Title of Invention

" A COMPOUND 2-(3-AMINOARYL) AMINO-4-ARYL-THIAZOLES OF FORMULA I."

Abstract The present invention relates to novel compounds selected from 2-(3-aminoaryl)amino-4-aryl-thiazoles of formula (I) that selectively modulate, regulate, and/or inhibit signal transductions mediated by certain native and/or mutant tyrosine kinases implicated in a variety of human and animal diseases such as cell proliferative, metabolic, allergic, and degenerative disorders. More particularly, these compounds are potent and selective c-kit inhibitors.
Full Text The present invention relates to novel compounds selected from 2-(3-aminoaryl)amino-4-aryl-thiazoles that selectively modulate, regulate, and/or inhibit signal transduction mediated by certain native and/or mutant tyrosine kinases implicated in a variety of human and animal diseases such as cell proliferative, metabolic, allergic, and degenerative disorders. More particularly, these compounds are potent and selective c-kit inhibitors.
Tyrosine kinases are receptor type or non-receptor type proteins, which transfer the terminal phosphate of ATP to tyrosine residues of proteins thereby activating or inactivating signal transduction pathways. These proteins are known to be involved in many cellular mechanisms, which in case of disruption, lead to disorders such as abnormal cell proliferation and migration as well as inflammation.
As of today, there are about 58 known receptor tyrosine kinases. Other tyrosine kinases are the well-known VEGF receptors (Kim et al, Nature 362, pp. 841-844,1993), PDGF receptors, c-kit and the FLK family. These receptors can transmit signals to other tyrosine kinases including Src, Raf, Frk, Btk, Csk, Abl, Fes/Fps, Fak, Jak, Ack. etc.
Among tyrosine kinase receptors, c-kit is of special interest. Indeed, c-kit is a key receptor activating mast cells, which have proved to be directly or indirectly implicated in numerous pathologies for which the Applicant filed WO 03/004007, WO 03/004006, WO 03/003006, WO 03/003004, WO 03/002114, WO 03/002109, WO 03/002108, WO 03/002107, WO 03/002106, WO 03/002105, WO 03/039550, WO 03/035050, WO 037035049, US 60/359,652.and US 60/359651.
It was found that mast cells present in tissues of patients are implicated in or contribute to the genesis of diseases such as autoimmune diseases (rheumatoid arthritis, inflammatory bowel diseases (IBD)) allergic diseases, tumor angiogenesis, inflammatory diseases, and interstitial cystitis. In these diseases, it has been shown that mast cells participate in the destruction of tissues by releasing a cocktail of different proteases and mediators such as histamine, neutral proteases, lipid-derived mediators (prostaglandins, thromboxanes and leucotrienes), and various cytokines (IL-I, EL-2, IL-3, IL-4, IL-5, EL-6, IL-8, TNF-α, GM-CSF, MlP-la, MlP-lb, MIP-2 and IFN-y).
The c-kit receptor also can be constitutively activated by mutations leading to abnormal cell proliferation and development of diseases such as mastocytosis and various cancers.
For this reason, it has been proposed to target c-kit to deplete the mast cells responsible for these disorders.
The main objective underlying the present invention is therefore to find potent and selective compounds capable of inhibiting wild type and/or mutated c-kit.
Many different compounds have been described as tyrosine kinase inhibitors, for example, bis monocyclic, bicyclic or heterocyclic aryl compounds (WO 92/20642), vinylene-azaindole derivatives (WO 94/14808) and l-cycloproppyl-4-pyridyl-quinolones (US 5,330,992), styryl compounds (US 5,217,999), styryl-substituted pyridyl compounds (US 5,302,606), selenoindoles and selenides (WO 94/03427), tricyclic polyhydroxylic compounds (WO 92/21660) and benzylphosphonic acid compounds (WO 91/15495), pyrimidine derivatives (US 5,521,184 and WO 99/03854), indolinone derivatives and pyrrole-substituted indolinones (US 5,792,783, EP 934 931, US 5,834,504, US
5,883,116, US 5,883,113, US 5, 886,020, WO 96/40116 and WO 00/38519), as well as bis monocyclic, bicyclie aryl and heteroaryl compounds (EP 584 222, US 5,656,643 and WO 92/20642), quinazoline derivatives (EP 602 851, EP 520 722, US 3,772,295 and US 4,343,940) and aryl and heteroaryl quinazoline (US 5,721,237, US 5,714,493, US 5,710,158 and WO 95/15758).
However, none of these compounds have been described as potent and selective inhibitors of c-kit or of the c-kit pathway.
In connection with the present invention, we have found that compounds corresponding to the 2-(3-aminoaryI)amitto-4-aryl-thiazoles are potent and selective inhibitors of c-kit or c-kit pathway. These compounds are good candidates for treating diseases such as autoimmunes diseases, inflammatory diseases, cancer and mastocytosis.
Description
Therefore, the present invention relates to compounds belonging to the 2-(3-amin6)arylamino-4-aryl-thiazoles. These compounds are capable of selectively inhibiting signal transduction involving the tyrosine phosphokinase c-kit and mutant forms thereof. In a first embodiment, the invention is aimed at compounds of formula I, which may represent either free base forms of the substances or pharmaceutically acceptable salts thereof:

(Formula Removed)
a) a linear of branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
b) an aryl substituted by an alkyl or aryl group substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
c) a -CO-NH-R, -CO-R", -CO-OR or a -CO-NRR' group, wherein R and R' are independently chosen from H or an aryl, heteroaryl, alkyl and cycloalkyl group, R" is chosen from an aryl, heteroaryl, and cycloalkyl group
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
R2 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifiuoromethyl or alkoxy;
R3 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifiuoromethyl or alkoxy;
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifiuoromethyl or alkoxy;
R5 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifiuoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifiuoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyI group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifiuoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy,
iv) H, a halogen selected from I, F, CI or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality;
and R7 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethylj and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyI group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazoIyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, a halogen selected from I, F, Clor Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl
Br and F, and / or bearing a pendant basic nitrogen functionality;
In another preferred embodiment, when R1 has the meaning depicted in c) above, the invention is directed to compounds of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F and / or bearing a pendant basic nitrogen functionality.
Among the particular compounds in which Rl has the meaning as depicted in c) above, the invention is directed to amide-aniline compounds of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl Br and F and / or bearing a pendant basic nitrogen functionality; or a a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl
or heteroaryl group optionally'substituted with a heteroatom, notably a halogen selected from I, Cl Br and F arid / or bearing a pendant basic nitrogen functionality; a -SO2-R group wherein R is an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with an heteroatom, notably a halogen selected from I, Cl Br and F and / or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are mdependently chosen from H,an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably selected from I, Cl Br and F, and / or bearing a pendant basic nitrogen functionality,
Among the particular compounds in which Rl has the meaning as depicted in c) above, the invention is directed to amide-benzylamine compounds of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl Br and F, and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl Br and F or bearing a pendant basic nitrogen functionality; or an alkyl, cycloalkyl, aryl or heteroaryl group substituted by a alkyl,cycloalkyl, aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl Br and F or bearing a pendant basic nitrogen functionality;
a -SO2- group wherein R is an alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H or an aryl heteroaryl,alkyl and cycloalkyl group optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality.
Among the particular compounds in which Rl has the meaning as depicted in c) above, the invention is directed to amide-phenol compounds of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
a cycloalkyl, aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F and / or bearing a pendant basic nitrogen functionality; or an alkyl, cycloalkyl, aryl or heteroaryl group substituted by a alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F and / or bearing a pendant basic nitrogen functionality;
a -SO2-R group wherein R is an alkyl, cyeloalkylj aryl of hetefdaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F and / or
bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H or an aryl, heteroaryl, alkyl and cycloalkyl group optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality.
Among the particular compounds in which Rl has the meaning as depicted in c) above, the invention is directed to urea compounds of the following formula:
(Formula Removed)
wherein R is H or1 an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality.
