The present invention covers 2-methyl-quinazoline compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, as a sole agent or in combination with other active ingredients.

BACKGROUND

The present invention covers 2-methyl-quinazoline compounds of general formula (I) which inhibit the Ras-Sos interaction.

In the 2-position substituted quinazoline compounds are described e.g. in EP 0326328, EP 0326329, WO93/007124, WO2003/087098 and US 5,236,925. These compounds are either not described as pharmaceutically active compounds or, if they are described as pharmacologically active compounds, they are described as compounds having affinity to the Epidermal Growth Factor Receptor (EGFR).

In the majority (45-100%) of patients receiving EGFR inhibitors skin toxicity is a class- specific side effect that is typically manifested as a papulopustular rash. The skin toxicity is related to the inhibition of EGFR in the skin, which is crucial for the normal development and physiology of the epidermis.

However, the state of the art does not describe:

the 2-methyl substituted quinazoline compounds of general formula (I) of the present invention as described and defined herein, i.e. compounds having a quinazoline core bearing a methyl group on the carbon atom 2 which effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor.

Ras proteins play an important role in human cancer. Mutations in Ras proteins can be found in 20-30% of all human tumors and are recognized as tumorigenic drivers especially in lung, colorectal and pancreatic cancers (Malumbres & Barbacid 2002 Nature Reviews Cancer, Pylayeva-Gupta et al. 2011 Nature Reviews Cancer). Three human Ras genes are known that encode four different Ras proteins of 21 kDa size: H-Ras, N-Ras, and two splice variants of K-Ras, namely K-Ras 4A and K-Ras-4B. All Ras isoforms are highly conserved within the GTP-binding domain and differ mainly in the hypervariable C-terminal region. The C-termini of the different Ras-isoforms are posttranslationally modified by lipidation (farnesylation, palmitoylation) to facilitate membrane anchorage. The localization of Ras-proteins at the cytoplasmic membrane provides vicinity to transmembrane growth receptors and has been shown to be essential for transmitting growth signals from extracellular growth factor binding to intracellular downstream pathways. A variety of upstream signals may activate Ras proteins depending on the cellular context, such as epidermal growth factor receptor (EGFR), platelet-derived growth factor receptor (PDGFR), nerve growth factor receptor (NGFR) and others. Activated Ras can signal through various downstream pathways, e.g. the Raf-MEK- ERK or the PI3K-PDK1 -Akt pathways.

On the molecular level, Ras proteins function as molecular switches. By binding GTP and GDP they exist in an active (GTP-bound) and inactive (GDP-bound) state in the cell. Active GTP-loaded Ras recruits other proteins by binding of their cognate Ras-binding domains (RBDs) resulting in activation of the effector protein followed by downstream signalling events of diverse functions, e.g. cytoskeletal rearrangements or transcriptional activation. The activity status of Ras is tightly regulated by guanine nucleotide exchange factors (GEFs) and GTPase activating proteins (GAPs). GEFs function as activators of Ras by promoting the nucleotide exchange from GDP to GTP. GAPs deactivate Ras-GTP by catalyzing the hydrolysis of the bound GTP to GDP. In a cancer cell, point mutations, typically within the GTP-binding region at codon 12, eliminate the ability of RAS to efficiently hydrolyse bound GTP, even in the presence of a GAP. Therefore, cancer cells comprise increased levels of active mutated Ras-GTP, which is thought to be a key factor for driving cancer cell proliferation.

Three main families of RAS-specific GEFs have been identified so far (reviewed in Vigil 2010 Nature Reviews Cancer; Rojas et al 2011, Genes & Cancer 2(3) 298-305). There are two son of sevenless proteins (SOS1 and SOS2), 4 different isoforms of Ras guanine nucleotide releasing proteins (Ras-GRP1 -4) and two Ras guanine nucleotide releasing factors (Ras-GRF1 and 2). The SOS proteins are ubiquitously expressed and are recruited to sites of activated growth factors. Ras-GRFs are expressed mainly in the nervous system, where they are involved in Calcium-dependent activation of Ras. In contrast, Ras GRP proteins are expressed in hematopoietic cells and act in concert with non-receptor tyrosine kinases. In the context of cancer, mainly SOS proteins have been found to be involved.

Targeting Ras for cancer therapy has been a dream since the 1990s (Downward 2002 Nature Reviews Cancer, Krens et al. 2010 Drug Discovery Today). Due to the compact nature, the high affinity towards GDP and GTP in combination with high intracellular GTP concentrations, the Ras protein itself has always been considered to be undruggable, i.e. the chance to identify small chemical molecules that would bind to and inhibit active Ras was rated extremely low. Alternative approaches have been undertaken to reduce Ras signaling, e.g. by addressing more promising drug targets such as enzymes involved in the posttranslational modification of Ras proteins, especially farnesyltransferase and geranylgeranyltransferase (Berndt 2011 Nature Reviews Cancer). Inhibitors of farnesyltransferase (FTIs) were identified and developed with promising antitumor effects in preclinical models. Unexpectedly, in clinical trials these inhibitors have been of limited efficacy. Targeting upstream and downstream kinases involved in Ras signaling pathways has been more successful. Several drugs are and have been in clinical trials that inhibit different kinases, e.g. EGFR, Raf, MEK, Akt, PI3K {Takashima & Falter 2013 Expert Opin. Ther. Targets). Marketed cancer drugs are available that inhibit Raf, EGFR or MEK.

Nevertheless, there is still a large unmet need for the treatment of Ras-dependent tumors that are resistant against current therapies. Many research groups have been active to identify small molecules that target Ras directly (Ras small molecules have been reviewed in: Cox et al. 2014 Nature Reviews Drug Discovery; Stephen et al. 2014 Cancer Cell; Hattum & Waldmann 2014 Chemistry & Biology, Spiegel et al. 2014 Nature Chemical Biology). One group of inhibitors comprises small molecules that inhibit the interaction of Ras with its effectors Raf or PI3K. Another group of compounds acts as covalent inhibitors of a specific cysteine mutant form of K-Ras (glycine to cysteine point mutation G12C). The specific targeting of the Ras-G12C mutant might have the benefit of reduced side effects, as the wildtype Ras proteins should not be affected. Furthermore, several reports show small molecules and peptides that interrupt the GEF assisted activation of Ras. There seem to be several different binding sites possible that result in this mode of action. Inhibitors may bind to Ras or to the GEF in an allosteric or orthosteric fashion. All these approaches of direct Ras-targeting are in preclinical research stage and the affinity of published small molecule inhibitors is still in the micromolar range. Stabilized peptides have been shown to be active in the nanomolar range. (Leshchiner et al. 2015 PNAS). Their usefulness as drugs in a clinical setting has to be awaited.

The Epidermal Growth Factor Receptor (EGFR) is a tyrosine kinase (TK) receptor that is activated upon binding to the Epidermal Growth Factor and other growth factor ligands, triggering several downstream pathways, including RAS/MAPK, PI3K/Akt and STAT that regulate different cellular processes, including DNA synthesis and proliferation (Russo A, Oncotarget.4254, 2015). The family of HER (ErbB) receptor tyrosine kinases consists of four members, ie, epidermal growth factor receptors [EGFR (HER1 or ErbB1 ), HER2 (ErbB2, neu), HER3 (ErbB3), and HER4 (ErbB4)]. Overexpression, mutation, or aberrant activity of these receptors has been implicated in various types of cancer (Feldinger K, Breast Cancer (Dove Med Press), 2015, 7, 147).

First-generation inhibitors

Erlotinib and Gefitinib are small molecule inhibitors of the EGFR/HER-1 (human epidermal growth factor receptor) tyrosine kinase. Erlotinib and Gefitinib were developed as reversible and highly specific small-molecule tyrosine kinase inhibitors that competitively block the binding of adenosine triphosphate to its binding site in the tyrosine kinase domain of EGFR, thereby inhibiting autophosphorylation and blocking downstream signaling (Cataldo VD, N Engl J Med, 201 1 , 364, 947).

Second-generation inhibitors

Afatinib is an oral tyrosine kinase inhibitor (TKI) approved for the first-line treatment of patients with NSCLC whose tumors are driven by activating mutations of genes coding for epidermal growth factor receptor (EGFR). Afatinib is also an inhibitor of a specific EGFR mutation (T790M) that causes resistance to first-generation EGFR-targeted TKIs in about half of patients receiving those drugs. (Engle JA, Am J Health Syst Pharm 2014, 71 (22), 1933).

Neratinib, a pan-HER inhibitor, irreversible tyrosine kinase inhibitor binds and inhibits the tyrosine kinase activity of epidermal growth factor receptors, EGFR (or HER1 ), HER2 and HER4, which leads to reduced phosphorylation and activation of downstream signaling pathways. Neratinib has been shown to be effective against HER2-overexpressing or mutant tumors in vitro and in vivo. Neratinib is currently being investigated in various clinical trials in breast cancers and other solid tumors, including those with HER2 mutation (Feldinger K, Breast Cancer (Dove Med Press), 2015, 7, 147).

Dacomitinib is an irreversible inhibitor of EGFR, HER2, and HER4. In preclinical cell lines and xenograft studies, dacomitinib demonstrated activities against both activating EGFR mutations and EGFR T790M (Liao BC, Curr Opin Oncol. 2015, 27(2), 94).

Third-generation inhibitors

The third-generation EGFR-TKIs were designed to inhibit EGFR T790M while sparing wild- type EGFR.

AZD9291 (AstraZeneca, Macclesfield, UK), a mono-anilino-pyrimidine compound, is an irreversible mutant selective EGFR-TKI. This drug is structurally different from the first and second-generation EGFR-TKIs. In preclinical studies, it potently inhibited phosphorylation of EGFR in cell lines with activating EGFR mutations (EGFR del19 and EGFR L858R) and EGFR T790M. AZD9291 also caused profound and sustained tumor regression in tumor xenograft and transgenic mouse models harboring activating EGFR mutations and EGFR T790M. AZD9291 was less potent in inhibiting phosphorylation of wild-type EGFR cell lines (Liao BC, Curr Opin Oncol. 2015, 27(2), 94).

Rociletinib (CO-1686) (Clovis Oncology, Boulder, Colo), a 2,4-disubstituted pyrimidine molecule, is an irreversible mutant selective EGFR-TKI. In preclinical studies, CO-1686 led to tumor regression in cell-lines, xenograft models, and transgenic mouse models harboring activating EGFR mutations and EGFR T790M (Walter AO, Cancer Discov, 2013, 3(12), 1404).

HM61713 (Hanmi Pharmaceutical Company Ltd, Seoul, South Korea) is an orally administered, selective inhibitor for activating EGFR mutations and EGFR T790M. It has low activity against wild-type EGFR (Steuer CE, Cancer. 2015, 121 (8), E1 ).

It has now been found, and this constitutes the basis of the present invention, that the compounds of the present invention have surprising and advantageous properties.

In particular, the compounds of the present invention have surprisingly been found to effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor and may therefore be used for the treatment or prophylaxis of hyper- proliferative disorders, in particular cancer.

DESCRIPTION of the INVENTION

In accordance with a first aspect, the present invention covers compounds of general formula (I):

in which R ¹ stands for

a substituent independently selected from: a hydrogen atom, a halogen atom, a hydroxy, cyano, nitro, Ci-C6-alkylsulfanyl or an amino group -N R ^a R ^b ,

wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci- Ce-alkyl,

a substituent selected from: a Ci-C6-alkyl, Ci-C6-alkoxy-, C2-C6-alkenyl, C2-C6- alkynyl, Cs-Cs-cycloalkyl, C4-C8-cycloalkenyl, 4- to 7-membered heterocycloalkyi, 5- to 10-membered heterocycloalkenyl, heterospirocycloalkyi, fused heterocycloalkyi, bridged heterocycloalkyi, phenyl, heteroaryl, Ci-C6-haloalkyl,

-C(=0)OH, -C(=0)OR ^c , and wherein R ^c stands for Ci-C ₆ -alkyl, C ₃ -C ₆ -alkenyl, C ₃ -C ₆ - alkynyl, Cs-Cs-cycloalkyl or C4-Cs-cycloalkenyl,

-N=S(=0)(R ^d )R ^e , and wherein R ^d and R ^e are selected independently from hydrogen, Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl or C4-Cs-cycloalkenyl,

-N H-C(0)-Ci-C ₆ -alkyl, -N H-C(0)-N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-Ce-alkyl, -N H-(CH ₂ )k-N H-C(0)-Ci-C6- alkyl, wherein k is 1 or 2, -N H-(CH2)i-R , wherein

I is 0, 1 or 2 and R stands for a 4- to 7-membered heterocycloalkyi, heteroaryl, Ci-C6-alkylsulfonyl,

whereby in all foregoing definitions the Ci-C6-alkyl-,Ci-C6-alkoxy-, the 4- to 7- membered heterocycloalkyi and the heteroaryl can be optionally substituted, one, two or three times, identically or differently, with:

a halogen atom, or a group selected from hydroxy, oxo (=0), a cyano, nitro, Ci-Ce-alkyl, C ₂ -C ₆ -alkenyl, C ₂ -C ₆ -alkynyl, Cs-Cs-cycloalkyl, 4- to 7- membered heterocycloalkyi, Ci-C6-alkoxy, Ci-C6-haloalkyl, C1-C6- haloalkoxy-, Ci-C6-alkylsulfonyl, phenyl, benzyl-, heteroaryl, -(CH2)- heteroaryl-, C3-Cs-cycloalkoxy-, phenyloxy-, heteroaryloxy-, -N H-C(0)-Ci- C6-alkyl or an amino group -N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-C6-alkyl, or

a substituent , wherein E and G each stands for an electron pair, or one of

E and G stands for an electron pair and the other for an oxygen atom or a group =NH or =N-Ci-C4-alkyl, or one of E and G stands for an oxygen atom and the other one for a group =N H or =N-Ci-C4-alkyl, or E and G each stands for an oxygen atom or each stands for a group =NH or =N-Ci-C4-alkyl, or a substituent -0-(CH ₂ ) _z -phenyl, -0-(CH ₂ )z-C4-C ₇ -heterocycloalkyl, -0-(CH ₂ ) _z - heteroaryl, whereby

z is 0, 1 or 2, and the phenyl, heterocycloalkyi and heteroaryl can optionally be substituted with a group selected from hydroxy, heterocycloalkyi or heterocycloalkenyl, which both can be substituted with a methyl- and/or oxo- group, or a substituent selected from the group of

and wherein x is 1 , 2 or 3,

A1 stands for a C ₄ to Ci2 carbocyclic, heterocyclic, optionally bicyclic, optionally aromatic or optionally heteroaromatic ring system, wherein in a bicyclic aromatic or heteroaromatic ring system one or two double bonds can be hydrogenated, R ² stands for

a hydrogen atom, a hydroxy group, oxo (=0), a halogen atom, a cyano group, a substituent selected from: a Ci-C6-alkyl, Ci-C6-alkoxy-, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8-cycloalkyl, C4-C8-cycloalkenyl, 4- to 7-membered heterocycloalkyi, -0-CH2-4- to 7-membered heterocycloalkyi, 5- to 10-membered heterocycloalkenyl, heterospirocycloalkyl, fused heterocycloalkyi, bridged heterocycloalkyi, phenyl, heteroaryl, Ci-C6-haloalkyl, Ci-C6-alkylsulfonyl,

-N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a d-Ce-alkyl,

-C(0)-N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a d-Ce-alkyl, -C(0)-0-R ⁹ , wherein R ⁹ is a hydrogen atom or a Ci-Ce-alkyl, -0-R ^h , wherein R ^h is a Ci-C6-alkyl or -CH2-N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-C6-alkyl,

and w is 1 or 2, and wherein

A2(R ³ ) _y stands either for a hydrogen atom or

A2 has the same meanings as the substituent A1 and

R ³ stands for

a hydrogen atom, a halogen atom, a hydroxy, oxo, cyano, nitro group, a substituent selected from a Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8- cycloalkyl, C4-C8-cycloalkenyl, C7-C8-cycloalkynyl, 4- to 7-membered heterocycloalkyi, 5- to 10-membered heterocycloalkenyl, phenyl, heteroaryl, C1-C6- haloalkyl,

which substituent is optionally substituted, one, two or three times, identically or differently, with a substituent selected from :

a halogen atom, or a group selected from hydroxy, oxo (=0), cyano, C1-C6- alkyl, Ci-C ₆ -alkoxy, Ci-C ₆ -haloalkyl, phenyl, -C(0)N R'R ^j , wherein

R' and R ^j are selected independently from a hydrogen atom or a C1-C6- alkyl, heteroaryl,

or with amino -N R ^k R', wherein R ^k and R' are selected independently from a hydrogen atom, a substituent selected from a Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, Ci-C6-alkylsulfonyl, phenyl, heteroaryl, 4- to 7-membered heterocycloalkyl, which are optionally substituted

one, two or three times, identically or differently, with a substituent selected from Ci-C6-haloalkyl, hydroxyl, oxo (=0), phenyl, cyano , Ci- C6-alkoxy, heteroaryl, wherein

the heteroaryl can optionally be substituted with a methyl group, or

-CH ₂ -C(0)-R ^m , wherein

R ^m is a bicyclic heteroaryl, which can be partially hydrogenated, a Ci- C6-alkoxy or a group -NR ⁿ R°, in which

R ⁿ and R° are selected independently from hydrogen, Ci-C6-alkyl, phenyl, wherein the Ci-C6-alkyl can optionally be substituted with a Ci-C6-alkoxy or a phenyl, or

-NR ⁿ R° stands for a 4- to 7-membered azacycloalkyi, bound via the nitrogen atom to the rest of the molecule and which optionally contains one more heteroatom selected from nitrogen and oxygen;

-C(=0)R ^p , wherein R ^p is selected from

the group of a C1 -C6-alkoxy, a C1 -C6-alkyl, which is optionally substituted, one, two or three times, identically or differently, with a substituent selected from hydroxyl or Ci-C6-alkoxy, a mono- or bicyclic heteroaryl, a 4- to 7-membered heterocycloalkyl or R ^p is a group -CH2-NR ^q R ^r ; wherein R ^q and R ^r are selected independently from hydrogen, phenyl or a Ci-C6-alkyl, which may optionally be substituted up to threefold with fluorine,

-NR ^s R' is

a 4- to 7-membered azacycloalkyi, bound via the nitrogen atom to the rest of the molecule, or a 6- to 10-membered azaspirocycloalkyl, which both may contain up to 2 further heteroatoms selected from nitrogen and oxygen and which both are optionally substituted one, two or three times, identically or differently, with a substituent selected from : hydroxy, oxo (=0), C1-C6- alkyl, d-Ce-hydroxyalkyl, -C(=0)OR ^u , wherein R ^u is a Ci-C ₆ -alkyl, halogen, -N(Ci-C ₆ -alkyl) ₂ , -CH ₂ -N(Ci-C ₆ -alkyl) ₂ , -C(0)NR ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-C6-alkyl, -C(=0)R ^v , -C(=0)NH ₂ , -C(=0)N(H)R ^v , -C(=0)N(R ^v )R ^w , -C(=0)OR ^v , wherein

R ^v and R ^w represent, independently from each other, a group selected from hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, phenyl, or a group -(CH2)2-NR ^x R ^y , wherein R ^x and R ^y independently from each other stand for hydrogen, a C1-C4- alkyl or a group -(CH ₂ )2N(CH ₃ )2;

-NH ₂ , -NHR ^Z , -N(R ^z )R ^za , -N(H)C(=0)R ^z , -N(H)C(=0)OR ^z , -N(H)S(=0) ₂ R ^z , 4- to 7- membered heterocycloalkyl, heteroaryl, heterospirocycloalkyl, fused heterocycloalkyl, bridged heterocycloalkyl, wherein

R ^z and R ^za represent, independently from each other, a group selected from Ci-

C4-alkyl, Ci-C4-haloalkyl and phenyl, d-Ce-alkoxy-, Ci-C ₆ - haloalkoxy-, -0-(CH ₂ )s-C3-Ce-cycloalkyl, -0-(CH ₂ ) _s -phenyl, -O- (CH ₂ )s-heterocycloalkyl, -0-(CH ₂ ) _s -heteroaryl, s is 0, 1 , 2 or 3,

-S(=0) ₂ R ^z , -S(=0) ₂ NH ₂ , -S(=0) ₂ NHR ^z , -S(=0) ₂ N(R ^z )R ^za , wherein R ^z and R ^za represent, independently from each other, a group selected from Ci-C4-alkyl, C1-C4- haloalkyl and phenyl,

wherein y is 1 , 2 or 3, and

L stands either for a bond or for -0-(CH ₂ )k, wherein k is 0, 1 , 2 or 3, or a group - CH =CH-(CH ₂ )n, wherein n is 0, 1 or 2, or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same. DEFINITIONS

When groups in the compounds according to the invention are substituted, it is possible for said groups to be mono-substituted or poly-substituted with substituent(s), unless otherwise specified. Within the scope of the present invention, the meanings of all groups which occur repeatedly are independent from one another. It is possible that groups in the compounds according to the invention are substituted with one, two or three identical or different substituents, particularly with one substituent. As used herein, an oxo substituent represents an oxygen atom, which is bound to a carbon atom or to a sulfur atom via a double bond.

The term "ring substituent" means a substituent attached to an aromatic or nonaromatic ring which replaces an available hydrogen atom on the ring.

Should a composite substituent be composed of more than one parts, e.g. (Ci-C4-alkoxy)-(Ci-C4-alkyl)-, it is possible for the position of a given part to be at any suitable position of said composite substituent, i.e. the Ci-C4-alkoxy part can be attached to any carbon atom of the Ci-C4-alkyl part of said (Ci-C4-alkoxy)-(Ci-C4-alkyl)- group. A hyphen at the beginning or at the end of such a composite substituent indicates the point of attachment of said composite substituent to the rest of the molecule. Should a ring, comprising carbon atoms and optionally one or more heteroatoms, such as nitrogen, oxygen or sulfur atoms for example, be substituted with a substituent, it is possible for said substituent to be bound at any suitable position of said ring, be it bound to a suitable carbon atom and/or to a suitable heteroatom.

The term "comprising" when used in the specification includes "consisting of".

If within the present text any item is referred to as "as mentioned herein", it means that it may be mentioned anywhere in the present text.

The terms as mentioned in the present text have the following meanings:

The term "halogen atom" means a fluorine, chlorine, bromine or iodine atom, particularly a fluorine, chlorine or bromine atom.

The term "Ci-C6-alkyl" means a linear or branched, saturated, monovalent hydrocarbon group having 1 , 2, 3, 4, 5 or 6 carbon atoms, e.g. a methyl, ethyl, propyl, isopropyl, butyl, sec-butyl, isobutyl, ie f-butyl, pentyl, isopentyl, 2-methylbutyl, 1 -methylbutyl, 1 -ethylpropyl, 1 ,2-dimethylpropyl, neo-pentyl, 1 ,1 -dimethylpropyl, hexyl, 1 -methylpentyl, 2-methylpentyl, 3-methylpentyl, 4-methylpentyl, 1 -ethylbutyl, 2-ethylbutyl, 1 ,1 -dimethylbutyl, 2,2-dimethylbutyl, 3,3-dimethylbutyl, 2,3-dimethylbutyl, 1 ,2-dimethylbutyl or 1 ,3-dimethylbutyl group, or an isomer thereof. Particularly, said group has 1 , 2, 3 or 4 carbon atoms ("Ci-C4-alkyl"), e.g. a methyl, ethyl, propyl, isopropyl, butyl, sec-butyl isobutyl, or ie f-butyl group, more particularly 1 , 2 or 3 carbon atoms ("Ci-C3-alkyl"), e.g. a methyl, ethyl, n-propyl or isopropyl group.

The term "Ci-C6-hydroxyalkyl" means a linear or branched, saturated, monovalent hydrocarbon group in which the term "Ci-C6-alkyl" is defined supra, and in which 1 , 2 or 3 hydrogen atoms are replaced with a hydroxy group, e.g. a hydroxymethyl, 1 -hydroxyethyl, 2-hydroxyethyl, 1 ,2-dihydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl, 1 -hydroxypropyl, 1 -hydroxypropan-2-yl, 2-hydroxypropan-2-yl, 2, 3-d i hydroxy propyl, 1 ,3-dihydroxypropan-2-yl,

3- hydroxy-2-methyl-propyl, 2-hydroxy-2-methyl-propyl, 1 -hydroxy-2-methyl-propyl group.

The term "Ci-C6-alkylsulfanyl" means a linear or branched, saturated, monovalent group of formula (Ci-C6-alkyl)-S-, in which the term "Ci-C6-alkyl" is as defined supra, e.g. a methylsulfanyl, ethylsulfanyl, propylsulfanyl, isopropylsulfanyl, butylsulfanyl, sec- butylsulfanyl, isobutylsulfanyl, ie f-butylsulfanyl, pentylsulfanyl, isopentylsulfanyl, hexylsulfanyl group.

The term "Ci-C6-alkylsulfonyl" means a linear or branched, saturated, monovalent group of formula (Ci-C6-alkyl)-SC>2-, in which the term "Ci-C6-alkyl" is as defined supra, e.g. a methylsulfonyl, ethylsulfonyl, propylsulfonyl, isopropylsulfonyl, butylsulfonyl, sec- butylsulfonyl, isobutylsulfonyl, ie f-butylsulfonyl, pentylsulfonyl, isopentylsulfonyl, hexylsulfonyl group.

The term "Ci-C6-alkoxy" means a linear or branched, saturated, monovalent group of formula (Ci-C6-alkyl)-0-, in which the term "Ci-C6-alkyl" is as defined supra, e.g. a methoxy, ethoxy, n-propoxy, isopropoxy, n-butoxy, sec-butoxy, isobutoxy, ie f-butoxy, pentyloxy, isopentyloxy or n-hexyloxy group, or an isomer thereof.

The term "C2-C6-alkenyl" means a linear or branched, monovalent hydrocarbon group, which contains one or two double bonds, and which has 2, 3, 4, 5 or 6 carbon atoms, particularly 2 or 3 carbon atoms ("C2-C3-alkenyl"), it being understood that in the case in which said alkenyl group contains more than one double bond, then it is possible for said double bonds to be isolated from, or conjugated with, each other. Said alkenyl group is, for example, an ethenyl (or "vinyl"), prop-2-en-1 -yl (or "allyl"), prop-1 -en-1 -yl, but-3-enyl, but-2-enyl, but-1 -enyl, pent-4-enyl, pent-3-enyl, pent-2-enyl, pent-1 -enyl, hex-5-enyl, hex-4-enyl, hex-3-enyl, hex-2-enyl, hex-1 -enyl, prop-1 -en-2-yl (or "isopropenyl"), 2-methylprop-2-enyl,

1 - methylprop-2-enyl, 2-methylprop-1 -enyl, 1 -methylprop-1 -enyl, 3-methylbut-3-enyl,

2- methylbut-3-enyl, 1 -methylbut-3-enyl, 3-methylbut-2-enyl, 2-methylbut-2-enyl, 1 -methylbut-2-enyl, 3-methylbut-1 -enyl, 2-methylbut-1 -enyl, 1 -methylbut-1 -enyl, 1 , 1 -dimethylprop-2-enyl, 1 -ethylprop-1 -enyl, 1 -propylvinyl, 1 -isopropylvinyl,

4- methylpent-4-enyl, 3-methylpent-4-enyl, 2-methylpent-4-enyl, 1 -methylpent-4-enyl, 4-methylpent-3-enyl, 3-methylpent-3-enyl, 2-methylpent-3-enyl, 1 -methylpent-3-enyl, 4-methylpent-2-enyl, 3-methylpent-2-enyl, 2-methylpent-2-enyl, 1 -methylpent-2-enyl, 4-methylpent-1 -enyl, 3-methylpent-1 -enyl, 2-methylpent-1 -enyl, 1 -methylpent-1 -enyl,

3- ethylbut-3-enyl, 2-ethylbut-3-enyl, 1 -ethylbut-3-enyl, 3-ethylbut-2-enyl, 2-ethylbut-2-enyl, 1 -ethylbut-2-enyl, 3-ethylbut-1 -enyl, 2-ethylbut-1 -enyl, 1 -ethylbut-1 -enyl, 2-propylprop-2-enyl, 1 -propylprop-2-enyl, 2-isopropylprop-2-enyl, 1 -isopropylprop-2-enyl, 2-propylprop-1 -enyl, 1 -propylprop-1 -enyl, 2-isopropylprop-1 -enyl, 1 -isopropylprop-1 -enyl, 3,3-dimethylprop-1 -enyl, 1 -(1 ,1 -dimethylethyl)ethenyl, buta-1 ,3-dienyl, penta-1 ,4-dienyl or hexa-1 ,5-dienyl group. Particularly, said group is vinyl or allyl.

The term "C2-C6-alkynyl" means a linear or branched, monovalent hydrocarbon group which contains one triple bond, and which contains 2, 3, 4, 5 or 6 carbon atoms, particularly 2 or 3 carbon atoms ("C2-C3-alkynyl"). Said C2-C6-alkynyl group is, for example, ethynyl, prop-1 -ynyl, prop-2-ynyl (or "propargyl"), but-1-ynyl, but-2-ynyl, but-3-ynyl, pent-1 -ynyl, pent-2-ynyl, pent-3-ynyl, pent-4-ynyl, hex-1 -ynyl, hex-2-ynyl, hex-3-ynyl, hex-4-ynyl, hex-5-ynyl, 1 -methylprop-2-ynyl, 2-methylbut-3-ynyl, 1 -methylbut-3-ynyl, 1 -methylbut-2-ynyl, 3-methylbut-1 -ynyl, 1 -ethylprop-2-ynyl, 3-methylpent-4-ynyl, 2-methylpent-4-ynyl, 1 -methyl- pent-4-ynyl, 2-methylpent-3-ynyl, 1 -methylpent-3-ynyl, 4-methylpent-2-ynyl, 1 -methyl- pent-2-ynyl, 4-methylpent-1 -ynyl, 3-methylpent-1-ynyl, 2-ethylbut-3-ynyl, 1 -ethylbut-3-ynyl, 1 -ethylbut-2-ynyl, 1 -propylprop-2-ynyl, 1 -isopropylprop-2-ynyl, 2,2-dimethylbut-3-ynyl, 1 ,1 -dimethylbut-3-ynyl, 1 ,1 -dimethylbut-2-ynyl or 3,3-dimethylbut-1 -ynyl group. Particularly, said alkynyl group is ethynyl, prop-1 -ynyl or prop-2-ynyl.

The term "Cs-Cs-cycloalkyl" means a saturated, monovalent, mono- or bicyclic hydrocarbon ring which contains 3, 4, 5, 6, 7 or 8 carbon atoms ("Cs-Cs-cycloalkyl"). Said Cs-Cs-cycloalkyl group is for example, a monocyclic hydrocarbon ring, e.g. a cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl group, or a bicyclic hydrocarbon ring, e.g. a bicyclo[4.2.0]octyl or octahydropentalenyl.

The term "C4-Cs-cycloalkenyl" means a monovalent, mono- or bicyclic hydrocarbon ring which contains 4, 5, 6, 7 or 8 carbon atoms and one double bond. Particularly, said ring contains 4, 5 or 6 carbon atoms ("C4-C6-cycloalkenyl"). Said C4-Cs-cycloalkenyl group is for example, a monocyclic hydrocarbon ring, e.g. a cyclobutenyl, cyclopentenyl, cyclohexenyl, cycloheptenyl or cyclooctenyl group, or a bicyclic hydrocarbon ring, e.g. a bicyclo[2.2.1]hept-2-enyl or bicyclo[2.2.2]oct-2-enyl.

The term "Cs-Cs-cycloalkoxy" means a saturated, monovalent, mono- or bicyclic group of formula (Cs-Cs-cycloalkyl)-O-, which contains 3, 4, 5, 6, 7 or 8 carbon atoms, in which the term "Cs-Cs-cycloalkyl" is defined supra, e.g. a cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, cyclohexyloxy, cycloheptyloxy or cyclooctyloxy group.

The term "spirocycloalkyl" means a saturated, monovalent bicyclic hydrocarbon group in which the two rings share one common ring carbon atom, and wherein said bicyclic hydrocarbon group contains 5, 6, 7, 8, 9, 10 or 1 1 carbon atoms, it being possible for said spirocycloalkyl group to be attached to the rest of the molecule via any one of the carbon atoms except the spiro carbon atom. Said spirocycloalkyl group is, for example, spiro[2.2]pentyl, spiro[2.3]hexyl, spiro[2.4]heptyl, spiro[2.5]octyl, spiro[2.6]nonyl, spiro[3.3]heptyl, spiro[3.4]octyl, spiro[3.5]nonyl, spiro[3.6]decyl, spiro[4.4]nonyl, spiro[4.5]decyl, spiro[4.6]undecyl or spiro[5.5]undecyl.

The terms "4- to 7-membered heterocycloalkyi" means a monocyclic, saturated heterocycle with 4, 5, 6 or 7 ring atoms in total, which contains one or two identical or different ring heteroatoms from the series N, O and S, it being possible for said heterocycloalkyi group to be attached to the rest of the molecule via any one of the carbon atoms or, if present, a nitrogen atom.

Said heterocycloalkyi group, without being limited thereto, can be a 4-membered ring, such as azetidinyl, oxetanyl or thietanyl, for example; or a 5-membered ring, such as tetrahydrofuranyl, 1 ,3-dioxolanyl, thiolanyl, pyrrolidinyl, imidazolidinyl, pyrazolidinyl, 1 ,1 -dioxidothiolanyl, 1 ,2-oxazolidinyl, 1 ,3-oxazolidinyl or 1 ,3-thiazolidinyl, for example; or a 6-membered ring, such as tetrahydropyranyl, tetrahydrothiopyranyl, piperidinyl, morpholinyl, dithianyl, thiomorpholinyl, piperazinyl, 1 ,3-dioxanyl, 1 ,4-dioxanyl or 1 ,2-oxazinanyl, for example, or a 7-membered ring, such as azepanyl, 1 ,4-diazepanyl or 1 ,4-oxazepanyl, for example.

Particularly, "4- to 6-membered heterocycloalkyi" means a 4- to 6-membered heterocycloalkyi as defined supra containing one ring nitrogen atom and optionally one further ring heteroatom from the series: N, O, S. More particularly, "5- or 6-membered heterocycloalkyi" means a monocyclic, saturated heterocycle with 5 or 6 ring atoms in total, containing one ring nitrogen atom and optionally one further ring heteroatom from the series: N, O.

The term "4- to 7-memebered azacycloalkyl" means a monocyclic saturated heterocycly with 4, 5, 6 or 7 ring atoms in total which is attached to the rest of the molecule via the nitrogen atom and which optionally contains one more heteroatom selected from nitrogen and oxygen.

Said 4- to 7-membered azacycloalkyl group, without being limited thereto, can be a 4- membered ring, such as azetidin-1 -yl, for example; or a 5-membered ring, such as pyrrolidin-

1 - yl, imidazolidin-1 -yl, pyrazolidin-1 -yl, 1 ,2-oxazolidin-2-yl or 1 ,3-oxazolidin-3-yl, for example; or a 6-membered ring, such as piperidin-1 -yl, morpholin-4-yl, piperazin-1 -yl or 1 ,2-oxazinan-

2- yl, for example, or a 7-membered ring, such as azepan-1 -yl, 1 ,4-diazepan-1 -yl or 1 ,4-oxazepan-4-yl, for example.

The term "5- to 10-membered heterocycloalkenyl" means a monocyclic, unsaturated, non- aromatic heterocycle with 5, 6, 7, 8, 9 or 10 ring atoms in total, which contains one or two double bonds and one or two identical or different ring heteroatoms from the series: N, O, S; it being possible for said heterocycloalkenyl group to be attached to the rest of the molecule via any one of the carbon atoms or, if present, a nitrogen atom. Said heterocycloalkenyl group is, for example, 4/-/-pyranyl, 2/-/-pyranyl, 2,5-dihydro-1 /-/-pyrrolyl, [1 ,3]dioxolyl, 4/-/-[1 ,3,4]thiadiazinyl, 2,5-dihydrofuranyl, 2,3-dihydrofuranyl, 2,5-dihydrothiophenyl, 2,3-dihydrothiophenyl, 4,5-dihydrooxazolyl or 4H-[1 ,4]thiazinyl.

The term "heterospirocycloalkyi" means a bicyclic, saturated heterocyde with 6, 7, 8, 9, 10 or 1 1 ring atoms in total, in which the two rings share one common ring carbon atom, which "heterospirocycloalkyi" contains one, two or three identical or different ring heteroatoms from the series: N, O, S; it being possible for said heterospirocycloalkyi group to be attached to the rest of the molecule via any one of the carbon atoms, except the spiro carbon atom, or, if present, a nitrogen atom.

Said heterospirocycloalkyi group is, for example, azaspiro[2.3]hexyl, azaspiro[3.3]heptyl, oxaazaspiro[3.3]heptyl, thiaazaspiro[3.3]heptyl, oxaspiro[3.3]heptyl, oxazaspiro[5.3]nonyl, oxazaspiro[4.3]octyl, azaspiro[4,5]decyl, oxazaspiro [5.5]undecyl, diazaspiro[3.3]heptyl, thiazaspiro[3.3]heptyl, thiazaspiro[4.3]octyl, azaspiro[5.5]undecyl, or one of the further homologous scaffolds such as spiro[3.4]-, spiro[4.4]-, spiro[2.4]-, spiro[2.5]-, spiro[2.6]-, spiro[3.5]-, spiro[3.6]-, spiro[4.5]- and spiro[4.6]-.

The term "6- to 10-membered azaspirocycloalkyl" means a bicyclic, saturated heterocyde with 6, 7, 8, 9 or 10 ring atoms in total, in which the two rings share one common ring carbon atom and which is bound to the rest of the molecule via the nitrogen atom and which azaspirocycloalkyl may contain up to 2 further heteroatoms selected from nitrogen and oxygen.

Said azaspirocycloalkyl is for example, azaspiro[2.3]hexyl, azaspiro[3.3]heptyl, oxaazaspiro[3.3]heptyl, oxazaspiro[5.3]nonyl, oxazaspiro[4.3]octyl, azaspiro[4,5]decyl, oxazaspiro[5.5]undecyl, diazaspiro[3.3]heptyl, triazaspiro[3.4]octyl or one of the further homologous scaffolds such as spiro[3.4]-, spiro[4.4]-, spiro[2.4]-, spiro[2.5]-, spiro[2.6]-, spiro[3.5]-, spiro[3.6]- and spiro[4.5]-, whereby these azaspirocycloalkyl groups are always bound via the nitrogen atom to the rest of the molecule. Of these groups preference is given to 2-oxa-6-azaspiro[3.3]hept-6-yl and 2,5,7- triazaspiro[3.4]octan-2-yl.

The term "fused heterocycloalkyi" means a bicyclic, saturated heterocyde with 6, 7, 8, 9 or 10 ring atoms in total, in which the two rings share two adjacent ring atoms, which "fused heterocycloalkyi" contains one or two identical or different ring heteroatoms from the series: N, O, S; it being possible for said fused heterocycloalkyi group to be attached to the rest of the molecule via any one of the carbon atoms or, if present, a nitrogen atom. Said fused heterocycloalkyl group is, for example, azabicyclo[3.3.0]octyl, azabicyclo[4.3.0]nonyl, diazabicyclo[4.3.0]nonyl, oxazabicyclo[4.3.0]nonyl, thiazabicyclo[4.3.0]nonyl or azabicyclo[4.4.0]decyl.

The term "bridged heterocycloalkyl" means a bicyclic, saturated heterocycle with 7, 8, 9 or 10 ring atoms in total, in which the two rings share two common ring atoms which are not adjacent, which "bridged heterocycloalkyl" contains one or two identical or different ring heteroatoms from the series: N, O, S; it being possible for said bridged heterocycloalkyl group to be attached to the rest of the molecule via any one of the carbon atoms, except the spiro carbon atom, or, if present, a nitrogen atom.

Said bridged heterocycloalkyl group is, for example, azabicyclo[2.2.1 ]heptyl, oxazabicyclo[2.2.1 ]heptyl, thiazabicyclo[2.2.1]heptyl, diazabicyclo[2.2.1]heptyl, azabicyclo- [2.2.2]octyl, diazabicyclo[2.2.2]octyl, oxazabicyclo[2.2.2]octyl, thiazabicyclo[2.2.2]octyl, azabi- cyclo[3.2.1]octyl, diazabicyclo[3.2.1]octyl, oxazabicyclo[3.2.1]octyl, thiazabicyclo[3.2.1 ]octyl, azabicyclo[3.3.1 ]nonyl, diazabicyclo[3.3.1]nonyl, oxazabicyclo[3.3.1]nonyl, thiazabicyclo[3.3.1 ]nonyl, azabicyclo[4.2.1 ]nonyl, diazabicyclo[4.2.1]nonyl, oxazabicyclo[4.2.1 ]nonyl, thiazabicyclo[4.2.1 ]nonyl, azabicyclo[3.3.2]decyl, diazabicyclo[3.3.2]decyl, oxazabicyclo[3.3.2]decyl, thiazabicyclo[3.3.2]decyl or azabicyclo[4.2.2]decyl.

The term "heteroaryl" means a monovalent, monocyclic, bicyclic or tricyclic aromatic ring having 5, 6, 8, 9, 10, 1 1 , 12, 13 or 14 ring atoms (a "5- to 14-membered heteroaryl" group), particularly 5, 6, 9 or 10 ring atoms, which contains at least one ring heteroatom and optionally one, two or three further ring heteroatoms from the series: N, O and/or S, and which is bound via a ring carbon atom or optionally via a ring nitrogen atom (if allowed by valency).

Said heteroaryl group can be a 5-membered heteroaryl group, such as, for example, thienyl, furanyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isoxazolyl, isothiazolyl, oxadiazolyl, triazolyl, thiadiazolyl or tetrazolyl; or a 6-membered heteroaryl group, such as, for example, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl or triazinyl; or a tricyclic heteroaryl group, such as, for example, carbazolyl, acridinyl or phenazinyl; a 8-membered heteroaryl group, such as for example 6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazolyl or a 9-membered heteroaryl group, such as, for example, benzofuranyl, benzothienyl, benzoxazolyl, benzisoxazolyl, benzimidazolyl, benzothiazolyl, benzothiadiazolyl, benzotriazolyl, indazolyl, indolyl, isoindolyl, indolizinyl, thienopyridinyl, 1 H-pyrrolo[2,3-b]pyridinyl or purinyl; or a 10-membered heteroaryl group, such as, for example, quinolinyl, quinazolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinoxalinyl or pteridinyl. In general, and unless otherwise mentioned, the heteroaryl or heteroarylene groups include all possible isomeric forms thereof, e.g.: tautomers and positional isomers with respect to the point of linkage to the rest of the molecule. Thus, for some illustrative non-restricting examples, the term pyridinyl includes pyridin-2-yl, pyridin-3-yl and pyridin-4-yl; or the term thienyl includes thien-2-yl and thien-3-yl.

A C4 to C12 carbocyclic, heterocyclic, optionally bicyclic, optionally aromatic or optionally heteroaromatic ring system, wherein in a bicyclic, aromatic or heteroaromatic ring system one or two double bonds can be hydrogenated is selected from the group of the substituents phenyl, naphthyl, 1 ,2,3,4-tetrahydronaphthyl, 1 ,3-benzodioxolyl, quinolinyl, isoquinolinyl, 2,3- dihydro-1 ,4-benzodioxinyl, imidazo[1 ,2-a]pyridinyl, furanyl, thienyl, pyridinyl, 21-1-1 ,4- benzoxazinyl-3(4H)-one, 2,1 ,3-benzothiadiazolyl, 1 -benzofuranyl, 1 -benzothienyl, 1 H- indazolyl, 1 H-indolyl, 1 H-benzimidazolyl, 1 ,3-benzothiazolyl, thieno[2,3-b]pyridinyl, thieno[2,3-c]pyridinyl, thieno[3,2-c]pyridinyl, pyrimidinyl, 1 H-pyrazolyl, 6,7-dihydro-5H- pyrrolo[1 ,2-a]imidazolyl, 1 ,2-oxazolyl, 1 H-imidazolyl, 1 ,3,4-oxadiazolyl, 1 H-tetrazolyl, 1 H- pyrrolyl, 1 H-pyrrolo[2,3-b]pyridinyl or 3,4-dihydro-2H-1 ,4-benzoxazinyl.

Particularly, the heteroaryl group is a quinolinyl, isoquinolinyl, imidazo[1 ,2-a]pyridinyl, furanyl, thienyl, pyridinyl, 2,1 ,3-benzothiadiazolyl, 1 -benzofuranyl, 1 -benzothiophenyl, 1 H-indazolyl, 1 H-indolyl, 1 H-benzimidazolyl, 1 ,3-benzothiazolyl, thieno[2,3-b]pyridinyl, thieno[2,3- c]pyridinyl, thieno[3,2-c]pyridinyl, pyrimidinyl, 1 H-pyrazolyl, 6,7-dihydro-5H-pyrrolo[1 ,2- a]imidazolyl, 1 ,2-oxazolyl, 1 H-imidazolyl, 1 ,3,4-oxadiazolyl, 1 H-tetrazolyl, 1 H-pyrrolyl, 1 H- pyrrolo[2,3-b]pyridinyl or 3, 4-dihydro-2H-1 ,4-benzoxazinyl group.

In composite substituents such as Ci-C6-haloalkyl, Ci-C4-haloalkyl, Ci-C6-haloalkoxy, -(CH2)- heteroaryl, heteroaryloxy, -0-(CH2) _x -heteroaryl, -0-(CH2) _z -heteroaryl, 0-(CH2)-4- to 7- membered heterocycloalkyl, bicyclic heteroaryl, Ci-C6-hydroxyalkyl, -0-(CH2)x-C3-Cs- cycloalkyl, 0-(CH2) _x -phenyl, -0-(CH2) _x -heterocyclyl and Cs-Cs-cycloalkyloxy the definition of the residue to which the further substituent is attached is the same as given for the residues which do not bear a further substituent, e.g. in Ci-C6-haloalkyl the Ci-C6-alkyl has the same meanings as given for the Ci-C6-alkyl earlier.

The term "Ο-ι-Οβ", as used in the present text, e.g. in the context of the definition of "Ci-C6-alkyl", "Ci-C6-haloalkyl", "Ci-C6-hydroxyalkyl", "Ci-C6-alkoxy" or "Ci-C6-haloalkoxy" means an alkyl group having a finite number of carbon atoms of 1 to 6, i.e. 1 , 2, 3, 4, 5 or 6 carbon atoms.

Further, as used herein, the term "C3-C8", as used in the present text, e.g. in the context of the definition of "Cs-Cs-cycloalkyl", means a cycloalkyl group having a finite number of carbon atoms of 3 to 8, i.e. 3, 4, 5, 6, 7 or 8 carbon atoms. When a range of values is given, said range encompasses each value and sub-range within said range.

For example:

"C1-C6" encompasses Ci , C2, C3, C ₄ , C5, C6, C1-C6, C1-C5, C1-C4, C1-C3, C1-C2, C2-C6, C2-C5, C2-C4, C2-C3, C3-C6, C3-C5, C3-C4, C4-C6, C4-C5, and C5-C6;

"C2-C6" encompasses C2, C3, C ₄ , C5, C6, C2-C6, C2-C5, C2-C4, C2-C3, C3-C6, C3-C5, C3-C4, C4-C6, C4-C5, and C5-C6;

"C3-C10" encompasses C3, C ₄ , C5, C6, C7, Ce, Cg, C10, C3-C10, C3-Cg, C3-C8, C3-C7,

C3-C6, C3-C5, C3-C4, C4-C10, C ₄ -Cg, C4-C8, C4-C7, C4-C6, C4-C5, C5-C10, Cs-Cg, Cs-Ce,

C5-C7, C5-C6, C6-C10, C6-Cg, C6-Ce, C6-C7, C7-C10, C7-Cg, C7-C8, Ce-Cio, Ce-Cg and

"C3-C8" encompasses C3, C ₄ , C5, C6, C7, Ce, C3-C8, C3-C7, C3-C6, C3-C5, C3-C4, C4-C8, C4-C7, C4-C6, C4-C5, Cs-Ce, C5-C7, C5-C6, C6-Ce, C6-C7 and C7-C8;

"C3-C6" encompasses C3, C ₄ , C5, C6, C3-C6, C3-C5, C3-C4, C4-C6, C4-C5, and C5-C6;

"C4-C8" encompasses C ₄ , C5, C6, C7, Ce, C4-C8, C4-C7, C4-C6, C4-C5, Cs-Ce, C5-C7, C5-C6, C6-Ce, C6-C7 and C7-C8;

"C4-C7" encompasses C ₄ , C5, C6, C7, C4-C7, C4-C6, C4-C5, C5-C7, C5-C6 and C6-C7;

"C4-C6" encompasses C ₄ , C5, C6, C4-C6, C4-C5 and C5-C6;

"C5-C10" encompasses C5, C6, C7, Ce, Cg, C10, C5-C10, Cs-Cg, C5-C8, C5-C7, C5-C6, C6-C10, Ce- Cg, C6-Ce, C6-C7, C7-C10, C7-Cg, C7-C8, Ce-Cio, Ce-Cg and Cg-Cio!

"C6-C10" encompasses C6, C7, C8, Cg, C10, C6-C10, C6-Cg, C6-Ce, C6-C7, C7-C10, C7-Cg, C7-C8, Ce-Cio, Ce-Cg and Cg-Cio-

As used herein, the term "leaving group" means an atom or a group of atoms that is displaced in a chemical reaction as stable species taking with it the bonding electrons. In particular, such a leaving group is selected from the group comprising: halide, in particular fluoride, chloride, bromide or iodide, (methylsulfonyl)oxy, [(trifluoromethyl)sulfonyl]oxy, [(nonafluorobutyl)sulfonyl]oxy, (phenylsulfonyl)oxy, [(4-methylphenyl)sulfonyl]oxy, [(4-bromophenyl)sulfonyl]oxy, [(4-nitrophenyl)sulfonyl]oxy, [(2-nitrophenyl)sulfonyl]oxy, [(4-isopropylphenyl)sulfonyl]oxy, [(2,4,6-triisopropylphenyl)sulfonyl]oxy, [(2,4,6-trimethylphenyl)sulfonyl]oxy, [(4-ie f-butylphenyl)sulfonyl]oxy and

[(4-methoxyphenyl)sulfonyl]oxy. It is possible for the compounds of general formula (I) to exist as isotopic variants. The invention therefore includes one or more isotopic variant(s) of the compounds of general formula (I), particularly deuterium-containing compounds of general formula (I).

The term "Isotopic variant" of a compound or a reagent is defined as a compound exhibiting an unnatural proportion of one or more of the isotopes that constitute such a compound.

The term "Isotopic variant of the compound of general formula (I)" is defined as a compound of general formula (I) exhibiting an unnatural proportion of one or more of the isotopes that constitute such a compound.

The expression "unnatural proportion" means a proportion of such isotope which is higher than its natural abundance. The natural abundances of isotopes to be applied in this context are described in "Isotopic Compositions of the Elements 1997", Pure Appl. Chem., 70(1 ), 217-235, 1998.

Examples of such isotopes include stable and radioactive isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorus, sulfur, fluorine, chlorine, bromine and iodine, such as ² H (deuterium), ³ H (tritium), ¹¹ C, ¹³ C, ¹⁴ C, ¹⁵ N, ¹⁷ 0, ¹⁸ 0, ³² P, ³³ P, ³³ S, ³⁴ S, ³⁵ S, ³⁶ S, ¹⁸ F, ³⁶ CI, ⁸² Br, ¹²³ l, ¹²⁴ l, ¹²⁵ l, ¹²⁹ l and ¹³¹ 1, respectively.

With respect to the treatment and/or prophylaxis of the disorders specified herein the isotopic variant(s) of the compounds of general formula (I) preferably contain deuterium ("deuterium- containing compounds of general formula (I)"). Isotopic variants of the compounds of general formula (I) in which one or more radioactive isotopes, such as ³ H or ¹⁴ C, are incorporated are useful e.g. in drug and/or substrate tissue distribution studies. These isotopes are particularly preferred for the ease of their incorporation and detectability. Positron emitting isotopes such as ¹⁸ F or ¹¹ C may be incorporated into a compound of general formula (I). These isotopic variants of the compounds of general formula (I) are useful for in vivo imaging applications. Deuterium-containing and ¹³ C-containing compounds of general formula (I) can be used in mass spectrometry analyses in the context of preclinical or clinical studies.

Isotopic variants of the compounds of general formula (I) can generally be prepared by methods known to a person skilled in the art, such as those described in the schemes and/or examples herein, by substituting a reagent for an isotopic variant of said reagent, preferably for a deuterium-containing reagent. Depending on the desired sites of deuteration, in some cases deuterium from D2O can be incorporated either directly into the compounds or into reagents that are useful for synthesizing such compounds. Deuterium gas is also a useful reagent for incorporating deuterium into molecules. Catalytic deuteration of olefinic bonds and acetylenic bonds is a rapid route for incorporation of deuterium. Metal catalysts (i.e. Pd, Pt, and Rh) in the presence of deuterium gas can be used to directly exchange deuterium for hydrogen in functional groups containing hydrocarbons. A variety of deuterated reagents and synthetic building blocks are commercially available from companies such as for example C/D/N Isotopes, Quebec, Canada; Cambridge Isotope Laboratories Inc., Andover, MA, USA; and CombiPhos Catalysts, Inc., Princeton, NJ, USA.

The term "deuterium-containing compound of general formula (I)" is defined as a compound of general formula (I), in which one or more hydrogen atom(s) is/are replaced by one or more deuterium atom(s) and in which the abundance of deuterium at each deuterated position of the compound of general formula (I) is higher than the natural abundance of deuterium, which is about 0.015%. Particularly, in a deuterium-containing compound of general formula (I) the abundance of deuterium at each deuterated position of the compound of general formula (I) is higher than 10%, 20%, 30%, 40%, 50%, 60%, 70% or 80%, preferably higher than 90%, 95%, 96% or 97%, even more preferably higher than 98% or 99% at said position(s). It is understood that the abundance of deuterium at each deuterated position is independent of the abundance of deuterium at other deuterated position(s).

The selective incorporation of one or more deuterium atom(s) into a compound of general formula (I) may alter the physicochemical properties (such as for example acidity [C. L. Perrin, et al., J. Am. Chem. Soc, 2007, 129, 4490], basicity [C. L. Perrin et al., J. Am. Chem. Soc, 2005, 127, 9641 ], lipophilicity [B. Testa et al., Int. J. Pharm., 1984, 19(3), 271]) and/or the metabolic profile of the molecule and may result in changes in the ratio of parent compound to metabolites or in the amounts of metabolites formed. Such changes may result in certain therapeutic advantages and hence may be preferred in some circumstances. Reduced rates of metabolism and metabolic switching, where the ratio of metabolites is changed, have been reported (A. E. Mutlib et al., Toxicol. Appl. Pharmacol., 2000, 169, 102). These changes in the exposure to parent drug and metabolites can have important consequences with respect to the pharmacodynamics, tolerability and efficacy of a deuterium-containing compound of general formula (I). In some cases deuterium substitution reduces or eliminates the formation of an undesired or toxic metabolite and enhances the formation of a desired metabolite (e.g. Nevirapine: A. M. Sharma et al., Chem. Res. Toxicol., 2013, 26, 410; Efavirenz: A. E. Mutlib et al., Toxicol. Appl. Pharmacol., 2000, 169, 102). In other cases the major effect of deuteration is to reduce the rate of systemic clearance. As a result, the biological half-life of the compound is increased. The potential clinical benefits would include the ability to maintain similar systemic exposure with decreased peak levels and increased trough levels. This could result in lower side effects and enhanced efficacy, depending on the particular compound's pharmacokinetic/ pharmacodynamic relationship. ML-337 (C. J. Wenthur et al., J. Med. Chem., 2013, 56, 5208) and Odanacatib (K. Kassahun et al., WO2012/1 12363) are examples for this deuterium effect. Still other cases have been reported in which reduced rates of metabolism result in an increase in exposure of the drug without changing the rate of systemic clearance (e.g. Rofecoxib: F. Schneider et al., Arzneim. Forsch. / Drug. Res., 2006, 56, 295; Telaprevir: F. Maltais et al., J. Med. Chem., 2009, 52, 7993). Deuterated drugs showing this effect may have reduced dosing requirements (e.g. lower number of doses or lower dosage to achieve the desired effect) and/or may produce lower metabolite loads.

A compound of general formula (I) may have multiple potential sites of attack for metabolism. To optimize the above-described effects on physicochemical properties and metabolic profile, deuterium-containing compounds of general formula (I) having a certain pattern of one or more deuterium-hydrogen exchange(s) can be selected. Particularly, the deuterium atom(s) of deuterium-containing compound(s) of general formula (I) is/are attached to a carbon atom and/or is/are located at those positions of the compound of general formula (I), which are sites of attack for metabolizing enzymes such as e.g. cytochrome P450.

In another embodiment the present invention concerns a deuterium-containing compound of general formula (I), in which one, two or three of the hydrogen atom(s) in either one or both of the methyl groups shown in general formula (I) is/are replaced with a deuterium atom. Also the hydrogen atom on the carbon atom between the nitrogen atom and the group A1 can be replaced with a deuterium atom either as the single replacement of a hydrogen by a deuterium or in addition to the beforementioned replacements in either one or both of the methyl groups shown in general formula (I).

Where the plural form of the word compounds, salts, polymorphs, hydrates, solvates and the like, is used herein, this is taken to mean also a single compound, salt, polymorph, isomer, hydrate, solvate or the like.

By "stable compound' or "stable structure" is meant a compound that is sufficiently robust to survive isolation to a useful degree of purity from a reaction mixture, and formulation into an efficacious therapeutic agent.

The compounds of the present invention contain at least one or optionally even more asymmetric centres, depending upon the location and nature of the various substituents desired. It is possible that one or more asymmetric carbon atoms are present in the (R) or (S) configuration, which can result in racemic mixtures in the case of a single asymmetric centre, and in diastereomeric mixtures in the case of multiple asymmetric centres. In certain instances, it is possible that asymmetry also be present due to restricted rotation about a given bond, for example, the central bond adjoining two substituted aromatic rings of the specified compounds.

Preferred isomers are those which produce the more desirable biological activity. Separated, pure or partially purified isomers and stereoisomers or racemic or diastereomeric mixtures of the compounds of the present invention are also included within the scope of the present invention. The purification and the separation of such materials can be accomplished by standard techniques known in the art.

The optical isomers can be obtained by resolution of the racemic mixtures according to conventional processes, for example, by the formation of diastereoisomeric salts using an optically active acid or base or formation of covalent diastereomers. Examples of appropriate acids are tartaric, diacetyltartaric, ditoluoyltartaric and camphorsulfonic acid. Mixtures of diastereoisomers can be separated into their individual diastereomers on the basis of their physical and/or chemical differences by methods known in the art, for example, by chromatography or fractional crystallisation. The optically active bases or acids are then liberated from the separated diastereomeric salts. A different process for separation of optical isomers involves the use of chiral chromatography (e.g., HPLC columns using a chiral phase), with or without conventional derivatisation, optimally chosen to maximise the separation of the enantiomers. Suitable HPLC columns using a chiral phase are commercially available, such as those manufactured by Daicel, e.g., Chiracel OD and Chiracel OJ, for example, among many others, which are all routinely selectable. Enzymatic separations, with or without derivatisation, are also useful. The optically active compounds of the present invention can likewise be obtained by chiral syntheses utilizing optically active starting materials.

In order to distinguish different types of isomers from each other reference is made to lUPAC Rules Section E (Pure Appl Chem 45, 1 1 -30, 1976).

The present invention includes all possible stereoisomers of the compounds of the present invention as single stereoisomers, or as any mixture of said stereoisomers, e.g. (R)- or (S)- isomers, in any ratio. Isolation of a single stereoisomer, e.g. a single enantiomer or a single diastereomer, of a compound of the present invention is achieved by any suitable state of the art method, such as chromatography, especially chiral chromatography, for example.

Further, it is possible for the compounds of the present invention to exist as tautomers. For example, any compound of the present invention which contains an imidazopyridine moiety as a heteroaryl group for example can exist as a 1 H tautomer, or a 3H tautomer, or even a mixture in any amount of the two tautomers, namely :

1 H tautomer 3H tautomer The present invention includes all possible tautomers of the compounds of the present invention as single tautomers, or as any mixture of said tautomers, in any ratio.

Further, the compounds of the present invention can exist as N-oxides, which are defined in that at least one nitrogen of the compounds of the present invention is oxidised. The present invention includes all such possible N-oxides.

The present invention also covers useful forms of the compounds of the present invention, such as metabolites, hydrates, solvates, prodrugs, salts, in particular pharmaceutically acceptable salts, and/or co-precipitates.

The compounds of the present invention can exist as a hydrate, or as a solvate, wherein the compounds of the present invention contain polar solvents, in particular water, methanol or ethanol for example, as structural element of the crystal lattice of the compounds. It is possible for the amount of polar solvents, in particular water, to exist in a stoichiometric or non-stoichiometric ratio. In the case of stoichiometric solvates, e.g. a hydrate, hemi-, (semi-), mono-, sesqui-, di-, tri-, tetra-, penta- etc. solvates or hydrates, respectively, are possible. The present invention includes all such hydrates or solvates.

Further, it is possible for the compounds of the present invention to exist in free form, e.g. as a free base, or as a free acid, or as a zwitterion, or to exist in the form of a salt. Said salt may be any salt, either an organic or inorganic addition salt, particularly any pharmaceutically acceptable organic or inorganic addition salt, which is customarily used in pharmacy, or which is used, for example, for isolating or purifying the compounds of the present invention.

The term "pharmaceutically acceptable salt" refers to an inorganic or organic acid addition salt of a compound of the present invention. For example, see S. M. Berge, et al. "Pharmaceutical Salts," J. Pharm. Sci. 1977, 66, 1-19.

A suitable pharmaceutically acceptable salt of the compounds of the present invention may be, for example, an acid-addition salt of a compound of the present invention bearing a nitrogen atom, in a chain or in a ring, for example, which is sufficiently basic, such as an acid-addition salt with an inorganic acid, or "mineral acid", such as hydrochloric, hydrobromic, hydroiodic, sulfuric, sulfamic, bisulfuric, phosphoric, or nitric acid, for example, or with an organic acid, such as formic, acetic, acetoacetic, pyruvic, trifluoroacetic, propionic, butyric, hexanoic, heptanoic, undecanoic, lauric, benzoic, salicylic, 2-(4-hydroxybenzoyl)-benzoic, camphoric, cinnamic, cyclopentanepropionic, digluconic, 3-hydroxy-2-naphthoic, nicotinic, pamoic, pectinic, 3-phenylpropionic, pivalic, 2-hydroxyethanesulfonic, itaconic, trifluoromethanesulfonic, dodecylsulfuric, ethanesulfonic, benzenesulfonic, para- toluenesulfonic, methanesulfonic, 2-naphthalenesulfonic, naphthalinedisulfonic, camphorsulfonic acid, citric, tartaric, stearic, lactic, oxalic, malonic, succinic, malic, adipic, alginic, maleic, fumaric, D-gluconic, mandelic, ascorbic, glucoheptanoic, glycerophosphoric, aspartic, sulfosalicylic, or thiocyanic acid, for example.

Further, another suitably pharmaceutically acceptable salt of a compound of the present invention which is sufficiently acidic, is an alkali metal salt, for example a sodium or potassium salt, an alkaline earth metal salt, for example a calcium, magnesium or strontium salt, or an aluminium or a zinc salt, or an ammonium salt derived from ammonia or from an organic primary, secondary or tertiary amine having 1 to 20 carbon atoms, such as ethylamine, diethylamine, triethylamine, ethyldiisopropylamine, monoethanolamine, diethanolamine, triethanolamine, dicyclohexylamine, dimethylaminoethanol, diethylaminoethanol, tris(hydroxymethyl)aminomethane, procaine, dibenzylamine, N- methylmorpholine, arginine, lysine, 1 ,2-ethylenediamine, /V-methylpiperidine, /V-methyl- glucamine, Λ/,/V-dimethyl-glucamine, /V-ethyl-glucamine, 1 ,6-hexanediamine, glucosamine, sarcosine, serinol, 2-amino-1 ,3-propanediol, 3-amino-1 ,2-propanediol, 4-amino-1 ,2,3- butanetriol, or a salt with a quarternary ammonium ion having 1 to 20 carbon atoms, such as tetramethylammonium, tetraethylammonium, tetra(n-propyl)ammonium, tetra(n- butyl)ammonium, /V-benzyl-/V,/V,/V-trimethylammonium, choline or benzalkonium.

Those skilled in the art will further recognise that it is possible for acid addition salts of the claimed compounds to be prepared by reaction of the compounds with the appropriate inorganic or organic acid via any of a number of known methods. Alternatively, alkali and alkaline earth metal salts of acidic compounds of the present invention are prepared by reacting the compounds of the present invention with the appropriate base via a variety of known methods.

The present invention includes all possible salts of the compounds of the present invention as single salts, or as any mixture of said salts, in any ratio.

In the present text, in particular in the Experimental Section, for the synthesis of intermediates and of examples of the present invention, when a compound is mentioned as a salt form with the corresponding base or acid, the exact stoichiometric composition of said salt form, as obtained by the respective preparation and/or purification process, is, in most cases, unknown.

Unless specified otherwise, suffixes to chemical names or structural formulae relating to salts, such as "hydrochloride", "trifluoroacetate", "sodium salt", or "x HCI", "x CF3COOH", "x Na ⁺ ", for example, mean a salt form, the stoichiometry of which salt form not being specified.

This applies analogously to cases in which synthesis intermediates or example compounds or salts thereof have been obtained, by the preparation and/or purification processes described, as solvates, such as hydrates, with (if defined) unknown stoichiometric composition.

As used herein, the term "in vivo hydrolysable ester" means an in vivo hydrolysable ester of a compound of the present invention containing a carboxy or hydroxy group, for example, a pharmaceutically acceptable ester which is hydrolysed in the human or animal body to produce the parent acid or alcohol. Suitable pharmaceutically acceptable esters for carboxy include for example alkyl, cycloalkyl and optionally substituted phenylalkyl, in particular benzyl esters, C1-C6 alkoxymethyl esters, e.g. methoxymethyl, C1-C6 alkanoyloxymethyl esters, e.g. pivaloyloxymethyl, phthalidyl esters, C3-C8 cycloalkoxy-carbonyloxy-Ci-C6 alkyl esters, e.g. 1 -cyclohexylcarbonyloxyethyl ; 1 ,3-dioxolen-2-onylmethyl esters, e.g. 5-methyl- 1 ,3-dioxolen-2-onylmethyl ; and Ci-C6-alkoxycarbonyloxyethyl esters, e.g. 1 - methoxycarbonyloxyethyl, it being possible for said esters to be formed at any carboxy group in the compounds of the present invention.

An in vivo hydrolysable ester of a compound of the present invention containing a hydroxy group includes inorganic esters such as phosphate esters and [alpha]-acyloxyalkyl ethers and related compounds which as a result of the in vivo hydrolysis of the ester breakdown to give the parent hydroxy group. Examples of [alpha]-acyloxyalkyl ethers include acetoxymethoxy and 2,2-dimethylpropionyloxymethoxy. A selection of in vivo hydrolysable ester forming groups for hydroxy include alkanoyl, benzoyl, phenylacetyl and substituted benzoyl and phenylacetyl, alkoxycarbonyl (to give alkyl carbonate esters), dialkylcarbamoyl and N-(dialkylaminoethyl)-N-alkylcarbamoyl (to give carbamates), dialkylaminoacetyl and carboxyacetyl. The present invention covers all such esters.

Furthermore, the present invention includes all possible crystalline forms, or polymorphs, of the compounds of the present invention, either as single polymorph, or as a mixture of more than one polymorph, in any ratio.

Moreover, the present invention also includes prodrugs of the compounds according to the invention. The term "prodrugs" here designates compounds which themselves can be biologically active or inactive, but are converted (for example metabolically or hydrolytically) into compounds according to the invention during their residence time in the body.

In accordance with a second embodiment of the first aspect, the present invention covers compounds of general formula (I), supra, in which:

R ¹ stands for a substituent independently selected from: a hydrogen atom, a halogen atom, a hydroxy, nitro, Ci-C6-alkylsulfanyl or an amino group -NR ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci- Ce-alkyl,

a substituent selected from: a Ci-C6-alkyl, Ci-C6-alkoxy-, Cs-Cs-cycloalkyl, 4- to 7- membered heterocycloalkyl, heteroaryl,

-C(=0)OH, -C(=0)OR ^c , and wherein R ^c stands for Ci-C ₆ -alkyl or C ₃ -C ₈ -cycloalkyl,

-N=S(=0)(R ^d )R ^e , and wherein R ^d and R ^e are selected independently from C1-C6- alkyl,

-NH-C(0)-Ci-C ₆ -alkyl, -NH-C(0)-N R ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-Ce-alkyl, -N H-(CH ₂ )k-N H-C(0)-Ci-C6- alkyl, wherein k is 2, -N H-(CH2)i-R , wherein

I is 0 or 2 and R stands for a 4- to 7-membered heterocycloalkyl or C1-C6- alkylsulfonyl,

whereby in all foregoing definitions the Ci-C6-alkyl-,Ci-C6-alkoxy-, the 4- to 7- membered heterocycloalkyl and the heteroaryl can be optionally substituted, one or two or three times, identically or differently, with:

a group selected from hydroxy, oxo (=0), Ci-C6-alkyl, Cs-Cs-cycloalkyl, 4- to 7-membered heterocycloalkyl, Ci-C6-alkoxy, Ci-C6-alkylsulfonyl, benzyl, -(CH2)-heteroaryl- or an amino group -N R ^a R ^b , wherein R ^a and R ^b are selected independently from Ci-C6-alkyl, or a substituent -0-(CH2) _z -phenyl, whereby z is 0, 1 or 2, or and wherein x is 1 , 2 or 3,

A1 stands for

a C ₄ to Ci2 carbocyclic, heterocyclic, optionally bicyclic, optionally aromatic or optionally heteroaromatic ring system, wherein in a bicyclic aromatic or

heteroaromatic ring system one or two double bonds can be hydrogenated,

R ² stands for

a hydrogen atom, a hydroxy group, oxo (=0), a halogen atom, a cyano group, a substituent selected from: a Ci-C6-alkyl, Ci-C6-alkoxy-, C2-C6-alkenyl, C3-C8- cycloalkyl, 4- to 7-membered heterocycloalkyi, -0-CH2-4- to 7-membered heterocycloalkyi, Ci-C6-alkylsulfonyl,

-C(0)-NR ^a R ^b , wherein R ^a and R ^b are both hydrogen atoms, -C(0)-0-R ⁹ , wherein R ⁹ is a Ci-C6-alkyl, or-CH2-N R ^a R ^b , wherein R ^a and R ^b are both hydrogen atoms, and w is 1 or 2, and wherein

A2(R ³ ) _y stands either for a hydrogen atom or

A2 has the same meanings as the substituent A1 and

R ³ stands for

a hydrogen atom, a halogen atom, a hydroxy, oxo, cyano, nitro group,

a substituent selected from a Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C3-C8- cycloalkyl, C4-C8-cycloalkenyl, Cz-Cs-cycloalkynyl, 4- to 7-membered

heterocycloalkyi, 5- to 10-membered heterocycloalkenyl, phenyl, heteroaryl, C1-C6- haloalkyl,

which substituent is optionally substituted, one, two or three times, identically or differently, with a substituent selected from :

a halogen atom, or a group selected from hydroxy, oxo (=0), cyano, C1-C6- alkyl, Ci-C ₆ -alkoxy, Ci-C ₆ -haloalkyl, phenyl, -C(0)NR'R ^j , wherein

R' and R ^j are selected independently from a hydrogen atom or a C1-C6- alkyl, heteroaryl,

or with amino -NR ^k R', wherein R ^k and R' are selected independently from

a hydrogen atom, a substituent selected from a Ci-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, Cs-Cs-cycloalkyl, Ci-C6-alkylsulfonyl, phenyl, heteroaryl, 4- to 7-membered heterocycloalkyi, which are optionally substituted one, two or three times, identically or differently, with a substituent selected from Ci-C6-haloalkyl, hydroxyl, oxo (=0), phenyl, cyano , Ci- C6-alkoxy, heteroaryl, wherein

the heteroaryl can optionally be substituted with a methyl group, or

-CH ₂ -C(0)-R ^m , wherein R ^m is a bicyclic heteroaryl, which can be partially hydrogenated, a Ci- C6-alkoxy or a group -NR ⁿ R°, in which

R ⁿ and R° are selected independently from hydrogen, Ci-C6-alkyl, phenyl, wherein the Ci-C6-alkyl can optionally be substituted with a Ci-C6-alkoxy or a phenyl, or

-NR ⁿ R° stands for a 4- to 7-membered azacycloalkyl, bound via the nitrogen atom to the rest of the molecule and which optionally contains one more heteroatom selected from nitrogen and oxygen;

-C(=0)R ^p , wherein R ^p is selected from

the group of a C1 -C6-alkoxy, a C1 -C6-alkyl, which is optionally substituted, one, two or three times, identically or differently, with a substituent selected from hydroxyl or Ci-C6-alkoxy,

a mono- or bicyclic heteroaryl, a 4- to 7-membered heterocycloalkyl or R ^p is a group -CH2-NR ^q R ^r ; wherein R ^q and R ^r are selected independently from hydrogen, phenyl or a Ci-C6-alkyl, which may optionally be substituted up to threefold with fluorine,

-NR ^s R' is

a 4- to 7-membered azacycloalkyl, bound via the nitrogen atom to the rest of the molecule, or a 6- to 10-membered azaspirocycloalkyl, which both may contain up to 2 further heteroatoms selected from nitrogen and oxygen and which both are optionally substituted one, two or three times, identically or differently, with a substituent selected from : hydroxy, oxo (=0), C1-C6- alkyl, d-Ce-hydroxyalkyl, -C(=0)OR ^u , wherein R ^u is a Ci-C ₆ -alkyl, halogen, -N(Ci-C ₆ -alkyl) ₂ , -CH ₂ -N(Ci-C ₆ -alkyl) ₂ , -C(0)NR ^a R ^b , wherein R ^a and R ^b are selected independently from a hydrogen atom or a Ci-C6-alkyl,

-C(=0)R ^v , -C(=0)NH ₂ , -C(=0)N(H)R ^v , -C(=0)N(R ^v )R ^w , -C(=0)OR ^v , wherein

R ^v and R ^w represent, independently from each other, a group selected from hydrogen, Ci-C4-alkyl, Ci-C4-haloalkyl, phenyl, or a group -(CH ₂ ) ₂ -NR ^x R ^y , wherein R ^x and R ^y independently from each other stand for hydrogen, a C1-C4- alkyl or a group -(CH ₂ ) ₂ N(CH ₃ ) ₂ ;

-NH ₂ , -NHR ^Z , -N(R ^z )R ^za , -N(H)C(=0)R ^z , -N(H)C(=0)OR ^z , -N(H)S(=0) ₂ R ^z , 4- to 7- membered heterocycloalkyl, heteroaryl, heterospirocycloalkyl, fused

heterocycloalkyl, bridged heterocycloalkyl, wherein R ^z and R ^za represent, independently from each other, a group selected from Ci- C4-alkyl, Ci-C4-haloalkyl and phenyl, d-Ce-alkoxy-, Ci-C ₆ - haloalkoxy-, -0-(CH ₂ )s-C ₃ -C8-cycloalkyl, -0-(CH ₂ ) _s -phenyl, -O- (CH ₂ )s-heterocycloalkyl, -0-(CH ₂ )s-heteroaryl, s is 0, 1 , 2 or 3,

-S(=0) ₂ R ^z , -S(=0) ₂ NH ₂ , -S(=0) ₂ NHR ^z , -S(=0) ₂ N(R ^z )R ^za , wherein R ^z and R ^za represent, independently from each other, a group selected from Ci-C4-alkyl, C1-C4- haloalkyl and phenyl, wherein y is 1 , 2 or 3, and

L stands either for a bond or for -0-(CH ₂ )k, wherein k is 0, 1 , 2 or 3, or a group - CH=CH-(CH ₂ )n, wherein n is 0, 1 or 2, or a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

In accordance with a third embodiment of the first aspect, the present invention covers compounds of general formula (I), supra, in which:

R ¹ is selected from the list of the following substituents

H, *-OCH ₃ „ *-OC ₂ H ₅ , , *-CH ₂ OH, *-C(0)OH, *-C(0)OCH ₃ , -Br, *-0-

CH(CH ₃ ) ₂ ., *-0-(CH ₂ ) ₂ CH(CH ₃ ) ₂ , *-0-(CH ₂ ) ₃ C , *-0-

CH ₂ -Phenyl, *. N=S (0)(CH ₃ ) ₂ , *-CH ₃ , , *-NH(CH ₃ ), *-N(CH ₃ ) ₂ , *-NH ₂ ,

O

*-NH-(CH ₂ )2-NH-C(0)-CH _3! . *-NH-(CH ₂ ) ₂ -morpholino, *-NH-C(0)-CH ₃ , *-NH-C(0)-NH-CH ₃ , *-NH-C(0)-N(CH ₃ ) ₂ , *-N0 ₂ , *-NH-S(0) ₂ -CH ₃ , *-N=S(0)(CH ₃ ) ₂ , *-OH, -0-(CH ₂ ) ₂ -S(0) ₂ -CH ₃ ,

*-fluorine,

and z is 1 or 2 and

x is 1 or 2 and wherein

A1 is selected from the group

and

R ² is selected from the group of hydrogen, hydroxy, oxo (=0), cyano, cyclopropyl, 1 , 1 - dimethylcyclopropyl,

-C(=CH ₂ )CH ₃ , -C(CH ₃ )=CHCH ₃ , -CH=CH-(CH ₂ ) ₂ CH ₃ , CH=CHCH ₃ , -CH=CH- cyclopropyl), -C(0)NH ₂ , C(0)OCH ₃ , -S(0) ₂ CH ₃ , -OCH ₃ , -CH ₂ NH ₂ , a halogen atom (F, CI; Br),and w is 1 or 2 and

A2 is selected from the group

and

R ³ is selected from the group of the following substituents

*-C(0)NH-(CH ₂ ) ₂ CH ₃

^* -C(0)-N(CH ₃ ) ₂

^* -C(0)-NH ₂

^* -C(0)-NH-(CH ₂ ) ₂ N(CH ₃ ) ₂

*-CH ₂ -C(0)-NH ₂

hydrogen

*-F, *-CI, ^* -Br

*-C≡N; ^* -CF ₃ , ^* -CH ₃ , ^* -C ₂ H ₅ , ^* -CH=CH ₂ ;

*-CH ₂ -CN; ^* -CH(CH ₃ )-NH ₂ ; ^* -CH=CH-CN;

-C(0)-OH; *-C(0)-OCH ₃ ; *-C(0)-CH ₃ ; ^* -C(CH ₃ ) ₂ -C(0)-OCH ₃ ; ^* -C(CH ₃ ) ₂ -CN; Oxo(=0); h droxy;

^* -NH ₂

^* -NH-C(0)CH ₃

*-NH-S0 ₂ -CH ₃ *- -C(0)-0-C(CH ₃ ) ₃

*-N

3) ₂

-O-CH2-CH3; *-0-(CH ₂ ) ₂ -CH ₃ ;

*-0(CH ₂ ) ₂

- o

*-OCH ₂ -Cyclopropyl; *-OCH ₃ ;

*-0(CH ₂ ) ₃ -CH ₃ ; *-OCH ₂ -P enyl; *-0-Phenyl;

*-(CH ₂ )-OH

*-(CH ₂ ) ₂ -OH

*-(CH ₂ )-0-CH ₃

*-(CH ₂ )-0-CH ₂ -CH ₃

*-CH(OH)-CH ₂ -P enyl

*-CH(OH)-CH ₂ -CH ₃

*-CH(OH)-(CH2)2-CH ₃ *-CH(OH)-(CH ₂ )3-CH ₃

*-CH(OH)-CH-(CH ₃ ) ₂

*-CH(OH)-Phenyl

*-CH(OH)-CN

*-CH(OH)-CH ₂ OH

*-CH(OH)-CF ₃

*-CH(OH)-(CH ₂ ) ₂ -Phenyl

*-CH(OH)-C≡CH ^* -CH(NH ₂ )-CH ₂ -COOH

^* -CH ₂ -NH-S0 ₂ -CH ₃

^* -CH ₂ -NH-CH ₃

^* -CH ₂ -N(CH ₃ ) ₂

*-CH ₂ -NH-C ₂ H ₅ ^* -CH(CH ₃ )-NH ₂

^* -CH ₂ -NH ₂

^* -(CH ₂ ) ₂ -NH ₂

^* -CH ₂ -NH-CH ₂ -Phenyl

^* -CH ₂ -N(C ₂ H ₅ ) ₂

^* -CH ₂ -NH-Cyclopropyl

^* -CH ₂ -NH-Cyclobutyl

^* -CH ₂ -NH-Cyclopentyl

^* -CH ₂ -NH-Pyridyl

^* -CH ₂ -NH-Phenyl

^* -CH ₂ -NH-(CH ₂ ) ₂ -OH

*-CH ₂ -N(CH ₃ )(CH ₂ ) ₂ OH ^* -CH ₂ -NH-CH ₂ -CN

^* -CH ₂ -N(CH ₃ )-CH ₂ -CN

^* -CH ₂ -N(CH ₃ )-CH ₂ -CF ₃

*-CH ₂ -N(CH ₃ )-CH ₂ -CF ₂ H

^* -CH ₂ -NH-CH ₂ -CF ₂ H

^* -CH ₂ -NH-CH ₂ -CF ₃

^* -CH ₂ -NH-(CH ₂ ) ₂ -OCH ₃ H ₃ *-CH ₂ — N N H -CH ₂ -N N-C H ₃

*-CH ₂ — N N-C(0)0-C(CH ₃ ) ₃ — CH ₂ — N O *_CH ₂ -N

^* -CH ₂ -NH-C(0)-0-C(CH ₃ ) ₃

^* -(CH ₂ ) ₂ -NH-C(0)-0-C(CH ₃ )3

^* -CH ₂ -NH-C(0)-CH ₂ -OH

^* -CH ₂ -NH-C(0)-CH ₂ -OCH ₃

^* -CH-(CH ₃ )-NH-C(0)-0-C(CH ₃ ) ₃

^* -CH ₂ -NH-C 0)-CH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH ₂

-CH ₂ -NH-CH ₂ -C(0)-N(CH ₃ ) ₂

-CH ₂ -NH-CH ₂ -C(0)-OCH ₃

-CH ₂ -NH-CH ₂ -C(0)-NHCH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH-(CH ₂ ) ₂ -0-CH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH-CH ₂ -Phenyl

*-CH ₂ -NH-CH ₂ -C(0) -N O

-CH ₂ -NH-CH ₂ -C(0)-NH-Phenyl

*-CH ₂ -NH-CH ₂ -C(0) -N r ^{Q *} -CH ₂ -NH-C(0)-CH ₂ -NH Phenyl

^* -CH ₂ -NH-C(0)-CH ₂ -NH CH ₂ -CF ₃

y is 1 or 2 and k is 1 or 2 and n is 0 or 1 and stereoisomers, tautomers, N-oxides, hydrates, solvates, and salts thereof, and mixtures of same.

