 150⁰C for 2 hours. Aqueous NaOH solution was then added to the reaction mixture to a pH 10 - 12. The solution was diluted with chloroform (50 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using EtOAc / Et₃N (1 :0.04) as eluent to give the desired 8,9-dimethoxy-2-melhyl-3-phenyl- 3H- 1,3,4,6- tctraaza-phcnalcnc as a yellow solid. ("Yield 20 mg, 62%).

Example 5 2- Ethyl- 8,9- dimcthoxy- 3-phcnyl-3#- 1 ,3,4,6- tctraaza-phcn alcnc

C₁₉H₁₈N₄O₂ MW 334.38

A solution of 6,7-dimethoxy-M-phenyl-quinazoline-4,5-diamine (130 mg, 0.44 mmol) (from Example 1, Step C, supra) in propionic anhydride (3 mL) (Aldrich) was healed at 170 °C for 2 hours. Aqueous NaOH solution was added to the rcaclion mixture to a pH 10 - 12. The solution was diluted with chloroform (50 mL). The organic layer was separated, dried over Na_JSO₄, and concentrated. This residue was purified by chromatography using EtOAc / Et₃N (1:0.05) as eluent to give the desired 2-ethyl-8,9- dimelhoxy-3-phenyl-3#-l,3,4,6-tetraaza-phenalene as an orange solid. (Yield 21 mg, 14%).

Example 6 3-(3-Bromo-phenyl)-8,9-dimethoxy-3/M ,3,4,6- tetraaza-phenalene

C_nH₁₃BrN₄O₂ MW 385.23

Step A: (3-Bromo-phenyl)-(6,7-dimethoxy-5-nitro-quinazolin-4-yl)-amine

Cu₁Hi₃BrN₄O₄ MW 405.22

To a solution of 6,7-dimelhoxy-5-nitiO-3W-quinazolin-4-one (1.0 g, 3.98 mmol) (from Example 1, Step A, supra) in SOCfc (20 mL) (Aldrich) was added a few drops of DMF (0.05 mL). The reaction mixture was then heated with stirring at 90⁰C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (30 mL), then 3-bromoaniline (0.69 g, 3.98 mmol) (Aldrich) was added. The reaction mixture was heated at 110 °C for 3 hours. The solvents were removed and the residue was purified by chromatography using EtOAc / CH₂CI₂ / NEt₃ (1:1:0.05) as eluent to give the desired (3-bromo-phenyl)-(6,7-dimethoxy-5-nitro- quinaz()]in-4-yl)-aminc as a yellow solid. (Yield 1.2 g, 74%). LB: Λf4-(3-BiOmo-phenyl)-6,7-dimclhoxy-quinazoIine-4,5-diamine

C₁₆H₁₅BrN₄O₂

MW 375.23

To a solution of (3-bromo-phcnyl)-(6,7-dimcthoxy-5-nitro-quinazolin-4-yl)- amine (0.2 g, 0.49 mmol) (from Example 6, Step A, supra) and NH₄Cl (0.26 g, 4.94 mmol) in a mixture of MeOH, H₂O and CHCI₃ (30 mL, 6:1:1) was added Zn powder (0.64 g, 9.87 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was then filtered, the filtrate was concentrated and then extracted with chloroform (100 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography using EtOAc / CH₂Cl₂ / NEt₃ (1 :1:0.05) as elucnt to give the desired Λf4-(3-biOmo-phcnyl)-6,7-dimcthoxy- quinazoline-4,5-diamine as a yellow gum. (Yield 0.1 g, 54%).

Step C: 3-(3-BiOmo-phenyl)-8,9-dimethoxy-3//- 1,3,4,6-tetraaza-phenalene

Ci₇H₁₃BrN₄O₂ MW 385.23

A solution of iV4-(3-bromo-phcnyl)-6,7-dimcthoxy-quinazolinc-4,5-diaminc (100 mg, 0.27 mmol) (from Example 6, Step B supra) in formic acid (5 mL) was heated at 110 ⁰C for 2 hours. Aqueous NaOH solution was added to the reaction mixture to a pH 10 - 12. The solution was diluted with chloroform (100 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography using EtOAc / Et₃N (1 :0.04) as eluenl to give the desired 3-(3-bromo-phenyl)-8,9- dimcthoxy-37J-l,3,4,6-tctraaza-phcnalcnc as a brown solid. (Yield 86 mg, 83%). Example 7 3-(3-Bromo-phenyl)-8,9-dimethoxy-l#,3#-l,3,4,6-tetraaza-phenalen-2-one

To a solution ofΛM--(3-bremo-phenyl)-6,7-dirnethoxy-quinazoline-4,5-diamine (0.15 g, 0.40 mmol) (from Example 6, Step B, supra) in 1,2-dichlorocthanc (50 mL) was added lj'-carbonyldiimidazolc (0.65 g, 4.0 mmol) (Aldrich). The reaction mixture was healed with stirring at 90⁰C for 4 hours. The solvents were evaporated and the residue was purified by chromatography using EtOAc / CH₂CI₂ / Et₃N (1:1:0.05) as eluent to give the desired 3-(3-bromo-phenyl)-8,9-dimcthoxy-lfl^r,3^-l,3,4,6-tctraaza-phcnalcn-2-onc as a brown solid. (Yield 0.12 g, 75%).

Example 8 3-(3-BiOmo-phenyl)-8,9-dimethoxy-2-melhyl-3W-l ,3A6-lelraaza-phenalene

C₁₈Hi₅BrN₄O₂ MW 399.26 A solution ofΛM-(3-biOmo-phenyl)-6,7-dimethoxy-quinazoline-4,5-diamine (120 mg, 0.32 mmol) (from Example 6, Step B, supra) in acetic anhydride (3 mL) was heated at 150 °C for 2 hours. Aqueous NaOH solution was added to the reaction mixture to a pH 10 - 12. The solution was extracted with chloroform (50 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography using EtOAc / El₃N (1 :0.05) as clucnt to give the desired 3-(3-bromo- phenyl)-8,9-dimethoxy-2-methyl-3#-l ,3,4,6-tetraaza-phenalene as a brown solid. (Yield 60 mg, 47%). Example 9 3-(3-Bromo-phenyl)-8,9-dimethoxy-l/^3F-l,3,4,6-tetraaza-phenalen-2-thione

To a solution of N4-(3-bromo-phenyl)-6,7-dimethoxy-quinazoline-4,5-diarnine (80 mg, 0.21mmol) (from Example 6, Step B, supra) in 1,2-dichloroethane (50 mL) was added l.r-thiocarbonyldiimidazolc (0.38 g, 2.13 mmol) (Huka). The reaction mixture was healed with stirring at 90⁰C for 4 hours. The solvents were evaporated and the residue was purified by chromatography using EtOAc / CH2CI2 /Et₃N (1 :2:0.05) as eluent to give the desired 3-(3-bromo-phcnyl)-8,9-dimcthoxy- liϊ,3iϊ- 1,3,4,6- tctraaza- phenalene-2-lhione as ayellow solid. (Yield 80 mg, 91 %).

Example 10

3-(3-BiOmo-phcnyl)~2-cthyI-8,9-dimcthoxy-3W-l, 3,4,6- lclraaza-phcn alone

CwHi₇BrN₄O₂ MW 413.28

A solution ofiV4-(3-biOmo-phenyl)-6,7-dimethoxy-quinazoline-4,5-diamine (120 mg, 0.32 mmol) (from Example 6, Step B, supra) in propionic anhydride (3 mL) (Aldrich) was healed at 170 °C for 2 hours Aqueous NaOH solution was added to the reaction mixture to a pH 10 - 12. The solution was extracted with chloroform (50 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography using EtOAc / Et₃N (1:0.05) as clucnt Io give the desired 3- (3-bromo-phenyl)-2-ethyl-8,9-dimethoxy-3#-l,3,4,6-tetraaza-phenalene as a brown solid. (Yield 50 mg, 38%).