Among the particular compounds in which Rl has the meaning as depicted in a) and b) above, the invention is directed to N-Aminoalkyl-N'-thiazol-2-yl-benzene-l,3-diamine compounds of the following formula;
(Formula Removed)
wherein Y is a linear or branched alkyl group containing from 1 to 10 carbon atoms; wherein Z represents an aryl or heteroaryl group, optionally substituted at one or more ring position with any permutation of the following groups:
- a halogen such as F, Cl, Br, I;
- a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group Optiorially substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, arid / or bearing a pendant basic nitrogen functionality;
- an O-FL, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
an NRaRb, where Ra and Rb represents a hydrogen, or a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality or a cycle; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;.
a COOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyli an aryl or heteroaryl group optionally substituted- with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
a CONRaRb, where Ra and Rb are a hydrogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
an NHCQR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / of bearing a pendant basic nitrogen functionality; a cycloalkyl, an afyl of heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; of a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl of heteroaryl group optionally substituted with an hetefoatOm, notably a halogen selected from t, Cl, Br and F, and / of bearing a pendant basic nitrogen functionality;
an NHCOOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / of bearing a pendant basic nitrogen functionality; a cycloalkyl, an afyl of heteroaryl group optionally substituted with at least one hetefoatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen fbnctionality; of a cycloalkyl, ah aryl Or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or hetefoafyl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and /of bearing a pendant basic nitrogen functionality;
an NHCONRaRb, where Ra and Rb are a hydrogen of a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / Of bearing a pendant basic nitrogen functionality;
- an OSO2R, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- an NRaOSO2Rb, where Ra and Rb are a linear or branched alkyfc group containing from 1 to 10 carbon atoms atoms optionally substituted with at least One heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; Ra can also be a hydrogen; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl of heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
R2 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R3 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R4 is hydrogen, halogen or a linear or branched alkyl group containing ftom 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring positionj of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, frifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which inay additionally bear
any combination of one or more substituents such as halogen, alkyl groups containmg
from 1 to 10 carbon atoms, triflubromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, a halogen selected from I, F, Cl or Br; NH2, NO2 or SO2-R5 wherein R is a linear
or branched alkyl gOup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heterOatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality;
and R7 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyI, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, an halogen selected from Is Fs Cl or Br; NH2, NO2 or SO2-R, wherein R is a
linear or branched alkyl goup containing one or more group such as 1 to 10 carbon
atoms, and optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and/or bearing a pendant basic nitrogen functionality.
An example of preferred compounds of the above formula is depicted below: Among the compounds of formula I, the invention is particularly embodied by the compounds of the following formula II:
(Formula Removed)
wherein X is R or NRR' and wherein R and R' are independently chosen from an aryl, a heteroaryl, or a cycloalkyl group optionally substituted with at least one heteroatom, such as for example a halogen chosen from F, I, Cl and Br and optionally
bearing a pendant basic nitrogen functionality; or an aryl, a heteroaryl, an alkyl or a
cycloalkyl group substituted with an aryl, a heteroaryl, an alkyl or a cycloalkyl group
optionally substituted with at least one heteroatom, such as for example a halogen
chosen from F, I, Cl and Br and optionally bearing a pendant basic nitrogen
functionality,
R2 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R3 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R5 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, a halogen selected from I, F, Cl or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality.
In another alternative, substituent R6, which in the formula II is connected to position 4 of the thiazole ring, may instead occupy position 5 of the thiazole ring.
Among the preferred compounds corresponding formula H the invention is directed to compounds in which X is a substituted alkyl, aryl or heteroaryl group bearing a pendant basic nitrogen functionality represented for example by the structures a to f shown below, wherein the wavy line corresponds to the point of attachment to core structure of formula II:
(Formula Removed)
Among group a to f, X (see formula IT) is preferentially group d.
Furthermore, among the preferred compounds of formula I or II, the invention concerns the compounds in which R2 and R3 are hydrogen. Preferentially, R4 is a methyl group and R5 is H In addition, R6 is preferentially a 3-pyridyl group (of. structure g below), or a 4-pyridyl group (cf structure h below). The wavy line in structure g and h correspond to the point of attachment to the core structure of formula I or II.
(Formula Removed)
Thus, the invention contemplates:
1- A compound of formula II as depicted above, wherein X is group d and R6 is a 3-pyridyl group.
2- A compound of formula II as depicted aboye, wherein X is group d and R4 is a methyl group.
3- A compound of formula I or II as depicted above, wherein R1 is group d and R2 is H.
4- A compound of formula I or II as depicted above, wherein R1 is group d and R3 is H.
5- A compound of formula I or II as depicted above, wherein R1 is group d and R2 and/or R3 and/or R5 is H.
6- A compound of formula I or II as depicted above, wherein R6 is a 3-pyridyl group and R3 is a methyl group.
7- A compound of formula I or II as depicted above, wherein R6 is a 3-pyridyl group and R2 is H.
8- A compound of formula I or II as depicted above, wherein R2 and/or R3 and/or R5 is H and R4 is a methyl group.
9- A compound of formula I or II as depicted above wherein R2 and/or R3 and/or R5 is H, R4 is a methyl group and R6 is a 3-pyridyl group.
Among the compounds of formula II, the invention is particularly embodied by the compounds wherein R2S R3, R5 are hydrogen, corresponding to the following formula II-l :
(Formula Removed)
wherein X is R or NRR' and wherein R and R' are independently chosen from H or an
organic group that can be selected for example from a linear or branched alkyl group
containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom
or bearing a pendant basic nitrogen functionality; a cycloalkyi, an aryl or heteroaryl
group optionally substituted with an heteroatom, notably a halogen selected from I, Cl,
Br and F or bearing a pendant basic nitrogen functionality; or a a cycloalkyl an aryl or
heteroaryl group optionally substituted with a cycloalkyi, an aryl or heteroaryl group
optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and
F or bearing a pendant basic nitrogen functionality;
a -SO2-R group wherein R is an alkyl, cycloalkyi, aryl or heteroaryl optionally
substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing
a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and
R' are independently chosen from H, an alkyl, a cycloalkyi, an aryl or heteroaryl group
optionally substituted with at least one heteroatom, notably selected from I, Cl, Br and F,
and / or bearing a pendant basic nitrogen functionality.
R4 is hydrogen, halogen of a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl,- 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, a halogen selected from I, F, CI or Br; NH2, NO2 or SO2-R, wherein R is a linear or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen fiinctionality.
In another alternative, substituent R6, which in the formula II is connected to position 4
of the thiazole ring, may instead occupy position 5 of the thiazole ring.