In accordance with a further embodiment of the first aspect, the present invention covers the following compounds of general formula (I), supra, namely:

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(naphthalen-1 -yl)ethyl]quinazolin-4- amine

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

methyl 4-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-1 - benzothiophene-2-carboxylate

N-[1 -(1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

N-[1 -(7-fluoro-1 H-indazol-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

N-[1 -(6-fluoro-1 H-indazol-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-methyl-1 H-indazol-4- yl)ethyl]quinazolin-4-amine 6 _! 7-dimethoxy-2-methyl-N-[1 -(2-methyl-2H-indazol-7- yl)ethyl]quinazolin-4-amine

6 _! 7-dimethoxy-2-methyl-N-[1 -(2-methyl-2H-indazol-4- yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(1 -methyl-1 H-indazol-7- yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5,6,7,8-tetrahydronaphthalen-1 - yl)ethyl]quinazolin-4-amine

N-[(1 R)-1 -(4-fluorophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

6,7-dimethoxy-2-methyl-N-[1 -(3-methyl-1 H-indazol-4- yl)ethyl]quinazolin-4-amine

N-[1 -(1 ,3-benzothiazol-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin -4 amine

N-[1 -(1 -benzothiophen-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4 amine

6,7-dimethoxy-2-methyl-N-[1 -(6-methyl-1 H-indazol-4- yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(1 -methyl-1 H-indazol-4- yl)ethyl]quinazolin-4-amine

N-[1 -(5-fluoro-1 H-indazol-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazol ^' 4-amine

N-[1 -(2,3-dihydro-1 ,4-benzodioxin-6-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[1 -(1 -benzofuran-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

N-[1 -(2,3-dimethoxyphenyl)ethyl]-6,7-dimethoxy-2-methylquinazoli n-' amine

N-[1 -(2,3-dihydro-1 -benzofuran-4-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[1 -(1 ,3-benzodioxol-5-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4 amine

N-[1 -(2,3-dihydro-1 -benzofuran-5-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5,6,7,8-tetrahydronaphthalen-2- yl)ethyl]quinazolin-4-amine 6,7-dimethoxy-2-methyl-N-[1 -(2-methylimidazo[1 ,2-a]pyridin-3- yl)ethyl]quinazolin-4-amine

N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4- amine

2-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-1 - benzofuran-7-ol

6-bromo-2-methyl-N-[(1 R)-1 -phenylethyl]quinazolin-4-amine

6-{[dimethyl(oxido)-lambda6-sulfanylidene]amino}-2-methyl -N-[(1 R)-1 - phenylethyl]quinazolin-4-amine

6-bromo-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2-methylquinazolin-4-amine 6-{[dimethyl(oxido)-lambda6-sulfanylidene]amino}-N-[(1 R)-1 -(4- fluorophenyl)ethyl]-2-methylquinazolin-4-amine

6,7-dimethoxy-N-[1 -(7-methoxy-1 -benzofuran-2-yl)ethyl]-2- methylquinazolin-4-amine

6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2H-1 ,4- benzoxazin-3(4H)-one

6,7-dimethoxy-N-[1 -(6-methoxy-2-naphthyl)ethyl]-2-methylquinazolin-4- amine

N-[(1 R)-1 -(5'-amino-2'-methylbiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(pyrimidin-5- yl)phenyl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3'-(cyclopropylmethoxy)biphenyl-3-yl]ethyl}-6,7-dimethoxy- 2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(isoquinolin-5-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[(1 R)-1 -(2'-chloro-6'-fluoro-3'-methylbiphenyl-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(5-methylpyridin-3- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(pyrimidin-5-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[4-(morpholin-4-yl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[3-(morpholin-4-yl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine N-{1 -[5-(isoquinolin-5-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(5-methylpyridin-3-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(2-propoxyphenyl)thiophen-2- yl]ethyl}quinazolin-4-amine

2- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)-N,N-dimethylbenzamide

6,7-dimethoxy-2-methyl-N-{1 -[5-(1 -methyl-1 H-indol-5-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-N-[1 -{5-[2-(methoxymethyl)phenyl]thiophen-2-yl}ethyl]-2- methylquinazolin-4-amine

3- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)-N,N-dimethylbenzamide

(5'-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,2'- bithiophen-5-yl)methanol

6,7-dimethoxy-2-methyl-N-{1 -[5-(3-methylpyridin-4-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

N-{1 -[5-(1 H-indol-6-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3'-(5-methyl-1 ,3,4-oxadiazol-2- yl)biphenyl-3-yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{3-[5-(methylsulfonyl)pyridin-3- yl]phenyl}ethyl]quinazolin-4-amine

5-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)-1 ,3-dihydro-2H-indol-2-one

N-{(1 R)-1 -[3-(2,2-dimethylcyclopropyl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4'-(5-methyl-1 ,3,4-oxadiazol-2- yl)biphenyl-3-yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrrolo[2,3-b]pyridin-5- yl)phenyl]ethyl}quinazolin-4-amine

3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-3-sulfonamide

N-{(1 R)-1 -[3-(2-aminopyrimidin-5-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine N-[(1 R)-1 -{3-[(E)-2-cyclopropylethenyl]phenyl}ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[2'-(ethoxymethyl)biphenyl-3-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[(1 R)-1 -(3'-fluoro-5'-methoxybiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-N-{(1 R)-1 -[3-(5-methoxy-1 -benzofuran-2- yl)phenyl]ethyl}-2-methylquinazolin-4-amine

N-[(1 R)-1 -(2'-butoxy-6'-fluorobiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

5-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)pyridin-2-ol

2-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-4-yl)-2-methylpropanenitrile

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylthiophen-2-yl)ethyl]quinazolin-' amine

N-[(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-3-yl)methyl]methanesulfonamide

N-[(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-4-yl)methyl]methanesulfonamide

3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N- propylbiphenyl-4-carboxamide

3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N-[2- (dimethylamino)ethyl]biphenyl-4-carboxamide

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-3- yl)phenyl]ethyl}quinazolin-4-amine

N-[(1 R)-1 -{3-[(2E)-but-2-en-2-yl]phenyl}ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[(1 R)-1 -(5'-chloro-2'-propoxybiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{3-[(1 E)-3-phenylprop-1 -en-1 - yl]phenyl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4'-(morpholin-4-yl)biphenyl-3- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3'-(morpholin-4-yl)biphenyl-3- yl]ethyl}quinazolin-4-amine N-{(1 R)-1 -[2'-(benzyloxy)biphenyl-3-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4'-(methylsulfonyl)biphenyl-3- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[2'-(trifluoromethoxy)biphenyl-3- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3'-(trifluoromethoxy)biphenyl-3- yl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(1 H-indol-5-yl)phenyl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(furan-3-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(1 -benzothiophen-3-yl)phenyl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-indol-2- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{3-[(1 E)-pent-1 -en-1 - yl]phenyl}ethyl]quinazolin-4-amine

N-[(1 R)-1 -{3-[(E)-2-cyclohexylethenyl]phenyl}ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(2'-phenoxybiphenyl-3- yl)ethyl]quinazolin-4-amine

tert-butyl (3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-4-yl)carbamate

(2E)-3-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-3-yl)prop-2-enenitrile

N-[(1 R)-1 -(2',4'-dimethylbiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

1 -[5-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)thiophen-2-yl]ethanone

N-{(1 R)-1 -[3-(1 ,3-benzodioxol-5-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[4'-(benzyloxy)biphenyl-3-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(2,3-dihydro-1 ,4-benzodioxin-6-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine 6,7-dimethoxy-N-[(1 R)-1 -(3'-methoxybiphenyl-3-yl)ethyl]-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3'-(trifluoromethyl)biphenyl-3- yl]ethyl}quinazolin-4-amine

3'-{(1 R)-1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N,N- dimethylbiphenyl-2-sulfonamide

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(2'-propoxybiphenyl-3- yl)ethyl]quinazolin-4-amine

3'-{(1 R)-1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N,N- dimethylbiphenyl-2-carboxamide

6,7-dimethoxy-N-{(1 R)-1 -[2'-(methoxymethyl)biphenyl-3-yl]ethyl}-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-indol-5- yl)phenyl]ethyl}quinazolin-4-amine

3'-{(1 R)-1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N,N- dimethylbiphenyl-3-carboxamide

[5-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)thiophen-2-yl]methanol

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(3-methylpyridin-4- yl)phenyl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(1 H-indol-6-yl)phenyl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(1 H-indol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-N-{(1 R)-1 -[3-(2-methoxypyrimidin-5-yl)phenyl]ethyl}-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3'-(methylsulfonyl)biphenyl-3- yl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(2,3-dihydro-1 -benzofuran-5-yl)phenyl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{3-[(E)-2- phenylethenyl]phenyl}ethyl]quinazolin-4-amine

3'-{(1 R)-1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-N,N- dimethylbiphenyl-4-carboxamide

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{3-[(1 E)-prop-1 -en-1 - yl]phenyl}ethyl]quinazolin-4-amine N-{(1 R)-1 -[3-(cyclopent-1 -en-1 -yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-3-yl)methanesulfonamide

N-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-2-yl)acetamide

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[2'-(methylsulfonyl)biphenyl-3- yl]ethyl}quinazolin-4-amine

N-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-2-yl)methanesulfonamide

N-{1 -[5-(3,5-dichlorophenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2 - methylquinazolin-4-amine

N-{(1 R)-1 -[3'-(benzyloxy)biphenyl-3-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[(1 R)-1 -(3',5'-dichlorobiphenyl-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(2,3-dihydro-1 ,4-benzodioxin-6-yl)phenyl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

ej-dimethoxy^-methyl-N-tl -iS-^-iS-methyl-I .S^-oxadiazol^- yl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

6 J-dimethoxy-2-methyl-N-[1 -{5-[5-(methylsulfonyl)pyridin-3-yl]thiophen- 2-yl}ethyl]quinazolin-4-amine

ej-dimethoxy^-methyl-N-tl -iS-^-iS-methyl-I .S^-oxadiazol^- yl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(1 H-pyrrolo[2,3-b]pyridin-5-yl)thiophen-

2- yl]ethyl}quinazolin-4-amine

3- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)benzenesulfonamide

N-{1 -[5-(2-aminopyrimidin-5-yl)thiophen-2-yl]ethyl}-6,7-dimethox y-2- methylquinazolin-4-amine

N-[1 -{5-[(E)-2-cyclopropylethenyl]thiophen-2-yl}ethyl]-6,7-dimet hoxy-2- methylquinazolin-4-amine

N-[1 -{5-[2-(ethoxymethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimetho xy-2- methylquinazolin-4-amine

N-{1 -[5-(3-fluoro-5-methoxyphenyl)thiophen-2-yl]ethyl}-6,7-dimet hoxy- 2-methylquinazolin-4-amine N-[1 -{5-[3-(benzyloxy)phenyl]thiophen-2-yl}ethyl]-6,7-dimethoxy- 2- methylquinazolin-4-amine

N-{1 -[5-(2-butoxy-6-fluorophenyl)thiophen-2-yl]ethyl}-6,7-dimeth oxy-2- methylquinazolin-4-amine

2-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]-2-methylpropanenitrile

N-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]acetamide

N-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]methanesulfonamide

N-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]methanesulfonamide

4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n- yl)-N-propylbenzamide

4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n- yl)-N-[2-(dimethylamino)ethyl]benzamide

N-[1 -{5-[(2E)-but-2-en-2-yl]thiophen-2-yl}ethyl]-6,7-dimethoxy-2 - methylquinazolin-4-amine

N-{1 -[5-(5-chloro-2-propoxyphenyl)thiophen-2-yl]ethyl}-6,7-dimet hoxy- 2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[(1 E)-3-phenylprop-1 -en-1 -yl]thiophen 2-yl}ethyl]quinazolin-4-amine

N-{1 -[5-(5-amino-2-methylphenyl)thiophen-2-yl]ethyl}-6,7-dimetho xy-2 methylquinazolin-4-amine

N-{1 -[5-(3,5-dimethyl-1 ,2-oxazol-4-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(methylsulfonyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[4-(methylsulfonyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(trifluoromethoxy)phenyl]thiophen-2 yl}ethyl]quinazolin-4-amine

6 ,7-dimethoxy-2-methyl-N-[1 -{5-[3-(trifluoromethoxy)phenyl]thiophen-2 yl}ethyl]quinazolin-4-amine

N-{1 -[5-(1 H-indol-5-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine N-{1 -[5-(furan-3-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(1 -benzothiophen-3-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(1 -methyl-1 H-indol-2-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[(1 E)-pent-1 -en-1 -yl]thiophen-2- yl}ethyl]quinazolin-4-amine

N-[1 -{5-[(E)-2-cyclohexylethenyl]thiophen-2-yl}ethyl]-6,7-dimeth oxy-2 methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(2-phenoxyphenyl)thiophen-2- yl]ethyl}quinazolin-4-amine

tert-butyl [4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]carbamate

(2E)-3-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]prop-2-enenitrile

N-{1 -[5-(2,4-dimethylphenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2 - methylquinazolin-4-amine

1 - (5'-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,2'- bithiophen-5-yl)ethanone

N-{1 -[5-(1 ,3-benzodioxol-5-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(4-methyl-3,4-dihydro-2H-1 ,4- benzoxazin-7-yl)thiophen-2-yl]ethyl}quinazolin-4-amine

N-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]methanesulfonamide

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]acetamide

6,7-dimethoxy-N-{1 -[5-(3-methoxyphenyl)thiophen-2-yl]ethyl}-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[3-(trifluoromethyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

2- (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n yl)-N,N-dimethylbenzenesulfonamide

N-[1 -{5-[3-(cyclopropylmethoxy)phenyl]thiophen-2-yl}ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine N-{1 -[5-(1 H-indol-4-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

6 J-dimethoxy-N-{1 -[5-(2-methoxypyrimidin-5-yl)thiophen-2-yl]ethyl}-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[3-(methylsulfonyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

N-{1 -[5-(2,3-dihydro-1 -benzofuran-5-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[(E)-2-phenylethenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

4-(5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)-N,N-dimethylbenzamide

6,7-dimethoxy-2-methyl-N-[1 -{5-[(1 E)-prop-1 -en-1 -yl]thiophen-2- yl}ethyl]quinazolin-4-amine

methyl 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzoate

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]piperidine-4-carboxamide

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethanol

2-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethanol

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(2-oxa-6-azaspiro[3.3]hept-6- ylmethyl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(pyrrolidin-1 - ylmethyl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

N-[1 -{5-[2-({2-[(dimethylamino)methyl]pyrrolidin-1 - yl}methyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethoxy-2-methyl quinazolin-

4-amine

2-methyl-N-[(1 R)-1 -(naphthalen-1 -yl)ethyl]quinazolin-4-amine

N-[(1 R)-1 -(4-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4- (methylsulfonyl)phenyl]ethyl}quinazolin-4-amine 4-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}benzonitrile

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(3-methylphenyl)ethyl]quinazolin-4 amine

N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4 amine

4-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}benzamide

N-[(1 R)-1 -(biphenyl-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}benzonitrile

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(4-methylphenyl)ethyl]quinazolin-4 amine

N-[(1 R)-1 -(biphenyl-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

N-[(1 R)-1 -(4-cyclopropylphenyl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3- (methylsulfonyl)phenyl]ethyl}quinazolin-4-amine

3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}benzamide

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4-(1 -methyl-1 ,2,3,6- tetrahydropyridin-4-yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 ,2,3,6- tetrahydropyridin-4-yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4-(prop-1 -en-2- yl)phenyl]ethyl}quinazolin-4-amine

N-[(1 R)-1 -(3-cyclopropylphenyl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[1 -(1 -benzothiophen-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -phenylethyl]quinazolin-4-amine 6,7-dimethoxy-2-methyl-N-[1 -(thiophen-2-yl)ethyl]quinazolin-4-amine N-[1 -(5-bromofuran-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4- amine

N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4- amine

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]pyrrolidin-3-ol

N-{1 -[5-(2-{[(3S)-3-fluoropyrrolidin-1 -yl]methyl}phenyl)thiophen-2- yl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-5-yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4- amine

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(3-phenoxyphenyl)ethyl]quinazolin-4- amine

6,7-dimethoxy-2-methyl-N-{1 -[3-(2H-tetrazol-5- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-8-yl)ethyl]quinazolin-4-amine 2-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-1 H-pyrazol-1 -yl]ethanol

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}- 6,7-dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-

4-yl}thiophen-2-yl)ethyl]quinazolin-4-amine

N-{1 -[5-(1 -cyclopentyl-1 H-pyrazol-4-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{1 -[5-(1 H-pyrazol-3-yl)thiophen-2- yl]ethyl}quinazolin-4-amine

N-[1 -(5-{2-[(3,3-difluoropyrrolidin-1 -yl)methyl]phenyl}thiophen-2- yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4- amine

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

2-[1 -(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}furan-2 - yl)-1 H-pyrazol-3-yl]ethanol 5-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}pyridin- 2(1 H) one

6,7-dimethoxy-2-methyl-N-[1 -(3-phenoxyphenyl)ethyl]quinazolin-4- amine

N-[1 -(2,1 _! 3-benzothiadiazol-5-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(quinolin-8-yl)ethyl]quinazolin-4- amine

N-{1 -[5-(cyclopent-1 -en-1 -yl)thiophen-2-yl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(2-ethoxyphenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(4-fluoronaphthalen-1 -yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-{1 -[5-(3,6-dihydro-2H-pyran-4-yl)thiophen-2-yl]ethyl}-6,7-dime thoxy- 2-methylquinazolin-4-amine

tert-butyl {[5-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)furan-2-yl]methyl}carbamate

methyl 3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-1 -methyl-1 H-pyrazole-5-carboxylate

N-{1 -[5-(2-{[3-(dimethylamino)pyrrolidin-1 -yl]methyl}phenyl)thiophen-2- yl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4- amine

2- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2 yl)benzamide

3- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2 yl)benzamide

4- (5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2 yl)benzamide

N-{1 -[5-(2-aminophenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

[2-(5-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen - 2-yl)phenyl]methanol 2-(5-{1 -[(6 J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)benzonitrile

N-{1 -[5-(1 H-indazol-7-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(1 H-indazol-4-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(2-ethenylphenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

2-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-1 H-pyrazol-1 -yl]acetamide

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-

[(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazoli n-4-amine 2-[4-(4-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-1 H-pyrazol-1 -yl]ethanol

N-[1 -{5-[2-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6 ,7-dimethoxy-2- methylquinazolin-4-amine

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-3-yl]ethyl}- 6,7-dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-

4-yl}thiophen-3-yl)ethyl]quinazolin-4-amine

N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-3-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

2-[4-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)-1 H-pyrazol-1 -yl]ethanol

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(3-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H- pyrazol-4-yl}phenyl)ethyl]quinazolin-4-amine

N-iil R^I -P'-iaminomethy biphenyl-S-y ethylJ-ej-dimethoxy^- methylquinazolin-4-amine

N-[1 -{5-[2-(aminomethyl)phenyl]thiophen-3-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(aminomethyl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-{(1 R)-1 -[3-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)phenyl]ethyl}- 6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7- dimethoxy-2-methylquinazolin-4-amine 6,7-dimethoxy-2-methyl-N-[1 -(5-{2-

[(methylamino)methyl]phenyl}thiophen-3-yl)ethyl]quinazoli n-4-amine

N-[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4- amine

N-[1 -{5-[3-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

N-[1 -{5-[4-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(4-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol- 3-yl}thiophen-2-yl)ethyl]quinazolin-4-amine

6J-dimethoxy-2-methyl-N-[(1 R)-1 -{2'-[(methylamino)methyl]biphenyl-3- yl}ethyl]quinazolin-4-amine

N-[1 -{4-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-[1 -{4-[2-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-

[(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazoli n-4-amine

N-{1 -[4-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-

6,7-dimethoxy-2-methylquinazolin-4-amine

2-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-3-yl)-1 H-pyrazol-1 -yl]ethanol

N-{(1 R)-1 -[2'-(aminomethyl)-4'-fluorobiphenyl-3-yl]ethyl}-6,7-dimetho xy-

2-methylquinazolin-4-amine

N-[1 -{5-[5-(aminomethyl)furan-2-yl]thiophen-2-yl}ethyl]-6,7-dime thoxy- 2-methylquinazolin-4-amine

N-il -^'-iaminomethyl^^'-bithiophen-S-y ethylJ-ej-dimethoxy^- methylquinazolin-4-amine

2- {[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]amino}-1 -(1 H-indol-3-yl)ethanone

3- amino-4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-1 -benzothiophene-2-carboxamide 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]glycinamide

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]-N,N-dimethylglycinamide methyl N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]glycinate

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]-N-methylglycinamide

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]-N-(2-methoxyethyl)glyci namide

N-benzyl-2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]glycinamide

2- {[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]amino}-1 -(morpholin-4-yl)ethanone

3- (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)-1 ,5-dimethyl-1 H-pyrrole-2-carbonitrile

5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,3'- bithiophene-4'-carbonitrile

N-[1 -(5-{2-[(diethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]-N-phenylglycinamide

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]piperidine-3-carboxamide

N-{1 -[5-(2-{[(2,2-difluoroethyl)(methyl)amino]methyl}phenyl)thio phen-2- yl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -{5-[2-(aminomethyl)-5-chlorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-1 H-imidazole-2- carboxamide

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-1 H-imidazole-5- carboxamide

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-N<sup&a mp;gt;2</sup>-

(2,2,2-trifluoroethyl)glycinamide

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-1 H-indole-2-carboxamide

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]amino}ethanol 2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl](methyl)amino}ethanol

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-N2-phenylglyci namide

6 _! 7-dimethoxy-2-methyl-N-{1 -[5-(2-{[(2 _! 2,2- trifluoroethyl)amino]methyl}phenyl)thiophen-2-yl]ethyl}quina zolin-4- amine

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(pyridin-2- ylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(1 H-pyrazol-3- ylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazolin-4-amine

1 -(3,4-dihydroisoquinolin-2(1 H)-yl)-2-{[2-(5-{1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl)benzyl]amino }ethano

N-[1 -{5-[4-fluoro-2-({[(1 -methyl-1 H-imidazol-2- yl)methyl]amino}methyl)phenyl]thiophen-2-yl}ethyl]-6 J-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(piperazin-1 - ylmethyl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine hydrochloride tert-butyl 4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]piperazine-1 -carboxylate

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]acetamide

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(4-methylpiperazin-1 - yl)methyl]phenyl}thiophen-2-yl)ethyl]quinazolin-4-amine

(3S)-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]amino}-1 -methylpyrrolidin-2-one

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-1 H-pyrazole-3- carboxamide

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(morpholin-4- ylmethyl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]azetidin-3-ol

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]-2,5,7-triazaspiro[3.4]o ctan-6-one

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-L-prolinamide N-{1 -[5-(2-{[(2,2-difluoroethyl)amino]methyl}phenyl)thiophen-2-y l]ethyl}

6,7-dimethoxy-2-methylquinazolin-4-amine

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-prolinamide

N-[1 -{5-[2-(azetidin-1 -ylmethyl)phenyl]thiophen-2-yl}ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

{1 -[(2S)-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]azetidin-2-yl}methanol

N-{1 -[5-(2-{[3-(dimethylamino)azetidin-1 -yl]methyl}phenyl)thiophen-2- yl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(3,3-difluoroazetidin-1 -yl)methyl]phenyl}thiophen-2-yl)ethyl]-

6,7-dimethoxy-2-methylquinazolin-4-amine

6 _! 7-dimethoxy-2-methyl-N-{1 -[5-(2-{[methyl(2,2,2- trifluoroethyl)amino]methyl}phenyl)thiophen-2-yl]ethyl}quina zolin-4- amine

N-[1 -(5-{2-[(3-fluoroazetidin-1 -yl)methyl]phenyl}thiophen-2-yl)ethyl]-6,7 dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{4-chloro-2-[(dimethylamino)methyl]phenyl}thiophen-2-yl) ethyl]-

6,7-dimethoxy-2-methylquinazolin-4-amine

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethanone

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[2-(pyrrolidin-1 - yl)ethoxy]phenyl}thiophen-2-yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-

[(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazoli n-4-amine, enantiomer 1

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-

[(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazoli n-4-amine, enantiomer 2

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl} 6,7-dimethoxy-2-methylquinazolin-4-amine, enantiomer 1

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl} 6,7-dimethoxy-2-methylquinazolin-4-amine, enantiomer 2

6,7-dimethoxy-2-methyl-N-[1 -(2-methyl-1 -benzothiophen-4- yl)ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(thieno[2,3-b]pyridin-4-yl)ethyl]quinazolin- 4-amine 6 J-dimethoxy-2-methyl-N-[1 -(thieno[2,3-c]pyridin-4-yl)ethyl]quinazolin- 4-amine

6,7-dimethoxy-2-methyl-N-[1 -(thieno[3,2-c]pyridin-4-yl)ethyl]quinazolin- 4-amine

N-{(1 R)-1 -[3-(3,5-dimethyl-1 H-pyrazol-4-yl)phenyl]ethyl}-6,7-dimethoxy- 2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(5-methyl-1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(3,5-dimethyl-1 ,2-oxazol-4-yl)phenyl]ethyl}-6,7-dimethoxy- 2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-5- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-pyrazol-5- yl)phenyl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(1 H-imidazol-1 -yl)phenyl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-1 - yl)phenyl]ethyl}quinazolin-4-amine

N-{(1 R)-1 -[3-(1 H-imidazol-4-yl)phenyl]ethyl}-6 J-dimethoxy-2- methylquinazolin-4-amine

6-(benzyloxy)-N-[(1 R)-1 -(3-bromophenyl)ethyl]-7-methoxy-2- methylquinazolin-4-amine

6- (benzyloxy)-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

7- methoxy-2-methyl-4-({(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}amino)quinazolin-6-ol

6- (cyclopropylmethoxy)-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol- 4-yl)phenyl]ethyl}quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(thiophen-2-yl)ethyl]quinazolin-4-amine

7- methoxy-6-(2-methoxyethoxy)-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

(1 R)-1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]propan-1 -ol

6-butoxy-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine 7-methoxy-2-methyl-6-(3-methylbutoxy)-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

tert-butyl {2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethyl}carbamate

7-methoxy-2-methyl-6-(propan-2-yloxy)-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

7-methoxy-2-methyl-6-(oxetan-3-ylmethoxy)-N-{(1 R)-1 -[3-(1 H-pyrazol- 4-yl)phenyl]ethyl}quinazolin-4-amine

6-ethoxy-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

6-ethoxy-N-{(1 R)-1 -[3-(1 -ethyl-1 H-pyrazol-4-yl)phenyl]ethyl}-7-methoxy- 2-methylquinazolin-4-amine

N-[1 -{5-[2-(2-aminoethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimetho xy-2- methylquinazolin-4-amine

tert-butyl {1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethyl}carbamate

N-[1 -(5-{2-[1 -aminoethyl]phenyl}thiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[1 -(5-{2-[1 -aminoethyl]phenyl}thiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(1 H-pyrazol-4-yl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-

[(phenylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazoli n-4-amine 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine N-[1 -(5-{2-[(cyclopentylamino)methyl]phenyl}thiophen-2-yl)ethyl] -6,7- dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(benzylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(butylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(ethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(1 H-tetrazol-5-yl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine 6,7-dimethoxy-N-{1 -[5-(2-{[(2- methoxyethyl)amino]methyl}phenyl)thiophen-2-yl]ethyl}-2- methylquinazolin-4-amine

N-[1 -(5-{2-[(cyclopropylamino)methyl]phenyl}thiophen-2-yl)ethyl] -6,7- dimethoxy-2-methylquinazolin-4-amine

methyl 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6- carboxylate

4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6- carboxylic acid

(4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazolin-6- yl)methanol

[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-

2-yl)phenyl](phenyl)methanol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]-3-phenylpropan-1 -ol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]-2-phenylethanol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]pentan-1 -ol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]prop-2-yn-1 -ol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]-2-methylpropan-1 -ol

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]-2,2,2-trifluoroethanol

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)-4-methylthiophen-

2-yl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-2-hydroxyaceta mide

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)-5-fluorobenzyl]-2-methoxyaceta mide

N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-

6,7-dimethoxy-2-methylquinazolin-4-amine

N-(1 -(5-(2-((Dimethylamino) methyl)-4-(trifluoromethyl) phenyl) thiophen-2-yl) ethyl)-6, 7-dimethoxy-2-methylquinazolin-4-amine

6,7-dimethoxy-2-methyl-N-(1 -{5-[2-methyl-4-(trifluoromethyl)phenyl]-2- thienyl}ethyl)quinazolin-4-amine tert-butyl [4-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

4- (3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}phenyl)pyridin-2-ol

N-{1 -[3-(benzyloxy)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazoli n-4- amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7- dimethoxy-2-methylquinazolin-4-amine (enantiomer 1 )

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7- dimethoxy-2-methylquinazolin-4-amine (enantiomer 2)

2-(4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazolin-6- yl)propan-2-ol

2-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}biphenyl-2-yl)acetamide

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]acetamide

5- (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)pyridin-2-ol

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,8-dimethylquinazolin-4- amine

N-[1 -{5-[2-(aminomethyl)-3-chlorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-[1 -{5-[2-(aminomethyl)-4-chlorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-(1 -{5-[2-(aminomethyl)-4-fluorophenyl]-4-methyl-2-thienyl}ethy l)-6,7- dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-4-methyl-2-thienyl)eth yl]-6,7- dimethoxy-2-methylquinazolin-4-amine

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-3- methyl-2-thienyl)benzyl](methyl)amino}ethanol

6,7-dimethoxy-2-methyl-N-[1 -(4-methyl-5-{2-[(methylamino)methyl]- phenyl}thiophen-2-yl)ethyl]quinazolin-4-amine

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]ethane-1 ,2-diol

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2,6-dimethylquinazolin-4-amine

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methyl-6-(1 H-pyrazol-4- yl)quinazolin-4-amine N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methyl-6-(1 -methyl-1 H-pyrazol-4- yl)quinazolin-4-amine

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-cyclopropyl-2-methylquinazolin-4- amine

tert-butyl [3-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

N-[1 -{5-[2-(aminomethyl)-6-chlorophenyl]thiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)pyridin-2-ol

4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)phenyl]azetidin-2-one

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,7-dimethylquinazolin-4- amine

4-(5-{1 -[(6 ,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2 yl)-3-[(dimethylamino)methyl]benzonitrile

N-[1 -(5-bromothiophen-2-yl)ethyl]-6-[3-(dimethylamino)pyrrolidin -1 -yl]- 2-methylquinazolin-4-amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl 6-(pyrrolidin-1 -yl)quinazolin-4-amine

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(4-methylpiperazin- 1 - yl)quinazolin-4-amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl

6-(4-methylpiperazin-1 -yl)quinazolin-4-amine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6- [3-

(dimethylamino)pyrrolidin-1 -yl]-2-methylquinazolin-4-amine

N-[(1 R)-1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(pyrrolidin-1 - yl)quinazolin-4-amine

N-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)acetamide

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl 6-nitroquinazolin-4-amine

6,7-dimethoxy-N-{1 -[5-(4-methoxy-2-methylphenyl)thiophen-2-yl]ethyl}- 2-methylquinazolin-4-amine

N4-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-2-met hyl- quinazoline-4,6-diamine N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-[4-(pyridin-3- ylmethyl)piperazin-1 -yl]quinazolin-4-amine

N4-[1 -(5-bromo-2-thienyl)ethyl]-2-methyl-N6-[2-(morpholin-4-yl)et hyl]- quinazoline-4,6-diamine

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl-

6-[4-(pyridin-3-ylmethyl)piperazin-1 -yl]quinazolin-4-amine

N-{2-[(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)amino]ethyl}acetamid e

N-[1 -(5-bromo-3-chlorothiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

tert-butyl [2-(4-chloro-5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

N-[1 -{5-[2-(aminomethyl)phenyl]-4-chlorothiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-[1 -(4-chloro-5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl) ethyl]- 6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-bromo-4-chlorothiophen-2-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine

N4-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-2-met hyl- N6-[2-(morpholin-4-yl)ethyl]quinazoline-4,6-diamine

4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2-methylquinazolin-6-yl) -1 - methylpiperazin-2-one

4-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)-1 -methylpiperazin-2-one methyl 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- thiophen-2-yl)phenyl]-2-methylpropanoate

N-[1 -{5-[2-(aminomethyl)phenyl]-3-chlorothiophen-2-yl}ethyl]-6,7 - dimethoxy-2-methylquinazolin-4-amine

N-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)methanesulfonamide

N-[1 -(5-{2-[(dimethylamino)methyl]-4-methoxyphenyl}thiophen-2- yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

3-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)-1 ,1 -dimethylurea

1 -benzyl-4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2- methylquinazolin-6-yl)piperazin-2-one N-[1 -(5-{2-[(dimethylamino)methyl]-4-methylphenyl}thiophen-2-y

6,7-dimethoxy-2-methylquinazolin-4-amine

N-[1 -(5-{4-cyclopropyl-2-[(dimethylamino)methyl]phenyl}thiophen- 2- yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

6 J-dimethoxy-2-methyl-N-[1 -(2-methyl-1 ,3-thiazol-4-yl)ethyl]quinazolin-

4-amine

6 J-dimethoxy-2-methyl-N-[1 -(4-methyl-1 ,3-thiazol-2-yl)ethyl]quinazolin- 4-amine

3-(5-{1 -[(6 J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)-1 -methyl-1 H-pyrazole-5-carboxylic acid

tert-butyl [(5'-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- 2,2'-bithiophen-5-yl)methyl]carbamate

7-methoxy-2-methyl-6-[2-(methylsulfonyl)ethoxy]-N-{(1 R)-1 -[3-(1 H- pyrazol-4-yl)phenyl]ethyl}quinazolin-4-amine

tert-butyl [5-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

tert-butyl [2-chloro-6-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

7-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-nitroquinazolin-4-a mine

methyl 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-7- carboxylate

3-amino-3-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-3-yl)phenyl]propanoic acid

N-[1 -{5-[2-(2-aminopropan-2-yl)phenyl]thiophen-2-yl}ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-

2-yl)benzyl](methyl)amino}acetonitrile

1 -(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)-3-methylurea and

1 -benzyl-4-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2- yl)ethyl]amino}-2-methylquinazolin-6-yl)piperazin-2-one

In another embodiment of the first aspect, the present invention covers compounds of formula (I), supra, in which the carbon atom between the nitrogen atom and the substituent A1 is in (R)-configuration. In yet another embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein R ¹ is selected from the list of the following substituents

^* -0-CH ₂ -^°

H, *-OCH ₃ ,,-OC ₂ H ₅ , , *-CH ₂ OH, -C(0)OH, *-C(0)OCH ₃ , -Br,

*-O-CH ₂ _ |

*-0-CH(CH ₃ ) ₂ ., *-0-(CH2)2CH(CH3)2, *-0-(CH2)3CH3, *-0-(CH ₂ )20-CH3, ,

*-0-CH ₂ -Phenyl, *-N=S (0)(CH ₃ ) ₂ , *-CH ₃ , , *-NH(CH ₃ ), *-N(CH ₃ ) ₂ , *-NH ₂ ,

*-NH-(CH ₂ ) ₂ -NH-C(0)-CH ₃ ,. *-NH-(CH ₂ ) ₂ -morpholino, *-NH-C(0)-CH ₃ , *-NH-C(0)-NH-CH ₃ , *-NH-C(0)-N(CH ₃ ) ₂ , *-N0 ₂ , *-NH-S(0) ₂ -CH ₃ , *-N=S(0)(CH ₃ ) ₂ , *-OH, *-0-(CH ₂ ) ₂ -S(0)2-CH ₃ ,

In a further embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein R ² is selected from the group of hydrogen, hydroxy, oxo (=0), cyano, cyclopropyl, 1 ,1 -dimethylcyclopropyl, -C(=CH2)CH3, - C(CH ₃ )=CHCH ₃ , -CH=CH-(CH ₂ ) ₂ CH ₃ , CH=CHCH ₃ , -CH=CH-cyclopropyl), -C(0)NH ₂ , C(0)OCH ₃ , -S(0) ₂ CH ₃ , -OCH ₃ , -CH ₂ NH ₂ , a halogen atom (F, CI; Br),

In an even further embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein A1 is selected from the group

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

In a further another embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein A1 is a phenyl ring or a thienyl ring.

In a particular embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein A2 is selected from the group

or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

In a further particular embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein A2 is a phenyl ring.

In another further particular embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein R ³ is selected from the group of the following substituents

^* -C(0)NH-(CH ₂ ) ₂ CH ₃

^* -C(0)-N(CH ₃ ) ₂

^* -C(0)-NH ₂

^* -C(0)-NH-(CH ₂ ) ₂ N(CH ₃ ) ₂

*-CH ₂ -C(0)-NH ₂

hydrogen

*-F, ^* -CI, ^* -Br

^* -C≡N; ^* -CF ₃ , ^* -CH ₃ , ^* -C ₂ H ₅ , ^* -CH=CH ₂ ;

*-CH ₂ -CN; ^* -CH(CH ₃ )-NH ₂ ; ^* -CH=CH-CN; *-C(0)-OH; *-C(0)-OCH ₃ ; *-C(0)-CH ₃ ; ^* -C(CH ₃ ) ₂ -C(0)-OCH ₃ ; ^* -C(CH ₃ ) ₂ -CN; Oxo(=0); hydroxy;

^* -NH ₂

*-NH-C(0)CH ₃

*-NH-S0 ₂ -CH ₃

*-NH- 0)-0-C(CH ₃ ) ₃

*-S0 ₂ -CH ₃

*-S0 ₂ -N(CH ₃ ) ₂

*-S0 ₂ -NH ₂

*-0-CH ₂ -CH ₃ ; *-0-(CH ₂ ) ₂ -CH ₃ ; ^* -0-CF ₃ ;

*-0(CH ₂ ) ₂

*-OCH ₂ -C -ycolopropyl; ^* -OCH ₃ ;

*-0(CH ₂ ) ₃ -CH ₃ ; *-OCH ₂ -Phenyl; ^* -0-Phenyl;

*-(CH ₂ )-OH

*-(CH ₂ ) ₂ -OH

*-(CH ₂ )-0-CH ₃

*-(CH ₂ )-0-CH ₂ -CH ₃

*-CH(OH)-CH ₂ -Phenyl

*-CH(OH)-CH ₂ -CH ₃

*-CH(OH)-(CH ₂ ) ₂ -CH ₃ *-CH(OH)-(CH ₂ ) ₃ -CH ₃ -CH(OH)-CH-(CH ₃ ) ₂

-CH(OH)-Phenyl

-CH(OH)-CN

-CH(OH)-CH ₂ OH

-CH(OH)-CF ₃

-CH(OH)-(CH ₂ ) ₂ -Phenyl

-CH(OH)-C≡CH

-CH(NH ₂ )-CH ₂ -COOH

-CH ₂ -NH-S0 ₂ -CH ₃

-CH ₂ -NH-(CH ₂ ) ₃ -CH ₃

-CH ₂ -N(CH ₃ ) ₂

-CH ₂ -NH-C ₂ H ₅ ^* -CH(CH ₃ )-NH ₂

-CH ₂ -NH ₂

-(CH ₂ ) ₂ -NH ₂

-CH ₂ -NH-CH ₂ -Phenyl

-CH ₂ -N(C ₂ H ₅ ) ₂

-CH ₂ -NH-Cyclopropyl

-CH ₂ -NH-Cyclobutyl

*-CH ₂ -NH-Cyclopentyl

*-CH ₂ -NH-Pyridyl

*-CH ₂ -NH-Phenyl

*-CH ₂ -NH-(CH ₂ ) ₂ -OH

*-CH ₂ -N(CH ₃ )(CH ₂ ) ₂ 0H ^* -CH ₂ -NH-CH ₂ -CN

*-CH ₂ -N(CH ₃ )-CH ₂ -CN

*-CH ₂ -N(CH ₃ )-CH ₂ -CF ₃

*-CH ₂ -N(CH ₃ )-CH ₂ -CF ₂ H

*-CH ₂ -NH-CH ₂ -CF ₂ H

*-CH ₂ -NH-CH ₂ -CF ₃

*-CH ₂ -NH-(CH ₂ ) ₂ -OCH ₃

^

-CH ₂ -NH-C(0)-0-C(CH ₃ ) ₃

-(CH ₂ ) ₂ -NH-C(0)-0-C(CH ₃ )3

-CH ₂ -NH-C(0)-CH ₂ -OH

-CH ₂ -NH-C(0)-CH ₂ -OCH ₃

-CH-(CH ₃ )-NH-C(0)-0-C(CH ₃ ) ₃

-CH ₂ -NH-C 0)-CH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH ₂

-CH ₂ -NH-CH ₂ -C(0)-N(CH ₃ ) ₂

-CH ₂ -NH-CH ₂ -C(0)-OCH ₃

-CH ₂ -NH-CH ₂ -C(0)-NHCH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH-(CH ₂ ) ₂ -0-CH ₃

-CH ₂ -NH-CH ₂ -C(0)-NH-CH ₂ -Phenyl *-CH ₂ -NH-CH ₂ -C(0) -N O

^* -CH ₂ -NH-CH ₂ -C(0)-NH-Phenyl

_! -NH-C(0)-CH ₂ -NH-Phen l

*-CH2-NH-C(0)-CH ₂ -NH-CH2-CF ₃

In yet another further particular embodiment of the first aspect, the present invention covers compounds of formula (I), supra, wherein R ³ is a Ci- or C2-alkyl substituted with an amino group -NR ^k R', wherein R ^k and R' can have all the meanings as defined supra within the definition of R ³ or wherein R ³ is a Ci- or C2-alkyl substituted with a hydroxyl or a Ci-C6-alkoxy or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

In even further particular embodiments of the first aspect, the present invention covers compounds of formula (I), supra, wherein x is 1 or 2 and/or y is 1 or 2 and/or z is 1 or 2 or a stereoisomer, a tautomer, an N-oxide, a hydrate, a solvate, or a salt thereof, or a mixture of same.

In a particular further embodiment of the first aspect, the present invention covers combinations of two or more of the above mentioned embodiments under the heading "further embodiments of the first aspect of the present invention".

The present invention covers any sub-combination within any embodiment or aspect of the present invention of compounds of general formula (I), supra.

The present invention covers any sub-combination within any embodiment or aspect of the present invention of intermediate compounds of general formula (II). The present invention covers the compounds of general formula (I) which are disclosed in the Example Section of this text, infra.

Synthesis of Compounds (Overview)

The compounds of the present invention can be prepared as described in the following section. The schemes and the procedures described below illustrate general synthetic routes to the compounds of general formula (I) of the invention and are not intended to be limiting. It is clear to the person skilled in the art that the order of transformations as exemplified in the schemes can be modified in various ways. The order of transformations exemplified in the schemes is therefore not intended to be limiting. In addition, interconversion of any of the substituents can be achieved before and/or after the exemplified transformations. These modifications can be such as the introduction of protecting groups, cleavage of protecting groups, exchange, reduction or oxidation of functional groups, halogenation, metallation, substitution or other reactions known to the person skilled in the art. These transformations include those which introduce a functionality which allows for further interconversion of substituents. Appropriate protecting groups and their introduction and cleavage are well- known to the person skilled in the art (see for example P.G.M. Wuts and T.W. Greene in "Protective Groups in Organic Synthesis", 4"' edition, Wiley 2006). Specific examples are described in the subsequent paragraphs. Further, it is possible that two or more successive steps may be performed without work-up being performed between said steps, e.g. a "one- pot" reaction, as is well-known to the person skilled in the art.

The syntheses of the compounds of the present invention are preferably carried out according to the general synthetic sequence, shown in schemes 1 -7.

Scheme 1 : Route for the preparation of compounds of general formula 8, wherein R ¹ and x have the meaning as given for general formula (I), supra and R is alkyl, Hal is chloro, bromo or iodo and LG has the meaning as a leaving group, preferably chloro, bromo or a sulfonate group as depicted in scheme 1 . Specific examples are described in the subsequent paragraphs.

Step 1 -> 7 (Scheme 1 )

Quinazoline formation

In the first step (scheme 1 ) amino benzoic acid ester derivative 1 (which is commercially available or described in the literature) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically acetonitrile and hydrochloric acid in organic solvent such as for example 1 ,4-dioxane at elevated temperatures is used. For example see ACS Medicinal Chemistry Letters, 2013, vol. 4, # 9 p. 846 - 851 ; Journal of Medicinal Chemistry, 2009, vol. 52, # 8 p. 2341 - 2351 or WO2015/54572 and references therein. Step 2 -> 7 (Scheme 1 )

Quinazoline formation

Alternatively halogen substituted benzoic acid derivative of general formula 2 (which is commercially available or described in the literature) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically derivative 2 is reacted with acetamidine, copper metal, a base such as for example potassium carbonate in an organic solvent such as for example DMF at elevated temperature. For example see WO2005/51410, US2008/107623 and references therein.

Step 3 -> 7 (Scheme 1 )

Quinalzoline formation

Alternatively amino substituted benzoic acid derivative of general formula 3 (which is commercially available or described in the literature) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically derivative 3 is reacted with acetyl chloride or acetic anhydride, an ammonia source such as for example ammonia or ammonium acetate, a base such as for example triethylamine or pyridine with or without DMAP in an organic solvent such as for example DMF, toluene, 1 ,4-dioxane / water at elevated temperature. For example see Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21 , # 4 p. 1270 - 1274; Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 7 p. 2330 - 2334; WO2008/1 17079 or WO2006/74187 and references therein.

Step 4 -> 7 (Scheme 1 )

Quinazoline formation

Alternatively benzoxazinone derivative of general formula 4 (which is commercially available or can be prepared in analogy to literature procedures) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically derivative 4 is reacted with ammonium acetate in a solvent at elevated temperature. For example see Bioorganic and Medicinal Chemistry Letters, 2011 , vol. 21 , # 4 p. 1270 - 1274 or US6350750 and references therein.

Step 5 -> 7 (Scheme 1 )

Quinazoline formation

Alternatively benzoic acid amide derivative of general formula 5 (which is commercially available or described in the literature) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically derivative 5 is reacted with a base such as for example sodium hydroxide in a solvent such as for example water at elevated temperature. For example, see Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 16 p. 4573 - 4577 and references therein.

Step 6 -> 7 (Scheme 1 )

Quinazoline formation

Alternatively amino benzoic acid amide derivative of general formula 6 (which is commercially available or described in the literature) can be converted to the corresponding quinazoline 7 in analogy to literature procedures. Typically derivative 6 is reacted with acetic acid at elevated temperature. For example see Bioorganic and Medicinal Chemistry Letters, 2008, vol. 18, # 3 p. 1037 - 1041 and references therein.

Step 7 -> 8 (Scheme 1 )

Conversion of hydroxyl group into leaving group

In the next step (scheme 1 ) hydroxy quinazoline derivative 7 can be converted to the corresponding quinazoline 8 in analogy to literature procedures.

For W = chloro typically trichlorophosphate or thionylchloride, with or without N,N- dimethylaniline or N,N- diisopropylethylamine with or without an organic solvent such as for example toluene at elevated temperatures is used. For examples see Bioorganic and Medicinal Chemistry Letters, 2011 , 1270; Journal of Medicinal Chemistry, 2009, 2341 ; ACS Medicinal Chemistry Letters, 2013, 846; Bioorganic and Medicinal Chemistry Letters, 2010, 2330; US6350750 or WO2015/54572 and references therein.

For W = bromo typically phosphorus oxytribromide, with or without Ν,Ν-dimethylaniline or N,N- diisopropylethylamine with or without an organic solvent such as for example toluene at elevated temperatures is used. For examples see US2012/53174; WO2012/30912 or WO2012/66122 and references therein.

For W = 2,4,6-triisopropylsulfonate typically 2,4,6-triisopropylbenzenesulfonyl chloride, a base such as for example triethylamine and/or DMAP in an organic solvent such as for example dichloromethane is used. For examples see WO2010/99379 US2012/53176 and references therein.

For W = tosylate typically 4-methylbenzene-1 -sulfonyl chloride, a base such as for example triethylamine or potassium carbonate and/or DMAP in an organic solvent such as for example dichloromethane or acetonitrile is used. For examples see Organic Letters, 2011 , 4374 or Bioorganic and Medicinal Chemistry Letters, 2013, 2663 and references therein. For W = trifluoromethanesulfonate typically N,N-bis(trifluoromethylsulfonyl)aniline or trifluoromethanesulfonic anhydride, a base such as for example triethylamine or 1 ,8- diazabicyclo[5.4.0]undec-7-ene and/or DMAP in an organic solvent such as for example dichloromethane is used. For examples see Journal of the American Chemical Society, 2015, 13433 or WO2014/10050 l and references therein.

o H ₃ C S

H ^ A 2

A1 (R L-A2(R ³ C H

A1 (R ² ) _W -L-A2(R ³ )

10

11 12

Scheme 2: Route for the preparation of compounds of general formula 12, wherein A1 , A2, L, R ² , R ³ , w and y have the meaning as given for general formula (I), supra. Specific examples are described in the subsequent paragraphs.

Step 9 -> 10 (Scheme 2)

Sulfinimine formation

In the first step (scheme 2) aldehyde derivative 9 (which is commercially available or described in the literature) can be converted to the corresponding sulfinimine 10 in analogy to the numerous literature procedures. For example the reaction can be performed at ambient temperature using Titanium(IV)ethoxide in an organic solvent as for example THF. For a review about sulfinimine chemistry see for example Chem. Rev. 2010, 1 10, 3600- 3740; Chem. Soc. Rev. 2009, 38, 1 162-1 186; Tetrahedron 2004, 60, 8003or WO2013030138 and the references therein.

Step 10 -» 11 (Scheme 2)

Sulfinamide formation

In the next step (scheme 2) sulfinimine 10 can be converted to the corresponding sulfinamide 11 in analogy to the numerous literature procedures. For example the reaction can be performed using methylmagnesium bromide in an organic solvent as for example THF. For a review about sulfinimine and sulfinamide chemistry see for example Chem. Rev. 2010, 1 10, 3600-3740; Chem. Soc. Rev. 2009, 38, 1 162-1 186; Tetrahedron 2004, 60, 8003 or WO2013030138 and the references therein.

Step 11 12 (Scheme 2)

Formation of amine

In the next step (scheme 2) sulfinamide 11 can be converted to the corresponding amine 12 in analogy to the numerous literature procedures. For example the reaction can be performed using acetylchloride in a protic organic solvent as for example methanol. For a review about sulfinimine and sulfonamide chemistry see for example Chem. Rev. 2010, 1 10, 3600-3740; Chem. Soc. Rev. 2009, 38, 1 162-1 186; Tetrahedron 2004, 60, 8003 or WO2013030138 and the references therein.

Alk ₀

Hal-A1 (R ² ) _W -L-A2(R ³ ) _y H ₂ C k A1 (R ² ) _W -L-A2(R ³ ) _y

H O

O H ^H , H

H†

H gC ^ AI fR ² ) _W -L-A2(R ³ ) _y ^► _{H 3} C M (R ² ) _W -L-A2(R ³ ) _y - ^H N \ _A 1 (R ² ) _W -L-A2(R ³ )

H

15 16 12

Scheme 3: An alternative route for the preparation of compounds of general formula 12, wherein A1 , A2, L, R ² , R ³ , w and y have the meaning as given for general formula (I), supra, Hal has the meaning as chloro, bromo or iodo and Alk has the meaning of alkyl, preferable ethyl as depicted in scheme 3. Specific examples are described in the subsequent paragraphs.

Step 13 -> 14 (Scheme 3)

Stille coupling

In the first step (scheme 3) halide derivative 13 (which is commercially available or described in the literature) can be converted to the corresponding enolester derivative 14 in analogy to literature procedures. Typically the reaction is performed with tributyl(1 - ethoxyethenyl)stannane, a palladium catalyst such as for example bis-triphenylphosphine- palladium(ll) chloride or dichloro(1 ,1 '-bis(diphenylphosphanyl)ferrocene)palladium(ll) dichloromethane adduct, with or without a base such as for example triethylamine in an organic solvent such as for example DMF, 1 ,4-dioxane or toluene at elevated temperature. For W = bromo see for example the literature references WO2010/1 16282, WO2004/214, WO2013/185093 or Journal of the American Chemical Society, 2002, 6343 and references therein.

For W = chloro see for example the literature references Angewandte Chemie - International Edition, 1999, 241 1 - 2413; Journal of the American Chemical Society, 2004, 16433, Organic Letters, 2004, 1421 ; Organic letters, 2001 , 4295 and references therein.

For W = iodo see for example the literature references Bioorganic and Medicinal Chemistry Letters, 2003, 637, WO201 1/100401 , WO2007/38613 or US2005/143401 and references therein.

Step 14 -> 15 (Scheme 3)

Formation of methylketone

In the next step (scheme 3) enolester derivative 14 can be converted to the corresponding methyl ketone 15 in analogy to literature procedures. Typically the reaction is performed with an acid such as for example aqueous hydrochloric acid in an organic solvent such as for example THF, 1 ,4-dioxane or acetone. See for example the literature references Journal of Organic Chemistry, 1992, 1486, WO2013/185103 or US7361789 (2008) and references therein.

Step 15 -> 16 (Scheme 3)

Formation of oxime

In the next step (scheme 3) methyl ketone derivative 15 can be converted to the corresponding oxime 16 in analogy to literature procedures. Typically the reaction is performed with hydroxylamine hydrochloride with or without the addition of a base such as for example sodium acetate, pyridine, or KOH aq. in an organic solvent such as for example ethanol, DMSO, THF, dimethylether or methanol. See for example the literature references US5332757 (1994); US2004/157849 or International Journal of Pharmaceutics, 2016, 205 and references therein.

Step 16 -> 12 (Scheme 3)

Reduction of oxime

In the next step (scheme 3) oxime derivative 16 can be reduced to the corresponding amine 12 in analogy to literature procedures. Typical reaction conditions include for example hydrogen, acetic acid, palladium on activated carbon in ethanol (see literature reference WO2006/82392 and references therein); ammonia, hydrogen, Raney nickel in methanol (see literature reference US201 1/263626 (2011 ) and references therein); hydrogen, acetic acid, palladium on activated carbon in ethanol (see literature references WO2006/82392 and references therein) or acetic acid, zinc in methanol (see literature reference WO2013/26914 and references therein).

Scheme 4: Route for the preparation of compounds of general formula 17 (a compound of general formula I), wherein R ¹ , R ² , R ³ ,L, w, x, y, A1 and A2 have the meaning as given for general formula (I), supra and LG has the meaning as a leaving group, preferably chloro, bromo or a sulfonate group as depicted in scheme 4. Specific examples are described in the subsequent paragraphs.

Step 12 + 8 -» 17 (Scheme 4)

Amine coupling

In the first step (scheme 4) amine derivative 12 and quinazoline derivative 8 are converted to amine 17 in analogy to literature procedures. Typically the reaction is performed in an organic solvent such as for example THF, DMF, acetonitrile dichloromethane or isopropyl alcohol with or without a base such as for example triethylamine, N-ethyl-N,N- diisopropylamine, potassium carbonate or potassium tert-butylate.

For LG = chloro see for example the literature references WO2008/86462; WO2008/86462 or European Journal of Medicinal Chemistry, 2015, 462 and references therein.

For LG = bromo see for example the literature references US2009/247519 or Journal of Organic Chemistry, 2009, 8460 and references therein.

For LG = tosylate see for example the literature references Synthetic Communications, 2012, 1715; Synthesis 2015, 2055 or Bioorganic and Medicinal Chemistry Letters, 2013, 2663 and references therein. For LG = triflate see for example the literature references Bioorganic and Medicinal Chemistry Letters, 2013, 3325 and references therein.

For LG = 2,4,6-triisopropylbenzenesulfonate see for example the literature reference WO2010/99379 and references therein.

19

Hal is CI, Br, I

OR

OR

Scheme 5: Alternative route for the preparation of compounds of general formula 12', wherein R ² , R ³ ,w, y, A1 and A2 have the meaning as given for general formula (I), supra, L' is a direct bond or an ethendiyl bridge and Hal has the meaning as chloro, bromo, iodo, and R is hydrogen or alkyl, preferably both R groups for a pinacolyl residue (as depicted in scheme 5). Specific examples are described in the subsequent paragraphs.

Step 18 + 20 -» 12 (Scheme 5)

C-C cross coupling reaction

Halogen comounds of general formula 18' (Scheme 5) can be reacted with a boronic acid derivative 20 to give a compound of formula 12'. The boronic acid derivative may be a boronic acid (R =— H) or an alkyl ester of the boronic acid, e.g. its isopropyl ester (R =— CH(CH3)2), preferably an ester derived from pinacol. The coupling reaction is catalyzed by palladium catalysts, e.g. by Pd(0) catalysts like tetrakis(triphenylphosphine)palladium(0) [Pd(PPh3)4], tris(dibenzylideneacetone)di-palladium(0) 15 [Pd&(dba)3], or by Pd(ll) catalysts like dichlorobis(triphenylphosphine)-palladium(ll) [Pd(PPh3)3CI], palladium(ll) acetate and triphenylphosphine or by [1 ,1 '-bis(diphenylphosphino)ferrocene]palladium dichloride. The reaction is preferably carried out in a mixture of a solvent like 1 ,2-dimethoxyethane, dioxane, DMF, DME, THF, or isopropanol with water and in the presence of a base like potassium carbonate, sodium bicarbonate or potassium phosphate. For a review see D.G. Hall, Boronic Acids, 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, ISBN 3-527-30991 -8 and references cited therein). The reaction is performed at temperatures ranging from room temperature to the boiling point of the solvent. Further on, the reaction can be performed at temperatures above the boiling point under pressure. The reaction is preferably completed after 1 to 36 hours.

Step 18 -> 19 (Scheme 5)

Formation of boronates / boronic acids

Halogogen derivative 18' are converted to boronic acid derivative 22 in analogy to literature procedures (scheme 5).

For Hal = bromo or iodo and ^* -B(OR)2 = boronic acid pinacol ester the reaction is typically performed with bis(pinacolato)diboron, a palladium catalyst as for example palladium diacetate or dichloro(1 ,1 '-bis(diphenylphosphanyl)ferrocene)palladium(ll) dichloromethane adduct a base as for example potassium acetate or triethylamine in an organic solvent as for example DMF, DMSO, acetonitrile. See for example the literature references WO2010/150192, WO2012/158795 or Journal of Medicinal Chemistry, 2006, 5671 and references therein.

For Hal = chloro and ^* -B(OR)2 = boronic acid pinacole ester see for example the literature references Organic Letters, 2002, 543 or Journal of Organic Chemistry, 2012, 3543 and references therein.

For Hal = bromo or iodo and ^* -B(OR)2 = boronic acid or boronic acid methyl ester the reaction is typically performed with butyllithium or magnesium / iodine, boronic acid trimethylester in an organic solvent as for example THF, hexane. See for example the literature references Organic and Biomolecular Chemistry, 2012, 6693, Journal of the American Chemical Society, 2009, 17500 or Organic Letters, 2011 , 4479 and references therein.

Step 19 + 21 ^ 12 (Scheme 5)

C-C cross coupling reaction

Halogen comounds of general formula 21 (Scheme 5) can be reacted with a boronic acid derivative 19 to give a compound of formula 12'. The boronic acid derivative may be a boronic acid (R =— H) or an alkyl ester of the boronic acid, e.g. its isopropyl ester (R =— CH(CH3)2), preferably an ester derived from pinacol. The coupling reaction is catalyzed by palladium catalysts, e.g. by Pd(0) catalysts like tetrakis(triphenylphosphine)palladium(0) [Pd(PPh3)4], tris(dibenzylideneacetone)di-palladium(0) 15 [Pd&(dba)3], or by Pd(ll) catalysts like dichlorobis(triphenylphosphine)-palladium(ll) [Pd(PPh3)3CI], palladium(ll) acetate and triphenylphosphine or by [1 ,1 '-bis(diphenylphosphino)ferrocene]palladium dichloride. The reaction is preferably carried out in a mixture of a solvent like 1 ,2-dimethoxyethane, dioxane, DMF, DME, THF, or isopropanol with water and in the presence of a base like potassium carbonate, sodium bicarbonate or potassium phosphate. For a review see D.G. Hall, Boronic Acids, 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, ISBN 3-527-30991 -8 and references cited therein). The reaction is performed at temperatures ranging from room temperature to the boiling point of the solvent. Further on, the reaction can be performed at temperatures above the boiling point under pressure. The reaction is preferably completed after 1 to 36 hours.

Hal is CI, Br, I

Scheme 6: Route for the preparation of compounds of general formula 22, wherein R ¹ , R ² , L, LG, w, x, A1 and A2 have the meaning as given for general formula (I), supra and Hal is chloro, bromo or iodo and W has the meaning as a leaving group, preferably chloro, bromo or a sulfonate group as depicted in scheme 4. Specific examples are described in the subsequent paragraphs.

Step 18 + 8 -> 22 (Scheme 6)

In the first step (scheme 6) amine derivative 18 and quinazoline derivative 8 are converted to amine 22 in analogy to literature procedures. Typically the reaction is performed in an organic solvent such as for example THF, DMF, acetonitrile dichloromethane or isopropyl alcohol with or without a base such as for example triethylamine, N-ethyl-N,N- diisopropylamine, potassium carbonate or potassium tert-butylate.

For LG = chloro see for example the literature references WO2008/86462; WO2008/86462 or European Journal of Medicinal Chemistry, 2015, 462 and references therein.

For LG = bromo see for example the literature references US2009/247519 or Journal of Organic Chemistry, 2009, 8460 and references therein.

For LG = tosylate see for example the literature references Synthetic Communications, 2012, 1715; Synthesis 2015, 2055 or Bioorganic and Medicinal Chemistry Letters, 2013, 2663 and references therein.

For LG = triflate see for example the literature references Bioorganic and Medicinal Chemistry Letters, 2013, 3325 and references therein.

For LG = 2,4,6-triisopropylbenzenesulfonate see for example the literature reference WO2010/99379 and references therein.

² ) _W -L ^' -A2(R ³ )

23

C H

OR O H 3

O-Alkyl ,C H ,

* -B is *— B * -B * -B

OR O H O-Alkyl -C H .

C H .

Hal is CI, Br, I

Scheme 7: Route for the preparation of compounds of general formula 17 (a compound of general formula I), wherein R ¹ , R ² , R ³ , w, x, y, A1 and A2 have the meaning as given for general formula (I), supra, L' is a direct bond or an ethendiyl bridge and Hal is chloro, bromo or iodo and R is hydrogen, alkyl or both R groups form a pinacolyl as depicted in scheme 7. Specific examples are described in the subsequent paragraphs.

Step 22 + 20 -» 17 (Scheme 7)

C-C cross coupling reaction

Halogen comounds of general formula 22 (Scheme 7) can be reacted with a boronic acid derivative 20 to give a compound of formula 17. The boronic acid derivative may be a boronic acid (R =— H) or an alkyl ester of the boronic acid, e.g. its isopropyl ester (R =— CH(CH3)2), preferably an ester derived from pinacol. The coupling reaction is catalyzed by palladium catalysts, e.g. by Pd(0) catalysts like tetrakis(triphenylphosphine)palladium(0) [Pd(PPh3)4], tris(dibenzylideneacetone)di-palladium(0) [Pd2 (dba)3], or by Pd(ll) catalysts like dichlorobis(triphenylphosphine)-palladium(ll) [Pd(PPh3)3CI], palladium(ll) acetate and triphenylphosphine or by [1 ,1 '-bis(diphenylphosphino)ferrocene]palladium dichloride. The reaction is preferably carried out in a mixture of a solvent like 1 ,2-dimethoxyethane, dioxane, DMF, DME, THF, or isopropanol with water and in the presence of a base like potassium carbonate, sodium bicarbonate or potassium phosphate. For a review see D.G. Hall, Boronic Acids, 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, ISBN 3-527-30991 -8 and references cited therein). The reaction is performed at temperatures ranging from room temperature to the boiling point of the solvent. Further on, the reaction can be performed at temperatures above the boiling point under pressure. The reaction is preferably completed after 1 to 36 hours.

Step 22 -> 23 (Scheme 7)

Formation of boronates / boronic acids

Halogogen derivative 22 are converted to boronic acid derivative 23 in analogy to literature procedures (scheme 7).

For Hal = bromo or iodo and ^* -B(OR)2 = boronic acid pinacole ester the reaction is typically performed with bis(pinacolato)diboron, a palladium catalyst as for example palladium diacetate or dichloro(1 ,1 '-bis(diphenylphosphanyl)ferrocene)palladium(ll) dichloromethane adduct a base as for example potassium acetate or triethylamine in an organic solvent as for example DMF, DMSO, acetonitrile. See for example the literature references WO2010/150192, WO2012/158795 or Journal of Medicinal Chemistry, 2006, 5671 and references therein.

For Hal = bromo or iodo and ^* -B(OR)2 = boronic acid or boronic acid methyl ester the reaction is typically performed with butyllithium or magnesium / iodine, boronic acid trimethylester in an organic solvent as for example THF, hexane. See for example the literature references Organic and Biomolecular Chemistry, 2012, 6693, Journal of the American Chemical Society, 2009, 17500 or Organic Letters, 2011 , 4479 and references therein.

Step 23 + 21 ^ 17 (Scheme 7)

C-C cross coupling reaction

Halogen comounds of general formula 21 (Scheme 7) can be reacted with a boronic acid derivative 23 to give a compound of formula 17. The boronic acid derivative may be a boronic acid (R =— H) or an alkyl ester of the boronic acid, e.g. its isopropyl ester (R =— CH(CH3)2), preferably an ester derived from pinacol. The coupling reaction is catalyzed by palladium catalysts, e.g. by Pd(0) catalysts like tetrakis(triphenylphosphine)palladium(0) [Pd(PPh3)4], tris(dibenzylideneacetone)di-palladium(0) 15 [Pd&(dba)3], or by Pd(ll) catalysts like dichlorobis(triphenylphosphine)-palladium(ll) [Pd(PPh3)3CI], palladium(ll) acetate and triphenylphosphine or by [1 ,1 '-bis(diphenylphosphino)ferrocene]palladium dichloride. The reaction is preferably carried out in a mixture of a solvent like 1 ,2-dimethoxyethane, dioxane, DMF, DME, THF, or isopropanol with water and in the presence of a base like potassium carbonate, sodium bicarbonate or potassium phosphate. For a review see D.G. Hall, Boronic Acids, 2005 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, ISBN 3-527-30991 -8 and references cited therein). The reaction is performed at temperatures ranging from room temperature to the boiling point of the solvent. Further on, the reaction can be performed at temperatures above the boiling point under pressure. The reaction is preferably completed after 1 to 36 hours.

In accordance with a further aspect, the present invention covers intermediate compounds which are useful in the preparation of compounds of the present invention of general formula (I), particularly in the methods described herein. In particular, the present invention covers compounds of general formula II,

II in which R ¹ , R ² , A1 , R ² , L', w and x have the same meanings as defined for the compound of general (I) supra, and Z is

Hal (iodo, bromo or chloro) or

C H,

OR O H O-Alkyl -C H,

*— B which is *— B *— B *— B

OR O H O-Alkyl -C H*

C H,

The present invention covers the intermediate compounds which are disclosed in the Example Section of this text, infra.

The present invention covers any sub-combination within any embodiment or aspect of the present invention of intermediate compounds of general formula (II), supra.

In accordance with another aspect, the present invention covers methods of preparing compounds of the present invention, said methods comprising the step as described below and / or the Experimental Section. In particular, the present invention covers a method to prepare compounds of general formula I supra,

X1

X2 characterized in that compounds of general formula X1 and X2, in which R ¹ , R ² , R ³ , L, w, x, y, A1 and A2 have the same meaning as defined for compounds of general formula (I) and LG is a leaving group as chloro, bromo, iodo, fluoro, triflate, tosylate, mesitylate or nonaflate, are reacted in an organic solvent at a temperature between -20°C and the boiling point of a solvent, preferably between ambient temperature and the boiling point of the solvent, with or without a base to obtain compounds of general formula I.

The preparation of compounds of general formula I can be performed in a protic or aprotic solvent, preferably in dioxan, tetrahydrofuran, Ν,Ν-dimethylformamide, dimethylsulfoxid, methanol, ethanol or 2-propanol.

Preferred bases which can be used for the preparation of compounds of the general formula I are N,N-diisopropylethylamin or triethylamin.

Said compound of general formula I can then optionally be converted into solvates, salts and/or solvates of such salts using the corresponding (i) solvents and/or (ii) bases or acids.

The present invention covers methods of preparing compounds of the present invention of general formula (I), said methods comprising the steps as described in the Experimental Section herein.

The compounds of general formula (I) of the present invention can be converted to any salt, preferably pharmaceutically acceptable salts, as described herein, by any method which is known to the person skilled in the art. Similarly, any salt of a compound of general formula (I) of the present invention can be converted into the free compound, by any method which is known to the person skilled in the art.

For the synthesis of deuterated intermediates and test compounds of the general formula I the same general procedures as described before can be applied by using the corresponding deuterated reagents. For example, compound 3 can be converted to compound 7D by using deuterated acetyl chloride. o

Scheme 8: To obtain deuterated methyl compounds of general formula 12D3 one can use the described general procedures using deuterated organo metal reagents such as for example CDsMgl , CDsMgBr, CDsMgCI, CD3L1 for the conversion of compound 10 to compound H D3.

10

H D3 I2 D3

Scheme 9: Deuterated compounds of general formula 12Di can be obtained for example by reduction of compound 16 with sodium borodeuteride, titanium tetrachloride in ethylene glycol dimethyl ether (see for example Acta Crystallographica Section B: Structural Science, 2000 56, pages 245 - 253). (R ² ) _W -L-A2(R ³ ) _y

16 12D ₃

One of the most fundamental characteristics of cancer cells is their ability to sustain chronic proliferation whereas in normal tissues the entry into and progression through the cell division cycle is tightly controlled to ensure a homeostasis of cell number and maintenance of normal tissue function. Loss of proliferation control is emphasized as one of the six hallmarks of cancer [Hanahan D and Weinberg 15 RA, Cell 100, 57, 2000; Hanahan D and Weinberg RA, Cell 144, 646, 201 1].

Compounds of general formula (I) of the present invention demonstrate a valuable pharmacological spectrum of action which could not have been predicted. Compounds of the present invention have surprisingly been found to effectively inhibit the Ras-Sos interaction and it is possible therefore that said compounds be used for the treatment or prophylaxis of diseases, preferably hyperproliferative disorders in humans and animals.

Compounds of the present invention can be utilized to inhibit, block, reduce, decrease, eic, cell proliferation and/or cell division, and/or produce apoptosis. This method comprises administering to a mammal in need thereof, including a human, an amount of a compound of general formula (I) of the present invention, or a pharmaceutically acceptable salt, isomer, polymorph, metabolite, hydrate, solvate or ester thereof, which is effective to treat the disorder.

Hyperproliferative disorders include, but are not limited to, for example: psoriasis, keloids, and other hyperplasias affecting the skin, benign prostate hyperplasia (BPH), solid tumours, such as cancers of the breast, respiratory tract, brain, reproductive organs, digestive tract, urinary tract, eye, liver, skin, head and neck, thyroid, parathyroid and their distant metastases. Those disorders also include lymphomas, sarcomas, and leukaemias.

Examples of breast cancers include, but are not limited to, invasive ductal carcinoma, invasive lobular carcinoma, ductal carcinoma in situ, and lobular carcinoma in situ.

Examples of cancers of the respiratory tract include, but are not limited to, small-cell and non-small-cell lung carcinoma, as well as bronchial adenoma and pleuropulmonary blastoma. Examples of brain cancers include, but are not limited to, brain stem and hypophtalmic glioma, cerebellar and cerebral astrocytoma, medulloblastoma, ependymoma, as well as neuroectodermal and pineal tumour.

Tumours of the male reproductive organs include, but are not limited to, prostate and testicular cancer.

Tumours of the female reproductive organs include, but are not limited to, endometrial, cervical, ovarian, vaginal, and vulvar cancer, as well as sarcoma of the uterus.

Tumours of the digestive tract include, but are not limited to, anal, colon, colorectal, oesophageal, gallbladder, gastric, pancreatic, rectal, small-intestine, and salivary gland cancers.

Tumours of the urinary tract include, but are not limited to, bladder, penile, kidney, renal pelvis, ureter, urethral and human papillary renal cancers.

Eye cancers include, but are not limited to, intraocular melanoma and retinoblastoma.

Examples of liver cancers include, but are not limited to, hepatocellular carcinoma (liver cell carcinomas with or without fibrolamellar variant), cholangiocarcinoma (intrahepatic bile duct carcinoma), and mixed hepatocellular cholangiocarcinoma.

Skin cancers include, but are not limited to, squamous cell carcinoma, Kaposi's sarcoma, malignant melanoma, Merkel cell skin cancer, and non-melanoma skin cancer.

Head-and-neck cancers include, but are not limited to, laryngeal, hypopharyngeal, nasopharyngeal, oropharyngeal cancer, lip and oral cavity cancer and squamous cell.

Lymphomas include, but are not limited to, AIDS-related lymphoma, non-Hodgkin's lymphoma, cutaneous T-cell lymphoma, Burkitt lymphoma, Hodgkin's disease, and lymphoma of the central nervous system.

Sarcomas include, but are not limited to, sarcoma of the soft tissue, osteosarcoma, malignant fibrous histiocytoma, lymphosarcoma, and rhabdomyosarcoma.

Leukemias include, but are not limited to, acute myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, chronic myelogenous leukemia, and hairy cell leukemia.

The present invention also provides methods of treating angiogenic disorders including diseases associated with excessive and/or abnormal angiogenesis.

Inappropriate and ectopic expression of angiogenesis can be deleterious to an organism. A number of pathological conditions are associated with the growth of extraneous blood vessels. These include, for example, diabetic retinopathy, ischemic retinal-vein occlusion, and retinopathy of prematurity [Aiello et al., New Engl. J. Med., 1994, 331 , 1480 ; Peer et al., Lab. Invest., 1995, 72, 638], age-related macular degeneration (AMD) [Lopez et al., Invest. Opththalmol. Vis. Sci., 1996, 37, 855], neovascular glaucoma, psoriasis, retrolental fibroplasias, angiofibroma, inflammation, rheumatoid arthritis (RA), restenosis, in-stent restenosis, vascular graft restenosis, etc. In addition, the increased blood supply associated with cancerous and neoplastic tissue, encourages growth, leading to rapid tumour enlargement and metastasis. Moreover, the growth of new blood and lymph vessels in a tumour provides an escape route for renegade cells, encouraging metastasis and the consequence spread of the cancer. Thus, compounds of general formula (I) of the present invention can be utilized to treat and/or prevent any of the aforementioned angiogenesis disorders, for example by inhibiting and/or reducing blood vessel formation; by inhibiting, blocking, reducing, decreasing, etc. endothelial cell proliferation, or other types involved in angiogenesis, as well as causing cell death or apoptosis of such cell types.

These disorders have been well characterized in humans, but also exist with a similar etiology in other mammals, and can be treated by administering pharmaceutical compositions of the present invention.

The term "treating" or "treatment" as stated throughout this document is used conventionally, for example the management or care of a subject for the purpose of combating, alleviating, reducing, relieving, improving the condition of a disease or disorder, such as a carcinoma.

The compounds of the present invention can be used in particular in therapy and prevention, i.e. prophylaxis, of tumour growth and metastases, especially in solid tumours of all indications and stages with or without pre-treatment of the tumour growth.

Generally, the use of chemotherapeutic agents and/or anti-cancer agents in combination with a compound or pharmaceutical composition of the present invention will serve to:

1 . yield better efficacy in reducing the growth of a tumour or even eliminate the tumour as compared to administration of either agent alone,

2. provide for the administration of lesser amounts of the administered chemotherapeutic agents,

3. provide for a chemotherapeutic treatment that is well tolerated in the patient with fewer deleterious pharmacological complications than observed with single agent chemotherapies and certain other combined therapies,

4. provide for treating a broader spectrum of different cancer types in mammals, especially humans,

5. provide for a higher response rate among treated patients, 6. provide for a longer survival time among treated patients compared to standard chemotherapy treatments,

7. provide a longer time for tumour progression, and/or

8. yield efficacy and tolerability results at least as good as those of the agents used alone, compared to known instances where other cancer agent combinations produce antagonistic effects.

In addition, the compounds of general formula (I) of the present invention can also be used in combination with radiotherapy and/or surgical intervention.

In a further embodiment of the present invention, the compounds of general formula (I) of the present invention may be used to sensitize a cell to radiation, i.e. treatment of a cell with a compound of the present invention prior to radiation treatment of the cell renders the cell more susceptible to DNA damage and cell death than the cell would be in the absence of any treatment with a compound of the present invention. In one aspect, the cell is treated with at least one compound of general formula (I) of the present invention.

Thus, the present invention also provides a method of killing a cell, wherein a cell is administered one or more compounds of the present invention in combination with conventional radiation therapy.

The present invention also provides a method of rendering a cell more susceptible to cell death, wherein the cell is treated with one or more compounds of general formula (I) of the present invention prior to the treatment of the cell to cause or induce cell death. In one aspect, after the cell is treated with one or more compounds of general formula (I) of the present invention, the cell is treated with at least one compound, or at least one method, or a combination thereof, in order to cause DNA damage for the purpose of inhibiting the function of the normal cell or killing the cell.

In other embodiments of the present invention, a cell is killed by treating the cell with at least one DNA damaging agent, i.e. after treating a cell with one or more compounds of general formula (I) of the present invention to sensitize the cell to cell death, the cell is treated with at least one DNA damaging agent to kill the cell. DNA damaging agents useful in the present invention include, but are not limited to, chemotherapeutic agents (e.g. cis platin), ionizing radiation (X-rays, ultraviolet radiation), carcinogenic agents, and mutagenic agents.