Example 11 3-(3-αiloro-phenyl)-8,9-dimelhoxy4#3tf43A6-(etraaza-phenalen-2-one

CnH₁₃ClN₄O₃

MW 356.77 Step A: (3-ChloiO-phenyl)-(6,7-dimelhoxy-5-niliO-quinazolin-4-y])-amine

Ci₆H₁₃ClN₄O₄ MW 360.76 A solution of 6,7-dimethoxy-5-nitro-3W-quinazolin-4-one (0.5 g, 1.99mmol)

(from Example 1, Step A, supra) in SOCl₂ (20 mL) (Aldrich) and a fcw drops of DMF (0.05 mL) was heated with stirring at 90⁰C for 3 hours. The solvents were then evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (30 mL), then 3-chloroaniline (0.25 g, 1.99 mmol) (Aldrich) was added. The reaction mixture was hcalcd at 110 ⁰C for 3 hours. The solvents were removed and the residue was purified by chromatography using EtOAc / CH2CI2 / NEt₃ (1:2:0.05) as eluent to give UiC desired (3-chloro-phcnyl)-(6,7-dimethoxy-5-nitro-quinazolin-4-yl)-aminc as a yellow solid. (Yield 0.4 g, 56%).

Lft Λ^P-Chloro-phenyD-δ^-dimethoxy-quinazolineΛS-diaminc

Ci₆Hi₅CIN₄O₂ MW 330.78

To a solution of (3-chloro-phcnyl)-(6,7-dimcthoxy-5-nitro-quinazolin-4-yl)- atnine (0.2 g, 0.55 rnmol) (from Example 11, Step A, supra) and NH₄Cl (0.24 g, 4.43 mmol) in a mixture of MeOH, H₂O and CHCI3 (50 mL, 2:1:12), was added Zn powder (0.72 g, 11 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was then filtered. The filtrate was concentrated and then extracted with chloroform (100 rnL). The organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using SOAc / CH₂Cl₂/ NEt₃ (1:1 :0.05) as eluent to give the desired yV4-(3-chloro-phenyl)-6,7-dimcthoxy- quinazoline-4,5-diamine as an orange gum. (Yield 0.1 g, 55%).

!_C: 3-(3-Chloro-phenyl)-8,9-dimethoxy- 1 H$H- 1 ,3,4,6- tetraaza-phenalen-2-one

Ci₇HoCiN₄O₃ MW 356.77

To a solution oW4-(3-chloro-phenyl)-6,7-dimelhoxy-quinazoline-4,5-diamine (80 mg, 0.24 mmol) (from Example 11, Step B, supra) in 1,2-dichlorocthanc (30 mL) was added lj'-carbonyldiimidazolc (0.2 g, 1.21 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The solvents were evaporated and the residue was purified by chromatography using EtOAc / CH₂Cl₂ / R₃N (1:1:0.05) as eluent to give the desired 3-(3-chloro-phenyl)-8,9-dimcthoxy-l#,3ff-l,3,4,6-lctraaza-phcnalcn-2-onc as a brown solid. (Yield 50 mg, 58%). Example 12 3-(3-Oiloro-phenyl)-8,9-dimethoxy-2-methyl-3i7-l,3,4,6-tetraaza-phenalene

5 Ci₈Hi₅ClN₄O₂

MW 354.80

A solution of Λ^4-(3-chloro-phcnyl)-6,7-dimcthoxy-quinazolinc-4,5-diaminc (0.2 g, 0.60mmol) (from Example 11, Step B siipra) in acetic anhydride (3 mL) was heated at

10 150 "C for 2 hours. Aqueous NaOH solution was added to the reaction mixture to a pH K) - 12. The solution was extracted with chloroform (5O mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using ROAc / CH₂Cl₂/ Et₃N (1 :1 :0.05) as eluenl to give the desired 3- (3-chloro-phcnyl)-8,9-dimcthoxy-2-methyl-3i?-l,3,4,6-tetraaza-phcnalcnc as a yellow

15 solid. (Yield 90 mg, 42%) .

Example 13 3-(4-Chloro-phcnyl)-8,9-dimcthoxy-3#-l,3,4,6-tctraaza-phcnalcnc

0 C_nHi₃ClN₄O₂

MW 340.77

Step A (4-Chloro-phcnyl)-(6,7-dimcthoxy-5-nilro-quinazolin-4-yl)-aminc

C₁₆H₁₃ClN₄O₄ MW 360.76

To a solution of 6,7-dimelhoxy-5-nilro-3//-quinazolin-4-one (0.5 g, 1.99 mmol) (from Example 1, Step A, supra) in SOCb (20 mL) (Aldrich) was added a few drops of DMF (0.05 mL). The reaction mixture was then heated with stirring at 90 °C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. This residue was dissolved in 2-propanol (30 mL), then 4-chloroaniline (0.25 g, 1.99 mmol) (Aldrich) was added. The reaction mixture was heated at 110 °C for 3 hours. The solvents were removed and the residue was purified by chromatography using EtOAc / CH₂CI₂/ NEt₃ (1:2:0.05) as eluent to give the desired (4-chloro-phenyl)-(6,7-dimelhoxy-5-nitro- quinazolin-4-yl)-amino as a yellow solid. (^"Weld 0.5 g, 70%).

Step B: Ar4-(4-Chloro-phcnvl1-6.7-dimcthoxv-αuinaroϋnc-4.5-diaminc

C₁₆H₁₅ClN₄O₂ MW 330.78

To a solution of (4-chloi"0-phenyl)-(6,7-dimelhoxy-5-nitro-quina/.olin-4-yl)- amine (0.2 g, 0.55 mmol) (from Example 13, Step A, supra) and NH₄Cl (0.24 g, 4.43 mmol) in a mixture ofMcOH, H₂O and CHCl₃ (50 mL, 2:1 :12) was added Zn powder (0.72 g, 11 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was then filtered, the filtrate was concentrated and then extracted with chloroform (100 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂/ NEt₃ (1:1:0.05) as eluent to give the desired Λ/4-(4-chloro-phenyl)-6,7-dimethoxy- quinazolinc-4,5-diaminc as a pale yellow gum. CMcId 0.16 g, 88%).

Step C: 3-(4-Chloro-phcnvl)-8.9-dimcthoxv-3#-l,3,4,6-tctraaza-phcnalcnc

C_nH₁₃ClN₄O₂ MW 340.77 A solution ol^"Λf4-(4-chloro-phcnyl)-6,7-dimcthoxy-quinazolinc-4,5-diaminc (160 mg, 0.48 mmol) (from Example 13, Step B, supra) in formic acid (2 mL) was heated at 110 °C for 2 hours. Aqueous NaOH solution was added to the reaction mixture to a pH 10 - 12. The solution was diluted with chloroform (100 mL). The organic layer was separated, dried over Na₂SO₄, and concentrated. This residue was purified by chromatography using EtOAc / Et₃N (1:0.05) as eluent to give the desired 3-(4-chloro- phcnyi)-8,9-dimcthoxy-3.ff-l,3,4,6-tctraaza-phcnalcnc as an off white solid. (^"McId 96 mg, 59%).

Example 14 3-(4-Chloro-phcnyl)-8,9-dimcthoxy-lff,3//-l,3,4,6-tclraaza-phcnalcn-2-thionc

Ci₇Hi₃CFN₄O₂S MW 372.84

To a solution of N4-(4-chloro-phenyl)-6,7-dimethoxy-quinazoline-4,5-diamine (120 mg, 0.36 mmol) (from Example 13, Step B, supra) in 1,2-dichlorocthanc (30 mL) was added l,r-lhiocarbonyldiimida/.ole (0.65 g, 3.63 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The solvents were evaporated and the residue was purified by chromatography using EtOAc / CH₂Cl₂Z Et₃N (1:3:0.05) as eluent to give the desired 3-(Φchloro-phenyl)-8,9-dirnethoxy-l#,3//-l,3,4,6-tetraaza- phenalenc-2-thione as a yellow solid. (Yield 110 mg, 82%).