Examples :
002 : N-(3-(4-(pyridin-3-yl)thiazol-2-ylamino)-4-methylphenyl)-4-((4'methylpiperazin-
1 -yl)methyl)benzamide
(Formula Removed)
003 : 4-(4-Methyl-piperazin-1 -ylmethyl)-N-[3-(4-pyridin-3 -yl-thiazol-2-ylamino)-phenylj-benzamide
(Formula Removed)
004 : N-[4-methyl-3-(4-phenyl-thiazol-2-ylamino)-phenyI]-4-(4-methyl-piperazin-l -ylmethyl)-benzamide
(Formula Removed)
005 : N-[3-([2,4']Bithiazolyl-2,-ylamino)-4-methyl-phenyl]-4-(4-methyl-piperazin-l-ylmethyl)-benzamide

(Formula Removed)
006 : 4-(4-Methyl-piperazm-l-ylmethyl)-N-[4-methyl-3-(4-pyrazin-2-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
027:2-(2-chloro-5-amino)phenyl-4-(3-pyridyI)-thiazole
(Formula Removed)
110: N-{3-[4-(4-Methoxy-phenyl)-thiazol-2-yIamino]-4-methyl-phenyl}-4-(4-methyl-piperazin-1 ylmethyl)-benzamide
(Formula Removed)
116: 4-(4-Methyl-piperazin4-ylmethyl)-N-{4-methyl-3-[4-(3-trifluoromethyl-phenyI)-thiazol-2-ylaraino]-phenyl}-benzamide
(Formula Removed)
124 :N-{3-[4-(2,5-Dimethyl-phenyl)-thiazol-2-ylarnino]-4-methyl-phenyl}-4-(4-methyl-piperazin-1 -ylmethyl)-benzamide
(Formula Removed)
108: N-{3-[4-(4-Chloro-phenyl)4hiazol-2-ylaminc>]-4-methyl-phenyl}-4-(4-methyl-piperazin-l-ylmetliyl)-benzamide
(Formula Removed)
113: N-{3-[4-(3-Me1hoxy-phenyl)-thiazoI-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-piperazin-l-ylmethyl)-benzamide
(Formula Removed)
063: N-[4-Methyl-3^4-pyridin-3-yl-1hiazoI-2-ylaniino)'-phenyl]-isonicotmamide
(Formula Removed)
064: 2,6-Dichloro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
(Formula Removed)
isonicotinamide
(Formula Removed)
092: Cyclohexanecarboxylic acid [4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylmethyl)-phenyl]-amide
(Formula Removed)
093: 5-[4-Methyl-3-(4-pyridin-3-yl4hiazol-2-yIamind)-phenylcarbamoyli-pentanoic acid ethyl ester

(Formula Removed)
094: 1-Methyl-cyclohexanecarboxylic acid [4-methyl-3-(4-pyridin-3-yI-thiazoI-2-ylmethyl)-phenyl]-amide
(Formula Removed)
095: 4-tert-Butyl-cyclohexanecarboxylic acid [4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-amide
(Formula Removed)
096: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-morpholin-4-yl-
butyramide
(Formula Removed)
beige powder mp:116-120°C
1H RMN (DMSO-d6) δ = 1.80-2.00 (m, 2H) ; 2.29 (s, 3H) ; 2.30-2.45 (m, 6H) ; 3.55-3.65 (m, 6H) ; 7.15-7.25 (m, 2H) ; 7.46-7.50 (m, 2H) ; 7.52 (s, 1H) ; 8.35 (d, J = 6.2 Hz, 1H); 8.55 (dd, J = 1.5 Hz, J = 4.7 Hz, 2H) ; 9.22 (s, 1H) ; 9.45 (s, 1H) ; 9.93 (s, 1H)
(Formula Removed)
Among the compounds of formula II, the invention is particularly embodied by the compounds wherein X is a urea group, a -CO-NRR' group, corresponding to the [3-(thiazol-2-ylamino)-phenyI]-urea family and the following formula II-2 : R6
(Formula Removed)
wherein Ra, Rb are independently chosen from H or an organic group that can be
selected for example from a linear or branched alkyl group containing from 1 to 10
carbon atoms optionally substituted with at least one heteroatom and / or bearing a
pendant basic nitrogen functionality; a cycloalkyi, an aryl or heteroaryl group optionally
substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing
a pendant basic nitrogen functionality; or a cycloalkyi, an aryl or heteroaryl group
optionally substituted with a cycloalkyi, an aryl or heteroaryl group optionally
substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing
a pendant basic nitrogen functionality;
a -SO2-R group wherein R is an alkyl, cycloalkyi, aryl or heteroaryl optionally
substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or
bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group,
wherein R and R' are independently chosen from H, an alkyl, a cycloalkyi, an aryl or
heteroaryl group optionally substituted with at least one heteroatom, notably selected
from I, Cl, Br and F, or bearing a pendant basic nitrogen functionality,
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluorornethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
iv) H, a halogen selected from I, F, Cl or Br; NH2, NO2 of SQ2-R, wherein R is a linear or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality.
Examples
009: l-(4-Methoxy-phenyl)-3-[4-memyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
urea
(Formula Removed)
010:1 -(4-Bromo-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-tliazol-2-ylamind)-phenyl]-urea
(Formula Removed)
011: 1 -[4-Memyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-(4-trifluoromethyl-phenyl)-urea
(Formula Removed)
012:1 -(4-FluorO'phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
013: 1 -[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-(3,4,5-trimethoxy-phenyl)-urea
(Formula Removed)
014: 4-{3-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-ureido}-benzoic acid ethyl ester

(Formula Removed)
015: l-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-thiophen-2-yl-urea

(Formula Removed)
016: l-Cyclohexyl-l-(N-Cyclohexyl-formamide)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
017: l-(2,4-Dimethoxy-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
018: H2-Iodo-phenyl)-l-(K-(2-Iddo-phenyl)-formamide)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-y!amino)-phenyl]-urea
(Formula Removed)
019: l-(3,5-Dimethyl-isoxazol-4-yl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
020: 1-(2-Iodo-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl] urea
(Formula Removed)
021:1 -(4-Difluoromethoxy-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-
(Formula Removed)
022: l-(4-Dimethylam{no-phenyI)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
023:1 -(2-Fluoro-phenyl)-3-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-urea
(Formula Removed)
light brown powder mp : 203-206°C
1H NMR (DMSO-d6) : δ= 2.24 (s, 3H) ; 6.98-7.00 (m5 2H) ; 7.10-7.23 (m, 3H) ; 7.40 (m, 1H) ; 7.48 (s, 1H) ; 8.25 (m, 1H) ; 8.37 (d,. J = 7.8 Hz, 1H); 8.51 (m, 3H) ; 9.03 (s, 1H) ; 9.19 (s, 1H); 9.39 (s, 1H)
024: l-(2-Chloro-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-urea
(Formula Removed)
025: l-(3-Fluoro-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-urea
(Formula Removed)
white powder mp:210-215°C
1H NMR (DMSO-d6) : δ 2.24 (s, 3H) ; 6.79 (t, J = 6.3 Hz, 1H); 6.99 (m, 1H) ; 7.09-7.14 (m, 2H) ; 7.30 (m, 1H) ; 7.41 (t, J = 4.7 Hz, 1H) ; 7.48 (s, 1H) ; 7.56 (d, J = 1.2 Hz, 1H); 8.39 (d, J = 8.0 Hz, 1H); 8.49-8.52 (m, 2H); 8.71 (s, 1H); 8.87 (s, 1H); 9.18 (s, 1H); 9.38 (s, 1H)
026: l-[4-Methyl-3-(4-pyridin-3-yl--thiazolr2-yIamino)-phenyl]-3-p-tolyl-urea
(Formula Removed)
white powder mp : 238-240°C
1H RMN (DMSO-d6) δ = 2.29 (s, 3H) ; 2.31 (s, 3H) ; 7.05 (d, J = 6.2 Hz, 1H) ; 7.10-1.16 (m, 3H); 7.42-7.49 (m, 3H) ; 7.53 (s, 1H) ; 8.35-8.62 (m, 5H) ; 9.22 (d, J = 1.6 Hz, 1H) ; 9.43 (s, 1H)
Among the compounds of formula II, the invention is particularly embodied by the compounds wherein X is a -substituted Aryl group, corresponding to the N-[3-(Thiazol-2-ylamino)-phenyl]-amide family and the following formula II-3 :
(Formula Removed)
wherein Ra, Rb, Re, Rd, Re are independently chosen from H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Bf and F or bearing a pendant basic nitrogen functionality;
a -SO2-R group wherein R is an alkyl, cycloalkyl^ aryl or heteroaryl optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a-CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H, an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably selected from I, Cl, Br and F, and or bearing a pendant basic nitrogeh functionality; Ra, Rb, Rc, Rd, Re may also be
- a halogen such as L Cl, Br and F
- a NRR' group where R and R' are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br
and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl., an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- an OR group where R is H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I> Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyV an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally., substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or. bearing a pendant basic nitrogen functionality; a -SO2-R' group wherein R' is an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with a heteroatonij notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- a NRaCORb group where Ra and Rb are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom^ notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- a NRaCONRbRc group where Ra and Rb are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; Or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl
group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- a COOR, where R is' a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Brand F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- a CONRaRb, where Ra and Rb are a hydrogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) arid / or bearing a pendant basic nitrogen functionality; a cycIoalkyL an aryl or heterbaryl group optionally substituted with at least one heteroatOffij notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nifrbgeh fuhctiohality;
- an NHCOOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- an OSO2R, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a eycloalkylj an aryl or heteroaiyl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkylj a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and;/ or bearing a pendant basic nitrogen functionality;
- an NRaOSO2Rb, where Ra and Rh are a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one.heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; Ra can also be a hydrogen; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, ail aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
-aCNgroup
- a trifluoromethyl group
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyI group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkdxy;
(iii) a five-menibered ring aromatic heterocyclic gr6Up such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, ah alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl and alkoxy;
iv) H, a halogen selected from I, F, CI Or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality.