In other embodiments, a cell is killed by treating the cell with at least one method to cause or induce DNA damage. Such methods include, but are not limited to, activation of a cell signalling pathway that results in DNA damage when the pathway is activated, inhibiting of a cell signalling pathway that results in DNA damage when the pathway is inhibited, and inducing a biochemical change in a cell, wherein the change results in DNA damage. By way of a non-limiting example, a DNA repair pathway in a cell can be inhibited, thereby preventing the repair of DNA damage and resulting in an abnormal accumulation of DNA damage in a cell.

In one aspect of the invention, a compound of general formula (I) of the present invention is administered to a cell prior to the radiation or other induction of DNA damage in the cell. In another aspect of the invention, a compound of general formula (I) of the present invention is administered to a cell concomitantly with the radiation or other induction of DNA damage in the cell. In yet another aspect of the invention, a compound of general formula (I) of the present invention is administered to a cell immediately after radiation or other induction of DNA damage in the cell has begun.

In another aspect, the cell is in vitro. In another embodiment, the cell is in vivo.

It is possible for the compounds according to the invention to have systemic and/or local activity. For this purpose, they can be administered in a suitable manner, such as, for example, via the oral, parenteral, pulmonary, nasal, sublingual, lingual, buccal, rectal, vaginal, dermal, transdermal, conjunctival, otic route or as an implant or stent.

For these administration routes, it is possible for the compounds according to the invention to be administered in suitable administration forms.

For oral administration, it is possible to formulate the compounds according to the invention to dosage forms known in the art that deliver the compounds of the invention rapidly and/or in a modified manner, such as, for example, tablets (uncoated or coated tablets, for example with enteric or controlled release coatings that dissolve with a delay or are insoluble), orally- disintegrating tablets, films/wafers, films/lyophylisates, capsules (for example hard or soft gelatine capsules), sugar-coated tablets, granules, pellets, powders, emulsions, suspensions, aerosols or solutions. It is possible to incorporate the compounds according to the invention in crystalline and/or amorphised and/or dissolved form into said dosage forms.

Parenteral administration can be effected with avoidance of an absorption step (for example intravenous, intraarterial, intracardial, intraspinal, intralumbal or intratumoral) or with inclusion of absorption (for example intramuscular, subcutaneous, intracutaneous, percutaneous or intraperitoneal). Administration forms which are suitable for parenteral administration are, inter alia, preparations for injection and infusion in the form of solutions, suspensions, emulsions, lyophylisates or sterile powders.

Examples which are suitable for other administration routes are pharmaceutical forms for inhalation [inter alia powder inhalers, nebulizers], nasal drops, nasal solutions, nasal sprays; tablets/films/wafers/capsules for lingual, sublingual or buccal administration; suppositories; eye drops, eye ointments, eye baths, ocular inserts, ear drops, ear sprays, ear powders, ear- rinses, ear tampons; vaginal capsules, aqueous suspensions (lotions, mixturae agitandae), lipophilic suspensions, emulsions, ointments, creams, transdermal therapeutic systems (such as, for example, patches), milk, pastes, foams, dusting powders, implants or stents.

The compounds according to the invention can be incorporated into the stated administration forms. This can be effected in a manner known per se by mixing with pharmaceutically suitable excipients. Pharmaceutically suitable excipients include, inter alia,

• fillers and carriers (for example cellulose, microcrystalline cellulose (such as, for example, Avicel®), lactose, mannitol, starch, calcium phosphate (such as, for example, Di-Cafos®)),

• ointment bases (for example petroleum jelly, paraffins, triglycerides, waxes, wool wax, wool wax alcohols, lanolin, hydrophilic ointment, polyethylene glycols),

• bases for suppositories (for example polyethylene glycols, cacao butter, hard fat),

• solvents (for example water, ethanol, isopropanol, glycerol, propylene glycol, medium chain-length triglycerides fatty oils, liquid polyethylene glycols, paraffins),

• surfactants, emulsifiers, dispersants or wetters (for example sodium dodecyl sulfate), lecithin, phospholipids, fatty alcohols (such as, for example, Lanette®), sorbitan fatty acid esters (such as, for example, Span®), polyoxyethylene sorbitan fatty acid esters (such as, for example, Tween®), polyoxyethylene fatty acid glycerides (such as, for example, Cremophor®), polyoxethylene fatty acid esters, polyoxyethylene fatty alcohol ethers, glycerol fatty acid esters, poloxamers (such as, for example, Pluronic®),

• buffers, acids and bases (for example phosphates, carbonates, citric acid, acetic acid, hydrochloric acid, sodium hydroxide solution, ammonium carbonate, trometamol, triethanolamine),

• isotonicity agents (for example glucose, sodium chloride),

• adsorbents (for example highly-disperse silicas),

• viscosity-increasing agents, gel formers, thickeners and/or binders (for example polyvinylpyrrolidone, methylcellulose, hydroxypropylmethylcellulose, hydroxypropyl- cellulose, carboxymethylcellulose-sodium, starch, carbomers, polyacrylic acids (such as, for example, Carbopol®); alginates, gelatine), • disintegrants (for example modified starch, carboxymethylcellulose-sodium, sodium starch glycolate (such as, for example, Explotab®), cross- linked polyvinylpyrrolidone, croscarmellose-sodium (such as, for example, AcDiSol®)),

• flow regulators, lubricants, glidants and mould release agents (for example magnesium stearate, stearic acid, talc, highly-disperse silicas (such as, for example, Aerosil®)),

• coating materials (for example sugar, shellac) and film formers for films or diffusion membranes which dissolve rapidly or in a modified manner (for example polyvinylpyrrolidones (such as, for example, Kollidon®), polyvinyl alcohol, hydroxypropylmethylcellulose, hydroxypropylcellulose, ethylcellulose, hydroxypropyl- methylcellulose phthalate, cellulose acetate, cellulose acetate phthalate, polyacrylates, polymethacrylates such as, for example, Eudragit®)),

• capsule materials (for example gelatine, hydroxypropylmethylcellulose),

• synthetic polymers (for example polylactides, polyglycolides, polyacrylates, polymethacrylates (such as, for example, Eudragit®), polyvinylpyrrolidones (such as, for example, Kollidon®), polyvinyl alcohols, polyvinyl acetates, polyethylene oxides, polyethylene glycols and their copolymers and blockcopolymers),

• plasticizers (for example polyethylene glycols, propylene glycol, glycerol, triacetine, triacetyl citrate, dibutyl phthalate),

• penetration enhancers,

• stabilisers (for example antioxidants such as, for example, ascorbic acid, ascorbyl palmitate, sodium ascorbate, butylhydroxyanisole, butylhydroxytoluene, propyl gallate),

• preservatives (for example parabens, sorbic acid, thiomersal, benzalkonium chloride, chlorhexidine acetate, sodium benzoate),

• colourants (for example inorganic pigments such as, for example, iron oxides, titanium dioxide),

• flavourings, sweeteners, flavour- and/or odour-masking agents.

The present invention furthermore relates to a pharmaceutical composition which comprise at least one compound according to the invention, conventionally together with one or more pharmaceutically suitable excipient(s), and to their use according to the present invention. In accordance with another aspect, the present invention covers pharmaceutical combinations, in particular medicaments, comprising at least one compound of general formula (I) of the present invention and at least one or more further active ingredients, in particular for the treatment and/or prophylaxis of a hyper-proliferative disorder, in particular cancer.

Particularly, the present invention covers a pharmaceutical combination, which comprises:

• one or more first active ingredients, in particular compounds of general formula (I) as defined supra, and

• one or more further active ingredients, in particular those used for treatment of hyper- proliferative disorder, in particular cancer.

The term "combination" in the present invention is used as known to persons skilled in the art, it being possible for said combination to be a fixed combination, a non-fixed combination or a kit-of-parts.

A "fixed combination" in the present invention is used as known to persons skilled in the art and is defined as a combination wherein, for example, a first active ingredient, such as one or more compounds of general formula (I) of the present invention, and a further active ingredient are present together in one unit dosage or in one single entity. One example of a "fixed combination" is a pharmaceutical composition wherein a first active ingredient and a further active ingredient are present in admixture for simultaneous administration, such as in a formulation. Another example of a "fixed combination" is a pharmaceutical combination wherein a first active ingredient and a further active ingredient are present in one unit without being in admixture.

A non-fixed combination or "kit-of-parts" in the present invention is used as known to persons skilled in the art and is defined as a combination wherein a first active ingredient and a further active ingredient are present in more than one unit. One example of a non-fixed combination or kit-of-parts is a combination wherein the first active ingredient and the further active ingredient are present separately. It is possible for the components of the non-fixed combination or kit-of-parts to be administered separately, sequentially, simultaneously, concurrently or chronologically staggered.

The compounds of the present invention can be administered as the sole pharmaceutical agent or in combination with one or more other pharmaceutically active ingredients where the combination causes no unacceptable adverse effects. The present invention also covers such pharmaceutical combinations. For example, the compounds of the present invention can be combined with known anti-tumor agents (cancer therapeutics). Examples of anti-tumor agents (cancer therapeutics) include:

131 1-chTNT, abarelix, abiraterone, aclarubicin, ado-trastuzumab emtansine, afatinib, aflibercept, aldesleukin, alectinib, alemtuzumab, alendronic acid, alitretinoin, altretamine, amifostine, aminoglutethimide, hexyl aminolevulinate, amrubicin, amsacrine, anastrozole, ancestim, anethole dithiolethione, anetumab ravtansine, angiotensin II, antithrombin III, aprepitant, arcitumomab, arglabin, arsenic trioxide, asparaginase, axitinib, azacitidine, basiliximab, belotecan, bendamustine, besilesomab, belinostat, bevacizumab, bexarotene, bicalutamide, bisantrene, bleomycin, blinatumomab, bortezomib, buserelin, bosutinib, brentuximab vedotin, busulfan, cabazitaxel, cabozantinib, calcitonine, calcium folinate, calcium levofolinate, capecitabine, capromab, carboplatin, carboquone, carfilzomib, carmofur, carmustine, catumaxomab, celecoxib, celmoleukin, ceritinib, cetuximab, chlorambucil, chlormadinone, chlormethine, cidofovir, cinacalcet, cisplatin, cladribine, clodronic acid, clofarabine, cobimetinib, copanlisib , crisantaspase, crizotinib, cyclophosphamide, cyproterone, cytarabine, dacarbazine, dactinomycin, daratumumab, darbepoetin alfa, dabrafenib, dasatinib, daunorubicin, decitabine, degarelix, denileukin diftitox, denosumab, depreotide, deslorelin, dianhydrogalactitol, dexrazoxane, dibrospidium chloride, dianhydrogalactitol, diclofenac, dinutuximab, docetaxel, dolasetron, doxifluridine, doxorubicin, doxorubicin + estrone, dronabinol, eculizumab, edrecolomab, elliptinium acetate, elotuzumab, eltrombopag, endostatin, enocitabine, enzalutamide, epirubicin, epitiostanol, epoetin alfa, epoetin beta, epoetin zeta, eptaplatin, eribulin, erlotinib, esomeprazole, estradiol, estramustine, ethinylestradiol, etoposide, everolimus, exemestane, fadrozole, fentanyl, filgrastim, fluoxymesterone, floxuridine, fludarabine, fluorouracil, flutamide, folinic acid, formestane, fosaprepitant, fotemustine, fulvestrant, gadobutrol, gadoteridol, gadoteric acid meglumine, gadoversetamide, gadoxetic acid, gallium nitrate, ganirelix, gefitinib, gemcitabine, gemtuzumab, Glucarpidase, glutoxim, GM-CSF, goserelin, granisetron, granulocyte colony stimulating factor, histamine dihydrochloride, histrelin, hydroxycarbamide, 1-125 seeds, lansoprazole, ibandronic acid, ibritumomab tiuxetan, ibrutinib, idarubicin, ifosfamide, imatinib, imiquimod, improsulfan, indisetron, incadronic acid, ingenol mebutate, interferon alfa, interferon beta, interferon gamma, iobitridol, iobenguane (1231), iomeprol, ipilimumab, irinotecan, Itraconazole, ixabepilone, ixazomib, lanreotide, lansoprazole, lapatinib, lasocholine, lenalidomide, lenvatinib, lenograstim, lentinan, letrozole, leuprorelin, levamisole, levonorgestrel, levothyroxine sodium, lisuride, lobaplatin, lomustine, lonidamine, masoprocol, medroxyprogesterone, megestrol, melarsoprol, melphalan, mepitiostane, mercaptopurine, mesna, methadone, methotrexate, methoxsalen, methylaminolevulinate, methylprednisolone, methyltestosterone, metirosine, mifamurtide, miltefosine, miriplatin, mitobronitol, mitoguazone, mitolactol, mitomycin, mitotane, mitoxantrone, mogamulizumab, molgramostim, mopidamol, morphine hydrochloride, morphine sulfate, nabilone, nabiximols, nafarelin, naloxone + pentazocine, naltrexone, nartograstim, necitumumab, nedaplatin, nelarabine, neridronic acid, netupitant/palonosetron, nivolumabpentetreotide, nilotinib, nilutamide, nimorazole, nimotuzumab, nimustine, nintedanib, nitracrine, nivolumab, obinutuzumab, octreotide, ofatumumab, olaparib, omacetaxine mepesuccinate, omeprazole, ondansetron, oprelvekin, orgotein, orilotimod, osimertinib, oxaliplatin, oxycodone, oxymetholone, ozogamicine, p53 gene therapy, paclitaxel, palbociclib, palifermin, palladium-103 seed, palonosetron, pamidronic acid, panitumumab, panobinostat, pantoprazole, pazopanib, pegaspargase, PEG-epoetin beta (methoxy PEG-epoetin beta), pembrolizumab, pegfilgrastim, peginterferon alfa-2b, pemetrexed, pentazocine, pentostatin, peplomycin, Perflubutane, perfosfamide, Pertuzumab, picibanil, pilocarpine, pirarubicin, pixantrone, plerixafor, plicamycin, poliglusam, polyestradiol phosphate, polyvinylpyrrolidone + sodium hyaluronate, polysaccharide-K, pomalidomide, ponatinib, porfimer sodium, pralatrexate, prednimustine, prednisone, procarbazine, procodazole, propranolol, quinagolide, rabeprazole, racotumomab, radium-223 chloride, radotinib, raloxifene, raltitrexed, ramosetron, ramucirumab, ranimustine, rasburicase, razoxane, refametinib , regorafenib, risedronic acid, rhenium-186 etidronate, rituximab, rolapitant, romidepsin, romiplostim, romurtide, roniciclib , samarium (153Sm) lexidronam, sargramostim, satumomab, secretin, siltuximab, sipuleucel-T, sizofiran, sobuzoxane, sodium glycididazole, sonidegib, sorafenib, stanozolol, streptozocin, sunitinib, talaporfin, talimogene laherparepvec, tamibarotene, tamoxifen, tapentadol, tasonermin, teceleukin, technetium (99mTc) nofetumomab merpentan, 99mTc-HYNIC-[Tyr3]-octreotide, tegafur, tegafur + gimeracil + oteracil, temoporfin, temozolomide, temsirolimus, teniposide, testosterone, tetrofosmin, thalidomide, thiotepa, thymalfasin, thyrotropin alfa, tioguanine, tocilizumab, topotecan, toremifene, tositumomab, trabectedin, trametinib, tramadol, trastuzumab, trastuzumab emtansine, treosulfan, tretinoin, trifluridine + tipiracil, trilostane, triptorelin, trametinib, trofosfamide, thrombopoietin, tryptophan, ubenimex, valatinib , valrubicin, vandetanib, vapreotide, vemurafenib, vinblastine, vincristine, vindesine, vinflunine, vinorelbine, vismodegib, vorinostat, vorozole, yttrium-90 glass microspheres, zinostatin, zinostatin stimalamer, zoledronic acid, zorubicin.

Based upon standard laboratory techniques known to evaluate compounds useful for the treatment of hyper-proliferative disorders, by standard toxicity tests and by standard pharmacological assays for the determination of treatment of the conditions identified above in mammals, and by comparison of these results with the results of known active ingredients or medicaments that are used to treat these conditions, the effective dosage of the compounds of the present invention can readily be determined for treatment of each desired indication. The amount of the active ingredient to be administered in the treatment of one of these conditions can vary widely according to such considerations as the particular compound and dosage unit employed, the mode of administration, the period of treatment, the age and sex of the patient treated, and the nature and extent of the condition treated.

The total amount of the active ingredient to be administered will generally range from about 0.001 mg/kg to about 200 mg/kg body weight per day, and preferably from about 0.01 mg/kg to about 20 mg/kg body weight per day. Clinically useful dosing schedules will range from one to three times a day dosing to once every four weeks dosing. In addition, it is possible for "drug holidays", in which a patient is not dosed with a drug for a certain period of time, to be beneficial to the overall balance between pharmacological effect and tolerability. It is possible for a unit dosage to contain from about 0.5 mg to about 1500 mg of active ingredient, and can be administered one or more times per day or less than once a day. The average daily dosage for administration by injection, including intravenous, intramuscular, subcutaneous and parenteral injections, and use of infusion techniques will preferably be from 0.01 to 200 mg/kg of total body weight. The average daily rectal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight. The average daily vaginal dosage regimen will preferably be from 0.01 to 200 mg/kg of total body weight. The average daily topical dosage regimen will preferably be from 0.1 to 200 mg administered between one to four times daily. The transdermal concentration will preferably be that required to maintain a daily dose of from 0.01 to 200 mg/kg. The average daily inhalation dosage regimen will preferably be from 0.01 to 100 mg/kg of total body weight.

Of course the specific initial and continuing dosage regimen for each patient will vary according to the nature and severity of the condition as determined by the attending diagnostician, the activity of the specific compound employed, the age and general condition of the patient, time of administration, route of administration, rate of excretion of the drug, drug combinations, and the like. The desired mode of treatment and number of doses of a compound of the present invention or a pharmaceutically acceptable salt or ester or composition thereof can be ascertained by those skilled in the art using conventional treatment tests.

EXPERIMENTAL SECTION

The following table 1 lists the abbreviations used in this paragraph and in the Examples section as far as they are not explained within the text body. Other abbreviations have their meanings customary per se to the skilled person. Table 1 : Abbreviations

BuLi Butyllithium

DCE Dichloroethane

DCM Dichloromethane

DMF Dimethylformamide

DMSO Dimethyl sulfoxide

EA Ethyl acetate

HPLC, LC high performance liquid chromatoc

h hour

□ HMDS Lithium bis(trimethylsilyl)amide

KHMDS Potassium bis(trimethylsilyl)amide

KOtBu Potassium ie f-butoxide

min minute

LDA Lithiumdiisopropylamid

MS mass spectroscopy

NMR nuclear magnetic resonance

NaHMDS Sodium bis(trimethylsilyl)amide

PE Petrol ether

Rac Racemate

R _f Retardiation factor

Rt Retention time

RT Room temperature

TFA Trifluoroacetic acid

THF Tetrahydrofuran

TLC thin-layer chromatography

Chemical names were generated using ACD/Name Batch Version 12.01 or Autonom 2000.

All reagents, for which the synthesis is not described in the experimental part, are either commercially available or synthesized as described in literature references.

The various aspects of the invention described in this application are illustrated by the following examples which are not meant to limit the invention in anyway.

The example testing experiments described herein serve to illustrate the present invention and the invention is not limited to the examples given. EXPERIMENTAL SECTION - GENERAL PART

All reagents, for which the synthesis is not described in the experimental part, are either commercially available, or are known compounds or may be formed from known compounds by known methods by a person skilled in the art.

The compounds and intermediates produced according to the methods of the invention may require purification. Purification of organic compounds is well known to the person skilled in the art and there may be several ways of purifying the same compound. In some cases, no purification may be necessary. In some cases, the compounds may be purified by crystallization. In some cases, impurities may be stirred out using a suitable solvent. In some cases, the compounds may be purified by chromatography, particularly flash column chromatography, using for example prepacked silica gel cartridges, e.g. Biotage SNAP cartidges KP-Sil ^® or KP-NH ^® in combination with a Biotage autopurifier system (SP4 ^® or Isolera Four ^® ) and eluents such as gradients of hexane/ethyl acetate or DCM/methanol. In some cases, the compounds may be purified by preparative HPLC using for example a Waters autopurifier equipped with a diode array detector and/or on-line electrospray ionization mass spectrometer in combination with a suitable prepacked reverse phase column and eluents such as gradients of water and acetonitrile which may contain additives such as trifluoroacetic acid, formic acid or aqueous ammonia.

In some cases, purification methods as described above can provide those compounds of the present invention which possess a sufficiently basic or acidic functionality in the form of a salt, such as, in the case of a compound of the present invention which is sufficiently basic, a trifluoroacetate or formate salt for example, or, in the case of a compound of the present invention which is sufficiently acidic, an ammonium salt for example. A salt of this type can either be transformed into its free base or free acid form, respectively, by various methods known to the person skilled in the art, or be used as salts in subsequent biological assays. It is to be understood that the specific form (e.g. salt, free base etc.) of a compound of the present invention as isolated and as described herein is not necessarily the only form in which said compound can be applied to a biological assay in order to quantify the specific biological activity. EXPERIMENTAL SECTION - EXAMPLES Analytical Methods

LC-MS Method 1 :

Column: Ascentis Express C18 2.7 μπι, 30x2.1 mm

Fragment, potential: 50 V

Mass range: 80-800 m/z

Solvent: A = H ₂ O + 0.1 %vol HCOOH

B = methanol + 0.1 %vol HCOOH

0-1 min 5% B, 1 -4 min 5-100% B 4-5 min 100% B, 5-6 min 100-

Gradient:

5% B, 6-6.5 min 5% B

Flow: 0.8 mL/min

Temperature: 30°C

Injection: 1 .0 μί.

Detection: MM-ES + APCI + DAD (254 nm)

System time delay: 0.2 min

LC-MS Method 2:MS instrument type: Micromass Quatro Micro; HPLC instrument type: Agilent 1100 Series; UV DAD; column: Chromolith Flash RP-18E 25-2 mm; mobile phase A: 0.0375% TFA in water, mobile phase B: 0.01875% TFA in acetonitrile; gradient: 0.0 min 100% A -» 1 .0 min 95% A -» 3.0 min 95% A -» 3.5 min 5% A -» 3.51 min 5% A -» 4.0 min 95% A; flow rate: 0.8 mL/min; column temp: 50°C; UV detection: 220 nm & 254 nm.

LC-MS Method 3:

Waters Acquity UPLC-MS: Binary Solvent Manager, Sample

System:

Manager/Organizer, PDA, ELSD

Column: Acquity UPLC BEH C18 1.7 m, 50x2.1 mm

Solvent: A = H ₂ 0 + H ₂ 0 + 0.1 %vol. HCOOC (99%)

B = acetonitrile

Gradient: 0-1 .6 min 1 -99% B, 1.6-2 min 99% B

Flow: 0.8 mL/min

Temperature: 60°C

Injection: 2.0 μί

Detection: DAD scan range 210-400 nm + ELSD

LC-MS Method 4: System: Shimadzu LC-MS: UFLC 20-AD and LCMS 2020 MS detector Column: Shim-pack XR-ODS 2.2 pm, 3.0x50 mm

Solvent: A = H ₂ 0 + 0.05%vol. HCOOC (99%)

B = acetonitrile+ 0.05%vol. HCOOC (99%)

LC-MS Method 5:

Waters Acquity UPLC-MS: Binary Solvent Manager, Sample

System:

Manager/Organizer, PDA, ELSD

Column: Acquity UPLC BEH C18 1.7 m, 50x2.1 mm

Solvent: A = H ₂ 0 + 0.2%vol. NH ₃ (32%)

B = acetonitrile

Gradient: 0-1 .6 min 1 -99% B, 1.6-2 min 99% B

Flow: 0.8 mL/min

Temperature: 60°C

Injection: 2.0 pL

Detection: DAD scan range 210-400 nm + ELSD

LC-MS Method 6:

Instrument HPLC: Waters UPLC Acquity; Instrument MS:

System:

Waters ZQ

Column: Acquity UPLC BEH C18 1 .7pm, 50x2.1 mm

Solvent: A = H ₂ 0 + 0.1 %vol. HCOOC (99%)

B = acetonitrile

Gradient: 0-1 .6 min 1 -99% B, 1.6-1 .8 min 99% B, 1 .81 -2 min 1 % B Flow: 0.8 mL/min

Temperature: 60°C

Detection: PDA scan range 210-400 nm

LC-MS Method 7:

System: Agilent 1290 UHPLC-MS Tof

Column: BEH C 18 (Waters) 1.7 pm, 50x2.1 mm

Solvent: A = H ₂ 0 + 0.05%vol. HCOOC (99%)

B = acetonitrile + 0.05%vol. HCOOC (99%)

Gradient: 0-1 .7 min 2-90% B, 1.7-2 min 90% B, 2-2.5 min 90-2% B Flow: 1 .2 mL/min

Temperature: 60°C Detection: DAD scan range 210-400 nm

LC-MS Method 8:

Waters Acquity UPLC-MS: Binary Solvent Manager, Sample

System:

Manager/Organizer, PDA, ELSD

Column: Acquity UPLC BEH C18 1.7 m, 50x2.1 mm

Solvent: A = H ₂ 0 + 0.1 %vol. HCOOC (99%)

B = acetonitrile

Gradient: 0-1 .6 min 1 -99% B, 1.6-2 min 99% B

Flow: 0.8 mL/min

Temperature: 60°C

Injection: 2.0 μί

Detection: DAD scan range 210-400 nm + ELSD

LC-MS Method 9:

System: Waters Acquity UPLC-MS SingleQuad

Column: Kinetex C 18 (Phenomenex) 2.6 μηι, 50x2.1 mm

Solvent: A = H ₂ 0 + 0.05%vol. HCOOC (99%)

B = acetonitrile + 0.05%vol. HCOOC (99%)

0-0.2 min 2% B, 0.2-1 .7 min 2-90% B, 1 .7-1 .9 min 90% B, 1 .9-2

Gradient:

min 90-2% B, 2-2.5 min 2% B

Flow: 1 .3 mL/min

Temperature: 60°C

Detection: DAD scan range 210-400 nm

LC-MS method 10:

System: Waters Acquity UPLC-MS SingleQuad

Column: Acquity UPLC BEH C18 1 .7 m, 50x2.1 mm

Solvent: A = H20 + 0.2%vol. NH3 (32%)

B = acetonitrile

Gradient: 0-1 .6 min 1 -99% B, 1.6-2 min 99% B

Flow: 0.8 mL/min

Temperature: 60°C

Detection: DAD scan range 210-400 nm

Preparative HPLC a) Autopurifier: acidic conditions

Waters Autopurification system: Pump 2545, Sample Manager

System:

2767, CFO, DAD 2996, ELSD 2424, SQD

Column: XBrigde C18 5.0 μηι 100x30 mm

Solvent: A = H ₂ 0 + 0.1 %vol. HCOOH (99%)

B = acetonitrile

0-0.5 min 5% B 25 mL/min, 0.51 -5.5 min 10-100% B 70 mL/min,

Gradient:

5.51 -6.5 min 100% B 70 mL/min

Temperature: RT

Solution: max. 250 mg / max. 2.5 mL DMSO or DMF

Injection: 1 x 2.5 mL

DAD scan range 210-400 nm, MS ESI+, ESI-, scan range 160-

Detection:

1000 m/z

Autopurifier: basic conditions

Waters Autopurification system: Pump 2545, Sample Manager

System:

2767, CFO, DAD 2996, ELSD 2424, SQD

Column: XBrigde C18 5.0 μηι 100x30 mm

Solvent: A = H ₂ 0 + 0.2%vol. NHs (32%)

B = acetonitrile

0-0.5 min 5% B 25 mL/min, 0.51 -5.5 min 10-100% B 70 mL/min,

Gradient:

5.51 -6.5 min 100% B 70 mL/min

Temperature: RT

Solution: max. 250 mg / max. 2.5 mL DMSO or DMF

Injection: 1 x 2.5 mL

DAD scan range 210-400 nm, MS ESI+, ESI-, scan range 160-

Detection:

1000 m/z

Method X1 :

Instrument: Labomatic HD5000, Labocord-5000; Gilson GX-241 , Labcol Vario 4000;

Column: Chiralpak IE 5 μηι 250x20 mm; Eluent A: MTBE + 0.1 %vol. Diethylamine Eluent B: Ethanol; Isocratic: 90%A + 10%B; Flow 30.0 mL/min; UV 254 nm.

Method X2:

Instrument: Labomatic HD5000, Labocord-5000; Gilson GX-241 , Labcol Vario 4000;

Column: Chiralpak IA 5 μηι 250x30 mm; Eluent A: MTBE + 0.1 %vol. Diethylamine Eluent B: Ethanol; Isocratic: 85%A + 15%B; Flow 40.0 mL/min; UV 254 nm. Method X3:

Instrument: Labomatic HD5000, Labocord-5000; Gilson GX-241 , Labcol Vario 4000, Column: Chiralpak IA 5.0 μηι 250x30 mm; Eluent: 100% Acetonitrile; Flow 50.0 mL/min; UV 280 nm.

Method X4:

Instrument: Waters Autopurification system; Column: Waters XBrigde C18 5.0 μηη 100x30 mm; Eluent A: H ₂ 0 + 0.2%vol. NH ₃ (32%), Eluent B: Acetonitrile; Gradient: 0.00-0.50 min 8% B (25->70mL/min), 0.51-5.50 min 8-15% B (70mL/min), DAD scan: 210-400 nm.

Method X5:

Instrument: Labomatic HD5000, Labocord-5000; Gilson GX-241 , Labcol Vario 4000, Column: Chiralpak IF 5.0 μηι 250x30 mm; Eluent A: Hexane + 0.1 %vol. Diethylamine (99%); Eluent B: Ethanol; Isocratic: 90%A + 10%B; Flow 50.0 mL/min; UV 280 nm.

Method X6:

Instrument: Waters Autopurification system; Column: Waters XBrigde C18 5.0 μηη 100x30 mm; Eluent A: H ₂ 0 + 0.2%vol. NH ₃ (32%), Eluent B: Acetonitrile; Gradient: 0.00-0.50 min 30% B (25->70mL/min), 0.51-5.50 min 30-45% B (70mL/min), DAD scan: 210-400 nm.

Method X7:

Instrument: Labomatic HD5000, Labocord-5000; Gilson GX-241 , Labcol Vario 4000,

Column: Chiralpak ID 5.0 μηι 250x30 mm; Eluent A: Hexane + 0.1 %vol Diethylamin (99%); Eluent B: 2-Propanol; Isocratic: 85%A + 15%B; Flow 50.0 mL/min; UV 254 nm.

Preparation of Intermediates

General remarks for the reparation of ethanamines of general formula I:

Aromatic or heteroaromatic ethanamines of general structure I have been prepared as described in the literature, for example in Synlett, 2015 (26) 201 -204 using commercially available aromatic or heteroaromatic methyl ketones. Not commercially available aromatic or heteroaromatic methyl ketones have been prepared as described in WO 2013/185103. Representative procedure for preparation of aryl-ethanamines from the corresponding bromides:

Intermediate INT-1

1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanamine

Step a:

5-(1 -ethoxyvinyl)-1 ,2,3,4-tetrahydronaphthalene

To 5-bromo-1 ,2,3,4-tetrahydronaphthalene (commercially available; 1 .00 g, 4.74 mmol) in 10 mL DMF were added tributyl(1 -ethoxyethenyl)stannane (2.1 ml_, 6.2 mmol) and tetrakis(triphenylphosphino)palladium(0) (1 .09 g, 0.95 mmol). The reaction mixture was heated to 1 10°C for 16 h. The reaction mixture was poured into brine. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over sodium sulfate and evaporated.

The obtained crude material was used without further purification in step b.

Step b:

1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanone

To the crude material from step a in 26 mL THF was added hydrochloric acid (7.1 mL, 2.0 M in water, 14 mmol). The mixture was stirred for 16 h. The reaction mixture was carefully poured into saturated aqueous sodium hydrogen carbonate solution. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and evaporated. The obtained crude product was purified by flash chromatography to give 1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanone (560 mg). LCMS (Method 5): R _t = 1 .26 min; MS (ESIpos): m/z = 174.9 [M+H] ⁺

Step c:

N-hydroxy-1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanimine

To 1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanone (560 mg, 3.21 mmol) in 1 1 mL ethanol were added sodium acetate (2.64 g, 32.1 mmol) and hydroxylamine hydrochloride (1 .12 g, 16.1 mmol). The mixture was stirred for 16 h at 40°C. The solvent was evaporated. Ethyl acetate and 6 mL of 2 M hydrochloric acid were carefully added. Brine was added. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated. The obtained crude material (780 mg) was used without further purification in step d.

Step d

1 -(5,6,7,8-tetrahydronaphthalen-1 -yl)ethanamine

To the crude material from step c (608 mg) in 46 mL methanol were added ammonium chloride (10.3 g, 193 mmol) and zinc powder (10.5 g, 161 mmol). The mixture was stirred at 60°C for 16 h. The precipitate was filtered off. The solution was concentrated under reduced pressure. The remaining material was suspended in water. Aqueous ammonia solution was added and ethyl acetate was added. The aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated. The obtained crude product was used without further purification in the subsequent step as described in the corresponding product examples.

Representative procedure for the preparation of aryl-ethanamines from the corresponding methyl ketones:

Intermediate INT-2

1 -(1 -methyl-1 H-indazol-4-yl)ethanamine

Step a:

N-hydroxy-1 -(1 -methyl-1 H-indazol-4-yl)ethanimine

1 -(1 -methyl-1 H-indazol-4-yl)ethanone (956 mg, 5.49 mmol), hydroxylamine hydrochloride (1 : 1 ) (1 .91 g, 27.4 mmol) and sodium acetate (4.50 g, 54.9 mmol) in 23 mL ethanol were stirred at 40°C for 19 h. The reaction mixture was diluted with ethyl acetate and water was added. The aqueous layer was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and evaporated. The obtained crude product was used without further purification in step b. LCMS (Method 5): R _t = 0.83 min; MS (ESIpos): m/z = 190.0 [M+H] ⁺ . Step b:

1 -(1 -methyl-1 H-indazol-4-yl)ethanamine

To N-hydroxy-1 -(1 -methyl-1 H-indazol-4-yl)ethanimine (crude material from step a) in 78 mL methanol were added ammonium chloride (17.6 g, 329 mmol) and zinc powder (17.9 g, 274 mmol). The resulting mixture was stirred at 60°C for 18 h. The remaining solid material was filtered off and washed with methanol. The obtained solution was concentrated. Water was added. The mixture was brought to basic pH by addition of aqueous ammonia (33% in water). The aqueous layer was extracted with ethyl acetate. The organic layer was washed with brine, dried over sodium sulfate and evaporated to give 908 mg of the title compound which was used without further purification. LCMS (Method 5): Rt = 0.74 min; MS (ESIpos): m/z = 175.9 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.21 (1 H), 7.50-7.40 (1 H), 7.36-7.27 (1 H), 7.20-7.10 (1 H), 4.47-4.36 (1 H), 4.02 (3H), 1 .36 (3H).

The following ethanamines have been prepared in analogy to the representative procedures described for the intermediates I NT-1 and I NT-2:

Starting Name of

Intermediate Structure

material Intermediate

6-Acetyl-2H-1 ,4-

N H ₂ H benzoxazin- 6-[1 -aminoethyl]-2H-

INT-3 3(4H)-one 1 ,4-benzoxazin- (commercially 3(4H)-one

available)

4-Bromo-3- methyMH- 1-(3-methyl-1H-

INT-20 indazole indazol-4- H

(commercially yl)ethanamine

available)

7-Acetyl-1- HoC

methyMH- 1-(1-methyl-1H- H ₂ N N-N

INT-21 indazole indazol-7- (commercially yl)ethanamine

available)

4-Acetyl-2- CH ₃ methyl-2H- 1-(2-methyl-2H- NH ₂ r-N

INT-22 indazole indazol-4- j . N

(commercially yl)ethanamine

available)

4-Bromo-5- methyMH- 1-(5-methyl-1H- H

INT-23 indazole indazol-4- (commercially yl)ethanamine

available)

4-Bromo-7- NH ₂ «-Ν fluoro-1 H- 1-(7-fluoro-1H- 1 1 NH

INT-24 indazole indazol-4- (commercially yl)ethanamine

available)

4-Bromo-6- fluoro-1 H- 1-(6-fluoro-1H- H

INT-25 indazole indazol-4- (commercially yl)ethanamine

available)

INT-28

1 -(5-bromothiophen-2-yl)ethanamine

N-[(E)-(5-bromothiophen-2-yl)methylidene]-2-methylpropane -2 -sulfinamide

A solution of 5-bromothiophene-2-carbaldehyde (2.5 mL, 21 mmol), 2-methylpropane-2- sulfinamide (3.06 g, 25.2 mmol) and Ti(OEt) ₄ (9.1 mL, 42 mmol) in THF (50 mL) was stirred at room temperature overnight. The reaction was quenched with brine (13 mL), diluted with EtOAc and filtered over a celite plug. The crude residue was then dissolved in DCM, filtered over a silica plug and the solvent then removed in vacuo to give the title compound as a yellow solid (6.37g, quantitative). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.24 (s, 1 H), 7.42 (d, 1 H), 6.92 (d, 1 H), 1 .16 (s, 9H).

Step b:

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide

To a solution of N-[(E)-(5-bromothiophen-2-yl)methylidene]-2-methylpropane-2- sulfinamide (2.00 g, 6.80 mmol) in THF (14 mL) was added methylmagnesiumbromide (6.8 ml_, 3.0 M, 20 mmol) dropwise and the mixture then stirred at room temperature during 1 hour. The reaction was quenched with NH4CI (sat.), the resulting mixture extracted with DCM and the solvent removed in vacuo to give the title compound as a brown oil (2.03g, 96%). Main diastereoisomer: ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.06 (d, 1 H), 6.83 (dd, 1 H), 5.67 (d, 1 H), 4.58 (quin, 1 H), 1.55-1 .51 (m, 3H), 1 .15 (s, 9H).

Step c:

1 -(5-bromothiophen-2-yl)ethanamine

To a solution of N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (1 .05 g, 3.40 mmol) in MeOH (7.0 mL) was added acetyl chloride (730 μΙ_, 10 mmol) dropwise and the mixture then stirred at room temperature during 1 hour. The solvent was removed in vacuo, ΕίβΝ (5.0 mL) and Et.20 (10 mL) added to the residue and the mixture stirred during 1 hour, then the precipitate filtered out and the solvent removed in vacuo to give the title compound as a brown oil (0.47 g, 67%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.01 (d, 1 H), 6.74 (dd, 1 H), 4.16 (qd, 1 H), 1.30 (d, 3H).

The following compounds were synthesized in analogy to intermediate INT-28:

Intermediate # Structure Analtical data Example 1

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(naphthalen-1 -yl)ethyl]quinazolin

Step a:

2-chloro-6,7-dimethoxy-N-[(1 R)-1 -(1 -naphthyl)ethyl]quinazolin-4-amine

To 2,4-dichloro-6,7-dimethoxyquinazoline (commercially available; 500 mg, 1.93 mmol) in 4 mL THF was added triethylamine (323 μΙ_, 2.32 mmol) and (1 R)-1 -(1 -naphthyl)ethanamine (commercially available; 354 mg, 2.12 mmol). The mixture was stirred at room temperature for 5 d. Saturated aqueous sodium hydrogen carbonate solution was added and the aqueous layer was extracted with ethyl acetate. The combined organic layers were dried over sodium sulfate and evaporated. The resulting solid material was digested with a mixture of dichloromethane and hexane to give 565 mg of the title compound as solid material. LCMS (Method 5): R _t = 1.34 min; MS (ESIpos): m/z = 394.3 [M+H] ⁺ . ¹ H-NMR (500 MHz, DMSO-d ₆ ), δ [ppm] = 1.73 (3H), 3.89 (6H), 6.25-6.33 (1 H), 7.08 (1 H), 7.52 (3H), 7.66-7.71 (1 H), 7.80 (1 H).

Step b:

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(naphthalen-1 -yl)ethyl]quinazolin-4-amine

2-chloro-6,7-dimethoxy-N-[(1 R)-1 -(1 -naphthyl)ethyl]quinazolin-4-amine (60 mg, 0.127 mmol) , methyl boronic acid (76 mg, 1 .27 mmol) tetrakis(triphenylphoshino)palladium(0) (147 mg,. 0.127 mmol) and 2.0 M aqueous sodium carbonate solution (0.76 mL, 1 .52 mmol) in 7 mL of 1 ,4-dioxane were heated to 100°C for 24 h. The reaction mixture was poured into a mixture of brine and aqueous sodium hydrogen carbonate solution. The aqueous layer was extracted with ethyl acetate, dried over sodium sulfate and evaporated. The obtained crude material was purified by preparative HPLC to give 8 mg of the title compound as solid material. LCMS (Method 5): R _t = 1.26 min; MS (ESIpos): m/z = 374.3 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .71 (3 H) 2.31 -2.35 (3 H) 3.87 (6 H) 6.44 (1 H) 7.03 1 H) 7.49-7.57 (3 H) 7.61 - 7.66 (1 H) 7.71 -7.73 (1 H) 7.84 (1 H) 7.95 (1 H) 8.10 (1 H) 8.29 (1 H).

Example 2

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-a mine

The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4-amine (example 1 1 ) using (1 R)-1 -(3-chloro- phenyl)ethanamine (commercially available; 286 mg, 1.84 μηιοΙ) to give 398 mg of the title compound. LCMS (Method 5): R _t = 1.24 min; MS (ESIpos): m/z = 358.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.59 (3 H) 2.35 (s, 3 H) 3.89 (6 H) 5.62 (1 H) 7.04 (1 H) 7.26- 7.31 (1 H) 7.36 (1 H) 7.39-7.44 (1 H) 7.50 (1 H) 7.70 (1 H) 8.01 (1 H).

Example 3

methyl 4-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-1 -benzothiophene-2- carboxylate

The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4-amine (example 1 1 ) using methyl 4-[1 - aminoethyl]-1 -benzothiophene-2-carboxylate (described in INT-27, 96.4 mg, 90 % purity, 369 μηιοΙ) to give 69 mg of the title compound. LCMS (Method 5): R _t = 1 .25 min; MS (ESIpos): m/z = 438.3 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .71 (3 H), 2.33-2.39 (3 H), 3.85 (3 H), 3.89 (6 H), 6.20 (1 H), 7.01 (1 H), 7.52-7.58 (1 H), 7.60-7.64 (1 H), 7.68 (1 H), 7.96 (1 H), 8.15 (1 H), 8.70 (1 H).

Example 4

N-[1-(1-benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazo lin-4-amine

The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1-yl)ethyl]quinazolin-4-amine (example 11) using 1-(1-benzofuran-7- yl)ethanamine (described in procedure INT-26, 59.4 mg, 369 μηηοΙ) to give 64 mg of the title compound. LCMS (method 5): R _t = 1.18 min; MS (ESIpos): m/z = 364.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.70 (3H), 2.29 (3H), 3.77-3.97 (6H), 6.14 (1H), 6.98 (1H), 7.03 (1H), 7.18-7.25 (1H), 7.36 (1H), 7.53 (1H), 7.78 (1H), 8.05 (1H), 8.11 (1H).

Example 5

N-[1-(7-fluoro-1H-indazol-4-yl)eth l]-6,7-dimethoxy-2-methylquinazolin-4-amine

Was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine (example 27) using 1-(7-fluoro-1 H-indazol-4-yl)ethanamine (described in procedure INT-24; 93.4 mg, 80 % purity, 417 μιτιοΙ) to give 34 mg of the title compound. LCMS (Method 5): R _t = 0.99 min; MS (ESIpos): m/z = 382.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.70 (3H), 2.31 (3H), 3.83-3.87 (3H), 3.89 (3H), 5.97-6.07 (1H), 7.01 (1H), 7.08-7.18 (2H), 7.71 (1H), 8.06-8.14 (1H), 8.33-8.41 (1H), 13.57-13.66 (1H).

Example 6

N-[1-(6-fluoro-1H-indazol-4-yl)ethyl]-6,7-dimethoxy-2-methyl quinazolin-4-amine H

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(6-fluoro-1 H-indazol-4- yl)ethanamine (described in procedure INT-25; 84.9 mg, 88 % purity, 417 μηιοΙ) to give 43 mg of the title compound. LCMS (Method 5): R _t = 0.99 min; MS (ESIpos): m/z = 382.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1.70 (3H), 2.31 (3H), 3.86 (3H), 3.91 (3H), 5.97-6.08 (1H), 7.02 (2H), 7.13-7.20 (1H), 7.72 (1H), 8.08-8.15 (1H), 8.29 (1H), 13.08-13.16 (1H).

Example 7

6,7-dimethoxy-2-methyl-N-[1-(5-meth l-1H-indazol-4-yl)ethyl]quinazolin-4-amine

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(5-methyl-1 H-indazol-4- yl)ethanamine (described in procedure INT-23; 61.7 mg, 85 % purity, 299 μηιοΙ) to give 53 mg of the title compound. LCMS (Method 5): R _t = 1.04 min; MS (ESIpos): m/z = 378.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1.70 (3H), 2.24 (3H), 2.65 (3H), 3.83 (3H), 3.97 (3H), 5.67-5.77 (1H), 6.96 (1H), 7.11 (1H), 7.20 (1H), 7.85 (1H), 8.21-8.27 (1H), 8.55 (1H), 12.81 (1H).

Example 8

6,7-dimethoxy-2-methyl-N-[1-(2-methyl-2H-indazol-7-yl)ethyl] quinazolin

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(2-methyl-2H-indazol-7- yl)ethanamine (described in procedure INT-27a; 87.5 mg, 84 % purity, 0419 μηιοΙ) to give 90 mg of the title compound. LCMS (Method 5): R _t = 1.07 min; MS (ESIpos): m/z = 378.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1.71 (3H), 2.29 (3H), 3.87 (3H), 3.94 (3H), 4.23 (3H), 6.12-6.22 (1H), 6.93-7.00 (1H), 7.03 (1H), 7.16-7.21 (1H), 7.52-7.58 (1H), 7.73- 7.78 (1H), 8.07-8.14 (1H), 8.36 (1H).

Example 9

6,7-dimethoxy-2-methyl-N-[1-2-methyl-2H-indazol-4-yl)ethyl]q uinazolin-4-amine

Was prepared in analogy to N-1-(1-benzothiophen-3-yl)ethyl]-6,7-dimethoxy-2- methylquinazolin-4-amine (example 27) using 1-(2-methyl-2H-indazol-4-yl)ethanamine (described in procedure INT-22; 81.6 mg, 90 % purity, 419 μιτιοΙ) to give 115 mg of the title compound. LCMS (Method 5): R _t = 0.97 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.68 (3H), 2.34 (3H), 3.84-3.87 (3H), 3.89 (3H), 4.14 (3H), 5.93-6.02 (1H), 7.02 (1H), 7.07 (1H), 7.18 (1H), 7.45 (1H), 7.73 (1H), 8.01-8.06 (1H), 8.45 (1H).

Example 10

6,7-dimethoxy-2-methyl-N-[1 -(1 -methyl-1 H-indazol-7-yl)ethyl]quinazolin

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1 -(1 -methyl-1 H-indazol-7- yl)ethanamine (described in procedure INT-21 ; 74.9 mg, 98 % purity, 419 μηιοΙ) to give 92 mg of the title compound. LCMS (Method 5): R _t = 1 .07 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1 .70 (3H), 2.29 (3H), 3.85 (3H), 3.91 (3H), 4.43 (3H), 6.34-6.44 (1 H), 7.01 (1 H), 7.10 (1 H), 7.55 (1 H), 7.62 (1 H), 7.74 (1 H), 8.01 (1 H), 8.20-8.27 (1 H).

Example 11

6,7-dimethoxy-2-methyl-N-[1 -(5,6,7, 8-tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4- amine

To 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 106 mg, 445 μιτιοΙ, commercially available) in 3 ml. DMSO was added 1 -(5,6,7, 8-tetrahydronaphthalen-1 - yl)ethanamine (described in procedure INT-1 ; 85.8 mg, 489 μιτιοΙ) and N-ethyl-N- isopropylpropan-2-amine (200 μΙ_, 1 .2 mmol). The resulting mixture was heated to 130°C for 2 h in a microwave oven. The reaction mixture was filtered and purified by preparative HPLC to give 63.4 mg of the title compound. LCMS (Method 5): R _t = 1 .37 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .50 (d, 3H), 1.69-1 .91 (m, 4H), 2.33 (s, 3H), 2.69-2.81 (m, 3H), 3.22-3.32 (m, 1 H), 3.82-3.95 (m, 6H), 5.68 (t, 1 H), 6.89 (d, 1 H), 6.98-7.07 (m, 2H), 7.32 (d, 1 H), 7.72 (s, 1 H), 8.05 (d, 1 H).

Example 12

N-[(1 R)-1 -(4-fluorophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using (1 R)-1 -(4-fluorophenyl)- ethanamine (commercially available; 170 μΙ_, 1 .3 mmol) to give 583 mg of the title compound. LCMS (Method 5): R _t = 1.15 min; MS (ESIpos): m/z = 342.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .57 (3H), 2.34 (3H), 3.86 (3H), 3.90 (3H), 5.63 (1 H), 7.02 (1 H), 7.10- 7.18 (2H), 7.44-7.51 (2H), 7.68 (1 H), 7.98 (1 H).

Example 13

6,7-dimethoxy-2-methyl-N-[1 -(3-methyl-1 H-indazol-4-yl)ethyl]quinazolin-4-amine H

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1 -(3-methyl-1 H-indazol-4- yl)ethanamine (described in procedure INT-20; 92.9 mg, 79 % purity, 419 μηιοΙ) to give 106 mg of the title compound. LCMS (Method 5): R _t = 0.97 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .63 (3H), 2.27 (3H), 2.77 (3H), 3.85 (3H), 3.92 (3H), 6.31 (1 H), 7.00 (1 H), 7.18-7.30 (3H), 7.76 (1 H), 8.17 (1 H), 12.61 (1 H).

Example 14

N-[1 -(1 ,3-benzothiazol-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin -4-amine

C H ₃ N=\ The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4-amine (example 1 1 ) using 1 -(1 ,3-benzothiazol- 4-yl)ethanamine (described in procedure INT-19; 82.2 mg, 461 μηιοΙ) to give 39 mg of the title compound. LCMS (Method 5): R _t = 1.15 min; MS (ESIpos): m/z = 381 .4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.71 (3 H), 2.24 (3 H), 3.87 (3 H), 3.95 (3 H), 6.45 (1 H), 7.03 (1 H), 7.37-7.48 (1 H), 7.57 (1 H), 7.81 (1 H), 8.04 (1 H), 8.19 (1 H), 9.47 (1 H).

Example 15

N-[1 -(1 -benzothiophen-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1 -(1 -benzothiophen-7- yl)ethanamine (described in procedure INT-18; 81 .7 mg, 461 μηιοΙ) to give 72 mg of the title compound. LCMS (Method 5): R _t = 1.22 min; MS (ESIpos): m/z = 380.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .71 (d, 3 H), 2.30 (s, 3 H), 3.88 (d, 6 H), 5.89 (t, 1 H), 7.03 (s, 1 H), 7.35-7.44 (m, 1 H), 7.45-7.52 (m, 2 H), 7.68-7.82 (m, 3 H), 8.18 (d, 1 H).

Example 16

6,7-dimethoxy-2-methyl-N-[1 -(6-meth l-1 H-indazol-4-yl)ethyl]quinazolin-4-amine

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1 -(6-methyl-1 H-indazol-4- yl)ethanamine (described in procedure INT-16; 88.5 mg, 83 % purity, 419 μιτιοΙ) to give 89 mg of the title compound. LCMS (Method 5): R _t = 1 .01 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ . 1 H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .68 (3H), 2.33 (3H), 2.41 (3H), 3.82-3.86 (3H), 3.88 (3H), 5.98-6.08 (1 H), 6.98-7.02 (2H), 7.16 (1 H), 7.71 (1 H), 8.05-8.1 1 (1 H), 8.14 (1 H), 12.85-12.90 (1 H).

Example 17 6,7-dimethoxy-2-methyl-N-[1 -1 -methyl-1 H-indazol-4-yl)ethyl]quinazolin-4-amine

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1 -(1 -methyl-1 H-indazol-4- yl)ethanamine (described in procedure INT-2; 73.4 mg, 99 % purity, 419 μηηοΙ) to give 107 mg of the title compound. LCMS (Method 5): R _t = 1.05 min; MS (ESIpos): m/z = 378.5 [M+H] ⁺ .1H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1.70 (3H), 2.30 (3H), 3.85 (3H), 3.90 (3H), 4.01 (3H), 5.99-6.08 (1H), 7.01 (1H), 7.19 (1H), 7.31-7.38 (1H), 7.48 (1H), 7.74 (1H), 8.09- 8.14 (1H), 8.25 (1H).

Example 18

N-[1-(5-fluoro-1H-indazol-4-yl)eth l]-6,7-dimethoxy-2-methylquinazolin-4-amine

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(5-fluoro-1 H-indazol-4- yl)ethanamine (described in procedure INT-17; 209 mg, 36 % purity, 419 μηηοΙ) to give 80 mg of the title compound. LCMS (Method 5): R _t = 1.01 min; MS (ESIpos): m/z = 382.1 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] = 1.75 (3H), 2.22 (3H), 3.84 (3H), 3.96 (3H), 5.93 (1H), 6.98 (1H), 7.19 (1H), 7.35 (1H), 7.85 (1H), 8.15 (1H), 8.23 (1H), 8.45 (1H), 13.02-13.12 (1H).

Example 19

N-[1-(2,3-dihydro-1,4-benzodioxin-6-yl)ethyl]-6,7-dimethoxy- 2-methylquinazolin-4- amine

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(2,3-dihydro-1,4-benzodioxin-6- yl)ethanamine (described in procedure INT-14; 84.4 mg, 89 % purity, 419 μηιοΙ) to give 125 mg of the title compound. LCMS (Method 5): R _t = 1.12 min; MS (ESIpos): m/z = 382.1 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] =1.52 (3H), 2.35 (3H), 3.86 (3H), 3.89 (3H), 4.19 (4H), 5.52-5.61 (1H), 6.78 (1H), 6.86-6.91 (1H), 6.93 (1H), 7.01 (1H), 7.66 (1H), 7.85- 7.90 (1H).

Example 20

N-[1-(1-benzofuran-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazo lin-4-amine

The title compound was prepared in analogy to N-[1-(1-benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using 1-(1-benzofuran-2-yl)ethanamine (described in procedure INT-15; 68.2 mg, 99 % purity, 419 μιτιοΙ) to give 48 mg of the title compound. LCMS (Method 5): R _t = 1.26 min; MS (ESIpos): m/z = 364.1 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1.68 (3H), 2.41 (3H), 3.87 (6H), 5.88-5.98 (1H), 6.77-6.81 (1H), 7.05 (1H), 7.17-7.28 (2H), 7.52 (1H), 7.58 (1H), 7.67 (1H), 8.12 (1H).

Example 21

N-[1-(2,3-dimethoxyphenyl)ethyl]-6,7-dimethoxy-2-methylquina zolin-4-amine

CH ₃

CH, O The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4-amine (example 1 1 ) using 1 -(2,3- dimethoxyphenyl)ethanamine (described in procedure INT-13; 92.8 mg, 90 % purity, 461 μηιοΙ) to give 86 mg of the title compound. LCMS (Method 5): R _t = 1 .12 min; MS (ESIpos): m/z = 384.3 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] 1 .48 (d, 3 H), 2.29 (s, 3 H), 3.80 (s, 3 H), 3.86 (s, 3 H), 3.93 (d, 6 H), 5.80-5.94 (m, 1 H), 6.84-6.92 (m, 1 H), 6.95-7.08 (m, 3 H), 7.77 (s, 1 H), 7.98 (s, 1 H).

Example 22

N-[1 -(2,3-dihydro-1 -benzofuran-4- l)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

The title compound was prepared in analogy to 6, 7-dimethoxy-2-methyl-N-[1 -(5,6,7,8- tetrahydronaphthalen-1 -yl)ethyl]quinazolin-4-amine (example 1 1 ) using 1 -(2, 3-d i hydro- 1 - benzofuran-4-yl)ethanamine (described in procedure INT-12; 83.6 mg, 90 % purity, 461 μηιοΙ) to give 78 mg of the title compound. LCMS (Method 5): R _t = 1 .12 min; MS (ESIpos): m/z = 366.3 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ) δ [ppm] 1 .56 (d, 3 H), 2.35 (s, 3 H), 3.23 (d, 1 H), 3.43 (d, 1 H), 3.79-3.93 (m, 6 H), 4.54 (t, 2 H), 5.52 (t, 1 H), 6.60 (d, 1 H), 6.96 (d, 1 H), 6.99-7.1 1 (m, 2 H), 7.70 (s, 1 H), 8.01 (d, 1 H).

Example 23

N-[1 -(1 ,3-benzodioxol-5-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

The title compound was prepared in analogy to 6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)-one (example 34) using 1 -(1 ,3-benzodioxol-5- yl)ethanamine (described in procedure INT-9; 1 12 mg, 74 % purity, 503 μιτιοΙ) to give 1 10 mg of the title compound. LCMS (Method 5): R _t = 1 .12 min; MS (ESIpos): m/z = 368 [M+H] ⁺ . ¹ H- NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .54 (3H), 2.36 (3H), 3.83-3.87 (3H), 3.90 (3H), 5.52- 5.63 (1 H), 5.96 (2H), 6.83 (1 H), 6.90 (1 H), 6.99-7.04 (2H), 7.67 (1 H), 7.85-7.92 (1 H).

Example 24

N-[1 -(2,3-dihydro-1 -benzofuran-5- l)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

The title compound was prepared in analogy to 6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)-one (example 34) using 1 -(2, 3-d i hydro- 1 - benzofuran-5-yl)ethanamine (described in procedure INT-8; 132 mg, 62 % purity, 503 μηηοΙ) to give 123 mg of the title compound. LCMS (Method 5): R _t = 1 .13 min; MS (ESIpos): m/z = 366 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .54 (3H), 2.36 (3H), 3.10-3.16 (2H), 3.85 (3H), 3.89 (3H), 4.47 (2H), 5.60 (1 H), 6.69 (1 H), 7.01 (1 H), 7.16 (1 H), 7.31 (1 H), 7.67 (1 H), 7.89 (1 H).

Example 25

6,7-dimethoxy-2-methyl-N-[1 -(5,6,7,8-tetrahydronaphthalen-2-yl)ethyl]quinazolin-4- amine

The tilte compound was prepared in analogy to 6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)-one (example 34) using 1 -(5,6,7,8- tetrahydronaphthalen-2-yl)ethanamine (described in procedure INT-7; 1 16 mg, 76 % purity, 503 μηιοΙ) to give 132 mg of the title compound. LCMS (Method 5): R _t = 0.91 min; MS (ESIpos): m/z = 378 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .54 (3H), 1 .70 (4H), 2.35 (3H), 2.62-2.72 (4H), 3.83-3.87 (3H), 3.89 (3H), 5.58 (1 H), 6.94-7.02 (2H), 7.09-7.17 (2H), 7.68 (1 H), 7.91 (1 H).

Example 26 6,7-dimethoxy-2-methyl-N-[1-(2-methylimidazo[1,2-a]pyridin-3 -yl)ethyl]quinazolin

The title compound was prepared in analogy to 6-{1-[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1,4-benzoxazin-3(4H)-one (example 34) using 1-(2-methylimidazo[1,2- a]pyridin-3-yl)ethanamine (described in procedure INT-6; 155 mg, 57 % purity, 503 μηιοΙ) to give 16.1 mg of the title compound. LCMS (Method 5): R _t = 0.91 min; MS (ESIpos): m/z = 378 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1.78 (3H), 2.32 (3H), 2.52-2.55 (3H), 3.81-3.86 (3H), 3.89 (3H), 5.85-5.96 (1H), 6.83-6.91 (1H), 7.00 (1H), 7.09-7.16 (1H), 7.38- 7.44 (1H), 7.68 (1H), 8.07-8.14 (1H), 8.60-8.66 (1H).

Example 27

N-[1-(1-benzothiophen-3-yl)eth l]-6,7-dimethoxy-2-methylquinazolin-4-amine

To 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 100 mg, 419 μηηοΙ) in 1.7 mL DMSO was added 1-(1-benzothiophen-3-yl)ethanamine (described in procedure INT-10; 137 mg, 65 % purity, 503 μηηοΙ) and N-ethyl-N-isopropylpropan-2-amine (190 μΙ_, 1.1 mmol). The resulting mixture was heated to 100°C for 16 h. The reaction mixture was filtered and purified by preparative HPLC to give 110 mg of the title compound. LCMS (Method 5): Rt = 1.24 min; MS (ESIpos): m/z = 380.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1.71 (3H), 2.44 (3H), 3.79-3.84 (3H), 3.86 (3H), 6.08-6.18 (1H), 7.04 (1H), 7.30-7.37 (2H), 7.62 (1H), 7.72 (1H), 7.87 (1H), 7.94-8.04 (2H).

Example 28 2-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-1 -benzofuran-7-ol

The title compound was prepared in analogy to N-[1 -(1 -benzothiophen-3-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (example 27) using [1 -aminoethyl]-1 -benzofuran-7-ol (described in procedure INT-1 1 ; 109 mg, 82 % purity, 503 μηηοΙ) to give 33 mg of the title compound. LCMS (Method 5): R _t = 0.86 min; MS (ESIpos): m/z = 380.5 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de), δ [ppm] = 1 .66 (3H), 2.42 (3H), 3.87 (6H), 5.84-5.96 (1 H), 6.65-6.74 (2H), 6.97 (1 H), 7.05 (1 H), 7.67 (1 H), 8.12 (1 H), 9.94 (1 H).

Example 29

6-bromo-2-methyl-N-[(1 R)-1 -phenylethyl]quinazolin-4-amine

The title compound was prepared in analogy to 6-bromo-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2- methylquinazolin-4-amine (example 31 ) using (1 R)-1 -phenylethanamine (commercially available; 170 μΙ_, 1 .3 mmol) to give 57 mg of the title compound from 90 mg of the title compound. LCMS (Method 5): R _t = 1 .30 min; MS (ESIpos): m/z = 343 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de) δ [ppm] = 1 .58 (d, 3H), 2.39 (s, 3H), 5.62 (t, 1 H), 7.17-7.26 (m, 1 H), 7.33 (t, 2H), 7.45 (d, 2H), 7.53 (d, 1 H), 7.84 (d, 1 H), 8.48 (d, 1 H), 8.71 (s, 1 H).

Example 30

6-{[dimethyl(oxido)-lambda6-sulfanylidene]amino}-2-methyl-N- [(1 R)-1 - phenylethyl]quinazolin-4-amine

The title compound was prepared in analogy 6-{[dimethyl(oxido)-lambda6- sulfanylidene]amino}-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2-methylquinazolin-4-amine (example 32) using 6-bromo-2-methyl-N-[(1 R)-1 -phenylethyl]quinazolin-4-amine ((described in example 29; 66.4 mg, 0.194 mmol,) to give 9 mg of the title compound. LCMS (Method 5): R _t = 0.96 min; MS (ESIpos): m/z = 355.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .57 (3 H), 2.35 (3 H), 3.28 (6 H), 5.57-5.71 (1 H), 7.21 (1 H), 7.31 (2 H), 7.38-7.49 (4 H), 7.75 (1 H), 8.19 (1 H).

Example 31

6-bromo-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2-methylquinazolin-4-amine

To 6-bromo-4-chloro-2-methylquinazoline (300 mg, 1 .16 mmol, commercially available) in 2 ml. DMF was added (1 R)-1 -(4-fluorophenyl)ethanamine (170 μΙ_, 1 .3 mmol, commercially available) and N-ethyl-N-isopropylpropan-2-amine (520 μΙ_, 3.0 mmol). The resulting mixture was heated for 1 h at 100°C in a microwave oven. The reaction was allowed to cool to room temperature. Brine was added, and the resulting mixture was extracted with ethyl acetate. The organic layer was separated and dried over magnesium sulfate. After evaporation of the solvent, 58 mg of the crude product was purified by preparative HPLC to give 37 mg of the title compound. LCMS (Method 5): R _t = 1 .31 min; MS (ESIpos): m/z = 361 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO- d ₆ ) δ [ppm] = 1 .57 (d, 3H), 2.39 (s, 3H), 5.59 (t, 1 H), 7.14 (t, 2H), 7.42- 7.57 (m, 3H), 7.84 (d, 1 H), 8.46 (d, 1 H), 8.68 (s, 1 H).

Example 32

6-{[dimethyl(oxido)-lambda6-sulfanylidene]amino}-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2- methylquinazolin-4-amine

To the crude material of 6-bromo-N-[(1 R)-1 -(4-fluorophenyl)ethyl]-2-methylquinazolin-4- amine (220 mg, 0.61 mmol, example 31 ) in 10 mL DMF were added sodium tert-butoxide (234 mg, 2.44 mmol), (R)-(+)-2,2'-bis(diphenylphosphino)-1 -1 '-binaphthyl (57 mg, 0.092mmol), bis(dibenzylideneacetone)palladium (35 mg, 0.061 mmol) and rac- methylsulfonimidoyl)methane (85 mg, 0.92mmol). The reaction mixture was heated to 100 C for 3 h in a microwave oven. Brine was added and the aqueous layer was extracted with ethyl acetate, dried over sodium sulfate and evaporated. LCMS (Method 5): Rt = 0.99 min; MS (ESIpos): m/z = 373.4 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .56 (3 H), 2.35 (3 H), 3.27 (6 H), 5.61 (1 H), 7.13 (2 H), 7.36-7.54 (4 H), 7.73 (1 H), 8.15 (1 H).

Example 33

6,7-dimethoxy-N-[1 -(7-methox -1 -benzofuran-2-yl)ethyl]-2-methylquinazolin-4-amine

The title compound was prepared in analogy to 6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)-one (example 34) using 1 -(7-methoxy-1 - benzofuran-2-yl)ethanamine (described in procedure INT-5; 134 mg, 66 % purity, 461 μηηοΙ) to give 141 ,4 mg of the title compound. LCMS (Method 5): R _t = 1 .24 min; MS (ESIpos): m/z = 404 [M+H] ⁺ . ¹ H-N MR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .68 (3H), 2.44 (3H), 3.86-3.90 (9H), 5.88-5.97 (1 H), 6.79 (1 H), 6.88 (1 H), 7.05 (1 H), 7.10-7.16 (2H), 7.70 (1 H), 8.26-8.37 (1 H).

Example 34

6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)- one

To 4-chloro-6,7-dimethoxy-2-methylquinazoline (100 mg, 419 μηηοΙ, commercially available) in 1 .7 mL DMSO was added 6-[1 -aminoethyl]-2H-1 ,4-benzoxazin-3(4H)-one (described in procedure INT-3; 1 14 mg, 78 % purity, 461 μηηοΙ) and N-ethyl-N-isopropylpropan-2-amine (190 μΙ_, 1 .1 mmol). The resulting mixture was stirred at 100°C overnight. The reaction mixture was filtered purified by preparative HPLC to give 151 mg of the title compound. LCMS (Method 5): R _t = 0.92 min; MS (ESIpos): m/z = 395 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de), δ [ppm] = 1 .56 (3H), 2.41 (3H), 3.86-3.89 (3H), 3.90 (3H), 4.52 (2H), 5.55-5.65 (1 H), 6.91 (1 H), 6.96-7.05 (3H), 7.74 (1 H), 8.26-8.36 (1 H), 10.68 (1 H). Example 35

6,7-dimethoxy-N-[1 -(6-methox -2-naphthyl)ethyl]-2-methylquinazolin-4-amine

The title compound was prepared in analogy to 6-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2H-1 ,4-benzoxazin-3(4H)-one (example 34) using 1 -(6-methoxynaphthalen-2- yl)ethanamine (described in procedure INT-4; 1 16 mg, 80 % purity, 461 μηηοΙ) to give 151 ,3 mg of the title compound. LCMS (Method 5): R _t = 1 .24 min; MS (ESIpos): m/z = 404 [M+H] ⁺ . ¹ H-N MR (400 MHz, DMSO-d ₆ ), δ [ppm] = 1 .69 (3H), 2.43 (3H), 3.85 (3H), 3.87-3.90 (3H), 3.92 (3H), 5.80-5.89 (1 H), 7.04 (1 H), 7.14 (1 H), 7.28 (1 H), 7.57 (1 H), 7.77-7.83 (3H), 7.86 (1 H), 8.54-8.67 (1 H).

Example 36

N-[(1 R)-1 -(5'-amino-2'-methylbiphenyl-3-yl)ethyl]-6,7-dimethoxy-2-met hylquinazolin-4- amine

To N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (prepared as described in example 191 ; 60.3 mg, 0.15 mmol) in 1 mL N MP were added 4-methyl-3- (4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)aniline (commercially available; 69.9 mg, 0.3 mmol) in 0.53 mL NMP, [1 , 1 '-bis-(diphenylphosphino)-ferrocene]dichloropalladium(l l) dichloromethane complex (25 mg, 0.03 mmol) in 1 mL N MP and potassium carbonate (62.2 mg, 0.45 mmol) in 0.5 mL water. The reaction mixture is heated to 100°C for 24 h. The reaction mixture is filtered over alumina N. The obtained mixture is purified by preparative HPLC to give 16 mg of the title compound as solid material. LCMS (Method 6): Rt = 0.78 min; MS (ESIpos): m/z = 429.3 [M+H] ⁺ . The compounds in the following table were prepared in analogy to example 36. All boronic acids for the Suzuki coupling are commercially available as free boronic acid or its corresponding pinacolate. The preparation of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine is described in example 209:

Example 178

methyl 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzoate

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 200 mg, 85 % purity, 416 μηηοΙ), [2- (methoxycarbonyl)phenyl]boronic acid (commercially available; 74.9 mg, 416 μηηοΙ), K2CO3 (230 mg, 1 .67 mmol) and Pd(PPh ₃ )4 (48.1 mg, 41.6 μηηοΙ) in dioxane (4.0 mL) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (61.5 mg, 36%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.61 -7.53 (m, 2H), 7.52-7.47 (m, 1 H), 7.45-7.40 (m, 1 H), 7.05 (s, 2H), 6.95 (d, 1 H), 5.93 (quin, 1 H), 3.87 (s, 6H), 3.62 (s, 3H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 464, Rt = 0.96 min.

Example 179

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]piperidine-4-carboxamide

Step a:

2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2-thie nyl)benzaldehyde

The title compound was prepared in analogy to example 178 using N-[1 -(5-bromothiophen-2- yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine (described in example 209; 10 g, 22.4 mmol) and 2-formylphenylboronic acid (commercially available; 3.37 g, 22.4 mmol) to give the title compound in 79 % yield (8.4 g). The crude product was recrystallized from diethylether and used directly in the next step.

Step b: 1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]piperidine-4-carboxamide

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(50.0 mg, 1 15 μηιοΙ), piperidine-4-carboxamide (29.6 mg, 231 μηιοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηιοΙ) and the solution stirred at room temperature during 5 hours. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as a white solid (19.5 mg, 31 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.65 (s, 1 H), 7.43-7.39 (m, 1 H), 7.38-7.35 (m, 1 H), 7.33-7.25 (m, 2H), 7.21 (d, 1 H), 7.19 (br s, 1 H), 7.08 (dd, 1 H), 7.04 (s, 1 H), 6.71 (br s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.39 (s, 2H), 2.76 (br t, 2H), 2.43 (s, 3H), 2.07-1.97 (m, 1 H), 1 .87 (br t, 2H), 1.71 (d, 3H), 1.63-1.55 (m, 2H), 1 .54-1 .42 (m, 2H). LC-MS (method 7): m/z: [M+H] ⁺ = 546, Rt = 0.58 min.

Example 180

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]ethanol

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 100 mg, 245 μηιοΙ), [2-(2-{[tert- butyl(dimethyl)silyl]oxy}ethyl)phenyl]boronic acid (68.6 mg, 245 μηιοΙ), K ₂ C0 ₃ (135 mg, 980 μηιοΙ) and Pd(PPh ₃ )4 (28.3 mg, 24.5 μιτιοΙ) in dioxane (2.5 mL) and H ₂ 0 (500 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (60.4 mg, 53%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.35-7.31 (m, 1 H), 7.30-7.25 (m, 2H), 7.23-7.18 (m, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 6.99 (d, 1 H), 5.96 (quin, 1 H), 4.67 (t, 1 H), 3.87 (s, 6H), 3.54 (td, 2H), 2.84 (t, 2H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 450, Rt = 0,89 min.

Example 181

2-[3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]ethanol

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 100 mg, 245 μηιοΙ), [3-(2-hydroxyethyl)phenyl]boronic acid (40.7 mg, 245 μηιοΙ), K ₂ C0 ₃ (135 mg, 980 μηιοΙ) and Pd(PPh ₃ ) ₄ (28.3 mg, 24.5 μηιοΙ) in dioxane (2.5 mL) and H2O (500 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a pale yellow solid (58.8 mg, 48%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.13 (d, 1 H), 7.65 (s, 1 H), 7.43-7.38 (m, 2H), 7.33 (d, 1 H), 7.26 (t, 1 H), 7.1 1 (br d, 1 H), 7.06 (dd, 1 H), 7.05 (s, 1 H), 5.93 (quin, 1 H), 4.64 (t, 1 H), 3.87 (s, 6H), 3.60 (td, 2H), 2.72 (t, 2H), 2.43 (s, 3H), 1.70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 450, Rt = 0.86 min.

Example 182

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(2-oxa-6-azaspiro[3.3]hept-6- ylmethyl)phenyl]thiophen-2-yl}ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (prepared in example 179a; 50.0 mg, 1 15 μιτιοΙ), 2-oxa-6-azaspiro[3.3]heptane (22.9 mg, 231 μηιοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (39.7 mg, 65%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.40-7.32 (m, 2H), 7.31 -7.23 (m, 2H), 7.12 (d, 1 H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 4.54 (s, 4H), 3.87 (s, 3H), 3.87 (s, 3H), 3.51 (s, 2H), 3.24 (s, 4H), 2.43 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 517, Rt = 0.60 min.

Example 183

N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin-4-amine

A solution of 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 789 mg, 3.30 mmol) and 1 -(5-bromo-4-methylthiophen-2-yl)ethanamine (procedure described in INT- 31 ; 800 mg, 3.63 mmol) in dioxane (15 mL) was heated to 1 10°C during 18 hours. MTBE (20 mL) was added, the mixture stirred at room temperature during 3 hours then the precipitate filtered and dried to give the HCI salt of the title compound as an off-white solid (1.56 g, 90% purity, 93%). Purification of a sample by preparative HPLC (basic conditions) gave the title compound as yellow solid (29.1 mg, 2%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.04 (d, 1 H), 7.60 (s, 1 H), 7.05 (s, 1 H), 6.88 (s, 1 H), 5.76 (quin, 1 H), 3.87 (s, 6H), 2.42 (s, 3H), 2.09 (s, 3H), 1 .64 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 422, Rt = 0.97 min.

Example 184

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(pyrrolidin-1 -ylmethyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen

(described in example 179a; 50.0 mg, 1 15 μηιοΙ), pyrrolidine (19 μΙ_, 230 μηιοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (39.8 mg, 71 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.44-7.41 (m, 1 H), 7.38-7.34 (m, 1 H), 7.32-7.25 (m, 2H), 7.18 (d, 1 H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.54 (s, 2H), 2.42 (s, 3H), 2.38 (br s, 4H), 1.72 (d, 3H), 1.60 (br s, 4H). LC-MS (method 7): m/z: [M+H] ⁺ = 489, Rt = 0,62 min.

Example 185

N-[1 -{5-[2-({(2S)-[(dimethylamino)methyl]pyrrolidin-1 -yl}methyl)phenyl]thi

yl}ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηιοΙ), N,N-dimethyl-1 -[(2S)-pyrrolidin-2- yl]methanamine (29.6 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηιοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (40.6 mg, 63%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.13 (dd, 1 H), 7.64 (s, 1 H), 7.51 -7.48 (m, 1 H), 7.32-7.22 (m, 3H), 7.14 (dd, 1 H), 7.08-7.06 (m, 1 H), 7.05 (s, 1 H), 5.96 (br quin, 1 H), 4.07 (d, 1 H), 3.87 (s, 6H), 3.36 (d, 1 H), 2.77-2.70 (m, 1 H), 2.42 (d, 3H), 2.08 (ddd, 1 H), 2.05-2.01 (m, 1 H), 2.00 (s, 3H), 1 .99 (s, 3H), 1 .88-1.75 (m, 1 H), 1 .72 (d, 3H), 1 .58-1 .43 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 546, Rt = 0,64 min.

Example 186

2-methyl-N-[(1 R)-1 -(naphthalen-1 -yl)ethyl]quinazolin-4-amine

To a solution of 4-chloro-2-methylquinazoline (commercially available; 95 mg, 0.53 mmol) and (R)-(+)-1 -(1 -naphthyl)ethylamine (commercially available; 91 mg, 0.53 mmol) in DMSO (1 mL) was added TEA (108 mg, 1 .1 mmol) was stirred at 50°C for 16h. The reaction mixture was filtered through a 0.45μηι Whatmann filter and purified by preparative HPLC (Autopurifier: basic conditions) to give the desired product (68 mg, 39%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 1 .71 (3H), 2.35 (3H), 6.42 (1 H), 7.42 (1 H), 7.46-7.62 (4H), 7.65-7.76 (2H), 7.82 (1 H), 7.89-7.99 (1 H), 8.31 (1 H), 8.41 (1 H), 8.46 (1 H).

Example 187

N-[(1 R)-1 -(4-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

Step a:

4-chloro-6,7-dimethoxy-2-methylquinazoline

2.50 g (1 1 .4 mmol) of 6,7-dimethoxy-2-methylquinazolin-4-ol were suspended in 1 1 .00 mL of thionyl chloride, admixed with 10 drops of /V,/V-dimethylformamide and stirred for 1 h at 80°C. The thionyl chloride was removed in vacuo. The residue was admixed twice with in each case 20 mL of toluene and evaporated to dryness in vacuo. With ice bath cooling, 20 mL of a 5N sodium hydroxide solution were added dropwise to the residue. The suspension was admixed with 20 mL of dichloromethane and vigorously stirred for 10 min. The phases were separated and the aqueous phase was extracted by shaking five times with in each case 20 mL of dichloromethane. The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. 2.71 g (100% of theory) of the title compound were isolated as a beige solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 2.79 (s, 3H), 4.04 (s, 3H), 4.05 (s, 3H), 7.25 (s, 1 H), 7.35 (s, 1 H). LC-MS (method 1 ): R _t = 3.19 min; MS (ESI/APCIpos) m/z = 239.1 [M+H] ⁺ .

Step b:

N-[(1 R)-1 -(4-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

In the microwave vessel, under argon, 2.70 g (1 1 .3 mmol) of 4-chloro-6,7-dimethoxy-2- methylquinazoline were dissolved in 15.0 mL of absolute 1 ,4-dioxane, admixed with 3.9 mL (22.6 mmol) of Λ/,/V-diisopropylethylamine and 2.72 g (13.6 mmol) of (R)-1 -(4- bromophenyl)ethylamine (commercially available) and stirred for 16 h at 100°C. The reaction solution was evaporated to dryness in vacuo. The residue was taken off in 30 mL of dichloromethane and 30 mL of water. The phases were separated and the aqueous phase was extracted by shaking three times with in each case 25 mL of dichloromethane. The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. The residue (4 g) was chromatographed [silica gel 60 (2 ^χ 80 g, 30 μηι); dichloromethane/methanol (96:4)]. 2.91 g (64% of theory) of the title compound were isolated as a beige solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 1.63 (d, 3H), 2.55 (s, 3H), 3.91 (d, 6H), 5.64 (m, 1 H), 5.78 (s, 1 H), 6.96 (s, 1 H), 7.1 1 (s, 1 H), 7.28-7.32 (m, 2H), 7.91 -7.43 (m, 2H). LC-MS (method 1 ): R _t = 3.19 min; MS (ESI/APCIpos) m/z = 402.1 [M+H] ⁺ .