Example 15 7,8-Dimethoxy-5-mcthyl-4-phcnyl-4#-l,3,4-triaza-phcnalcne

Ci₉H₁₇N₃O₂ MW 319.37

!_A: 6-Acetoxy-7-methoxy-4-phenylamino-quinazoline

C_nHi₅N₃O₃ MW 309.33 6-Acctoxy-7-mclhoxy-quinazolin-4-onc was synthesized according to the literature procedure of Gibson, K. H. et al. Bioorganic & Medicinal Chemistry Letters, 1997, 7(21), 2723 - 2728. To a solution of 6-acctoxy-7-mcthoxy-quinazolm-4-onc (1.2 g, 5.13 mmol) hi SOCl₂ (30 mL) (Aldrich) was added a few drops of DMF (0.1 mL). The reaction mixture was then heated with stirring at 100 °C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (30 mL), then aniline (0.47 mL, 5.13 mmol) (Aldrich) was added. The reaction mixture was heated at 110⁰C for 3 hours, then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give 6-acetoxy-7-methoxy-4- phcnylamino-quinazolinc as a white solid. (Yield 1.0 g, 63%).

7-Mcthoxy-4-phenylamino-quinazolin -6-ol

C₁₅H₁₃N₃O₂ MW 267.29

To a solution of 6-acctoxy-7-methoxy-4-phcnylamino-quinazolinc (1.01 g, 3.27 mmol) (from Example 15, Step A, supra) in MeOH (30 mL) was added an aqueous solution of NH₄OH (29%, 2.0 g, 31.4 mmol). The reaction mixture was stirred at room temperature for 18 hours, and then heated at 10O⁰C for 1.5 hours. The mixture was then cooled to room temperature and Gltcrcd. The precipitate was collected and dried in vacuo to give the desired 7-methoxy-4-phenylamino-quinazolin-6-ol as a white solid. (Yield 0.6 g, 69%).

Step C: (6-A11v1oxy-7-methoxv-quinazolin-4-vl)-phenyl-arnine

Ci₈Hi₇N₃O₂ MW 307.36

To a solution of 7-mcthoxy-4-phcnylamino-quinazolin-6-ol (0.56 g, 2.1 mmol) (from Example 15, Step B, supra) in acetone (50 mL) was added K₂CO₃ (1.45 g, 10 mmol), and allyl bromide (0.2 mL, 2.3 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography usingElOAc / CH₂Cl₂ / Et₃N (1 :4:0.04) as eluent to give the desired (6-allyloxy-7- methoxy-quinazolin-4-yl)-phenyl-amine as a yellow solid. (Yield 0.6 g, 93%). i D: 5-AUvl-7-methoxy-4-phenvlamino-quinazolin-6-ol

Ci₈Hi₇N₃O₂ MW 307.36

A solution of (6-a11yloxy-7-methoxy-quinazolin-4-y])-phenyl-amine (0.30 g, 0.98 mmol) (from Example 15, Step C, supra) in o-xylcnc (50 mL) was heated at 150 °C for 7 hours. Al the end of this period, TLC analysis indicated almost complete consumption of the starting material and the formation of the desired product as the major spot. The solvent was evaporated and the residue was purified by chromatography using EtOAc / Et₃N (1:0.04) as olucnt to give the desired 5-allyl-7-mcthoxy-4-phcnyIamino-quinazolin- 6-ol as an off while solid. (Yield 0.26 g, 87%).

Step E: (5-AUvl-6,7-dimcthoxv-ciuinazolin-4-vl)-phcnyl-ajminc

Ci₉Hi₉N₃O₂ MW 321.38

To a solution of 5-allyl-7-methoxy-4-phenylarnino-quinazolin-6-ol (0.16 g, 0.524 mmol) (from Example 15, Step D, supra) in acetone (30 mL) was added K₂CO₃ (0.36 g, 2.62 mmol) and methyl iodide (0.15 g, 1.05 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / R₃N (1:5:0.05) as clucnl Io give the desired (5-allyl-6,7- dimelhoxy-quinazolin -4-yl)-phenyl-amine as a pale yellow solid. (Yield 0.13 g, 77%).

Step F: 5-Iodomethyl-7,8-dimethoxy-4-phenyl-5,6-dihydiO-4tf- 1 ,3,4-triaza-phenalene

To a solution of (5-allyl-6,7-dimethoxy-quinazolin -4-yl)-phenyl-amine (0.12 g,

0.37 mmol) (from Example 15, Step E, supin) in dichloromcthanc (20 mL) was added h (0.24 g, 1.87 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was diluted with chloroform (100 mL), and washed with a saturated aqueous Na₂SO.! solution. The organic layer was separated, dried over Na₂SO^ and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / H₃N (1 :2:0.05) as eluent to give the desired 5-iodomethyl-7,8-dimelhoxy-4-phenyl-5,6- dihydro-4#- 1,3,4- triaza-phenalene as a pale yellow solid. (Yield 0.11 g, 66%).

Stcρ G: 7,8-Dimethoxv-5-mcthvl-4-phcnvl-4#-l,3,4-triaza-phcnalcnc

Ci₉H_nN₃O₂ MW 319.37

To a solution 5- iodomclhyl-7,8-dimcthoxy-4- phenyl- 5,6-dihydro-4H- 1,3,4- triaza- phenalene (0.1 g, 0.22 mmol) (from Example 15, Step F, supra) in toluene (20 mL) was added DBU (73 μL, 0.49 mmol) (Fluka). The reaction mixture was heated at 120 °C for 1 hour. The mixture was then diluted with chloroform (KX) mL), and washed with H₂O. The organic layer was separated, dried over Na₂Sθ₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / Et₃N (1:1:0.05) as eluent to give the desired 7,8-dimcthoxy-5-mcthyl-4-phcnyl-4H-l,3,4-triaza-phcnalcnc as a pale yellow solid. (Yield 50 mg, 71%). Example 16 4-(4-Chloro-phenyl)-7,8-dimcthoxy-5-methyl-4#-l,3,4-triaza-phenalene

Ci₉H₁₆CIN₃O₂ MW 353.81

Step A 6-Accloxy-4-(4-chloro-phcnylamino)-7-mclhoxy-quinazoline

Ci₇Hi₄ClN₃O₃

MW 343.76

To a solution of 6-acetoxy-7-methoxy-quinazolin-4-one (1.0 g, 4.26 mmol) (from Example 15, Step A, supra) in SOCl₂ (12.5 mL) (Aldricli) was added a few drops ofDMF (0.1 mL). The reaction mixture was then healed with stirring at 100 ⁰C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (20 mL), then 4-chloroanilinc (0.6 g, 4.69 mmol) (Fluka) was added. The reaction mixture was healed at 110⁰C for 3 hours. The reaction mixture was cooled to room temperature and filtered. The precipitate was collected and dried /n vacuo to give 6- acctoxy-4-(4-chloro-phcnylamino)-7-mcthoxy-quinazolinc as a gray solid. (Yield 1.45 g, 99%).

Ster)^: 4-(4-Chloro-phenylamino)-7-meth()xy-quinazolin-6-ol

Ci₅Hi₂ClN₃O₂ MW 301.73

To a solution of 6-acetoxy-4-(4-chloro-phenylamino)-7-methoxy-quinazoline (1.4 g, 4.07 mmol) (from Example 16, Step A, supm) in MeOH (35 mL) was added an aqueous solution of NH₄OH (29%, 0.82 mL, 12.2 mmol). The reaction mixture was stirred at room temperature for 18 hours, then heated at 100 ⁰C for 1.5 hours. The mixture was then cooled to room temperature an d filtered. The precipitate was collected and dried in vacuo to give the desired 4-(4-chloro-phcnylamino)-7-mcthoxy-quinazolin- 6-0I as a gray solid. (Yield 0.67 g, 55%).

Step C: (6-Allvloxv-7-mcthoxv-quinazolin-4-yl)-(4-chloro-phenvl)-aminc

C₁₈H₁₆ClN₃O₂ MW 341.79

To a solution of 4-(4-chloro-phcnylamino)-7-mcthoxy-quinazolin-6-ol (0.61 g, 2.02 mmol) (from Example 16, Step B, supra) in acetone (50 mL) was added K₂CO₃ (0.84 g, 6.06 mmol), and allyl bromide (0.52 ml, 6.06 mmol) (Aldrich). The reaction mixture was healed with stirring at 90 °C for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / Et₃N (1:1:0.01) as eluent to give the desired (6- allyloxy-7-mcthoxy-quinazolin-4-yl)-(4-chloro-phcnyl)-aminc as a white solid. (^"Meld 0.5 g, 72%).