Examples 028:3-Bromo-N-[4-methyl-3^(4-pyridin^yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
029:3-Iodo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-benzamide
(Formula Removed)
030: 4-Hydroxymethyl-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-
benzamide
(Formula Removed)
031:4-Amino-N-[4-methyl-3-(4-pyridin-3-yl-diiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
032:2-lodo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzsmide
(Formula Removed)
033: 4-Iodo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamidef
034:4-(3-{4-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenylcarbamoyl]-phenyl}-ureido)-benzoic acid ethyl ester
(Formula Removed)
035: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-[3-(4-trifluoromethyl-phenyl)-ureido]-benzamide
(Formula Removed)
036: 4-[3K4-Bromo-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazQl-2-ylamino)-phenyl]-benzamide
(Formula Removed)
037:4-Hydroxy-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-benzamide
f038: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-(3-thiophen-2-yl-
ureido)-benzamide
(Formula Removed)
039: 4-[3-(3,5-Dimethyl4soxazol-4-yl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
(Formula Removed)
040: 4-[3-(4-Methoxy-phenyl)-ureido]-N-[4-metfayI-3-(4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide
(Formula Removed)
041: 4-[3-(4-Difluoromethoxy-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
042: Thiophene-2-sulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenylcarbamoyl]-phenyl ester
(Formula Removed)
043: 4-Iodo-benzenesulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenylcarbamoylj-phenyl ester
(Formula Removed)
044: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-4-(thiophene-2-
suIfonylamino)-benzamide
(Formula Removed)
brown powder mp:230-233°C
1H NMR (DMSO-d6) δ = 2.29 (s, 3H) ; 7.15-7.18 (m, 2H) ; 7.22-7.32 (m, 3H) ; 7.48 (m, 2H) ; 7.67 (dd, J = 1.3 Hz, J = 3.7 Hz, 1H) ; 7.90-7.96 (m, 3H) ; 8.38-8.42 (m, 1H) ; 8.51 (m, 1H) ; 8.57 (d, J = 1.9 Hz, 1H); 9.17 (d, J = 1.7 Hz, 1H); 9.44 (s, 1H) ; 10.12 (s, 1H) ; 10.82 (s, 1H)
045:3-Fluoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
off-white foam mp : 184-186°C .
1H NMR (CD3OD-d4) : δ = 2.23 (s, 3H) ; 7.12-7.14 (m, 2H) ; 7.20-7.23 (m,,2H) ; 7.30 (m, 1H) ; 7.43 (m, 1H) ; 7.50 (m, 1H) ; 7.66 (d, J = 1.0 Hz, 1H) ; 8.23 (m, 1H) ; 8.33 (m,. 1H) ; 8.38 (s, 1H) ; 8.98 (s, 1H)
046: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-4-pyridin-4-yl-
benzamide
(Formula Removed)
yellow powder mp : 254-256°C
1H NMR (DMSO-d6) : δ 2.34 (s, 3H) ; 7.28 (d, J = 8.0 Hz, 1H) ; 7.45-7.49 (m5 2H) ; 7.54 (s, 1H) ; 7.78 (t, J = 7.6 Hz, 1H); 7.89-7.91 (m, 2H) ; 8.10 (t, J = 7.8 Hz, 2H) ; 8.37-8.42 (m, 2H) ;' 8.55 (d, J = 4.7 Hz, 1H); 8.73-8.77 (m, 3H) ; 9.24 (s, 1H) ; 9.52 (s, 1H) ; 10.43 (s, 1H)
047: 4-Dimethylaminoi-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yiamino)-phenyl]-
benzamide
(Formula Removed)
beige powder mp : 147-150°C
'H NMR (DMSO-d6): 5 2.25 (s, 3H) ; 2.99 (s, 6H); 6.76 (d, J = 8.9 Hz, 2H); 7.16 (d, J = 8.3 Hz, 1H) ; 7.35 (d, J = 2.0 Hz, 1H) ; 7.44-7.47 (m, 2H); 7.86-7.89 (m, 2H) ; 8.34-8.36 (m, 1H) ; 8.48-8.50 (m, 1H); 8.56-8.57 (m, 1H) ; 9.16 (s, 1H) ; 9.44 (s, 1H) ; 9.85 (s,lH)
048: 2-Fluoro-5-methyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamuio)-phenyl]-
benzamide
(Formula Removed)
brown orange powder mp : 103-106°C
1H RMN (DMSO-d6) δ = 2.26 (s, 3H) ; 2.35 (s, 3H) ; 7.17-7.47 (m, 7H) ; 8.29 (dd, J = 1.6 Hz, J = 7.9 Hz, 1H) ; 8.47 (d, J= 3.5 Hz, 1H) ; 8.57 (s, 1H) ; 9.15 (d, J = 2.0 Hz, 1H) ; 9.44 (s, 1H) ; 10.33 (s, 1H)
049:4-tert-ButyI-N-[4-methyl-3-(4-pyridm-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
brown powder mp : 145-150°C
1H RMN (DMSO-d6) δ = 1.32 (s, 9H) ; 2.04 (s, 3H) ; 7.18 (d, J = 8.4 Hz, 1H) ; 7.35-7.44 (m, 2H) ; 7.46 (s, 1H) ; 7.55 (d, J = 8.5 Hz, 1H) ; 7.90 (d, J = 8.5 Hz, 1H) ; 8.32 (d, J -7.9 Hz, 1H) ; 8.47 (dd, J = 1.5 Hz, J = 4.7 Hz, 1H) ; 8.60 (d, J = 2.0 Hz, 1H) ; 9.15 (d, J = 1.7 Hz, 1H) ; 9.43 (s, 1H); 10.15 (s, 1H)
050: 4-Isopropoxy-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIniethyI)-phenyl3-
benzamide
(Formula Removed)
brown powder mp : 154-155°C
1H RMN (DMSO-d6) δ = 1.34 (d, J = 5.9 Hz, 6H) ; 4.72 (hept, J = 5.9 Hz, 1H); 7.01 (d, J = 7.0 Hz, 2H) ; 7.18 (d, J = 8.5 Hz, 1H) ; 7.35-7.44 (m, 2H) ; 7.46 (s, 1H); 7.94 (dd, J = 2.0 Hz, J = 6.7 Hz, 2H) ; 8.32 (d, J = 8.3 Hiz, 1H) ; 8.48 (dd, J = 3.3 Hz, J = 4.8 Hz, 1H) ; 8.58 (d, J = 2.0 Hz, 1H) ; 9.15 (d, J = 1.8 Hz, 1H) ; 9.43 (s, 1H); 10.4 (s, 1H)
051: Benzo[l,3]dioxole-5-carboxyllc acid [4-rnethyI-3-(4-pyridin-3-yl-thiazol-2-ylmethyl)-phenyl]-amide
(Formula Removed)
brown orange powder rap: 130-132°C
1H RMN (DMSO-d6) δ = 2.23 (s, 3H) ; 6.10 (s, 2H) ; 7.03 (d, J = 8.1 Hz, 1H) ; 7.15 (d, J - 8.3 Hz, 1H) ; 7.25-7.55 (m, 6H) ; 8.26 (s, 1H) ; 8.45 (dd, J = 1.5 Hz, J = 4.7, 1H) ; 8.55 (d, J = 2.0 Hz, 1H) ; 9.12 (d, J = 1.7 Hz, 1H) ; 9.40 (s, 1H) ; 10.01 (s, 1H)
052: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-(2-morphoIin-4-yl-ethoxy)-benzamide
(Formula Removed)
beige yellow powder mp : 75-80°C
1H RMN (DMSO-d6) δ = 2.10-2.25 (m, 4H) ; 2.50-2.60 (m, 2H) ; 3.19 (s, 3H) ; 3.41-3.48 (m, 4H) ; 4.00-4.06 (m, 2H) ; 7.00-7.11 (m, 2H) ; 7.22-7.35 (m, 6H), 8.18 (d, J = 8.0 Hz, 1H) ; 8.33 (d, J = 0.9 Hz, 1H) ; 8.49 (d, J = 1.7 Hz, 1H) ; 9.03 (s> 1H); 9.31 (s, 1H) ; 10.05 (s, 1H)
053: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylme11iyl).phenyl]4-pyridin-4-yl-
benzamide
(Formula Removed)
brown powder mp : dec. 250°C
1H RMN (DMSO-d6) δ = 2.28 (s, 3H) ; 7.21 (d, J = 7.9 Hz, 1H) ; 7.30-7.50 (m, 3H) ; 7.81 (d, J = 4.7 Hz, 1H) ; 7.98 (d, J = 7.5 Hz, 2H) ; 8.13 (d, J = 7.9 Hz, 2H) ; 8.32 (d, J = 7.7 Hz, 1H) ; 8.48 (d, J = 4.9 Hz, 1H) ; 8.62-8.69 (m, 3H) ; 9.16 (s, 1H); 9.45 (s, 1H) ; 10.34 (s, 1H)
054:3-Cyano-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-benzamide
(Formula Removed)
055: 2-FIuoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylainino)-phenyI]-3-
trifluoromethyl-benzamide
(Formula Removed)
056: 3-FIuoro-benzenesulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenylcarbamoyl]-phenyl ester
(Formula Removed)
057: 4-Aminomethyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
058: 2-Fluoro-benzenesulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-pheriylcarbamoyl]-phenyI ester