Example 188

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4-(methylsulfonyl)phenyl]ethyl}quinazolin-4-amine

In the microwave vessel, 200 mg (0.50 mmol) of [(R)-1 -(4-bromophenyl)ethyl](6,7-dimethoxy- 2-methylquinazolin-4-yl)amine, 102 mg (0.99 mmol; prepared as described in example 187) of sodium sulphinate, 36 mg (99 μηηοΙ) of copper(ll) trifluoromethanesulphonate and 23 mg (199 μιηοΙ) of (+-)-trans-1 ,2-diaminocyclohexane were dissolved in 3.0 mL of absolute dimethylsulphoxide and stirred for 21 h at 120°C and for 7 h at 130°C. The reaction solution was evaporated to dryness in vacuo. The residue was admixed with 3 mL of water and extracted by shaking three times with in each case 5 mL of dichloromethane. The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. The residue was chromatographed [silica gel 60 (25 g, 30 μηι); ethyl acetate/methanol (97:3)]. 122 mg (55% of theory) of the title compound were isolated as a beige solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 1.67 (d, 3H), 2.50 (s, 3H), 3.92 (s, 3H), 3.95 (s, 3H), 5.71 (m, 1 H), 6.15 (s, 1 H), 7.12 (m, 2H), 7.59 (d, 2H), 7.79 (s, 2H). LC-MS (method 1 ): R _t = 2.72 min; MS (ESI/APCIpos) m/z = 402.2 [M+H] ⁺ .

Example 189

4-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}benzoni trile

In the microwave vessel, under argon, 300 mg (1 .26 mmol) of 4-chloro-6,7-dimethoxy-2- methylquinazoline were dissolved in 3.00 mL of absolute 1 ,4-dioxane, admixed with 1 .10 mL (6.29 mmol) of Λ/,/V-diisopropylethylamine and 344 mg (1.00 mmol) of (R)-4-(1 - aminoethyl)benzonitrile hydrochloride and stirred for 16 h at 100°C. The batch was evaporated to dryness in vacuo. The residue was chromatographed three times [1 ^st column, silica gel 60 (40 g, 30 μηη); dichloromethane/methanol (98:2 to 1 :1 ); 2 ^nd column, silica gel 60 (25 g, 30 m); dichloromethane/methanol (98:2 to 95:5); 3 ^rd column, silica gel 60 (25 g, 30 μηη); ethyl acetate/methanol (95:5)]. 172 mg (39% of theory) of the title compound were isolated as a beige solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 1 .67 (d, 3H), 2.50 (s, 3H), 3.94 (s, 3H), 3.96 (s, 3H), 5.67 (m, 1 H), 5.78 (s, 1 H), 6.98 (s, 1 H), 7.13 (s, 1 H), 7.52-7.58 (m, 4H). LC-MS (method 1 ): R _t = 2.73 min; MS (ESI/APCIpos) m/z = 402.2 [M+H] ⁺ .

Example 190

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(3-methylphenyl)ethyl]quinazolin-4-amine

Under argon, a suspension of 100 mg (0.258 mmol) of [(R)-1 -(3-bromophenyl)ethyl](6,7- dimethoxy-2-methylquinazolin-4-yl)amine (described in example 191 ) and 86 mg (0.386 mmol) of methylboronic acid in 1 mL of 1 ,2-dimethoxyethane and 0.3 mL of water was admixed with 18 mg (0.026 mmol) of bis(triphenylphosphine)palladium(ll) dichloride and 107 mg (0.773 mmol) of potassium carbonate. The reaction mixture was degassed three times and stirred for 4 h at 90°C. The solution was admixed with 5 mL of water. The aqueous phase was extracted four times with in each case 20 mL of dichloromethane. The combined organic phases were dried over sodium sulphate and then evaporated to dryness. The residue was chromatographed on the Flashmaster [silica gel 60 (25 g, 50 μηη); dichloromethane/methanol (98:2)]. 55 mg (30% of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, DMSO): δ [ppm] = 1 .65-1 .68 (m, 3H), 2.35 (s, 3H), 2.59 (s, 3H), 3.91 -3.94 (m, 6H), 5.61 -5.72 (m, 2H), 6.88 (s, 1 H), 7.08-7.10 (m, 1 H), 7.14 (s, 1 H), 7.23-7.27 (m, 3H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 338.3, R _t = 3.14 min.

Example 191

N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

Step a:

6,7-Dimethoxy-2-methylquinazolin-4-ol

1 .25 g (6.34 mmol) of 2-amino-4,5-dimethoxybenzoic acid, 1 .2 g (12.68 mmol) of acetamidine hydrochloride and 1.04 g (12.678 mmol) of sodium acetate anhydrous were suspended in 20 mL of 2-methoxyethanol and stirred for 6 h under reflux. LCMS reveals complete conversion. After cooling to room temperature, the batch was admixed with 50 mL of water. The solid that has precipitated out in the process was filtered off with suction, washed three times with in each case 10 mL of cold water and evaporated to dryness in vacuo. 768 mg (55% of theory) of 6,7-dimethoxy-2-methylquinazolin-4-ol were isolated as a colourless solid. LC-MS (method 1 ): m/z: [M+H] ⁺ = 221.2, R _t = 2.28 min. Step b:

4-Chloro-6,7-dimethoxy-2-methylquinazoline

2.5 g (1 1.35 mmol) of 6,7-dimethoxy-2-methylquinazolin-4-ol were suspended in the Teflon vessel in 10 mL (137.1 mmol) of thionyl chloride and stirred with 10 drops of N,N- dimethylformamide and for 1 h at 85°C. The progress of the reaction was controlled by means of LC-MS. Complete conversion was detected. The reaction solution was evaporated to dryness in vacuo. The residue was taken up five times in 20 mL of toluene and evaporated to dryness in vacuo. Under ice cooling, 5 N sodium hydroxide solution was added until pH 8 was reached. Then, the aqueous phase was extracted four times with in each case 30 mL of chloroform. The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. 2.5 g (95% of theory) of 4-chloro-6,7-dimethoxy-2- methylquinazoline were isolated as a colourless solid. LC-MS (method 1 ): m/z: [M+H] ⁺ = 239.1 , R _t = 3.17 min.

Step c:

N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

2.57 g (10.77 mmol) of 4-chloro-6,7-dimethoxy-2-methylquinazoline were dissolved in 30 mL of 1 ,4-dioxane, admixed with 3.23 g (16.15 mmol) of (R)-3-bromo-alpha-methylbenzylamine (commercially available) and 3.75 mL (21.54 mmol) of Hunig's base and stirred for 18 h at 100°C. The progress of the reaction was monitored by means of LC-MS. Still no complete conversion was detected. A further 3.23 g (16.15 mmol) of (R)-3-bromo-alpha- methylbenzylamine and 3.75 mL (21.54 mmol) of Hunig's base were added and the mixture was stirred for 18 h at 100°C. The solvent was removed in vacuo. The residue was taken up in 50 mL of dichloromethane and washed with 20 mL of saturated sodium hydrogencarbonate solution and 20 mL of 1 .0 N hydrochloric acid. The organic phase was evaporated to dryness in vacuo. The residue was chromatographed on the Flashmaster [silica gel 60 (120 g, 30 m); dichloromethane/methanol (98:2)]. 2.79 g (64% of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, CDC ): δ [ppm] = 1 .61 -1.63 (m, 3H), 2.55 (s, 3H), 3.89-3.90 (m, 6H), 5.63-5.70 (m, 1 H), 5.86-5.88 (m, 1 H), 7.00 (s, 1 H), 7.1 1 (s, 1 H), 7.14-7.18 (m, 1 H), 7.34-7.37 (m, 2H), 7.55-7.56 (m, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 403.1 , R _t = 3.19 min.

Example 192

4-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}benzami de

In the microwave vessel, 137 mg (0.39 mol) of 4-[(R)-1 -(6,7-dimethoxy-2-methylquinazolin-4- ylamino)ethyl]benzonitrile (described in example 189) and 3 mg of hydrido(dimethyl- phosphinous acid-kP)[hydrogen bis(dimethylphosphinito-kP)]platinum(ll) were suspended in 2.00 mL of ethanol and 2.00 mL of water and stirred for 5 h at 100°C. The reaction solution was evaporated to dryness in vacuo. The residue was chromatographed twice [1 ^st column silica gel 60 (25 g, 30 μηι); ethyl acetate/methanol (95:5); 2 ^nd column silica gel 60 (25 g, 30 μιτι); dichloromethane/methanol (85:15)]. 73 mg (51 % of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.59 (d, 3H), 2.33 (s, 3H), 3.86 (s, 3H), 3.1 (s, 3H), 5.66 (m, 1 H), 7.02 (s, 1 H), 7.25 (s, 1 H), 7.50 (d, 2H), 7.71 (s, 1 H), 7.80-7.85 (m, 2H), 7.86 (s, 1 H), 7.99 (d, 1 H). LC-MS (method 1 ): R _t = 2.68 min; MS (ESI/APCIpos) m/z = 367.2 [M+H] ⁺ .

Example 193

N-[(1 R)-1 -(biphenyl-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

Under argon, a suspension of 200 mg (0.497 mmol) of [(R)-1 -(3-bromophenyl)ethyl](6,7- dimethoxy-2-methylquinazolin-4-yl)amine (described in example 191 ) and 152 mg (0.746 mmol) of phenylboronic acid pinacol ester in 2 mL of 1 ,2-dimethoxyethane and 0.6 mL of water was admixed with 35 mg (0.05 mmol) of bis(triphenylphosphine)palladium(ll) dichloride and 275 mg (1 .99 mmol) of potassium carbonate. The reaction mixture was degassed three times and stirred for 6 h at 90°C. The solution was admixed with 5 mL of water. The aqueous phase was extracted four times with in each case 20 mL of dichloromethane. The combined organic phases were dried over sodium sulphate and then evaporated to dryness. The residue was chromatographed twice on the Flashmaster [silica gel 60 (2 ^χ 25 g, 50 m); dichloromethane/methanol (98:2)]. 39 mg (19% of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, DMSO): δ [ppm] = 1 .72-1.74 (m, 3H), 2.60 (s, 3H), 3.92-3.94 (m, 6H), 5.65-5.67 (m, 1 H), 5.77-5.80 (m, 1 H), 6.88 (s, 1 H), 7.14 (s, 1 H), 7.32-7.36 (m, 1 H), 7.40-7.47 (m, 3H), 7.49-7.52 (m, 1 H), 7.55-7.56 (m, 2H), 7.70 (s, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 400.3, R _t = 3.35 min.

Example 194

3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}benzoni trile

Under argon, a suspension of 400 mg (0.99 mmol) of [(R)-1 -(3-bromophenyl)ethyl](6,7- dimethoxy-2-methylquinazolin-4-yl)amine (described in example 191 ) and 1 17 mg, (0.99 mmol) of zinc cyanide in 2.5 mL of absolute dimethylformamide was admixed with 81 mg (0.09 mmol) of [1 ,1 '-bis(diphenylphosphino)ferrocene]dichloropalladium(ll) complex in CH2CI2. The reaction mixture was stirred for 5 h at 100°C. For the work-up, the batch was admixed with a mixture of 10 mL of water and 10 mL of 25 per cent ammonia. The aqueous phase was extracted three times using in each case 30 mL of dichloromethane. The combined organic phases were dried over sodium sulphate and then evaporated to dryness. The residue was chromatographed five times on the Flashmaster [silica gel 60 (5 ^χ 25 g, 30 μηη); chloroform/methanol (98:2)]. 70 mg (19% of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, DMSO): δ [ppm] = 1 .64-1 .65 (m, 3H), 2.51 (s, 3H), 3.91 -3.94 (m, 6H), 5.63-5.70 (m, 1 H), 5.98-5.99 (m, 1 H), 7.06 (s, 1 H), 7.10 (s, 1 H), 7.38-7.42 (m, 1 H), 7.47-7.50 (m, 1 H), 7.60-7.71 (m, 2H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 349.2, R _t = 2.87 min.

Example 195 6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(4-methylphenyl)ethyl]quinazolin-4-amine

In the microwave vessel under argon, 200 mg (0.50 mmol) of [(R)-1 -(4-bromo- phenyl)ethyl](6,7-dimethoxy-2-methylquinazolin-4-yl)amine (described in example 187), 89 mg (1 .49 mmol) of methylboronic acid, 36 mg (0.05 mmol) of [bis(diphenyl- phosphino)ferrocene]dichloropalladium(ll) and 486 mg (1 .49 mmol) of caesium carbonate were dissolved in 10.0 mL of absolute 1 ,4-dioxane, degassed three times, aerated with argon and stirred for 20 min at 100°C. The reaction solution was evaporated to dryness in vacuo. The residue was taken up in 50 mL of dichloromethane and washed three times with in each case 10 mL of water. The organic phase was dried over sodium sulphate and evaporated to dryness in vacuo. The residue was chromatographed [silica gel 60 (40 g, 30 μηι); dichloromethane/methanol (96:4)]. 95 mg (54% of theory) of the title compound were isolated as an orange solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 1.66 (d, 3H), 2.34 (s, 3H), 2.59 (s, 3H), 3.93 (d, 6H), 5.68 (s, 1 H), 5.68 (m, 1 H), 6.86 (s, 1 H), 7.15-7.17 (m, 3H), 7.35-7.37 (m, 2H). LC-MS (method 1 ): R _t = 3.16 min; MS (ESI/APCIpos) m/z = 338.3 [M+H] ⁺ .

Example 196

N-[(1 R)-1 -(biphenyl-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

In the microwave vessel under argon, 250 mg (0.62 mmol) of [(R)-1 -(4-bromophenyl)- ethyl](6,7-dimethoxy-2-methylquinazolin-4-yl)amine (described in example 187), 190 mg (0.93 mmol) of phenylboronic acid pinacol ester, 44 mg (0.062 mmol) of bis(triphenylphosphine)palladium(ll) chloride and 264 mg (1.24 mmol) of potassium phosphate were dissolved in 12 mL of absolute dimethoxyethane and 1.20 mL of water and stirred for 30 min at 90°C. The reaction solution was evaporated to dryness in vacuo. The residue was admixed with 30 mL of water and extracted by shaking five times with in each case 20 mL of dichloromethane. The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. The residue was chromatographed [silica gel 60 (40 g, 30 μηι); dichloromethane/methanol (95:5)]. 98 mg (38% of theory) of the title compound were isolated as a colourless solid. ¹ H-NMR (400 MHz, CDC ): δ [ppm] = 1 .73 (d, 3H), 2.61 (s, 3H), 3.97 (s, 6H), 5.61 (s br, 1 H), 5.76 (m, 1 H), 6.89 (m, 1 H), 7.20 (m, 1 H); 7.32-7.36 (m, 1 H), 7.41 -7.45 (m, 2H), 7.53-7.60 (m, 6H). LC-MS (method 1 ): R _t = 3.44 min; MS (ESI/APCIpos) m/z = 400.3 [M+H] ⁺ .

Example 197

N-[(1 R)-1 -(4-cyclopropylphenyl)ethyl]-6,7-dimethoxy-2-methylquinazoli n-4-amine

In the microwave vessel under argon, 200 mg (0.50 mmol) of [(R)-1 -(4-bromophenyl)- ethyl](6,7-dimethoxy-2-methylquinazolin-4-yl)amine (described in example 187), 128 mg (1 .49 mmol) of cyclopropyl boronic acid, 36 mg (0.05 mmol) of [bis(diphenylphosphino)ferrocene]dichloro-palladium(ll) and 485 mg (1 .49 mmol) caesium carbonate were dissolved in 10.0 mL of absolute 1 ,4-dioxane, degassed three times, aerated with argon and stirred for 30 min at 100°C. The reaction solution was evaporated to dryness in vacuo. The residue was taken up in 50 mL of dichloromethane and washed three times with in each case 10 mL of water. The organic phase was dried over sodium sulphate and evaporated to dryness in vacuo. The residue was chromatographed [silica gel 60 (40 g, 30 μιτι); dichloromethane/methanol (96:4)]. 1 16 mg (61 % of theory) of the title compound were isolated as an orange solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 0.66-0.70 (m, 2H), 0.93- 0.97 (m, 2H), 1.66 (d, 3H), 1.88 (m, 1 H), 2.60 (s, 3H), 3.94 (d, 6H), 5.57 (s, 1 H), 5.67 (m, 1 H), 6.83 (s, 1 H), 7.05-7.07 (m, 2H), 7.26 (s, 1 H), 7.26-7.37 (m, 2H). LC-MS (method 1 ): R _t = 3.31 min; MS (ESI/APCIpos) m/z = 364.3 [M+H] ⁺ .

Example 198

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(methylsulfonyl)phenyl]ethyl}quinazolin-4-amine

A solution of 200 mg (0.497 mmol) of [(R)-1 -(3-bromophenyl)ethyl](6,7-dimethoxy-2- methylquinazolin-4-yl)amine (described in example 191 ), 56 mg (0.547 mmol) of sodium methanesulphinate, 18 mg (0.05 mmol) of copper(ll) trifluoromethanesulphonate and 12 mg (0.099 mmol) of (±)-irans-1 ,2-diaminocyclohexane in 3 mL of dimethylsulphoxide was stirred at 100°C for 1 week. The crude batch was purified five times by column chromatography on the Flashmaster [Puri-Flash, silica gel 60 (1 ^χ 40 g, 4 ^x 25 g, 30 μηη), chloroform/methanol 98:2]. 47 mg (21 % of theory) of the title compound were isolated as colourless solid. ¹ H-NMR (400 MHz, CDCIs): δ [ppm] = 1 .63-1 .65 (m, 3H), 2.5 (s, 3H), 3.01 -3.93 (m, 3H), 5.68-5.71 (m, 1 H), 6.04-6.06 (m, 1 H), 7.05 (s, 3H), 7.1 1 (s, 1 H), 7.47-7.51 (m, 1 H), 7.74-7.79 (m, 2H), 8.03- 8.04 (m, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 402.2, R _t = 2.73 min.

Example 199

3-{(1 R)-1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}benzamide

In the microwave vessel, 1 14 mg (0.327 mmol) of 3-[(R)-1 -(6,7-dimethoxy-2-methyl- quinazolin-4-ylamino)ethyl]benzonitrile (described in example 194) and 3 mg (5.76 μηηοΙ) of hydrido(dimethylphosphinous acid-kP)[hydrogenbis(dimethylphosphinito-kP)]platinum(ll) were suspended in 2 mL of ethanol and 2 mL of water and stirred for 5 h at 100°C. The progress of the reaction was monitored by means of LC-MS. The reaction solution was brought to room temperature. The ethanol was removed in vacuo. During this, a solid precipitated out. The aqueous phase was extracted by shaking five times with in each case 2 mL of a mixture of dichloromethane:2-propanol (4:1 ). The combined organic phases were dried over sodium sulphate, filtered and evaporated to dryness in vacuo. The residue was chromatographed on the Flashmaster [silica gel 60 (40 g, 30 μιτι); dichloromethane/methanol (9:1 )]. 79 mg (59% of theory) of the title compound were isolated as a colourless solid. ¹ H- NMR (400 MHz, DMSO): δ [ppm] = 1 .56-1 .58 (m, 3H), 2.5 (s, 3H), 3.78 (s, 3H), 3.84 (s, 3H), 5.66-5.73 (m, 1 H), 6.15 (s, 1 H), 6.51 -6.57 (m, 1 H), 7.00 (s, 1 H), 7.12 (s, 1 H), 7.27-7.31 (m, 2H), 7.55-7.59 (m, 2H), 7.94 (s, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 367.2, R _t = 2.72 min.

Example 200

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}quinazolin-4-amine

Under argon a suspension of 2.0 M sodiumcaronate solution (644 mL, 1 .288 mmol), [(R)-1 - (3-Bromphenyl)ethyl]-(6,7-dimethoxychinazolin-4-ylamine (described in example 191 ; 200 mg, 0.515 mmol), 4-pyrazoleboronic acid pinacolester (200 mg, 1.03 mmol) and Tetrakis(triphenylphosphine)palladium(0) (60 mg, 0.052 mmol) in DMF (2 mL) was stirred at 130°C for 2 hours. Water (5 mL) was added to the reaction and the aqueous layer was extracted with dichloromethane:isopropanol 4:1 (4x 40 mL). The combined organic layers were dried over sodium sulfate, evaporated and the crude product was purified via Flashmaster column chromatography (silica gel 60, 30μη"ΐ, eluent: dichloromethane: methanol 98:2) to obtain the title compound in 8% yield (15 mg). ¹ H-NMR (400 MHz, DMSO): δ [ppm] =1 .61 -1 .63 (m, 3H), 3.89 (s, 3H), 3.94 (s, 3H), 5.62-5.65 (m, 1 H), 7.08 (s, 1 H), 7.25- 7.30 (m, 2H), 7.43-7.46 (m, 1 H), 7.66 (s, 1 H), 7.77 (s, 1 H), 8.06-8.07 (m, 1 H), 8.28 (s, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 376.3, R _t = 2.78 min.

Example 201

6,7-dimethoxy-2-methyl-N-{(1 R)-1.[4-(i -methyl-1 ,2,3,6-tetrahydropyridin-4- yl)phenyl]ethyl}quinazolin-4-amine

In the microwave vessel under argon, 200 mg (0.5 mmol) of [(R)-1 -(4-bromophenyl)- ethyl](6,7-dimethoxy-2-methylquinazolin-4-yl)amine (described in example 187), 221 mg (0.99 mmol) of 1 -methyl-1 ,2,3, 6-tetrahydropyridine-4-boronic acid pinacol ester, 36 mg (0.05 mmol) of [bis(diphenylphosphino)ferrocene]dichloropalladium(ll) and 486 mg (1 .49 mmol) of caesium carbonate were dissolved in 10.0 mL of absolute 1 ,4-dioxane, degassed three times, aerated with argon and stirred for 1 h at 120°C. The reaction solution was evaporated to dryness in vacuo. The residue was taken up in 50 mL of dichloromethane and washed three times with in each case 10 mL of water. The organic phase was dried over sodium sulphate and evaporated to dryness in vacuo. The residue was chromatographed [silica gel 60 (40 g, 30 m); dichloromethane/methanol (90:5 to 1 :1 )]. 102 mg (49% of theory) of the title compound were isolated as a brown solid. ¹ H-NMR (400 MHz, CDC ): δ [ppm] = 1 .69 (d, 2H), 2.43 (s, 3H), 2.56-2.59 (m, 5H), 2.70 (m, 2H), 3.14 (s, 2H), 3.92 (d, 6H), 5.18 (m, 1 H), 5.90-6.10 (m, 2H), 7.00 (s, 1 H), 7.15 (s, 1 H), 7.36 (d, 2H), 7.41 (d, 2H). LC-MS (method 1 ): R _t = 2.47 min; MS (ESI/APCIpos) m/z = 419.3 [M+H] ⁺ .

Example 202

6,7-dimethoxy-2-methyl-N-{(1 R)-1.[3.(1 -methyl-1 ,2,3,6-tetrahydropyridin-4- yl)phenyl]ethyl}quinazolin-4-amine

Under argon a suspension of [(R)-1 -(3-bromphenyl)ethyl]-(6,7-dimethoxy-2-methylchinazolin- 4-yl)amin (described in example 191 ; 300 mg, 0.746 mmol), 1 -methyl-1 ,2,3,6- tetrahydropyridine-4-boronic acid pinacol ester (250 mg, 1 .1 19 mmol), 1 ,2-dimethoxyethane (3 mL), water (0.9 mL), bis(triphenylphosphine)palladium(ll)dichloride (53 mg, 0.075 mmol) and potassium carbonate (310 mg, 2.237 mmol) was prepared. The reaction mixture was degassed three times and stirred at 90°C for 4 h. The course of the reaction was monitored by LC/MS. Mainly product was observed. The residue was dissolved in water (5 mL) und dichloromethane (10 mL) and the solution was extracted three times with 20 mL of dichlormethane. The combined organic layers were dried over sodium sulfate and then concentrated in vacuo. The crude product was purified by flash chromatography [silica gel 60 (25 g, 30 μηι); chloroform/methanol 95 : 5]. 101 mg (32 % d. Th.) of the title compound was isolated in form of a solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 1 .67-1 .69 (m, 3H), 2.39 (s, 3H), 2.58 (s, 5H), 2.64-2.67 (m, 2H), 3.08-3.1 1 (m, 2H), 3.91 -3.93 (m, 6H), 5.61 -5.71 (m, 2H), 6.03-6.04 (m, 1 H), 6.88 (s, 1 H), 7.12 (s, 1 H), 7.28-7.36 (m, 3H), 7.50 (s, 1 H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 419.3, R _t = 2.46 min.

Example 203

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[4-(prop-1 -en-2-yl)phenyl]ethyl}quinazolin-4-amine

A microwave vial was charged with 200 mg (0.5 mmol) N-[(1 R)-1 -(4-bromophenyl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine (described in example 187; 186 mg, 0.99 mmol) 2- isopropenyl-4,4,5,5-tetramethyl-1 ,3,2-dioxaborolane, 41 mg (0.05 mmol) [1 ,1 - bis(diphenylphosphino)ferrocene]dichloropalladium and 486 mg (1 .50 mmol) caesium carbonate. The vial was sealed with a Teflon cap and the mixture was dissolved in 10.0 mL of dry 1 ,4-dioxane. The vial was degassed three times, refilled with argon, and the mixture was stirred at 100°C for 2 h. The course of the reaction was monitored by LC/MS. Mainly product was observed. The mixture was concentrated in vacuo. The residue was dissolved in 100 ml. of dichloromethane and the solution was washed three times with 50 ml. of water. The combined organic layers were dried over sodium sulfate and then concentrated in vacuo. The crude product was purified by flash chromatography [silica gel 60, first column (40 g, 30 μηι); dichloromethane /methanol (95 : 5 ), second column (12 g, 30 μηι); ethyl acetate (100 %)]. 42 mg (21 %) of the title compound were obtained in form of a white- coloured solid. LC-MS (method 1 ): m/z: [M+H] ⁺ = 364.3, R _t = 3.39 min.

Example 204

N-[(1 R)-1 -(3-cyclopropylphenyl)ethyl]-6,7-dimethoxy-2-methylquinazoli n-4-amine

A microwave vial was charged with [(R)-1 -(3-Bromphenyl)ethyl]-(6,7-dimethoxy-2- methylchinazolin-4-yl)amine (described in example 191 ; 396 mg, 0.984 mmol) and cyclopropylboronic acid pinacol ester (496 mg, 2.953 mmol), [1 ,1 - bis(diphenylphosphino)ferrocene]-dichloropalladium (72 mg, 0.098 mmol) and caesium carbonate (962 mg, 2.953 mmol). The vial was sealed with a teflon cap and the mixture was dissolved in dry 1 ,4-dioxane (3 ml_). The vial was degassed three times, refilled with argon, and the mixture was stirred at 100°C for 30 min. The course of the reaction was monitored by LC/MS. The mixture was concentrated in vacuo. The residue was dissolved in dichloromethane (50 mL) and the solution was washed with water (3 x 50 mL). The combined organic layers were dried over sodium sulfate and then concentrated in vacuo. The crude product was purified by flash chromatography [silica gel 60 (40 g, 30 μηι); dichloromethane/methanol 95:5]. The thus obtained 95 mg of crude product was purified by preparative HPLC (column: Luna 5μηι phenyl-hexyl; acetonitrile/water/DEA; 250 x 30 mm; 65 : 35 : 0.1 ) to yield the title compound (13 mg, 3 %) as yellow solid. ¹ H-NMR (400 MHz, CDCIs): δ [ppm] = 0.68-0.72 (m, 2H), 0.94-0.99 (m, 2H), 1 .67-1 .69 (m, 3H), 1 .87-1.92 (m, 1 H), 2.61 (s, 3H), 3.95-3.96 (m, 6H), 5.50-5.68 (m, 2H), 6.84 (s, 1 H), 6.95-6.98 (m, 1 H), 7.18- 7.25 (m, 4H). LC-MS (method 1 ): m/z: [M+H] ⁺ = 364.2, R _t = 3.81 min.

Example 205

N-[1 -(1 -benzothiophen-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

The title compound was prepared in analogy to 1 -(5,6,7, 8-tetrahydronaphthalen-1 - yl)ethanamine (INT-1 ) from 4-bromo-1 -benzothiophene (commercially available, 1 .00 g, 4.69 mmol) and used directly in step b.

Step b:

N-[1 -(1 -benzothiophen-4-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 1 .02 g, 4.27 mmol), 1 -(1 -benzothiophen-4-yl)ethanamine (832 mg, 4.69 mmol), N,N-diisopropylethylamine (1 .9 ml_, 1 1 mmol) and DMSO (17 ml_). The reaction mixture was heated to 130°C during 2.5 hours in the microwave. The mixture was diluted with H2O, extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (234 mg, 14%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.10 (s, 1 H), 7.90 (d, 1 H), 7.78 (d, 1 H), 7.77-7.75 (m, 1 H), 7.71 (s, 1 H), 7.51 (d, 1 H), 7.37 (t, 1 H), 7.02 (s, 1 H), 6.18 (quin, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 2.33 (s, 3H), 1 .69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 380, R _t = 1 .25 min.

Example 206

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -phenylethyljquinazolin

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 1 .00 g, 4.19 mmol), (1 R)-1 -phenylethanamine (commercially available; 590 μΙ_, 4.6 mmol), N,N-diisopropylethylamine (1 .9 mL, 1 1 mmol) and DMSO (17 mL). The reaction mixture was heated to 130°C during 2.5 hours in the microwave. The mixture was diluted with H2O, extracted with DCM and the solvent removed in vacuo. The crude residue was purified by column chromatography (silica gel, hexane/EtOAc 50-100%). The resulting residue was stirred in Et.20 over the weekend then filtered to give the title compound as a pale yellow solid (909 mg, 66%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.99 (d, 1 H), 7.71 (s, 1 H), 7.46 (s, 1 H), 7.44 (s, 1 H), 7.32 (t, 2H), 7.22 (tt, 1 H), 7.02 (s, 1 H), 5.67 (quin, 1 H), 3.90 (s, 3H), 3.86 (s, 3H), 2.35 (s, 3H), 1 .59 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 324,

Example 207

6,7-dimethoxy-2-methyl-N-[1 -(thiophen-2-yl)ethyl]quinazolin-4-amine

Step a:

1 -(thiophen-2-yl)ethanamine The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from thiophene-2-carbaldehyde (commercially available, 1 12 mg, 1.00 mmol) to give 24.3 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(thiophen-2-yl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 41.4 mg, 174 μηιοΙ), 1 -(thiophen-2-yl)ethanamine (24.3 mg, 191 μηιοΙ), Ν,Ν- diisopropylethylamine (77 μΙ_, 450 μηιοΙ) and DMSO (1 .3 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (17 mg, 30%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.09 (d, 1 H), 7.64 (s, 1 H), 7.36 (dd, 1 H), 7.08 (d, 1 H), 7.05 (s, 1 H), 6.98 (dd, 1 H), 5.94 (quin, 1 H), 3.87 (d, 6H), 2.42 (s, 3H), 1.69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 330, R _t = 0.72 min.

Example 208

N-[1 -(5-bromofuran-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

Step a:

1 -(5-bromofuran-2-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 5-bromo-2-furaldehyde (commercially available, 3.00 g, 17.1 mmol) to give 1.67 g of the title compound.

Step b:

N-[1 -(5-bromofuran-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 343 mg, 1 .44 mmol), 1 -(5-bromofuran-2-yl)ethanamine (300 mg, 1.58 mmol), N,N- diisopropylethylamine (640 μΙ_, 3.7 mmol) and DMSO (10 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (basic conditions) gave the title compound as a beige solid (1 .13 g, 45%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.01 (d, 1 H), 7.63 (s, 1 H), 7.05 (s, 1 H), 6.51 (d, 1 H), 6.41 (dd, 1 H), 5.75 (quin, 1 H), 3.87 (s, 6H), 2.42 (s, 3H), 1 .55 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 392, R _t = 0.85 min.

Example 209

N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 2.39 g, 10.0 mmol), 1 -(5-bromothiophen-2-yl)ethanamine (described in procedure INT-28; 2.27 g, 1 1 .0 mmol), N,N-diisopropylethylamine (4.5 ml_, 26 mmol) and DMSO (20 ml_). The reaction mixture was heated to 130°C during 6 hours in the microwave. The mixture was added to H2O, extracted with DCM and the solvent removed in vacuo. The residue was stirred in Et.20 during 20 minutes then filtered to give the title compound as a beige solid (3.00 g, 73%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.09 (d, 1 H), 7.60 (s, 1 H), 7.06 (d, 1 H), 7.05 (s, 1 H), 6.92 (dd, 1 H), 5.78 (quin, 1 H), 3.87 (d, 6H), 2.43 (s, 3H), 1.66 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 408, R _t = 0.91 min.

Example 210

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]pyrrolidin-3-ol H

To 2-(5-{1-[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(described in example 179a; 50.0 mg, 115 μηιοΙ), pyrrolidin-3-ol (19 μΙ_, 230 μηιοΙ) and acetic acid (13 μΙ_, 230 μπιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (38.8 mg, 66%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1H), 7.65 (s, 1H), 7.44 (dd, 1H), 7.37-7.33 (m, 1H), 7.33-7.24 (m, 2H), 7.20 (d, 1H), 7.07 (dd, 1H), 7.05 (s, 1H), 5.97 (quin, 1H), 4.64 (dd, 1H), 4.18-4.09 (m, 1H), 3.87 (s, 6H), 3.55 (d, 1H), 3.51 (d, 1H), 2.66-2.62 (m, 1H), 2.57-2.53 (m, 1H), 2.43 (s, 3H), 2.40-2.35 (m, 1H), 2.30-2.24 (m, 1H), 1.95-1.84 (m, 1H), 1.71 (d, 3H), 1.52-1.43 (m, 1H). LC-MS (method 7): m/z: [M+H] ⁺ = 505, Rt = 0,59 min.

Example 211

N-{1-[5-(2-{[(3S)-3-fluoropyrrolidin-1-yl]methyl}phenyl)thio phen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1-[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl} thiophen-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 115 μηηοΙ), 3-fluoropyrrolidine (20.6 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (31.6 mg, 54%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1H), 7.65 (s, 1H), 7.45 (dd, 1H), 7.38-7.35 (m, 1H), 7.34-7.27 (m, 2H), 7.18 (dd, 1H), 7.08 (dd, 1H), 7.05 (s, 1H), 5.97 (quin, 1H), 5.13 (br d, 1H), 3.87 (s, 3H), 3.87 (s, 3H), 3.59 (d, 1H), 3.56 (dd, 1H), 2.79-2.68 (m, 2H), 2.65-2.53 (m, 1H), 2.42 (s, 3H), 2.28 (br q, 1H), 2.13- 1.95 (m, 1H), 1.88-1.74 (m, 1H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 507, Rt = 0,62 min.

Example 212

6,7-dimethoxy-2-methyl-N-[1-(quinolin-5-yl)ethyl]quinazolin

The title compound was prepared in analogy to 1-(5-bromothiophen-2-yl)ethanamine (INT- 28) from quinoline-8-carbaldehyde (commercially available, 1.00 g, 6.36 mmol) to give 206 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1-(quinolin-5-yl)ethyl]quinazolin- 4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 50.0 mg, 209 μηηοΙ), 1-(quinolin-5-yl)ethanamine (39.7 mg, 230 μηηοΙ), Ν,Ν- diisopropylethylamine (93 μΙ_, 540 μηηοΙ) and DMSO (1.5 mL). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a white solid (14.6 mg, 19%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.91 (dd, 1H), 8.77 (d, 1H), 8.19 (d, 1H), 7.94 (dd, 1H), 7.81-7.73 (m, 2H), 7.70 (s, 1H), 7.58 (dd, 1H), 7.03 (s, 1H), 6.40 (quin, 1H), 3.88 (s, 3H), 3.86 (s, 3H), 2.31 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 375, R _t = 0.58 min. Example 213

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4-amine

Step a:

1 -(5-phenylfuran-2-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 5-phenyl-2-furaldehyde (commercially available, 300 mg, 1 .74 mmol) to give 25 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 29.0 mg, 121 μηιοΙ), 1 -(5-phenylfuran-2-yl)ethanamine (25.0 mg, 134 μηιοΙ), Ν,Ν- diisopropylethylamine (54 μΙ_, 320 μmol) and DMSO (900 μΙ_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light orange solid (9.4 mg, 20%). ¹ H-NMR (500 MHz, DMSO-de): δ [ppm] = 7.68 (s, 1 H), 7.64 (d, 1 H), 7.62 (d, 1 H), 7.38 (t, 2H), 7.27-7.22 (m, 1 H), 7.04 (s, 1 H), 6.88 (d, 1 H), 6.44 (d, 1 H), 5.84 (quin, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 2.45 (s, 3H), 1 .63 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 390, R _t = 0.95 min.

Example 214

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

Step a:

1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 5-bromo-2,3-dihydro-1 -benzofuran-7-carbaldehyde (commercially available, 1 .00 g, 4.40 mmol) to give 65 mg of the title compound.

Step b:

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 64.1 mg, 268 μηηοΙ), 1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethanamine (65.0 mg, 268 mol), N,N-diisopropylethylamine (120 μΙ_, 700 mol) and DMSO (2.0 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a yellow solid (51.9 mg, 44%). ¹ H-NMR (500 MHz, DMSO-de): δ [ppm] = 7.93 (d, 1 H), 7.71 (s, 1 H), 7.26 (s, 2H), 7.02 (s, 1 H), 5.66 (quin, 1 H), 4.65-4.55 (m, 2H), 3.91 (s, 3H), 3.86 (s, 3H), 3.20 (br t, 2H), 2.32 (s, 3H), 1.50 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 444, R _t = 0.93 min.

Example 215

6,7-dimethoxy-2-methyl-N-[1 -(3-phenoxyphenyl)ethyl]quinazolin-4-amine

Step a:

1 -(3-phenoxyphenyl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 3-phenoxybenzaldehyde (commercially available, 1.00 g, 5.05 mmol) to give 18 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(3-phenoxyphenyl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 18.3 mg, 76.7 μηηοΙ), 1 -(3-phenoxyphenyl)ethanamine (18.0 mg, 84.4 μηηοΙ), Ν,Ν- diisopropylethylamine (34 μΙ_, 200 μηηοΙ) and DMSO (600 μΙ_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (6.00 mg, 19%). ¹ H-NMR (500 MHz, DMSO-de): δ [ppm] = 7.98 (d, 1 H), 7.67 (s, 1 H), 7.38-7.32 (m, 3H), 7.23 (d, 1 H), 7.14- 7.10 (m, 2H), 7.03 (s, 1 H), 6.99-6.98 (m, 1 H), 6.98-6.96 (m, 1 H), 6.83 (dd, 1 H), 5.61 (quin, 1 H), 3.89 (s, 3H), 3.87 (s, 3H), 2.33 (s, 3H), 1.58 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 416, R _t = 0.99 min.

Example 216

6 -dimethoxy-2-methyl-N-{1 -[3-(2H-tetrazol-5-yl)phenyl]ethyl}quinazolin

1 -[3-(2H-tetrazol-5-yl)phenyl]ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 3-(2H-tetrazol-5-yl)benzaldehyde (commercially available, 1.00 g, 4.69 mmol) to give 165 mg of the title compound.

Step b:

6 -dimethoxy-2-methyl-N- 1 -[3-(2H-tetrazol-5-yl)phenyl]ethyl}quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 57.8 mg, 242 μηιοΙ), 1 -[3-(2H-tetrazol-5-yl)phenyl]ethanamine (168 mg, 30 % purity, 266 mol), N,N-diisopropylethylamine (1 10 μΙ_, 630 mol) and DMSO (1 .8 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (4.00 mg, 4%). ¹ H-NMR (500 MHz, DMSO-de): δ [ppm] = 8.48 (br d, 1 H), 8.18-8.1 1 (m, 1 H), 7.87 (dt, 1 H), 7.79 (s, 1 H), 7.50 (br d, 1 H), 7.45 (t, 1 H), 7.03 (s, 1 H), 5.75 (quin, 1 H), 3.92 (s, 3H), 3.88 (s, 3H), 2.41 (s, 3H), 1.66 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 392, R _t = 0.64 min.

Example 217

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-8-yl)ethyl]quinazolin-4-amine

Step a:

1 -(quinolin-8-yl)ethanamine hydrochloride (1 :1)

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from quinoline-8-carbaldehyde (commercially available, 1 .00 g, 4.69 mmol) to give 50 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-8-yl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 52.0 mg, 218 μηιοΙ), 1 -(quinolin-8-yl)ethanamine hydrochloride (1 :1 ) (50.0 mg, 240 μηιοΙ), N,N-diisopropylethylamine (130 μΙ_, 780 μηιοΙ) and DMSO (1 .6 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (4.3 mg, 5%). ¹ H- NMR (600 MHz, DMSO-de): δ [ppm] = 9.04 (dd, 1 H), 8.40 (dd, 1 H), 8.24 (br d, 1 H), 7.88-7.85 (m, 1 H), 7.83 (br s, 1 H), 7.82 (s, 1 H), 7.60 (dd, 1 H), 7.57 (t, 1 H), 7.03 (s, 1 H), 6.75 (quin, 1 H), 3.98 (s, 3H), 3.88 (s, 3H), 2.21 (s, 3H), 1.71 (d, 3H). LC-MS (method 8): m/z: [M+H] ⁺ = 375, R _t = 0.96 min.

Example 218

2-[4-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl )-1 H- pyrazol-1 -yl]ethanol

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 50.0 mg, 122 μηιοΙ), 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)-1 H-pyrazol-1 -yl]ethanol (29.2 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μπιοΙ) and Pd(PPh ₃ ) ₄ (7.08 mg, 6.12 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (26.4 mg, 49%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.53 (br s, 1 H), 7.95 (s, 1 H), 7.71 (s, 1 H), 7.66 (d, 1 H), 7.07 (s, 1 H), 7.04-7.01 (m, 1 H), 7.01 -6.98 (m, 1 H), 5.94 (quin, 1 H), 4.92 (br s, 1 H), 4.1 1 (t, 2H), 3.90 (s, 2H), 3.91 -3.89 (m, 1 H), 3.89 (s, 3H), 3.72 (br d, 2H), 2.49 (s, 3H), 1.70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 440, R _t = 0.67 min.

Example 219

N-{1 -[5-(6 -dihydro-5H^yrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6 -dim

2-methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine hydrochloride (1 :1 ) (described in example 209; 300 mg, 674 μηηοΙ), 6,7-dihydro-5H- pyrrolo[1 ,2-a]imidazol-3-ylboronic acid (102 mg, 674 μηιοΙ), K2CO3 (373 mg, 2.70 mmol) and Pd(PPh ₃ ) ₄ (39.0 mg, 33.7 μηιοΙ) in dioxane (6.9 mL) and H ₂ 0 (1 .4 mL) were stirred at 1 10°C overnight. 6,7-Dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-ylboronic acid (50 mg, 330 μηηοΙ) and Pd(PP i3) ₄ (30.0 mg, 25.9 μηηοΙ) were then added again and the reaction mixture further stirred at 1 10°C during 10 hours. H2O was added, the mixture extracted with DCM, dried (hydrophobic filtration) and the solvent removed in vacuo. The crude residue was purified by preparative HPLC (basic conditions). The resulting residue was stirred in Et20 during 20 minutes then filtered to give the title compound as a white solid (1 17 mg, 38%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.63 (s, 1 H), 7.03 (t, 4H), 5.89 (quin, 1 H), 4.06 (t, 2H), 3.87 (s, 6H), 2.77-2.71 (m, 2H), 2.59-2.53 (m, 2H), 2.43 (s, 3H), 1.68 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 436, R _t = 0.49 min.

Example 220

6,7-dimethoxy-2-methyl-N-[1 -(5-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-4-yl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 50.0 mg, 122 μηιοΙ), 1 -[2-(pyrrolidin-1 -yl)ethyl]-4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole (35.7 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μιτιοΙ) and Pd(PPh ₃ )4 (7.08 mg, 6.12 μιτιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (27.5 mg, 46%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.10 (d, 1 H), 7.99 (s, 1 H), 7.65 (d, 2H), 7.05 (s, 1 H), 7.00 (d, 1 H), 6.97 (dd, 1 H), 5.90 (quin, 1 H), 4.17 (t, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.81 (t, 2H), 2.47-2.40 (m, 7H), 1 .68 (d, 3H), 1 .64 (dt, 4H). LC-MS (method 7): m/z: [M+H] ⁺ = 493, R _t = 0.54 min.

Example 221

N-{1 -[5-(1 -cyclopentyl-1 H-pyrazol-4-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηηοΙ), 1 -cyclopentyl-4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)-1 H-pyrazole (12.8 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (4.70 mg, 21 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 8.01 (s, 1 H), 7.64 (s, 1 H), 7.64 (d, 1 H), 7.05 (s, 1 H), 7.01 (d, 1 H), 6.96 (dd, 1 H), 5.90 (quin, 1 H), 4.65 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 2.43 (s, 3H), 2.10-2.00 (m, 2H), 1 .95-1 .85 (m, 2H), 1 .83-1 .71 (m, 2H), 1.68 (d, 3H), 1.65-1 .56 (m, 2H). LC-MS (method 7): m/z: [M+H] ⁺ = 464, R _t = 0.95 min.

Example 222

6,7-dimethoxy-2-methyl-N-{1 -[5-(1 H-pyrazol-3-yl)thiophen-2-yl]ethyl}quinazolin-4- amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), 3-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)-1 H-pyrazole (9.50 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μιτιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C over the weekend. 3- (4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole (9.50 mg, 49.0 μιτιοΙ) and Pd(PP i3) ₄ (2.83 mg, 2.45 μηηοΙ) were then added again and the reaction mixture further stirred at 1 10°C during 24 hours. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as an off-white solid (3.10 mg, 16%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 12.78 (br s, 1 H), 8.14 (s, 1 H), 7.71 (br s, 1 H), 7.66 (s, 1 H), 7.21 (d, 1 H), 7.06 (s, 1 H), 7.01 (br d, 1 H), 6.53 (br s, 1 H), 5.92 (quin, 1 H), 3.88 (s, 6H), 2.44 (s, 3H), 1.70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 396, R _t = 0.71 min.

Example 223

N-[1 -(5-{2-[(3,3-difluoropyrrolidin-1 -yl)methyl]phenyl}thiophen-2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen

(described in example 179a; 50.0 mg, 1 15 μηηοΙ), 3,3-difluoropyrrolidine hydrochloride (1 :1 ) (33.1 mg, 231 μηιοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (41.6 mg, 69%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.46-7.42 (m, 1 H), 7.40-7.36 (m, 1 H), 7.35-7.29 (m, 2H), 7.15 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.60 (s, 2H), 2.83 (t, 2H), 2.64 (t, 2H), 2.42 (s, 3H), 2.21 -2.09 (m, 2H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 525, Rt = 1.00 min.

Example 224

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4-amine, enantiomer 1

Step a:

1 -(5-phenylfuran-2-yl)ethanamine, enantiomer 1

The title compound was prepared by first synthesising the sulfinamide analogous to N-[1 -(5- bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (INT-28b) from 5-phenyl-2- furaldehyde (commercially available, 300 mg, 1 .74 mmol), separating the two diastereoisomers obtained by preparative HPLC (Method X3) and then deprotecting diastereoisomer 1 in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT-28c) to give 43 mg of the title compound.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(5-phenylfuran-2-yl)ethyl]quinazolin-4-amine, enantiomer 1

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 35.9 mg, 151 μηιοΙ), 1 -(5-phenylfuran-2-yl)ethanamine (enantiomer 1 , 31.0 mg, 166 μηιοΙ), N,N-diisopropylethylamine (67 μΙ_, 390 μmol) and DMSO (1 .1 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (19.0 mg, 30%). ¹ H- NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (s, 1 H), 7.68 (s, 1 H), 7.66 (d, 1 H), 7.64 (d, 1 H), 7.39 (t, 2H), 7.29-7.23 (m, 1 H), 7.06 (s, 1 H), 6.89 (d, 1 H), 6.45 (dd, 1 H), 5.85 (quin, 1 H), 3.88 (s, 3H), 3.87 (s, 3H), 2.45 (s, 3H), 1 .65 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 390, R _t = 0.93 min.

Example 225

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

Step a:

1 -(5-bromo-2,3-dihydro-1 -benzofuran-7- l)ethanamine, enantiomer 1

The title compound was prepared by first synthesising the sulfinamide analogous to N-[1 -(5- Bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (INT-28b) from 5-bromo-2,3- dihydro-1 -benzofuran-7-carbaldehyde (commercially available, 1.00 g, 4.40 mmol), separating the two diastereoisomers obtained by preparative HPLC (Method X3) and then deprotecting diastereoisomer 1 in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT-28c) to give 60 mg of the title compound. Step b:

N-[1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 48.4 mg, 203 μηηοΙ), 1 -(5-bromo-2,3-dihydro-1 -benzofuran-7-yl)ethanamine (enantiomer 1 , 54.0 mg, 223 μηηοΙ), N,N-diisopropylethylamine (90 μΙ_, 530 μmol) and DMSO (1 .5 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (33.7 mg, 36%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (s, 1 H), 7.74 (s, 1 H), 7.28 (d, 2H), 7.04 (s, 1 H), 5.68 (quin, 1 H), 4.62 (td, 2H), 3.93 (s, 3H), 3.88 (s, 3H), 3.21 (t, 2H), 2.35 (s, 3H), 1.52 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 444, R _t = 0.90 min.

Example 226

2- [1 -(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}furan-2 -yl)-1 H-pyrazol-

3- yl]ethanol

Step a:

1 -(5-bromo-2-furyl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 5-bromo-2-furaldehyde (commercially available, 3.00 g, 17.1 mmol) to give 300 mg of the title compound.

Step b:

N-[1 -(5-bromo-2-furyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 343 mg, 1 .44 mmol), 1 -(5-bromo-2-furyl)ethanamine (300 mg, 1 .58 mmol), N,N- diisopropylethylamine (639 μΙ_, 3.74 mmol) and DMSO (10.0 mL). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (basic conditions) gave the title compound as a beige solid (227 mg, 40%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.01 (d, 1 H), 7.63 (s, 1 H), 7.05 (s, 1 H), 6.51 (d, 1 H), 6.41 (dd, 1 H), 5.75 (quin, 1 H), 3.87 (s, 6H), 2.42 (s, 3H), 1 .55 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 392, R _t = 0.82 min.

Step c:

2- [1 -(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}furan-2 -yl)-1 H-pyrazol-

3- yl]ethanol

Under argon, N-[1 -(5-bromo-2-furyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4- amine (20.0 mg, 51 .0 mol), 2-(1 H-pyrazol-3-yl)ethanol (5.72 mg, 51 .0 mol), Cs ₂ C0 ₃ (33.2 mg, 102 mol) and Cu(OAc) ₂ (460 Mg, 2.5 Mmol) in DMF (500 μί) were stirred at 1 10°C for a week. The crude reaction mixture was filtered through celite. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (7.60 mg, 35%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.03 (d, 1 H), 7.92 (s, 1 H), 7.64 (s, 1 H), 7.60 (s, 1 H), 7.04 (s, 1 H), 6.46 (dd, 1 H), 6.34 (d, 1 H), 5.79 (quin, 1 H), 4.69 (t, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 3.59- 3.52 (m, 2H), 2.59 (t, 2H), 2.43 (s, 3H), 1 .60 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 424,

Example 227

5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}pyridin -2(1 H)-one,

enantiomer 1

Step a:

5-[1 -aminoethyl]pyridin-2(1 H)-one, enantiomer 1

The title compound was prepared by first synthesising the sulfinamide analogous to N-[1 -(5- Bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (INT-28b) from 6-oxo-1 ,6- dihydropyridine-3-carbaldehyde (commercially available, 1 .00 g, 8.12 mmol), separating the two diastereoisomers obtained by preparative HPLC (Method X4) and then deprotecting diastereoisomer 1 in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT-28c) to give the title compound which was used directly in step b.

Step b:

5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}pyridin -2(1 H)-one,

enantiomer 1

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 72.5 mg, 304 μηηοΙ), 5-[1 -aminoethyl]pyridin-2(1 H)-one (enantiomer 1 , 46.1 mg, 334 μηηοΙ), N,N-diisopropylethylamine (210 μΙ_, 1 .2 mmol) and DMSO (3.0 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions followed by basic conditions) gave the title compound as a light yellow solid (1 1 .5 mg, 1 1 %). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 1 .42 (br s, 1 H), 7.82 (d, 1 H), 7.61 (s, 1 H), 7.55 (dd, 1 H), 7.31 (br s, 1 H), 7.03 (s, 1 H), 6.32 (d, 1 H), 5.39 (quin, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 2.39 (s, 3H), 1.51 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 341 , R _t = 0.49 min.

Example 228 6,7-dimethoxy-2-methyl-N- 1 -(3-phenoxyphenyl)ethyl]quinazolin-4-amine, enantiomer 1

Step a:

1 -(3-phenoxyphenyl)ethanamine, enantiomer 1

The title compound was prepared by first synthesising the sulfinamide analogous to N-[1 -(5- Bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (INT-28b) from 3- phenoxybenzaldehyde (commercially available, 1 .00 g, 5.05 mmol), separating the two diastereoisomers obtained by preparative HPLC (Method X5) and then deprotecting diastereoisomer 1 in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT-28c) to give the title compound which was used directly in step b.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(3-phenoxyphenyl)ethyl]quinazolin-4-amine, enantiomer 1

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 75.3 mg, 315 μηηοΙ), 1 -(3-phenoxyphenyl)ethanamine (enantiomer 1 , 74.0 mg, 347 μηιοΙ), N,N-diisopropylethylamine (220 μΙ_, 1 .3 mmol) and DMSO (3.2 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions followed by basic conditions) gave the title compound as a light yellow solid (57.9 mg, 43%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 9.12 (br s, 1 H), 7.92 (s, 1 H), 7.40-7.33 (m, 3H), 7.26 (d, 1 H), 7.17-7.10 (m, 3H), 7.00 (br d, 1 H), 6.98 (br d, 1 H), 6.88-6.83 (m, 1 H), 5.70 (quin, 1 H), 3.93 (s, 3H), 3.92 (s, 3H), 2.46 (s, 3H), 1 .64 (d, 3H). LC- MS (method 7): m/z: [M+H] ⁺ = 416, R _t = 0.96 min.

Example 229

N-[1 -(2,1 ,3-benzothiadiazol-5-yl)ethyl]-6,7-dimethoxy-2-methylquinazo lin-4-amine

Step a:

1 -(2,1 ,3-benzothiadiazol-5-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 2,1 ,3-benzothiadiazole-5-carbaldehyde (commercially available, 500 mg, 3.05 mmol) and used directly in step b.

Step b:

N-[1 -(2 ,3-benzothiadiazol-5-yl)ethyl]-6,7-dimethoxy-2-methylquinazo lin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 23.9 mg, 100 μηιοΙ), 1 -(2,1 ,3-benzothiadiazol-5-yl)ethanamine (19.7 mg, 1 10 μηιοΙ), N,N-diisopropylethylamine (68 μΙ_, 400 μηιοΙ) and DMSO (1 .0 mL). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions followed by basic conditions) gave the title compound as a light yellow solid (1 1 .6 mg, 29%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.30 (br s, 1 H), 8.07 (d, 1 H), 8.06 (s, 1 H), 7.86 (dd, 1 H), 7.77 (s, 1 H), 7.04 (s, 1 H), 5.82 (quin, 1 H), 3.94 (s, 3H), 3.88 (s, 3H), 2.36 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 382, R _t = 0.75 min.

Example 230

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-8-yl)ethyl]quinazolin-4-amine, enantiomer 1

The title compound was prepared by first synthesising the sulfinamide analogous to N-[1 -(5- Bromothiophen-2-yl)ethyl]-2-methylpropane-2-sulfinamide (INT-28b) from quinoline-8- carbaldehyde (commercially available, 1.00 g, 4.69 mmol), separating the two diastereoisomers obtained by preparative HPLC (Method X6) and then deprotecting diastereoisomer 1 in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT-28c) to give the title compound which was used directly in step b.

Step b:

6,7-dimethoxy-2-methyl-N-[1 -(quinolin-8-yl)ethyl]quinazolin-4-amine, enantiomer 1

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 45.6 mg, 191 μηηοΙ), 1 -(quinolin-8-yl)ethanamine (enantiomer 1 , 36.2 mg, 210 μηιοΙ), N,N-diisopropylethylamine (130 μΙ_, 760 μηιοΙ) and DMSO (2.0 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions followed by basic conditions) gave the title compound as a light yellow solid (6.30 mg, 9%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 9.03 (dd, 1 H), 8.39 (dd, 1 H), 8.24 (d, 1 H), 7.86 (d, 1 H), 7.84-7.80 (m, 2H), 7.60 (dd, 1 H), 7.56 (t, 1 H), 7.02 (s, 1 H), 6.74 (quin, 1 H), 3.97 (s, 3H), 3.87 (s, 3H), 2.19 (s, 3H), 1.70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 375, R _t = 0.81 min.

Example 231 N-{1 -[5-(cyclopent-1 -en-1 -yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-methylquinazolin

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), cyclopent-1 -en-1 -ylboronic acid (5.48 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μπιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μί) and H2O (100 μί) were stirred at 1 10°C over the weekend. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (1 .50 mg, 8%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.07 (d, 1 H), 7.64 (s, 1 H), 7.05 (s, 1 H), 6.94 (d, 1 H), 6.84 (d, 1 H), 5.91 -5.86 (m, 1 H), 3.87 (s, 6H), 2.63-2.56 (m, 2H), 2.45-2.40 (m, 5H), 1.97-1 .86 (m, 2H), 1.66 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 396, R _t = 1 .01 min.

Example 232

N-{1 -[5-(2-ethoxyphenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-met hylquinazolin-4- amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), (2-ethoxyphenyl)boronic acid (8.13 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as an off-white solid (1 1.8 mg, 54%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.12 (d, 1 H), 7.66 (s, 1 H), 7.64 (dd, 1 H), 7.45 (d, 1 H), 7.22 (td, 1 H), 7.08-7.04 (m, 3H), 6.96 (td, 1 H), 5.94 (quin, 1 H), 4.10 (q, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.44 (s, 3H), 1.71 (d, 3H), 1 .33 (t, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 450, R _t = 1 .00 mm.

Example 233 N-{1 -[5-(4-fluoronaphthalen-1 -yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηηοΙ), (4-fluoronaphthalen-1 -yl)boronic acid (9.31 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μπιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as an off-white solid (12.6 mg, 54%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.22-8.17 (m, 2H), 8.16-8.10 (m, 1 H), 7.73-7.65 (m, 3H), 7.53 (dd, 1 H), 7.37 (dd, 1 H), 7.20 (dd, 1 H), 7.18 (d, 1 H), 7.06 (s, 1 H), 6.01 (quin, 1 H), 3.88 (s, 3H), 3.87 (s, 3H), 2.44 (s, 3H), 1 .76 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 474, R _t = 1 .09 min.

Example 234

N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 2.00 mg, 4.90 μηηοΙ), [2-(aminomethyl)-4-fluorophenyl]boronic acid hydrochloride (1 :1 ) (1 .01 g, 4.90 mmol), K2CO3 (2.71 mg, 19.6 mmol) and Pd(PPh ₃ ) ₄ (566 mg, 490 μηηοΙ) in dioxane (50 mL) and H2O (10 mL) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (1 .26 g, 50%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.25 (s, 1 H), 8.16 (d, 1 H), 7.65 (s, 1 H), 7.45 (dd, 1 H), 7.34 (dd, 1 H), 7.14-7.07 (m, 2H), 7.05 (s, 1 H), 7.04 (d, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.84 (s, 2H), 2.44 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 453, R _t = 0.55 min. Example 235

N-{1 -[5-(3,6-dihydro-2H-pyran-4-yl)thiophen-2-yl]ethyl}-6,7-dime thoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηηοΙ), 4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)-3,6-dihydro-2H-pyran (10.3 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μπιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (5.40 mg, 27%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.08 (d, 1 H), 7.64 (s, 1 H), 7.05 (s, 1 H), 6.96 (dd, 1 H), 6.92 (d, 1 H), 6.02 (br s, 1 H), 5.87 (quin, 1 H), 4.14 (br d, 2H), 3.87 (s, 6H), 3.76 (t, 2H), 2.42 (s, 3H), 2.41 -2.36 (m, 2H), 1.66 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 412, R _t = 0.81 min.

Example 236

tert-butyl {[5-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)furan-2-yl]methyl}carbamate

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 40.0 mg, 98.0 μηηοΙ), (5-{[(tert- butoxycarbonyl)amino]methyl}furan-2-yl)boronic acid (23.6 mg, 98.0 μηηοΙ), K2CO3 (54.2 mg, 392 μηιοΙ) and Pd(PPh ₃ ) ₄ (5.66 mg, 4.90 μηιοΙ) in dioxane (1 .0 mL) and H ₂ 0 (200 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (29.0 mg, 55%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.35 (br t, 1 H), 7.14 (d, 1 H), 7.06 (s, 1 H), 7.03 (dd, 1 H), 6.56 (d, 1 H), 6.23 (d, 1 H), 5.92 (quin, 1 H), 4.10 (br d, 2H), 3.88 (s, 3H), 3.88-3.87 (m, 3H), 2.43 (s, 3H), 1 .70 (d, 3H), 1 .36 (s, 9H). LC-MS (method 7): m/z: [M+H] ⁺ = 525, R _t = 0.97 min.

Example 237

methyl 3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-1 - methyl-1 H-pyrazole-5-carbox late

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), methyl 1 -methyl-3-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole-5-carboxylate (13.0 mg, 49.0 μηηοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (1 .60 mg, 7%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.13 (d, 1 H), 7.65 (s, 1 H), 7.35 (d, 1 H), 7.21 (s, 1 H), 7.06 (s, 1 H), 7.03 (dd, 1 H), 5.92 (quin, 1 H), 4.05 (s, 3H), 3.88 (s, 6H), 3.84 (s, 3H), 2.43 (s, 3H), 1.70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 468, R _t = 0.88 min.

Example 238

N-{1 -[5-(2-{[3-(dimethylamino)pyrrolidin-1 -yl]methyl}phenyl)thiophen-2-yl]ethyl}-6 dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), N,N-dimethylpyrrolidin-3-amine (26.3 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηιοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a pale yellow solid (43.5 mg, 70%). ¹ H-NMR (400 MHz, DMSO- d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.43-7.39 (m, 1 H), 7.38-7.34 (m, 1 H), 7.32-7.25 (m, 2H), 7.17 (d, 1 H), 7.07 (d, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.54 (d, 1 H), 3.46 (dd, 1 H), 2.65-2.58 (m, 1 H), 2.43 (s, 3H), 2.41 -2.35 (m, 1 H), 2.26-2.20 (m, 1 H), 1 .98 (s, 6H), 1 .71 (d, 3H), 1.70-1 .64 (m, 1 H), 1.53-1 .42 (m, 1 H). LC-MS (method 7): m/z: [M+H] ⁺ = 532, Rt = 0,61 min.

Example 239

N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 895 mg, 3.75 mmol), 1 -(5-bromothiophen-3-yl)ethanamine (described in procedure INT-30; 850 mg, 4.12 mmol), N,N-diisopropylethylamine (1 .7 mL, 9.7 mmol) and DMSO (19 mL). The reaction mixture was heated to 130°C during 2.5 hours in the microwave. The mixture was diluted with H2O, extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light brown solid (541 mg, 35%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.94 (d, 1 H), 7.64 (s, 1 H), 7.41 -7.35 (m, 1 H), 7.24 (d, 1 H), 7.04 (s, 1 H), 5.70 (quin, 1 H), 3.88 (s, 3H), 3.87 (s, 3H), 2.40 (s, 3H), 1 .56 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 408, R _t = 0.90 min.

Example 240

2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzamide

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-ai (described in example 209; 20 mg, 49.0 μηιοΙ), (2-carbamoylphenyl)boronic acid (8.08 49.0 μη-ιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μί) and H2O (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (8.50 mg, 39%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.79 (s, 1 H), 7.65 (s, 1 H), 7.44-7.38 (m, 3H), 7.35-7.32 (m, 2H), 7.13 (d, 1 H), 7.06-7.04 (m, 2H), 5.95 (quin, 1 H), 3.87 (s, 6H), 2.44 (s, 3H), 1 .70 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 449, R _t = 0.77 min.

Example 241

3-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzamide

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), (3-carbamoylphenyl)boronic acid (8.08 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (14.2 mg, 61 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 8.08 (s, 1 H), 8.06 (t, 1 H), 7.78-7.71 (m, 2H), 7.66 (s, 1 H), 7.48-7.42 (m, 3H), 7.1 1 (dd, 1 H), 7.06 (s, 1 H), 5.96 (quin, 1 H), 3.88 (s, 6H), 2.44 (s, 3H), 1 .72 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 449, R _t = 0.81 min.

Example 242

4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzamide

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), (4-carbamoylphenyl)boronic acid (8.08 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μί) and H2O (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (3.80 mg, 17%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.98 (s, 1 H), 7.89-7.87 (m, 1 H), 7.86-7.84 (m, 1 H), 7.68- 7.64 (m, 3H), 7.50 (d, 1 H), 7.36 (s, 1 H), 7.12 (dd, 1 H), 7.06 (s, 1 H), 5.95 (quin, 1 H), 3.88 (s, 6H), 2.44 (s, 3H), 1.72 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 449, R _t = 0.80 min.

Example 243

N-{1 -[5-(2-aminophenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-meth ylquinazolin-4-amin

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), (2-aminophenyl)boronic acid (6.71 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. The crude residue was purified by preparative HPLC (basic conditions). The resulting residue was stirred in Et.20 during 2 hours then filtered to give the title compound as a light brown solid (7.50 mg, 36%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.13 (d, 1 H), 7.65 (s, 1 H), 7.1 1 -7.07 (m, 3H), 7.05 (s, 1 H), 7.04-6.99 (m, 1 H), 6.76 (dd, 1 H), 6.57 (td, 1 H), 5.95 (quin, 1 H), 5.03 (s, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.44 (s, 3H), 1.71 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 421 , R _t = 0.92 min.

Example 244

[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]methanol

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μιτιοΙ), [2-(hydroxymethyl)phenyl]boronic acid (7.44 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 }L) and H2O (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (13.2 mg, 62%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.65 (s, 1 H), 7.56 (d, 1 H), 7.35 (dd, 1 H), 7.33 (s, 1 H), 7.30-7.25 (m, 1 H), 7.12 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 5.24 (t, 1 H), 4.54 (d, 2H), 3.88 (s, 6H), 2.44 (s, 3H), 1.72 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 436,

Example 245

2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzonitri

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), (2-cyanophenyl)boronic acid (7.20 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (5.00 mg, 22%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.20 (d, 1 H), 7.91 (d, 1 H), 7.74-7.69 (m, 1 H), 7.68-7.64 (m, 2H), 7.53- 7.48 (m, 2H), 7.21 (dd, 1 H), 7.06 (s, 1 H), 5.97 (quin, 1 H), 3.88 (s, 6H), 2.45 (s, 3H), 1 .74 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 431 , R _t = 0.97 min.

Example 246

N-{1 -[5-(1 H-indazol-7-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-methylqu inazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μιτιοΙ), 7-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)-1 H-indazole (12.0 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μιτιοΙ) in dioxane (500 μί) and H2O (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (12.0 mg, 53%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 13.22 (br s, 1 H), 8.19 (br d, 2H), 7.72 (d, 1 H), 7.67 (s, 1 H), 7.55 (br d, 1 H), 7.42 (br d, 1 H), 7.19 (br d, 1 H), 7.14 (br t, 1 H), 7.06 (s, 1 H), 5.99 (quin, 1 H), 3.88 (s, 3H), 3.88 (s, 3H), 2.45 (s, 3H), 1.75 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 446, R _t = 0.92 min.

Example 247

N-{1 -[5-(1 H-indazol-4-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-methylqu inazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηηοΙ), 4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)-1 H-indazole (12.0 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μιτιοΙ) in dioxane (500 μΙ_) and H2O (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (7.20 mg, 32%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 13.29 (br s, 1 H), 8.34 (s, 1 H), 8.18 (d, 1 H), 7.67 (s, 1 H), 7.55 (d, 1 H), 7.48 (d, 1 H), 7.35 (t, 1 H), 7.28 (d, 1 H), 7.17 (d, 1 H), 7.06 (s, 1 H), 5.98 (quin, 1 H), 3.88 (s, 3H), 3.88 (s, 3H), 2.46 (s, 3H), 1.75 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 446, R _t = 0.90 min.

Example 248

N-{1 -[5-(2-ethenylphenyl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-me thylquinazolin-4- amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 200 mg, 85 % purity, 416 μηιοΙ), (2-ethenylphenyl)boronic acid (61 .6 mg, 416 μηιοΙ), K ₂ C0 ₃ (230 mg, 1.67 mmol) and Pd(PPh ₃ ) ₄ (48.1 mg, 41.6 μηιοΙ) in dioxane (4.0 mL) and H2O (800 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (92.9 mg, 51 %). ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.66-7.62 (m, 2H), 7.38-7.28 (m, 3H), 7.10 (dd, 1 H), 7.05 (s, 1 H), 6.91 (dd, 1 H), 6.95 (d, 1 H), 5.96 (quin, 1 H), 5.77 (dd, 1 H), 5.29 (dd, 1 H), 3.87 (s, 6H), 2.43 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 432, Rt = 1 .09 min.

Example 249

2-[4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-1 H- pyrazol-1 -yl]acetamide

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηιοΙ), 2-[4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)-1 H-pyrazol-1 -yl]acetamide (12.3 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (1 .50 mg, 6%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (br s, 1 H), 7.94 (s, 1 H), 7.67 (d, 1 H), 7.65 (s, 1 H), 7.51 (s, 1 H), 7.27 (s, 1 H), 7.05 (s, 1 H), 7.03 (d, 1 H), 6.98 (dd, 1 H), 5.91 (quin, 1 H), 4.73 (s, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.44 (s, 3H), 1 .69 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 453, R _t = 0.71 min.

Example 250

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 200 mg, 490 μηιοΙ), N-methyl-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)phenyl]methanamine (121 mg, 490 μηιοΙ), K2CO3 (271 mg, 1 .96 mmol) and Pd(PPh ₃ ) ₄ (56.6 mg, 49.0 mol) in dioxane (5.0 mL) and H ₂ 0 (1 .0 mL) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed bycolumn chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a light orange solid (104 mg, 47%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.49 (d, 1 H), 7.35-7.28 (m, 2H), 7.28-7.23 (m, 1 H), 7.15 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.65 (s, 2H), 2.44 (s, 3H), 2.25 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 449, R _t = 0.54 min.

Example 251

2-[4-(4-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-1 H- pyrazol-1 -yl]ethanol

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 20.0 mg, 49.0 mol), 2-[4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)-1 H-pyrazol-1 -yl]ethanol (1 1 .7 mg, 49.0 mol), K2CO3 (27.1 mg, 196 Mmol) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 Mmol) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (1 1.8 mg, 53%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 7.99 (s, 1 H), 7.96 (d, 1 H), 7.68 (d, 1 H), 7.67 (s, 1 H), 7.18 (d, 1 H), 7.18-7.16 (m, 1 H), 7.04 (s, 1 H), 5.75 (quin, 1 H), 4.91 (t, 1 H), 4.12 (t, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 3.73 (q, 2H), 2.41 (s, 3H), 1.59 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 440, R _t = 0.66 min.

Example 252

N-[1 -{5-[2-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 200 mg, 490 μηιοΙ), 1-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)phenyl]methanamine (1 14 mg, 490 μηιοΙ), K ₂ C0 ₃ (271 mg, 1 .96 mmol) and Pd(PPh ₃ )4 (56.6 mg, 49.0 μηιοΙ) in dioxane (5.0 mL) and H2O (1.0 mL) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a pink solid (163 mg, 77%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.56 (br d, 1 H), 7.33 (td, 1 H), 7.29 (dd, 1 H), 7.26-7.21 (m, 1 H), 7.1 1 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.77 (s, 2H), 2.44 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 435, R _t = 0.61 min.

Example 253

N-{1 -[5-(6 -dihydro-5H^yrrolo[1 ,2-a]imidazol-3-yl)thiophen-3-yl]ethyl}-6 -dim

2-methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 20.0 mg, 49.0 μηιοΙ), 6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3- ylboronic acid (7.44 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. The crude residue was purified by preparative HPLC (basic conditions). The resulting residue was stirred in Et.20 during 2 hours then filtered to give the title compound as a pale yellow solid (4.20 mg, 19%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 7.96 (d, 1 H), 7.66 (s, 1 H), 7.29 (t, 1 H), 7.25 (d, 1 H), 7.10 (s, 1 H), 7.04 (s, 1 H), 5.74 (quin, 1 H), 4.08 (t, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.79-2.73 (m, 2H), 2.61 -2.54 (m, 2H), 2.41 (s, 3H), 1 .61 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 436, R _t = 0.56 min. Example 254

6,7-dimethoxy-2-methyl-N-[1.(5-{i -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-4-yl}thiophen-3- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 20.0 mg, 49.0 μηιοΙ), 1 -[2-(pyrrolidin-1 -yl)ethyl]-4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole (14.3 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μπιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μπιοΙ) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. The crude residue was purified by preparative HPLC (basic conditions). The resulting residue was stirred in Et.20 during 2 hours then filtered to give the title compound as an off-white solid (800 μς, 3%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.04 (d, 1 H), 7.97 (d, 1 H), 7.67 (d, 2H), 7.18-7.16 (m, 2H), 7.04 (s, 1 H), 5.74 (quin, 1 H), 4.18 (t, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.81 (t, 2H), 2.46-2.42 (m, 4H), 2.41 (s, 3H), 1 .64 (dt, 4H), 1 .59 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 493, R _t = 0.61 min.

Example 255

N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-3-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 50.0 mg, 122 μηηοΙ), [2-(aminomethyl)-4-fluorophenyl]boronic acid hydrochloride (1 :1 ) (25.2 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (7.08 mg, 6.12 μηιοΙ) in dioxane (1 .2 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C during 36 hours. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a pale yellow solid (17.4 mg, 31 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 7.98 (d, 1 H), 7.66 (s, 1 H), 7.44 (dd, 1 H), 7.41 (t, 1 H), 7.34 (dd, 1 H), 7.20 (d, 1 H), 7.08 (td, 1 H), 7.03 (s, 1 H), 5.77 (quin, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 3.76 (s, 2H), 2.41 (s, 3H), 1.62 (d, 3H). LC-MS (Method 8): m/z: [M+H] ⁺ = 453, R _t = 0.69 min.

Example 256

2-[4-(3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}phenyl) -1 H- pyrazol-1 -yl]ethanol

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ; 100 mg, 249 μηιοΙ), 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)-1 H-pyrazol-1 -yl]ethanol (59.2 mg, 249 μηιοΙ), K ₂ C0 ₃ (137 mg, 994 μπιοΙ) and Pd(PPh ₃ ) ₄ (14.4 mg, 12.4 μιτιοΙ) in dioxane (2.5 mL) and H ₂ 0 (500 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification preparative HPLC (basic conditions) gave the title compound as a pale yellow solid (10.4 mg, 10%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.1 1 (d, 1 H), 7.99 (d, 1 H), 7.84 (d, 1 H), 7.71 (s, 1 H), 7.65 (s, 1 H), 7.41 (dt, 1 H), 7.30 (d, 1 H), 7.28-7.24 (m, 1 H), 7.02 (s, 1 H), 5.67 (quin, 1 H), 4.92 (t, 1 H), 4.15 (t, 2H), 3.90 (s, 3H), 3.86 (s, 3H), 3.75 (q, 2H), 2.36 (s, 3H), 1.61 (d, 3H) . LC-MS (Method 8): m/z: [M+H] ⁺ = 434, R _t = 0.81 min.

Example 257

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -(3-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-4- yl}phenyl)ethyl]quinazolin-4-amine

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ; 100 mg, 249 μηηοΙ), 1 -[2-(pyrrolidin-1 -yl)ethyl]-4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole (72.4 mg, 249 μηιοΙ), K ₂ C0 ₃ (137 mg, 994 μηηοΙ) and Pd(PPh ₃ ) ₄ (14.4 mg, 12.4 μηηοΙ) in dioxane (2.5 mL) and H ₂ 0 (500 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification preparative HPLC (basic conditions) gave the title compound as a white solid (73.2 mg, 59%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (s, 1 H), 7.98 (d, 1 H), 7.83 (d, 1 H), 7.71 (s, 1 H), 7.64 (br s, 1 H), 7.41 (dt, 1 H), 7.30 (d, 1 H), 7.28-7.24 (m, 1 H), 7.02 (s, 1 H), 5.67 (quin, 1 H), 4.21 (t, 2H), 3.90 (s, 3H), 3.86 (s, 3H), 2.82 (t, 2H), 2.47- 2.41 (m, 4H), 2.36 (s, 3H), 1 .66-1 .59 (m, 7H). LC-MS (Method 8): m/z: [M+H] ⁺ = 487, R _t = 0.68 min.

Example 258

N-{(1 R)-1 -[2'-(aminomethyl)biphenyl-3-yl]ethyl}-6,7-dimethoxy-2-methy lquinazolin-4- amine

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ; 100 mg, 249 μηιοΙ), 1-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)phenyl]methanamine (57.9 mg, 249 μηιοΙ), K ₂ C0 ₃ (137 mg, 994 μηιοΙ) and Pd(PPh ₃ ) ₄ (28.7 mg, 24.9 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a yellow solid (95.0 mg, 88%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.03 (d, 1 H), 7.69 (s, 1 H), 7.58 (d, 1 H), 7.48 (br d, 1 H), 7.45-7.34 (m, 5H), 7.26-7.21 (m, 2H), 7.01 (s, 1 H), 5.71 (quin, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 3.81 -3.77 (m, 2H), 2.35 (s, 3H), 1 .63 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 429, R _t = 0.55 min.

Example 259

N-[1 -{5-[2-(aminomethyl)phenyl]thiophen-3-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 50.0 mg, 122 μηιοΙ), 1-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)phenyl]methanamine (28.5 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μιτιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a yellow solid (33.1 mg, 59%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.99 (d, 1 H), 7.66 (s, 1 H), 7.57 (br d, 1 H), 7.41 (t, 1 H), 7.37-7.30 (m, 2H), 7.28-7.25 (m, 2H), 7.03 (s, 1 H), 5.78 (quin, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 3.79 (s, 2H), 2.41 (s, 3H), 1.63 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 435, R _t = 0.55 min.

Example 260

N-{(1 R)-1 -[3-(aminomethyl) henyl]ethyl}-6,7-dimethoxy-2-methylquinazolin

To 3-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}benzoni trile (described in example 194; 300 mg, 861 mol) and NiCI ₂ .6H ₂ 0 (40.9 mg, 172 mol) in MeOH (9.0 ml.) was carefully added NaBH ₄ (163 mg, 4.31 mmol) and the reaction mixture stirred 10 minutes at room temperature. H2O was added carefully, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (140 mg, 46%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 7.97 (d, 1 H), 7.70 (s, 1 H), 7.41 (s, 1 H), 7.28 (dt, 1 H), 7.24 (t, 1 H), 7.18 (br d, 1 H), 7.01 (s, 1 H), 5.65 (quin, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 3.69 (s, 2H), 2.35 (s, 3H), 1.57 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 353, R _t = 0.41 min.

Example 261

N-{(1 R)-1 -[3-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 1 91 ; 1 00 mg, 249 mol), 6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3- ylboronic acid (37.8 mg, 249 Mmol), K2CO3 (1 37 mg, 994 Mmol) and Pd(PPh ₃ ) ₄ (28.7 mg, 24.9 Mmol) in dioxane (2.5 ml.) and H2O (500 M L) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification preparative HPLC (basic conditions) gave the title compound as a yellow solid (26.9 mg, 25%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.02 (d, 1 H), 7.71 (s, 1 H), 7.60 (s, 1 H), 7.41 - 7.32 (m, 3H), 7.17 (s, 1 H), 7.02 (s, 1 H), 5.68 (quin, 1 H), 4.10 (qt, 2H), 3.90 (s, 3H), 3.86 (s, 3H), 2.78-2.72 (m, 2H), 2.56-2.52 (m, 2H), 2.35 (s, 3H), 1 .61 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 430, R _t = 0.52 min.

Example 262

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7-dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 20.0 mg, 49.0 μηηοΙ), {2-[(dimethylamino)methyl]phenyl}boronic acid (8.77 mg, 49.0 μηιοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (5.66 mg, 4.90 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM, dried (hydrophobic filtration) and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (12.5 mg, 55%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.65 (s, 1 H), 7.43- 7.40 (m, 1 H), 7.38-7.34 (m, 1 H), 7.31 -7.27 (m, 2H), 7.17 (d, 1 H), 7.08 (dd, 1 H), 7.04 (s, 1 H), 5.96 (quin, 1 H), 3.86 (s, 6H), 2.43 (s, 3H), 2.10 (s, 6H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 463, R _t = 0.60 min.