Step D: 5- Allyl-4- (4-chloro-phcnylamino)-7-mcthoxy-quinazolin -6-0I

C₈H₁₆ClN₃O₂ MW 341.79 A solution of (6-allyloxy-7-methoxy^LquinazoKn-4-yl)-(4-chloro-phenyl)-amine (0.50 g, 1.46 mmol) (from Example 16, Step C, supra) in o xylene (50 mL) was heated at 150⁰C for 7 hours. At the end of this period, TLC analysis indicated almost complete consumption of the starting material and the formation of desired product as the major spot. The solvent was evaporated and the residue was purified by chromatography using EtOAc / Et₃N (1:0.04) as clucnt to give the desired 5-allyl-4-(4-chloiO-phenylamino)-7- methoxy-quinazolin-6-ol as an off white solid. (Yield 0.4 g, 80%).

Step E: (5-Allyl-6,7-dimethoxy-quinazolin-4-yl)-(4-chloro-phenyl)-amine

Ci₉HiSClN₃O₂ MW 355.82 To a solution of 5-allyl-4-(4-chloro-phcnylaniino)-7-rnclhoxy-quinazolin -6-ol

(0.45 g, 1.32 mmol) (from Example 16, Step D, supra) in acetone (30 mL) was added K₂CO₃ (0.36 g, 2.6 mmol) and methyl iodide (0.75 g, 5.3 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / Et₃N ( 1 :2:0.()l) as cluent to give the desired (5- allyl-6,7-dimcthoxy-quinazoHii-4-yl)-(4-chloro-phcnyl)-amine as a white solid. (Yield 0.3 g, 84%).

Step F: 4-(4-Chloro-phcnγl)-5-iodomcthvl-7,8-dimcthoxy-5,6-dihvdro-4ff- 1,3,4-triaza- phenalene

Ci₉Hi₇CUN₃O₂ MW 481.71 To a solution of (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-(4-chloro-phenyl)-amine (0.3 g, 0.85 mmol) (from Example 16, Step E, supra) in dichloromethanc (50 mL) was added k (0.53 g, 4.2 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was diluted with chloroform (100 mL), and washed with a saturated aqueous Na₂SO₃ solution. The organic layer was separated, dried over Na₂SO₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂CI₂ / EI₃N (2:1:0.01) as eluent to give the desired 4-(4-chloro-phenyl)-5-iodomethyl-7,8- dimcthoxy-5,6-dihydro-4ff-l,3,4-triaza-phcnalenc as a white solid. (^"Held 0.15 g, 37%).

Step G: 4-(4-Chloro-pricnvl)-7,8-dimethoxy-5-mcthvl-4fl^r- 1,3,4- triaza-phenalenc

C₁₉H₁₆ClN₃O₂ MW 353.81

To a solution of 4-(4-chloro-phenyl)-5-iodomethyl-7,8-dimethoxy-5,6-dihydro- 15 4//-l,3,4-triaza-phenalene (0.15 g, 0.31 mmol) (from Example 16, Step F, supra) in toluene (50 mL) was added DBU (0.46 mL, 3.1 mmol) (Fluka). The reaction mixture was heated at 120 °C for 1 hour. The mixture was then diluted with chloroform (100 mL), and washed with H₂O. The organic layer was separated, dried over Na₂SO^, and concentrated. The residue was purified by chromatography using EtOAc / CH₂CI₂ / Et₃N 20 (1 :l:0.05) as eluent to give the desired 4-(4-chloiO-phenyl)-7,8-dimethoxy-5-methyl-4//- 1,3,4-triaza-phenalene as a pale yellow solid. (Yield 0.1 g, 91 %).

Example 17 4-(3-Bromo-phenyl)-7,8-dimethoxy-5-methy^]-4#-l,3,4-triaza-phenalene

C₉H₁₆BrN₃O₂ MW 398.25 Step A 6-Acetoxy-4-(3-bromo-phenylamino)-7-methoxy-quinazoline

C_nHi₄BrN₃O₃ MW 388.22

To a solution of 6-acctoxy-7-metlioxy-quinazolin-4-onc (1.0 g, 4.26 mmol) (from K) Example 15, Step A, supra) in SOCl₂ (12.5 mL) (Aldrich) was added a few drops of DMF (0.1 mL). The reaction mixture was then heated with stirring at 100 °C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (20 mL), then 3-bromoanilinc (0.806 g, 4.69 mmol) (Aldrich) was added. The reaction mixture was heated at 110 ⁰C for 3 hours. The reaction mixture was cooled 15 to room temperature and filtered. The precipitate was collected and dried in vacuo to give 6-acctoxy-4-(3-bromo-phcnylamino)-7-mcthoxy-quinazolinc as a gray solid. (Yield 1.65 g, 100%).

Step B: 4-(3-Bromo-phenylamino)-7-methoxy-quinazolin-6-ol 20

Ci₅Hi₂BrN₃O₂ MW 346.18

25 To a solution of 6-acetoxy-4-(3-biOmo-phenylamino)-7-melhoxy-quinazoline

(1.59 g, 4.11 mmol) (from Example 17, Step A supra) in McOH (30 mL) was added an aqueous solution OfNH₄OH (29%, 0.83 mL, 12.3 mmol). The reaction mixture was stirred at room temperature for 18 hours, then heated at 100 ⁰C for 1.5 hours. The mixture was then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give the desired 4-(3-bromo-phenylamino)-7-mefhoxy-quinazolin- 6-ol as a gray solid, (^"ϊield 1.25 g, !

Step C: (6-AUyloxy-7-mcthoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-amine

To a solution of 4-(3-bromo-phenylamino)-7-methoxy-quinazolin-6-ol (1.24 g,

3.58 mmol) (from Example 17, Step B, supra) in acetone (250 mL) was added K₂CO₃ (0.99 g, 7.16 mmol), and allyl bromide (1.55 mL, 17.9 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using ElOAc / CH₂Cl₂ / Et₃N (2:3:0.02) as clucnt to give the desired (6- allyloxy-7-methoxy-quinazolin-4-yl)-(3-bromo~phenyl)-amine as a yellow oil. (Yield 0.55 g, 40%).

1 D: 5-Allγl-4-(3-bromo-phcnvlamino)-7-mcthoxy-quinazolin-6-ol

Ci₈Hi₆BrN₃O₂ MW 388.24 A solution of (6-allyloxy-7-mcthoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-aminc

(0.54 g, 1.39 mmol) (from Example 17, Step C, mpra) in o- xylene (75 mL) was heated at 150 ^CC for 4.5 hours, during which time TLC analysis indicated almost complete consumption of the starting material and the formation of desired product as the major spot. The solution was concentrated and filtered. The solid was collected and dried in vacuo to give the desired 5-allyl-4-(3-bromo-phenylamino)-7-methoxy-quinazolin-6-ol as an off white solid. (Yield 0.33 g, 61%).

Step E: (5-Allyl-6,7-dimethoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-aminc

Ci₉H₁₈BrN₃O₂ MW 400.27

To a solution of 5-allyl-4-(3-biOmo-phenylamino)-7-methoxy-quinazolin-6-ol (0.27 g, 0.7 mmol) (from Example 17, Step D, supra) in acetone (30 mL) was added K₂CO₃ (0.48 g, 3.5 mmol) and methyl iodide (0.4 g, 2.8 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered, and the filtrate was concentrated. Theresidue waspurified by chromatography using EtOAc / CH₂CI₂ / Et₃N ( 1 :3:().O1) as clucnt to give the desired (5- allyl-6,7-dimcthoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-aminc as a yellow solid. (Yield 0.14 g, 50%).