(Formula Removed)
059:3-Methoxy-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2Tylme1b.yl)-phenyl]-benzamide
(Formula Removed)
white powder mp : 76-79°C
1H RMN (DMSO-d6) δ = 2.32 (s, 3H); 3.89 (s, 3H); 7.22-7.25 (m, 2H), 7.44-7.58 (m, 4H), 8.28-8.35 (m, 1H); 8.52 (dd, J- 1.6 Hz, J = 4.7 Hz, 1H); 8.66 (d, J = 2.0Hz, 1H); 9.20 (d, J = 1.4 Hz, 1H); 9.50 (s, 1H); 10.25 (s, 1H)
060: 4-(4-methyJ-piperazin-l-yl)-N-f4-methyl-3-(4-pyridin-3-yi-thiazol-2-ylaniino)-
ph eny) ]-benzam ide
(Formula Removed)
beige brown powder mp: 128-130°C
!H RMN (DMSO-d6) δ = 2.15 (s, 3H) ; 2.18 (s, 3H) ; 2.35-2.41 (m, 4H) ; 3.18-3.3.24 (m, 4H); 6.94 (d, J = 8.9 Hz, 2H); 7.09 (d, J = 8.4 Hz, 1H); 7.28-7.38 (m, 3H); 7.81 (d, J = 8.9 Hz, 2H) ; 8.20-8.25 (m, 1H); 8.40 (dd, J = 1.6 Hz, J = 4.7, 1H); 8.48 (d, J = 1.9 Hz, 1H); 9.07 (d, J =1.5 Hz, 1H); 9.35 (s, 1H); 9.84 (s, 1H)
061: 3-Methyl-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
062: Biphenyl-3-carboxyiic acid [4-methyl-3-(4-pyridin-3-yl-trdazol-2-ylamino)-phenyl]-amide
(Formula Removed)
065: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylarnino)-phenyl]-3-trifluoromethyl-
benzamide
(Formula Removed)
099: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl] -4-pyrrolidin-1 -ylmethyl-
benzamide
(Formula Removed)
100: 4-[3-(2,4-Dimethoxy-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide
(Formula Removed)
101: 4-[3-2-Iodo-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
102: 4-[3-(4-Fluoro-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
105: 3-Bromo-4-methyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
(Formula Removed)
106:4-Fluoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
103:4-Cyano-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-benzamide
(Formula Removed)
104:4-Fluoro-N-[4-memyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
Among compounds of formula II, the invention is particularly embodied by the compounds wherein X is a -substituted-aryl group, corresponding to the 4-(4-substituted-l-ylmethyl)-N-[3-(miazol-2-ylatnino)-phenyl]-benzamide family and the following formula II-4 :

(Formula Removed)
wherein X is a heteroatom, such as 0 or N
wherein Ra, Rb, Rd, Re, Rf, Rg, Rh are independently chosen from H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a NRR' group where R and R' are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F of bearing a pendant basic nitrogen functionality;
- or an OR group where R is H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a
pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality* or a cyctoalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; a -SO2-R' group wherein R' is an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a NRaCORb group where Ra and Rb are H or a linear of branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; Or a cyclbalkylj an aryl or heteroaryl group optionally substituted with a cycloalkylj an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a NRaCONRbRc group where Ra arid Rb are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a COOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / of bearing a pendant basic nitrogen functionality; a cycloalkyl, aft aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected
from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or a CONRaRb, where Ra and Rb are a hydrogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or an NHCOOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- an OSO2R, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or
heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or an NRaOSO2Rb, where Ra and Rb are a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; Ra can also be a hydrogen; a cycloalkyl* an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or a -SO2-R group wherein R is an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen front H, an alkyl, a cycloalkyL an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality.
Ra, Rb, Rd, Re can also be halogen such as Cl, F, Br, I or trifluoromethyl;
R4 is hydrogen, halogen or a linear of branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of One or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one of more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a flye-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thiehyl, 2-thiazoIyl, 4-thiazolyl, 5-thiazolyl, Which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl] and alkoxy]-
iv) H, a halogen selected from I, F, CI or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality.
Examples
066: 4-(4-memyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide
(Formula Removed)
067: 3,5-Dibromo-4-(4-memyl'piperazin-l-ylmetliyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
068: 4-Diethylaminomethyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
069: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-morpholin-4-
ylmethyl-benzamide
(Formula Removed)
070: 4-Dipropylaminomethyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phen benzamide
(Formula Removed)
071: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylambo)-phenyl]-4-piperidm-l-ylmethyl-benzamide
(Formula Removed)
072: 4-[(Diisopropylamino)-methyl]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
073: {4-[4-Mefliyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenylcarbamoyl]-benzyl} -carbamic acid tort-butyl ester
(Formula Removed)
074: 3-Fluoro-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
075: 4-(4-Methyl-piperazin-l-yImethyl)-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-
ylmethyl)-phenyI]-3-tri£luoromethyl-berizainide
(Formula Removed)
yellow crystals mp:118-120°C
1H RMN (DMSO-d6) δ - 2.22 (s, 3H) ; 2.33 (s, 3H) ; 2.34-2.50 (m, 8H) ; 3.74 (s, 2H) ;
7.26 (d, J = 8.3Hz, 1H) ; 7.41-7.49 (m, 2H) ; 7.53 (s, 1H) ; 7.99 (d, J = 8.0 Hz, 1H) ;
8.28-8.31 (m, 2H); 8.38 (d, J = 7.9 Hz, 1H); 8.53 (dd, J = 1.3 Hz, J - 4.7 Hz, 1H) ; 8.68
(d, J = 1.9 Hz, 1H); 9.21 (d, J = 2.0 Hz, 1H) ; 9.53 (s, 1H) ; 10.49 (s, 1H)
076: 2,3,5,6-Tetrafluoro-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
077: N-{3-[4-(4-Fluoro-phenyl)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-
piperazin- l-ylmethyl)-benzamide
(Formula Removed)
081: N-{3-[4-(4-cyano-phenyl)-thiazol-2-ylamino]}-4-methyl-phenyl-4-(4-methyl-piperazin-1 -ylmethyl)-benzamide.