Example 263

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(methylamino)methyl]phenyl}thiophen-3- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-3-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 239; 50.0 mg, 122 μηιοΙ), N-methyl-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)phenyl]methanamine (30.3 mg, 122 μηιοΙ), K2CO3 (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a pale yellow solid (30.9 mg, 56%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.01 (d, 1 H), 7.66 (s, 1 H), 7.46 (dd, 1 H), 7.41 (t, 1 H), 7.38-7.34 (m, 2H), 7.34-7.25 (m, 2H), 7.02 (s, 1 H), 5.79 (quin, 1 H), 3.86 (s, 6H), 3.60 (s, 2H), 2.40 (s, 3H), 2.15 (s, 3H), 1 .63 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 449, R _t = 0.59 min.

Example 264

N-[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 500 mg, 2.09 mmol), 1 -(4-bromothiophen-2-yl)ethanamine hydrochloride (1 :1 ) (described in procedure INT-29; 559 mg, 2.30 mmol), N,N-diisopropylethylamine (930 μΙ_, 5.4 mmol) and DMSO (4.0 mL). The reaction mixture was heated to 130°C during 6 hours in the microwave. H2O was added, the mixture extracted with DCM, dried (hydrophobic filtration) and the solvent removed in vacuo. The crude residue was stirred in Et.20 during 30 minutes then filtered to give the title compound as a pale yellow solid (668 mg, 71 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.09 (d, 1 H), 7.61 (s, 1 H), 7.48 (d, 1 H), 7.07 (t, 1 H), 7.05 (s, 1 H), 5.87 (quin, 1 H), 3.87 (s, 6H), 2.41 (s, 3H), 1 .67 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 408, R _t = 0.86 min.

Example 265

N-[1 -{5-[3-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 100 mg, 225 μηιοΙ), 1-[3-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)phenyl]methanamine hydrochloride (1 :1 ) (60.6 mg, 225 μηιοΙ), K ₂ C0 ₃ (124 mg, 899 μηιοΙ) and Pd(PPh ₃ )4 (13.0 mg, 1 1 .2 μιτιοΙ) in dioxane (2.3 mL) and H ₂ 0 (460 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM, dried (hydrophobic filtration) and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (78.6 mg, 79%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.54 (s, 1 H), 7.42- 7.39 (m, 1 H), 7.34 (d, 1 H), 7.28 (t, 1 H), 7.21 (br d, 1 H), 7.06 (dd, 1 H), 7.05 (s, 1 H), 5.93 (quin, 1 H), 3.87 (s, 6H), 3.70 (s, 2H), 2.43 (s, 3H), 1 .70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 435, R _t = 0.57 min.

Example 266

N-[1 -{5-[4-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 100 mg, 225 μηηοΙ), [4-(aminomethyl)phenyl]boronic acid hydrochloride (1 :1 ) (42.1 mg, 225 μηιοΙ), K ₂ C0 ₃ (124 mg, 899 μmol) and Pd(PPh ₃ ) ₄ (13.0 mg, 1 1.2 μιτιοΙ) in dioxane (2.3 mL) and H2O (460 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (48.5 mg, 47%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.13 (d, 1 H), 7.64 (s, 1 H), 7.53-7.47 (m, 2H), 7.34-7.28 (m, 3H), 7.07-7.03 (m, 2H), 5.92 (quin, 1 H), 3.87 (s, 6H), 3.68 (s, 2H), 2.43 (s, 3H), 1.69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 435, R _t = 0.57 min. Example 267

6,7-dimethoxy-2-methyl-N-[1 -(4-{1 -[2-(pyrrolidin-1 -yl)ethyl]-1 H-pyrazol-3-yl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηηοΙ), 1 -[2-(pyrrolidin-1 -yl)ethyl]-4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole (35.7 mg, 122 μmol), K ₂ C0 ₃ (67.7 mg, 490 μmol) and Pd(PPh ₃ )4 (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (32.5 mg, 53%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.10 (d, 1 H), 8.04 (d, 1 H), 7.73 (d, 1 H), 7.64 (s, 1 H), 7.33 (d, 1 H), 7.28 (t, 1 H), 7.04 (s, 1 H), 5.92 (quin, 1 H), 4.18 (t, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 2.85-2.76 (m, 2H), 2.45-2.41 (m, 7H), 1 .70 (d, 3H), 1 .64 (dt, 4H). LC-MS (method 7): m/z: [M+H] ⁺ = 493, R _t = 0.55 min.

Example 268

6,7-dimethoxy-2-methyl-N-[(1 R)-1 -{2'-[(methylamino)methyl]biphenyl-3- yl}ethyl]quinazolin-4-amine

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ; 100 mg, 249 μηιοΙ), N-methyl-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)phenyl]methanamine (61 .4 mg, 249 μηηοΙ), K2CO3 (137 mg, 994 μηηοΙ) and Pd(PPh ₃ ) ₄ (28.7 mg, 24.9 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (32.0 mg, 28%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.01 (d, 1 H), 7.69 (s, 1 H), 7.49 (dd, 2H), 7.44 (br d, 1 H), 7.38 (t, 1 H), 7.30 (dtd, 2H), 7.23 (dt, 1 H), 7.19 (dd, 1 H), 7.01 (s, 1 H), 5.69 (quin, 1 H), 3.88 (s, 3H), 3.86 (s, 3H), 3.45 (s, 2H), 2.34 (s, 3H), 2.08 (s, 3H), 1.62 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 443, R _t = 0.58 min.

Example 269

N-[1 -{4-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηηοΙ), [2-(aminomethyl)-4-fluorophenyl]boronic acid hydrochloride (1 :1 ) (25.2 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μιτιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (32.2 mg, 55%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.40 (dd, 1 H), 7.36 (d, 1 H), 7.27 (dd, 1 H), 7.17 (t, 1 H), 7.09-7.03 (m, 2H), 5.95 (quin, 1 H), 3.87 (s, 6H), 3.71 (s, 2H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 453, R _t = 0.70 min.

Example 270

N-[1 -{4-[2-(aminomethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimethox y-2- methylquinazolin-4-amine

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηιοΙ), 1 -[2-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)phenyl]methanamine (28.5 mg, 122 μηηοΙ), K2CO3 (67.7 mg, 490 μηηοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (5.20 mg, 9%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.53 (d, 1 H), 7.41 (d, 1 H), 7.33-7.28 (m, 1 H), 7.27-7.23 (m, 2H), 7.21 (t, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.71 (s, 2H), 2.43 (s, 3H), 1 .72 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 435, R _t = 0.69 min.

Example 271

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηιοΙ), N-methyl-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)phenyl]methanamine (30.3 mg, 122 μηηοΙ), K2CO3 (67.7 mg, 490 μηηοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (15.4 mg, 28%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.47-7.43 (m, 2H), 7.32-7.25 (m, 4H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.56 (s, 2H), 2.43 (s, 3H), 2.22 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 449, R _t = 0.71 min.

Example 272

N-{1 -[4-(6 -dihydro-5H^yrrolo[1 ,2-a]imi

2-methylquinazolin-4-amine

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηηοΙ), 6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3- ylboronic acid (18.6 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H2O (250 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (16.0 mg, 30%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.63 (s, 1 H), 7.35 (d, 1 H), 7.31 (t, 1 H), 7.13 (s, 1 H), 7.04 (s, 1 H), 5.91 (quin, 1 H), 4.1 1 (t, 2H), 3.87 (s, 6H), 2.77-2.71 (m, 2H), 2.61 -2.52 (m, 2H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 436, R _t = 0.49 min.

Example 273

2-[3-(5^1 -[(6,7-dimethoxy-2-methylquinazolin^-yl)amino]ethyl}thiophen -3-yl)-1 H- pyrazol-1 -yl]ethanol

Under argon, -[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 264; 50.0 mg, 122 μηιοΙ), 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan- 2-yl)-1 H-pyrazol-1 -yl]ethanol (29.2 mg, 122 μηιοΙ), K ₂ C0 ₃ (67.7 mg, 490 μηιοΙ) and Pd(PPh ₃ ) ₄ (14.2 mg, 12.2 μηιοΙ) in dioxane (1 .3 mL) and H ₂ 0 (250 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (28.1 mg, 51 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 8.00 (d, 1 H), 7.74 (s, 1 H), 7.64 (s, 1 H), 7.33 (d, 1 H), 7.28 (t, 1 H), 7.04 (s, 1 H), 5.91 (quin, 1 H), 4.92 (t, 1 H), 4.1 1 (t, 2H), 3.86 (d, 6H), 3.73 (q, 2H), 2.42 (s, 3H), 1 .70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 440, R _t = 0.67 min.

Example 274

N-{(1 R)-1 -[2'-(aminomethyl)-4'-fluorobiphenyl-3-yl]ethyl}-6,7-dimetho xy-2- methylquinazolin-4-amine

Under argon, N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ; 100 mg, 249 μηηοΙ), [2-(aminomethyl)-4-fluorophenyl]boronic acid hydrochloride (1 :1 ) (51 .1 mg, 249 μηιοΙ), K ₂ C0 ₃ (137 mg, 994 μΓηο βΓ^ Pd(PPh ₃ ) ₄ (14.4 mg, 12.4 μηηοΙ) in dioxane (2.5 mL) and H2O (500 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification preparative HPLC (basic conditions) followed twice by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (15.6 mg, 14%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.00 (d, 1 H), 7.68 (s, 1 H), 7.47-7.36 (m, 4H), 7.23- 7.16 (m, 2H), 7.13-7.06 (m, 1 H), 7.02 (s, 1 H), 5.68 (quin, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 3.65-3.54 (m, 2H), 2.35 (s, 3H), 1.62 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 447, R _t = 0.57 min.

Example 275

N-[1 -{5-[5-(aminomethyl)furan-2-yl]thiophen-2-yl}ethyl]-6,7-dime thoxy-2- methylquinazolin-4-amine

To tert-butyl {[5-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)furan-2-yl]methyl}carbamate (described in example 236; 1 10 mg, 210 μιτιοΙ) in MeOH (4.2 mL) was added dropwise acetyl chloride (45 μί, 630 μηηοΙ) and the reaction mixture stirred at room temperature over the weekend. The reaction was quenched with NaHC03 (sat.), diluted with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (MeOH/EtOAc 0-20% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as an off-white solid (17.5 mg, 18%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.14 (d, 1 H), 7.05 (s, 1 H), 7.02 (d, 1 H), 6.56 (d, 1 H), 6.28 (d, 1 H), 5.91 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.71 (s, 2H), 2.42 (s, 3H), 1 .69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 425, R _t = 0.51 min.

Example 276

N-{1 -[5'-(aminomethyl)-2,2'-bithiophen-5-yl]ethyl}-6,7-dimethoxy -2-methylquinazolin-4- amine

Step a:

tert-butyl [(5'-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,2'-bithiop hen- 5-yl)methyl]carbamate

Under argon, N-[1 -(5-bromo-2-thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine (described in example 209; 20.0 mg, 50.0 μηιοΙ), (5-{[(tert-butoxycarbonyl)amino]methyl}-2- thienyl)boronic acid (12.6 mg, 50.0 mol), K ₂ C0 ₃ (27.1 mg, 196 mol) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.44 mol) in dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. H ₂ 0 was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification preparative HPLC (basic conditions) gave the title compound as a light yellow solid (15.6 mg, 14%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.12 (d, 1 H), 7.64 (s, 1 H), 7.50 (t, 1 H), 7.07 (d, 1 H), 7.06 (s, 1 H), 7.03-7.00 (m, 2H), 6.82 (d, 1 H), 5.89 (quin, 1 H), 4.22 (br d, 2H), 3.88 (s, 6H), 2.43 (s, 3H), 1 .69 (d, 3H), 1 .39 (s, 9H). LC-MS (method 9): m/z: [M+H] ⁺ = 541 , Rt = 1 .09 min.

Step b:

N^I -IS'-iaminomethylJ^^'-bithiophen-S-yllethy^-e. -dimethoxy^-methylquinazolin^- amine

To tert-butyl [(5'-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,2'-b ithiophen-5- yl)methyl]carbamate (100 mg, 185 mol) in MeOH (3.7 mL) was added dropwise acetyl chloride (79 μΙ_, 1 .1 mmol) and the reaction mixture stirred at room temperature over the weekend. The reaction was quenched with NaHCC>3 (sat.), diluted with Η ₂ 0, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (MeOH/EtOAc 0-20% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a yellow solid (39.6 mg, 47%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.12 (d, 1 H), 7.64 (s, 1 H), 7.06 (d, 1 H), 7.05 (s, 1 H), 7.03 (d, 1 H), 7.00 (dd, 1 H), 6.86 (d, 1 H), 5.88 (quin, 1 H), 3.91 -3.88 (m, 2H), 3.87 (s, 6H), 2.43 (s, 3H), 1 .68 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 441 , Rt = 0.53 min.

Example 277

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]amino}-1 -(1 H-indol-3-yl)ethanone

Under argon, 2-(5-{1 -[(6,7-Dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηιοΙ) and 2-amino-1 -(1 H-indol- 3-yl)ethanone hydrochloride (1 :1 ) (24.3 mg, 1 15 μηιοΙ) in MeOH (1 .2 mL) were stirred at room temperature overnight. NaBH(OAc)3 (48.9 mg, 231 μιτιοΙ) was then added and the reaction mixture stirred at room temperature during 15 minutes. The reaction was quenched with NaOH (1 .0 M), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (acidic conditions) gave the title compound as an off-white solid (2.20 mg, 3%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 1 1 .97 (br s, 1 H), 8.33 (d, 1 H), 8.29-8.21 (m, 1 H), 8.19-8.12 (m, 2H), 7.63 (s, 1 H), 7.59 (d, 1 H), 7.46 (dd, 1 H), 7.37-7.31 (m, 2H), 7.31 -7.25 (m, 1 H), 7.24-7.15 (m, 3H), 7.05-7.02 (m, 2H), 5.94 (quin, 1 H), 3.94-3.90 (m, 2H), 3.86 (s, 3H), 3.85 (s, 3H), 3.84-3.81 (m, 2H), 2.42 (s, 3H), 1 .69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 592, R _t = 0.67 min.

Example 278

3-amino-4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-1 - benzothiophene-2-carboxamide

Step a:

(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2-thie nyl)boronic acid

Under argon, N-[1 -(5-bromo-2-thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine (described in example 209; 500 mg, 1 .23 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi-1 ,3,2- dioxaborolane (466 mg, 1.84 mg), KOAc (361 mg, 3.67 mmol) and PdCI ₂ (dppf) (89.6 mg, 122 μηηοΙ) in dioxane (12.5 mL) were stirred at 80°C overnight) and the solvent then removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (157 mg, 34%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.09 (s, 2H), 7.64 (s, 1 H), 7.50 (d, 1 H), 7.08 (dd, 1 H), 7.04 (s, 1 H), 6.55 (s, 1 H), 5.95 (quin, 1 H), 3.86 (s, 6H), 2.40 (s, 3H), 1 .74-1 .61 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 374, R _t = 0.59 min.

Step b:

3-amino-4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n benzothiophene-2-carboxamide

Under argon, (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)boronic acid (30.0 mg, 80.4 μηηοΙ), 3-amino-4-bromo-1 -benzothiophene-2-carboxamide (21 .8 mg, 80.4 μηιοΙ), K ₂ C0 ₃ (44.4 mg, 322 μηιοΙ) and Pd(PPh ₃ ) ₄ (9.29 mg, 8.04 μηιοΙ) in dioxane (500 μΙ_) and H2O (100 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions, repeated twice) gave the title compound as a pale yellow solid (1 .00 mg, 2%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.20 (d, 1 H), 7.90 (dd, 1 H), 7.65 (s, 1 H), 7.44 (dd, 1 H), 7.22 (dd, 1 H), 7.19-7.13 (m, 3H), 7.05 (t, 2H), 6.19-6.10 (m, 2H), 5.97 (quin, 1 H), 3.89-3.87 (m, 3H), 3.87-3.86 (m, 3H), 2.43 (s, 3H), 1.75 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 520, Rt = 0.86 min.

Example 279

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)- benzyljglycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηιοΙ) and glycinamide hydrochloride (1 :1 ) (12.7 mg, 1 15 μηιοΙ) in MeOH (1 .2 mL) was stirred at room temperature overnight. NaBH(OAc)3 (48.9 mg, 231 μηιοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (28.5 mg, 47%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.64 (s, 1 H), 7.54 (d, 1 H), 7.35-7.30 (m, 2H), 7.29- 7.25 (m, 1 H), 7.25-7.21 (m, 1 H), 7.12 (d, 1 H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 7.01 (br s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.72 (s, 2H), 3.03 (s, 2H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 492, Rt = 0.55 min.

Example 280

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzyl]- N,N-dimethylglycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and N,N- dimethylglycinamide (1 1.8 mg, 1 15 μηηοΙ) in MeOH (1.2 mL) was stirred at room temperature overnight. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (28.5 mg, 47%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.54-7.49 (m, 1 H), 7.35-7.30 (m, 2H), 7.29-7.24 (m, 1 H), 7.15 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.73 (s, 2H), 3.30 (s, 2H), 2.83 (s, 3H), 2.79 (s, 3H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 520, Rt = 0.57 min.

Example 281

methyl N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]glycinate

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and methyl glycinate hydrochloride (1 :1 ) (14.5 mg, 1 15 μηηοΙ) in MeOH (1 .2 mL) was stirred at room temperature overnight. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (28.5 mg, 47%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.51 -7.48 (m, 1 H), 7.34-7.29 (m, 2H), 7.29-7.24 (m, 1 H), 7.15 (d, 1 H), 7.08 (dd, 1 H), 7.04 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.74 (s, 2H), 3.57 (s, 3H), 3.31 (s, 2H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 507, Rt = 0.60 min.

Example 282 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzyl]-N- methylglycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and N-methylglycinamide hydrochloride (1 :1 ) (14.4 mg, 1 15 μηηοΙ) in MeOH (1 .2 mL) was stirred at room temperature during 5 hours. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (26.0 mg, 45%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.67 (br d, 1 H), 7.64 (s, 1 H), 7.55 (d, 1 H), 7.35-7.29 (m, 2H), 7.29-7.24 (m, 1 H), 7.10 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.70 (s, 2H), 3.04 (s, 2H), 2.56 (d, 3H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 506, Rt = 0.56 min.

Example 283

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzyl]-N- (2-methoxyethyl)glycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and N-(2- methoxyethyl)glycinamide hydrochloride (1 :1 ) (19.4 mg, 1 15 μηηοΙ) in MeOH (1 .2 mL) was stirred at room temperature during 5 hours. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (15.5 mg, 24%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.80 (t, 1 H), 7.64 (s, 1 H), 7.53 (d, 1 H), 7.36-7.30 (m, 2H), 7.29-7.24 (m, 1 H), 7.10 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.70 (br s, 2H), 3.30-3.26 (m, 2H), 3.22-3.17 (m, 5H), 3.06 (br s, 2H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 550, Rt = 0.59 min.

Example 284

N-benzyl-2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]glycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and N-benzylglycinamide hydrochloride (1 :1 ) (23.1 mg, 1 15 μηηοΙ) in MeOH (1 .2 mL) was stirred at room temperature during 5 hours. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (27.3 mg, 40%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.26 (t, 1 H), 8.15 (d, 1 H), 7.64 (s, 1 H), 7.55 (d, 1 H), 7.33 (dd, 1 H), 7.30 (s, 1 H), 7.29-7.24 (m, 3H), 7.21 -7.16 (m, 3H), 7.10 (d, 1 H), 7.07-7.04 (m, 2H), 5.96 (quin, 1 H), 4.26 (d, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 3.74 (s, 2H), 3.14 (s, 2H), 2.43 (s, 3H), 1 .70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 582, Rt = 0.68 min.

Example 285

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]amino}-1 -(morpholin-4-yl)ethanone A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) and 2-amino-1 -(morpholin- 4-yl)ethanone hydrochloride (1 :1 ) (20.8 mg, 1 15 μηιοΙ) in MeOH (1 .2 mL) was stirred at room temperature during 5 hours. NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as a white solid (32.4 mg, 50%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.54-7.49 (m, 1 H), 7.35-7.30 (m, 2H), 7.29-7.24 (m, 1 H), 7.15 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.74 (s, 2H), 3.54-3.48 (m, 4H), 3.43-3.37 (m, 2H), 3.33-3.29 (m, 4H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 562, Rt = 0.58 min.

Example 286

3-(5^1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-1 ,5- dimethyl-1 H-pyrrole-2-carbonitrile

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine hydrochloride (1 :1 ) (described in example 209; 100 mg, 225 μηηοΙ), 1 ,5-dimethyl-3-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-pyrrole-2-carbonitrile (55.3 mg, 225 μηιοΙ), K2CO3 (124 mg, 899 μηιοΙ) and Pd(PPh ₃ ) ₄ (13.0 mg, 1 1 .2 μηιοΙ) in dioxane (2.5 mL) and H ₂ 0 (500iL) were stirred at 1 10°C during 8 hours. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (87.5 mg, 87%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.63 (s, 1 H), 7.19 (d, 1 H), 7.06-7.04 (m, 2H), 6.22 (d, 1 H), 5.89 (quin, 1 H), 3.87 (s, 6H), 3.58 (s, 3H), 2.43 (s, 3H), 2.21 (s, 3H), 1.69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 448, Rt = 0.90 min.

Example 287

5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,3'-b ithiophene-4'- carbonitrile

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine hydrochloride (1 :1 ) (described in example 209; 100 mg, 225 μηιοΙ), 4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)thiophene-3-carbonitrile (52.9 mg, 225 μηιοΙ), K ₂ C0 ₃ (124 mg, 899 μιτιοΙ) and Pd(PPh ₃ )4 (13.0 mg, 1 1 .2 μιτιοΙ) in dioxane (2.3 mL) and H ₂ 0 (460 μί) were stirred at 1 10°C during 8 hours. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (69.5 mg, 71 %). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.68 (d, 1 H), 8.15 (d, 1 H), 7.86 (d, 1 H), 7.64 (s, 1 H), 7.35 (d, 1 H), 7.14 (dd, 1 H), 7.05 (s, 1 H), 5.92 (quin, 1 H), 3.87 (s, 6H), 2.44 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 437, Rt = 0.87 min.

Example 288

N-[1 -(5-{2-[(diethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 20.0 mg, 46.1 μηηοΙ), N-ethylethanamine (5.8 μί, 55 μηηοΙ) and acetic acid (5.3 μΙ_, 92 μηιοΙ) in 1 ,2-dichloroethane (500 μΙ_) was added NaBH(OAc) ₃ (19.6 mg, 92.3 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (5.10 mg, 22%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.57-7.51 (m, 1 H), 7.33-7.28 (m, 2H), 7.27-7.22 (m, 1 H), 7.09 (d, 1 H), 7.06 (dd, 1 H), 7.04 (s, 1 H), 5.95 (quin, 1 H), 3.87 (s, 6H), 3.54 (s, 2H), 2.42 (s, 3H), 2.39 (q, 4H), 1 .71 (d, 3H), 0.86 (t, 6H). LC-MS (method 7): m/z: [M+H] ⁺ = 491 , Rt = 0.59 min.

Example 289

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzyl]-N- phenylglycinamide

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηιοΙ) and N-phenylglycinamide hydrochloride (1 :1 ) (21 .5 mg, 1 15 μηιοΙ) in MeOH (1 .2 ml.) was stirred at room temperature during 5 hours. NaBH(OAc)3 (48.9 mg, 231 μηιοΙ) was added and the solution stirred at room temperature during 15mn. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 ml_), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-50% then MeOH) followed by preparative HPLC (basic conditions) gave the title compound as an off-white solid (1 .40 mg, 2%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 9.91 (br s, 1 H), 7.68 (s, 1 H), 7.61 (br d, 1 H), 7.55 (br d, 2H), 7.43- 7.24 (m, 6H), 7.14 (d, 1 H), 7.09-7.02 (m, 3H), 5.95 (quin, 1 H), 4.05-3.90 (m, 2H), 3.88 (s, 3H), 3.87 (s, 3H), 2.46 (s, 3H), 1 .69 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 568, Rt = 0.67 min.

Example 290

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]piperidine-3-carboxamide

To 2-(5-{1-[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}t hiophen-2-yl)benza (described in example 179a; 50.0 mg, 115 μηιοΙ), piperidine-3-carboxamide (29.6 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature during 5 hours. The reaction was quenched with aqueous NaOH (1.0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (8.90 mg, 14%). 1H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (dd, 1H), 7.65 (s, 1H), 7.41 (dt, 1H), 7.38-7.34 (m, 1H), 7.33- 7.27 (m, 2H), 7.21 (brs, 1H), 7.19 (t, 1H), 7.08 (d, 1H), 7.05 (s, 1H), 6.72 (brs, 1H), 5.97 (br t, 1H), 3.87 (s, 6H), 3.47 (dd, 1H), 2.75 (brd, 1H), 2.43 (s, 3H), 2.28-2.18 (m, 1H), 1.96 (br t, 1H), 1.92-1.82 (m, 1H), 1.71 (d, 3H), 1.69-1.64 (m, 1H), 1.59-1.46 (m, 1H), 1.41-1.25 (m, 2H). LC-MS (method 7): m/z: [M+H] ⁺ = 546, Rt = 0.57 min.

Example 291

N-{1-[5-(2-{[(2,2-difluoroethyl)(methyl)amino]methyl}phenyl) thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1-[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl} thiophen-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 115 μηηοΙ), 2,2-difluoro-N-methylethanamine (21.9 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηηοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (29.6 mg, 50%).1H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1H), 7.65 (s, 1H), 7.51 (d, 1H), 7.36-7.26 (m, 3H), 7.13-7.11 (m, 1H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 6.05 (tt, 1 H), 3.87 (s, 6H), 3.63 (s, 2H), 2.74 (td, 2H), 2.43 (s, 3H), 2.19 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 513, Rt = 0.94 min.

Example 292

N-[1 -{5-[2-(aminomethyl)-5-chlorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

Step a:

1 -(2-bromo-4-chlorophenyl)methanamine

Borane tetrahydrofuran complex (55 mL, 1 .0 M in THF) were provided with ice cooling, then slowly a solution of 2-bromo-4-chlorobenzonitrile (4.00 g, 18.5 mmol) in THF (10 mL) was added. Thereafter the reaction-mixture was heated under reflux for 16 hours. The reaction was quenched by addition of methanol. 20 mL of hydrochloric acid (1 .0 N) were added dropwise with ice cooling. The solution was rendered alkaline with 1 .0 M sodium hydroxide solution and extracted with dichloromethane. The organic phase was dried over sodium sulfate and evaporated to yield 2.10 g (36%) of the title compound as the off-white solid. The reaction was monitored by TLC (ethyl acetate/petroleum ether=1 :1 , Rf = 0.3). MS (ESIpos): m/z = 220 [M+H] ⁺ .

Step b:

tert-butyl (2-bromo-4-chlorobenzyl)carbamate

1 -(2-bromo-4-chlorophenyl)methanamine (1 .60 g, 7.3 mmol), di-tert-butyl dicarbonate (2.06 g, 9.4 mmol), and triethylamine (1 .84 g, 18.1 mmol), were added into 25 mL of dichloromethane. The resulting mixture was stirred at room temperature for four hours. The resulting mixture was washed with water and the combined organic layers were concentrated on a rotary evaporator. The reaction was purified by silica gel chromatography column (EA/PE = 1 :19, Rf = 0.2) to give 1 .90 g (74%) of the title compound as a light yellow oil. MS (ESIpos): m/z = 319 [M+H] ⁺ .

Step c:

tert-butyl [4-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

tert-butyl (2-bromo-4-chlorobenzyl)carbamate (1 .0 g, 2.8 mmol), 4,4,4',4',5,5,5',5'-octamethyl- 2,2'-bi(1 ,3,2-dioxaborolane) (1 .78 g, 7.0 mmol), potassium acetate (0.83 g, 8.4 mmol) and 1 ,1 '-bis(diphenylphosphino)ferrocenepalladiumdichloride CH2CI2 (0.23 g, 0.3 mmol), were added in 15 mL of 1 ,4-dioxane under N2 atmosphere. The resulting mixture was stirred at 100°C for 15 h. The solvent was removed in vacuo and was diluted by addition of water. The mixture was extracted with ethyl acetate, was washed with water and the combine organic layers was concentrated under vacuum. The residue was purified by silica gel column on chromatography (ethyl acetate / petroleum ether=3:7) to 500 mg (36%) of the product as a light yellow oil. MS (ESIpos): m/z = 368 [M+H] ⁺ .

Step d: tert-butyl [4-chloro-2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)benzyl]carbamate

N-[1 -(5-bromo-2-thienyl)ethyl]-6 ,7-dimethoxy-2-methylquinazolin-4-amine (described in example 209; 150 mg, 0.3 mmol) was dissolved in 1 ,4-dioxane (10 mL) and water (2 ml_), then tert-butyl [4-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate (430 mg, 0.9 mmol), potassium carbonate (199 mg, 1 .4 mmol) and tetrakis(triphenylphosphine)palladium(0) (36 mg, 0.03 mmol) were added under N2 atmosphere. The reaction was stirred at 100°C for 16 h. The solvent was removed in vacuo and was diluted by addition of water. The mixture was extracted with dichloromethane, was washed with water and the combined organic layers were concentrated under vacuum. The residue was purified by silica gel column on chromatography (dichloromethane:methanol=13:1 , Rf = 0.3) to yield 150 mg (63%) of the title compound as a light yellow solid. MS (ESIpos): m/z = 569 [M+H] ⁺ .

Step e:

N-[1 -{5-[2-(aminomethyl)-5-chlorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

tert-butyl [4-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)benzyl]carbamate,(100 mg, 0.14 mmol), was dissolved in 1 ,4-dioxane (3 mL), then hydrochloric acid (4.0 M, 3 mL) was added at 0°C. The resulting mixture was stirred at room temperature for 3 hours. By addition of saturated sodium carbonate solution the pH value was adjusted to pH = 7. The water layer was extracted with ethyl acetate, washed with water and the combined organic layers were concentrated under vacuum. The residue was purified by preparative HPLC (Column: XBridge Prep C18 OBD Column 19x150mm δμηη; Mobile Phase A: Water (10 mM NH4HCO3), Mobile Phase B: Acetonitrile; Flow rate: 20 mL/min; Gradient: 25% B to 50% B in 7 min; Detector: 254 nm, 220 nm) to give 17.9 mg (25%) of the title compound as an off-white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.24 (s, 2H), 8.16 (d, 1 H), 7.66 (s, 1 H), 7.62 (d, 1 H), 7.47 (m, 1 H), 7.36 (m, 1 H), 7.19-7.1 1 (m, 2H), 7.06 (s, 1 H), 6.03-5.90 (m, 1 H), 3.88 (m, 6H), 2.44 (s, 3H), 1.73 (d, 3H).

Example 293

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-1 H-imidazole-2-carboxamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μιτιοΙ), 1 H-imidazole-2- carboxylic acid (12.4 mg, 1 10 μιτιοΙ), PyBOP (1 15 mg, 221 μιτιοΙ) and N,N- diisopropylethylamine (95 μί, 550 μηιοΙ) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (24.1 mg, 39%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 13.02 (br s, 1 H), 9.04 (t, 1 H), 8.17 (d, 1 H), 7.65 (s, 1 H), 7.37 (dd, 1 H), 7.29 (br s, 1 H), 7.14-7.06 (m, 5H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 4.52 (d, 2H), 3.87 (s, 6H), 2.44 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 547, Rt = 0.83 min.

Example 294

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-1 H-imidazole-5-carboxamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μιτιοΙ), 1 H-imidazole-5- carboxylic acid (12.4 mg, 110 μηιοΙ), PyBOP (115 mg, 221 μηιοΙ) and N,N- diisopropylethylamine (95 μί, 550 μηιοΙ) in DMF (1.0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (22.8 mg, 37%).1H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 12.52 (br s, 1H), 8.55 (brt, 1H), 8.17 (d, 1H), 7.74 (d, 1H), 7.65 (s, 1H), 7.63 (d, 1H), 7.36 (dd, 1H), 7.13-7.05 (m, 4H), 7.05 (s, 1H), 5.97 (quin, 1H), 4.50 (s, 1H), 4.49 (s, 1H), 3.87 (s, 6H), 2.43 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 547, Rt = 0.77 min.

Example 295

N-[2-(5-{1-[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth yl}thiophen-2-yl)-5- fluorobenzyl]-N<sup>2</sup>-(2,2 ,2-trifluoroethyl)glycinamide

A solution of N-[1-{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl] -6,7-dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 110 μηηοΙ), N-(2,2,2- trifluoroethyl)glycine (17.4 mg, 110 μηιοΙ), PyBOP (115 mg, 221 μιτιοΙ) and N,N- diisopropylethylamine (95 μί, 550 μηηοΙ) in DMF (1.0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (35.0 mg, 50%).1H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.31 (t, 1H), 8.15 (d, 1H), 7.64 (s, 1H), 7.36 (dd, 1H), 7.17-7.11 (m, 2H), 7.09 (dd, 1H), 7.05 (s, 1H), 7.03 (d, 1H), 5.96 (quin, 1H), 4.36 (d, 2H), 3.87 (s, 6H), 3.28 (d, 2H), 2.96 (dt, 1H), 2.85 (quin, 1H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 592, Rt = 0.92 min.

Example 296

N-[2-(5-{1-[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth yl}thiophen-2-yl)-5- fluorobenzyl]-1H-indole-2-carboxamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), 1 H-indole-2- carboxylic acid (17.8 mg, 1 10 μιτιοΙ), PyBOP (1 15 mg, 221 μηιοΙ) and N,N- diisopropylethylamine (95 μΙ_, 550 μmol) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (32.8 mg, 49%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 1 .64-1 1.57 (m, 1 H), 9.02 (t, 1 H), 8.17 (d, 1 H), 7.65 (s, 1 H), 7.62 (d, 1 H), 7.44-7.38 (m, 2H), 7.21 -7.18 (m, 2H), 7.18-7.15 (m, 1 H), 7.15-7.1 1 (m, 3H), 7.08-7.01 (m, 2H), 5.97 (quin, 1 H), 4.58 (d, 2H), 3.87 (s, 6H), 2.43 (s, 3H), 1.73 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 596, Rt = 0.99 min.

Example 297

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]amino}ethanol

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2-aminoethanol (14 μί, 230 μηηοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1.0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (12.5 mg, 23%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.52-7.48 (m, 1 H), 7.34-7.28 (m, 2H), 7.28-7.23 (m, 1 H), 7.16 (d, 1 H), 7.08 (d, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 4.45 (t, 1 H), 3.87 (s, 6H), 3.72 (s, 2H), 3.41 (q, 2H), 2.56-2.53 (m, 2H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 479, Rt = 0.55 min.

Example 298

2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl](methyl)amino ethanol

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2-(methylamino)ethanol (18 μΙ_, 230 μmol) and acetic acid (13 μΙ_, 230 μιτιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (31 .6 mg, 56%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.51 (dd, 1 H), 7.35-7.29 (m, 2H), 7.29-7.24 (m, 1 H), 7.18 (d, 1 H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 4.35 (t, 1 H), 3.87 (s, 6H), 3.52-3.48 (m, 2H), 3.48-3.42 (m, 2H), 2.43 (s, 3H), 2.40 (t, 2H), 2.10 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 493, Rt = 0.56 min.

Example 299

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-N ² -phen lglycinamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 20.0 mg, 44.2 μηηοΙ), N-phenylglycine (13.4 mg, 88.4 μηιοΙ), PyBOP (46.0 mg, 88.4 μηιοΙ) and N,N-diisopropylethylamine (38 μΙ_, 220 μηιοΙ) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (3.50 mg, 14%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.59 (t, 1 H), 8.14 (d, 1 H), 7.63 (s, 1 H), 7.42- 7.38 (m, 2H), 7.35-7.27 (m, 3H), 7.26-7.21 (m, 1 H), 7.10-7.03 (m, 3H), 6.97 (dd, 1 H), 6.95 (dt, 1 H), 5.94 (quin, 1 H), 4.40 (s, 1 H), 4.34-4.29 (m, 2H), 3.87 (s, 3H), 3.86-3.85 (m, 3H), 2.42 (s, 3H), 1 .70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 586, Rt = 0.69 min.

Example 300

6,7-dimethoxy-2-methyl-N-{1 -[5-(2-{[(2,2,2- trifluoroethyl)amino]methyl}phenyl)thiophen-2-yl]ethyl}quina zolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2,2,2-trifluoroethanamine (18 μΙ_, 230 μηηοΙ) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (26.9 mg, 45%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.53 (d, 1 H), 7.36-7.25 (m, 3H), 7.13 (d, 1 H), 7.08 (d, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.83 (d, 2H), 3.20 (qd, 2H), 2.76 (quin, 1 H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 517, Rt = 0.98 min.

Example 301

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(pyridin-2-ylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen

(described in example 179a; 50.0 mg, 1 15 μηηοΙ), pyridin-2-amine (21.7 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (15.5 mg, 26%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.89 (ddd, 1 H), 7.64 (s, 1 H), 7.42 (dd, 1 H), 7.36-7.23 (m, 4H), 7.09 (s, 2H), 7.05 (s, 1 H), 6.93 (t, 1 H), 6.49-6.43 (m, 2H), 5.96 (quin, 1 H), 4.51 (d, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 512, Rt = 0.65 min.

Example 302

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(1 H^yrazol-3-ylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 1 H-pyrazol-3-amine (19.2 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (17.0 mg, 28%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 1 1.52- 1 1 .32 (m, 1 H), 8.16 (d, 1 H), 7.64 (s, 1 H), 7.52 (d, 1 H), 7.34-7.27 (m, 3H), 7.26-7.21 (m, 1 H), 7.10-7.07 (m, 2H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 5.52 (br s, 1 H), 5.39 (br s, 1 H), 4.28 (br d, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 501 , Rt = 0.79 min.

Example 303 1 -(3,4-dihydroisoquinolin-2(1 H)-yl)-2-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thio hen-2-yl)benzyl]amino}ethanone

To 2-(5-{1 -[(6 J-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2-y l)ben

(described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2-amino-1 -(3,4-dihydroisoquinolin-2(1 H)- yl)ethanone hydrochloride (1 :1 ) (52.3 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μmol) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature during 5 hours. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (28.5 mg, 41 %). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.64 (s, 1 H), 7.52 (t, 1 H), 7.34-7.24 (m, 3H), 7.19-7.1 1 (m, 5H), 7.05-7.02 (m, 2H), 5.95 (br quin, 1 H), 4.58 (s, 1 H), 4.54 (s, 1 H), 3.86 (s, 6H), 3.76 (s, 2H), 3.64 (t, 1 H), 3.55 (t, 1 H), 3.44 (s, 2H), 2.79 (t, 1 H), 2.73 (t, 1 H), 2.43 (s, 3H), 1.70 (br d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 608, Rt = 0.69 min.

Example 304

N-[1 -{5-[4-fluoro-2-({[(1 -methyl-1 H-imidazol-2-yl)methyl]amino}methyl)phenyl]thiophen- 2-yl}ethyl]-6,7-dimethox -2-methylquinazolin-4-amine

To N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), 1 -methyl-1 H- imidazole-2-carbaldehyde (12.2 mg, 1 10 μηιοΙ) and acetic acid (13 μί, 230 μηιοΙ) in 1 ,2- dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid solid (4.90 mg, 8%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.64 (s, 1 H), 7.39 (dd, 1 H), 7.34 (dd, 1 H), 7.09 (td, 1 H), 7.06-7.03 (m, 2H), 7.01 (d, 1 H), 6.98 (dd, 1 H), 6.71 (dd, 1 H), 5.94 (quin, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 3.70 (br d, 3H), 3.55 (s, 3H), 3.20 (s, 1 H), 2.43 (s, 3H), 1 .70 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 547, Rt = 0.64 min.

Example 305

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(piperazin-1 -ylmethyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine hydrochloride

To tert-butyl 4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]piperazine-1 -carboxylate (described in example 306; 70.0 mg, 1 16 μηιοΙ) in MeOH (1 .1 mL) and H2O (200 μί) was added dropwise acetyl chloride (100 μί, 1 .4 mmol). The solution was stirred at room temperature overnight and the solvent then removed in vacuo. The residue was stirred in Et.20 then filtered to give the title compound as a yellow solid (57.6 mg, 85%). NMR is broad. Selected peaks : ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 14.48 (br s, 1 H), 10.08 (br d, 1 H), 8.07 (s, 1 H), 7.21 (s, 1 H), 7.20 (s, 2H), 6.1 1 (quin, 1 H), 3.96 (s, 3H), 3.95 (s, 3H), 2.66 (s, 3H), 1 .81 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 504, Rt = 0.63 mm.

Example 306

tert-butyl 4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]piperazine-1 -carboxylate

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(described in example 179a; 50.0 mg, 1 15 μηιοΙ), tert-butyl piperazine-1 -carboxylate (43.0 mg, 231 μmol) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification of 30.0 mg of the crude residue by preparative HPLC (basic conditions) gave the title compound as an off-white solid (1 1 .4 mg, 16%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.43-7.35 (m, 2H), 7.33-7.27 (m, 2H), 7.17 (d, 1 H), 7.07 (dd, 1 H), 7.04 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.42 (s, 2H), 3.19 (br s, 4H), 2.42 (s, 3H), 2.26 (br s, 4H), 1 .71 (d, 3H), 1 .37 (s, 9H). LC- MS (method 7): m/z: [M+H] ⁺ = 604, Rt = 0.79 min.

Example 307

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyljacetamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 100 mg, 221 μηηοΙ), acetic acid (19 μί, 330 μηιοΙ), PyBOP (230 mg, 442 μιτιοΙ) and N,N-diisopropylethylamine (190 μί, 1.1 mmol) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (66.5 mg, 57%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.34 (t, 1 H), 8.16 (d, 1 H), 7.64 (s, 1 H), 7.36 (dd, 1 H), 7.16- 7.1 1 (m, 2H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 7.02 (d, 1 H), 5.95 (quin, 1 H), 4.30 (d, 2H), 3.87 (s, 6H), 2.43 (s, 3H), 1 .87 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 495, Rt = 0.81 min.

Example 308

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(4-methylpiperazin-1 -yl)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μιτιοΙ), 1 -methylpiperazine (26 μί, 230 μιτιοΙ) and acetic acid (13 μΙ_, 230 μπιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature during 5 hours. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light brown solid (36.2 mg, 61 %). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.65 (s, 1 H), 7.38 (dt, 2H), 7.29 (dd, 2H), 7.18 (d, 1 H), 7.06 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.37 (s, 2H), 2.42 (s, 3H), 2.31 -2.22 (m, 4H), 2.19-2.07 (m, 4H), 2.03 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 518, Rt = 0.64 min.

Example 309

(3S)-{[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)benzyl]amino}-1 -meth lpyrrolidin-2-one

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), (3S)-3-amino-1 -methylpyrrolidin-2-one (26.3 mg, 231 μιτιοΙ) and acetic acid (13 μί, 230 μιτιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature during 5 hours. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (8.70 mg, 14%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (dd, 1 H), 7.66-7.64 (m, 1 H), 7.63-7.54 (m, 2H), 7.33- 7.26 (m, 2H), 7.16 (dd, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.85- 3.75 (m, 2H), 3.23-3.04 (m, 2H), 2.67 (d, 3H), 2.43 (s, 3H), 2.17 (br s, 1 H), 2.08-1.97 (m, 1 H), 1 .71 (d, 3H), 1 .56 (dq, 1 H). LC-MS (method 7): m/z: [M+H] ⁺ = 532, Rt = 0.59 min.

Example 310

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-1 H-pyrazole-3-carboxamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), 1 H-pyrazole-3- carboxylic acid (12.4 mg, 1 10 μηιοΙ), PyBOP (1 15 mg, 221 μιτιοΙ) and N,N- diisopropylethylamine (95 μί, 550 μηηοΙ) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as an off-white solid (31.6 mg, 51 %). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 13.29 (br s, 1 H), 8.77 (br s, 1 H), 8.17 (d, 1 H), 7.87-7.78 (m, 1 H), 7.65 (s, 1 H), 7.40-7.34 (m, 1 H), 7.14-7.07 (m, 4H), 7.05 (s, 1 H), 6.70-6.59 (m, 1 H), 5.97 (quin, 1 H), 4.51 (d, 2H), 3.87 (s, 6H), 2.43 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 547, Rt = 0.83 min.

Example 311

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(morpholin-4-ylmethyl)phenyl]thiophen-2- yl}ethyl]quinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(described in example 179a; 50.0 mg, 1 15 μηιοΙ), morpholine (20 μΙ_, 230 μηιοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (24.9 mg, 43%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.16 (d, 1 H), 7.65 (s, 1 H), 7.43-7.36 (m, 2H), 7.32-7.27 (m, 2H), 7.19 (d, 1 H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.43 (br t, 4H), 3.41 (s, 2H), 2.42 (s, 3H), 2.30 (br s, 4H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 505, Rt = 0.60 min.

Example 312

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl]azetidin-3-ol

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), azetidin-3-ol hydrochloride (1 :1 ) (25.3 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a light orange solid (28.3 mg, 48%). 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.19-8.1 1 (m, 1 H), 7.65 (s, 1 H), 7.40 (dd, 1 H), 7.35-7.32 (m, 1 H), 7.31 -7.23 (m, 2H), 7.16 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 5.27 (d, 1 H), 4.15 (sxt, 1 H), 3.87 (s, 6H), 3.58 (s, 2H), 3.47 (dt, 2H), 2.76-2.70 (m, 2H), 2.44 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 491 , Rt = 0.56 min.

Example 313

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzyl]- 2,5,7-triazaspiro[3.4]octan-6-one

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μιτιοΙ), 2,5,7-triazaspiro[3.4]octan-6-one (29.3 mg, 231 μmol) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light orange solid (19.3 mg, 29%). 1 H-NMR (400 MHz, DMSO- d ₆ ): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.41 (dd, 1 H), 7.35-7.24 (m, 3H), 7.14 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 6.82 (s, 1 H), 6.24 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 6H), 3.58 (s, 2H), 3.46 (s, 2H), 3.31 -3.28 (m, 2H), 2.99 (dd, 2H), 2.43 (s, 3H), 1 .75-1 .70 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 545, Rt = 0.54 min.

Example 314

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-L-prolinamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), L-proline (12.7 mg, 1 10 μηιοΙ), PyBOP (1 15 mg, 221 μηιοΙ) and N,N-diisopropylethylamine (95 μΙ_, 550 μmol) in DMF (1.0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0- 20% then MeOH) gave the title compound as a white solid (9.40 mg, 15%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.42 (br td, 1 H), 8.15 (d, 1 H), 7.64 (s, 1 H), 7.35 (dd, 1 H), 7.14- 7.00 (m, 5H), 5.95 (quin, 1 H), 4.33 (d, 2H), 3.87 (s, 6H), 3.54 (dd, 1 H), 2.85-2.70 (m, 2H), 2.43 (s, 3H), 1 .97-1.87 (m, 1 H), 1 .71 (d, 3H), 1 .67-1.51 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 550, Rt = 0.64 min.

Example 315

N-{1 -[5-(2-{[(2,2-difluoroethyl)amino]methyl}phenyl)thiophen-2-y l]ethyl}-6 -di

2-methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2,2-difluoroethanamine (16 μί, 230 μηηοΙ) and acetic acid (13 μί, 230 μηιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (12.0 mg, 20%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.54-7.50 (m, 1 H), 7.35-7.30 (m, 2H), 7.29-7.24 (m, 1 H), 7.15 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.97 (tt, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.78 (br d, 2H), 2.84 (br t, 2H), 2.43 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 499, Rt = 0.70 min.

Example 316

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzylj-prolinamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), D-proline (12.7 mg, 1 10 μηιοΙ), PyBOP (1 15 mg, 221 μηιοΙ) and N,N-diisopropylethylamine (95 μΙ_, 550 μmol) in DMF (1.0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0- 20% then MeOH) gave the title compound as a white solid (7.30 mg, 12%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.45-8.39 (m, 1 H), 8.15 (d, 1 H), 7.64 (s, 1 H), 7.35 (dd, 1 H), 7.14- 7.00 (m, 5H), 5.95 (quin, 1 H), 4.33 (d, 2H), 3.87 (s, 6H), 3.54 (dd, 1 H), 2.85-2.71 (m, 2H), 2.43 (s, 3H), 1 .98-1.86 (m, 1 H), 1 .71 (d, 3H), 1 .68-1.50 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 550, Rt = 0.64 min.

Example 317

N-[1 -{5-[2-(azetidin-1 -ylmethyl)phenyl]thiophen-2-yl}ethyl]-6 -dimethoxy-2- methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), azetidine (13.2 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηιοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc) ₃ (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (26.1 mg, 48%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.40 (dd, 1 H), 7.35-7.32 (m, 1 H), 7.31 -7.23 (m, 2H), 7.17 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.53 (s, 2H), 3.09 (t, 4H), 2.44 (s, 3H), 1 .93 (quin, 2H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 475, Rt = 0.57 min. Example 318

{1 -[(2S)-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)benzyl]azetidin-2-yl}methanol

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(described in example 179a; 50.0 mg, 1 15 μηιοΙ), (2S)-azetidin-2-ylmethanol (20.1 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μmol) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (32.3 mg, 55%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (d, 1 H), 7.48-7.44 (m, 1 H), 7.34-7.29 (m, 1 H), 7.29-7.22 (m, 3H), 7.07 (ddd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 4.35 (td, 1 H), 3.88-3.86 (m, 6H), 3.82 (d, 1 H), 3.47 (dd, 1 H), 3.30-3.26 (m, 2H), 3.25-3.18 (m, 1 H), 3.17-3.10 (m, 1 H), 2.75-2.68 (m, 1 H), 2.43 (d, 3H), 1 .96-1 .87 (m, 1 H), 1.80 (quin, 1 H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 505, Rt = 0.56 min.

Example 319

N-{1 -[5-(2-{[3-(dimethylamino)azetidin-1 -yl]methyl}phenyl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), N,N-dimethylazetidin-3-amine dihydrochloride (39.9 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηιοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (22.3 mg, 36%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.41 -7.37 (m, 1 H), 7.37-7.33 (m, 1 H), 7.31 -7.24 (m, 2H), 7.15 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.88-3.87 (m, 3H), 3.87-3.85 (m, 3H), 3.55 (s, 2H), 3.30-3.25 (m, 2H), 2.77-2.70 (m, 2H), 2.70-2.67 (m, 1 H), 2.43 (s, 3H), 1 .95 (s, 6H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 518, Rt = 0.57 min.

Example 320

N-[1 -(5-{2-[(3,3-difluoroazetidin-1 -yl)methyl]phenyl}thiophen-2-yl)ethyl]-6 -d

2-methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 3,3-difluoroazetidine hydrochloride (1 :1 ) (29.9 mg, 231 μιτιοΙ) and acetic acid (13 μί, 230 μιτιοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (29.1 mg, 49%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.48-7.44 (m, 1 H), 7.38-7.35 (m, 1 H), 7.35-7.27 (m, 2H), 7.16 (d, 1 H), 7.10 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.75 (s, 2H), 3.59 (t, 4H), 2.43 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 51 1 , Rt = 0.90 min.

Example 321

6,7-dimethoxy-2-methyl-N-{1 -[5-(2-{[methyl(2,2,2- trifluoroethyl)amino]methyl}phenyl)thiophen-2-yl]ethyl}quina zolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]eth^

(described in example 179a; 50.0 mg, 1 15 μηηοΙ), 2,2,2-trifluoro-N-methylethanamine hydrochloride (1 :1 ) (34.5 mg, 231 μηηοΙ) and acetic acid (13 μΙ_, 230 μηηοΙ) in 1 ,2- dichloroethane (1 .0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (25.4 mg, 42%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.54-7.49 (m, 1 H), 7.38-7.27 (m, 3H), 7.08 (s, 2H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.74 (s, 2H), 3.20 (q, 2H), 2.43 (s, 3H), 2.25 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 531 , Rt = 1 .09 min.

Example 322

N-[1 -(5-{2-[(3-fluoroazetidin-1 -yl)methyl]phenyl}thiophen-2-yl)ethyl]-6 -dimet^ methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ), 3-fluoroazetidine hydrochloride (1 :1 ) (25.7 mg, 231 μηηοΙ) and acetic acid (13 μί, 230 μηηοΙ) in 1 ,2-dichloroethane (1.0 mL) was added NaBH(OAc)3 (48.9 mg, 231 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (28.6 mg, 50%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.42 (dd, 1 H), 7.37-7.33 (m, 1 H), 7.33-7.25 (m, 2H), 7.16 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 5.13 (dquin, 1 H), 3.87 (s, 6H), 3.65 (s, 2H), 3.57-3.47 (m, 2H), 3.18-3.13 (m, 1 H), 3.12-3.06 (m, 1 H), 2.43 (s, 3H), 1 .72 (d, 3H). LC- MS (method 7): m/z: [M+H] ⁺ = 493, Rt = 0.58 min.

Example 323

N-[1 -(5-{4-chloro-2-[(dimethylamino)methyl]phenyl}thiophen-2-yl) ethyl]-6,7-dimethoxy- 2-methylquinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine hydrochloride (1 :1 ) (described in example 209; 100 mg, 225 μηηοΙ), 1 -[5-chloro-2-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]-N,N-dimethylmethanamine (66.5 mg, 225 μηηοΙ), K ₂ C0 ₃ (124 mg, 899 μηιοΙ) and Pd(PPh ₃ ) ₄ (26.0 mg, 22.5 μπιοΙ) in dioxane (2.3 mL) and H ₂ 0 (460 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH, repeated twice) followed by preparative HPLC (basic conditions) gave the title compound as a yellow solid (37.5 mg, 33%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.64 (s, 1 H), 7.50 (d, 1 H), 7.37 (d, 1 H), 7.34 (dd, 1 H), 7.15 (d, 1 H), 7.09 (dd, 1 H), 7.05 (s, 1 H), 5.95 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.38 (s, 2H), 2.43 (s, 3H), 2.1 1 (s, 6H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 497, Rt = 0.60 min.

Example 324

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]ethanone

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (described in example 209; 200 mg, 85 % purity, 416 μηιοΙ), (2-acetylphenyl)boronic acid (68.3 mg, 416 μηιοΙ), K ₂ C0 ₃ (230 mg, 1.67 mmol) and Pd(PPh ₃ ) ₄ (48.1 mg, 41.6 μηιοΙ) in dioxane (4.0 mL) and H2O (800 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (71 .3 mg, 38%). ¹ H- NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.64 (s, 1 H), 7.53-7.40 (m, 4H), 7.07 (dd, 1 H), 7.05 (s, 1 H), 6.89 (d, 1 H), 5.93 (quin, 1 H), 3.87 (s, 6H), 2.43 (s, 3H), 2.21 (s, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 448, Rt = 0.92 min.

Example 325

6 -dimethoxy-2-methyl-N-[1 -(5-{2-[2-(pyrrolidin-1 -yl)ethoxy]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine hydrochloride (1 :1 ) (described in example 209; 100 mg, 225 μιτιοΙ), {2-[2-(pyrrolidin-1 - yl)ethoxy]phenyl}boronic acid (52.9 mg, 225 μιτιοΙ), K ₂ C0 ₃ (124 mg, 899 μιτιοΙ) and Pd(PPh ₃ ) ₄ (26.0 mg, 22.5 μηιοΙ) in dioxane (2.3 mL) and H ₂ 0 (460 μΙ_) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a off- white solid (81.1 mg, 70%). 1 H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.12 (d, 1 H), 7.67-7.63 (m, 2H), 7.47 (d, 1 H), 7.24-7.19 (m, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 7.03 (dd, 1 H), 6.96 (td, 1 H), 5.96 (quin, 1 H), 4.10 (t, 2H), 3.87 (s, 6H), 2.77-2.69 (m, 2H), 2.43 (s, 3H), 2.35-2.31 (m, 4H), 1.70 (d, 3H), 1.51 (ddd, 4H). LC-MS (method 7): m/z: [M+H] ⁺ = 519, Rt = 0.62 min.

Example 326

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine, enantiomer 1

Enantiopure 6J-Dimethoxy-2-methyl-N-[1 -(4-{2-[(methylamino)methyl]phenyl}thio yl)ethyl]quinazolin-4-amine was obtained from racemic 6,7-dimethoxy-2-methyl-N-[1 -(4-{2- [(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazolin-4 -amine (described in example 271 ) by chiral HPLC purification (method X1 ). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.46 (d, 1 H), 7.46-7.43 (m, 1 H), 7.32-7.24 (m, 4H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.57 (s, 2H), 2.43 (s, 3H), 2.22 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 449, Rt = 0.55 min. [a] _D = -93.9° +/- 1 .16°.

Example 327

6,7-dimethoxy-2-methyl-N-[1 -(4-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine, enantiomer 2

Enantiopure 6,7-Dimethoxy-2-methyl-N-[(1 -(4-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine was obtained from racemic 6,7-dimethoxy-2-methyl-N-[1 -(4-{2- [(methylamino)methyl]phenyl}thiophen-2-yl)ethyl]quinazolin-4 -amine (described in example 271 ) by chiral HPLC purification (method X1 ). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.46 (d, 1 H), 7.46-7.42 (m, 1 H), 7.32-7.24 (m, 4H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.57 (s, 2H), 2.43 (s, 3H), 2.22 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 449, Rt = 0.55 min. [a] _D = +89.4° +/- 1.91 °.

Example 328

N-{1 -[5-(6 -dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy- 2-methylquinazolin-4-amine, enantiomer 1

Enantiopure N-{1 -[5-(6,7-Dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine was obtained from racemic N-{1 -[5-(6,7-Dihydro-5H- pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-meth ylquinazolin-4-amine (described in example 219) by chiral HPLC purification (method X2). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.63 (s, 1 H), 7.05-7.02 (m, 4H), 5.90 (quin, 1 H), 4.06 (t, 2H), 3.87 (s, 6H), 2.77-2.71 (m, 2H), 2.59-2.53 (m, 2H), 2.43 (s, 3H), 1.69 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 436, Rt = 0.58 min. [a] _D = -92.7° +/- 31 .06°.

Example 329

N-{1 -[5-(6 -dihydro-5H^yrrolo[1 ,2-a]imidaz

2-methylquinazolin-4-amine, enantiomer 2

Enantiopure N-{1 -[5-(6,7-Dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine was obtained from racemic N-{1 -[5-(6,7-Dihydro-5H- pyrrolo[1 ,2-a]imidazol-3-yl)thiophen-2-yl]ethyl}-6,7-dimethoxy-2-meth ylquinazolin-4-amine (described in example 219) by chiral HPLC purification (method X2). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.63 (s, 1 H), 7.06-7.02 (m, 4H), 5.90 (quin, 1 H), 4.06 (t, 2H), 3.87 (s, 6H), 2.77-2.71 (m, 2H), 2.59-2.53 (m, 2H), 2.43 (s, 3H), 1.68 (d, 3H). LC-MS (method 9): m/z: [M+H] ⁺ = 436, Rt = 0.58 min. [a] _D = +154.0° +/- 34.5°.

Example 330

6,7-dimethoxy-2-methyl-N-[1 - 2-methyl-1 -benzothiophen-4-yl)ethyl]quinazolin-4-amine

Step a:

4-bromo-2 -methyl benzo[b]thiophene

4-Bromobenzo[b]thiophene, 5.00 g (23.5 mmol), was dissolved in 100 mL of tetrahydrofuran. Then lithium diisopropylamide, 14.08 mL (28.2 mmol), was added dropwise at -78°C. The resulting mixture was stirred at this temperature for 30 min. Then iodomethane, 7.30 mL (1 17.3 mmol), was added dropwise at -78°C and the resulting mixture was stirred at this temperature for 1 hour. Aq. ammonium chloride was added and the resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to give 4.00 g (71 %) of the product as a yellow solid. ¹ H-NMR (400 MHz, CDCIs): δ [ppm] = 2.63 (d, 3H), 7.08-7.19 (m, 2H), 7.49 (d, 1 H), 7.69 (d, 1 H).

Step b:

1 -(2 -methyl benzo[b]thiophen-4-yl)ethanone

Synthesis of the enolether: 4-Bromo-2-methylbenzo[b]thiophene, 1 .50 g (6.6 mmol), tributyl(1 -ethoxyvinyl)stannane, 3.12 g (8.6 mmol), 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 483 mg (0.7 mmol) and potassium carbonate, 2.74 g (19.8 mmol), were added into 30 mL of 1 ,4-dioxane. The resulting mixture was stirred at 60°C for overnight under nitrogen.

Hydrolysis of the enolether: Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to give 1.00 g (64%) of the product as a yellow solid. MS (ESIpos): m/z = 191 [M+H] ⁺ ; LC-MS (method 4, gradient Acetonitrile-Water-0.05%HCOOH-5%B): R _t = 1.58 min.

Step c:

(E)-1 -(2-methylbenzo[b]thiophen-4-yl)ethanone oxime

1 -(2-Methylbenzo[b]thiophen-4-yl)ethanone, 500 mg (2.6 mmol), hydroxylamine hydrochloride, 274 mg (3.9 mmol), and sodium acetate, 323 mg (3.9 mmol), were dissolved in 10 mL of methanol. The resulting mixture was stirred at room temperature for 2 hours. The solid was removed by filtration and the filtrate was concentrated in vacuo to give 500 mg (81 %) of the product as an off-white solid. MS (ESIpos): m/z = 206 [M+H] ⁺ ; LC-MS (method 4, gradient Acetonitrile-Water-0.05%HCOOH-5%B): R _t = 1.49 min.

Step d:

1 -(2-methylbenzo[b]thiophen-4-yl)ethanamine

(E)-1 -(2-Methylbenzo[b]thiophen-4-yl)ethanone oxime, 500 mg (2.4 mmol), and Raney Nickel, 500 mg (8.5 mmol), were dissolved in 10 mL of 7.0 M ammonium/methanol solution. The resulting mixture was stirred under hydrogen (3 atm) at room temperature for overnight. The solid was removed by filtration and the filtrate was concentrated in vacuo to give 300 mg (53%) of the product as a grey solid. MS (ESIpos): m/z = 192 [M+H] ⁺ ; LC-MS (method 4, gradient acetonitrile-water-0.05%TFA-5%B): R _t = 1 .07 min.

Step e:

6,7-dimethoxy-2-methyl-N-[1 - 2-methyl-1 -benzothiophen-4-yl)ethyl]quinazolin-4-amine

1 - (2-Methylbenzo[b]thiophen-4-yl)ethanamine, 100 mg (0.52 mmol), 4-chloro-6,7-dimethoxy-

2- methylquinazoline, 137 mg (0.58 mmol, commercially available), and triethylamine, 132 mg (1 .31 mmol), were dissolved in 5 mL of Ν,Ν-dimethylformamide. The resulting solution was stirred at 100°C for overnight under nitrogen. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 1 1.60 mg (6%) of the product as a light yellow solid. MS (ESIpos): m/z = 394 [M+H] ⁺ ; LC-MS (method 4, gradientAcetonitrile-Water-0.05%TFA-5%B): R _t = 1 .19 min. ¹ H- NMR (400 MHz, CD ₃ OD): δ [ppm] = 2.44 (s, 3H), 2.57 (d, 3H), 3.92 (s, 3H), 3.93 (s, 3H), 6.12-6.18 (m, 1 H), 7.01 (s, 1 H), 7.22 (t, 1 H), 7.33 (s, 1 H), 7.41 -7.43 (m, 1 H), 7.61 -7.65 (m, 2H). Example 331

6 -dimethoxy-2-methyl-N-[1 -(thieno[2,3-b]pyridin-4-yl)ethyl]quinazolin-4-amine

Step a:

4-(1 -ethoxyvinyl)thieno[2,3-b]pyridine

This compound was synthesized by the same method as described in example 330 (step b; synthesis of enolether) to give 400 mg (63%) of the title compound as a yellow solid. MS (ESIpos): m/z = 206 [M+H] ⁺ ; LC-MS (method 4, gradient Acetonitrile-Water-0.05%HCOOH- 5%B): R _t = 1 .86 min.

Step b:

1 -(thieno[2,3-b]pyridin-4-yl)ethanone

4-(1 -Ethoxyvinyl)thieno[2,3-b]pyridine, 400 mg (2.0 mmol), was dissolved in 10 mL of tetrahydrofuran. Then 5 mL of hydrochloric acid (4.0 M) was added. The resulting mixture was stirred at 50°C for 2 hours. The mixture was extracted with ethyl acetate and the combined organic phase was dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 250 mg (72%) of the product as a yellow solid. MS (ESIpos): m/z = 178 [M+H] ⁺ ; LC-MS (method 4, gradient Acetonitrile-Water-0.1 %HCOOH-10%B): R _t = 0.79 min.

Step c:

(E)-1 -(thieno[2,3-b]pyridin-4-yl)ethanone oxime

This compound was synthesized by the same method as described in example 330 (step c) to give 300 mg (75%) of the product as a yellow oil. MS (ESIpos): m/z = 193 [M+H] ⁺ ; LC-MS (mehod 4, Acetonitrile-Water-0.05%TFA-5%B): R _t = 1.08 min.

Step d:

1 -(Thieno[2,3-b]pyridin-4-yl)ethanamine

This compound was synthesized by the same method as described in example 330 (step d) to give 200 mg (48%) of the product as a yellow solid. MS (ESIpos): m/z = 179 [M+H] ⁺ ; LC- MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.66 min. Step e:

6,7-dimethoxy-2-methyl-N-[1 -(thieno[2,3-b]pyridin-4-yl)ethyl]quinazolin-4-amine

This compound was synthesized by the same method as described in example 330 (step e) to give 21 .2 mg (10%) of the product as a light yellow solid. MS (ESIpos): m/z = 381 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.90 min. ¹ H-NMR (400 MHz, CD ₃ OD): δ [ppm] = 1 .77 (d, 3H), 2.33 (s, 3H), 3.94 (s, 3H), 4.01 (s, 3H), 6.09-6.14 (m, 1 H), 7.02 (s, 1 H), 7.47 (d, 1 H), 7.67 (s, 1 H), 7.72-7.76 (m, 2H), 8.45 (d, 1 H).

Example 332

6,7-dimethoxy-2-methyl-N-[1 -(thieno[2,3-c]pyridin-4-yl)ethyl]quinazolin-4-amine

Step a:

ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate

3,5-Dibromoisonicotinaldehyde, 2.00 g (7.6 mmol), ethyl 2-mercaptoacetate, 0.91 g (7.6 mmol), and cesium carbonate, 2.46 g (7.6 mmol), were added into 40 mL of tetrahydrofuran. The resulting mixture was stirred at 60°C for overnight. After evaporation in vacuo, water was added and the mixture was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give 1 .8 g (82%) of the product as a yellow solid. MS (ESIpos): m/z = 286 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%HCOOH-5%B): R _t = 1 .47 min.

Step b:

4-bromothieno[2,3-c]pyridine-2-carboxylic acid

Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate, 1 .80 g (6.3 mmol), and sodium hydroxide, 1 .13 g (28.3 mmol), were dissolved in 50 mL of methanol and 25 mL of water. The resulting mixture was stirred at room temperature for overnight. After evaporation in vacuo, hydrochloric acid (4.0 M) was added to adjust the pH = 2 and the precipitated solid was collected by filtration. The filter cake was washed with water and dried in vacuo to give 1.50 g (74%) of the product as a yellow solid. MS (ESIpos): m/z = 258 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%HCOOH-5%B): R _t = 1 .17 min.

Step c:

4-bromothieno[2,3-c]pyridine

4-Bromothieno[2,3-c]pyridine-2-carboxylic acid, 1 .30 g (5.0 mmol), silver carbonate, 139 mg (0.5 mmol), and acetic acid, 0.04 ml. (0.6 mmol), were dissolved in 13 ml. of N,N- dimethylformamide. The resulting mixture was stirred at 120°C for overnight. Water was added and the resulting mixture was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to give 400 mg (35%) of the product as a yellow solid. MS (ESIpos): m/z = 214 [M+H] ⁺ ; LC-MS (Acetonitrile-Water- 0.05%HCOOH-5%B): R _t = 1 .16 min.

Step d:

4-(1 -ethoxyvinyl)thieno[2,3-c]pyridine

C H ₃

This compound was synthesized by the same method as described in example 330 (step b, synthesis of enolether) to give 380 mg (73%) of the product as a yellow oil. MS (ESIpos): m/z = 206 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B):

Step e:

1 -(thieno[2,3-c]pyridin-4-yl)ethanone

This compound was synthesized by the same method as described in example 330 (step b) to give 200 mg (59%) of the product as yellow oil. MS (ESIpos): m/z = 178 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.44 min.

Step f:

1 -(thieno[2,3-c]pyridin-4-yl)ethanamine

1 -(Thieno[2,3-c]pyridin-4-yl)ethanone, 200 mg (1 .9 mmol), and 1 .2 mL of acetic acid were dissolved in 10 mL of 7 M ammonium/methanol solution. Then sodium cyanoborohydride, 284 mg (4.5 mmol), was added and the resulting mixture was stirred at 40°C for overnight. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 150 mg (59%, 82% purity) of the product as a yellow oil and the product was used directly for next step. MS (ESIpos): m/z = 179 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.61 min.

Step g:

6,7-dimethoxy-2-methyl-N-[1 -(thieno[2,3-c]pyridin-4-yl)ethyl]quinazolin

1 -(Thieno[2,3-c]pyridin-4-yl)ethanamine, 50 mg (0.28 mmol), 4-chloro-6,7-dimethoxy-2- methylquinazoline, 74 mg (commercially available; 0.31 mmol), triethylamine, 85 mg (0.84 mmol), were dissolved in 3 mL of methanol. The resulting mixture was stirred at room temperature for 3 days under nitrogen and the solid was removed by filtration. The filtrate was purified by preparative HPLC to give 13.80 mg (13%) of the product as a light yellow solid. MS (ESIpos): m/z = 381 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile- Water-0.05%TFA-5%B): R _t = 0.66 min. ¹ H-NMR (400 MHz, CD ₃ OD): δ [ppm] = 1 .84 (d, 3H), 2.43 (s, 3H), 3.95 (s, 3H), 3.96 (s, 3H), 6.20-6.25 (m, 1 H), 7.02 (s, 1 H), 7.66 (s, 1 H), 7.83 (d, 1 H), 8.04 (d, 1 H), 8.51 (s, 1 H), 9.06 (s, 1 H).

Example 333

6,7-dimethoxy-2-methyl-N-[1 -(thieno[3,2-c]pyridin-4-yl)ethyl]quinazolin-4-amine

Step a: 4-bromothieno[3,2-c]pyridine

Thieno[3,2-c]pyridin-4(5H)-one, 700.00 mg (4.6 mmol), was dissolved in 30 mL of toluene. Then phosphoryl bromide, 1 .59 g (5.6 mmol), and 0.1 mL of Ν,Ν-dimethylformamide were added successively. The resulting mixture was stirred at 1 10°C for 2 hours. The reaction was quenched with water and the resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 600 mg (56%) of the product as a light yellow solid. MS (ESIpos): m/z = 214 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%HCOOH-5%B): R _t = 0.83 min. Step b:

4-(1 -ethoxyvinyl)thieno[3,2-c]pyridine

This compound was synthesized by the same method as described in example 330 (step b, synthesis of enolether) to give 430 mg (70%) of the product as yellow oil. MS (ESIpos): m/z = 206 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.1 %HCOOH- 10%B): R _t = 0.57 min.

Step c:

1 -(thieno[3,2-c]pyridin-4-yl)ethanone

This compound was synthesized by the same method as described in example 330 (step b, hydrolysis of enolether) to give 350.00 mg (82%) of the product as a yellow solid. MS (ESIpos): m/z = 178 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water- 0.05%TFA-5%B): R _t = 0.79 min.

Step d:

1 -(thieno[3,2-c]pyridin-4-yl)ethanamine

This compound was synthesized by the same method as described in example 332 (step f) to give 200.00 mg (55%) of the product as a yellow solid. MS (ESIpos): m/z = 179 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.52 min. Step e:

6,7-dimethoxy-2-methyl-N-[1 -(thieno[3,2-c]pyridin-4-yl)ethyl]quinazolin-4-amine

This compound was synthesized by the same method as described in example 332 (step g) to give 12.70 mg (6%) of the product as a white solid. MS (ESIpos): m/z = 381 [M+H] ⁺ ; LC-MS (method 4, gradient starting with Acetonitrile-Water-0.05%TFA-5%B): R _t = 0.82 min. ¹ H-NMR (300 MHz, DMSO-de): δ [ppm] = 1.69 (d, 3H), 2.31 (s, 3H), 3.85 (d, 6H), 6.27 (m, 1 H), 6.99 (s, 1 H), 7.71 (s, 1 H), 7.82-7.91 (m, 2H), 7.97(d, 1 H), 8.24 (d, 1 H), 8.39 (d, 1 H).

Example 334

N-{(1 R)-1 -[3-(3,5-dimethyl-1 H-pyrazol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

N-[(1 R)-1 -(3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine

4-Chloro-6,7-dimethoxy-2-methylquinazoline, 1.20 g (5.0 mmol, commercially available) was dissolved in 5 mL of 2-propanol, then (R)-1 -(3-bromophenyl)ethanamine, 1 .31 g (6.5 mmol, commercially available), was added at room temperature. The resulting mixture was stirred at 1 10°C for 6 hours. The reaction was cooled to room temperature and water was added. The resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to give 1 .70 g (66%) of the product as a light yellow solid. MS (ESIpos): m/z = 402 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 5%B]: Rt = 1 .59 min. 1 H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.55-1 .57 (d, 3H), 2.33 (s, 3H), 3.85 (s, 3H), 3.90 (s, 3H), 5.57-5.61 (m, 1 H), 7.01 (s, 1 H), 7.26-7.30 (m, 1 H), 7.39-7.44 (m, 2H), 7.61 -7.62 (d, 1 H), 7.67 (s, 1 H), 7.97-7.99 (m, 1 H). Step b:

N-{(1 R)-1 -[3-(3,5-dimethyl-1 H-pyrazol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2- methylquinazolin-4-amine

This compound was synthesized by the same method as described in example 335 to give 37.4 mg (30%) of the product as a yellow solid. MS (ESIpos): m/z = 418 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1 .01 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.63 (d, 3H), 2.14 (s, 6H), 2.35 (s, 3H), 3.88 (d, 6H), 5.71 (m, 1 H), 7.03 (d, 1 H), 7.10-7.17 (m, 1 H), 7.35 (m, 3H), 7.71 (s, 1 H), 7.99 (d, 1 H), 12.23 (s, 1 H). Example 335

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(5-methyl-1 H-pyrazol-4-yl)phenyl]ethyl}quinazolin- 4-amine

(R)-N-(1 -(3-bromophenyl)ethyl)-6 ,7-dimethoxy-2-methylquinazolin-4-amine (described in example 191 ), 120 mg (0.30 mmol), 5-methyl-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)- 1 H-pyrazole, 186 mg (0.90 mmol), cesium carbonate, 486 mg (1 .49 mmol), and tetrakis(triphenylphosphine)palladium(0), 34 mg (0.03 mmol), were dissolved in 2 mL of N,N- dimethylformamide/water (5:2). The resulting mixture was stirred at 80°C for overnight under nitrogen atmosphere. The reaction was cooled to room temperature and water was added. The resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 43.4 mg (36%) of the product as a white solid. MS (ESIpos): m/z = 404 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)- Acetonitrile, 5%B]: Rt = 1 .06 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .62 (d, 3H), 2.29 (s, 3H), 2.32 (s, 3H), 3.88 (d, 6H), 5.71 (m, 1 H), 7.03 (d, 1 H), 7.31 (m, 3H), 7.52 (s, 1 H), 7.71 (s, 2H), 7.99 (d, 1 H), 12.59 (s, 1 H).

Example 336

N-{(1 R)-1 -[3-(3,5-dimethyl-1 ,2-oxazol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2-methyl- quinazolin-4-amine

3

This compound was synthesized by the same method as described in example 338 to give 35.2 mg (27%) of the product as an off-white solid. MS (ESIpos): m/z = 419 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 2.66 min. ¹ H- NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1.59 (d, 3H), 2.14 (s, 3H), 2.31 (d, 6H), 3.84 (d, 6H), 5.64 (m, 1 H), 6.98 (s, 1 H), 7.20 (d, 1 H), 7.32-7.47 (m, 3H), 7.66 (s, 1 H), 7.97 (d, 1 H).

Example 337

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-5-yl)phenyl]ethyl}quinazolin-4-amine

This compound was synthesized by the same method as described in example 338 to give 52.3 mg (43%) of the product as a white solid. MS (ESIpos): m/z = 390 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 2.70 min. ¹ H- NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .59 (d, 3H), 2.31 (s, 3H), 3.84 (d, 6H), 5.66 (m, 1 H), 6.62 (s, 1 H), 6.98 (s, 1 H), 7.31 (m, 2H), 7.50-8.08 (m, 5H), 12.80-13.48 (m, 1 H).

Example 338

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-pyrazol-4-yl)phenyl]ethyl}quinazolin- 4-amine

(R)-N-(1 -(3-bromophenyl)ethyl)-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ), 120 mg (0.30 mmol), 3,5-dimethylisoxazol-4-ylboronic acid, 310 mg (1 .49 mmol), potassium carbonate, 206 mg (1 .49 mmol), and 1 ,1 '- Bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 44 mg (0.06 mmol), were dissolved in 2 mL of Ν,Ν-dimethylformamide. The resulting mixture was stirred at 80°C for overnight under nitrogen atmosphere. The reaction was cooled to room temperature and water was added. The resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 45.5 mg (37%) of the product as a grey solid. MS (ESIpos): m/z = 404 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1.13 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.60 (d, 3H), 2.36 (s, 3H), 3.81 -3.94 (m, 9H), 5.63-5.71 (m, 1 H), 7.01 (s, 1 H), 7.22-7.33 (m, 2H), 7.39 (d, 1 H), 7.48-7.62 (m, 2H), 7.72 (s, 1 H), 7.80 (s, 1 H), 8.08 (s, 1 H).

Example 339

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 -methyl-1 H-pyrazol-5-yl)phenyl]ethyl}quinazolin- 4-amine

This compound was synthesized by the same method as described in example 338 to give 52.3 mg (43%) of the product as a white solid. MS (ESIpos): m/z = 404 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1 .13 min. ¹ H- NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1.59 (d, 3H), 2.31 (s, 3H), 3.73-3.90 (m, 9H), 5.66 (m, 1 H), 6.33 (d, 1 H), 6.98 (s, 1 H), 7.29-7.58 (m, 5H), 7.66 (s, 1 H), 7.99 (d, 1 H),

Example 340

N-{(1 R)-1 -[3-(1 H-imidazol-1 -yl)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazolin-4-amine

This compound was synthesized by the same method as described in example 341 to give 52.7 mg (36%) of the product as a white solid. MS (ESIpos): m/z = 390 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 0.83 min. ¹ H- NMR (300 MHz, CD30D): δ [ppm] = 1 .60 (d, 3H), 2.31 (s, 3H), 3.85 (d, 6H), 5.66 (m, 1 H), 6.99 (s, 1 H), 7.03-7.1 1 (m, 1 H), 7.34-7.51 (m, 3H), 7.63-7.71 (m, 3H), 7.96 (d, 1 H), 8.19 (d, 1 H).

Example 341

6,7-dimethoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-1 -yl)phenyl]ethyl}quinazolin-4-amine

(R)-N-(1 -(3-bromophenyl)ethyl)-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 191 ), 150 mg (0.37 mmol), 1 H-pyrazole, 127 mg (1 .86 mmol), copper (I) iodide, 7 mg (0.04 mmol), potassium carbonate, 258 mg (1 .86 mmol), and (S)-(-)-proline, 9 mg (0.08 mmol), were dissolved in 2 ml. of dimethyl sulfoxide. The resulting mixture was stirred at 80°C for 4 days under nitrogen atmosphere. The reaction was cooled to room temperature and water was added. The resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 7.8 mg (5%) of the product as a colorless oil. MS (ESIpos): m/z = 390 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1.17 min. ¹ H-NMR (300 MHz, CD ₃ OD): δ [ppm] = 1 .68 (d , 3H), 2.41 (s, 3H), 3.93 (d, 6H) 5.72 (m, 1 H), 6.48 (m, 1 H), 6.99 (s, 1 H), 7.37-7.45 (m, 2H), 7.47-7.59 (m, 1 H), 7.59-7.71 (m, 2H), 7.82 (s, 1 H), 8.15 (d, 1 H). Example 342

N-{(1 R)-1 -[3-(1 H-imidazol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazol in-4-amine

5-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)-1 H-imidazole

5-iodo-I H-imidazole, 200 mg (1 .03 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2- dioxaborolane), 524 mg (2.06 mmol), potassium acetate, 304 mg (3.09 mmol), and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll)chloride, 75 mg (0.10 mmol), were dissolved in 5ml_ of Ν,Ν-dimethylformamide. The resulting mixture was stirred at 90°C for overnight under nitrogen atmosphere. The reaction was cooled to room temperature and water was added. The resulting solution was extracted with ethyl acetate. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give 600 mg (crude) of the product as a grey solid and it was used directly for next step. MS (ESIpos): m/z = 195 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1.53 min.