Step F: 4-(3-Bromo-phcnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6-dihydro-4g- 1,3,4-triaza- phenalene

Ci₉H₁₇BrIN₃O₂ MW 526.17

To a solution of (5-allyl-6,7-dimcthoxy-quinazolin-4-yl)-(3-bromo-phcnyl)-aminc (0.14 g, 0.35 mmol) (from Example 17, Step E, supra) in dichloromelhane (20 mL) was added I₂ (0.23 g, 1.75 mmol). The reaction mixture was stirred at room temperature for 3 hours. The mixture was diluted with chloroform (100 mL) and washed with a saturated aqueous NSaSO₃ solution. The organic layer was separated, dried over Na₂SO^ and concentrated. The residue was purified by chromatography using EtOAc / CH₂Ck/ Et₃N (1:2:0.01) as elucnt to give the desired 4-(3-bromo-phcnyl)-5-iodomethyl-7,8- dimethoxy-5,6-dihydro-4#-l,3,4-triaza-phenalene as a pale yellow foam. (Yield 0.12 g, 66%). Step G: 4-(3-Bromo-phenyl)-7,8-dirnethoxy-5-melhyl-4.ft^r-l ,3,4-triaza-pheπalene

Ci₉Hi₆BrN₃O₂ MW 398.25

To a solution of 4-(3-bromo-phcnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6-dihydro- 4//-l,3,4-triaza-phenalene (0.12 g, 0.23 mmol) (from Example 17, Step F, supra) in toluene (20 mL) was added DBU (0.075 mL, 0.5 mmol) (Fluka). The reaction mixture was heated at 120 °C for 1 hour. The mixture was then diluted with chloroform (100 mL), and washed with H₂O. The organic layer was separated, dried over Na₂Sθ₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / Et₃N (1:2:0.05) as cluenl to give the desired 4-(3-bromo-phenyl)-7,8-dimcthoxy-5-mcthyl-4i?- 1 ,3,4-lriaza-phenalene as a pale yellow solid. (Yield 0.09 g, 100%).

Example 18 4-(3-Chloro-4-fluoro-phcnyl)-7,8-dimethoxy-5-methyl-4ftf-l,3,4-triaza-ρhenalene

Ci₉Hi₅ClFN₃O₂ MW 371.80 Step A: 6-Acetoxy-4-(3-chloro-4-fluoiO-phenylamino)-7-methoxy-quinazoline

Ci₇Hi₃ClEN₃O₃ MW 361.76 To a solution of 6-accloxy-7-mclhoxy-quinazolin-4-onc (1.0 g, 4.26 mmol) (from

Example 15, Step A, supra) in SOCh (12.5 mL) (Aldrich) were added a few drops of DMF (0.1 mL). The reaction mixture was then heated with stirring at 100 °C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (20 mL), followed by addition of 4-chloro-3-riuoiOaniline (0.682 g, 4.69 mmol) (Aldrich). The reaction mixture was heated at 110⁰C for 3 hours. The reaction mixture was cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give 6-acctoxy-4-(3-chloiO-4-fluoiO-phcnylamino)-7-mclhoxy- quinazoline as a gray solid. (Yield 1.54 g, 100%).

Step B: 4-(4-Chloro-4-fluoro-phenylamino)-7-methoxv-quinazolin-6-ol

C i₅HuClEN₃O₂

MW 319.72

To a solution of 6-acctoxy-4-(3-chloro-4-fluoro-phcny]amino)-7-rncthoxy- quinazoline (1.54 g, 4.26 mmol) (from Example 18, Step A, supra) in MeOH (30 mL) was added an aqueous solution OfNH₄OH (29%, 0.86 mL, 12.7 mmol). The reaction mixture was stirred at room temperature for 18 hours, then heated at 100 °C for 1.5 hours. The mixture was then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give the desired 4-(3-chloro-4-fluoro-phcnylamino)- 7-mcthoxy-quinazolin-6-ol as a gray solid. (Yield 1.21 g, 89%).

Step C: (6-Allyloxy-7-methoxy-quinazolin-4-yl)-(3-chloro-4-fluoro-phenyl)-amine

Ci₈Hi₅ClEN₃O₂ MW 359.78

To a solution of 4-(3-chloro-4-fluoro-phenylamino)-7-mcthoxy-quinazo]in-6-ol

(0.70 g, 2.18 mmol) (from Example 18, Step B, supra) in acetone (140 mL) was added K₂CO₃ (0.61 g, 10.9 mmol) and allyl bromide (0.94 mL, 10.9 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 4 hours. The mixture was cooled to room temperature, filtered, and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂ / Et₃N ( 1 :l:0.02) as eluent to give the desired (6-aUyloxy-7-methoxy-quinazolm-4-yl)-(3-ehloro-4-fluoro-phcnyl)-aminc as an off white solid. (Yield 0.64 g, 82%).

Sterj r2: 5-Allyl-4-(3-chloiO-4-fluoiO-phenylamino)-7-methoxy-quina7.olin-6-ol

CiSHi₅ClEN₃O₂ MW 359.78

A solution of (6-allyloxy-7-methoxy-quinazolin-4-yl)-(3-chloro-4-fluoiO-phenyl)- aminc (0.92 g, 2.55 mmol) (from Example 18, Step C, supra) in o-xylcnc (150 mL) was healed at 150 ⁰C for 7 hours. Al the end of this period, TLC analysis indicated almost complete consumption of the starting material and the formation of desired product as the major spot. The solution was concentrated and filtered. The solid was collected and dried in vacuo to give the desired 5-allyl-4-(3-chloro-4-fluoiO-phenylamino)-7-methoxy- quinazoIin-6-ol as an off white solid. (Yield 0.65 g, 71%). i E: (5-AUyl-6,7-dimethoxy-quinazotin-4-yl)-(3-chloro-4-fluoro-phenyl)-arnine

Ci₉H_nClFN₃O₂ MW 373.81

To a solution of 5-allyl-4-(3-chloro-4-iluoro-phcnylamino)-7-methoxy- quinazolin-6-ol (0.59 g, 1.63 mmol) (from Example 18, Step D, supra) in acetone (175 ml_) was added K₂CO₃ (0.68 g, 4.91 mmol) and methyl iodide (2.32 g, 16.4 mmol) (Aldrich). The reaction mixture was heated with stirring at 90⁰C for 3 hours. The mixture was cooled to room temperature, filtered and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂CI₂ / Et₃N (1 :3:0.01) as eluent to give the desired (5-allyl-6,7-dimcthoxy-quinazolin-4-yl)-(3-chloro-4-fluoro-phcnyl)- aminc as an off while solid. (Yield 0.29 g, 48%). Step F: 4-(3-Chloro-4-rluoro-phenvl)-5-iodomethvl-7,8-dimethoxv-5,6-dihydro-4fl'- 1 ,3 ,4-triaza-phen alen e

C _IC)Hi₆ClFIN₃O₂ MW 499.70

To a solution of (5-allyl-6,7-dimethoxy-quinazoh^'n-4-yl)-(3-chloiO-4-fluoro- phcnyl)-aminc (0.102 g, 0.27 mmol) (from Example 18, Step E, siφm) in dichloromethane (20 mL) was added I₂ (0.69 g, 2.7 mmol). The reaction mixture was stirred at room temperature for 2 hours. The mixture was diluted with chloroform ( KX) mL) and washed with a saturated aqueous Na₂SO₃ solution. The organic layer was separated, dried over Na₂SO^, and concentrated to give the desired 4-(3-chloiO-4-fluoro- phenyl)-5-iodomethyl-7,8-dimethoxy-5,6-dihydro-4#-l,3,4-triaza-phenalene as a yellow foam. (Yield 0.134 g, 99%).

StC2_G: 4-(3-Bromo-phcnyl)-7,8-dimcthoxy-5-methyl-4iϊ-l,3,4-triaza-phcnalene

To a solution of 4-(3-chloiO-4-fluoiO-phenyl)-5-iodomethyl-7,8-dirnethoxy-5,6- dihydro-4//-l,3,4-triaza-phenalene (0.125 g, 0.25 mmol) (from Example 18, Step F, supra) in toluene (25 mL) was added DBU (0.37 mL, 2.5 mmol) (Fluka). The reaction mixture was heated at 120 °C for 1 hours. The mixture was then diluted with chloroform (100 mL) and washed with H₂O. The organic layer was separated, dried over Na₂Sθ₄, and concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂/ Et₃N (3:1 :0.05) as clucnt to give the desired 4-(3-ch]oro-4-fIuoiO-phcnyl)-7,8- dimelhoxy-5-melhyl-4//- 1 ,3,4-lriaza-phenalene as a white solid. (Yield 0.093 g, 100%).