(Formula Removed)
082: 4-[l-(4-Methyl-piperazin-l-y])-ethyl]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylmethy])-phenyl]-benzamide
(Formula Removed)
beige powder mp : 153-155°C
1H RMN (DMSO-d6) δ = 1.29 (d, J = 6.6 Hz, 3H); 2.15 (s, 3H); 2.26 (s, 3H); 3.15-3.25 (m, 9H); 7.18 (d, J = 8.4 Hz, 1H); 7.35-7.47 (m, 5H); 7.91 (d, J = 8.2 Hz, 2H); 8.31 (d, J = 8.0 Hz, 1H); 8.47 (dd, J = 1.6 Hz, J = 4.7 Hz, 1H); 8.60 (d, J = 2.0, 1H); 9.15 (d, J = 0.6, 1H); 9.45 (s, 1H); 10.18 (s, 1H)
(Formula Removed)
078: 3-Bromo-4-(4-methy!-pipeiazin-l-ylmethyl)-N-[4-methyl-3-(pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide

(Formula Removed)
079: 3-Chloro-4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
(Formula Removed)
080: 4-(4-Methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridia-4-yl-thiazol-2-
ylamino)-phenyl]~benzamide
(Formula Removed)
084:N-{4-Methyl-3-[4-(5-methyl-pyridin-3-yl)-thiazoI-2-ylamino]-phenyl)-4-(4-methyl-piperazin-l-ylmethyl)-benzamide

(Formula Removed)
085: 3-Iodo-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylmethyl)-phenyl]-benzamide
(Formula Removed)
086: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-[3-(4-trifluoromethyl-phenyl)-ureidomethyl]-benzamide
(Formula Removed)
087: 3, -Dibromo-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-4-[(3-
morpholin-4-yl-propylamino)-methyl]-benzamide
(Formula Removed)
107: 3,5-Dibromo-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-4-
piperidin-1-ylmethyl-benzamide
(Formula Removed)
122: 4-(4-Methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-2-yI-thiazol-2-
ylammo)-phenyl]-benzamide
(Formula Removed)
111: N-{3-[4-(3-Fluoro-phenyl)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-
piperazin-l-ylmethyl)-benzamide
(Formula Removed)
118: N-{3-[4-(2-Fluoro-phenyl)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-
piperazin-1 -ylmethyl)-benzamides
(Formula Removed)
Among compounds of formula II, the invention is particularly embodied by the compounds wherein X is a -aryl-substitiited group, corresponding to the 3-Disubstituted-amino-N-[3-(thiazol-2-ylamino)-phenyl]-benzamide family and the following formula II-5:
(Formula Removed)
wherein Ra, Kb, Rc, Re, Rf, Rg are independently chosen from H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1
to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycioalkyl; an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Brand F or bearing a pendant basic nitrogen functionality; or at cycioalkyl, an aryl or heteroaryl group optionally substituted with a cycioalkyl, an aryl or heteroaryl group optionally substituted with an hetefoatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nifrogen tunetionality;
- or a NRR' group where R and R' are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycioalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom;, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycioalkyl, an aryl or heteroaryl group optionally substituted with a cycioalkyl, an aryl or heteroaryl group optionally substituted with an heteroatonij notably a halogen selected from I, Cl,, Br and F or bearing a pendant basic nitrogen functionality;
- or an OR group where R is H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen funcstionality; a cycioalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycioalkyl, an aryl or heteroaryl group optionally substituted with a cycioalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; a -SO2-R' group wherein R' is an alkyl, cycioalkyl, aryl or heteroaryl optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a NRaCORb group where Ra and Rb are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycioalkyl, an aryl Or heteroaryl
group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a NRaCONRbRe group where Ra and Rb are H or a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with' a heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with, a cycloalkyl, an aryl Or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I* Cl, Br and F or bearing a pendant basic nitrogen functionality;
- or a COOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkylj an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I> CL Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkylj a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or a CONRaRb, where Ra and Rb are a hydrogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen), and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br arid F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl of heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted
with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or an NHCOOR, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- an OSO2R, where R is a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or an NRaOSO2Rb, where Ra and Rb are a linear or branched alkyl group containing from 1 to 10 carbon atoms atoms optionally substituted with at least one heteroatom (for example a halogen) and / or bearing a pendant basic nitrogen functionality; Ra can also be a hydrogen; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / Or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatonij notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality;
- or a -SO2-R group wherein R is an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H, an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality.
Ra, Rb, Re, Re can also be halogen such as Cl, F, Br, I or trifluoromethyl;
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substituents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substituents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyI, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substituents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
iv) H, a halogen selected from I, F, CI or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality.
Examples
088: 3-Dimethylamino-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
(Formula Removed)
beige powder mp: 197-19S°C
1H NMR (DMSO-d6) : 8 = 2.32 (s, 3H) ; 3.03 (s, 6H) ; 6.97 (d, J = 6.4 Hz, 1H) ; 7.23-7.56 (m, 7H) ; 8.37 (d, J = 7.3 Hz, 1H) ; 8.53 (d, J = 4.7 Hz, 1H) ; 8.63 (s, 1H) ; 9.20 (s, lH);9.48(s, 1H) ; 10.15 (s, 1H)
089: 3-(4-Methyl-piperazinrl-yl)-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyI]-benzamide
(Formula Removed)
beige powder mp:274-246°C
1H RMN (DMSO-d6) δ = 2.23 (s, 3H) ; 2.24-2.30 (m, 4H); 3.22-3.27 (m, 4H); 7.07-7.20 (m, 2H); 7.36-7.53 (m, 6H) ; 8.31 (d, J - 7.5 Hz, 1H); 8.47 (d, J = 3.7 Hz, 1H) ; 8.58 (s, 1H) ; 9.12 (d, J= 7.8 Hz, 1H) ; 9.44 (s, 1H) ; 10.12 (s, 1H)
090: N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-inorpholin-4-yl-
benzamide
(Formula Removed)
beige powder mp:247-248°C
1H RMN (CDCl3) δ = 1.50 (s, 3H) ; 3.15-3.18 (m, 4H) ; 3.79-3.82 (m, 3H) ; 6.85 (s, 1H) ; 7.00-7.30 (m, 7H) ; 7.41 (s, 1H) ; 7.75 (s, 1H) ; 8.08 (d, J = 7.9 Hz, 1H); 8.22 (d, J = 1.7 Hz, 1H) ; 8.46 (dd, J = 1.3 Hz, J = 4.7 Hz, 1H) ; 9.01 (d, J = 1.6 Hz, 1H)
Among the compounds of formula n, the invention is particularly embodied by the compounds wherein X is a -OR group, corresponding to the family [3-(ThiazoI-2-ylamino)-phenyl]-carbamate and the following formula II-6
(Formula Removed)
wherein R is independently chosen from an organic group mat can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom and / or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F and / or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with a heteroatom, notably a halogen selected from I, Cl, Br and F and / or bearing a pendant basic nitrogen functionality;
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination,
at any one ring position, of one or more substiruents such as halogen, alkyl groups
containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear
any combination of one or more substiruents such as halogen, alkyl groups containing
from 1 to 10 carbon atoms, trifluoromethyl and alkoxy;
(iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-
thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally bear any
combination of one or more substiruents such as halogen, an alkyl group containing from
1 to 10 carbon atoms, trifluoromethyl, and alkoxy;s
iv) H, a halogen selected from I, F, Cl or Br; NH2, NO2 or SO2-R, wherein R is a linear
or branched alkyl goup containing one or more group such as 1 to 10 carbon atoms, and
optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl,
Br and F, and / or bearing a pendant basic nitrogen functionality.
Examples
097: [4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-carbamic acid isobutyl
ester
(Formula Removed)
098:2-(2-methyl-5-tert-butoxycarbonylamino)phenyl-4-(3-pyridyl)-thiazole
(Formula Removed)
In a second embodiment, the invention is directed to a process for manufacturing a compound of formula I depicted above. This entails the condensation of a substrate of general formula 10 with a thiourea of the type 11.
(Formula Removed)
Substituent "L" in formula 10 is a nucleofugal leaving group in nucleophilic substitution reactions (for example, L can be selected from chloro, bromo, iodo, toluenesulfonyloxy,
methanesulfonyloxy, trifluoromethanesulfonyloxy, etc., with 1, being preferentially a
bromo group),
Group Rl in formula 1 la corresponds to group Rl as described in formula L
Group "PG" in formula 1 lc is a suitable protecting group of a type commonly utilized by
the person skilled in the art.
The reaction of 10 with 1 a-d leads to a thiozole-type product of formula 12a-d.
(Formula Removed)
NO2 Formula 12a is the same as formula I. Therefore, Rl in 12a corresponds to Rl in formula I.
Formula 12b describes a precursor to compounds of formula I which lack substituent Rl. Therefore, in a second phase of the synthesis, substituent Rl is connected to the free amine group in 12b, leading to the complete structure embodied by formula 1:
12b + "Rl" → I The introduction of Rl, the nature of which is as described on page 3 for the general formula I, is achieved by the use of standard reactions that are well known to the person skilled in the art, such as alkylation, acylation, sulfonylation, formation of ureas, etc.
Formula 12c describes an N-protected variant of compound 12b. Group "PG" in formula 12c represents a protecting group of the type commonly utilized by the person
skilled in the art. Therefore, in a second phase of the synthesis, group PG is cleaved to transform compound 12c into compound 12b. Compound 12b is subsequently advanced to structures of formula I as detailed above.
Formula 12d describes a nitro analogue of compound 12b. In a second phase of the synthesis, the nitro group of compound 12d is reduced by any of the several methods utilized by the person skilled in the art to produce the corresponding amino group, namely compound 12b. Compound 12b thus obtained is subsequently advanced to structures of formula I as detailed above.