Step b:

N-{(1 R)-1 -[3-(1 H-imidazol-4-yl)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazol in-4-amine

This compound was synthesized by the same method as described in example 335 to give 3.6 mg (3%) of the product as a white solid. MS (ESIpos): m/z = 390 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water (0.05% TFA)-Acetonitrile, 5%B]: Rt = 1 .07 min. ¹ H-NMR (300 MHz, CD30D): δ [ppm] = 1 .70 (d, 3H), 2.50 (s, 3H), 3.95 (d, 6H), 5.76 (m, 1 H), 7.00 (s, 1 H), 7.25-7.34 (m, 2H), 7.38-7.48 (m, 1 H), 7.64 (m, 1 H), 7.72 (s, 1 H), 7.90 (s, 2H), 8.49 (s, 1 H).

Example 343

6-(benzyloxy)-N-[(1 R)-1 -(3-bromophenyl)ethyl]-7-methoxy-2-methylquinazolin-4-amine

methyl 5-(benzyloxy)-4-methoxy-2-aminobenzoate

Methyl 5-(benzyloxy)-4-methoxy-2-nitrobenzoate, 3.00 g (9.5 mmol), and iron powder, 5.28 g (94.5 mmol), were added into 70 ml. of ethanol. Then ammoniumchloride, 5.06 (94.5 mmol), in 15 mL of water was added dropwise at 90°C and the resulting mixture was stirred at this temperature for 4 hours. After cooling to room temperature, excess iron powder was removed by filtration. The filtrate was concentrated under vacuum and the residue was purified by silica gel column chromatography to give 2.50 g (91 %) of the product as a light yellow solid. MS (ESIpos): m/z = 287 [M+H] ⁺ . LC-MS [method4, Water (0.05%TFA)- Acetonitrile, 5%B]: Rt = 1 .01 min.

Step b: 6-(benzyloxy)-7-methoxy-2-methylquinazolin-4(3H)-one

Dry hydrochloric acid gas was passed (until the clear solution observed) to a solution of 5- bromo-2,4-dichloro-7-(phenylsulfonyl)-7H-pyrrolo[2,3-d]pyrim idine, 2.00 g (6.9 mmol) in 50 mL of acetonitrile for 2 hours at room temperature. The precipitated solid was collected by filtration and the filter cake was dissolved in water. The solution was neutralized with 10% aqueous sodium bicarbonate and the precipitated solid was collected by filtration, washed with ice cold water and dried in oven to give 1 .0 g (71 %) of the product as an off-white solid. MS (ESIpos): m/z = 297 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)- Acetonitrile, 5%B]: Rt = 1.06 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 2.31 (s, 3H), 3.89 (s, 3H), 5.19 (s, 2H), 7.08 (s, 1 H), 7.33-7.50 (m, 6H), 12.02 (s, 1 H).

Step c:

6-(benzyloxy)-4-chloro-7-methoxy-2-methylquinazoline

6-(Benzyloxy)-7-methoxy-2-methylquinazolin-4(3H)-one, 1.45 g (4.9 mmol), was added to 13 mL of thionyl chloride at 0°C. Then 1 .0 mL of Ν,Ν-dimethylformamide was added at room temperature. The resulting mixture was stirred at reflux for 10 hours. After cooling to room temperature, the mixture was poured into ice water. Aqueous sodium bicarbonate was added to pH = 7 and the resulting solution was extracted with dichloromethane. The combined organic phase was dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give 900 mg (54%) of the product as a light brown solid. MS (ESIpos): m/z = 315 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .05 min.

Step d:

6-(benzyloxy)-N-[(1 R)-1 -(3-bromophenyl)ethyl]-7-methoxy-2-methylquinazolin-4-amine

Br 6-(Benzyloxy)-4-chloro-7-methoxy-2-methylquinazoline, 350 mg (1 .0 mmol), and (R)-1 -(3- bromophenyl)ethanamine, 271 mg (1 .4 mmol), were dissolved in 5 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for 6 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 490 mg (98%) of the product as a light brown solid. MS (ESIpos): m/z = 478 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .51 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .56 (s, 3H), 2.34 (s, 3H), 3.85 (s, 3H), 5.16-5.20 (m, 2H), 5.60-5.62 (m, 1 H), 7.04 (s, 1 H), 7.26-7.28 (m, 1 H), 7.30-7.42 (m, 5H), 7.44-7.45 (m, 2H), 7.55 (s, 1 H), 7.99 (s, 1 H), 8.01 (m, 1 H).

Example 344

6-(benzyloxy)-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}- quinazolin-4-amine

6-(Benzyloxy)-N-[(1 R)-1 -(3-bromophenyl)ethyl]-7-methoxy-2-methylquinazolin-4-amine (described in example 343), 300 mg (0.6 mmol), tert-butyl 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)-1 H-pyrazole- 1 -carboxylate, 518 mg (1 .8 mmol), tetrakis(triphenylphosphine)palladium(0), 68 mg (0.1 mmol) and cesium carbonate, 574 mg (1 .8 mmol), were added into 10 mL of Ν,Ν-dimethylformamide and 4 mL of water. The resulting mixture was stirred at 80°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the resulting solution was extracted with ethyl acetate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 240 mg (87%) of the product as a yellow solid. MS (ESIpos): m/z = 466 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.29 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .60-1 .62 (d, 3H), 2.35 (s, 3H), 3.85 (s, 3H), 5.16-5.17 (s, 2H), 5.66-5.69 (m, 1 H), 7.03 (s, 1 H), 7.24-7.29 (m, 2H), 7.30-7.45 (m, 4H), 7.52-7.54 (m, 2H), 7.68 (s, 1 H), 7.89 (s, 2H), 7.96-7.98 (m, 1 H), 8.14 (s, 1 H), 12.92 (s, 1 H).

Example 345

7-methoxy-2-methyl-4-({(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}amino)quinazolin-6-ol

6-(Benzyloxy)-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}quinazolin-4- amine (described in example 344), 800 mg (1 .6 mmol), 10% palladium carbon, 80 mg, and 0.5 mL of hydrochloric acid (2.0 M), were added into 20 mL of methanol. The resulting mixture was stirred at room temperature for 13 hours under hydrogen (2 atm) atmosphere. Then palladium carbon was filtered out and washed with methanol. The filtrate was concentrated in vacuo to give 580 mg (89%) of the product as a light brown solid. MS (ESIpos): m/z = 376 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)- Acetonitrile, 5%B]: Rt = 2.41 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .56-1 .58 (d, 3H), 2.34 (s, 3H), 3.90 (s, 3H), 5.57-5.64 (m, 1 H), 7.01 (s, 1 H), 7.26-7.29 (s, 2H), 7.42-7.43 (s, 1 H), 7.66-7.69 (m, 2H), 7.82-7.84 (m, 1 H), 8.00 (s, 2H), 8.18 (s, 1 H).

Example 346

6-(cyclopropylmethoxy)-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

This compound was synthesized by the same method as described in example 355 to give 13.3 mg of the product as an off-white solid. MS (ESIpos): m/z = 430 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.21 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 0.32-0.35 (m, 2H), 0.62-0.64 (m, 2H), 1 .29-1 .34 (m, 1 H), 1 .60- 1 .62 (d, 3H), 2.35 (s, 3H), 3.87 (s, 3H), 3.93-3.95 (m, 2H), 5.66-5.71 (m, 1 H), 7.01 (s, 1 H), 7.24-7.31 (m, 2H), 7.43-7.45 (d, 1 H), 7.66-7.67 (d, 2H), 7.87-7.93 (m, 2H), 8.13 (br, 1 H), 12.92 (br, 1 H).

Example 347

6,7-dimethoxy-2-methyl-N-[1 -(thiophen-2-yl)ethyl]quinazolin-4-amine

N-[1 -(5-bromo-2-thienyl)ethyl]-6 ,7-dimethoxy-2-methylquinazolin-4-amine (described in example 209, 200 mg, 0.5 mmol), was dissolved in 10 mL of tetrahydrofuran, n-butyllithium, 0.43 mL (1.1 mmol), was added to the above solution at -78°C and the resulting mixture was stirred at this temperature for 30 min under nitrogen atmosphere. Then tri-isopropoxyborane, 181 mg (1 .0 mmol), was added at at -78°C the resulting mixture was stirred at this temperature for 1 hour under nitrogen atmosphere. Aq. ammonium chloride was added and the organic solvent was removed in vacuo. 3.0 M hydrogen chloride was added to adjust the pH value to 3 and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 39 mg of a product B as an off- white solid. For B: MS (ESIpos): m/z = 330 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .13 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .67-1 .69 (d, 3H), 2.33 (s, 3H), 3.87 (s, 6H), 5.90-5.97 (m, 1 H), 6.96-6.97 (m, 1 H), 6.98 (s, 1 H), 7.04-7.08 (m, 1 H), 7.35-7.36 (d, 1 H), 7.63 (s, 1 H), 8.06-8.08 (d, 1 H).

Example 348

7-methoxy-6-(2-methoxyethoxy)-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]- ethyl}quinazolin-4-amine

This compound was synthesized by the same method as described in example 355 to give 5.4 mg of the product as a brown solid. MS (ESIpos): m/z = 434 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.10 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 3.75 (s, 3H), 3.74-3.76 (m, 2H), 3.87-3.97 (s, 3H), 4.21 -4.22 (m, 2H), 5.66-5.69 (m, 1 H), 7.01 -7.03 (s, 1 H), 7.25-7.31 (m, 3H), 7.44-7.46 (m, 1 H), 7.55-7.68 (m, 1 H), 7.73-7.89 (s, 1 H), 8.09-8.1 1 (d, 1 H), 8.12-8.13 (m, 1 H), 12.93 (br, 1 H).

Example 349 (1 R)-1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]propan-1 -ol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a) 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1.0 mL) was added chloro(ethyl)magnesium (130 μΙ_, 2.0 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (27.6 mg, 52%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (dd, 1 H), 7.65 (s, 1 H), 7.56 (d, 1 H), 7.38-7.33 (m, 1 H), 7.26-7.22 (m, 2H), 7.08 (dd, 1 H), 7.05 (d, 1 H), 6.92 (dd, 1 H), 5.95 (quin, 1 H), 5.05 (d, 1 H), 4.76-4.66 (m, 1 H), 3.87 (s, 6H), 2.43 (s, 3H), 1 .72 (d, 3H), 1.61 -1 .47 (m, 2H), 0.82-0.73 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 464, Rt = 0.93 min.

Example 350

6-butoxy-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}quinazolin-4- amine

This compound was synthesized by the same method as described in example 355 to give 3.3 mg of the product as an off-white solid. MS (ESIpos): m/z = 432 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.27 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 0.94-0.97 (m, 3H), 1 .43-1 .46 (m, 2H), 1.51 -1 .55 (d, 3H), 1.71 - 1 .80 (m, 2H), 2.31 -2.35 (s, 3H), 3.81 -3.83 (s, 3H), 4.06-4.10 (m, 2H), 5.65-5.68 (m, 1 H), 7.02 (s, 1 H), 7.23-7.26 (m, 2H), 7.43-7.46 (m, 1 H), 7.65-7.69 (m, 2H), 7.83-7.86 (s, 1 H), 7.92-7.95 (d, 1 H), 8.1 1 -8.15 (s, 1 H), 12.89-12.93 (br, 1 H).

Example 351

This compound was synthesized by the same method as described in example 355 to give 4.3 mg of the product as a light yellow solid. MS (ESIpos): m/z = 446 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.35 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 0.96-0.98 (d, 6H), 1.66-1 .69 (m, 5H), 1.71 -1 .73 (m, 1 H), 2.33 (s, 3H), 3.90 (s, 3H), 4.12-4.13 (m, 2H), 5.72-5.76 (m, 1 H), 7.04 (s, 1 H), 7.26-7.33 (m, 2H), 7.46- 7.48 (d, 1 H), 7.69 (s, 1 H), 7.77-7.79 (s, 1 H), 7.81 -7.90 (s, 1 H), 8.15 (s, 1 H), 12.94 (br, 1 H).

Example 352

tert-butyl {2-[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)phenyl]ethyl}carbamate

N-[1 -(5-bromo-2-thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin- 4-amine

4-Chloro-6,7-dimethoxy-2-methylquinazoline, 1.50 g (6.3 mmol), and 1 -(5-bromothiophen-2- yl) ethanamine, 1 .68 g (8.2 mmol), were added into 15 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for overnight. After cooled to room temperature, the solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 1 .80 g (70%) of the product as a brown solid. MS (ESIpos): m/z = 408 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1 .12 min. Step b:

tert-butyl [2-(2-bromophenyl)ethyl]carbamate

2-(2-Bromophenyl)ethanamine, 1 .00 g (5.0 mmol), di-tert-butyl dicarbonate, 2.18 g (10.0 mmol), and triethylamine, 1 .52 g (15.0 mmol), were added into 15 mL of dichloromethane. The resulting mixture was stirred at room temperature for 13 hours. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 1 .10 g (73%) of the product as a light yellow solid. MS (ESIpos): m/z = 300 [M+H] ⁺ , LC-MS [method 4, gradient starting with Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .83 min. Step c:

tert-butyl {2-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]ethyl}carbamate

Tert-butyl [2-(2-bromophenyl)ethyl]carbamate, 500 mg (1.7 mmol), was dissolved in 15 mL of 1 ,4-dioxane, then bis(pinacolato) diboron 1.69 g (6.7 mmol), potassium acetate, 654 mg (6.7 mmol) and 1 ,1 '-bis(diphenylphosphino)ferrocenepalladiumdichloride CH2CI2, 272 mg (0.3 mmol), were added successively to the above solution. The resulting mixture was stirred at 100°C for overnight under nitrogen atmosphere. After cooled to room temperature, the solvent was removed in vacuo and water was added. The resulting mixture was extracted with ethyl acetate, washed with water and the combined organic layers were concentrated under vacuum. The residue was purified by silica gel column chromatography to give 370 mg (58%) of the product as a light yellow solid. MS (ESIpos): m/z = 348 [M+H] ⁺ , LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .30 min.

Step d:

tert-butyl {2-[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)phenyl]ethyl}carbamate

N-[1 -(5-bromo-2-thienyl)ethyl]-6J-dimethoxy-2-methylquinazolin-4 -amin 200 mg (0.5 mmol), tert-butyl {2-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]ethyl}carbamate, 370 mg (1 .0 mmol), potassium carbonate, 135 mg (1 .0 mmol) and tetrakis(triphenylphosphine) palladium(O), 1 13 mg (0.1 mmol), were added into 12 mL of 1 ,4- dioxane/water (5:1 , v:v). The resulting mixture was stirred at 1 10°C for overnight under nitrogen atmosphere. After cooled to room temperature, the solvent was removed in vacuo and water was added. The resulting mixture was extracted with dichloromethane, washed with water and the combine organic layers was concentrated under vacuum. The residue was purified by silica gel column chromatography to give 190 mg (30%) of the product as a light yellow solid. 90 mg of the product was purified by preparative HPLC to give 32.8 mg of the product as an off-white solid. MS (ESIpos): m/z = 549 [M+H] ⁺ , LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .50 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 1 .15-1.34 (s, 9H), 1 .71 -1.73 (d, 3H), 2.44 (s, 3H), 2.79-2.82 (m, 2H), 3.09-3.14 (m, 2H), 3.87 (s, 6H), 5.95-6.00 (m, 1 H), 6.88-6.91 (s, 1 H), 6.99-7.00 (s, 1 H), 7.05- 7.08 (m, 2H), 7.20-7.31 (m, 4H), 7.65 (s, 1 H), 8.14-8.19 (m, 1 H).

Example 353

7-methoxy-2-methyl-6-(propan-2-yloxy)-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

This compound was synthesized by the same method as described in example 355 to give 2.9 mg of the product as an off-white solid. MS (ESIpos): m/z = 418 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.18 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 1 .32-1 .33 (m, 6H), 1 .60-1.62 (d, 3H), 2.35 (s, 3H), 3.85 (s, 3H), 4.78-4.82 (m, 1 H), 5.66-5.70 (s, 1 H), 7.02 (s, 1 H), 7.24-7.31 (m, 2H), 7.44-7.45 (m, 1 H), 7.55-7.60 (m, 2H), 7.68-7.69 (s, 1 H), 7.94 (s, 1 H), 7.96 (m, 1 H), 8.01 (s, 2H), 12.79 (br, 1 H).

Example 354

7-methoxy-2-methyl-6-(oxetan-3-ylmethoxy)-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

This compound was synthesized by the same method as described in example 355 to give 3.2 mg of the product as a light yellow solid. MS (ESIpos): m/z = 446 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.08 min. ¹ H-NMR (400 MHz, DMSO-de) : δ [ppm] = 1 .62-1 .64 (d, 2H), 2.02-2.04 (m, 1 H), 2.33-2.36 (s, 3H), 3.86 (s, 3H), 4.31 -4.38 (m, 2H), 4.41 -4.48 (m, 2H), 4.71 -4.76 (m, 2H), 5.70-5.71 (m, 1 H), 7.03 (s, 1 H), 7.26-7.32 (m, 2H), 7.44-7.46 (m, 1 H), 7.69 (s, 1 H), 7.80 (s, 1 H), 7.99-8.02 (m, 2H), 8.32 (br, 2H).

Example 355

6-Ethoxy-7-methoxy-2-methyl-N-{(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}-quinazolin-4- amine

7-Methoxy-2-methyl-4-({(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}amino)quinazolin-6-ol (described in example 345), 55 mg (0.14 mmol), potassium carbonate, 29 mg (0.21 mmol), bromoethane, 20 mg (0.18 mmol), and potassium iodide, 5 mg (0.03 mmol), were added into 2 mL of Ν,Ν-dimethylformamide. The resulting mixture was stirred at room temperature for 14 hours. The solid was removed by filtration and the filtrate was purified by preparative HPLC to give 1 .4 mg of the product as an off-white solid. MS (ESIpos): m/z = 404 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.15 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ) : δ [ppm] = 1 .39-1 .43 (m, 3H), 1 .60-1.62 (m, 3H), 2.34- 2.35 (s, 3H), 3.89 (s, 3H), 4.14-4.16 (m, 2H), 5.64-5.71 (m, 1 H), 7.01 (s, 1 H), 7.25-7.31 (m, 2H), 7.44-7.46 (m, 1 H), 7.66-7.72 (d, 2H), 7.97-8.02 (m, 2H), 8.37-8.45 (br, 2H).

Example 356

6-ethoxy-N-{(1 R)-1 -[3-(1 -ethyl-1 H-pyrazol-4-yl)phenyl]ethyl}-7-methoxy-2- methylquinazolin-4-amine

H ₃ C

7-Methoxy-2-methyl-4-({(1 R)-1 -[3-(1 H-pyrazol-4-yl)phenyl]ethyl}amino)quinazolin-6-ol (described in example 345), 55 mg (0.14 mmol), potassium carbonate, 29 mg (0.21 mmol), bromoethane, 20 mg (0.18 mmol), and potassium iodide, 5 mg (0.03 mmol), were added into 2 mL of Ν,Ν-dimethylformamide. The resulting mixture was stirred at room temperature for 14 hours. The solid was removed by filtration and the filtrate was purified by preparative HPLC to give 5.0 mg of the product as a light yellow solid. For B: MS (ESIpos): m/z = 432 [M+H] ⁺ . LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .25 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ) : δ [ppm] = 1 .40-1.44 (m, 6H), 1 .66-1 .68 (d, 3H), 2.51 (s, 3H), 3.92-3.96 (s, 3H), 4.14-4.23 (m, 4H), 5.76-5.79 (m, 1 H), 7.08 (s, 1 H), 7.26-7.35 (m, 2H), 7.44-7.46 (s, 1 H), 7.48-7.68 (s, 1 H), 7.70 (s, 1 H), 7.85-7.93 (s, 1 H), 8.18 (s, 1 H), 14.13 (br, 1 H).

Example 357

N-[1 -{5-[2-(2-aminoethyl)phenyl]thiophen-2-yl}ethyl]-6,7-dimetho xy-2-methyl- quinazolin-4-amine

Tert-butyl{2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)phenyl]ethyl}carbamate (described in example 352), 50 mg (0.1 mmol), was dissolved in 1 .5 mL of 1 ,4-dioxane, then 1 .5 mL of 3.0 M hydrochloric acid/dioxane solution was added into the above solution at 0°C. The resulting mixture was stirred at room temperature for 3 hours. Saturated sodium bicarbonate solution was added to adjust the pH value to 7. The resulting mixture was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent removed in vacuo and the residue was purified by preparative HPLC to give 30.1 mg (73%) of the product as an off-white solid. MS (ESIpos): m/z = 449 [M+H] ⁺ , LC-MS [method 4, gradient starting with Water (0.1 %HCOOH)- Acetonitrile, 10%B]: R _t = 0.75 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 -1 .73 (d, 3H), 2.44 (s, 3H), 2.67-2.84 (m, 4H), 3.12 (br, 2H), 3.87 (s, 6H), 5.93-6.00 (m ,1 H), 6.97-7.08 (m, 3H), 7.18-7.31 (m, 4H), 7.65 (s, 1 H), 8.16-8.18 (d, 1 H).

Example 358

tert-butyl {1 -[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)phenyl]ethyl}carbamate

Step a:

tert-butyl {(1 R)-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl]ethyl}carbamate

This compound was synthesized by the same method as described in example 352 (step c) to give 800 mg (41 %) of the product as a light brown solid. MS (ESIpos): m/z = 348 [M+H] ⁺ , LC-MS [method 4, gradient starting with Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .56 min. Step b: tert-butyl {1 -[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2- yl)phenyl]ethyl}carbamate

This compound was synthesized by the same method as described in example 352 (step d) to give 7.1 mg of the product as an off-white solid. MS (ESIpos): m/z = 549 [M+H] ⁺ . LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.48 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.17-1.23 (d, 3H), 1.32 (s, 9H), 1.72-1.73 (d, 3H), 2.44 (s, 3H), 3.87 (s, 6H), 5.01 (m, 1H), 5.95-5.99 (m, 1H), 7.05-7.10 (m, 3H), 7.21-7.22 (m, 2H), 7.35-7.36 (m, 1H), 7.51-7.53 (d, 2H), 7.65 (s, 1H), 8.21 (d, 1H).

Example 359

N-[1-(5-{2-[1-aminoethyl]phenyl}thiophen-2-yl)ethyl]-6,7-dim ethoxy-2- methylquinazolin-4-amine

This compound was synthesized by the same method as described in example 357 to give 6.0 mg (36%) of the product as an off-white solid. MS (ESIpos): m/z = 449 [M+H] ⁺ , LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.30 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.32-1.35 (m, 3H), 1.72-1.74 (d, 3H), 2.44 (s, 3H), 3.87 (s, 6H), 4.40-4.41 (s, 1H), 5.93-6.00 (m, 1H), 6.97-6.98 (s, 1H), 7.05 (s, 1H), 7.11 (s, 1H), 7.28-7.32 (m, 2H), 7.41-7.45 (m, 1H), 7.65 (s, 1H), 7.72-7.74 (d, 1H), 8.18-8.20 (d, 1H), 8.32 (br, 2H).

Example 360

N-[1-(5-{2-[1-aminoethyl]phenyl}thiophen-2-yl)ethyl]-6,7-dim ethoxy-2- methylquinazolin-4-amine

Step a:

tert-butyl {(1 S)-1 -[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)phenyl]ethyl}carbamate

This compound was synthesized by the same method as described in example 352 (step c) to give 400 mg (38%) of the product as a light brown solid. MS (ESIpos): m/z = 348 [M+H] ⁺ , LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .53 min. Step b:

tert-butyl rel-{(1 R)-1 -[2-(5-{(1 R)-1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- 2-thienyl)phenyl]ethyl}carbamate

This compound was synthesized by the same method as described in example 352 (step d) to give 50 mg (7%) of the product as a light yellow solid. MS (ESIpos): m/z = 549 [M+H] ⁺ . LC- MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .44 min. Step c:

N-[1 -(5-{2-[1 -aminoethyl]phenyl}thiophen-2-yl)ethyl]-6 -dimethoxy-2- methylquinazolin-4-amine

This compound was synthesized by the same method as described in example 357 to give 6.6 mg (60%) of the product as an off-white solid. MS (ESIpos): m/z = 449 [M+H] ⁺ , LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .30 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .28-1 .39 (d, 3H), 1 .72-1 .74 (d, 3H), 2.33 (s, 3H), 3.87 (s, 6H), 4.42 (m, 1 H), 5.94-5.98 (m, 1 H), 6.98 (s, 1 H), 7.05 (s, 1 H), 7.1 1 (s, 1 H), 7.28-7.33 (m, 2H), 7.42-7.46 (m, 1 H), 7.66 (s, 1 H), 7.74-7.75 (d, 1 H), 8.20-8.23 (d, 1 H), 8.25-8.35 (br, 2H).

Example 361

6 -dimethoxy-2-methyl-N-[1 -{5-[2-(1 H-pyrazol-4-yl)phenyl]thiophen-2-yl}ethyl]- quinazolin-4-amine

Step a:

tert-butyl 4-bromo-1 H-pyrazole-1 -carboxylate

4-Bromo-1 H-pyrazole, 5.00 g (34.0 mmol), di-tert-butyl dicarbonate, 8.17 g (37.4 mmol), and triethylamine, 7.57 g (74.8 mmol), were added into 50 mL of dichloromethane. The resulting mixture was stirred at room temperature for overnight. The resulting mixture was purified by silica gel column chromatography to give 8.00 g (93%) of the product as an off-white solid. MS (ESIpos): m/z = 247 [M+H] ⁺ . LC-MS [method 4, gradient starting with water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 1 .75 min.

Step b:

4-(2-bromophenyl)-1 H-pyrazole

2-Bromophenylboronic acid, 6.00 g (29.9 mmol), tert-butyl 4-bromo-1 H-pyrazole-1 - carboxylate, 3.69 g (14.9 mmol), potassium carbonate, 8.26 g (59.8 mmol), and tetrakis(triphenylphosphine) palladium(O), 1 .22 g (1 .5 mmol), were added into 60 ml. of 1 ,4- dioxane/water (5:1 , v:v). The resulting mixture was stirred at 1 10°C for overnight under nitrogen atmosphere. After cooled to room temperature, water was added and the resulting mixture was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 2.00 g (26%) of the product as a light yellow solid. MS (ESIpos): m/z = 223 [M+H] ⁺ . LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.96 min.

Step c:

tert-butyl 4-(2-bromophenyl)-1 -pyrazole-1 -carboxylate

4-(2-Bromophenyl)-1 H-pyrazole, 2.00 g (7.8 mmol), di-tert-butyl dicarbonate, 1 .87 g (8.6 mmol), and triethylamine, 1 .74 g (17.2 mmol), were added into 30 ml. of dichloromethane. The resulting mixture was stirred at room temperature for overnight. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 1 .10 g (54%) of the product as a light yellow oil. MS (ESIpos): m/z = 323 [M+H] ⁺ , LC-MS [method 4, gradient starting with water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 1 .27 min. Step d:

tert-butyl 4-[2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]-1 H-pyrazole- 1 -carboxylate

This compound was synthesized by the same method as described in example 352 (step c) to give 550 mg (52%) of the product as a light yellow oil. MS (ESIpos): m/z = 371 [M+H] ⁺ , LC- MS [method 4, gradient starting with water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .30 min.

Step e:

6 -dimethoxy-2-methyl-N-[1 -{5-[2-(1 H-pyrazol-4-yl)phenyl]thiophen-2-yl}ethyl]- quinazolin-4-amine

This compound was synthesized by the same method as described in example 352 (step d) to give 73.5 mg (45%) of the product as an off-white solid. MS (ESIpos): m/z = 472 [M+H] ⁺ , LC-MS [method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .28 min. ¹ H-N MR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .66-1 .68 (d, 3H), 2.41 (s, 3H), 3.87 (s, 6H), 5.89- 5.92 (m, 1 H), 6.77-6.78 (s, 1 H), 6.97-6.98 (s, 1 H), 7.04 (s, 1 H), 7.24-7.28 (m, 2H), 7.33-7.36 (m, 2H), 7.44-7.46 (s, 1 H), 7.57 (s, 1 H), 7.63 (s, 1 H), 8.09-8.1 1 (d, 1 H), 12.80 (br, 1 H).

Example 362

6,7-dimethoxy-2-methyl-N-[1 -(5-{2-[(phenylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

C H A mixture of N-[1 -(5-Bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(N- Phenylaminomethyl)phenylboronic acid (commercially available; 58.5 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and Tetrakis(triphenylphosphin)palladium(0) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 48% of the title compound (64 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.64 (s, 1 H), 7.48-7.45 (m, 1 H), 7.38-7.26 (m, 3H), 7.12-7.08 (m, 2H), 7.05 (s, 1 H), 6.99 (t, 2H), 6.51 -6.44 (m, 3H), 6.13 (t, 1 H), 5.96 (t, 1 H), 4.26 (d, 2H), 3.87 (s, 3H), 3.86 (s, 3H), 2.43 (s, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 51 1.2, R _t = 1 .07 min.

Example 363

6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine

A solution of 6-bromo-4-chloro-2-methylquinazoline (commercially available; 5g, 19.4 mmol), (R)-1 -(3-chlorophenyl)ethylamine (3.66 g, 23.3 mmol, commercially available) and N,N- diisopropylethylamine (6.76 mL) in dioxane (75 mL) was stirred overnight at 100°C. After cooling to ambient temperature the reaction mixture was evaporated and the crude material was purified via Isolera flash chromatography (silica gel, gradient hexanes 100% -> ethylacetate 100%) to obtain the title compound in quantitative yield (7.35 g). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.67 (d, 1 H), 8.47 (d, 1 H), 7.84 (dd, 1 H), 7.55-7.48 (m, 2H), 7.42- 7.38 (m, 1 H), 7.35 (t, 1 H), 7.30-7.27 (m, 1 H), 5.57 (t, 1 H), 2.54-2.52 (m, 1 H), 2.38 (s, 3H), 1 .57 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 378.0, R _t = 0.87 min.

Example 364

N-[1 -(5-{2-[(cyclopentylamino)methyl]phenyl}thiophen-2-yl)ethyl] -6,7-dimethoxy-2- methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2- (cyclopentylaminomethyl)phenylboronoc acid, pinacol ester (commercially available; 76.8 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis- (triphenylphosphin)palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 49% of the title compound (62 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.93 (d, 1 H), 8.44 (s, 1 H), 8.27 (d, 1 H), 8.1 1 -8.01 (m, 3H), 7.97 (d, 1 H), 7.87 (d, 1 H), 7.84 (s, 1 H), 6.75 (t, 1 H), 4.46 (s, 2H), 4.12 (s, 6H), 3.76-3.69 (m, 1 H), 3.22 (s, 3H), 2.52 (s, 2H), 2.51 -2.49 (m, 1 H), 2.44-2.28 (m, 4H), 2.22-2.10 (m, 2H), 2.09-1.99 (m, 2H). LC-MS (method 7): m/z: [M+H] ⁺ = 503.3, R _t = 0.64 min.

Example 365

N-[1 -(5-{2-[(benzylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7- dimethoxy-2- methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(N- benzylaminomethyl)phenylboronic acid, pinacol ester (commercially available; 80.8 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 48% of the title compound (63 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.54 (d, 1 H), 7.34-7.22 (m, 7H), 7.22-7.14 (m, 1 H), 7.1 1 (d, 1 H), 7.06-7.03 (m, 2H), 5.96 (t, 1 H), 3.86 (d, 6H), 3.73-3.61 (m, 4H), 2.54-2.52 (m, 1 H), 2.44-2.40 (m, 3H), 1.71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 525.2, R _t = 0.66 min.

Example 366

N-[1 -(5-{2-[(butylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6 -dimethoxy-2- methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(N- butylaminomethyl)phenylboronic acid, pinacol ester (commercially available; 73.8 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 46% of the title compound (56 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.49 (d, 1 H), 7.33-7.22 (m, 3H), 7.16 (d, 1 H), 7.07 (d, 1 H), 7.05 (s, 1 H), 5.96 (t, 1 H), 3.68 (s, 2H), 3.33 (s, 3H), 2.43 (s, 5H), 1.71 (d, 3H), 1.36-1 .19 (m, 4H), 0.82-0.77 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 491.3, R _t = 0.63 min.

Example 367

N-[1 -(5-{2-[(ethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6,7-d imethoxy-2- methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2- (ethylaminomethyl)phenylboronic acid, pinacol ester (commercially available; 66.6 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 ml.) and water (0.5 ml.) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 31 % of the title compound (36 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (d, 1 H), 7.65 (s, 1 H), 7.49 (d, 1 H), 7.33-7.22 (m, 3H), 7.16 (d, 1 H), 7.05 (s, 1 H), 5.96 (t, 1 H), 3.68 (s, 2H), 3.33 (s, 3H), 2.43 (s, 3H), 1 .71 (d, 3H), 0.95 (t, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 463.2, R _t = 0.59 min.

Example 368

6,7-dimethoxy-2-methyl-N-[1 -{5-[2-(1 H-tetrazol-5-yl)phenyl]thiophen-2-yl}ethyl]- quinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(tetrazole-5-yl)- phenylboronic acid (commercially available; 49 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 ml.) and water (0.5 ml.) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 28% of the title compound (33 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.45 (br d, 1 H), 7.66 (s, 1 H), 7.61 -7.53 (m, 2H), 7.51 -7.43 (m, 2H), 7.04 (s, 1 H), 6.94 (dd, 1 H), 6.62 (d, 1 H), 5.86 (t, 1 H), 3.88 (d, 6H), 2.48-2.45 (m, 3H), 1 .64 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 474.2, R _t = 0.76 min.

Example 369

6,7-dimethoxy-N-{1 -[5-(2-{[(2-methoxyethyl)amino]methyl}phenyl)thiophen-2-yl]e thyl}- 2-methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(2- methoxyethyl)aminomethylpphenylboronic acid, pinacol ester (commercially available; 74.3 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin)palladium(0) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 50% of the title compound (61 mg). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.48 (d, 1 H), 7.33-7.23 (m, 3H), 7.15 (d, 1 H), 7.08 (d, 1 H), 7.06-7.06 (m, 1 H), 7.05 (s, 1 H), 5.96 (t, 1 H), 3.71 (s, 2H), 3.33 (s, 3H), 3.33-3.29 (m, 2H), 3.16 (s, 3H), 2.60 (t, 2H), 2.43 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 493.2, R _t = 0.58 min.

Example 370

N-[1 -(5-{2-[(cyclopropylamino)methyl]phenyl}thiophen-2-yl)ethyl] -6,7-dimethoxy-2- methylquinazolin-4-amine

A mixture of N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (prepared as described in example 209; 100 mg, 0.24 mmol), 2-(N- cyclopropylaminoethyl)penylboronic acid, pinacol ester (commercially available; 47.7 mg, 0.24 mmol), potassium carbonate (135.4 mg, 0.98 mmol) and tetrakis(triphenylphosphin) palladium(O) (28.3 mg, 0.025 mmol) in dioxane (2.5 mL) and water (0.5 mL) was stirred at 1 10°C overnight. The reaction mixture was evaporated and the crude product was purified via HPLC to yield 3 % of the title compound (3.6 mg). LC-MS (method 7): m/z: [M+H] ⁺ = 475.2, R _t = 0.58 min.

Example 371

methyl 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6-carboxyl ate

In an autoclave a solution of 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4- amine (prepared as described in example 363; 9.5g, 25.22 mmol) was dissolved in a 10:1 methanokTHF mixture (440 mL) and 1 , 1 -Bis- (diphenylphosphino)-ferrocen- palladium(ll)dichloride (1 g, 1 .26 mmol), triethylamine (7 mL, 50.44 mmol) were added. At ambient temperature the reaction mixture was flushed with CO gas (3x) and then carbonylated at 14.77 bar CO at 80°C overnight. The reaction mixture was evaporated and the crude product was purified via Isolera flash chromatography (Silica column; eluent: gradient hexanes 100% -» ethylacetate 100%) to yield the title compound (8.9 g, 95%). ¹ H- NMR (400 MHz, DMSO-de): δ [ppm] = 9.10 (d, 1 H), 8.90 (d, 1 H), 8.18 (dd, 1 H), 7.64 (d, 1 H), 7.53 (t, 1 H), 7.44-7.40 (m, 1 H), 7.36 (t, 1 H), 7.31 -7.26 (m, 1 H), 5.63 (t, 1 H), 3.93 (s, 3H), 2.42 (s, 3H), 1 .60 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 356.1 , R _t = 0.82 min.

Example 372

4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6-carboxyl ic acid

To a solution of methyl 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6- carboxylate (prepared as described in example 371 ; 1 .5g, 4.22 mmol) in ethanol (40 mL) was added NaOH beads (674 mg, 16.9 mmol) and the reaction was stirred at ambient temperature for two hours. Water was added (100 mL) and the pH value was adjusted to pH3 by the addition of 1 .0 N aqueous HCI. The precipitate was collected by filtration and the product was dried under reduced pressure to yield the title compound in 95% yield (1 .38g). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 13.33-13.06 (m, 1 H), 9.09 (d, 1 H), 8.87 (d, 1 H), 8.17 (dd, 1 H), 7.62 (d, 1 H), 7.53 (t, 1 H), 7.44-7.41 (m, 1 H), 7.35 (t, 1 H), 7.30-7.26 (m, 1 H), 5.62 (quin, 1 H), 2.45-2.40 (m, 3H), 1.59 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 342.1 , R _t = 0.75 min.

Example 373

(4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazolin-6-yl)methan ol

To a solution of 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6-carboxyl ic acid (prepared as described in example 372; 600 mg, 1 .75 mmol) in THF (30 mL) was added UAIH4 solution (2.0 M in THF, 3.5 mL) at ambient temperature. The reaction was allowed to stir at ambient temperature for 30 minutes, then methanol (5 mL) was added and the reaction mixture was poured carefully into saturated aqueous ammoniumchloride solution. The reaction mixture was extracted with butanol (3x 10 mL), the combined organic layers were evaporated and the crude product was purified via HPLC chromatography to yield the title compound (74 mg, 13 % yield). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 9.35-8.77 (m, 1 H), 8.41 (s, 1 H), 8.13 (s, 1 H), 7.82-7.71 (m, 1 H), 7.61 (d, 1 H), 7.53 (s, 1 H), 7.42 (s, 1 H), 7.36 (s, 1 H), 7.31 (s, 1 H), 5.82-5.55 (m, 1 H), 5.55-5.29 (m, 1 H), 4.66 (br d, 2H), 1 .60 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 328.1 , R _t = 0.72 min.

Example 374

[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)- phenyl](phenyl)methanol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1 .0 mL) was added bromo(phenyl)magnesium (250 μί, 1 .0 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (16.5 mg, 27%). ¹ H-NMR (500 MHz, DMSO-de): δ [ppm] = 8.14 (dd, 1 H), 7.65 (d, 1 H), 7.44 (d, 1 H), 7.36-7.32 (m, 1 H), 7.30-7.24 (m, 2H), 7.22-7.17 (m, 2H), 7.16-7.12 (m, 1 H), 7.12-7.09 (m, 2H), 7.07 (d, 1 H), 7.05 (s, 1 H), 6.91 (d, 1 H), 5.97 (t, 1 H), 5.95-5.90 (m, 1 H), 5.86 (dd, 1 H), 3.87 (s, 6H), 2.42 (d, 3H), 1 .71 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 512, Rt = 0.98 min.

Example 375

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)phenyl]-3 phenylpropan-1 -ol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηιοΙ) in anhydrous THF (1 .0 ml.) was added chloro(2-phenylethyl)magnesium (250 μΙ_, 1 .0 M, 250 μηιοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (32.7 mg, 51 %). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.14 (dd, 1 H), 7.65 (s, 1 H), 7.62 (d, 1 H), 7.36 (dt, 1 H), 7.24 (d, 2H), 7.20-7.07 (m, 3H), 7.06-7.00 (m, 3H), 6.99-6.94 (m, 1 H), 6.76 (t, 1 H), 5.95 (br t, 1 H), 5.20 (t, 1 H), 4.88-4.76 (m, 1 H), 3.88-3.83 (m, 6H), 2.70-2.61 (m, 1 H), 2.43 (s, 3H), 1 .80 (br d, 2H), 1 .71 (dd, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 540, Rt = 1 .06 min.

Example 376

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)phenyl]-2- phenylethanol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1 .0 mL) was added benzyl(chloro)magnesium (130 μΙ_, 2.0 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (19.5 mg, 32%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.70-7.64 (m, 2H), 7.43-7.37 (m, 1 H), 7.29-7.20 (m, 2H), 7.10-7.04 (m, 5H), 7.00-6.93 (m, 2H), 6.82 (dd, 1 H), 6.02-5.91 (m, 1 H), 5.17 (dd, 1 H), 5.00 (dt, 1 H), 3.89-3.85 (m, 6H), 2.84 (dt, 1 H), 2.73 (dd, 1 H), 2.42 (d, 3H), 1.73 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 526, Rt = 1.02 min.

Example 377

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]pentan-1 -ol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1 .0 mL) was added butyl(chloro)magnesium (130 μΙ_, 2.0 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (22.0 mg, 39%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.13 (br d, 1 H), 7.65 (s, 1 H), 7.57 (d, 1 H), 7.35 (dt, 1 H), 7.24-7.21 (m, 2H), 7.07 (dd, 1 H), 7.04 (s, 1 H), 6.90 (d, 1 H), 5.99-5.90 (m, 1 H), 5.03 (d, 1 H), 4.83-4.75 (m, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 2.42 (s, 3H), 1 .72 (d, 3H), 1.54- 1 .45 (m, 2H), 1 .33-1 .21 (m, 1 H), 1 .18-1 .05 (m, 3H), 0.76-0.65 (m, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 492, Rt = 1.03 min. Example 378

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]prop-2-yn-1 -ol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1 .0 mL) was added bromo(ethynyl)magnesium (510 μΙ_, 0.50 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (23.6 mg, 45%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.76 (d, 1 H), 7.65 (s, 1 H), 7.44- 7.38 (m, 1 H), 7.36-7.29 (m, 2H), 7.12 (d, 1 H), 7.10 (dd, 1 H), 7.05 (s, 1 H), 6.08 (br s, 1 H), 5.96 (quin, 1 H), 5.41 (br s, 1 H), 3.87 (s, 6H), 3.51 (t, 1 H), 2.44 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 460, Rt = 0.88 min.

Example 379

1 -[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl )phenyl]-2- methylpropan-1 -ol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μηηοΙ) in anhydrous THF (1 .0 mL) was added lithium chloride - chloro(propan-2-yl)magnesium (1 :1 :1 ) (85 μί, 3.0 M, 250 μηηοΙ) dropwise and the reaction mixture stirred during 30 minutes at room temperature. The reaction was quenched with H2O, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (8.10 mg, 14%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (br d, 1 H), 7.65 (s, 1 H), 7.53 (d, 1 H), 7.35 (dt, 1 H), 7.23 (dd, 2H), 7.06 (d, 1 H), 7.05 (s, 1 H), 6.93 (d, 1 H), 5.95 (br quin, 1 H), 5.02 (d, 1 H), 4.58 (dd, 1 H), 3.87 (s, 6H), 2.42 (d, 3H), 1 .79-1 .74 (m, 1 H), 1.72 (d, 3H), 0.82 (dd, 3H), 0.61 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 478, Rt = 0.99 min.

Example 380

1 -[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)phenyl]- 2,2,2-trifluoroethanol

To a solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (described in example 179a; 50.0 mg, 1 15 μιτιοΙ) and trimethyl(trifluoromethyl)silane (82 μΙ_, 575 μηιοΙ) in THF (1 .0 mL) was added TBAF (200 μΙ_, 1 .0 M, 200 μηηοΙ) and the mixture stirred at room temperature during 1 hour. The reaction was quenched with HCI (1 .0 M, 3.0 mL) and stirred at room temperature during 30 minutes, then extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a yellow solid (34.2 mg, 59%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.17 (dd, 1 H), 7.68 (d, 1 H), 7.64 (s, 1 H), 7.47 (td, 1 H), 7.42 (td, 1 H), 7.37-7.33 (m, 1 H), 7.12 (d, 1 H), 7.05 (s, 1 H), 6.91 (dd, 1 H), 5.95 (quin, 1 H), 5.30 (qd, 1 H), 3.87 (s, 6H), 3.20-3.1 1 (m, 1 H), 2.43 (d, 3H), 1 .73 (dd, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 504, Rt = 0.97 min.

Example 381

N-{1 -[5-(6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3-yl)-4-methylthiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

Step a:

N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin-4-amine hydrochloride (1 :1)

A solution of 4-chloro-6,7-dimethoxy-2-methylquinazoline (commercially available; 789 mg, 3.30 mmol) and 1 -(5-bromo-4-methyl-2-thienyl)ethanamine (described in procedure INT-31 ; 800 mg, 3.63 mmol) in dioxane (15 mL) was heated to 1 10°C during 18 hours. MTBE (20 mL) was added at room temperature, the mixture stirred during 3 hours and the precipitate then filtered to give the title compound as an off-white solid (1 .56 g, 93%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.04 (d, 1 H), 7.60 (s, 1 H), 7.05 (s, 1 H), 6.88 (s, 1 H), 5.76 (quin, 1 H), 3.87 (s, 6H), 2.42 (s, 3H), 2.09 (s, 3H), 1.64 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 422, R _t = 0.97 min.

Step b:

N-{1 -[5-(6 -dihydro-5H^yrrolo[1 ,2-a]imidazol-3-yl)-4-methylthiophen-2-yl]ethyl}-6,7- dimethoxy-2-methylquinazolin-4-amine

Under argon, N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin- 4-amine hydrochloride (1 :1 ) (100 mg, 218 μηιοΙ), 6,7-dihydro-5H-pyrrolo[1 ,2-a]imidazol-3- ylboronic acid (33.1 mg, 218 mol), K ₂ C0 ₃ (120 mg, 872 mol) and Pd(PPh ₃ ) ₄ (25.2 mg, 21 .8 mol) in dioxane (2.0 mL) and H2O (400 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (23.8 mg, 24%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.08 (d, 1 H), 7.63 (s, 1 H), 7.04 (s, 1 H), 6.95 (s, 2H), 5.87 (quin, 1 H), 3.93 (t, 2H), 3.86 (s, 6H), 2.75 (t, 2H), 2.43 (s, 3H), 2.18 (s, 3H), 1 .67 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 450, Rt = 0.54 min.

Example 382

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-2-hydroxyacetamide

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 100 mg, 221 μηηοΙ), hydroxyacetic acid (16.8 mg, 221 μηιοΙ), PyBOP (230 mg, 442 μηιοΙ) and N,N-diisopropylethylamine (190 μΙ_, 1 .1 mmol) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (61 .7 mg, 54%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.35 (t, 1 H), 8.16 (d, 1 H), 7.64 (s, 1 H), 7.35 (dd, 1 H), 7.13-7.07 (m, 3H), 7.06-7.03 (m, 2H), 5.96 (quin, 1 H), 5.56 (t, 1 H), 4.38 (d, 2H), 3.90-3.85 (m, 8H), 2.43 (s, 3H), 1 .72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 51 1 , Rt = 0.80 min.

Example 383

N-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-5- fluorobenzyl]-2-methoxyacetamide

C H ₃

A solution of N-[1 -{5-[2-(aminomethyl)-4-fluorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine (described in example 234; 50.0 mg, 1 10 μηηοΙ), methoxyacetic acid (8.5 μΙ_, 1 10 μηιοΙ), PyBOP (1 15 mg, 221 μηιοΙ) and N,N-diisopropylethylamine (95 μΙ_, 550 μηηοΙ) in DMF (1 .0 mL) was stirred at room temperature overnight. Purification by preparative HPLC (basic conditions) gave the title compound as a pale brown solid (30.0 mg, 52%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.38 (t, 1 H), 8.16 (d, 1 H), 7.64 (s, 1 H), 7.35 (dd, 1 H), 7.14-7.06 (m, 3H), 7.06-7.03 (m, 2H), 5.96 (quin, 1 H), 4.37 (d, 2H), 3.87 (s, 8H), 3.31 (s, 3H), 2.43 (s, 3H), 1.72 (d, 3H). LC-MS (method 7): m/z: [M+H] ⁺ = 525, Rt = 0.88 min.

Example 384 N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-6,7-dimeth 2-meth lquinazolin-4-amine

4-Bromo-1 -iodo-2-methylbenzene, 5.00 g (16.8 mmol), and N-bromosuccinimide, 3.06 g (20.2 mmol), were dissolved into 50 mL of 1 ,2-dichloroethane. 2,2'-Azobisisobutyronitrile, 0.28 g (1 .7 mmol), was added to the above solution at 85°C and the resulting mixture was stirred at this temperature for 3 hours under nitrogen atmosphere. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 3.01 g (48%) of the product as a white solid. ¹ H-NMR (400 MHz, CDCI ₃ ): δ [ppm] = 4.54 (s, 2H), 7.13-7.16 (m, 1 H), 7.63 (d, 1 H), 7.73 (d, 1 H).

Step b:

(5-bromo-2-iodophenyl)-N,N-dimethylmethanamine

4-Bromo-2-(bromomethyl)-1 -iodobenzene, 2.00 g (5.3 mmol), was dissolved into 10 mL of tetrahydrofuran and 5.3 mL of dimethylamine/THF solution (2.0 M). The resulting mixture was stirred at room temperature for 3 hours. The solvent was removed in vacuo and water was added. The mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 1 .46 g (80%) of the product as a colourless oil. MS (ESIpos): m/z = 340 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.72 min.

Step c: 1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thanone

(5-Bromo-2-iodophenyl)-N,N-dimethylmethanamine, 1.41 g (4.1 mmol), 5-acetylthiophen-2- ylboronic acid, 1 .06 g (6.2 mmol), sodium carbonate, 1 .76 g (16.6 mmol) and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 0.30 g (0.4 mmol), were added into 12 mL of 1 ,4-dioxane/H20 (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 48 hours under nitrogen atmosphere. After cooled to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by silica gel column chromatography to give 0.67 g (30%) of the product as a yellow oil. MS (ESIpos): m/z = 338 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 5%B]: R _t = 2.17 min.

Step d:

N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thylidene)-2- methylpropane-2-sulfinamide

1 -(5-(4-Bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thanone, 620.0 mg (1 .8 mmol), 2-methylpropane-2-sulfinamide, 444.3 mg (3.7 mmol), and titanium(IV) ethoxide, 836.2 mg (3.7 mmol), were dissolved into 20 mL of tetrahydrofuran and the resulting mixture was stirred at 70°C for 36 hours under nitrogen atmosphere. After cooled to room temperature, 10% sodium chloride solution was added and the precipitated solid was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 0.51 g (51 %) of the product as a yellow oil. MS (ESIpos): m/z = 441 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%TFA)-Acetonitrile, 5%B]: Rt = 0.83 min.

Step e: N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-2- methylpropane-2 -sulfinamide

N-(1 -(5-(4-Bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thylidene)-2- methylpropane-2-sulfinamide, 512.0 mg (1.2 mmol), was dissolved in 10 mL of tetrahydrofuran. Sodium borohydride, 87.8 mg (2.3 mmol), was added to the above solution portionwise. The resulting mixture was stirred at room temperature for 2 hours. Water was added and the resulting solution was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography to give 0.33 g (59%) of the product as a yellow oil. MS (ESIpos): m/z = 443 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.88 min.

Step f:

1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thanamine

N-(1 -(5-(4-Bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-2-methylpropane-2- sulfinamide, 331.0 mg (0.7 mmol), was dissolved into 10 mL of tetrahydrofuran. Then 5 mL of cone, hydrochloric acid was added and the resulting mixture was stirred at room temperature for 24 hours. The solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The resulting mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 98.0 mg (42%) of the product as a brown oil. MS (ESIpos): m/z = 339 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 5%B]: R _t = 1 .96 min.

Step g: N-(1 -(5-(4-bromo-2-((dimethylamino)methyl^

2-methylquinazolin-4-amine

1 -(5-(4-Bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e than 93.0 mg (0.3 mmol), and 4-chloro-6,7-dimethoxy-2-methylquinazoline, 98.1 mg (0.4 mmol), were dissolved into 2 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for 6 hours. After cooled to room temperature, the solvent was removed in vacuo and the residue was purified by preparative HPLC to give 58.4 mg (38%) of the product as a light yellow solid. MS (ESIpos): m/z = 541 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .1 1 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .72 (d, 3H), 2.1 1 (s, 6H), 2.43 (s, 3H), 3.38 (s, 2H), 3.87 (s, 6H), 5.94-5.97 (m, 1 H), 7.05 (s, 1 H), 7.09 (s, 1 H), 7.15 (d, 1 H), 7.30 (d, 1 H), 7.46 (d, 1 H), 7.63-7.64 (m, 2H), 8.16 (d, 1 H).

Example 385

N-(1 -(5-(2-((dimethylamino) methyl)-4-(trifluoromethyl) phenyl) thiophen-2-yl) ethyl)-6, 7-dimethoxy-2-methylquinazolin-4-amine

Step a:

4,4,5,5-tetramethyl-2-(2 -meth -4-(trifluoromethyl)phenyl)-1 , 3, 2-dioxaborolane

1 -Bromo-2-methyl-4-(trifluoromethyl)benzene, 200.0 mg (0.8 mmol), 4,4,4',4',5,5,5',5'- octamethyl-2,2'-bi(1 , 3, 2-dioxaborolane), 424.9 mg (1 .7 mmol), potassium acetate, 328.5 mg (3.3 mmol), and 1 ,1 '-bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 61 .2 mg (0.08 mmol), were added into 6 mL of 1 ,4-dioxane. The resulting mixture was stirred at 100°C for overnight. After cooled to room temperature, water was added and the resulting mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 198.0 mg (83%) of the product as a white solid. ¹ H-NMR (400 MHz, CDCIs): δ [ppm] = 1 .38 (s, 12H), 2.61 (s, 3H), 7.42-7.43 (m, 2H), 7.88 (d, 1 H). Step b:

2-(2-(bromomethyl)-4-(trifluoromethyl) phenyl)-4, 4, 5, 5-tetramethyl-1 , 3, 2- dioxaborolane

4,4,5,5-Tetramethyl-2-(2-methyl-4-(trifluoromethyl)phenyl)-1 ,3,2-dioxaborolane, 198.0 mg (0.7 mmol), and N-bromosuccinimide, 135.5 mg (0.8 mmol), were dissolved into 10 mL of

I , 2-dichloroethane. The resulting mixture was heated to 80°C and 2,2'-azobisisobutyronitrile,

I I .4 mg (0.07 mmol), was added successively. The resulting mixture was stirred at 80°C for 3 hours under nitrogen. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography to give 165.0 mg (65%) of the product as a colorless oil. ¹ H-NMR (400 MHz, CDCIs): δ [ppm] = 1 .39 (s, 12H), 4.92 (s, 2H), 7.52 (d, 1 H), 7.63 (s, 1 H), 7.93 (d, 1 H).

Step c:

2-((dimethylamino)methyl)-4-(trifluoromethyl)phenylboronic acid

2-(2-(Bromomethyl)-4-(trifluoromethyl)phenyl)-4, 4, 5, 5-tetramethyl-1 , 3, 2-dioxaborolane, 165.0 mg (0.5 mmol), was added into 1 .1 mL of dimethylamine/THF (2.0 M). The resulting mixture was stirred at room temperature for 3 hours. The solvent was removed in vacuo to give 121 .0 mg (crude) of the product as a light yellow solid. MS (ESIpos): m/z = 248 [M+H] ⁺ ; LC-MS [Water(0.1 %HCOOH)-Acetonitrile, 5%B)]: R _t = 0.60 min.

Step d:

N-(1 -(5-(2-((dimethylamino)methyl)-4-(trifluoromethyl)phenyl)thi ophen-2-yl)ethyl) dimethoxy-2-methylquinazolin-4-amine

2-((Dimethylamino)methyl)-4-(trifluoromethyl)phenylboronic acid, 100.0 mg (0.4 mmol), N-(1 - (5-bromothiophen-2-yl)ethyl)-6,7-dimethoxy-2-methylquinazoli n-4-amine, 165.3 mg (0.4 mmol), sodium carbonate, 171.6 mg (1 .6 mmol) and tetrakis(triphenylphosphine)palladium(0), 46.8 mg (0.04 mmol), were added into 3 mL of 1 ,4- dioxane/h O (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 6 hours under nitrogen atmosphere. After cooled to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 34.8 mg (16%) of the product as a white solid. MS (ESIpos): m/z = 531 [M+H] ⁺ ; LC-MS [method 4, gradient starting with Water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .10 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 2.14 (s, 6H), 2.45 (s, 3H), 3.51 (s, 2H), 3.88 (s, 6H), 5.96-6.00 (m, 1 H), 7.05 (s, 1 H), 7.14 (d, 1 H), 7.26 (d, 1 H), 7.58-7.67 (m, 3H), 7.80 (s, 1 H), 8.26 (d, 1 H).

Example 386

6 -dimethoxy-2-methyl-N-(1 -{5-[2-methyl-4-(trifluoromethyl)phenyl]-2- thienyl}ethyl)quinazolin-4-amine

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (50.0 mg, 122 μηιοΙ), 4,4,5,5-tetramethyl-2-[2-methyl-4-(trifluoromethyl)phenyl]-1 ,3,2- dioxaborolane (70.1 mg, 245 μηηοΙ), Na ₂ C0 ₃ (51 .9 mg, 490 μηηοΙ) and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride (8.96 mg, 12.2 μηηοΙ) in 1 ,4-dioxane (2.5 mL) and H2O (500 μΙ_) were stirred at 100°C during 6 hours. H2O was added, the mixture extracted with EtOAc, dried over anhydrous sodium sulphate and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an off- white solid (8.40 mg, 14 %). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.17 (br d, 1 H), 7.68 (br s, 1 H), 7.66 (s, 1 H), 7.56 (s, 2H), 7.21 (br d, 1 H), 7.16 (br d, 1 H), 7.06 (s, 1 H), 5.98 (quin, 1 H), 3.88 (s, 6H), 2.48 (s, 3H), 2.44 (s, 3H), 1 .74 (br d, 3H). LC-MS (Method 4): m/z: [M+H] ⁺ = 488, R _t = 1 .63 min.

Example 387

tert-butyl [4-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- thiophen-2-yl)benzyl]carbamate

Step a:

1 -(2-bromo-4-chlorophenyl)methanamine

This compound was synthesized by the same method as described in example 408 (step a) to give 1 .47 g (36%) of the product as an off-white solid. MS (ESIpos): m/z = 220 [M+H] ⁺ . LC- MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 0.62 min.

Step b:

ferf-butyl (2-bromo-4-chlorobenzyl)carbamate

This compound was synthesized by the same method as described in example 428 (step a) to give 1 .71 g (74%) of the product as a light yellow solid. MS (ESIpos): m/z = 320 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .21 min. Step c:

ferf-butyl [4-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

H ₃

This compound was synthesized by the same method as described in example 428 (step b) to give 375 mg (36%) of the product as a light yellow solid. MS (ESIpos): m/z = 368 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .42 min.

Step d:

tert-butyl [4-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- thiophen-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 429 to give 150 mg (63%) of the product as a light yellow solid. MS (ESIpos): m/z = 569 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .56 min. ¹ H-NMR (400 MHz, DMSO- d ₆ ): δ [ppm] = 1 .37 (s, 9H), 1 .72 (d, 3H), 2.44 (s, 3H), 3.87 (s, 6H), 4.20 (d, 2H), 5.95-5.99 (m, 1 H), 7.05 (s, 1 H), 7.10-7.12 (m, 2H), 7.32-7.44 (m, 4H), 7.65 (s, 1 H), 8.17 (d, 1 H).

Example 388

4-(3-{(1 R)-1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}phenyl)pyridi n-2-ol

To a solution of 2-hydroxypyridine-4-boronic acid (46.8 mg, 0.32 mmol) and N-[(1 R)-1 -(3- bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine (described in example 191 , 100 mg, 0.25 mmol) in DMF (10 mL) were added potassium phosphate solution (0.5 M in water, 1 .49 mL) and the second generation RuPhos precatalyst (chloro(2- dicyclohexylphosphino-2',6'-diisopropoxy-1 ,1 '-biphenyl)[2-(2'-amino-1 ,1 '- biphenyl)]palladium(ll), 38.6 mg, 0.05 mmol). The reaction mixture was stirred at 75°C for two hours. More 2-hydroxypyridine-4-boronic acid (46.8 mg, 0.32 mmol), chloro(2- dicyclohexylphosphino-2',6'-diisopropoxy-1 ,1 '-biphenyl)[2-(2'-amino-1 ,1 '- biphenyl)]palladium(ll) (38.6 mg, 0.05 mmol) and potassium phosphate solution (0.5 M in water, 1.49 mL) were added and the reaction was stirred at 75°C overnight. The reaction mixture was filtered and the filtrate was evaporated. The title compound was obtained in 12% yield (12.4 mg) after HPLC chromatography. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 12.07- 1 1.09 (m, 1 H), 8.02 (d, 1 H), 7.78 (s, 1 H), 7.70 (s, 1 H), 7.58-7.49 (m, 2H), 7.48-7.38 (m, 2H), 7.02 (s, 1 H), 6.56 (d, 1 H), 6.47 (dd, 1 H), 5.69 (t, 1 H), 3.91 (s, 3H), 3.86 (s, 3H), 2.39-2.28 (m, 3H), 1.63 (d, 3H). LC-MS (Method 8): m/z: [M+H] ⁺ = 417, R _t = 0.78 min.

Example 389

N-{1 -[3-(benzyloxy)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazoli n-4-amine

Step a: 1 -[3-(benzyloxy)phenyl]-N-hydroxyeth

A solution of 3-benzyloxyacetophenon (commercially available, 10.5 g, 46.4 mmol), hydroxylamine hydrochloride (16.1 g, 232 mmol), sodium acetate (464 mmol) in ethanol (250 mL) was stirred at 40°C overnight. The solvent was distilled off under reduced pressure and the residue was extracted once with ethyl acetate / HCI (1 .0 M in water). The aqueous phase was extracted with ethyl acetate (3 x 100 mL) and the combined organic layers were dried over sodium sulfate. The crude product was obtained in quantitative yield (1 1 .5 g) and used without further purification in the next step. LC-MS (Method 7): m/z: [M+H] ⁺ = 242.1 , R _t = 1 .15 & 1 .20 min. (E/Z isomers in ratio - 2:1 )

Step b:

1 -[3-(benzyloxy)phenyl]ethanamine

To a solution of 1 -[3-(benzyloxy)phenyl]-N-hydroxyethanimine (5.5 g, 22.79 mmol) in methanol (500 mL) was added Zn powder (44.7 g, 684 mmol) and ammonium chloride (42.7 g, 797.8 mmol) and the reaction was stirred at 60°C overnight. The suspension was filtered and the residue was washed with methanol (3 x 100 mL). The filtrate was evaporated, water and basified by addition of ammonia solution (in water). The aqueous phase was extracted with ethyl acetate (3 x 100 mL) and the combined organic layers were dried over magnesium sulfate. After evaporation of the solvent the crude product was purified via Isolera flash chromatography (SNAP KP NH, 375g column; eluent gradient hexanes (100% -> hexanes / ethyl acetate (60:40)) to yield the title compound in 25% yield (1 .35 g). LC-MS (Method 8): m/z: ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 7.50-7.43 (m, 2H), 7.42-7.27 (m, 3H), 7.19 (t, 1 H), 7.06-7.01 (m, 1 H), 6.92 (d, 1 H), 6.82 (ddd, 1 H), 3.93 (q, 1 H), 1.80 (br s, 2H), 1.21 (d, 3H). [M+H] ⁺ = 228, R _t = 0.76 min.

Step c:

N-{1 -[3-(benzyloxy)phenyl]ethyl}-6,7-dimethoxy-2-methylquinazoli n-4-amine

A solution of 1 -[3-(benzyloxy)phenyl]ethanamine (200 mg, 0.88 mmol), 4-chloro-6,7- dimethoxy-2-methylquinazoline (commercially available, 191 mg, 0.80 mmol), N,N- diisopropylethylamine (0.28 mL) in 1 ,4-dioxane (4.17 mL) was heated in a microwave oven for 7 hours at 120°C. The solvent was distilled off under reduced pressure and the residue purified by HPLC. The title compound was obtained in 45% yield (173 mg). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.13 (s, 2H), 7.73 (s, 1 H), 7.44-7.20 (m, 6H), 7.09 (s, 1 H), 7.03 (s, 2H), 6.93-6.84 (m, 1 H), 5.83-5.41 (m, 1 H), 5.07 (s, 2H), 3.90 (s, 3H), 3.87 (s, 3H), 2.36 (s, 3H), 1.57 (br d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 430.2, R _t = 0.99 min.

Example 390

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7-dimethoxy-2- methylquinazolin-4-amine (enantiomer 1 )

Enantiopure N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-6,7-d imethoxy-2- methylquinazolin-4-amine was obtained from racemic N-[1 -(5-{2- [(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-6,7-dimethox y-2-methylquinazolin-4-amine (described in example 262) by chiral HPLC purification (Method X7). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.44-7.40 (m, 1 H), 7.38-7.35 (m, 1 H), 7.33- 7.26 (m, 2H), 7.18 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.36 (s, 2H), 2.43 (s, 3H), 2.10 (s, 6H), 1 .72 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 463, R _t = 0.58 min. [a] _D = +163.8° +/- 1 .76°.

Example 391

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7-dimethoxy-2- methylquinazolin-4-amine (enantiomer 2)

Enantiopure N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-6J-di m methylquinazolin-4-amine was obtained from racemic N-[1 -(5-{2- [(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-6,7-dimethox y-2-methylquinazolin-4-amine (described in example 262) by chiral HPLC purification (Method X7). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.15 (d, 1 H), 7.65 (s, 1 H), 7.44-7.40 (m, 1 H), 7.38-7.35 (m, 1 H), 7.33- 7.26 (m, 2H), 7.18 (d, 1 H), 7.08 (dd, 1 H), 7.05 (s, 1 H), 5.96 (quin, 1 H), 3.87 (s, 6H), 3.36 (s, 2H), 2.43 (s, 3H), 2.10 (s, 6H), 1 .72 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 463, R _t = 0.58 min. [a] _D = -158.1 ° +/- 2.00°.

Example 392

2-(4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazolin-6-yl)propan -2-ol

To a solution of methyl 4-{[(1 R)-1 -(3-chlorophenyl)ethyl]amino}-2-methylquinazoline-6- carboxylate (described in example 371 , 300 mg, 0.84 mmol) in THF was added at 0°C methyl magnesium chloride (3.0 M in THF, 1 .69 ml_, 5.06 mmol). The reaction was allowed to warm to ambient temperature and stirred for three hours at room temperature. More methyl magnesium chloride (3.0 M in THF, 1 .69 ml_, 5.06 mmol) was added at ambient temperature and the reaction was stirred at RT for another 16 hours. The reaction mixture was poured into saturated ammonium chloride solution and extracted with dichloromethane (3 x 50 ml_). The combined organic layers were evaporated and the residue purified via HPLC chromatography to yield the title compound (108 mg, 35%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.45-8.39 (m, 1 H), 8.36 (d, 1 H), 8.15 (s, 1 H), 7.85 (dd, 1 H), 7.56-7.49 (m, 2H), 7.41 (s, 1 H), 7.35 (t, 1 H), 7.29 (dd, 1 H), 5.64 (s, 1 H), 5.28-5.13 (m, 1 H), 2.37 (s, 3H), 1 .59 (d, 3H), 1 .53 (s, 6H). LC-MS (Method 7): m/z: [M+H] ⁺ = 356.2, R _t = 0.83 min. Example 393

2-(3'-{(1 R)-1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}bipheny l-2- yl)acetamide

The title compound was prepared in analogy to 4-(3-{(1 R)-1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}phenyl)pyridin-2-ol (described in example 388) using 2- (aminocarbonylmethyl)phenylboronic acid; pinacol ester (243 mg, 0.93 mmol) and N-[(1 R)-1 - (3-bromophenyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-ami ne (described in example 191 , 150 mg, 373 mol). Yield: 102 mg (58%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.02-7.96 (m, 1 H), 7.69 (s, 1 H), 7.49-7.42 (m, 2H), 7.38 (t, 1 H), 7.34-7.27 (m, 4H), 7.26-7.18 (m, 2H), 7.02 (s, 1 H), 6.91 (br s, 1 H), 5.70 (t, 1 H), 3.89 (s, 3H), 3.86 (s, 3H), 3.35 (d, 2H), 2.36 (s, 3H), 1 .62 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 457.2, R _t = 0.80 min.

Example 394

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]acetamide

The title compound was prepared in analogy to 4-(3-{(1 R)-1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}phenyl)pyridin-2-ol (described in example 388) using 2- (aminocarbonylmethyl)phenylboronic acid; pinacol ester (240 mg, 0.92 mmol) and N-[1 -(5- bromo-2-thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-am ine (described in example 209, 150 mg, 367 mol). Yield: 1 .1 mg (0.59%). LC-MS (Method 7): m/z: [M+H] ⁺ = 463.2, R _t = 0.77 min.

Example 395

5-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)pyridin-^

The title compound was prepared in analogy to 4-(3-{(1 R)-1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}phenyl)pyridin-2-ol (described in example 388) using 6- hydroxypyridine-3-boronic acid; pinacol ester (128 mg, 918 mol) and N-[1 -(5-bromo-2- thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine (described in example 209, 150 mg, 367 mol). Yield: 16 mg (10%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 1.71 (br s, 1 H), 8.09 (d, 1 H), 7.69 (dd, 1 H), 7.63 (s, 1 H), 7.58 (s, 1 H), 7.14 (d, 1 H), 7.04 (s, 1 H), 7.01 (dd, 1 H), 6.37 (d, 1 H), 5.89 (t, 1 H), 3.87 (s, 6H), 2.43 (s, 3H), 1 .68 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 423.2, R _t = 0.65 min.

Example 396

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,8-dimethylquinazolin-4-a mine

Step a:

6-methoxy-2, 8-dimethylquinazolin-4(3H)-one

Methyl 2-amino-5-methoxy-3-methylbenzoate, 500 mg (2.6 mmol, commercially available) was dissolved in 20 mL of acetonitrile and dry hydrogen chloride gas was passed into the above solution at room temperature until a clear solution was observed. The resulting mixture was stirred at reflux for overnight. The precipitated solid was collected by filtration, washed with acetonitrile and re-dissolved with water. Saturated aqueous sodium carbonate was added to adjust the pH value to 8 and the precipitated solid was collected by filtration. The filter cake was washed with ice cold water and dried in vacuo to give 212 mg (40%) of the product as a white solid. MS (ESIpos): m/z = 205 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .12 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 2.31 (s, 3H), 2.44 (s, 3H), 3.80 (s, 3H), 7.21 (s, 1 H), 7.28 (s, 1 H), 12.10 (br, 1 H).

Step b:

4-chloro-6-methoxy-2,8-dimethyl uinazoline

6-Methoxy-2, 8-dimethylquinazolin-4(3H)-one, 120 mg (0.60 mmol), was dissolved in 20 mL of phosphoryl trichloride. The resulting mixture was stirred at 1 10°C for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 97.0 mg (74%) of the product as a yellow solid. MS (ESIpos): m/z = 223 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B)]: Rt = 1 .1 1 min.

Step c: N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,8-dimethylquinazolin-4-a mine

4-Chloro-6-methoxy-2,8-dimethylquinazoline, 60.0 mg (0.30 mmol), and (R)-1 -(3- chlorophenyl)ethanamine, 46.1 mg (0.30 mmol, commercially available), were dissolved into 1 .0 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for 6 hours. After cooling to room temperature, the solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give 41 .3 mg (44%) of the product as a light yellow solid. MS (ESIpos): m/z = 342 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .31 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .59 (d, 3H), 2.39 (s, 3H), 2.49 (s, 3H), 3.88 (s, 3H), 5.60-5.64 (m, 1 H), 7.24-7.29 (m, 2H), 7.33-7.42 (m, 2H), 7.49 (s, 1 H), 7.58 (s, 1 H), 8.10 (d, 1 H).

Example 397

N-[1 -{5-[2-(aminomethyl)-3-chlorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

This compound was synthesized from tert-butyl [2-chloro-6-(5-{1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl)benzyl]carba mate (described in example 450) by the same method as described in example 437 to give 26.2 mg (63%) of the product as an off-white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .55 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .72- 1 .74 (d, 3H), 2.43 (s, 3H), 3.84-3.87 (m, 8H), 5.95-5.98 (m, 1 H), 7.05 (s, 1 H), 7.12-7.13 (m, 1 H), 7.23 (s, 1 H), 7.30-7.31 (m, 2H), 7.46-7.47 (m, 1 H), 7.65 (s, 1 H), 8.16-8.18 (m, 3H).

Example 398 N-[1 -{5-[2-(aminomethyl)-4-chlorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

This compound was synthesized from tert-butyl [5-chloro-2-(5-{1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl)benzyl]carba mate (described in example 449) by the same method as described in example 437 to give 1 1 .1 mg (33%) of the product as an off-white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)- Acetonitrile, 5%B]: R _t = 1.36 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.72 (d, 3H), 2.43 (s, 3H), 3.87-3.89 (m, 8H), 5.94-5.97 (m, 1 H), 7.05 (s, 1 H), 7.08-7.12 (m, 2H), 7.34-7.37 (m, 2H), 7.64-7.68 (m, 2H), 8.16 (d, 1 H), 8.23-8.24 (m, 2H).

Example 399

N-(1 -{5-[2-(aminomethyl)-4-fluorophenyl]-4-methyl-2-thienyl}ethy l)-6,7-dimethoxy-2- methylquinazolin-4-amine

Under argon, N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin- 4-amine hydrochloride (1 :1 ) (100 mg, 218 μιτιοΙ, described in example 183), [2- (aminomethyl)-4-fluorophenyl]boronic acid hydrochloride (1 :1 ) (44.8 mg, 218 μηηοΙ), K2CO3 (120 mg, 872 μηιοΙ) and Pd(PPh ₃ ) ₄ (25.2 mg, 21.8 μπιοΙ) in 1 ,4-dioxane (2.0 mL) and H ₂ 0 (400 μί) were stirred at 1 10°C during 36 hours. Additional [2-(aminomethyl)-4- fluorophenyl]boronic acid hydrochloride (1 :1 ) (44.8 mg, 218 μηηοΙ) was added and the mixture stirred at 1 10°C over the weekend. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (9.90 mg, 10%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.1 1 (d, 1 H), 7.64 (s, 1 H), 7.42 (dd, 1 H), 7.17 (dd, 1 H), 7.07-7.01 (m, 3H), 6.93 (d, 1 H), 5.91 (sxt, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 2.42 (s, 3H), 1 .90 (s, 3H), 1 .68 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 467, R _t = 0.60 min. Example 400

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-4-methyl-2-thienyl)eth yl]-6 -dimethoxy-2- methylquinazolin-4-amine

Step a:

2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde

Under argon, N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin- 4-amine hydrochloride (1 :1 ) (500 mg, 1 .09 mmol, described in example 183), 2- formylphenylboronic acid (163 mg, 1 .09 mmol), K ₂ C0 ₃ (602 mg, 4.36 mmol) and Pd(PPh ₃ )4 (126 mg, 109 mol) in 1 ,4-dioxane (10 mL) and H ₂ 0 (2.0 mL) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as an orange solid (340 mg, 63%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 9.84 (d, 1 H), 8.14 (d, 1 H), 7.88 (dd, 1 H), 7.72 (td, 1 H), 7.45 (dd, 1 H), 7.05 (s, 1 H), 7.03 (d, 1 H), 5.95 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 2.42 (s, 3H), 1 .99 (s, 3H), 1.71 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 448, R _t = 0.97 min.

Step b:

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-4-methyl-2-thienyl)eth yl]-6 -dimethoxy-2- methylquinazolin-4-amine

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethy^

(50.0 mg, 1 15 μηιοΙ), N-methylmethanamine (1 10 μΙ, 2.0 M, 220 μηιοΙ) and acetic acid (13 μΙ, 230 μmol) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc) ₃ (47.4 mg, 223 μηιοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1 .0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (31 .3 mg, 57%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.1 1 (d, 1 H), 7.65 (s, 1 H), 7.52 (d, 1 H), 7.36 (td, 1 H), 7.25 (td, 1 H), 7.16 (dd, 1 H), 7.04 (s, 1 H), 6.91 (d, 1 H), 5.92 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.23 (s, 2H), 2.41 (s, 3H), 2.03 (s, 6H), 1.90 (s, 3H), 1 .68 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 477, R _t = 0.61 min.

Example 401

2-{[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-3-methyl-2- thienyl)benzyl](methyl)amino}ethanol

To 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)benzaldehyde (50.0 mg, 1 15 μηιοΙ, described in example 400 [step a]), 2-(methylamino)ethanol (18 μΙ, 220 μηηοΙ) and acetic acid (13 μΙ, 230 μηηοΙ) in 1 ,2-dichloroethane (1 .0 mL) was added NaBH(OAc)3 (47.4 mg, 223 μηηοΙ) and the solution stirred at room temperature overnight. The reaction was quenched with aqueous NaOH (1.0 M, 1 .0 mL), the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (34.6 mg, 55%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.1 1 (d, 1 H), 7.64 (s, 1 H), 7.59 (dd, 1 H), 7.36 (td, 1 H), 7.24 (td, 1 H), 7.14 (dd, 1 H), 7.04 (s, 1 H), 6.91 (d, 1 H), 5.92 (quin, 1 H), 4.30 (br s, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 3.44- 3.37 (m, 3H), 2.42 (s, 3H), 2.30 (t, 2H), 2.04 (s, 3H), 1 .90 (s, 3H), 1 .68 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 507, R _t = 0.61 min.

Example 402

6,7-dimethoxy-2-methyl-N-[1 -(4-methyl-5-{2-[(methylamino)methyl]phenyl}thiophen-2- yl)ethyl]quinazolin-4-amine

Under argon, N-[1 -(5-bromo-4-methylthiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin- 4-amine hydrochloride (1 :1 ) (100 mg, 218 μηιοΙ, described in example 183), N-methyl-1 -[2- (4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]methanamine (53.9 mg, 218 μmol), K2CO3 (120 mg, 872 μηιοΙ) and Pd(PPh ₃ ) ₄ (25.2 mg, 21.8 μπιοΙ) in 1 ,4-dioxane (2.0 mL) and H2O (400 μΙ_) were stirred at 1 10°C during 36 hours. Additional N-methyl-1 -[2-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)phenyl]methanamine (53.9 mg, 218 μηηοΙ) was added and the mixture stirred at 1 10°C over the weekend. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) followed by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound as a white solid (33.5 mg, 33%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.12 (d, 1 H), 7.65 (s, 1 H), 7.53 (d, 1 H), 7.35 (td, 1 H), 7.24 (t, 1 H), 7.15 (dd, 1 H), 7.04 (s, 1 H), 6.92 (s, 1 H), 5.92 (quin, 1 H), 3.87 (s, 6H), 3.48 (s, 2H), 2.42 (s, 3H), 2.14 (s, 3H), 1 .92 (s, 3H), 1 .68 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 463, R _t = 0.60 min.

Example 403

1 -[2-(5-{(1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]ethane-1 ,2-diol

A solution of N-{1 -[5-(2-ethenylphenyl)thiophen-2-yl]ethyl}-6 J-dimethoxy-2-methylquinazolin- 4-amine (40.0 mg, 92.7 μηηοΙ, described in example 248), osmium tetroxide (94 μΙ, 2.5%w in tert-butanol, 9.3 μηηοΙ) and N-methylmorpholine N-oxide (32.6 mg, 278 μηηοΙ) in acetone (1.0 mL) and H2O (200 μΙ_) was stirred at room temperature overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light brown solid (33.5 mg, 33%). ¹ H- NMR (400 MHz, DMSO-de): δ [ppm] = 8.16 (d, 1 H), 7.65 (d, 1 H), 7.56 (d, 1 H), 7.35 (ddd, 1 H), 7.28-7.23 (m, 2H), 7.10-7.07 (m, 1 H), 7.05 (s, 1 H), 7.00 (dd, 1 H), 6.02-5.92 (m, 1 H), 5.17 (dd, 1 H), 4.90-4.81 (m, 1 H), 4.74 (td, 1 H), 3.87 (s, 6H), 3.46-3.39 (m, 1 H), 2.43 (s, 3H), 1 .72 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 466, R _t = 0.76 min.