Example 19 4-(4-Bromo-2-fiuoro-phcny])-7,8-dimclhoxy-5-mcthyl-4//-l ,3,4-lriaza-phcnalcnc

Ci₉Hi₅BrFN₃O₂

MW 416.24

Step A: 6-Aceloxy- 4-(4-biOino-2-fluoro-phenylamino)-7-methoxy-quinazoline

CnHi₃ClFN₃O₃ MW 361.76 To a solution of 6-acetoxy-7-methoxy-quinazolin-4-onc (1.0 g, 4.26 mmol) (from

Example 15, Step A, siipra) in SOCl₂ (12.5 mL) (Aldrich) were added a few drops of DMF (0.1 mL). The reaction mixture was then heated with stirring at 100 ⁰C for 3 hours. The solvents were evaporated and the residue was dried in vacuo. The residue was dissolved in 2-propanol (20 mL), then 4-bromo-2-fluoiOaniline (0.891 g, 4.69 mmol) (Aldrich) was added. The reaction mixture was heated at 110 °C for 3 hours. The reaction mixture was cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give 6-accloxy-4-(4-biOmo-2-fluoiO-phcnylamino)-7-mcthoxy-quinazolinc as a gray solid. (Yield 1.42 g, 82%).

Step B: 4-(4-Bromo-2-fluoro-phenylamino)-7-methoxy-quinayχ>1in-6-o1

Ci₅HnBrFN₃O₂

MW 364.17

To a solution of 6-acctoxy-4-(4-biOmo-2-fluoro-phcny]amino)-7-mclhoxy- quinazoline (1.36 g, 3.34 mmol) (from Example 19, Step A, supra) in MeOH (30 mL) was added an aqueous solution of NH₄OH (29%, 0.68 mL, K) mmol). The reaction mixture was stirred at room temperature for 18 hours, then healed at 100 ⁰C for 1.5 hours. The mixture was then cooled to room temperature and filtered. The precipitate was collected and dried in vacuo to give the desired 4-(4-bromo-2-fluoro-phenylamino)-7-methoxy- quinazolin-6-ol as a gray solid. (Yield 0.93 g, 77%). ) C: (6-Myloxy-7-methoxy-quhazoh^'n-4-vl)-(4-bromo-2-fluoro-phenyr)-amine

Ci₈Hi₅BrEN₃O₂ 5 MW 404.23

To a solution of 4-(4-bromo-2-fluoro-phcnylamino)-7-mcthoxy-quinazolin-6-ol (0.50 g, 1.37 mmol) (from Example 19, Step B, supra) in acetone (100 mL) was added K₂CO₃ (0.38 g, 2.74 mmol), and allyl bromide (0.59 mL, 6.86 mmol) (Aldrich). The K) reaction mixture was heated with stirring at 90⁰C for 2 hours. The mixture was cooled to room temperature, Gltered, and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂Cl₂/ Et₃N (1:1:0.02) as eluent to give the desired (6-allyloxy-7-mcthoxy-quinazorJn-4-yl-(4-bromo-2-fluoro-phcnyl)-amine as a pale yellow solid. (Yield 0.52 g, 95%). i D: 5-AUvl-4-(4-bromo-2-fluoro-phenylamino)-7-methoxy-quinazolin-6-oI

Ci₈Hi₅BrEN₃O₂

MW 404.23 20

A solution of (6-allyIoxy-7-methoxy-quinazolin-4-yl)-(4-bromo-2-fluoro-phenyl)- aminc (0.46 g, 1.13 mmol) (from Example 19, Step C, supra) in o- xylene (75 mL) was heated at 150 ⁰C for 4hours. At the end of this period, TLC analysis indicated almost complete consumption of the starting material and the formation of desired product as 25 the major spot. The solution was concentrated to a small volume and filtered. The solid was collected and dried in vacuo to give the desired 5-allyl-4-(4-bromo-2-πuoiO- phenylamino)-7-methoxy-quinazo1in-6-o1 as an off white solid. (Yield 0.35 g, 76%). ) E: (5-AUyl-6,7-dimcthoxy-quinazolin-4-yl)-(4-bromo-2-fluoro-phenyl)-atnine

Ci₉Hi₇BrFN₃O₂

MW 418.26

To a solution of 5-aUyl~4-(4-bromo-2-fluoro-phcnylamino)-7-mcthoxy- quinazolin-6-ol (0.34 g, 0.84 mmol) (from Example 19, Step D, supm) in acetone (100 mL) was added K₂CO₃ (0.35 g, 2.52 mrnol) and methyl iodide (1.19 g, 8.41 mmol) (Aldrich). The reaction mixture was heated with stirring at 90 °C for 4.5 hours. The mixture was cooled to room temperature, filtered, and the filtrate was concentrated. The residue was purified by chromatography using EtOAc / CH₂CI₂ / Et₃N (1 :4:0.01) as eluent to give the desired (5-allyl-6,7-dimcthoxy-quinazo]in-4-yl)-(4-bromo-2-fluoro-phcnyl)- amine as a yellow solid. (Yield 0.33 g, 94%).

Step F: 4-(4-Bromo-2-fluoro-phenyl)-5-iodomethyl-7,8-dirnethoxv-5,6-dihydro-4.fl^r- 1 ,3,4-lriaza-phenalene

Ci₉Hi₆BrFIN₃O₂

MW 544.16

To a solution of (5-allyl-6,7-dimethoxy-quinazolin-4-yl)-(4-biOrno-2-fluoiO- phenyl)-amine (0.236 g, 0.564 mmol) (from Example 19, Step E, supra) in dichloromcthanc (30 mL) was added I₂ (1.43 g, 5.64 mmol). The reaction mixture was stirred at room temperature for 4 hours. The mixture was diluted with chloroform (100 mL), and washed with a saturated aqueous Na₂SO₃ solution. The organic layer was separated, dried over Na₂Sθ₄, and concentrated to give the desired 4-(4-bromo-2-tluoro- phenyl)-5-iodomethyl-7,8-dimethoxy-5,6-dihydro-4//-l,3,4-triaza-phenalene as an off white oil. (Yield 0.034 g, 11%).

Step G: 4-(4-Bromo-2-πuoro-phcnγl)-7,8-dimcthoxv-5-methvl-4.tf-l,3₁4-ti-iaza- phenalene

Ci₉Hi₅BrEN₃O₂ MW 416.24 To a solution of 4-(4-bromo-2-fluoro-phcnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6- dihydro-4//- 1 ,3,4-lria7.a-phenalene (33 mg, 0.06 mmol) (from Example 19, Step F, supra) in toluene (7 mL) was added DBU (0.09 mL, 0.6 mmol) (Ruka). The reaction mixture was heated at 120 ⁰C for 1 hour. The mixture was then diluted with chloroform (100 mL), and washed with H₂O. The organic layer was separated, dried over Na₂SO^ and concentrated. The residue was purified by chromatography using ROAc / CH₂CI₂/ Et₃N (1:1:0.05) as clucnt to give the desired 4-(4-bromo-2-fluoro-phcnyl)-7,8- dimclhoxy-5-methyl-4#^'-l,3,4-triaza-phcnalcnc as a white solid. (Yield 0.027 g, 100%).

Example 20 7,8-Dimelhoxy-4-phenyl-4//-l,3,4-triaza-phenalene

Ci₈H₁₅N₃O₂ MW 305.33 i A: 7,8-Dimethox^4-phenyl-5,6-dihydro-4//-l,3,4-triaza-phenalen-5-ol

To a solution of (5-a11y]-6,7-dimethoxy-quinazolin-4-yl)-pheny1-amine (0.35 g, 1.09 mmol) (from Example 15, Step E jsupnx) in methanol (50 mL) at -78 ⁰C was passed a continuous stream of O₃ until the color of the solution became blue. The reaction solution was then purged with argon, and mclhyl sulfide (5 mL) (Aldrich) was added. The reaction mixture was slowly warmed to room temperature and stirred overnight. The solution was concentrated, the residue was dried in vacuo to give the desired 7,8- dimclhoxy-4-phcnyl-5,6-dihydro-4//-l ,3,4-triaza-phcnalcn-5-oI as a crude yellow solid. (Yield 0.17 g, 48%).