Examples of Compound synthesis
General: All chemicals used were commercial reagent grade products. Dimethylformamide (DMF), methanol (MeOH) were of anhydrous commercial grade and were used without further purification. Dichloromethane and tetrahydrofuran (THF) were freshly distilled under a stream of argon before use. The progress of the reactions was monitored by thin layer chromatography using precoated silica gel 60F 254, Fluka TLC plates, which were visualized under UV light. Multiplicities in 1H NMR spectra are indicated as singlet (s), broad singlet (br s), doublet (d), triplet (t), quadruplet (q), and multiplet (m) and the NMR spectrum were realized on a 300MHz Broker spectrometer.
3-Bromoacetyl-pyridine, HBr salt
(Formula Removed)
Dibromine (17.2g, 108 mmol) was added dropwise to a cold (0°C) solution of 3-acetyl-pyridine (12 g, 99 mmol) in acetic acid containing 33% of HBr (165 mL) under vigourous stirring. The vigorously stirred mixture was warmed to 40°C for 2h and then
to 75°C. After 2h at 75°C, the mixture was cooled and diluted With ether (400 mL) to precipitate the product, which was recovered by filtration and washed with ether and acetone to give white crystals (100%), This material may be recrystallised from methanol and ether.
IR (neat) : 3108, 2047,2982, 2559,1709,1603, 1221,1035, 798 cm-' - 1H NMR (DMSO-d6) δ = 5.09 (s, 2H, CH2Br); 7.88 (ms IB, pyridyl-H); 8M (m, lH, pyrldyl-H); 8.96 (m, 1H, pyridyl-H); 9.29 (m, 1H, pyridyl-H).
Methyl-[4-(l-N-methyl-piperazino)-methyl]-benzoate
To methyl-4-formyl benzoate (4.92 g, 30 mmol) and N-methyl-piperazine (3.6 mL, 32 mmol) in acetonitrile (100 mL) was added dropwise 2.5 mL of trifluoroacetic acid. The reaction mixture was stirred at room temperature for lh. After slow addition of sodium cyanoborohydride ( 2 g, 32 mmol), the solution was left stirring overnight at room temperature. Water (10 mL) was then added to the mixture, which was further acidified with 1N HCI to pH=6-7. The acetonitrile was removed under reduced pressure and the residual aqueous solution was extracted with diethyl ether (4x30 mL). These extracts were discarded. The aqueous phase was then basified (pH>12) by addition of 2.5N aqueous sodium hydroxyde solution. The crude product was extracted with ethyl acetate (4x30 mL). The combined organic layers were dried over MgSC>4 and concentrated under reduced pressure to afford a slightly yellow oil which became colorless after purification by Kugelrohr distillation (190°C) in 68% yield.
IR(neat) : 3322, 2944,2802,1721,1612,1457,1281, 1122,1012 - 1HNMR (CDC13) δ = 2.27 (s, 3H, NCH3); 2.44 (m, 8H, 2xNCH2CH2N); 3.53 (s, 2H, ArCH2N); 3.88 (s, 3H,
OCH3); 7.40 (d, 2H, J= 8.3 Hz,2xArH); 7.91 (d, 2H, J= 8.3 Hz, 2xArH) - 13C NMR (CDCl3) δ = 45.8 (NCH3); 51.8 (OCH3); 52.9 (2xCH2N); 54.9 (2xCH2N); 62.4 (A1CH2N); 128.7 (2xArC); 129.3 (2xArC); 143.7(ArC); 166.7 (ArCO2CH3) - MS CI (m/z) (%) : 249 (M+l, 100%).
2-Methyl-5-tert-butoxycarbonylamino-aniline
(Formula Removed)
A solution of di-tert-butyldicarbonate (70 g, 320 mmol) in methanol (200 mL) was added over 2 h to a cold (—10°C) solution of 2,4-diaminotoIuene (30 g, 245 mmol) and triethylamine (30 mL) in methanol (15 mL). The reaction was followed by thin layer chromatography (hexane/etliyl acetate, 3 :1) and stopped after 4h by adding 50 mL of water. The mixture was concentrated in vacuo and the residue was dissolved in 500 mL of ethyl acetate. This organic phase was washed with water (1x150 mL) and brine (2x150 mL), dried over MgSO4, and concentrated under reduced pressure. The resulting light brown solid was washed with small amounts of diethyl ether to give off-white crystals of 2-methyl-5-tert-butoxycarbonylamino-aniline in 67% yield.
IR (neat): 3359; 3246; 2970; 1719; 1609; 1557; 1173; 1050 cm"1- !H NMR (CDCI3): 5 = 1.50 (s, 9H, tBu); 2.10 (s, 3H, ArCH3); 3.61 (br s, 2H, NH2); 6.36 (br s, 1H, NH); 6.51 (dd, 1H, /= 7.9 Hz, 2.3 Hz, ArH); 6.92 (d, 1H, J= 7.9 Hz, ArH); 6.95 (s, 1H, ArH) - 13C NMR (CDC13) δ = 16.6 (ArCH3); 28.3 (C(CH3)3); 80.0 (C(CH3)3); 105.2 (ArC); 108.6 (ArC); 116.9 (ArC); 130.4 (ArC-CH3); 137.2 (ArC-NH); 145.0 (ArC-NH2); 152.8 (COOtBu)
MS ESI (m/z) (%) : 223 (M+l), 167 (55,100%).
N-(2-methyl-5-tert-butoxycarbonylamino)phenyl-thiourea
(Formula Removed)
Benzoyl chloride (5.64 g, 80 mmol) was added dropwise to a well-stirred solution of ammonium thiocyanate (3.54 g, 88 mmol) in acetone (50 mL). The mixture was refluxed for 15 min, then, the hydrobromide salt of 2-methyl-5-tert-butoxycarbonyIamino-aniline (8.4g, 80 mmol) was added slowly portionswise. After lh, the reaction mixture was poured into ice-water (350 mL) and the bright yellow precipitate was isolated by filtration. This crude solid was then refluxed for 45 min in 70 mL of 2.5 N sodium hydroxide solution. The mixture was cooled down and basified with ammonium hydroxide. The precipitate of crude thiourea was recovered by filtration and dissolved in 150 mL of ethyl acetate. The organic phase was washed with brine, dried over Na2SO4, and concentrated under reduced pressure. The residue was purified by column chromatography (hexane/ethyl acetate, 1 :1) to afford 63 % of N -(2-methyl-5-tert-butoxycarbony!amino)phenyl-thiourea as a white solid.
IR (neat): 3437, 3292, 3175, 2983, 1724, 1616, 1522, 1161, 1053 cm-1- 1H NMR (DMSO-d6) δ = 1.46 (s, 9H, tBu) ; 2.10 (s, 3H, ArCH3) ; 3.60 (br s, 2H, NH2) ; 7.10 (d, 1H, J= 8.29 Hz, ArH); 7.25 (d, 1H, J= 2.23 Hz, ArH); 7,28 (d, 1H, J= 2.63 Hz, ArH); 9.20 (s, 1H, ArNH); 9.31 (s, 1H, ArNH) - 13C NMR (DMSO-d6) δ = 25.1 (ArCH3); 28.1 (C(CH3)3); 78.9 (C(CH3)3); 116.6 (ArC); 117.5 (ArC); 128.0 (ArC); 130.4 (ArC-CH3); 136.5 (ArC-NH); 137.9 (ArC-NH); 152.7 (COOtBu); 181.4 (C=S) -MS CI(m/z) : 282 (M+l, 100%) ; 248 (33) ; 226 (55) ; 182 (99) ; 148 (133); 93 (188).