Example 404

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2,6-dimethylquinazolin-4-amine

To a solution of 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine (described in example 363, 100 mg, 265 μηηοΙ), methyl boronic acid (20 mg, 319 μηηοΙ) and [1 ,1 -bis(diphenylphosphino)ferrocene]dichloropalladium(ll), complex with dichloromethane (43.3 mg, 0.053 mmol)in 1 ,4-dioxane (3.0 mL) was added sodium carbonate solution (1 .0 M in water, 0.25 mL) and the reaction was stirred at 80°C for 4 hours. The reaction was filtered and the filtrate evaporated. The crude product was purified by HPLC chromatography to yield the title compound (10 mg, 1 1 %). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.24 (d, 1 H), 8.16 (s, 1 H), 7.58-7.45 (m, 3H), 7.43-7.38 (m, 1 H), 7.34 (t, 1 H), 7.30-7.23 (m, 1 H), 5.59 (quin, 1 H), 2.47 (s, 3H), 2.37 (s, 3H), 1.57 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 312.1 ,

Example 405

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methyl-6-(1 H-pyrazol-4-yl)quinazolin

To a solution of 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine (described in example 363, 150 mg, 0.398 mmol), 4-pyrazoleboronic acid 222.7 mg, 1.99 mmol) and [1 ,1 -Bis(diphenylphosphino)ferrocene]dichloropalladium(ll), complex with dichloromethane (81 .3 mg, 99.0 μηιοΙ) in DMF (4.0 mL) was added sodium carbonate solution (2.0 M in water, 0.54 mL) and the reaction was stirred at 80°C for 3 hours. The reaction was filtered and the filtrate evaporated. The crude product was purified by HPLC chromatography to yield the title compound (62.0 mg, 41 %). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 13.04 (br s, 1 H), 8.54 (s, 1 H), 8.35-7.94 (m, 4H), 7.57 (d, 1 H), 7.52 (s, 1 H), 7.46- 7.41 (m, 1 H), 7.37 (t, 1 H), 7.32-7.27 (m, 1 H), 5.65 (br t, 1 H), 2.38 (s, 3H), 1.62 (br d, 3H). LC- MS (Method 7): m/z: [M+H] ⁺ = 364.1 , R _t = 0.80 min.

Example 406

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methyl-6-(1 -methyl-1 H-pyrazol-4-yl)quinazolin-4- amine

To a solution of 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine (described in example 363, 150 mg, 0.398 mmol), 1 -methyl-1 H-pyrazole-4-boronic acid, pinacol ester (414 mg, 1 .99 mmol) and [1 ,1 -bis(diphenylphosphino)- ferrocene]dichloropalladium(ll), complex with dichloromethane (81.3 mg, 99.0 μηιοΙ) in DMF (4.0 mL) was added sodium carbonate solution (2.0 M in water, 0.54 mL) and the reaction was stirred at 80°C for 3 hours. The reaction was filtered and the filtrate evaporated. The crude product was purified by HPLC chromatography to yield the title compound (69.0 mg, 45 %). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.51 (br s, 1 H), 8.33-8.16 (m, 2H), 8.06-7.87 (m, 2H), 7.65-7.23 (m, 6H), 5.65 (br s, 1 H), 3.91 (br s, 3H), 2.38 (br s, 3H), 1.61 (br d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 378.2, R _t = 0.84 min.

Example 407

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-cyclopropyl-2-methylquinazolin-4-a mine

To a solution of 6-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine (described in example 363, 150 mg, 0.398 mmol), cyclopropyl boronic acid (171 mg, 1.99 mmol) and [1 ,1 -bis(diphenylphosphino)ferrocene]dichloropalladium(ll), complex with dichloromethane (81.3 mg, 99.0 μηηοΙ) in DMF (4.0 mL) was added sodium carbonate solution (2.0 M in water, 0.54 mL) and the reaction was stirred at 80°C for 3 hours. The reaction was filtered and the filtrate evaporated. The crude product was purified by HPLC chromatography to yield the title compound (20 mg, 14 %). LC-MS (Method 7): m/z: [M+H] ⁺ = 338.1 , R _t = 0.93 min.

Example 408

tert-butyl [3-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

Step a:

1 -(2-bromo-3-chlorophenyl)methanamine

To 25 ml. of borane tetrahydrofuran complex (1 .0 M in THF) was added a solution of 2- bromo-3-chlorobenzonitrile, 1.00 g (4.6 mmol, commercially available), in 5.0 ml. of THF at 0°C and the resulting mixture was stirred at reflux for 15 hours under nitrogen atmosphere. After cooling to room temperature, methanol and hydrochloric acid were added dropwise to the above solution at 0°C and the resulting mixture was stirred at room temperature for 30 minutes. Sodium hydroxide solution (1 .0 M) was added to adjust the pH value to 7 and the resulting mixture was extracted with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated in vacuo to give 610 mg (60%) of the product as a light yellow oil. MS (ESIpos): m/z = 220 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)- Acetonitrile, 10%B]: R _t = 0.51 min.

Step b:

ferf-butyl (2-bromo-3-chlorobenzyl)carbamate

This compound was synthesized by the same method as described in example 428 (step a) to give 720 mg (81 %) of the product as an off-white solid. MS (ESIpos): m/z = 320 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.18 min.

Step c:

ferf-butyl [3-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 428 (step b) to give 408 mg (49%) of the product as a light yellow oil. MS (ESIpos): m/z = 368 [M+H] ⁺ . LC- MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .25 min.

Step d:

ferf-butyl [3-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 429 to give 160 mg (51 %) of the product as an off-white solid. MS (ESIpos): m/z = 569 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .50 min. ¹ H-NMR (400 MHz, DMSO- d ₆ ): δ [ppm] = 1 .37 (s, 9H), 1 .73 (d, 3H), 2.43 (s, 3H), 3.87 (s, 6H), 3.94 (d, 2H), 5.97-6.01 (m, 1 H), 6.86-6.87 (m, 1 H), 7.05 (s, 1 H), 7.10 (d, 1 H), 7.23-7.34 (m, 2H), 7.39-7.45 (m, 2H), 7.66 (s, 1 H), 8.19 (d, 1 H).

Example 409

N-[1 -{5-[2-(aminomethyl)-6-chlorophenyl]thiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

This compound was synthesized from tert-butyl [3-chloro-2-(5-{1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl)benzyl]carba mate (described in example 408) by the same method as described in example 430 to give 18.2 mg (33%) of the product as an off-white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)- Acetonitrile, 5%B]: Rt = 1 .05 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 2.33 (s, 3H), 3.50 (s, 2H), 3.87 (s, 6H), 5.95-6.00 (m, 1 H), 6.87 (s, 1 H), 7.05-7.09 (m, 2H), 7.39- 7.43 (m, 2H), 7.52-7.54 (m, 1 H), 7.55-7.66 (m, 1 H), 8.19 (d, 1 H). Example 410

4-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2-thienyl)py ridin-2-ol

The title compound was prepared in analogy to 4-(3-{(1 R)-1 -[(6,7-dimethoxy-2- methylquinazolin-4-yl)amino]ethyl}phenyl)pyridin-2-ol (described in example 388) using 2- hydroxypyridine-4-boronic acid, pinacol ester (203 mg, 0.918 mmol) and N-[1 -(5-bromo-2- thienyl)ethyl]-6,7-dimethoxy-2-methylquinazolin-4-amine (150 mg, 0.367 mmol, described in example 209). Yield: 3.3 mg (1.7 %). LC-MS (Method 7): m/z: [M+H] ⁺ = 423.1 , R _t = 0.63 min.

Example 411

4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]azetidin-2-one

Step a:

N-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2-thie nyl)- phenyl]methylene}-2-methylpropane-2-sulfinamide H ₃ C C H ₃

A solution of 2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzaldehyde (500 mg, 1 .15 mmol, described in example 179 [step b]), 2-methylpropane- 2-sulfinamide (168 mg, 1 .38 mmol) and Ti(OEt) ₄ (480 μΙ, 2.3 mmol) in THF (1 .0 mL) was stirred at room temperature overnight. The reaction was quenched with brine (0.7 mL), diluted with EtOAc and filtered over a celite plug. Purification by column chromatography (silica gel, MeOH/EtOAc 0-20% then MeOH) gave the title compound which was used directly in step b. LC-MS (Method 10): m/z: [M+H] ⁺ = 537, R _t = 1 .45 min.

Step b:

4-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]azetidin-2-one

A solution of N-{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]methylidene}-2-methylpropane-2-sulfinamide (50.0 mg, 93.2 μηηοΙ) and malonic acid (19.4 mg, 186 μηηοΙ) in acetic acid (1 .0 mL) was stirred at 120°C overnight. The solvent was removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (9.60 mg, 22%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.19 (d, 1 H), 7.83 (d, 1 H), 7.77 (d, 1 H), 7.64 (s, 1 H), 7.45-7.37 (m, 3H), 7.16 (dd, 1 H), 7.05 (s, 1 H), 6.92 (d, 1 H), 6.49 (d, 1 H), 5.98 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 2.44 (s, 3H), 1.73 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 475, R _t = 0.89 min.

Example 412

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,7-dimethylquinazolin-4-a mine

Step a:

methyl 5-methoxy-4-methyl-2-nitrobenzoate; P OS589-1

5-Methoxy-4-methyl-2-nitrobenzoic acid, 500 mg (2.4 mmol), and 0.5 mL of cone, sulfuric acid were dissolved in 20 mL of methanol. The resulting mixture was stirred at 65°C overnight. After cooling to room temperature, the solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The resulting mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified with silica gel column chromatography to give 465 mg (87%) of the product as a light yellow solid. MS (ESIpos): m/z = 226 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .03 min.

Step b:

methyl 2-amino-5-methoxy-4-methylbenzoate

Methyl 5-methoxy-4-methyl-2-nitrobenzoate, 465 mg (2.1 mmol), and 0.1 g of palladium/carbon (10%), were added into 10 mL of methanol. The resulting slurry was stirred at room temperature for overnight under hydrogen atmosphere (3 atm). Catalyst was removed by filtration and the filtrate was concentrated in vacuo to give 393 mg (94%) of the product as a light yellow solid. MS (ESIpos): m/z = 196 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: Rt = 0.82 min.

Step c:

6-methoxy-2,7-dimethylquinazolin-4(3H)-one

Methyl 2-amino-5-methoxy-4-methylbenzoate, 393 mg (2.0 mmol), was dissolved into 20 mL of acetonitrile and dry hydrogen chloride gas was introduced into the above solution at room temperature until a clear solution was observed. Then the resulting mixture was stirred at reflux for overnight. The precipitated solid was collected by filtration, washed with acetonitrile and re-dissolved with water. Saturated aqueous sodium carbonate was added to adjust the pH value to 8 and the precipitated solid was collected by filtration, washed with ice cold water and dried in vacuo to give 308 mg (74%) of the product as a white solid. MS (ESIpos): m/z = 205 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.76 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 2.25 (s, 3H), 2.41 (s, 3H), 3.86 (s, 3H), 7.37 (s, 1 H), 7.38 (s, 1 H), 12.02 (br, 1 H).

Step d:

4-chloro-6-methoxy-2,7-dimeth lquinazoline

6-Methoxy-2,7-dimethylquinazolin-4(3H)-one, 130 mg (0.6 mmol), was dissolved into 10 mL of phosphoryl trichloride. The resulting mixture was stirred at 1 10°C for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 121 mg (68%) of the product, as a yellow solid. MS (ESIpos): m/z = 223 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .01 min.

Step e:

N-[(1 R)-1 -(3-chlorophenyl)ethyl]-6-methoxy-2,7-dimethylquinazolin-4-a mine

4-Chloro-6-methoxy-2,7-dimethylquinazoline, 60.0 mg (0.3 mmol), and (R)-1 -(3- chlorophenyl)ethanamine, 46.1 mg (0.3 mmol), were dissolved in 1 .0 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for 6 hours. After cooling to room temperature, the solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give 44.5 mg (48%) of the product, as a white solid. MS (ESIpos): m/z = 342 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.33 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .61 (d, 3H), 2.29 (s, 3H), 2.36 (s, 3H), 3.96 (s, 3H), 5.59-5.69 (m, 1 H), 7.28 (d, 1 H), 7.34- 7.41 (m, 3H), 7.43 (s, 1 H), 7.68 (s, 1 H), 8.16 (s, 1 H).

Example 413

4-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-3- dimethylamino)methyl]benzonitrile

4-Bromo-3-methylbenzonitrile, 500 mg (2.55 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'- bi(1 ,3,2-dioxaborolane), 712 mg (2.81 mmol), potassium acetate, 751 mg (7.65 mmol), 1 ,1 '- bis(diphenylphosphino)ferrocene-palladium(ll)dichloride dichloromethane complex, 208 mg (0.26 mmol), were added into 5.0 mL of Ν,Ν-dimethylformamide. The resulting mixture was stirred at 100°C for 24 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative TLC to give 480 mg (77%) of the product as a green solid. ¹ H-NMR (400 MHz, DMSO): δ [ppm] = 1.12 (s, 12H), 2.46 (s, 3H), 7.57-7.58 (d, 1 H), 7.62 (s, 1 H), 7.69-7.72 (d, 1 H).

Step b:

3-(bromomethyl)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile

3-Methyl-4-(4 _! 4 _! 5 _! 5-tetramethyl-1 _! 3,2-dioxaborolan-2-yl)benzonitrile _! 200 mg (0.82 mmol), was dissolved into 2 mL of 1 ,2-dichloroethane. Then 2,2'-azobisisobutyronitrile, 14 mg (0.08 mmol), and N-bromosuccinimide, 176 mg (0.99 mmol), were added into the above solution at reflux and the resulting mixture was stirred at this temperature for 12 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by preparative TLC to give 140 mg (52%) of the product as a yellow solid. ¹ H-NMR (400 MHz, DMSO): δ [ppm] 1 .27 (s, 12H), 4.90 (s, 2H), 7.73-7.78 (m, 2H), 7.94 (s, 1 H).

Step c:

3-((dimethylamino)methyl)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile

3- (Bromomethyl)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile, 100 mg (0.31 mmol), was dissolved into 1 .7 mL of dimethylamine/THF (2.0 M) solution. The resulting solution was stirred at room temperature for 12 hours. The solvent was removed in vacuo to give 90 mg (crude) of the product as a yellow solid. It was used directly for next step without further purification. MS (ESIpos): m/z = 205 (M of bonic acid+H) ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.52 min.

Step d:

4- (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2-yl)-3- [(dimethylamino)methyl]benzonitrile

N-(1 -(5-bromothiophen-2-yl)ethyl)-6,7-dimethoxy-2-methylquinazol in-4-amine, 50 mg (0.15 mmol), 3-((dimethylamino)methyl)-4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzonitrile, 87 mg (0.30 mmol), tetrakis(triphenylphosphine)palladium, 18 mg (0.02 mmol), and potassium carbonate, 84 mg (0.61 mmol), were added into 1 .4 mL of 1 ,4-dioxane/water (v:v = 5:2). The resulting mixture was stirred at 100°C. After cooling to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 5.8 mg (10%) of the final product as a white solid. MS (ESIpos): m/z = 488 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.96 min; ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] 1 .70-1 .72 (d, 3H), 2.10 (s, 6H), 2.41 (s, 3H), 3.31 (s, 2H), 3.85 (s, 6H), 5.93-5.97 (m, 1 H), 7.04 (s, 1 H), 7.13-7.14 (d, 1 H), 7.31 -7.32 (d, 1 H), 7.56-7.58 (d, 1 H), 7.63 (s, 1 H), 7.72 -7.74 (d, 1 H), 7.84 (s, 1 H), 8.14-8.16 (d, 1 H).

Example 414

N-[1 -(5-bromothiophen-2-yl)ethyl]-6-[3-(dimethylamino)pyrrolidin -1 -yl]-2- methylquinazolin-4-amine

Step a:

methyl 5-(3-(dimethylamino)pyrrolidin-1 -yl)-2-nitrobenzoate

This compound was synthesized by the same method as described in example 419 (step b) to give 580 mg (71 %) of the product as a yellow solid. MS (ESIpos): m/z = 294 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B)]: Rt = 1 .63 min.

Step b: methyl 2-amino-5-(3-(dimeth lamino)pyrrolidin-1 -yl)benzoate

This compound was synthesized by the same method as described in example 419 (step c) to give 470 mg (81%) of the product as a grey solid. MS (ESIpos): m/z = 264 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1.41 min. Step c:

6-(3-(dimethylamino)pyrrolidin-1- l)-2-methylquinazolin-4(3H)-one

This compound was synthesized by the same method as described in example 419 (step d) to give 305.6 mg (71%) of the product as a white solid. MS (ESIpos): m/z = 273 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1.15 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1.80-1.90 (m, 1H), 2.15-2.17 (m, 1H), 2.21 (s, 3H), 2.22 (s, 3H), 2.28 (s, 3H), 2.79-2.84 (m, 1H), 3.07-3.13 (m, 1H), 3.26-3.33 (m, 1H), 3.41- 3.54 (m, 2H), 6.97 (s, 1H), 7.08 (d, 1H), 7.42 (d, 1H), 11.89 (s, 1H).

1-(4-chloro-2-methylquinazolin-6-yl)-N,N-dimethylpyrrolid in-3-amine

This compound was synthesized by the same method as described in example 419 (step e) to give 530 mg (81%) of the product as a white solid. MS (ESIpos): m/z = 291 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1.60 min. Step e:

N-[1-(5-bromothiophen-2-yl)ethyl]-6-[3-(dimethylamino)pyrrol idin-1-yl]-2- methylquinazolin-4-amine

This compound was synthesized by the same method as described in example 419 (step f) to give 180 mg (40%) of the product as a yellow solid. MS (ESIpos): m/z = 460 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 2.05 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .67 (d, 3H), 1 .82-1 .88 (m, 1 H), 2.18-2.19 (m, 1 H), 2.21 (s, 3H), 2.23 (s, 3H), 2.41 (s, 3H), 2.83-2.87 (m, 1 H), 3.10-3.16 (m, 1 H), 3.32-3.34 (m, 1 H), 3.45-3.56 (m, 2H), 5.79-5.83 (m, 1 H), 6.91 (s, 1 H), 7.05 (d, 1 H), 7.06 (d, 1 H), 7.16 (d, 1 H), 7.47 (d, 1 H), 8.03 (d, 1 H).

Example 415

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl-6-(pyrrolidi yl)quinazolin-4-amine

N-(1 -(5-bromothiophen-2-yl)ethyl)-2-methyl-6-(pyrrolidin-1-yl)qu inazolin-4-amine formate, 30 mg (0.14 mmol, described in example 419), 2-((dimethylamino)methyl)phenylboronic acid, 38.6 mg (0.2 mmol), tetrakis(triphenylphosphine)palladium(0), 8.3 mg (0.01 mmol), and potassium carbonate, 39.7 mg (0.3 mmol), were added into 1.2 mL of 1 ,4-dioxane/water (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo the residue was purified by preparative HPLC to give 5.2 mg of the product as a yellow solid. MS (ESIpos): m/z = 473 [M+H] ⁺ ; LC-MS [Method 4, starting with gradient water (0.05%NH ₄ HCO ₃ )- Acetonitrile, 50%B]: R _t = 1 .38 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.73 (d, 3H), 1 .99-2.01 (m, 4H), 2.12(s, 6H), 2.42 (s, 3H), 3.32-3.33 (m, 4H), 3.37 (s, 2H), 5.96-6.02 (m, 1 H), 7.09-7.10 (m, 2H), 7.18-7.19 (m, 2H), 7.30-7.31 (m, 3H), 7.46 (d, 1 H), 7.49 (s, 1 H), 8.13

(d, 1 H).

Exemple 416 N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(4-methylpiperazin- 1 -yl)quinazolin-4- amine

Step a:

methyl 5-(4-methylpiperazin-1 -yl)-2-nitrobenzoate

This compound was synthesized by the same method as described in example 419 (step b) to give 0.58 g (83%) of the product as a yellow solid. MS (ESIpos): m/z = 280 [M+H] ⁺ ; LC-MS [Method 4, Water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .54 min.

Step b:

methyl 2-amino-5-(4-methyl iperazin-1 -yl)benzoate

This compound was synthesized by the same method as described in example 419 (step c) to give 0.48 g (83%) of the product as a grey solid. MS (ESIpos): m/z = 250 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .22 min. Step c:

2-methyl-6-(4-methylpiperazin-1 - l)quinazolin-4(3H)-one

This compound was synthesized by the same method as described in example 419 (step d) to give 199.1 mg (40%) of the product as a white solid. MS (ESIpos): m/z = 259 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1.03 min. ¹ H-N MR (300 MHz, DMSO-d ₆ ): δ [ppm] = 2.23 (s, 3H), 2.30 (s, 3H), 2.46-2.50 (m, 4H), 3.19-3.22 (m, 4H), 7.36 (s, 1 H), 7.42-7.53 (m, 2H), 12.01 (s, 1 H).

Step d:

4-chloro-2 -methyl -6-(4-meth lpiperazin-1 -yl)quinazoline

This compound was synthesized by the same method as described in example 419 (step e) to give 420 mg (78%) of the product as a white solid. MS (ESIpos): m/z = 277 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.65 min.

Step e:

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(4-methylpiperazin- 1 -yl)quinazolin-4- amine

This compound was synthesized by the same method as described in example 419 (step f) to give 130 mg (40%) of the product as a light yellow solid. MS (ESIpos): m/z = 446 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1 .94 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .67 (d, 3H), 2.24 (s, 3H), 2.43 (s, 3H), 2.49-2.51 (m, 4H), 3.22-3.26 (m, 4H), 5.78-5.83 (m, 1 H), 6.92 (d, 1 H), 7.06 (d, 1 H), 7.46 (s, 1 H), 7.50-7.54 (m, 2H), 8.19 (d, 1 H).

Example 417

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl-6-(4- methylpiperazin-1 -yl)quinazolin-4-amine

This compound was synthesized from N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(4- methylpiperazin-1 -yl)quinazolin-4-amine (described in example 416) by the same method as described in example 415 to give 45.3 mg (67%) of the product as a yellow solid. MS (ESIpos): m/z = 501 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)- Acetonitrile, 5%B]: R _t = 0.85 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .72 (d, 3H), 2.08 (s, 3H), 2.10 (s, 3H), 2.24 (s, 3H), 2.43 (s, 3H), 2.47-2.49 (m, 4H), 3.24-3.26 (m, 4H), 3.35- 3.36 (m, 2H), 5.96-6.01 (m, 1 H), 7.08 (d, 1 H), 7.18 (d, 1 H), 7.29-7.49 (m, 4H), 7.51 -7.54 (m, 3H), 8.26 (d, 1 H).

Example 418

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6- [3- (dimethylamino)pyrrolidin-1 -yl]-2-methylquinazolin-4-amine

This compound was synthesized from N-[1 -(5-bromothiophen-2-yl)ethyl]-6-[3- (dimethylamino)pyrrolidin-1 -yl]-2-methylquinazolin-4-amine (described in example 414) by the same method as described in example 415 to give 33.4 mg (29%) of the product as a yellow solid. MS (ESIpos): m/z = 515 [M+H] ⁺ ; LC-MS [Method 4, starting with gradient water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.89 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 1 .82-1 .86 (m, 1 H), 2.10 (s, 6H), 2.18-2.19 (m, 1 H), 2.22 (s, 3H), 2.23 (s, 3H), 2.33 (s, 3H), 2.82-2.84 (m, 1 H), 3.12-3.13 (m, 1 H), 3.28 (m, 1 H), 3.34 (s, 2H), 3.48-3.49 (m, 2H), 5.99-6.01 (m, 1 H), 7.07 (d, 2H), 7.15 (d, 2H), 7.27-7.32 (m, 2H), 7.35 (d, 1 H), 7.41 -7.43 (m, 1 H), 7.47 (d, 1 H), 8.08 (d, 1 H).

Example 419

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(pyrrolidin-1 -yl)quinazolin-4-amine

Step a:

methyl 5-fluoro-2-nitrobenzoate

To a solution of 5-fluoro-2-nitrobenzoic acid, 10 g (54 mmol), in 100 mL of methanol was added 20 mL of sulfuric acid at 0°C and the resulting mixture was stirred at 60°C for 16 hours. After cooling to room temperature, aq. potassium carbonate solution was added to adjust the pH value to 8 and methanol was removed in vacuo. The resulting solution was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 9.25 g (77%) of the product as a red oil. MS (ESIpos): m/z = 200 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.98 min.

Step b:

methyl 2-nitro-5-(pyrrolidin-1 -yl)benzoate

Methyl 5-fluoro-2-nitrobenzoate, 500 mg (2.5 mmol), pyrrolidine, 357 mg (5 mmol), and potassium carbonate, 694 mg (5 mmol), were added into 5 mL of N,N-dimethylformamide. The resulting mixture was stirred at reflux for 4 hours. After cooling to room temperature, water was added and the resulting solution was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo to give 550 mg (85%) of the product as a grey solid. MS (ESIpos): m/z = 251 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .85 min.

Step c:

methyl 2-amino-5-(pyrrolidin-1 -yl)benzoate

Methyl 2-nitro-5-(pyrrolidin-1 -yl)benzoate, 550 mg (2.2 mmol), and palladium on carbon (10%), 233 mg (0.2 mmol), were added into 10 mL of methanol. The resulting mixture was stirred under hydrogen atmosphere (2 atm) for 3 hours at room temperature. The catalyst was removed by filtration and the filtrate was concentrated in vacuo to give 450 mg (84%) of the product as a grey solid. MS (ESIpos): m/z = 221 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1 .74 min.

Step d:

2-methyl-6-(pyrrolidin-1 -yl)quinazolin-4(3H)-one

Dry HCI gas was passed (until the clear solution observed) to a solution of methyl 2-amino-5- (pyrrolidin-l -yl)benzoate, 450 mg (2 mmol), in 10 mL of acetonitrile for 3 hours at room temperature. Then the resulting mixture was stirred at reflux for 10 hours and cooled down to room temperature. The precipitated solid was collected by filtration and the filter cake was re- dissolved with water. The solution was neutralized with aqueous sodium bicarbonate and the precipitated solid was collected by filtration, washed with ice cold water and dried in vacuo to give 324 mg (69%) of the product as a white solid. MS (ESIpos): m/z = 230 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .36 min. ¹ H-N MR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .97-2.01 (m, 4H), 2.27 (s, 3H), 3.28-3.30 (m, 4H), 6.98 (s, 1 H), 7.08 (d, 1 H), 7.42 (d, 1 H), 1 1 .89 (br, 1 H).

Step e:

4-chloro-2 -methyl -6-(pyrrolidin-1 -yl)quinazoline

2-Methyl-6-(pyrrolidin-1 -yl)quinazolin-4(3H)-one, 680 mg (3 mmol), was dissolved in 20 mL of phosphorus oxychloride and the resulting mixture was stirred at 110°C for 2 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was re- dissolved with dichloromethane. Saturated sodium bicarbonate solution was added to adjust the pH value to 8. The resulting mixture was extracted with dichloromethane and the combine organic layer was concentrated in vacuo to give 720 mg (crude) of the product as a red solid. MS (ESIpos): m/z = 248 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .90 min.

Step f:

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-(pyrrolidin-1 -yl)quinazolin-4-amine

4-Chloro-2-methyl-6-(pyrrolidin-1 -yl)quinazoline, 200 mg (0.8 mmol), and 1 -(5- bromothiophen-2-yl)ethanamine, 166 mg (0.8 mmol, described in example INT-28), were dissolved into 6 ml. of propan-2-ol. The resulting mixture was stirred at 1 10°C for 16 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified with silica gel column chromatography to give 190 mg (33%) of the product as a yellow solid. MS (ESIpos): m/z = 417 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .48 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .67 (d, 3H), 1 .98-2.01 (m, 4H), 2.41 (s, 3H), 3.32-3.34 (m, 4H), 5.77-5.84 (m, 1 H), 6.91 (s, 1 H), 7.05 (d, 2H), 7.15 (d, 1 H), 7.47 (d, 1 H), 8.05 (d, 1 H).

Example 420

N-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6-yl)acetamide

/V4-(1 -(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)-2- methylquinazoline-4,6- diamine, 100 mg (0.24 mmol, described in example 423) and triethylamine, 73 mg (0.72 mmol), were dissolved into 3.0 ml. of dichloromethane. Then acetyl chloride, 24 mg (0.31 mmol), was added dropwise to the above solution at 0°C and the resulting mixture was stirred at room temperature for 2 hours. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give 32.9 mg (29%) of the product as a white solid. MS (ESIpos): m/z = 460 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1 .87 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 (d, 3H), 2.07 (s, 3H), 2.13 (s, 6H), 2.46 (s, 3H), 3.36 (s, 2H), 5.93-5.96 (m, 1 H), 7.08 (d, 1 H), 7.17 (d, 1 H), 7.26-7.33 (m, 2H), 7.35-7.37 (m, 1 H), 7.41 -7.43 (m, 1 H), 7.56 (d, 1 H), 7.68 (d, 1 H), 8.40 (s, 1 H), 8.46 (d, 1 H), 10.08 (s, 1 H). Example 421

N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-2- methyl-6- nitroquinazolin-4-amine

/V-(1 -(5-bromothiophen-2-yl)ethyl)-2-m 1.90 g (4.8 mmol, described in example 452), 2-((dimethylamino)methyl)phenylboronic acid, 2.60 g (14.5 mmol), potassium carbonate, 2.67 g (19.3 mmol), and tetrakis(triphenylphosphine)palladium(0), 0.56 g (0.5 mmol), were added into 60 mL of 1 ,4- dioxane/water (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 10 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified with silica gel column chromatography to give 1 .01 g (47%) of the product as a yellow solid. MS (ESIpos): m/z = 448 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 2.29 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .75 (d, 3H), 2.23-2.38 (m, 6H), 2.54 (s, 3H), 3.33 (s, 2H), 5.95-6.02 (m, 1 H), 7.14- 7.17 (m, 2H), 7.35-7.43 (m, 3H), 7.48-7.54 (br, 1 H), 7.76 (d, 1 H), 8.45 (d, 1 H), 9.27 (d, 1 H), 9.47 (s, 1 H).

Example 422

6,7-dimethoxy-N-{1 -[5-(4-methoxy-2-methylphenyl)thiophen-2-yl]ethyl}-2- methylquinazolin-4-amine

Step a: 2-(4-methoxy-2-methylphen l)-4,4,5,5-tetramethyl-1 ,3,2-dioxaborolane

To a solution of 1 -bromo-4-methoxy-2-methylbenzene, 0.50 g (2.5 mmol), in 10 mL of 1 ,4- dioxane were added 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane), 1 .26 g (5.0 mmol), potassium acetate, 0.98 g (10.0 mmol), and 1 ,1 '-bis(diphenyl- phosphino)ferrocenepalladium(ll) chloride, 0.18 g (0.25 mmol). The resulting mixture was stirred at 100°C for 10 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with water. The resulting mixture was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography (petroleum ether: ethyl acetate = 10: 1 ) to give 0.51 g (78%) of the product as a yellow solid. MS (ESIpos): m/z = 249 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .34 min.

Step b:

6,7-dimethoxy-yV-(1 -(5-(4-methoxy-2-methylphenyl)thiophen-2-yl)ethyl)-2- methylquinazolin-4-amine

To a solution of /V-(1 -(5-bromothiophen-2-yl)ethyl)-6,7-dimethoxy-2-methylquinazol in-4- amine, 25 mg (0.06 mmol, described in example 209), in 3 mL of 1 ,4-dioxane/water (v:v = 5: 1 ) were added 2-(4-methoxy-2-methylphenyl)-4,4,5,5-tetramethyl-1 ,3,2-dioxaborolane, 30.0 mg (0.1 mmol), sodium carbonate, 25.6 mg (0.2 mmol) and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 4.0 mg (6 μηηοΙ). The resulting mixture was stirred at 100°C for 6 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with water. The resulting mixture was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by preparative HPLC [Column: XBridge Prep C18 OBD, 5 μηη, 19 x 150 mm; Mobile Phase A: water (0.01 % NH4HCO3), Mobile Phase B: acetonitrile; Gradient: 10 % B to 25 % B in 5 min] to give 2.4 mg (9%) of the product as an off-white solid. MS (ESIpos): m/z = 450 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1.49 min. ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 1.70 (d, 3H), 2.34 (s, 3H), 2.43 (s, 3H), 3.75 (s, 3H), 3.87 (s, 6H), 5.93-5.96 (m, 1 H), 6.76-6.79 (m, 1 H), 6.86 (d, 1 H), 6.94-6.95 (m, 1 H), 7.05 (s, 2H), 7.24 (d, 1 H), 7.65 (s, 1 H), 8.13 (d, 1 H).

Example 423

N4-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-2-met hylquinazoline-4,6- diamine

/V-(1 -(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl)-2- m

amine, 1.01 g (2.3 mmol, described in example 421 ), and palladium carbon (10%), 0.24 g (0.2 mmol), were added into 30 ml. of methanol. The resulting mixture was stirred at room temperature for 3 hours under hydrogen atmosphere (3 atm). The catalyst was removed by filtration and the filtrate was concentrated in vacuo to give 0.71 g (54%) of the product as a light yellow solid. MS (ESIpos): m/z = 418 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.76 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .69 (d, 3H), 2.10 (s, 6H), 2.39 (s, 3H), 3.36 (s, 2H), 5.26 (s, 2H), 5.86-5.91 (m, 1 H), 7.09 (d, 1 H), 7.12 (d, 1 H), 7.16-7.18 (m, 2H), 7.26-7.36 (m, 4H), 7.41 -7.43 (m, 1 H), 7.97 (d, 1 H).

Example 424

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-[4-(pyridin-3-ylmet hyl)piperazin-1 - yl]quinazolin-4-amine

Step a:

methyl 2-nitro-5-(4-(pyridin-3-ylmethyl)piperazin-1 -yl)benzoate

This compound was synthesized by the same method as described in example 419 (step b) to give 0.95 g (73%) of the product as a yellow solid. MS (ESIpos): m/z = 357 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .66 min. Step b:

methyl 2-amino-5-(4-(pyridin-3-ylmethyl)piperazin-1 -yl)benzoate

This compound was synthesized by the same method as described in example 419 (step c) to give 1 g (85%) of the product as a grey solid. MS (ESIpos): m/z = 327 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1.42 min. Step c:

2-methyl-6-(4-(pyridin-3-ylmethyl)piperazin-1 -yl)quinazolin-4(3H)-one

This compound was synthesized by the same method as described in example 419 (step d) to give 1.2 mg (84%) of the product as a white solid. MS (ESIpos): m/z = 336 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .55 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 2.29 (s, 3H), 2.54-2.56 (m, 4H), 3.21 -3.24 (m, 4H), 3.58 (s, 2H), 7.36-7.38 (m, 2H), 7.44 (d, 1 H), 7.51 (d, 1 H), 7.75 (d, 1 H), 8.48-8.53 (m, 1 H), 8.54 (s, 1 H).

Step d:

4-chloro-2 -methyl -6-(4-(pyridin-3-ylmethyl)piperazin-1 -yl)quinazoline

This compound was synthesized by the same method as described in example 419 (step e) to give 470 mg (63%) of the product as a white solid. MS (ESIpos): m/z = 355 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.56 min.

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-[4-(pyridin-3-ylmet hyl)piperazin-1 - yl]quinazolin-4-amine

This compound was synthesized by the same method as described in example 419 (step f) to give 160 mg (51 %) of the product as a yellow solid. MS (ESIpos): m/z = 523 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 50%B]: R _t = 1.07 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .67 (d, 3H), 2.42 (s, 3H), 2.56-2.58 (m, 4H), 3.24- 3.25 (m, 4H), 3.60 (s, 2H), 5.78-5.82 (m, 1 H), 6.92 (d, 1 H), 7.07 (d, 1 H), 7.36-7.40 (m, 1 H), 7.47-7.53 (m, 3H), 7.76 (d, 1 H), 8.17 (d, 1 H), 8.48 (d, 1 H), 8.54 (s, 1 H).

Example 425

N4-[1 -(5-bromo-2-thienyl)ethyl]-2-methyl-N6-[2-(morpholin-4-yl)et hyl]quinazoline-4,6- diamine

Step a:

methyl 5-(2-morpholinoethylamino -2-nitrobenzoate

This compound was synthesized by the same method as described in example 419 (step b) to give 1.1 g (70%) of the product as a yellow solid. MS (ESIpos): m/z = 310 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1 .48 min. Step b:

methyl 2-amino-5-(2-morpholinoethylamino)benzoate

This compound was synthesized by the same method as described in example 419 (step c) to give 0.9 g (76%) of the product as a grey solid. MS (ESIpos): m/z = 327 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1.23 min. Step c:

2-methyl-6-(2-morpholinoethylamino)quinazolin-4(3H)-one

This compound was synthesized by the same method as described in example 419 (step d) to give 0.79 g (79%) of the product as a white solid. MS (ESIpos): m/z = 289 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1 .04 min. ¹ H-N MR (400 MHz, DMSO-d ₆ ): δ [ppm] = 2.26 (s, 3H), 2.33-2.36 (m, 4H), 2.53-2.54 (m, 2H), 3.16-3.20 (m, 2H), 3.58-3.61 (m, 4H), 5.91 -5.93 (m, 1 H), 7.02 (s, 1 H), 7.12 (d, 1 H), 7.32 (d, 1 H), 1 1 .85 (s, 1 H).

Step d:

4-chloro-2-methyl-N-(2-morpholinoeth l)quinazolin-6-amine

2-Methyl-6-(2-morpholinoethylamino)quinazolin-4(3H)-one, 300 mg (1 .0 mmol), and N,N- diisopropylethylamine, 2 mL (21 .5 mmol), were dissolved into 10 mL of toluene. The resulting mixture was stirred at 1 10°C for 1 hour under nitrogen atmosphere. After cooling to 80°C, 3.0 mL of phosphorus oxychloride was added dropwise to the above solution and the resulting mixture was stirred at this temperature for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved with dichloromethane. Aq. potassium carbonate solution was added to adjust pH value to 7-8 and the resulting mixture was extracted with dichloromethane. The combined organic layers were dried with anhydrous sodium sulfate and concentrated in vacuo to give 210 mg (39%) of the product as a brown solid. MS (ESIpos): m/z = 307 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.53 min.

Step e:

N4-[1 -(5-bromo-2-thienyl)ethyl]-2-methyl-N6-[2-(morpholin-4-yl)et hyl]quinazoline-4,6- diamine

This compound was synthesized from 1 -(5-bromothiophen-2-yl)ethanamine (described in example INT-28) by the same method as described in example 419 (step f) to give 180 mg (57%) of the product as a yellow solid. MS (ESIpos): m/z = 523 [M+H] ⁺ ; LC-MS [Method 4, starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1.91 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .66 (d, 3H), 2.40 (s, 3H), 2.44-2.46 (m, 4H), 2.57-2.58 (m, 2H), 3.19- 3.22 (m, 2H), 3.58-3.61 (m, 4H), 5.68-5.70 (m, 1 H), 5.77-5.80 (m, 1 H), 6.91 (d, 1 H), 7.02 (s, 1 H), 7.06 (d, 1 H), 7.18 (d, 1 H), 7.36 (d, 1 H), 7.95 (d, 1 H).

Example 426

N-[1 -(5-{2-[(dimethylamino)methyl]phe^

ylmethyl)piperazin-1 -yl]quinazolin-4-amine

This compound was synthesized from N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-[4- (pyridin-3-ylmethyl)piperazin-1 -yl]quinazolin-4-amine (described in example 424) by the same method as described in example 415 to give 8.2 mg (24%) of the product as a yellow solid. MS (ESIpos): m/z = 579 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water (0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 2.13 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .72 (d, 3H), 2.10 (s, 3H), 2.13 (s, 3H), 2.43 (s, 3H), 2.56-2.58 (m, 4H), 3.25-3.26 (m, 4H), 3.32-3.35 (m, 2H), 3.58-3.60 (m, 2H), 5.96-6.00 (m, 1 H), 7.07 (d, 1 H), 7.17 (d, 1 H), 7.29 (d, 2H), 7.32-7.40 (m, 3H), 7.41 -7.52 (m, 3H), 7.52 (d, 1 H), 8.24 (d, 1 H), 8.48 (d, 1 H), 8.54 (d, 1 H). Example 427

N-{2-[(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6- l)amino]ethyl}acetamide

/V4-(1-(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)eth yl)-2-m

diamine, 100 mg (0.24 mmol, described in example 423), and /V-(2-chloroethyl)acetamide, 35 mg (0.29 mmol), were dissolved into 3.0 mL of toluene. The resulting mixture was stirred at 1 10°C for 24 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by preparative HPLC to give 1 1 .4 mg (8%) of the product as an off-white solid. MS (ESIpos): m/z = 503 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 3.56 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 1 .84 (s, 3H), 2.1 1 (s, 6H), 2.41 (s, 3H), 3.17-3.21 (m, 2H), 3.28-3.30 (m, 2H), 3.37 (s, 2H), 5.88-5.96 (m, 2H), 7.07-7.08 (m, 1 H), 7.1 1 -7.14 (m, 2H), 7.17-7.18 (m, 1 H), 7.28-7.32 (m, 2H), 7.34-7.45 (m, 3H), 8.01 -8.04 (m, 2H).

Example 428

N-[1 -(5-bromo-3-chlorothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin-4-amine

Step a:

1 -(5-bromo-3-chloro-2-thienyl)ethanone

To a solution of 1 -(3-chlorothiophen-2-yl)ethanone, 1.00 g (6.2 mmol), in 15 mL of chloroform was added aluminum trichloride, 2.49 g (18.7 mmol), and the resulting mixture was stirred at room temperature for 30 min. Then bromine, 1 .49 g (9.3 mmol), was added to the above solution at 0°C and the resulting mixture was stirred at reflux for 15 hours under nitrogen atmosphere. Saturated sodium sulfite solution was added and the precipitated solid was removed by filtration. The filtrate was extracted with dichloromethane and the combined organic layers were washed water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give 1 .26 g (85%) of the product as a light yellow solid. MS (ESIpos): m/z = 239 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .09 min. ¹ H-NMR (300 MHz, CDCI ₃ ): δ [ppm] = 2.73 (s, 3H), 7.64 (s, 1 H).

Step b:

W-[1 -(5-bromo-3-chloro-2-thienyl)eth lidene]-2-methylpropane-2-sulfinamide

To a solution of 1 -(5-bromo-3-chloro-2-thienyl)ethanone, 1 .26 g (5.3 mmol), in 20 mL of tetrahydrofuran was added 2-methylpropane-2-sulfinamide, 0.83 g (6.8 mmol), and titanium(IV) ethoxide, 2.40 g (10.5 mmol). The resulting mixture was stirred at 75°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with ethyl acetate. Water was added and the precipitated solid was removed by filtration. The filtrate was extracted with ethyl acetate and combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give 1 .4 g (76%) of the product as a brown oil. MS (ESIpos): m/z = 342 [M+H] ⁺ . LC- MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile,10%B]: R _t = 1.21 min.

Step c:

yV-[1 -(5-bromo-3-chloro-2-thienyl)eth l]-2-methylpropane-2-sulfinamide

To a solution of /V-[1 -(5-bromo-3-chloro-2-thienyl)ethylidene]-2-methylpropane-2-s ulfinamide, 1 .40 g (4.1 mmol), in 15 mL of tetrahydrofuran was added sodium borohydride, 0.31 g (8.2 mmol), and the resulting mixture was stirred at room temperature for 30 min. Saturated sodium bicarbonate solution was added and the resulting mixture was stirred vigorously until gas evolution ceased. The resulting mixture was extracted with ethyl acetate and the combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give 1.06 g (75%) of the product as a brown oil. MS (ESIpos): m/z = 344 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 1.12 min.

Step d:

1 -(5-bromo-3-chloro-2-thienyl)ethanamine

To a solution of /V-[1-(5-bromo-3-chloro-2-thienyl)ethyl]-2-methylpropane-2-s ulfinamide, 1.06 g (3.08 mmol), in 10 mL of tetrahydrofuran was added 3 ml. of hydrochloric acid (3.0 M) and the resulting mixture was stirred at room temperature for 1 hour. Sodium hydroxide solution (6.0 M in water) was added to the above solution to adjust the pH value to 8 and the organic solvent was removed in vacuo. The resulting mixture was extracted with dichloromethane and the combined organic layers were washed water, brine, dried over anhydrous sodium sulfate and evaporated in vacuo to give 520 mg (71 %) of the product as a light yellow oil. MS (ESIpos): m/z = 240 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 0.54 min.

Step e:

N-[1 -(5-bromo-3-chlorothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin-4-amine

To a solution of 1 -(5-bromo-3-chloro-2-thienyl)ethanamine, 520 mg (2.2 mmol), in 8 mL of 2- propanol was added 4-chloro-6,7-dimethoxy-2-methylquinazoline, 673 mg (2.8 mmol), and the resulting mixture was stirred at 1 10°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was re- dissolved with dichloromethane. The resulting solution was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (dichloromethane:methanol = 13:1 ) to give 280 mg (29%) of the product as a yellow solid. MS (ESIpos): m/z = 442 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .33 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .64 (d, 3H), 2.36 (s, 3H), 3.87 (s, 3H), 3.91 (s, 3H), 5.79-5.86 (m, 1 H), 7.05 (s, 1 H), 7.69-7.71 (m, 2H), 8.17 (d, 1 H).

Example 429

tert-butyl [2-(4-chloro-5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

ferf-butyl (2-bromobenzyl)carbamate

To a solution of 2-bromophenylmethanamine, 1 .50 g (8.1 mmol), in 15 mL of dichloromethane were added di-ie f-butyl dicarbonate, 2.29 g (10.5 mmol), and triethylamine, 2.45 g (24.2 mmol). The resulting mixture was stirred at room temperature for 5 hours. Upon completion of the reaction, the reaction mixture was washed with water and dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate = 19:1 ) to give 2.08 g (79%) of the product as a light yellow oil. MS (ESIpos): m/z = 286 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 1 .94 min.

Step b:

ieri-butyl [2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

To a solution of terf-butyl (2-bromobenzyl)carbamate, 2.08 g (7.3 mmol), in 25 mL of 1 ,4- dioxane were added 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(1 ,3,2-dioxaborolane), 3.75 g (14.5 mmol), potassium acetate, 1.43 g (14.5 mmol), and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladiumdichloride, 0.59 g (0.7 mmol). The resulting mixture was stirred at 100°C for 15 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with water. The resulting mixture was extracted with ethyl acetate and the combined organic layers were concentrated in vacuo. The residue was purified by silica gel column chromatography (petroleum ethenethyl acetate = 7:3) to give 1 .26 g (52%) of the product as a light yellow oil. MS (ESIpos): m/z = 334 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 1 .35 min.

Step c:

tert-butyl [2-(4-chloro-5-{1 -[(6,7-dimethoxy-2-methylquinazolin

ethyl}thiophen-2-yl)benzyl]carbamate

To a solution of /V-[1 -(5-bromo-3-chloro-2-thienyl)ethyl]-6,7-dimethoxy-2-methylqu inazolin-4- amine, 160 mg (0.36 mmol, described in example 428), in 15 mL of 1 ,4-dioxane/water (v:v = 5:1 ) were added ierf-butyl [2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate, 240 mg (0.72 mmol), potassium carbonate, 150 mg (1.1 mmol) and tetrakis(triphenylphosphine)palladium(0), 42 mg (0.04 mmol). The resulting mixture was stirred at 1 10°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with water. The resulting mixture was extracted with dichloromethane and the combined organic layers were concentrated in vacuo. The residue was purified by silica gel column chromatography (dichloromethane:methanol = 13: 1 ) to give 180 mg (63%) of the product as a light yellow solid. MS (ESIpos): m/z = 569 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .10 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .37 (s, 9H), 1 .71 (d, 3H), 2.41 (s, 3H), 3.89 (s, 3H), 3.93 (s, 3H), 4.01 -4.07 (m, 2H), 5.87-5.91 (m, 1 H), 7.06 (s, 1 H), 7.16 (d, 1 H), 7.27-7.44 (m, 5H), 7.77 (s, 1 H), 8.55 (br, 1 H).

Example 430

N-[1 -{5-[2-(aminomethyl)phenyl]-4-chlorothiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

Step a:

ieri-butyl-2-(3-chloro-5-(1 -(6,7-dimethoxy-2-methylquinazolin-4- ylamino)ethyl)thio hen-2-yl)benzylcarbamate

To a solution of /V-(1 -(5-bromo-4-chlorothiophen-2-yl)ethyl)-6,7-dimethoxy-2- methylquinazolin-4-amine, 100 mg (0.23 mmol described in example 432), in 6.0 ml. of 1 ,4- dioxane/water (v:v =5: 1 ) were added 2-((ie f-butoxycarbonylamino)methyl)phenylboronic acid, 90.7 mg (0.36 mmol), tetrakis(triphenylphosphine)palladium(0), 41 .8 mg (36.1 μιτιοΙ), and potassium carbonate, 199.8 mg (1 .4 mmol). The resulting mixture was stirred at 100°C for 10 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by silica gel column chromatography (dichloromethane/methanol = 10: 1 ) to give 120 mg (58%) of the product as a yellow solid. MS (ESIpos): m/z = 569 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 3.39 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .36 (s, 9H), 1 .71 (d, 3H), 2.43 (s, 3H), 3.87 (s, 3H), 3.88 (s, 3H), 4.05 (d, 2H), 5.88-5.91 (m, 1 H), 7.06 (s, 1 H), 7.14 (s, 1 H), 7.21 (d, 1 H), 7.27-7.35 (m, 3H), 7.42-7.44 (m, 1 H), 7.63 (s, 1 H), 8.16 (d, 1 H).

Step b:

ieri-butyl-2-(3-chloro-5-(1 -(6,7-dimethoxy-2-methylquinazolin-4- ylamino)ethyl)thio hen-2-yl)benzylcarbamate

To a solution of ie f-butyl-2-(3-chloro-5-(1 -(6,7-dimethoxy-2-methylquinazolin-4- ylamino)ethyl)thiophen-2-yl)benzylcarbamate, 50 mg (0.09 mmol), in 1 .0 mL of 1 ,4-dioxane was added 1 .0 mL of hydrochloric acid (4.0 M) at 0°C and the resulting mixture was stirred at room temperature for 6 hours. Saturated sodium carbonate solution was added to adjust the pH value to 7 and the resulting mixture was extracted with ethyl acetate. The combined organic layers were washed with water, brine and concentrated in vacuo. The residue was purified by preparative HPLC [Mobile Phase A: Water (0.1 % NH4HCO3), Mobile Phase B: Acetonitrile; Gradient: 20% B to 45% B in 7 min] to give 27.3 mg (66%) of the product as a white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ ; LC-MS [Method 4, Water(0.05% NH ₄ HC0 ₃ )- Acetonitrile, 10%B]: R _t = 1 .85 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 (d, 3H), 2.43 (s, 3H), 3.60 (s, 2H), 3.87 (s, 3H), 3.88 (s, 3H), 5.87-5.92 (m, 1 H), 7.05 (s, 1 H), 7.12 (s, 1 H), 7.18 (d, 1 H), 7.24 (t, 1 H), 7.42 (t, 1 H), 7.61 -7.63 (m, 2H), 8.16 (d, 1 H).

Example 431

N-[1 -(4-chloro-5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl) ethyl]-6,7-dimethoxy- 2-methylquinazolin-4-amine

To a solution of /V-(1-(5-bromo-4-chlorothiophen-2-yl)ethyl)-6,7-dimethoxy-2- methylquinazolin-4-amine, 50 mg (0.1 1 mmol, described in example 432), in 2.4 mL of 1 ,4- dioxane/water (v:v = 5:1 ) were added 2-((dimethylamino)methyl)phenylboronic acid, 20 mg (0.1 1 mmol), tetrakis(triphenylphosphine)palladium(0), 13 mg (1 1.3 μηηοΙ), and potassium carbonate, 62.4 mg (0.45 mmol). The resulting mixture was stirred at 100°C for 10 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by preparative HPLC [Mobile Phase A: Water (0.1 % HCOOH), Mobile Phase B: Acetonitrile; Gradient: 30% B to 70% B in 8 min] to give 20.3 mg (35%) of the product as a yellow solid. MS (ESIpos): m/z = 497 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 2.15 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 2.02 (s, 6H), 2.43 (s, 3H), 3.26 (s, 2H), 3.88 (s, 3H), 3.89 (s, 3H), 5.84- 5.92 (m, 1 H), 7.06 (s, 1 H), 7.1 1 (s, 1 H), 7.22 (d, 1 H), 7.30 (t, 1 H), 7.41 (t, 1 H), 7.53 (d, 1 H), 7.64 (s, 1 H), 8.15 (d, 1 H).

Example 432

N-[1 -(5-bromo-4-chlorothio hen-2-yl)ethyl]-6 -dimethoxy-2-methylquinazolin-4-amine

Step a:

1 -(5-bromo-4-chlorothiophen-2-yl)ethanone

To a solution of 1 -(4-chlorothiophen-2-yl)ethanone, 1.00 g (6.2 mmol), in 15 mL of chloroform was added aluminum trichloride, 2.49 g (18.7 mmol). Then bromine, 1 .49 g (9.3 mmol), was added dropwise to the above solution at 0°C and the reaction mixture was stirred at 60°C for 1 hour. After cooling to room temperature, saturated sodium sulfite solution was added and the resulting mixture was extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give 1.28 g (69%) of the product as a light yellow oil. MS (ESIpos): m/z = 238 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.15 min.

Step b:

W-(1 -(5-bromo-4-chlorothiophen-2-yl)ethylidene)-2-methylpropane- 2-sulfinamide

To a solution of 1-(5-bromo-4-chlorothiophen-2-yl)ethanone, 600 mg (2.5 mmol), in 10 mL of tetrahydrofuran were added 2-methylpropane-2-sulfinamide, 395 mg (3.3 mmol), and titanium(IV) ethoxide, 1 143 mg (5.0 mmol). The resulting mixture was stirred at 75°C for 15 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved with ethyl acetate. Water was added and the precipitated solid was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 0.72 g (83%) of the product as a yellow oil. MS (ESIpos): m/z = 342 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.28 min.

Step c:

W-(-1 -(5-bromo-4-chlorothiophen-2- l)ethyl)-2-methylpropane-2-sulfinamide

To a solution of /V-(1 -(5-bromo-4-chlorothiophen-2-yl)ethylidene)-2-methylpropane- 2- sulfinamide, 720 mg (2.08 mmol), in 10 mL of tetrahydrofuran was added sodium borohydride, 199 mg (5.3 mmol), and the resulting mixture was stirred at this temperature for 5 hours. Saturated sodium bicarbonate solution was added and the resulting mixture was stirred vigorously until gas evolution ceased. The resulting mixture was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 740 mg (82%) of the product as a yellow oil. MS (ESIpos): m/z = 344 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1 .17 min.

Step d:

1 -(5-bromo-4-chlorothiophen-2-yl)ethanamine

To a solution of /V-(1 -(5-bromo-4-chlorothiophen-2-yl)ethyl)-2-methylpropane-2-sul finamide, 200 mg (0.6 mmol), in 5 mL of tetrahydrofuran was added 0.5 mL of hydrochloric acid (3.0 M) and the resulting mixture was stirred at room temperature for 1 hour. Sodium hydroxide solution (6M) was added to adjust the pH value to 7-8 and the resulting mixture was concentrated under vacuum. The residue was purified by silica gel column chromatography (dichloromethane:methanol = 8:1 ) to give 100 mg (52%) of the product as a yellow oil. MS (ESIpos): m/z = 240 [M+H] ⁺ ; LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.72 min.

Step e:

N-[1 -(5-bromo-4-chlorothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methy lquinazolin-4-amine

To a solution of 4-chloro-6,7-dimethoxy-2-methylquinazoline, 100 mg (0.4 mmol), in 2.0 mL of 2-propanol was added 1-(5-bromo-4-chlorothiophen-2-yl)ethanamine, 100.8 mg (0.4 mmol) and the resulting mixture was stirred at 1 10°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by silica gel column chromatography (dichloromethane/methanol = 13:1 ) to give 100 mg (53%) of the product as a yellow solid. MS (ESIpos): m/z = 442 [M+H] ⁺ ; LC- MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 2.1 1 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.68 (d, 3H), 2.44 (s, 3H), 3.88 (s, 6H), 5.74-5.77 (m, 1 H), 7.07 (s, 1 H), 7.12 (s, 1 H), 7.61 (s, 1 H), 8.1 1 (d, 1 H).

Example 433

N4-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-2-met hyl-N6-[2-(morpholin 4-yl)ethyl]quinazoline-4,6-diamine

This compound was synthesized by the same method as described in example 415 to give 14.4 mg (40%) of the product as a yellow solid. MS (ESIpos): m/z = 531 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 2.03 min. ¹ H-N MR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 (d, 3H), 2.10 (s, 6H), 2.33 (s, 3H), 2.40-2.44 (m, 4H), 2.55-2.59 (m, 2H), 3.20-3.23 (m, 2H), 3.25-3.36 (m, 2H), 3.58-3.59 (m, 4H), 5.66- 5.69 (m, 1 H), 5.94-5.98 (m, 1 H), 7.07 (d, 2H), 7.17 (d, 2H), 7.26-7.36 (m, 4H), 7.42 (d, 1 H), 8.02 (d, 1 H).

Example 434

4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2-methylquinazolin-6-yl) -1 - methylpiperazin-2-one

Step a:

methyl 5-(4-methyl-3-oxopiperazin-1 -yl)-2-nitrobenzoate

This compound was synthesized by the same method as described in example 419 (step b) to give 0.9 g (71 %) of the product as a yellow solid. MS (ESIpos): m/z = 294 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.1 %HCOOH)-Acetonitrile, 5%B)]: R _t = 0.99 min. Step b:

methyl 2-amino-5-(4-methyl-3-oxopiperazin-1 -yl)benzoate

This compound was synthesized by the same method as described in example 419 (step c) to give 0.76 g (91 %) of the product as a grey solid. MS (ESIpos) : m/z = 264 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1 .16 min. Step c: 2-methyl-6-(4-methyl-3-oxopiperazin-1 -yl)quinazolin-4(3H)-one

This compound was synthesized by the same method as described in example 419 (step d) to give 470 mg (60%) of the product as a light yellow solid. MS (ESIpos): m/z = 273 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.62 min. ¹ H-NMR (300 MHz, DMSO-d ₆ ): δ [ppm] = 2.30 (s, 3H), 2.91 (s, 3H), 3.43-3.50 (m, 2H), 3.56- 3.60 (m, 2H), 3.84 (s, 2H), 7.35 (s, 1 H), 7.50 (d, 2H), 12.04 (s, 1 H).

Step d:

4-(4-chloro-2-methylquinazolin-6-yl)-1 -methylpiperazin-2-one

This compound was synthesized by the same method as described in example 425 (step d) to give 100 mg (76%) of the product as a brown solid. MS (ESIpos): m/z = 291 [M+H] ⁺ ; LC- MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 1.03 min.

Step e:

4-(4-(1 -(5-bromothiophen-2-yl)ethylamino)-2-methylquinazolin-6-yl)- 1 -methylpiperazin- 2-one

This compound was synthesized from 1 -(5-bromothiophen-2-yl)ethanamine (described in example INT-28) by the same method as described in example 419 (step f) to give 180 mg (57%) of the product as a yellow solid. MS (ESIpos) : m/z = 461 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(5 mM NH ₄ HC03)-Acetonitrile, 10%B)]: R _t = 1 .85 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm]= 1.67 (d, 3H), 2.33 (s, 3H), 2.96 (s, 3H), 3.47-3.49 (m, 2H), 3.58-3.61 (m, 2H), 3.87-3.89 (m, 2H), 5.80-5.83 (m, 1 H), 6.92 (d, 1 H), 7.07 (d, 1 H), 7.43 (s, 1 H), 7.52 (d, 1 H), 7.58 (d, 1 H), 8.27 (d, 1 H). Example 435

4-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6- l)-1 -methylpiperazin-2-one

This compound was synthesized from 4-(4-(1 -(5-bromothiophen-2-yl)ethylamino)-2- methylquinazolin-6-yl)-1-methylpiperazin-2-one (described in example 434) by the same method as described in example 415 to give 3.3 mg (5%) of the product as a yellow solid. MS (ESIpos): m/z = 516 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .95 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .74 (d, 3H), 2.08(s, 3H), 2.12(s, 3H), 2.44 (s, 3H), 2.67 (s, 3H), 3.35-3.37 (m, 2H), 3.47-3.49 (m, 2H), 3.58-3.60 (m, 2H), 3.88-3.90 (m, 2H), 5.98-6.02 (m, 1 H), 7.09 (d, 1 H), 7.18 (d, 1 H), 7.31 (d, 2H), 7.36-7.38 (m, 1 H), 7.43 (d, 1 H), 7.50-7.51 (m, 1 H), 7.52 (s, 1 H), 7.59 (d, 1 H), 8.38 (d, 1 H).

Example 436

methyl 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]-2-methylpropanoate

To a solution of methyl 2-(2-bromophenyl)acetate, 5.00 g (21.8 mmol), in 100 ml. of tetrahydrofuran were added 18-crown-6, 1.44 g (5.5 mmol), iodomethane, 7.35 g (65.5 mmol), and potassium ie f-butoxide, 15.49 g (109.1 mmol). The resulting mixture was stirred at this temperature for 26 hours. The solvent was removed in vacuo and the residue was diluted with ethyl acetate. The resulting solution was washed with water, brine, dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate = 6:1 ) to give 2.73 g (49%) of the product as a yellow oil. MS (ESIpos): m/z = 257 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 1 .14 min.

Step b:

methyl 2-[2-(5-acetyl-2-thienyl)phenyl]-2-methylpropanoate

To a solution of methyl 2-(2-bromophenyl)-2-methylpropanoate, 2.50 g (7.4 mmmol), in 24 ml. of 1 ,4-dioxane/water (v:v = 5:1 ) were added 5-acetylthiophen-2-ylboronic acid, 1.26 g (7.4 mmol), 1 ,1 '-bis(diphenylphosphino)ferrocenepalladiumdichloride CH2CI2, 0.60 g (0.7 mmol), and sodium carbonate, 1 .57 g (14.8 mmol). The resulting mixture was stirred at 100°C for 22 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with ethyl acetate. The resulting solution was washed water and concentrated in vacuo. The residue was purified by silica gel column chromatography (petroleum ether:ethyl acetate = 7:1 ) to give 400 mg (17%) of the product as a light yellow solid. MS (ESIpos): m/z = 303 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 1 .15 min.

Step c:

methyl 2-(2-{5-[yV-(feri-butylsulfinyl)ethanimidoyl]-2-thienyl}phen yl)-2- methylpropanoate

To a solution of methyl 2-[2-(5-acetyl-2-thienyl)phenyl]-2-methylpropanoate, 400 mg (1.33 mmol), in 10 mL of tetrahydrofuran were added 2-methylpropane-2-sulfinamide, 21 1 mg (1 .73 mmol), and titanium(IV) ethoxide, 610 mg (2.7 mmol). The resulting mixture was stirred at 75°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with ethyl acetate. Water was added and the solid was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 500 mg (93%) of the product as a brown oil. MS (ESIpos): m/z = 406 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 2.25 min. Step d:

methyl (2-{5-[1 -{[tert-butylsulfinyl]amino}ethyl]-2-thienyl}phenyl)-2-methy lpropanoate

To a solution of methyl 2-(2-{5-[/V-(ie f-butylsulfinyl)ethanimidoyl]-2-thienyl}phenyl)-2- methylpropanoate, 500 mg (1 .5 mmol), in 10 mL of tetrahydrofuran was added sodium borohydride, 115 mg (3.0 mmol), and the resulting mixture was stirred at room temperature for 5 hours. Saturated sodium bicarbonate was added and the resulting mixture was stirred vigorously until gas evolution ceased. The resulting mixture was extracted with ethyl acetate and the combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo to give 455 mg (74%) of the product as a brown oil. MS (ESIpos): m/z = 408 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 2.03 min.

Step e:

methyl 2-{2-[5-(1 -aminoethyl)-2-thien l]phenyl}-2 -methylpropanoate

To a solution of methyl (2-{5-[1-{ie f-butylsulfinyl]amino}ethyl]-2-thienyl}phenyl)-2- methylpropanoate, 455 mg (1.11 mmol), in 10 mL of tetrahydrofuran was added 2.0 mL of hydrochloric acid (3.0 M) at 0°C and the resulting mixture was stirred at room temperature for 1 hour. Sodium hydroxide solution (6.0 M) was added to adjust the pH value to 8 and the organic solvent was removed in vacuo. The resulting mixture was extracted with dichloromethane and the combined organic layers were washed with water, brine, dried over anhydrous sodium sulfate and evaporated to dryness to give 240 mg (71 %) of the product as a light yellow solid. MS (ESIpos): m/z = 304 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 0.77 min.

Step f:

methyl 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)phenyl]-2-meth lpropanoate

To a solution of methyl 2-{2-[5-(1 -aminoethyl)-2-thienyl]phenyl}-2-methylpropanoate, 240 mg (0.8 mmol), in 6.0 mL of 2-propanol was added 4-chloro-6,7-dimethoxy-2-methylquinazoline, 189 mg (0.8 mmol), and the resulting mixture was stirred at 110°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was diluted with dichloromethane. The resulting solution was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by silica gel column chromatography (dichloromethane:methanol = 13: 1 ) to give 300 mg (60%) of the product as a yellow solid. MS (ESIpos): m/z = 506 [M+H] ⁺ . LC-MS [Water Method 4, (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .45 min. ¹ H-NMR (400 MHz, DMSO- d ₆ ): δ [ppm] = 1 .44 (s, 6H), 1 .71 (d, 3H), 2.42 (s, 3H), 3.26 (s, 3H), 3.87 (s, 6H), 5.90-5.96 (m, 1 H), 6.70 (s, 1 H), 6.95 (s, 1 H), 7.04 (s, 1 H), 7.13 (d, 1 H), 7.25 (t, 1 H), 7.38 (t, 1 H), 7.51 (d, 1 H), 7.65 (s, 1 H), 8.12 (d, 1 H).

Example 437

N-[1 -{5-[2-(aminomethyl)phenyl]-3-chlorothiophen-2-yl}ethyl]-6,7 -dimethoxy-2- methylquinazolin-4-amine

To a solution of ierf-butyl [2-(4-chloro-5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}-2-thienyl)benzyl]carbamate, 80 mg (0.14 mmol, described in example 429), in 3.0 mL of 1 ,4-dioxane was added 3.0 mL of hydrochloric acid (4.0 M), and the resulting mixture was stirred at room temperature for 6 hours. Saturated sodium carbonate solution was added to adjust the pH value to 7 and the resulting mixture was extracted with ethyl acetate. The combined organic layers were washed with water and concentrated in vacuo. The residue was purified by preparative HPLC [Mobile Phase A: Water (0.1 % NH4HCO3), Mobile Phase B: Acetonitrile; Gradient: 25% B to 50% B in 7 min] to give 19.6 mg (28%) of the product as an off-white solid. MS (ESIpos): m/z = 469 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1.82 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .69 (d, 3H), 2.50 (s, 3H), 3.66-3.74 (m, 2H), 3.92 (s, 3H), 3.95 (s, 3H), 5.84-5.91 (m, 1 H), 7.05 (s, 1 H), 7.19 (d, 1 H), 7.33-7.37 (m, 1 H), 7.41 -7.46 (m, 2H), 7.60 (d, 1 H), 7.72 (s, 1 H), 8.19 (d, 1 H), 8.25 (s, 1 H).

Example 438

N-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6-yl)methanesulfonamide

Step a:

N-(4-(1 -(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethylamin o)-2- methylquinazolin-6-yl)-N-(methylsulfonyl)methanesulfonamide

/V4-(1 -(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethyl^^

diamine, 100 mg (0.24 mmol, described in example 423), and triethylamine, 121 mg (1 .2 mmol), were dissolved into 3.0 mL of dichloromethane. Then methanesulfonyl chloride, 82 mg (0.72 mmol), was added dropwise to the above solution at 0°C and the resulting mixture was stirred at room temperature for 2 hours. The solvent was removed in vacuo to give 140 mg (crude) of the product as a yellow solid and it was used directly for next step without further purification. MS (ESIpos): m/z = 574 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.78 min.

Step b:

N-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6-yl methanesulfonamide

To a solution of /V-(4-(1 -(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)ethylamin o)-2- methylquinazolin-6-yl)-N-(methylsulfonyl)methanesulfonamide, 140 mg (0.24 mmol), in 2.0 mL of tetrahydrofuran was added sodium hydroxide solution, 30 mg (0.73 mmol) (in 2.0 mL of water). The resulting mixture was stirred at room temperature for 3 hours. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give 36.0 mg (29%) of the product as a light yellow solid. MS (ESIpos): m/z = 496 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 1 .86 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .73 (d, 3H), 2.10 (s, 6H), 2.47 (s, 3H), 3.05 (s, 3H), 3.36 (s, 2H), 5.95-5.98 (m, 1 H), 7.09 (d, 1 H), 7.18 (d, 1 H), 7.27-7.43 (m, 4H), 7.54 (d, 1 H), 7.61 (d, 1 H), 8.01 (s, 1 H), 8.57 (d, 1 H), 9.78 (br, 1 H).

Example 439

N-[1 -(5-{2-[(dimethylamino)methyl]-4-methoxyphenyl}thiophen-2-yl )ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

(2-Bromo-5-methoxyphenyl)-/V, /V-dimethylmethanamine, 200 mg (0.8 mmol), 5- acetylthiophen-2-ylboronic acid, 279 mg (1 .6 mmol), sodium carbonate, 347 mg (3.3 mmol) and 1 , 1 '-bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 60 mg (0.08 mmol), were added into 6.0 mL of 1 ,4-dioxane/H20 (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 48 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified with silica gel column chromatography to give 60 mg (22%) of the product as a brown solid. MS (ESIpos): m/z = 290 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.77 min.

Step b:

-(5-(2 -((d i methy I am i no)methy I ) -4-m

methylpropane-2-sulfinamide

1-(5-(2-((Dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-y l)ethanone, 80 mg (0.28 mmol), was dissolved into 3.0 mL of tetrahydrofuran. 2-methylpropane-2-sulfinamide, 44 mg (0.36 mmol), and titanium(IV) ethoxide, 252 mg (1.11 mmol), were added successively. The resulting mixture was stirred at 70°C for 36 hours under nitrogen atmosphere. Sodium chloride solution was added and the precipitated solid was removed by filtration. The filtrate was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo and the residue was purified with silica gel column chromatography to give 50 mg (44%) of the product as a brown solid. MS (ESIpos): m/z = 393 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)- Acetonitrile, 5%B]: R _t = 0.86 min.

Step c:

W-(1 -(5-(2-((dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-yl )ethyl)-2- methylpropane-2-sulfinamide

/V-(1 -(5-(2-((dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-yl )ethylidene)-2- methylpropane-2-sulfinamide, 50.0 mg (0.13 mmol), was dissolved into 3.0 mL of tetrahydrofuran. Sodium borohydride, 9.6 mg (0.26 mmol), was added successively to the above solution and the resulting mixture was stirred at room temperature for 2 hours. Water was added and the resulting solution was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate. The solvent was removed in vacuo to give 50.0 mg (crude) of the product as a yellow solid and it was used directly for next step without further purification. MS (ESIpos): m/z = 395 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.88 min.

Step d:

(1 -(5-(2-((dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-yl )ethanamine

/V-(1 -(5-(2-((dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-yl )ethyl)-2-methylpropane- 2-sulfinamide, 50.0 mg (0.13 mmol), was dissolved in 3.0 mL of tetrahydrofuran and 1 .0 mL of hydrochloric acid/1 ,4-dioxane (4.0 M). The resulting mixture was stirred at room temperature for 2 hours. The solvent was removed in vacuo and saturated aqueous sodium carbonate was added to adjust the pH value to 8. The resulting mixture was extracted with dichloromethane and the combined organic layers were dried over anhydrous sodium sulfate. The residue was purified with silica gel column chromatography to give 40 mg (84%) of the product as a light yellow solid. MS (ESIpos): m/z = 291 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO3)-Acetonitrile, 5%B]: R _t = 1 .62 min.

Step e:

N-[1 -(5-{2-[(dimethylamino)methyl]-4-methoxyphenyl}thiophen-2-yl )ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

(1 -(5-(2-((Dimethylamino)methyl)-4-methoxyphenyl)thiophen-2-yl )ethanamine, 40 mg (0.14 mmol), and 4-chloro-6,7-dimethoxy-2-methylquinazoline, 33 mg (0.14 mmol, commercially available), were dissolved into 3.0 mL of 2-propanol. The resulting mixture was stirred at 1 10°C for 10 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by preparative HPLC to give 0.9 mg of the product as a light yellow solid. MS (ESIpos): m/z = 493 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 5%B]: R _t = 2.08 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 (d, 3H), 2.1 1 (s, 6H), 2.43 (s, 3H), 3.34 (s, 2H), 3.76 (s, 3H), 3.87 (s, 6H), 5.90- 6.00 (m, 1 H), 6.85-6.87 (m, 1 H), 7.00-7.05 (m, 4H), 7.28 (d, 1 H), 7.65 (s, 1 H), 8.14 (d, 1 H).

Example 440

3-(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6-yl)-1 ,1 -dimethylurea

/V4-(1-(5-(2-((dimethylamino)methyl)phenyl)thiophen-2-yl)eth yl^

diamine, 100 mg (0.24 mmol, described in example 423), and triethylamine, 121 mg (1 .20 mmol), were dissolved into 3.0 mL of dichloromethane. Then dimethylcarbamic chloride, 129 mg (1 .20 mmol), was added dropwise to the above solution at 0°C and the resulting mixture was stirred at room temperature for 36 hours. The solvent was removed in vacuo and the residue was purified by preparative HPLC to give 18.9 mg (14%) of the product as a light yellow solid. MS (ESIpos): m/z = 489 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 1 .93 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .64 (d, 3H), 2.04 (s, 6H), 2.38 (s, 3H), 2.88 (s, 6H), 3.29 (s, 2H), 5.85-5.89 (m, 1 H), 7.00 (d, 1 H), 7.10 (d, 1 H), 7.19-7.26 (m, 2H), 7.29 (d, 1 H), 7.35 (d, 1 H), 7.44 (d, 1 H), 7.63 (d, 1 H), 8.13-8.17 (m, 3H), 8.30 (d, 1 H), 8.43 (s, 1 H).

Example 441

1 -benzyl -4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2-methylquinazolin-6- yl)piperazin-2-one

Step a:

methyl 5-fluoro-2-nitrobenzoate

To a solution of 5-fluoro-2-nitrobenzoic acid, 4 g (21 .6 mmol), in 40 mL of methanol was added 8.0 mL of sulfuric acid at 0°C and the resulting mixture was stirred at 60°C for 16 hours. After cooling to room temperature, aqueous potassium carbonate solution was added to adjust the pH value to 8 and the organic solvent was removed in vacuo. The resulting solution was extracted with ethyl acetate and the combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give 3.6 g (82%) of the product as a red oil. MS (ESIpos): m/z = 200 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 10%B]: R _t = 1 .01 min.

Step b:

methyl 5-(4-benzyl-3-oxopiperazin-1 -yl)-2-nitrobenzoate

To a solution of methyl 5-fluoro-2-nitrobenzoate, 0.8 g (4.0 mmol), in 10 mL of N,N- dimethylformamide was added 1 -benzylpiperazin-2-one, 1.53 g (8.0 mmol), and potassium carbonate, 1 .1 1 g (8.0 mmol). The resulting mixture was stirred at reflux for 4 hours. After cooling to room temperature, water was added and the resulting solution was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give 1 .2 g (81 %) of the product as a yellow solid. MS (ESIpos): m/z = 370 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 10%B]: R _t = 1 .77 min.

Step c:

methyl 2-amino-5-(4-benzyl-3-oxopiperazin-1 -yl)benzoate

To a solution of methyl 5-(4-benzyl-3-oxopiperazin-1 -yl)-2-nitrobenzoate, 1 .20 g (3.2 mmol), in 20 mL of methanol was added palladium/carbon (10%), 0.34 g (0.3 mmol), and the resulting mixture was stirred at room temperature for 3 hours under hydrogen atmosphere (2 atm). The catalyst was removed by filtration and the filtrate was concentrated in vacuo to give 0.8 g (67%) of the product as a grey solid. MS (ESIpos): m/z = 340 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 1 .64 min. Step d: 6-(4-benzyl-3-oxopiperazin-1 -yl)-2-methylquinazolin-4(3H)-one

Dry hydrochloric acid gas was passed (until the clear solution observed) to a solution of methyl 2-amino-5-(4-benzyl-3-oxopiperazin-1 -yl)benzoate, 0.8 g (2.4 mmol), in 20 mL of acetonitrile for 3 hours at room temperature. Then the resulting mixture was stirred at reflux for 10 hours and attained to room temperature. The precipitated solid was collected by filtration and the filter cake was dissolved with water. The resulting solution was neutralized with aqueous sodium bicarbonate solution (10%) and the precipitated solid was collected by filtration. The filter cake was washed with ice cold water and dried in air to give 0.68 g (79%) of the product as a white solid. MS (ESIpos): m/z = 349 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 2.02 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 2.30 (s, 3H), 3.36-3.38 (m, 2H), 3.56-3.59 (m, 2H), 3.97 (s, 2H), 4.61 (s, 2H), 7.26-7.29 (m, 3H), 7.32-7.37 (m, 3H), 7.46-7.53 (m, 2H), 12.04 (br, 1 H).

Step e:

1 -benzyl -4-(4-chloro-2-methylquinazolin-6-yl)piperazin-2 -one

To a solution of 6-(4-benzyl-3-oxopiperazin-1 -yl)-2-methylquinazolin-4(3H)-one, 300 mg (0.9 mmol), in 12 mL of toluene was added Λ/,/V-diisopropylethylamine, 0.6 mL (3.4 mmol), and the resulting mixture was stirred at 1 10°C for 1 hour. Then 1 .8 mL of phosphorus oxychloride was added to the above solution at 80°C and the resulting mixture was stirred at this temperature for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was dissolved in 10 mL of dichloromethane. Saturated potassium carbonate solution was added to adjust the pH value to 7-8 and the resulting mixture was extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo to give 240 mg (55%) of the product as a brown solid. MS (ESIpos): m/z = 367 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 1 .03 min.

Step f:

1 -benzyl -4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2-methylquinazolin-6- yl)piperazin-2-one

To a solution of 1 -benzyl-4-(4-chloro-2-methylquinazolin-6-yl)piperazin-2-one, 200 mg (0.7 mmol), in 4.0 mL of 2-propanol was added 1 -(5-bromothiophen-2-yl)ethanamine, 134 mg (0.7 mmol). The resulting mixture was stirred at 1 10°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was purified by silica gel column chromatography (dichloromethane:methanol = 13:1 ) to give 120 mg (41 %) of the product as a yellow solid. MS (ESIpos): m/z = 537 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 2.16 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .68 (d, 3H), 2.44 (s, 3H), 3.39-3.42 (m, 2H), 3.57-3.60 (m, 2H), 4.01 (s, 2H), 4.63 (s, 2H), 5.78-5.85 (m, 1 H), 6.92-6.93 (m, 1 H), 7.07-7.08 (m, 1 H), 7.28- 7.30 (m, 3H), 7.34-7.37 (m, 2H), 7.46-7.47 (m, 1 H), 7.51 -7.58 (m, 2H), 8.30 (br, 1 H).

Example 442

N-[1 -(5-{2-[(dimethylamino)methyl]-4-methy^

2-methylquinazolin-4-amine

N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-6,7-dimethoxy-2- methylquinazolin-4-amine, 20.0 mg (0.04 mmol, described in example 384), methylboronic acid, 6.6 mg (0.1 mmol), sodium carbonate, 15.7 mg (0.1 mmol) and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 2.2 mg (0.004 mmol), were added into 1 .2 mL of 1 ,4-dioxane/H20 (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 12 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 12.3 mg (69%) of the product as an off-white solid. MS (ESIpos): m/z = 477 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: R _t = 3.25 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .71 (d, 3H), 2.10 (s, 6H), 2.31 (s, 3H), 2.43 (s, 3H), 3.33 (s, 2H), 3.87 (s, 6H), 5.94- 5.97 (m, 1 H), 7.05-7.13 (m, 4H), 7.24-7.26 (m, 2H), 7.65 (s, 1 H), 8.14 (d, 1 H).