!_B: 7,8-Dimethoxy-4-phenyl-4#- 1,3,4-triaza-phcnalcnc

Ci₈H₁₅N₃O₂ MW 305.33

To a solution of 7,8-dimctJH)xy-4-phcnyl-5,6-dUτydro-4#-l,3,4-triaza-phcnalcn-5- ol (91 mg, 0.28 mrnol) (from Example 20, Step A, supra) and Iriclhylaminc (0.23 mL, 1.69 mmol) in dichloromethane (50 mL) at 0⁰C was added methanesulfonyl chloride (0.087 mL, 1.12 mmol) (Aldrich). The reaction solution was the stirred at room temperature for 2 hours. The solution was then concentrated, the residue was purified by chromatography using EtOAc / CH₂Cl₂ / NH₃ ( 1 :4:0.05) as eluenl to give the desired 7,8- dimethoxy-4-phenyl-4iϊ-l,3,4-triaza-phenalene as a white solid. (Yield 47 mg, 55%).

Example 21

4-(4-ChloiO-phenyl)-7,8-dimethoxy-4//- l,3,4-triaza-phenalene

C₁₈Hi₄ClN₃O₂ MW 339.78

Step A: 7,8-Dimcthoxv-4-phcny1-5,6-dihvdiO-4//-l ,3.4-triaza-phcnalcn-5-ol

C₁₈H₁₆CIN₃O₃ MW 360

To a solution of (5-aUyl-6,7-dimethoxy-quinazolin-4-yl)-(4-chloro-phenyl)-amine (0.14 g, 0.39 mmol) (from Example 16, Step E, supra) in methanol (50 mL) at -78⁰C was passed a continuous stream of O₃ until the color of the solution became blue. The reaction solution was then purged with argon, and methyl sulfide (5 mL) (Aldrich) was added. The reaction mixture was slowly warmed to room temperature and stirred overnight. The solution was concentrated, the residue was dried in vacuo to give the desired 7,8-dimelhoxy-4-(4-chloiO-phenyl)-5,6-dihydro-4#-l,3,4-lriaza-phenalen-5-ol as a crude yellow solid. (Yield 0.14 g, 100%).

Step B: 4-(4-Chloro-phenyl)-7,8-dimelhoxv-47/-l,3,4-triaza-phenalene

C₁₈H₁₄ClN₃O₂ MW 339.78

To a solution of 7,8-dimcthoxy-4-(4-chloro-phcnyl)-5,6-dihydro-4.ff-l,3,4-triaza- phenalen-5-ol (140 mg, 0.39 mmol) (from Example 21, Step A, supra) and trielhylamine (0.32 mL, 2.33 mmol) in dichloromethane (50 mL) at 0 ^CC was added methanesulfonyl chloride (0.12 mL, 1.55 mmol) (Aldrich). The reaction solution was the stirred at room temperature for 2 hours. The solution was then concentrated, the residue was purified by chromatography using EtOAc / CH₂CI₂/ NEt₃ (1 :1 :0.01) as eluent to give the desired 4- (4-cliloro-phcnyl)-7,8-dimethoxy-4iϊ-l,3,4-triaza-phcnalcnc as a yellow solid. (Yield 47 mg, 55%).

Example 22

4-(3-BiOmo-phenyl)-7,8-dimethoxy-4//-l,3,4-triaza-phenalene

Ci₈H₁₄BrN₃O₂ MW 384.23 > A 7,8-Dimcthoxy-4-(3- bromo-phcnyl)-5,6-dihvdiO-4ff-l,3,4-triaza-phenalcn-5-ol

C₁₈H₁₆BrN₃O₃

MW 402.24 To a solution of (5-allyl-6,7-dimcthoxy-quinazo]in-4-yl)-(3-bromo-phcnyl)-aminc

(0.17 g, 0.42 mmol) (from Example 17, Step E, siiprά) in methanol (50 mL) at -78⁰C was passed a conlinuous stream of O₃ until the color of the solution became blue. The reaction solution was then purged with argon, and methyl sulfide (5 mL) (Aldrich) was added. The reaction mixture was slowly warmed to room temperature and stirred overnight. The solution was concentrated, the residue was dried in vacuo to give the desired 7,8-dimcthoxy-4-(3-bromo-phcnyl)-5,6-diliydro-4ff- 1,3,4- triaza-phcnalcn-5-ol as a crude brown oil. (Yield ().16g, 100%).

_B: 4-(3-BiOmo-phcnyl)-7,8-dimethoxy-4J?-l,3,4-triaza-phenalcnc

C₁₈H₁₄BrN₃O₂ MW 384.23 To a solution of 7,8-dimethoxy-4-(3-bromo-phenyl)-5,6-dihydro-4#-l,3,4-triaza- phcnalcn-5-ol (0.17 g, 0.42 mmol) (from Example 22, Step A, supra) and triethylaminc (0.35 mL, 2.53 mmol) in dichloromethane (30 mL) at 0 ⁰C was added methanesulfonyl chloride (0.13 mL, 1.68 mmol) (Aldrich). The reaction solution was stirred at room temperature for 2 hours. The solution was then concentrated, the residue was purified by chromatography using BlOAc / CH₂Cl₂ / NH₃ (1:1:0.01) as clucnt to give the desired A- (3-biOmo-phenyl)-7,8-dimethoxy-4//-l,3,4-triaza-phenalene as an off while solid. (Yield 81 mg, 50%).

The pharmacological properties of the compounds of this invention maybe confirmed by a number of pharmacological assays. The exemplified pharmacological assay that follows was carried out with the compounds according to the invention and their salts.

Example 23: Kinase Inhibition Assay To determine the ability of test compounds according to the invention to inhibit

EGFR activity, kinase assays were conducted using an HTRF (Homogeneous Time Resolved Fluorescence) assay. This assay is described in A. J. KoIb ct. al., Drug Discovery Today, 1998, 3(7), p 333.

Kinase activity assays were performed in 96- well polypropylene plates (Falcon) with a total volume of 90 μLin each well. Each well contained 1 μM EGFR substrate (Biotin-EEEEYEELV), 1.5 nM EGFR, and a test compound with one of 8 assay concentrations ranging from 100 μM to 128 pM (1 :5 serial dilution). The kinase activity assay was done in the presence of 100 niM HEPES, pH 7.4, 1 mM DTT, 5 mM MgCl₂, 2 mM MnCl₂, 1% DMSO, 0.5 μM ATP (K_1n for EGFR), 0.1 mM Na₂VO₄, and 0.02% BSA. The reaction was incubated at 37⁰C for 30 minutes. To slop the EGFR reaction, 72 μL of reaction mixture was transferred into a STOP plate containing 18 μL of revelation buffer (20 mM EDTA, 50 mM HEPES, pH 7.4, 0.02% BSA, 10 nM Eu -labelled anti-pY antibody (final cone. 2 nM), and 100 nM strcptavidin (final cone. 20 nM)). Alter mixing, 35 μL of solution was Iran sferred into duplicate wells of a 384- well black plate (Costai'), and read at 615/665 nm on a Wallac Victor 5 reader.

Test compound IC50 values were determined from duplicate sets of data, and calculated by usingExcel and fitting data to equation Y=[(a-b)/{l+(X/c)^d]+b, where a and b arc enzyme activity in the presence of no lest compound and an infinite amount of test compound, respectively, c is the IC₅₀ and d is the hill constant of the compound response. The IC₅₀ value is the concentration of test compound that reduces by 50% the enzyme activity under the test conditions described.

The compounds of the invention had IC50 values of less than 1 μM when tested in the above-described assay. Those compounds thus exhibited BGFR kinase inhibition activity.

EGFR IC 50 (micro molar)

Example 1 0.04788

Example 2 0.06069

Example 4 0.04006

Example 9 0.00468

Example 10 0.00994

Example 11 C 0.00268

Example 19 G 0.02600

Claims

Claims

1. Acompound of the formula

I wherein

Z is C or N;

R¹ and R² arc independently selected from H, lower alkyl, lower alkyl substituted with

K) OR⁶, NR⁶R⁷, hctcrocyclc, andhclcroaryl;

R³ and R⁴ are each independently selected from H, F, Cl, and Br;

R= is selected from H, OH, SH, oxo, thionc, and Ci - C₃ alkyl; and

R⁶ and R⁷ are each independently selected from H, and lower alkyl or, alternately NR⁶R⁷ together can form a ring having 3 to 7 atoms, said ring optionally including up

15 to three additional heteroatoms and being optionally substituted by one or more lower alkyl; or the pharmaceutically acceptable salts or esters thereof.

2. The compound of claim 1 wherein Z is C.

20 3. The compound of claim 1 wherein Z is N.

4. The compound of formula I, claim 1, wherein Rl and R2 are independently selected from lower alkyl.

25 5. The compound of claim 4 wherein either Rl or R2 is methyl.

6. The compound of claim 4 wherein both Rl and R2 are methyl.

7. The compound of formula I, claim 1, wherein R3 and R4 are independently selected from H, Br, Cl and F.

8. The compound ofclaim 7 wherein either R3 or R4is H.

9. The compound ofclaim 7 wherein R3 and R4 arc both H.

10. The compound of formula I, claim 1, wherein R5 is selected from

=O, =S, H and lower alkyl.

11. The compound ofclaim 10 wherein R⁵ is selected from H and lower alkyl.

12. The compound of formula I, claim 1, wherein Z is N, R¹ and R² are methyl, and R³ and R⁴ are H.

13. The compound of formula I, claim 1, wherein Z is N, R¹ and R² are methyl, one of R³ and R⁴ is H and the other is Cl or Br.

14. The compound of formula I, claim 1, wherein Z is C, R¹ and R² arc methyl, one of R³ and R⁴ is H and the other is Cl or Br.

15. The compound of formula I, claim 1 , wherein Z is C, R¹ and R² arc methyl, one of R³ and R⁴ is F and the other is Cl or Br.

16. A compound selected from the group

8,9-Dimcthoxy-3-phcnyl-l.ff,37ϊ-l,3,4,6-tctraaza-phcnalcn-2-onc;

8,9-Dimcthoxy-3-phcnyl-lfl^r,3fl^r- l,3,4,6-tctraaza-phcnalcne-2-thionc; 8,9-Dimethoxy-3-phenyl-3//-l,3,4,6-tetraaza-phena1ene; 8,9-Diinethoxy- 2-melhyl-3-phenyl-3//-l , 3,4,6- telraaza-phenalene; and 2-Elhyl-8,9-dimethoxy-3-phenyl-3//-l ,3,4,6-tetraaza-phenalene.

17. A compound selected from the group 3-(3-Bromo-phenyl)-8,9-dimethoxy-3H-l,3,4,6-tetraaza-phenalene; 3-(3-BiOmo-phenyl)-8,9-dimethoxy-lH,3H-l,3,4,6-tetraaza-phenalen-2-one; 3-(3-Bromo-phenyl)-8,9-dimelhoxy-2-melhyl-3H- 1,3,4,6- letraaza-phenalene; 3-(3-Bramo-phcnyI)-8,9-dimethoxy-lH,3H-l,3,4,6-tetraaza-phcnalcn-2-lhionc; 3-(3-Bromo-ρhcnyl)-2-cthyl-8,9-dimcthoxy-3H-l,3,4,6-tclraaza-phcnalcnc; and 3-(3-Chloro-pheπyl)-8,9-dimcthoxy-lH,3H-l,3,4,6-tctraaza-phcnalcn-2-onc.

18. A compound selected from the group

3-(3-Chloro-phenyl)-8,9-dimethoxy-2-methyl-3H-l,3,4,6-tetraaza-phenalene; 3-(4-ChloiO-pheny1)-8,9-dimelhoxy-3H-l,3,4,6-lelraaza-phenalene;

3-(4-Chloro-phcnyl)-8,9-dimclhoxy-lH,3H- ] ,3,4,6-tctraaza-phcnalcn-2-thionc;

7,8-Dimcthoxy-5-mcthyl-4-phcnyl-4H- 1,3,4- triaza-phenalene;

4-(4-Chloro-phcnyl)-7,8-dimcthoxy-5-methyl-4H- 1,3,4- triaza-phcnalcnc;

4-(3-Bromo-phcnyl)-7,8-dimcthoxy-5-methyl-4H- 1,3,4- triaza-phcnalcnc; and 4-(3-Bromo-phenyl)-7,8-dimethoxy-5-methyl-4//-l,3,4-triaza-phenalene.

19. A compound selected from the group

4-(4-BiOmo-2-πuoiO-phenyl)-7,8-dimethoxy-5-methyl-4Λ^r-l ,3,4-lriaκa-phenalene; 7,8-Dimcthoxy-4-phenyl-4ff-l,3,4- triaza-phcnalcnc; 4-(4-Chloro-phcnyl)-7,8-dimcthoxy-4ff- 1,3,4-triaza-phenalcnc; and 4-(3-Bromo-phcnyl)-7,8-dimethoxy-4iϊ-l,3,4-triaza-phcnalcnc.

20. A compound selected from the group (5-Ally1-6,7-dimethoxy-quina/.olin-4-yl)-phenyl-amine; 5-Iodomethyl-7,8-dimethoxy-4-phenyl-5,6-dihydro-4H-l,3,4-triaza-phenalene;

5-AUyl-4-(4-chloiO-phenylamino)-7-methoxy-quinazolin-6-ol;

(5-AUyl-6,7-dimethoxy-quiiiazolin-4-yI)-(4-chloro-phenyl)-amine;

4-(4-ChloiO-phcnyl)-5-iodomGthyl-7,8-dimcthoxy-5,6-dihydro-4H-l,3,4-triaza- phenalene;

5-Allyl-4-(3-biOmo-phenylamino)-7-methoxy-quinazolin-6-ol; (5-Allyl-6,7-dimclhoxy-quinazoKn-4-yl)-(3-bromo-phcnyl)-aminc; and

4-(3-Bromo-phcnyl)-5-iodomclhyl-7,8-dimcthoxy-5,6-dih.ydro-4H-l,3,4-triaza- phenalene.

21. A compound selected from the group

5-A11yl-4-(3-ch]oiO-4-πuoro-pheny]amino)-7-methoxy-quinazolin-6-ol; (5-A11yl-6,7-dimelhoxy-quinazolin-4-yl)-(3-chloiO-4-πuoro-phenyl)-amine;

4-(3-ChloiO-4-iluoiO-ρhcnyl)-5-iodomclhyl-7,8-dimethoxy-5,6-diliydiO-4H-l,3,4- triaza-phenalene;

5-A11y1-4-(4-biOmo-2-πuoro-phenylamino)-7-methoxy-quinazolin-6-ol; 5-Ally]-6,7-dimcthoxy-quinazolin-4-yl)-(4-biOmo-2-nuoro-phcnyl)-aminc;

4-(4-Bromo-2-fluoro-plicnyl)-5-iodomcthyl-7,8-dimcthoxy-5,6-dihydro-4H-l,3,4- triaza-phenalene; 7,8-Dimcthoxy-4-phcnyl-5,6-dihydiO-4H-l ,3,4-tπaza-phcnaIcn-5-o]; 7,8-Dimcthoxy-4-phcnyl-5,6-dihydro-4H- 1,3,4- triaza-ρhcnalcn-5-ol; and 7,8-Dimcthoxy-4-(3-bromo-phcnyl)-5,6-diliydro-4H-l,3,4-triaza-phcnalcn-5-ol.

22. A pharmaceutical composition comprising as an active ingredient an effective amount of a compound according to anyone of claims 1 to 21 and a pharmaceutically acceptable carrier or excipienl.

23. The pharmaceutical composition of claim 22 which is suitable for parenteral administration.

24. Compounds according to anyone of claims 1 to 23 as medicament.

25. Use of a compound according to anyone of claims 1 to 23 for the preparation of a medicament for the treatment of a solid tumor

26. Use accordingto claim 25 wherein the solid tumor is a breast, colon, prostate or lung tumor.

27. The invention as described above.