Example 443

N-[1 -(5-{4-cyclopropyl-2-[(dimethylamino)methyl]phenyl}thiophen- 2-yl)ethyl]-6,7- dimethoxy-2-methylquinazolin-4-amine

N-(1 -(5-(4-bromo-2-((dimethylamino)methyl)phenyl)thiophen-2-yl)e thyl)-6,7-dimethoxy-2- methylquinazolin-4-amine, 20.0 mg (0.04 mmol, described in example 384), cyclopropylboronic acid, 9.5 mg (0.1 mmol), sodium carbonate, 15.7 mg (0.1 mmol) and 1 ,1 '- bis(diphenylphosphino)ferrocenepalladium(ll) chloride, 2.2 mg (0.004 mmol), were added into 1 .2 mL of 1 ,4-dioxane/H20 (v:v = 5:1 ). The resulting mixture was stirred at 100°C for 12 hours under nitrogen atmosphere. After cooling to room temperature, water was added and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified by preparative HPLC to give 12.5 mg (67%) of the product as an off-white solid. MS (ESIpos): m/z = 503 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%NH ₄ HCO ₃ )-Acetonitrile, 10%B]: Rt = 3.45 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 0.65-0.66 (m, 2H), 0.95-0.96 (m, 2H), 1 .71 (d, 3H), 1 .89-1 .96 (m, 1 H), 2.10 (s, 6H), 2.43 (s, 3H), 3.32 (s, 2H), 3.87 (s, 6H), 5.93-5.97 (m, 1 H), 6.95 (d, 1 H), 7.04-7.05 (m, 2H), 7.1 1 (s, 1 H), 7.12 (s, 1 H), 7.23 (d, 1 H), 7.65 (s, 1 H), 8.13 (d, 1 H).

Example 444

N-[1 -(2-methyl-1 ,3-thiazol-4-yl)ethyl]quinazolin-4-amine

Step a:

1 -(2-methyl-1 ,3-thiazol-4-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 2-methyl-1 ,3-thiazole-4-carbaldehyde (commercially available, 1.00 g, 7.86 mmol) to give 300 mg of the title compound.

Step b:

N-[1 -(2-methyl-1 ,3-thiazol-4-yl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (50.0 mg, 209 μηηοΙ, commercially available), 1 -(2-methyl-1 ,3-thiazol-4-yl)ethanamine (32.8 mg, 230 μηηοΙ), N,N-diisopropylethylamine (93 μΙ_, 540 μmol) and DMSO (1 .5 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a white solid (24.1 mg, 33%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.08 (br d, 1 H), 7.71 (s, 1 H), 7.25 (d, 1 H), 7.03 (s, 1 H), 5.77 (quin, 1 H), 3.88 (s, 3H), 3.87 (s, 3H), 2.64 (s, 3H), 2.39 (s, 3H), 1.60 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 345, R _t = 0.68 min.

Example 445

6 -dimethoxy-2-methyl-N-[1 -(4-methyl-1 ,3-thiazol-2-yl)ethyl]quinazolin-4-amine

Step a:

1 -(4-methyl-1 ,3-thiazol-2-yl)ethanamine

The title compound was prepared in analogy to 1 -(5-bromothiophen-2-yl)ethanamine (INT- 28) from 4-methyl-1 ,3-thiazole-2-carbaldehyde (commercially available, 1.00 g, 7.86 mmol) to give 530 mg of the title compound.

Step b:

6 -dimethoxy-2-methyl-N-[1 -(4-methyl-1 ,3-thiazol-2-yl)ethyl]quinazolin-4-amine

To a microwave vial were added 4-chloro-6,7-dimethoxy-2-methylquinazoline (50.0 mg, 209 μηηοΙ, commercially available), 1 -(4-methyl-1 ,3-thiazol-2-yl)ethanamine (32.8 mg, 230 μηηοΙ), N,N-diisopropylethylamine (93 μΙ_, 540 μmol) and DMSO (1 .5 ml_). The reaction mixture was heated to 130°C during 2 hours in the microwave. Purification by preparative HPLC (acidic conditions) gave the title compound as a light yellow solid (19.8 mg, 27%). ¹ H-NMR (400 MHz, DMSO-de): δ [ppm] = 8.32 (br d, 1 H), 7.69 (s, 1 H), 7.10 (d, 1 H), 7.07 (s, 1 H), 5.90 (quin, 1 H), 3.88 (d, 6H), 2.40 (s, 3H), 2.35 (d, 3H), 1 .71 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 345, R _t = 0.67 min.

Example 446

3-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophen-2-yl )-1 -methyl- 1 H-pyrazole-5-carboxylic acid

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (20.0 mg, 49.0 μηιοΙ, described in example 209), methyl 1 -methyl-3-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)-1 H-pyrazole-5-carboxylate (13.0 mg, 49.0 μηηοΙ), K ₂ C0 ₃ (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in 1 ,4-dioxane (500 μΙ_) and H ₂ 0 (100 μΙ_) were stirred at 1 10°C overnight. Brine was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (1 .40 mg, 6%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.20 (br d, 1 H), 7.66 (s, 1 H), 7.31 (d, 1 H), 7.08 (s, 1 H), 7.07 (s, 1 H), 7.02 (dd, 1 H), 5.92 (quin, 1 H), 4.03 (s, 3H), 3.88 (s, 3H), 3.88 (s, 3H), 2.44 (s, 3H), 1.70 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 454, R _t = 0.73 min.

Example 447

tert-butyl [(5'-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2,2'-bithiop hen- 5-yl)methyl]carbamate

Under argon, N-[1 -(5-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (20.0 mg, 49.0 μηιοΙ, described in example 209), (5-{[(tert- butoxycarbonyl)amino]methyl}thiophen-2-yl)boronic acid (12.6 mg, 49.0 μηηοΙ), K2CO3 (27.1 mg, 196 μηιοΙ) and Pd(PPh ₃ ) ₄ (2.83 mg, 2.45 μηιοΙ) in 1 ,4-dioxane (500 μΙ_) and H ₂ 0 (100 μί) were stirred at 1 10°C overnight. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a light yellow solid (1 1.1 mg, 41 %). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.12 (d, 1 H), 7.64 (s, 1 H), 7.50 (t, 1 H), 7.07 (d, 1 H), 7.06 (s, 1 H), 7.03-7.00 (m, 2H), 6.82 (d, 1 H), 5.89 (quin, 1 H), 4.22 (br d, 2H), 3.88 (s, 6H), 2.43 (s, 3H), 1 .69 (d, 3H), 1 .39 (s, 9H). LC- MS (Method 9): m/z: [M+H] ⁺ = 541 , R _t = 1 .09 min. Example 448

7-methoxy-2-methyl-6-[2-(methylsulfonyl)ethoxy]-N-{(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}quinazolin-4-amine

This compound was synthesized from 7-methoxy-2-methyl-4-({(1 R)-1 -[3-(1 H-pyrazol-4- yl)phenyl]ethyl}amino)quinazolin-6-ol (described in example 345) by the same method as described in example 355 to give 9.9 mg of the product as a brown solid. MS (ESIpos): m/z = 482 [M+H] ⁺ . LC-MS [Method 4, gradient starting with water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .04 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ) : δ [ppm] = 1 .23 (s, 3H), 1 .56-1 .58 (d, 3H), 2.34 (s, 3H), 2.87 (s, 3H), 3.73 (m, 2H), 3.90 (s, 3H), 4.55-4.58 (m, 2H), 5.58-5.61 (m, 1 H), 7.01 (s, 1 H), 7.28-7.31 (d, 2H), 7.39-7.40 (d, 1 H), 7.65-7.66 (d, 2H), 7.82-7.84 (d, 1 H), 7.92 (s, 1 H), 8.23 (s, 1 H), 9.20 (br, 1 H).

Example 449

tert-butyl [5-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-2-yl)benzyl]carbamate

Step a:

1 -(2-bromo-5-chlorophenyl)methanamine

This compound was synthesized by the same method as described in example 408 (step a) to give 1 .17 g (38%) of the product as the light yellow oil. MS (ESIpos): m/z = 220 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: R _t = 0.34 min.

Step b:

ferf-butyl (2-bromo-5-chlorobenzyl)carbamate

This compound was synthesized by the same method as described in example 429 (step a) to give 360 mg (21 %) of the product as a light yellow solid. MS (ESIpos): m/z = 320 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: Rt = 2.16 min.

Step c:

ieri-butyl[5-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

C H -

This compound was synthesized by the same method as described in example 429 (step b) to give 190 mg (46%) of the product as a light yellow oil. MS (ESIpos): m/z = 368 [M+H] ⁺ . LC- MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .34 min.

Step d:

tert-butyl [5-chloro-2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]- ethyl}thiophen-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 429 (step c) to give 160 mg (82%) of the product as an off-white solid. MS (ESIpos): m/z = 569 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .58 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .38 (s, 9H), 1 .72 (d, 3H), 2.43 (s, 3H), 3.87 (s, 6H), 4.22 (d, 2H), 5.96- 5.97 (m, 1 H), 7.05-7.07 (m, 2H), 7.10-7.1 1 (m, 1 H), 7.33-7.34 (m, 3H), 7.49-7.51 (m, 1 H), 7.64 (s, 1 H), 8.16 (d, 1 H).

Example 450

tert-butyl [2-chloro-6-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- thiophen-2-yl)benzyl]carbamate

Step a:

1 -(2-bromo-6-chlorophenyl)methanamine

This compound was synthesized by the same method as described in example 408 (step a) to give 1 .00 g (32%) of the product as the light yellow oil. MS (ESIpos): m/z = 220 [M+H] ⁺ . LC-MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 0.54 min.

Step b:

ferf-butyl (2-bromo-6-chlorobenzyl)carbamate

This compound was synthesized by the same method as described in example 429 (step a) to give 1 .17 g (81 %) of the product as a light yellow solid. MS (ESIpos): m/z = 320 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: R _t = 1 .18 min.

Step c:

ieri-butyl[6-chloro-2-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 429 (step b) to give 400 mg (33%) of the product as a light yellow oil. MS (ESIpos): m/z = 368 [M+H] ⁺ . LC- MS [Method 4, Water (0.1 %HCOOH)-Acetonitrile, 10%B]: Rt = 1 .43 min.

Step d:

tert-butyl [2-chloro-6-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}- thiophen-2-yl)benzyl]carbamate

This compound was synthesized by the same method as described in example 429 (step c) to give 250 mg (79%) of the product as an off-white solid. MS (ESIpos): m/z = 569 [M+H] ⁺ . LC-MS [Method 4, Water (0.05%TFA)-Acetonitrile, 5%B]: Rt = 1 .55 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .36 (s, 9H), 1 .71 (d, 3H), 2.43 (s, 3H), 3.87 (s, 6H), 4.19 (d, 2H), 5.91 - 6.02 (m, 1 H), 7.05-7.07 (m, 2H), 7.09-7.10 (m, 2H), 7.30-7.33 (m, 2H), 7.45-7.48 (m, 1 H), 7.64 (s, 1 H), 8.16 (d, 1 H).

Example 451

7-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin

A solution of 7-bromo-2-methylquinazolin-4-ol (520 mg, 2.17 mmol, prepared as described in patent US2004/29901 A1 , 2004, page 13), 2,4,6-triisopropylbenzenesulfonyl chloride (1 .32 g, 4.35 mmol), triethylamine (1 .21 mL, 8.70 mmol) and 4-dimethylaminopyridine (53.2 mg, 0.44 mmol) in DMF (18.6 mL) was stirred at ambient temperature for 3 hours. (1 R)-1 -(3- chlorophenyl)ethanamine (812 mg, 5.22 mmol, commercially available) was added and the reaction was stirred overnight at room temperature. The solvent was distilled off under reduced pressure and the residue was extracted with ethylacetate (3x) / water. The combined organic layers were washed with brine, dried over sodium sulfate, filtered and the solvent evaporated. The residue was purified via Isolera flash chromatography (100g silica, eluent hexanes / ethylacetate) to yield the title compound (713 mg, 78%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.51 (d, 1 H), 8.34 (d, 1 H), 7.78 (d, 1 H), 7.64 (dd, 1 H), 7.50 (t, 1 H), 7.44-7.38 (m, 1 H), 7.35 (t, 1 H), 7.31 -7.25 (m, 1 H), 5.59 (quin, 1 H), 2.39 (s, 3H), 1 .56 (d, 3H). LC-MS (Method 8): m/z: [M+H] ⁺ = 378, R _t = 0.93 min.

Example 452

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-nitroquinazolin-4-a mine

Step a:

2-methyl-6-nitroquinazolin-4(3H)-one

Dry HCI gas was passed (until the clear solution observed) to a solution of methyl 2-amino-5- nitrobenzoate, 5.00 g (25.5 mmol), in 100 mL of acetonitrile at room temperature for 3 hours and the resulting mixture was heated to reflux for overnight. After cooling to room temperature, the precipitated solid was collected by filtration. The filter cake was washed with acetonitrile and re-dissolved with water. The resulting solution was neutralized with saturated sodium bicarbonate solution and the precipitated solid was collected by filtration. The filter cake was washed with ice cold water and dried in air to give 4.75 g (90%) of the product as a light brown solid. MS (ESIpos): m/z= 206 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.70 min.

Step b:

4-chloro-2 -methyl -6-nitroquinazoline

2-Methyl-6-nitroquinazolin-4(3H)-one, 2.00 g (9.7 mmol), and 4.82 mL of N,N- diisopropylethylamine were dissolved into 50 mL of toluene. The resulting mixture was stirred at 120°C for 1 hour. After cooling to 80°C, 1 .00 mL of phosphorus oxychloride (10.7 mmol), was added dropwise to the above solution and the mixture was heated at this temperature for 3 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved with dichloromethane. Aq. potassium carbonate solution was added to adjust pH value to 7-8 and the resulting mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate and the solvent was removed in vacuo. The residue was purified with silica gel column chromatography to give 1 .50 g (68%) of the product as a yellow solid. MS (ESIpos): m/z = 224 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.1 %HCOOH)-Acetonitrile, 5%B]: R _t = 1 .01 min.

Step c:

N-[1 -(5-bromothiophen-2-yl)ethyl]-2-methyl-6-nitroquinazolin-4-a mine

4-Chloro-2-methyl-6-nitroquinazoline, 1 .50 g (6.7 mmol), and 1-(5-bromothiophen-2- yl)ethanamine, 1.38 g (6.7 mmol), were dissolved into 30 mL of 2-propanol. The resulting mixture was stirred at 110°C for 10 hours. After cooling to room temperature, the solvent was removed in vacuo to give 2.50 g (crude) of the product as a yellow solid and it was used directly for next step without further purification. MS (ESIpos): m/z = 393 [M+H] ⁺ ; LC-MS [Method 4, gradient starting with water(0.05%TFA)-Acetonitrile, 5%B]: R _t = 0.95 min. ¹ H- NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1.69 (d, 3H), 2.53 (s, 3H), 5.78-5.85 (m, 1 H), 6.97 (d, 1 H), 7.09 (d, 1 H), 7.76 (d, 1 H), 8.45 (d, 1 H), 9.19 (d, 1 H), 9.42 (s, 1 H).

Example 453

methyl 4-{[(1 R)-1 -(3-chloro henyl)ethyl]amino}-2-methylquinazoline-7-carboxylate

To a solution of 7-bromo-N-[(1 R)-1 -(3-chlorophenyl)ethyl]-2-methylquinazolin-4-amine (described in example 451 , 700 mg, 1 .86 mmol) in methanol/THF (10:1 , 33 mL) was added 1 ,1 -bis- (diphenylphosphino)-ferrocen-palladium(ll)dichloride (151 mg, 0.19 mmol) and trimethylamine (0.52 mL) and reacted in an autoclave with carbon monoxide (15.5 bar) at 80°C for 25 hours. The reaction mixture was evaporated and the crude product was purified by Isolera flash chromatography (1 10g NH phase; eluent gradient hexanes:ethyl acetate 5- 90%). The title compound was obtained in 75% yield (523 mg). 1 H-NMR (400 MHz, DMSO- d6): d [ppm] = 8.61 (d, 1 H), 8.50 (d, 1 H), 8.12 (d, 1 H), 7.94 (dd, 1 H), 7.52 (t, 1 H), 7.45-7.40 (m, 1 H), 7.35 (t, 1 H), 7.31 -7.26 (m, 1 H), 5.60 (quin, 1 H), 3.91 (s, 3H), 2.42 (s, 3H), 1.58 (d, 3H). LC-MS (Method 7): m/z: [M+H] ⁺ = 356.1 , R _t = 0.82 min.

Example 454

3-amino-3-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-3- thienyl)phenyl]propanoic acid

A solution of 3-amino-3-(2-bromophenyl)propanoic acid (59.8 mg, 245 μηηοΙ), di-tert-butyl dicarbonate (53.5 mg, 245 μηηοΙ) and N,N-diisopropylethylamine (47 μΙ, 270 μmol) in THF (1 .0 mL) and H2O (200 μΙ_) was stirred at room temperature for 2 hours. The solvent was removed in vacuo to give the title compound which was used directly in step c. LC-MS (Method 10): m/z: [M+H] ⁺ = 344, R _t = 0.67 min.

Step b:

(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-3-yl)boronic acid

Under argon, N-[1 -(4-bromothiophen-2-yl)ethyl]-6,7-dimethoxy-2-methylquinazol in-4-amine (100 mg, 245 μηηοΙ, described in example 264), tetrahydroxydiborane (73.2 mg, 816 μηηοΙ), potassium acetate (80.1 mg, 816 μηιοΙ), XPhos (2.34 mg, 4.90 μηιοΙ) and XPhos Pd G2 (2.18 mg, 2.78 μηηοΙ) in degassed ethanol (5.0 mL) were stirred at 100°C in the microwave for 1 hour. The solvent was removed in vacuo to give the title compound which was used directly in step c. LC-MS (Method 10): m/z: [M+H] ⁺ = 373, R _t = 0.81 min.

Step c:

3-[(tert-butoxycarbonyl)amino]-3-[2-(5-{1 -[(6 -dimethoxy-2-methylquinazolin-4- yl)amino]ethyl}thiophen-3-yl)phenyl]propanoic acid

Under argon, (5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-3- yl)boronic acid (91 .4 mg, 245 μηηοΙ), 3-(2-bromophenyl)-3-[(tert- butoxycarbonyl)amino]propanoic acid (84.3 mg, 245 μηιοΙ), K2CO3 (135 mg, 980 μmol) and Pd(PPh ₃ ) ₄ (28.3 mg, 24.5 μηιοΙ) in 1 ,4-dioxane (2.5 mL) and H ₂ 0 (500 μΙ_) were stirred at 1 10°C over the weekend. H2O was added, the mixture extracted with DCM and the solvent removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound (136 mg, 35%) which was used directly in step d.

Step d:

3-amino-3-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-3- thienyl)phenyl]propanoic acid

To a solution of 3-[(tert-butoxycarbonyl)amino]-3-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin- 4-yl)amino]ethyl}thiophen-3-yl)phenyl]propanoic acid (136 mg, 229 μηιοΙ) in DCM (2.0 mL) was slowly added trifluoroacetic acid (180 μΙ, 2.3 mmol) and the reaction mixture stirred at room temperature overnight. Trifluoroacetic acid (180 μΙ, 2.3 mmol) was slowly added and the reaction mixture stirred for 3 hours. The solvent was removed in vacuo. Purification by preparative HPLC (basic conditions) gave the title compound as a white solid (19.6 mg, 17%). ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.23 (dd, 1 H), 7.69-7.64 (m, 2H), 7.41 (td, 1 H), 7.36-7.30 (m, 2H), 7.27-7.21 (m, 1 H), 7.14 (dt, 1 H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 4.40 (dt, 1 H), 3.87 (s, 3H), 3.86 (s, 3H), 2.43 (d, 3H), 2.39 (ddd, 1 H), 2.26 (ddd, 1 H), 1.71 (d, 3H). LC-MS (Method 10): m/z: [M+H] ⁺ = 493, R _t = 0.73 min.

Example 455 N-[1 -{5-[2-(2-aminopropan-2-yl)phenyl]thiophen-2-yl}ethyl]-6,7-d imethoxy-2- methylquinazolin-4-amine

Step a:

2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2-thie nyl)phenyl]-2- methylpropanoic acid

To a solution of methyl 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)phenyl]-2-methylpropanoate, 208 mg (0.41 mmol, described in example 436), in 10 mL of methanol was added 1 .0 mL of sodium hydroxide (2.0 M), at 0°C and the resulting mixture was stirred at 60°C for 60 hours. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved with water. The resulting mixture was washed with ethyl acetate and the pH value was adjusted to 4 with hydrochloric acid (6.0 M). The resulting solution was extracted with ethyl acetate and the combined organic layers were concentrated in vacuo to give 120 mg (59%) of the product as yellow solid. MS (ESIpos): m/z = 492 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH ₄ HC0 ₃ )-Acetonitrile, 10%B]: R _t = 1.35 mm.

Step b:

N-[1 -{5-[2-(2-aminopropan-2-yl)phenyl]thiophen-2-yl}ethyl]-6,7-d imethoxy-2- methylquinazolin-4-amine

To a solution of 2-[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}-2- thienyl)phenyl]-2-methylpropanoic acid, 85 mg (0.17 mmol), in 5.0 mL of toluene were added diphenyl phosphoroazidate, 95 mg (0.35 mmol), and triethylamine, 35 mg (0.35 mmol). The resulting mixture was stirred at 50°C for 16 hours under nitrogen atmosphere. After cooling to room temperature, the solvent was removed in vacuo and the residue was re-dissolved with ethyl acetate. The resulting mixture was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was dissolved in 5.0 mL of 1 ,4- dioxane and to this solution was added 1 .0 mL of hydrochloric acid (3.0 M). The resulting mixture was stirred at room temperature for 5 hours. Saturated sodium carbonate solution was added to adjust the pH value to 8 and the solvent was removed in vacuo. The residue was purified by preparative HPLC [Mobile Phase A: Water (0.1 % NH ₄ HC0 ₃ ), Mobile Phase B: Acetonitrile; Gradient: 15% B to 45% B in 7 min] to give 2.3 mg of the product as an off- white solid. MS (ESIpos): m/z = 463 [M+H] ⁺ . LC-MS [Method 4, Water (0.05% NH4HCO3)- Acetonitrile, 10%B]: R _t = 1 .92 min. ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 1 .30 (s, 6H), 1 .70 (d, 3H), 2.32 (s, 3H), 3.86 (s, 6H), 5.89-5.93 (m, 1 H), 6.53 (d, 1 H), 6.87 (d, 1 H), 7.03 (s, 1 H), 7.06 (d, 1 H), 7.17 (t, 1 H), 7.30 (t, 1 H), 7.64 (s, 1 H), 7.73 (d, 1 H), 8.12 (d, 1 H).

Example 456

{[2-(5-{1 -[(6,7-dimethoxy-2-methylquinazolin-4-yl)amino]ethyl}thiophe n-2- yl)benzyl](methyl)amino}acetonitrile

A solution of N-[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]-6, 7-dimethoxy-2- methylquinazolin-4-amine (40.0 mg, 86.5 μηηοΙ), trimethylsilylcyanide (69 μί, 520 μηηοΙ) and rose bengal (880 μg, 0.86 μηηοΙ) in acetonitrile (940 μί) was lit with a fluorescent household lightbulb and stirred under an O2 atmosphere overnight. The reaction mixture was quenched with NaHCC>3 (aq., sat.) and extracted with DCM. Purification by preparative HPLC (basic conditions) gave the title compound (6.1 mg, 13%). ¹ H-NMR (400 MHz, DMSO-c/ ₆ ): δ [ppm] = 8.16 (br d, 1 H), 7.65 (s, 1 H), 7.44-7.28 (m, 4H), 7.12-7.07 (m, 2H), 7.05 (s, 1 H), 5.97 (quin, 1 H), 3.87 (s, 3H), 3.87 (s, 3H), 3.61 (d, 3H), 2.43 (s, 3H), 2.20 (s, 2H), 2.1 1 (s, 1 H), 1.72 (d, 3H). LC-MS (Method 10): m/z: [M+H] ⁺ = 488, R _t = 1 .35 min. Example 457

1 -(4-{[1 -(5-{2-[(dimethylamino)methyl]phenyl}thiophen-2-yl)ethyl]ami no}-2- methylquinazolin-6-yl)-3-methylurea

N4-[1 -(5-{2-[(dimethylamino)methyl]phenyl}-2-thienyl)ethyl]-2-met h

100 mg (0.24 mmol, described in example 423), was dissolved in 3.0 mL of dichloromethane. Triethylamine, 73 mg (0.72 mmol), and methylcarbamic chloride, 67 mg (0.14 mmol), were added. The resulting mixture was stirred at room temperature for 3 days. After evaporation in vacuo, the residue was purified by preparative HPLC (Column: Xbridge Prep C18, 5 m,19 ^* 150mm; Mobile Phase A: Waters(0.1 % HCOOH), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 10% B to 36% B in 8 min; 254 nm & 220 nm), the solvent was lyophilized to give 34.3 mg (26%) of the product as a yellow solid. MS (ESIpos): m/z = 475 [M+H] ⁺ . ¹ H-NMR (400 MHz, DMSO-d ₆ ): δ [ppm] = 8.62 (s, 1 H), 8.43-8.32 (m, 1 H), 8.17 (s, 3H), 7.70 (dd, 1 H), 7.52 (d, 1 H), 7.47-7.25 (m, 5H), 7.18 (d, 1 H), 7.08 (d, 1 H), 6.19 (br d, 1 H), 5.95 (br t, 1 H), 2.68 (d, 3H), 2.45 (s, 3H), 2.13 (s, 6H), 1.72 (d, 3H).

Example 458

1 -benzyl -4-(4-{[1 -(5-{2 -[(dimethylamino)methyl]phenyl}thiophen-2 -yl )ethyl]amino}-2- methylquinazolin-6-yl iperazin-2-one

1 -benzyl-4-(4-{[1 -(5-bromothiophen-2-yl)ethyl]amino}-2-methylquinazolin-6-yl) piperazin-2- one, 70 mg (130.5 μηηοΙ, described in example 441 ), 2- ((dimethylamino)methyl)phenylboronic acid, 23.4 mg (130.5 μηηοΙ), tetrakis(triphenylphosphine)palladium(0), 15.1 mg (13 μηηοΙ), and potassium carbonate, 72.1 mg (521 .9 μηηοΙ), were dissolved in 4.8 mL of 1 ,4- dioxane/ water (v:v=5:1 ) at room temperature. The resulting mixture was stirred at 100°C for 10 hours under nitrogen. The solvent was removed in vacuo the residue was purified by preparative HPLC (Column: XBridge Prep C18 OBD Column 19x150mm 5μηι; Mobile Phase A:Water(0.1 % HCOOH), Mobile Phase B: ACN; Flow rate: 20 mL/min; Gradient: 30% B to 70% B in 8 min; Detector: 254 nm, 220 nm) to give 7.2 mg (9%) of the product as a light yellow solid. MS (ESIpos) : m/z = 591 [M+H] ⁺ .

EXPERIMENTAL SECTION - BIOLOGICAL ASSAYS

Examples were tested in selected biological assays one or more times. When tested more than once, data are reported as either average values or as median values, wherein

• the average value, also referred to as the arithmetic mean value, represents the sum of the values obtained divided by the number of times tested, and

• the median value represents the middle number of the group of values when ranked in ascending or descending order. If the number of values in the data set is odd, the median is the middle value. If the number of values in the data set is even, the median is the arithmetic mean of the two middle values.

Examples were synthesized one or more times. When synthesized more than once, data from biological assays represent average values or median values calculated utilizing data sets obtained from testing of one or more synthetic batch.

6,7-dimethoxy-N-[(1 R)-1 -(1 -naphthyl)ethyl]quinazolin-4-amine, which was used to calibrate the assay, was prepared as follows:

To 4-chloro-6,7-dimethoxyquinazoline (100 mg, 0.445 mmol, commercially available) in 1 .7 mL DMSO was added (1 R)-1 -(1 -naphthyl)ethanamine (76 mg, 0.445 mmol, commercially available) and N-ethyl-N-isopropylpropan-2-amine (202 μΙ, 1 .16 mmol). The reaction was stirred at 100°C overnight, cooled to ambient temperature and filtered. After removal of the solvent under reduced pressure the crude product was purified via HPLC chromatography to yield the title compound (1 18 mg, 73%). ¹ H-NMR (400 MHz ,DMSO-d6), d [ppm]= 1 .72 (3H), 3.90 (6H), 6.32-6.41 (1 H), 7.09 (1 H), 7.46-7.58 (3H), 7.64-7.69 (1 H), 7.78 (2H), 7.92-7.97 (1 H), 8.18-8.24 (2H), 8.28 (1 H).

The in vitro activity of the compounds of the present invention can be demonstrated in the following assays:

Biochemical assay 1 : K-Ras ^G12C interaction assay with hSOS1

This assay quantifies the equilibrium interaction of human SOS1 with K-Ras ^G12C . Detection of the interaction is achieved by measuring homogenous time-resolved fluorescence resonance energy transfer (HTRF) from antiGST-Europium (FRET donor) bound to GST-K- Ras ^G12C to anti-6His-XL665 bound to His-tagged hSOS1 (FRET-acceptor).

The assay buffer contained 5 mM HEPES pH 7.4 (Applichem), 150 mM NaCI (Sigma), 10 mM EDTA (Promega), 1 mM DTT (Thermofisher), 0.05% BSA Fraction V, pH 7.0, (ICN Biomedicals), 0.0025% (v/v) Igepal (Sigma) and 100 mM KF (FLUKA).

The expression and purification of N-terminal GST-tagged human K-RasG12C and N- terminal His-tagged human SOS1 is described below. Concentrations of protein batches used were optimized to be within the linear range of the HTRF signal. A Ras working solution was prepared in assay buffer containing typically 10 nM GST-hK-RasG12C and 2 nM antiGST-Eu(K) (Cisbio, France). A SOS working solution was prepared in assay buffer containing typically 20nM His-hSOS1 and 10 nM anti-6His-XL665 (Cisbio, France). An inhibitor control solution was prepared in assay buffer containing 10 nM anti-6His-XL665 without hSOS1.

Fifty nl of a 100-fold concentrated solution of the test compound in DMSO were transferred into a black microtiter test plate (384 or 1536, Greiner Bio-One, Germany). For this, either a Hummingbird liquid handler (Digilab, MA, USA) or an Echo acoustic system (Labcyte, CA, USA) was used.

All steps of the assay were performed at 20°C. A volume of 2.5 μΙ of the Ras working solution was added to all wells of the test plate using a Multidrop dispenser (Thermo Labsystems). After 2 min preincubation, 2.5 μΙ of the SOS working solution were added to all wells except for those wells at the side of the test plate that were subsequently filled with 2.5 μΙ of the inhibitor control solution. After 60 min incubation the fluorescence was measured with a Pherastar (BMG, Germany) using the HTRF module (excitation 337nm, emission 1 : 620nm, emission 2: 665nm). The ratiometric data (emission 2 divided by emission 1 ) were normalized using the controls (DMSO = 0% inhibition, inhibition control wells with inhibitor control solution = 100% inhibition). Compounds were tested in duplicates at up to 1 1 concentrations (for example 20 μΜ, 5,7 μΜ, 1 ,6 μΜ, 0,47 μΜ, 0,13 μΜ, 38 ηΜ, 1 1 ηΜ, 3,1 ηΜ, 0,89 ηΜ, 0,25 ηΜ and 0,073 ηΜ). IC50 values were calculated by 4-Parameter fitting using a commercial software package (Genedata Screener, Switzerland).

Biochemical assay 2: K-Ras activation assay by hSOS1 at high GTP concentration

This assay quantifies human SOS1 -mediated nucleotide exchange of K-Ras ^G12C preloaded with a fluorescent GTP-analog and in presence of an excess of free GTP. Loaded hK- Ras ^G12C generates a high HTRF-signal by energy transfer from antiGST-Terbium (FRET donor) bound to K-Ras to the loaded fluorescent GDP analog (FRET-acceptor). SOS1 activity exchanges the fluorescent GDP for non-fluorescent GTP and therefore leads to a reduction of the HTRF signal.

The fluorescent GDP-analog EDA-GDP-Dy647P1 (273'-0-(2-Aminoethyl-carbamoyl)- guanosine-5'-diphosphate labelled with Dy647P1 (Dyomics GmbH, Germany)) was synthesized by Jena Biosciences GmbH (Germany) and supplied as a 1 mM aqueous solution.

The expression and purification of N-terminal GST-tagged human K-RasG12C and N- terminal His-tagged human SOS1 is described below. Concentrations of protein batches used were optimized to be within the linear range of the HTRF signal.

Preparation of GST-tagged hK-Ras ^G12C loaded with fluorescent nucleotide was performed as follows: incubation of 1 1 .5 μΜ hK-Ras ^G12C with 5-fold excess GDP-Dy647 nucleotide (54 μΜ) in 500 μΙ NLS-buffer (RAS activation Kit Jena Bioscience, Kat. #PR-950) for 10 min at 37°C. Addition of 20 μΙ 1 M MgC (Sigma) to final 40 mM and store on ice. Purification into buffer (10 mM HEPES pH 7.4 (Applichem), 150 mM NaCI (Sigma), 5 mM MgCI ₂ (Sigma)) by use of a PD-Minitrap desalting column (GE Healthcare). Concentration of 1 ml purified hK-Ras- GDP-Dy647 is approx. 4-5 μΜ.

The assay buffer contained 10 mM HEPES pH 7.4 (Applichem), 150 mM NaCI (Sigma), 5 mM MgC (Sigma), 1 mM DTT (Thermofisher), 0.05% BSA Fraction V, pH 7.0, (ICN Biomedicals), 0.0025% (v/v) Igepal (Sigma).

A Ras working solution was prepared in assay buffer containing typically 80 nM loaded GST- hK-RasG12C-EDA-GDP-Dy647P1 and 2 nM antiGST-Tb (Cisbio, France). A hSOS1 working solution was prepared in assay buffer containing typically 8nM His-hSOS1 and 100 μΜ GTP (Jena Bioscience, Germany). An inhibitor control solution was prepared in assay buffer containing the same concentration of hSOS1 without GTP. Alternatively, the inhibitor control solution was prepared by supplementing the hSOS1 working solution with 20 μΜ of 6,7-dimethoxy-N-[(1 R)-1 -(1 -naphthyl)ethyl]quinazolin-4-amine which was used to calibrate the assay.

Fifty nl of a 100-fold concentrated solution of the test compound in DMSO were transferred into a black microtiter test plate (384 or 1536, Greiner Bio-One, Germany). For this, either a Hummingbird liquid handler (Digilab, MA, USA) or an Echo acoustic system (Labcyte, CA, USA) was used.

All steps of the assay were performed at 20°C. A volume of 2.5 μΙ of the Ras working solution was added to all wells of the test plate using a Multidrop dispenser (Thermo Labsystems). After 2 min preincubation, 2.5 μΙ of the hSOS1 working solution were added to all wells except for those wells at the side of the test plate that were subsequently filled with 2.5 μΙ of the inhibitor control solution. After 20 min incubation the fluorescence was measured with a Pherastar (BMG, Germany) using the HTRF module (excitation 337nm, emission 1 : 620nm, emission 2: 665nm).

The ratiometric data (emission 2 divided by emission 1 ) were normalized using the controls (DMSO = 0% inhibition, inhibition control wells with inhibitor control solution = 100% inhibition). Compounds were tested in duplicates at up to 1 1 concentrations (for example 20 μΜ, 5,7 μΜ, 1 ,6 μΜ, 0,47 μΜ, 0,13 μΜ, 38 ηΜ, 1 1 ηΜ, 3,1 ηΜ, 0,89 ηΜ, 0,25 ηΜ and 0,073 ηΜ). IC50 values were calculated by 4-Parameter fitting using a commercial software package (Genedata Screener, Switzerland).

Biochemical assay 3: K-Ras ^G12C activation assay by hSOS1

K-Ras is a small GTPase that can bind GDP and GTP. The guanine nucleotide exchange factor SOS catalyzes the activation of K-Ras by promoting the exchange of GDP to GTP. SOS binds to K-Ras-GDP thereby opening the GDP-binding pocket to facilitate GDP release. Rebinding of excess nucleotide leads to dissociation of the K-Ras-SOS intermediate complex leaving K-Ras loaded with the nucleotide.

This assay quantifies human SOS1 -mediated loading of human K-Ras ^G12C -GDP with a fluorescent GTP-analog. Detection of successful loading is achieved by measuring homogenous time-resolved fluorescence resonance energy transfer (HTRF) from antiGST- Terbium (FRET donor) bound to GST-K-RasG12C to the loaded fluorescent GTP analog (FRET-acceptor).

The fluorescent GTP-analog EDA-GTP-Dy647P1 (273'-0-(2-Aminoethyl-carbamoyl)- guanosine-5'-triphosphate labelled with Dy647P1 (Dyomics GmbH, Germany)) was synthesized by Jena Biosciences GmbH (Germany) and supplied as a 1 mM aqueous solution.

The assay buffer contained 10 mM HEPES pH 7.4 (Applichem), 150 mM NaCI (Sigma), 5 mM MgC (Sigma), 1 mM DTT (Thermofisher), 0.05% BSA Fraction V, pH 7.0, (ICN Biomedicals), 0.0025% (v/v) Igepal (Sigma).

The expression and purification of N-terminal GST-tagged human K-RasG12C and N- terminal His-tagged human SOS1 is described below. Concentrations of protein batches used were optimized to be within the linear range of the HTRF signal. A Ras working solution was prepared in assay buffer containing typically 100 nM GST-hK-RasG12C and 2 nM antiGST-Tb (Cisbio, France). A hSOS1 working solution was prepared in assay buffer containing typically 20nM hSOS1 and 200 nM EDA-GTP-Dy647P1. An inhibitor control solution was prepared in assay buffer containing 200 nM EDA-GTP-Dy647P1 without hSOS1 .

Fifty nl of a 100-fold concentrated solution of the test compound in DMSO were transferred into a black microtiter test plate (384 or 1536, Greiner Bio-One, Germany). For this, either a Hummingbird liquid handler (Digilab, MA, USA) or an Echo acoustic system (Labcyte, CA, USA) was used.

All steps of the assay were performed at 20°C. A volume of 2.5 μΙ of the Ras working solution was added to all wells of the test plate using a Multidrop dispenser (Thermo Labsystems). After 10 min preincubation, 2.5 μΙ of the hSOS1 working solution were added to all wells except for those wells at the side of the test plate that were subsequently filled with 2.5 μΙ of the inhibitor control solution. After 30 min incubation the fluorescence was measured with a Pherastar (BMG, Germany) using the HTRF module (excitation 337nm, emission 1 : 620nm, emission 2: 665nm).

The ratiometric data (emission 2 divided by emission 1 ) were normalized using the controls (DMSO = 0% inhibition, inhibition control wells with inhibitor control solution = 100% inhibition). Compounds were tested in duplicates at up to 1 1 concentrations (for example 20 μΜ, 5,7 μΜ, 1 ,6 μΜ, 0,47 μΜ, 0,13 μΜ, 38 nM, 1 1 nM, 3,1 nM, 0,89 nM, 0,25 nM and 0,073 nM). IC50 values were calculated by 4-Parameter fitting using a commercial software package (Genedata Screener, Switzerland).

EGFR kinase assay

EGFR inhibitory activity of compounds of the present invention was quantified employing the TR-FRET based EGFR assay as described in the following paragraphs. Epidermal Growth Factor Receptor (EGFR) affinity purified from human carcinoma A431 cells (Sigma-Aldrich, # E3641 ) was used as kinase. As substrate for the kinase reaction the biotinylated peptide biotin-Ahx-AEEEEYFELVAKKK (C-terminus in amid form) was used which can be purchased e.g. form the company Biosyntan GmbH (Berlin-Buch, Germany).

For the assay 50 nl_ of a 10Ofold concentrated solution of the test compound in DMSO was pipetted into a black low volume 384well microtiter plate (Greiner Bio-One, Frickenhausen, Germany), 2 μΙ_ of a solution of EGFR in aqueous assay buffer [50 mM Hepes/HCI pH 7.0, 1 mM MgC , 5 mM MnC , 0.5 mM activated sodium ortho-vanadate, 0.005% (v/v) Tween- 20] were added and the mixture was incubated for 15 min at 22°C to allow pre-binding of the test compounds to the enzyme before the start of the kinase reaction. Then the kinase reaction was started by the addition of 3 μΙ_ of a solution of adenosine-tri-phosphate (ATP, 16.7 μΜ => final cone, in the 5 μΙ_ assay volume is 10 μΜ) and substrate (1.67 μΜ => final cone, in the 5 μΙ_ assay volume is 1 μΜ) in assay buffer and the resulting mixture was incubated for a reaction time of 20 min at 22°C. The concentration of EGFR was adjusted depending of the activity of the enzyme lot and was chosen appropriate to have the assay in the linear range, typical concentration were about 3 U/ml. The reaction was stopped by the addition of 5 μΙ of a solution of HTRF detection reagents (0.1 μΜ streptavidine-XL665 [Cis Biointernational] and 1 nM PT66-Tb-Cryptate, an terbium-cryptate labelled anti-phospho- tyrosine antibody from Cis Biointernational [instead of the PT66-Tb-cryptate PT66-Eu-Chelate from Perkin Elmer can also be used]) in an aqueous EDTA-solution (80 mM EDTA, 0.2 % (w/v) bovine serum albumin in 50 mM HEPES pH 7.5).

The resulting mixture was incubated 1 h at 22°C to allow the binding of the biotinylated phosphorylated peptide to the streptavidine-XL665 and the PT66-Eu-Chelate. Subsequently the amount of phosphorylated substrate was evaluated by measurement of the resonance energy transfer from the PT66-Tb-Cryptate to the streptavidine-XL665. Therefore, the fluorescence emissions at 620 nm and 665 nm after excitation at 337 nm were measured in a HTRF reader, e.g. a Pherastar (BMG Labtechnologies, Offenburg, Germany) or a Viewlux (Perkin-Elmer). The ratio of the emissions at 665 nm and at 622 nm was taken as the measure for the amount of phosphorylated substrate. The data were normalised (enzyme reaction without inhibitor = 0 % inhibition, all other assay components but no enzyme = 100 % inhibition). Usually the test compounds were tested on the same microtiterplate in 1 1 different concentrations in the range of 20 μΜ to 0.072 nM (e.g. 20 μΜ, 5.7 μΜ, 1.6 μΜ, 0.47 μΜ, 0.13 μΜ, 38 ηΜ, 1 1 ηΜ, 3.1 ηΜ, 0.89 ηΜ, 0.25 nM and 0.072 nM, the dilution series prepared separately before the assay on the level of the 10Ofold concentrated solutions in DMSO by serial dilutions, the exact concentrations may vary depending on the pipettor used) in duplicate values for each concentration and IC50 values were calculated by a 4 parameter fit.

Biochemical assay 4: K-Ras activation assay by hSOS2

This assay quantifies human SOS2-mediated loading of K-Ras ^G12C -GDP with a fluorescent GTP-analog. Detection of successful loading is achieved by measuring homogenous time- resolved fluorescence resonance energy transfer (HTRF) from antiGST-Terbium (FRET donor) bound to GST-hK-RasG12C to the loaded fluorescent GTP analog (FRET-acceptor).

The fluorescent GTP-analog EDA-GTP-Dy647P1 (273'-0-(2-Aminoethyl-carbamoyl)- guanosine-5'-triphosphate labelled with Dy647P1 (Dyomics GmbH, Germany)) was synthesized by Jena Biosciences GmbH (Germany) and supplied as a 1 mM aqueous solution.

The assay buffer contained 10 mM HEPES pH 7.4 (Applichem), 150 mM NaCI (Sigma), 5 mM MgC (Sigma), 1 mM DTT (Thermofisher), 0.05% BSA Fraction V, pH 7.0, (ICN Biomedicals), 0.0025% (v/v) Igepal (Sigma).

The expression and purification of N-terminal GST-tagged human K-RasG12C and N- terminal His-tagged human SOS1 is described below. Concentrations of protein batches used were optimized to be within the linear range of the HTRF signal. A Ras working solution was prepared in assay buffer containing typically 100 nM GST-hK-RasG12C and 2 nM antiGST-Tb (Cisbio, France). A hSOS2 working solution was prepared in assay buffer containing typically 20nM hSOS2 and 200 nM EDA-GTP-Dy647P1. An inhibitor control solution was prepared in assay buffer containing 200 nM EDA-GTP-Dy647P1 without hSOS2.

Fifty nl of a 100-fold concentrated solution of the test compound in DMSO were transferred into a black microtiter test plate (384 or 1536, Greiner Bio-One, Germany). For this, either a Hummingbird liquid handler (Digilab, MA, USA) or an Echo acoustic system (Labcyte, CA, USA) was used.

All steps of the assay were performed at 20°C. A volume of 2.5 μΙ of the Ras working solution was added to all wells of the test plate using a Multidrop dispenser (Thermo Labsystems). After 10 min preincubation, 2.5 μΙ of the hSOS2 working solution were added to all wells except for those wells at the side of the test plate that were subsequently filled with 2.5 μΙ of the inhibitor control solution. After 30 min incubation the fluorescence was measured with a Pherastar (BMG, Germany) using the HTRF module (excitation 337nm, emission 1 : 620nm, emission 2: 665nm). The ratiometric data (emission 2 divided by emission 1 ) were normalized using the controls (DMSO = 0% inhibition, inhibition control wells with inhibitor control solution = 100% inhibition). Compounds were tested in duplicates at up to 1 1 concentrations (for example 20 μΜ, 5,7 μΜ, 1 ,6 μΜ, 0,47 μΜ, 0,13 μΜ, 38 ηΜ, 1 1 ηΜ, 3,1 ηΜ, 0,89 ηΜ, 0,25 ηΜ and 0,073 ηΜ). IC50 values were calculated by 4-Parameter fitting using a commercial software package (Genedata Screener, Switzerland).

KRAS cellular assays

3D-Softagar MiaPaca-2 (ATCC CRL-1420) and NCI-H1792 (ATCC CRL-5895)

Day 1 : Softagar (Select Agar, Invitrogen, 3% in ddH20 autoclaved) is boiled and tempered at 48°C. Medium (MiaPaca-2: DMEM/Ham's F12; [Biochrom; # FG 4815, with stable Glutamine] 10% FCS and 2.5% Horse Serum, H1792: RPMI 1640; [Biochrom; # FG 1215, with stable Glutamine and 10%FCS]) is tempered to 37°C; Agar (3%) is diluted 1 :5 in medium (=0.6%) and 50 μΙ/well plated into 96 well plates (Corning, #3904), wait at room temperature until the agar is solid. 3% agar is diluted to 0.25% in medium (1 :12 dilution) and tempered at 42°C. Cells are trypsinized, counted and tempered at 37°C; cells (MiaPaCa-2: 125-150, NCI- HI 792: 1000) are resuspended in 100 μΙ 0.25% Agar and plated. Wait at room temperature until the agar is solid. Overlay wells with 50 μΙ medium. Plate sister wells in separate plate for time zero determination. All plates are incubated overnight 37°C and 5% C02.

Day 2: Measurement of time zero values: Add 40 μΙ Cell Titer 96 Aqueous Solution (Promega) per well, (light sensitive) and incubate in the dark at 37°Cand 5% C02. Absorption is measured at 490 nm and reference wavelength 660 nm. DMSO-prediluted test compounds are added with HP Dispenser to a final DMSO concentration of 0.3%.

Day 10: Measurement of test compound and control treated wells with Cell Titer 96 AQueous according to time zero. The IC50 values were determined using the four parameter fit.

Active RAS in Calu-1 cells (CLS 300141 )

40.000 Calu-1 cells are seeded in 96well plate (NUNC161093) for 48h at 37°C/5%C02 (10%FBS (S0615), DMEM/Ham's F-12 (Biochrom; # FG 4815), 2mM L-Glutamine). After that, medium is changed to FBS-free medium and the cells were incubated for further 24h at 37°C/5%C02. Cells are treated with varying concentrations of DMSO-prediluted test compounds (final 0.1 %) for 30 min at 37°C/5%C02. Supernatant with test compounds is discarded and, after that, treated cells are stimulated with 100ng/ml EGF (Sigma#E9644, diluted in serum free medium) for 3 minutes. Cells were treated with lysis buffer and all next steps were performed on ice according to the supplier's manual of G-LISA Kit (Cytoskeleton BK131 , Ras Activation Assay). Finally, the content of active Ras is measured by detecting the absorbance at 490 nm (Tecan Sunrise). The value of EGF-stimulated cells is set as 100%, whereas the value of untreated cells is set as 0%. The IC50 values were determined using the four parameter fit.

P-EGR assay (In-Cell Western) in Hela cells (ATCC CCL-2)

After stimulation with EGF, the EGF receptor autophosphorylates at Y1 173. In-cell Western assay simultaneously detect two targets at 700 and 800nm using two spectrally distinct near- infrared dyes. With a specific antibody, phosphorylated EGFR can be quantified and the samples can be normalized with total EGFR antibody parallel.

25000 Hela cells are seeded in 96well plate (NUNC161093) for 24 h at 37°C/5%C02 (10%FBS (S0615), D MEM/Ham's F-12 (Biochrom; # FG 4815), 2mM L-Glutamine). After that, medium is changed to FBS-free medium and the cells were incubated for further 24h at 37°C/5%C02.

Cells are treated with varying concentrations of DMSO-prediluted test compounds (final 0.1 %) for 30 minutes and finally with 100ng/ml EGF (Sigma#E9644, diluted in serum free medium) for 2 minutes.

Cells are treated according the manual of EGFR Near Infrared In-Cell ELISA Kit (Pierce #62210). If not specified, all buffers and antibodies are part of this kit.

Cells are fixed with 4% formaldehyde, washed twice with 100μΙ per well with TRIS-buffered saline with Surfact-Amps 20, permeabilized with 100μΙ TRIS-buffered saline with Surfact- Amps X-100, wash again with 100μΙ TRIS-buffered saline, and finally 200μΙ blocking buffer are added for 60 minutes at room temperature. Fixed and washed cells are incubated with primary antibody mix (P-EGFR; EGFR) overnight at 2-8°C. After washing with 100μΙ TRIS- buffered saline with Surfact-Amps 20, secondary IRDye-labeled antibody mix (DyLight 800 Goat Anti-Rabbit IgG, Pierce SA5-35571 ; DyLight 680 Goat Anti-Mouse IgG, Pierce 35518) is added for 1 h at room temperature and washed again. Plates are scanned with LiCor Odyssey Infrared Imager at 800nm for P-EGFR and at 700nm for total EGFR. The quotient of 800nm and 700nm for EGF only treated cells is set as 100% and the quotient of 800nm and 700nm of untreated cells is set as 0%. The IC50 values were determined using the four parameter fit.

Table 1 : I C50 values of the compounds of examples 1 to 458 in in vitro assays 1 to 3 and the EGFR-assay ("n.d." means "not determined") Assay 2 Assay 3

Assay 1

(KRAS- (KRAS- (KRAS-SOS

Activation by Activation by

Interaction)

SOS high GTP) SOS no GTP)

Example activity EGFR kinase activity activity

No. (expressed as inhibition IC50

(expressed as (expressed as

IC50, or as %

IC50, or as % IC50, or as %

inhibition at 20

inhibition at 20 inhibition at 20

μΜ)

μΜ) μΜ)

Reference

compound 3,04 E-07 2,63 E-07 6,93 E-07 5,53 E-07 above

1 1.33E-87 3.03E-07 3JOE-0? > 20 M

2 1.27E-87 2.07E-07 5.37B-0? L63E-05

3 1.13E-87 1.15E-07 2 1 B~0? > 20 pM

4 1.81 E-87 2.43E-07 4J9B-0? > 20 pM

5 1.71 E-88 1.3QE-06 5-08B-O8 > 20 pM

6 2.28E-8S 1.8SE-0S 4.98E-06 > 20 pM

7 44% 18% 33% > 20 pM

8 1.82E-05 1.9SE-05 14% > 20 pM

9 1.52E-8S 1.37E-08 5.96E-06 > 20 pM

10 1.18E-8S 1.27E-08 S.14E-06 > 20 pM

1 1 2.83E-87 2.21 E-07 5.49E-07 > 20 pM

12 3.3SE-87 5.78E-07 1.29E-06 > 20 pM

13 2.82E-8S 2.85E-08 7J3E-06 > 20 pM

14 8.SSE-87 6.08E-07 1.83E-06 > 20 pM

15 1.2SE-87 9.11 E-08 3.24E-07 > 20 pM 3.25E-98 3.02E-0S 8,17E-96 > 20 pM

2.70E-0? 2.97E-07 7,12E-97 > 20 pM

6.50E-06 7.88E-0S 1 ,G5E-G5 > 20 pM

7.78E-Q8 6.55E-88 44% > 20 pM

8.42E-Q8 8.28E-88 41 % > 20 pM

3.18E-Q8 3.23E-88 1.11 E-05 > 20 pM

1.77E-Q7 2.19E-87 5.89E-07 > 20 pM

2.72E-Q8 1.85E-88 8.82E-06 > 20 pM

7.Q1 E-Q7 1.22E-08 2.45E-06 > 20 pM

5.41 E-Q7 8.58E-87 1.50E-06 > 20 pM

9.55E-Q8 52% 8.96E-06 > 20 pM

3.88E-Q7 4.82E-87 4.98E-07 > 20 pM

40% 8% 46% > 20 pM

1.Q2E-Q5 1.09E-05 44% > 20 pM

1.34E-Q8 1.19E-88 2.91 E-06 > 20 pM

8.59E-0S 9.51 E-08 49% > 20 pM

1.87E-88 1.48E-08 2.59E-06 > 20 pM

53% 24% 9% > 20 pM

4.23E-0S 3.71 E-08 1.68E-05 > 20 pM 4.72E-98 4.78E-08 48% > 20

5.42E-97 1.00E-08 6,96E-07 n.d.

1.54E-06 1.85E-08 2,69E-06 n.d. n.d. n.d. η,ύ. n.d.

1.48E-Q8 1.83E-98 3.05E-06 n.d.

3.85E-Q8 1.75E-98 4.55E-06 n.d.

9.72E-Q7 1.48E-98 1.87E-06 n.d.

4.27E-Q8 5.58E-98 48% n.d.

30% 14% 16% n.d.

55% 47% 25% n.d.

1.51 E-Q8 2.17E-98 1.16E-06 n.d.

2.37E-Q8 3.82E-98 4.16E-06 n.d.

40% 22% 17% n.d.

2.12E-Q8 3.27E-98 4.52E-06 n.d.

1.98E-Q5 35% 36% n.d.

9.85E-88 2.08E-05 23% n.d.

5.83E-0S 5.98E-08 52% n.d.

4.29E-0S 5.48E-08 43% n.d.

8.89E-07 1.28E-08 1.08E-08 n.d. 4.19E-98 4.13E-0S 4.97E-96 n.d.

8.74E-97 6.29E-07 7.24E-97 n.d.

1.47E-98 1.79E-0S 2.56E-96 n.d.

4.14E-Q7 4.01 Ε-Θ7 8.29E-97 n.d.

1.77E-Q8 1.64Ε-Θ8 3.11 E-96 n.d.

1.59E-Q8 7.78E-87 9.85E-97 n.d.

5.85E-Q7 4.48E-87 1.94E-96 n.d.

3.74E-Q7 7.17E-87 8.95E-97 n.d.

1.28E-Q8 2.77E-88 2.83E-96 n.d.

1.13E-Q8 1.88E-88 1.88E-06 n.d.

1.40E-Q8 1.98E-88 2.21 E-06 n.d.

5.78E-Q8 8.34E-88 1.35E-95 n.d.

3.48E-Q8 4.55E-88 8.8GE-96 n.d.

9.98E-Q8 1.98E-85 54% n.d.

1.37E-Q7 4.88E-87 4.71 E-07 8.92E-88

3.92E-88 5.41 E-08 9.97E-98 rs.d.

8.82E-88 8.82E-08 47% rs.d.

3.93E-07 8.43E-07 8.8QE-97 rs.d.

7.37E-07 6.88E-07 8.82E-97 rs.d. 73 4.27E-9? 5.54E-07 4,95E-Q7 n.d.

74 1.49E-9? 2.23E-07 2,61 E-97 n.d.

75 5.S8E-0? 1.15E-08 1 ,91 E-96 n.d.

76 4.71 E-Q7 1.19E-88 9.52E-97 n.d.

77 7.88E-Q8 9.83E-88 1.99E-95 n.d.

78 8.55E-Q8 45% 31 % n.d.

79 1.55E-Q8 9.37E-87 1.85E-96 n.d.

80 7.21 E-Q7 7.11 E-87 1.12E-96 n.d.

81 42% 33% 24% n.d.

P'? 5.98E-Q7 8.57E-87 1.9GE-96 n.d.

83 8.50E-Q8 7.85E-88 1.74E-95 n.d.

84 5.33E-Q8 7.20E-08 1.1GE-05 n.d.

85 8.87E-Q7 7.58E-87 1.26E-96 n.d.

86 5.81 E-Q7 9.35E-87 8.93E-97 n.d.

87 4.42E-Q8 3.48E-88 7.42E-96 n.d.

88 3.58E-08 2.58E-08 8.18E-08 rs.d.

89 1.88E-08 2.88E-08 4.26E-06 rs.d.

90 1.1 E-85 48% 33% rs.d.

91 1.5 E-85 38% 38% rs.d. 92 4.70E-06 3.87E-0S 9.26E-Q6 η,ύ.

93 1.S5E-06 1.5SE-08 2.89E-Q6 η,ύ.

94 2.42E-06 3.14E-08 4.28E-Q6 η,ύ.

95 8.91 E-97 4.73Ε-Θ7 1.88E-86 si.d.

96 1.84E-88 1.Θ9Ε-Θ8 1.39E-86 si.d.

97 39% 28% 38% si.d.

98 1.81 E-85 43% 24% si.d.

99 2.18E-88 1.42E-88 2.83E-86 si.d.

100 5.35E-88 4.51 E-88 8.52E-86 si.d.

101 7.15E-87 8.97E-87 1.8GE-86 si.d.

102 6.38E-88 3.58E-88 1.15E-G5 si.d.

103 1.44E-88 2.48E-88 2.74E-G6 si.d.

104 1.82E-88 1.98E-88 2.52E-86 si.d.

105 2.40E-88 1.39E-88 2.77E-86 si.d.

106 1.41 E-88 1.53E-88 2.85E-86 si.d.

107 3.19E-87 4.87E-87 4.38E-87 si.d.

108 8.21 E-07 9.01 E-07 1.23E-08 n.d.

109 1.00E-06 3.92E-07 1.41 E-08 ri.d.

1 10 1.Q4E-Q6 9.08E-07 1.19E-08 ri.d. 111 2.10E-98 1.87E-08 3.34Ε-Θ6 n.d.

112 6.96E-0? 9.48E-07 1.12E-96 n.d.

113 1.35E-98 8.39E-07 2.1GE-96 n.d.

114 5.28E-98 2.39E-88 9.21 E-96 n.d.

115 8.85E-97 8.02E-87 1.57E-96 n.d.

116 1.98E-98 1.15E-08 1.72E-06 n.d.

117 1.85E-Q8 1.35E-08 3.08E-06 n.d.

118 5.29E-97 4.81 E-07 7.74E-07 n.d.

119 8.58E-97 1.28E-08 1.48E-06 n.d.

120 1.59E-98 2.82E-88 3.53E-06 n.d.

121 4.52E-97 6.79E-87 7.91 E-07 n.d.

122 48% 17% 21% n.d.

123 52% 1.31E-05 42% n.d.

124 1.83E-95 9.38E-88 37% n.d.

125 2.93E-98 1.09E-08 2.94E-96 n.d.

126 52% 31% 11% rs.d.

127 1.78E-05 44% 42% rs.d.

128 1.39E-05 1.89E-05 18% rs.d.

129 1.48E-0S 2.38E-08 3.45E-08 rs.d. 130 3.43E-98 4.31 E~0S 1.17E-05 η,ύ.

131 2.23E-06 3.37E-0S 5,94B-06 n„d.

132 6.58E-06 8.05E-0S 46% n„d.

133 4.30E-Q8 4.83E-88 5.87E-06 rs.d.

134 43% 23% 27% rs.d.

135 28% 5% 13% rs.d.

136 37% 28% 18% rs.d.

137 48% 38% 32% rs.d.

138 5.57E-Q8 7.43E-08 40% rs.d.

139 4.70E-Q8 6.13E-88 41 % rs.d.

140 5.33E-Q8 5.28E-88 33% rs.d.

141 5.83E-Q8 25% 1.11 E-05 rs.d.

142 1.Q1 E-Q6 1.81 E-08 1.02E-06 rs.d.

143 7.84E-Q8 8.78E-88 1.78E-05 rs.d.

144 30% 12% 19% rs.d.

145 40% 18% 11 % rs.d.

146 9.11 E-07 1.50E-QS 1.48E-06 rs.d.

1 7 3.97E-97 7.87E-07 δ.58Ε-07 rs.d.

148 1.41 E-0S 3.40E-08 3.08E-08 rs.d. 149 2.38E-98 4.39E-0S 17% n.d.

150 7.38E-98 1.32E-05 1 ,32E-G5 n.d.

151 1.04E-05 51 % 1 ,33E-G5 n.d.

152 5.48E-Q8 7.33E-98 1.11 E-05 n.d.

153 2.35E-Q8 2.73E-98 4.1GE-06 n.d.

154 7.82E-Q8 8.78E-98 1.29E-05 n.d.

155 9.92E-Q7 1.47E-98 1.84E-06 n.d.

156 4.12E-Q8 5.78E-98 1.08E-05 n.d.

157 44% 19% 12% n.d.

158 29% 4% 10% n.d.

159 43% 27% 35% n.d.

160 1.81 E-Q5 33% 13% n.d.

161 4.17E-Q8 3.97E-98 7.0GE-06 n.d.

162 8.78E-Q8 1.18E-95 1.8GE-05 n.d.

163 1.38E-Q5 42% 35% n.d.

164 41 % 19% 22% rs.d.

165 1.88E-85 1.64E-05 32% rs.d.

166 1.8ΘΕ-88 3.88E-08 4.99E-08 rs.d.

167 1.89E-85 48% 37% rs.d. 168 1.22E-95 38% 32% n.d.

169 2.16E-06 3.79E-0S 4,53E-Q6 n.d.

170 45% 7% 15% n.d.

171 5.59E-98 3.37E-88 7.18E-06 n.d.

172 4.97E-98 7.33E-88 9.19E-86 n.d.

173 6.88E-98 8.85E-88 48% n.d.

174 6.92E-98 9.28E-88 1.83E-05 n.d.

175 1.78E-95 58% 44% n.d.

176 3.49E-98 5.82E-88 42% n.d.

177 5.77E-98 6.78E-88 49% n.d.

178 1.43E-98 5.11 E-88 7.12E-06 > 20 pM

179 9.94E-98 2.45E-87 2.14E-07 > 20 pM

180 2.41 E-97 9.21 E-87 8.20E-07 > 20 pM

181 3.50E-Q8 6.51 Ε-Θ8 45% > 20 pM

182 5.10E-Q8 1.23E-87 1.21 E-07 > 20 pM

183 2.11 E-0S 4.29E-08 9.14E-06 > 20 pM

184 4.1 SE-08 1.08E-07 1.22E-07 > 20 pM

185 7.88E-88 3.44E-07 3.23E-07 > 20 pM

186 9.94E-0S 3.31 E-08 22% > 20 pM 187 4.78E-97 5.82E-07 1.26E-06 > 20 pM

188 1.57E-95 1.87E-05 38% > 20 pM

189 9.98E-97 1.17E-0S 2J6E-86 > 20 pM

190 1.75E-Q7 1.53Ε-Θ7 5.53E-07 > 20 pM

191 1.74E-Q7 2.45Ε-Θ7 3.82E-07 > 20 pM

192 4.59E-Q8 4.Θ9Ε-Θ8 1.42E-05 > 20 pM

193 4.18E-Q7 4.Θ5Ε-Θ7 8.20E-07 > 20 pM

194 4.93E-Q7 5.94Ε-Θ7 2.43E-06 > 20 pM

195 3.Q0E-Q7 6.35E-97 7.49E-07 > 20 pM

196 2.42E-Q8 1.99E-98 8.10E-06 > 20 pM

197 2.88E-Q7 3.93E-97 8.38E-07 > 20 pM

198 2.91 E-Q7 5.18E-97 1.09E-06 > 20 pM

199 1.73E-Q8 1.42E-98 8.70E-06 > 20 pM

200 1.39E-Q7 2.38E-97 4.04E-07 > 20 pM

201 1.97E-Q5 28% 50% > 20 pM

202 1.42E-8S 9.79E-07 5.32E-88 > 20 pM

203 1.37E-8S 1.38E-08 3.38E-88 > 20 pM

204 2.29E-87 2.85E-07 8.4QE-87 > 20 pM

205 7.38E-88 8.72E-08 1.28E-87 > 20 pM 206 4.81 E-97 1.09E-0S 1 J5E-G6 > 20 pM

207 2.73E-98 2.27E-0S 1.23E-G5 > 20 pM

208 5.97E-98 ri.d. 47% > 20 pM

209 1.98E-98 ri.d. 4.95E-06 > 20 pM

210 3.85E-98 1.89E-87 1.00E-07 > 20 pM

21 1 1.33E-97 2.92E-87 2.33E-07 > 20 pM

212 8.48E-97 ri.d. 2.84E-06 > 20 pM

213 6.78E-Q8 6.31 E-88 42% > 20 pM

214 3.33E-98 3.98E-88 1.36E-05 > 20 pM

215 9.98E-97 1.18E-88 2.95E-06 2.57Ξ-Θ8

216 8.58E-98 1.78E-85 1.81 E-05 > 20 pM

217 8.80E-98 59% 45% > 20 pM

218 1.98E-98 1.37E-08 3.78E-06 > 20 pM

219 4.15E-97 5.78E-87 9.08E-07 > 20 pM

220 3.79E-97 3.81 Ε-Θ7 1.01 E-06 > 20 pM

221 3.0SE-0S 4.65E-08 4.81 E-08 > 20 pM

3.88E-0S 4.44E-08 1.35E-05 > 20 pM

223 2.11 E-0S 5.80E-0S 7.18E-08 > 20 pM

224 3.80E-88 2.55E-08 9.37E-08 > 20 pM 225 1.54E-08 2.27E-0S 4,δ8Ε-0δ > 20 pM

228 43% 37% 24.00% > 20 pM

227 48% 24% 34% > 20 pM

228 5.89E-07 6.47E-97 1.43E-96 3.41 Ε-Θ7

229 8.95E-08 7.82E-98 29% > 20 pM

230 4.90E-08 6.89Ε-98 1.33E-05 > 20 pM

231 58% 53% 24% > 20 pM

232 9.01 E-08 9.29E-98 4.94E-96 > 20 pM

233 1.04E-05 2.98E-98 1.81 E-95 > 20 pM

234 7.58E-08 6.54E-98 9.21 E-08 > 20 pM

235 5.47E-08 4.72E-98 5.27E-96 > 20 pM

236 37% 3.82E-98 17% > 20 pM

237 31 % 32% 10% > 20 pM

238 8.18E-08 2.17E-07 2.16E-97 > 20 pM

239 7.07E-08 3.83E-98 1.43E-95 > 20 pM

240 3.21 E-88 3.19E-08 7.57E-98 > 20 pM

2 1 1.12E-88 1.44E-08 1.31 E-98 > 20 pM

242 1.83E-88 1.58E-08 3.91 E-98 > 20 pM

243 2.52E-87 3.25E-07 4.18E-97 > 20 pM 244 2.82E-97 4.01 E-07 4,44E-07 > 20 pM

245 5.92E-97 9.0QE-07 9,18E-07 > 20 pM

246 7.59E-98 4.21 E-08 44% > 20 pM

247 5.91 E-Q7 8.87E-07 2.70E-06 > 20 pM

248 1.49E-Q8 8.08E-08 8.43E-06 > 20 pM

249 6.10E-Q8 5.31 E-08 8.79E-06 > 20 pM

250 5.Q0E-Q8 5.81 E-08 7.04E-08 > 20 pM

251 4.57E-Q8 5.84E-08 52% > 20 pM

252 8.Q2E-Q8 7.41 E-08 1.03E-07 > 20 pM

253 1.31 E-Q8 2.33E-08 5.80E-06 > 20 pM

254 8.14E-Q7 1.59E-08 3.45E-G6 > 20 pM

255 2.48E-Q7 3.17E-07 3.9GE-07 > 20 pM

256 4.73E-Q7 8.28E-07 1.35E-06 > 20 pM

257 3.83E-Q7 7.54E-07 8.52E-07 > 20 pM

258 2.Q E-Q7 1.98E-07 2.45E-07 > 20 pM

259 4.02E-07 4.35E-07 8.5QE-07 > 20 pM

260 4.88E-0S 2.04E-08 5.68E-08 > 20 pM

261 8.39E-07 8.73E-07 1.1 QE-08 > 20 pM

262 4.03E-08 4.40E-08 5.11 E-08 > 20 pM 263 2.37E-97 2.32E-07 3,24E-G7 > 20 pM

264 5.94E-06 1.87E-0S 4,81 E-06 > 20 pM

265 2.77E-98 1.47E-0S 1 ,11 E-06 > 20 pM

266 3.81 E-Q8 1.78E-08 3.74E-06 > 20 pM

267 3.39E-Q8 1.52E-88 1.78E-06 > 20 pM

268 1.88E-Q7 1.51 E-07 1.89E-07 > 20 pM

269 1.82E-Q7 1.15E-07 1.35E-07 > 20 pM

270 9.14E-Q8 8.22E-88 9.80E-08 > 20 pM

271 6.Q5E-Q8 7.28E-08 7.59E-08 > 20 pM

272 1.82E-Q8 1.58E-88 2.50E-06 > 20 pM

273 2.32E-Q8 2.38E-88 3.83E-06 > 20 pM

274 1.30E-Q7 1.41 E-07 2.14E-07 > 20 pM

275 2.80E-Q8 2.97E-88 8.37E-06 > 20 pM

276 1.41 E-Q8 1.88E-08 2.16E-06 > 20 pM

277 2.14E-Q7 2.37Ε-Θ7 2.83E-07 > 20 pM

278 1.25E-05 3.71 E-08 43% > 20 pM

279 1.7SE-07 1.88E-07 1.8QE-07 > 20 pM

280 1.48E-07 1.28E-07 1.35E-07 > 20 pM

281 5.59E-07 4.47E-07 3.67E-07 > 20 pM 282 2.57E-97 2.65E-07 2,12E-07 > 20 pM

283 4.18E-9? 3.71 E~07 3,44E-G7 > 20 pM

284 1.06E-06 8.79E-07 8,89E-07 > 20 pM

285 2.Q3E-Q7 1.58E-87 1.81 E-07 > 20 pM

286 1.87E-Q5 1.74E-85 36% > 20 pM

287 5.88E-Q8 1.88E-88 5.76E-06 > 20 pM

288 1.70E-Q7 1.48E-97 2.47E-07 > 20 pM

289 2.11 E-Q8 1.18E-98 2.73E-06 > 20 pM

290 1.78E-Q7 1.18Ε-Θ7 1.59E-07 > 20 pM

291 1.12E-Q8 1.32E-98 2.23E-06 > 20 pM

292 3.15E-Q8 3.87E-98 4.13E-08 > 20 pM

293 2.75E-Q8 3.92Ε-Θ8 8.20E-06 > 20 pM

294 3.10E-Q8 3.93Ε-Θ8 8.58E-06 > 20 pM

295 9.80E-Q7 1.47E-08 2.78E-06 > 20 pM

296 34% 48% 1.18E-05 > 20 pM

297 4.80E-O8 5.78E-08 8.06E-08 > 20 pM

298 4.72E-08 4.93E-08 5.88E-08 > 20 pM

299 9.48E-07 1.23E-08 1.88E-08 > 20 pM

300 3.15E-08 3.07E-08 5.08E-06 > 20 pM 301 7.99E-87 9.31 E~07 1.93E-96 > 20 pM

302 7.87E-87 1.2SE-0S 1.54E-96 > 20 pM

303 7.24E-87 8.49E-07 8,8GE-97 > 20 pM

304 4.17E-87 4.89E-87 3.99E-07 > 20 pM

305 8.18E-88 5.52E-88 5.84E-88 > 20 pM

306 45% 4.28E-88 7.94E-96 > 20 pM

307 5.89E-87 5.93E-07 7.88E-87 > 20 pM

308 2.80E-87 2.29E-07 2.2GE-97 > 20 pM

309 1.32E-88 6.98E-87 8.8GE-07 > 20 pM

310 5.82E-88 1.34E-08 5.76E-96 > 20 pM

31 1 7.83E-87 5.13E-07 8.29E-97 > 20 pM

312 6.82E-98 6.85E-88 7.32E-88 > 20 pM

313 1.87E-87 1.82E-07 1.58E-97 > 20 pM

314 1.84E-87 8.73E-08 9.91 E-98 > 20 pM

315 7.77E-87 9.67E-87 1.28E-86 > 20 pM

316 2.71 E-87 2.84E-07 3.98E-97 > 20 pM

317 7.8ΘΕ-88 8.27E-08 8.84E-98 > 20 pM

318 1.71 E-87 1.87E-07 2.21 E-97 > 20 pM

319 1.84E-87 1.19E-07 1.27E-97 > 20 pM 320 2.26E-06 1.39E-0S 3,49E-Q6 > 20 pM

321 1.48E-95 6.24E-08 1.28E-G5 > 20 pM

4.98E-9? 2.47E-07 2,68E-Q7 > 20 pM

323 3.95E-Q8 7.29E-98 6.84E-08 > 20 pM

324 1.29E-Q8 3.38E-98 6.84E-06 > 20 pM

325 2.28E-Q7 4.43E-97 4.38E-07 > 20 pM

326 1.29E-Q8 2.91 E-98 2.77E-08 > 20 pM

327 1.38E-Q8 1.94E-98 2.56E-06 > 20 pM

328 1.42E-Q7 5.28E-97 6.89E-07 > 20 pM

329 2.41 E-Q8 6.47E-98 1.06E-05 > 20 pM

330 2.27E-Q7 3.65E-97 5.47E-07 > 20 pM

331 9.19E-Q7 9.92E-97 3.17E-06 > 20 pM

332 2.25E-Q8 2.62E-98 1.14E-05 > 20 pM

333 1.30E-Q5 6.28E-98 1.48E-05 1.64Ε-Θ5

334 3.62E-Q7 7.73E-97 1.41 E-06 > 20 pM

335 1.45E-87 3.71 E-07 5.64E-07 > 20 pM

336 8.87E-87 1.26E-08 1.99E-06 > 20 pM

337 3.44E-87 8.O8E-07 1.35E-08 > 20 pM

338 3.25E-87 8.38E-07 1.39E-08 > 20 pM 339 S.15E-0? 1.38E-0S 1 ,99E-96 > 20 pM

340 3.44E-97 9.09E-07 1 ,39E-96 > 20 pM

341 2.83E-98 3.73E-0S 1.22E-05 > 20 pM

342 5.44E-Q7 9.93Ε-Θ7 1.13E-96 > 20 pM

343 1.88E-Q8 1.61 Ε-Θ8 4.33E-96 > 20 pM

344 9.31 E-Q7 1.19E-88 1.86E-96 > 20 pM

345 1.48E-Q5 7.84E-08 ! 2.94E-5 > 20 pM

346 3.42E-Q7 3.95E-87 5.76E-97 > 20 pM

347 1.58E-Q5 9.05E-08 48% > 20 pM

348 8.93E-Q7 8.18E-87 7.53E-97 > 20 pM

349 2.31 E-97 6.49E-87 7.40E-97 > 20 pM

350 8.88E-97 7.38E-87 8.50E-97 > 20 pM

351 1.71 E-Q8 1.28E-88 1.31 E-96 > 20 pM

352 1.80E-Q5 1.22E-05 1.82E-05 > 20 pM

353 3.80E-97 4.28E-07 4.53E-07 > 20 pM

354 3.13E-07 5.18E-07 8.77E-07 > 20 pM

355 4.85E-07 5.71 E-07 7.14E-97 > 20 pM

356 8.55E-07 7.77E-07 9.33E-97 > 20 pM

357 5.12E-08 4.88E-08 8.92E-98 > 20 pM 358 1.44E-98 1.53E-0S 2,45E-86 > 20 pM

359 2.34E-97 2.09E-07 2,99E-87 > 20 pM

360 1.95E-97 1.41 E-07 1 ,9GE-87 > 20 pM

361 2.48E-98 4.85E-88 8.8GE-06 > 20 pM

362 28% 27% 30% > 20 pM

363 1.24E-Q5 1.13E-85 1.72E-05 > 20 pM

364 1.29E-97 1.58E-87 2.17E-07 > 20 pM

365 4.89E-97 2.99E-87 3.53E-07 > 20 pM

366 9.78E-98 9.69E-88 1.36E-07 > 20 pM

367 7.18E-98 6.13E-88 9.9GE-08 > 20 pM

368 41 % 39% 8% > 20 pM

369 9.95E-88 1.52E-87 1.89E-07 > 20 pM

370 2.70E-97 3.52E-87 3.83E-07 > 20 pM

371 1.89E-98 2.42E-88 3.35E-06 > 20 pM

372 28% 33% 19% > 20 pM

373 1.52E-0S 8.29E-06 9.21 E-oe > 20 pM

374 1.8 E-88 2.55E-08 8.50E-06 > 20 pM

375 48% 17% 35% > 20 pM

376 5.48E-88 1.84E-05 1.79E-05 > 20 pM 377 5.14E-06 9.75E-0S 1,51Β-85 > 20

378 4.30E-8? 1.05Ε-08 1,45Ε-0δ > 20

379 5.88E-0? 1.35E-0S 1,83Ε-0δ > 20

380 9.37E-07 1.60Ε-06 2.74Ε-06 > 20 Μ

381 4.90E-Q7 1.98Ε-88 2.33Ε-06 > 20 Μ

382 2.53E-07 9.31 Ε-97 7.48Ε-07 > 20 Μ

383 9.84E-07 3.82Ε-88 5.11Ε-06 > 20 Μ

384 1,23 Ξ-7 8,85 Ξ-8 8,48 Ε-8 η, d,

385 7,32 Ξ-7 3,29 Ε-7 3,88 Ε-7 η, d,

386 8,77 Ξ-δ 3,86 Ξ-8 1,81 Ε-5 η, d,

387 1,17 Ξ-δ 1,86 Ξ-8 8,32 Ε ^» 6 > 2,00 Ε-5

388 2,05 Ξ-7 8,01 Ε-7 7,57 Ε-7 > 2,00 Ε-5

389 8,89 Ξ-6 1,49 Ε-5 1,89 Ε-5 > 2,00 Ε-5

390 5,09 Ξ-6 8,25 Ε-8 1,29 Ε-5 > 2,00 Ε-5

391 1,55 Ξ-8 3,87 Ε-8 3,79 Ε-8 > 2,00 Ε-5

392 3,38 Ε-7 1,19 Ε-8 1,52 Ε-8 > 2,00 Ε-5

393 2,44 Ε-7 9,75 Ε-7 1,04 Ε-8 > 2,00 Ε-5

394 4,05 Ε-7 1,82 Ε-8 > 2,00 Ε-5

395 9,84 Ε-7 1,08 Ε-8 1,02 Ε-8 7,07 Ε-δ 396 2,24 E-6 1,15 B-8 3,13 E~6 > 2,00 E~5

397 2,97 E-7 2,09 B~? 2,49 E~7 > 2,00 E~5

398 1,04 E-7 6,34 B-8 7,21 E~8 > 2,00 E~5

399 3,33 E-7 1,92 E-7 2,96 E-7 > 2,00 E-5

400 7,87 E-8 6,88 E-8 7,66 E-8 > 2,00 E-5

401 7,83 E-8 6,52 E-8 8,23 E-8 > 2,00 E-5

402 8,28 E-8 7,52 E-8 9,81 E-8 > 2,00 E-5

403 4,42 E-7 5,48 E-7 8,32 E-7 > 2,00 E-5

404 4,88 E-6 1,45 E-8 9,30 E-8 > 2,00 E-5

405 1 ,11 E-6 4,48 E-7 1 ,31 E-8 > 2,00 E-5

406 7,27 E-7 4,00 E-7 8,55 E-7 > 2,00 E-5

407 1 ,25 E-6 1,06 E-8 2,14 E-8 > 2,00 E-5

408 5,33 E-7 5,60 E-7 1 ,02 E-8 > 2,00 E-5

409 4,92 E-8 2,80 E-8 3,16 E-8 > 2,00 E-5