2-(2-methyl-5-tert-butoxycarbonyIamino)phenyI-4-(3-pyridyl)-thiazoIe
(Formula Removed) A mixture of 3-brbmoacetyl-pyridine, HBr salt (0.8lg, 2.85 mmol), N-(2-methyl-5-tert-butoxycarbonyIamino)phenyl-thiourea (0.8g, 2.85 mmol) and KHCO3 (~0.4g) in ethanol (40 mL) was heated at 75°C for 20h. The mixture was cooled, filtered (removal of KHCO3) and evaporated under reduced pressure. The residue was dissolved in CHCl3 (40 mL) and washed with saturated aqueous sodium hydrogen carbonate solution and with water. The organic layer was dried over Na2SO4 and concentrated. Colum chromatographic purification of the residue (hexane/ethyl acetate, 1:1) gave the desired thiazole in 70% yield as an orange solid
IR(neat) : 3380, 2985, 2942, 1748, 1447, 1374, 1239, 1047, 938 - 1HNMR (CDCl3) δ = 1.53 (s, 9H, tBu); 2.28 (s, 3H, ArCH3); 6.65 (s, 1H, thiazole-H); 6.89 (s, 1H); 6.99 ( dd, 1H, J= 8.3 Hz, 2.3 Hz); 7.12 ( d, 2H, J =8.3 Hz) ; 7.35 (dd, 1H, J = 2.6 Hz, 4.9 Hz); 8.03 ( s, 1H); 8.19 (dt, 1H, J= 1.9 Hz, 7.9 Hz); 8.54 (br s, 1H, NH); 9.09 (s, 1H, NH)
- 13C NMR (CDCl3) δ = 18.02 (ArCH3); 29.2 (C(CH3)3); 81.3 (C(CH3)3); 104.2 (thiazole-C); 111.6; 115.2; 123.9; 124.3; 131.4; 132.1; 134.4; 139.5; 148.2; 149.1 ; 149.3 ; 153.6; 167.3 (C=0) - MS CI (m/z) (%) : 383 (M+l, 100%) ; 339 (43); 327 (55) ; 309 (73) ; 283 (99) ; 71 (311).
2-(2-methyl-5-amino)phenyI-4-(3-pyridyl)-thiazoIe
(Formula Removed)
2-(2-methyl-5-tert-butoxycarbonyIamino)phenyI-4-(3-pyridyl)-thiazole (0.40g, 1.2 mmol) was dissolved in 10 mL of 20% TFA/CH2Cl2. The solution was stirred at rool temperature for 2h, then it was evaporated under reduced pressure. The residue was dissolved in ethyl acetate. The organic layer was washed with aqueous 1N sodium hydroxide solution, dried over MgSO4, and concentrated to afford 2-(2-methyl-5-amino)phenyl-4-(3-pyridyl)-thiazoIe as a yellow-orange solid in 95% yield. This crude product was used directly in the next step.
A 2M solution of trimethyl aluminium in toluene ( 2.75 mL) was added dropwise to a cold (0° C) solution of 2-(2-methyl-5-amino)phenyl-4-(3-pyridyl)-thiazole (0.42 g, 1.5 mmol) in anhydrous dichloromethane (10 mL) under argon atmosphere. The mixture was warmed to room temperature and stirred at room temperature for 30 min. A solution of methyl-4-(l-N-methyl-piperazino)-methyl benzoate (0.45 g, 1.8 mmol) in anhydrous dichloromethane (1 mL) and added slowly, and the resulting mixture was heated at reflux for 5h. The mixture was cooled to 0°C and quenched by dropwise addition of a 4N aqueous sodium hydroxide solution (3 mL). The mixture was extracted with dichloromethane (3x20 mL). The combined organic layers were washed with brine
(3x20 mL) and dried over anhydrous MgSO4. (2-(2-methyl-5-amino)phenyl-4-(3-pyridyl)-thiazoIe) is obtained in 72% after purification by column chromatography (dichloromethane/methanol, 3 :1)
IR (neat) : 3318,2926,1647, 1610, 1535, 1492, 1282, 1207, 1160, 1011, 843 - 1HNMR (CDC13) δ = 2.31 (br s, 6H, ArCH3+NCH3) ; 2.50 ( br s, 8H, 2xNCH2CH2N) ; 3.56 (s, 2H, ArCH2N) ; 6.89 (s, 1H, thiazoleH); 7.21-7.38 (m, 4H); 7.45 (m, 2H) ; 7.85 ( d, 2H, J = 8.3Hz) ; 8.03 ( s, 1H ) ; 8.13 (s, 1H) ; 8.27 (s, 1H) ; 8.52 (br s, 1H); 9.09 (s, 1H, NH) - ,3C NMR (CDCI3) δ = 17.8 (ArCH3); 46.2 ( NCH3); 53.3 (NCH2); 55.3 (NCH2); 62.8 (ArCH2N) ; 99.9 (thiazole-C) ; 112.5 ; 123.9 ; 125.2; 127.5 ; 129.6; 131.6 ; 133.7 ; 134.0; 137.6; 139.3; 142.9; 148.8; 149.1; 166.2 (C=0); 166.7 (thiazoleC-NH) -MS CI (m/z) (%) : 499 (M+H, 100%); 455 (43); 430 (68) ; 401 (97); 374 (124) ; 309 (189); 283 (215) ; 235 (263) ; 121 (377) ; 99 (399).
In a third embodiment, the invention relates to a pharmaceutical composition comprising a compound as depicted above.
Such medicament can take the form of a pharmaceutical composition adapted for oral administration, which can be formulated using pharmaceutically acceptable carriers well known in the art in suitable dosages. Such carriers enable the pharmaceutical compositions to be formulated as tablets, pills, dragees, capsules, liquids, gels, syrups, slurries, suspensions, and the like, for ingestion by the patient. In addition to the active ingredients, these pharmaceutical compositions may contain suitable pharmaceutically-acceptable carriers comprising excipients and auxiliaries which facilitate processing of the active compounds into preparations which can be used pharmaceutically. Further details on techniques for formulation and administration may be found in the latest edition of Remington's Pharmaceutical Sciences (Maack Publishing Co., Easton, Pa.).
The composition of the invention can also take the form of a pharmaceutical or cosmetic composition for topical administration.
Such compositions may be presented in the form of a gel, paste, ointment, cream, lotion, liquid suspension aqueous, aqueous-alcoholic or, oily solutions, or dispersions of the lotion or serum type, or anhydrous or lipophilic gels, or emulsions of liquid or semi-solid consistency of the milk type, obtained by dispersing a fatty phase in an aqueous phase or vice versa, or of suspensions or emulsions of soft, semi-solid consistency of the cream or gel type, or alternatively of microemulsions, of microcapsules, of microparticles or of vesicular dispersions to the ionic and/or nonionic type. These compositions are prepared according to standard methods.
The composition according to the invention comprises any ingredient commonly used in dermatology and cosmetic. It may comprise at least one ingredient selected from hydrophilic or lipophilic gelling agents, hydrophilic or lipophilic active agents, preservatives, emollients, viscosity enhancing polymers, humectants, surfactants, preservatives, antioxidants, solvents, and fillers, antioxidants, solvents, perfumes, fillers, screening agents, bactericides, odor absorbers and coloring matter.
As oils which can be used in the invention, mineral oils (liquid paraffin), vegetable oils (liquid fraction of shea butter, sunflower oil), animal oils, synthetic oils, silicone oils (cyclomethicone) and fluorinated oils may be mentioned. Fatty alcohols, fatty acids (stearic acid) and waxes (paraffin, carnauba, beeswax) may also be used as fatty substances.
As emulsifiers which can be used in the invention, glycerol stearate, polysorbate 60 and the PEG-6/PEG-32/glycol stearate mixture are contemplated.
As hydrophilic gelling agents, carboxyvinyl polymers (carbomer), acrylic copolymers such as acrylate/alkylacrylate copolymers, polyacrylamides, polysaccharides such as hydroxypropylcellulose, clays and natural gums may be mentioned, and as lipophilic gelling agents, modified clays such as bentones, metal salts of fatty acids such as aluminum stearates and hydrophobic silica, or alternatively ethylcellulose and polyethylene may be mentioned.
As hydrophilic active agents, proteins or protein hydrolysates, amino acids, polyols, urea, allantoin, sugars and sugar derivatives, vitamins, starch and plant extracts, in particular those of Aloe vera may be used.
As lipophilic active, agents, retinol (vitamin A) and its derivatives, tocopherol (vitamin E) and its derivatives, essential fatty acids, ceramides and essential oils may be used. These agents add extra moisturizing or skin softening features when utilized.
In addition, a surfactant can be included in the composition so as to provide deeper penetration of the compound capable of depleting mast cells, such as a tyrosine kinase inhibitor, preferably a c-kit inhibitor.
Among the contemplated ingredients, the invention embraces penetration enhancing agents selected for example from the group consisting of mineral oil, water, ethanol, triacetin, glycerin and propylene glycol; cohesion agents selected for example from the group consisting of polyisobutylene, polyvinyl acetate and polyvinyl alcohol, and thickening agents.
Chemical methods of enhancing topical absorption of drugs are well known in the art. For example, compounds with penetration enhancing properties include sodium lauryl sulfate (Dugard, P. H. and Sheuplein, R. J., "Effects of Ionic Surfactants on the
Permeability of Human Epidermis: An Electrometric Study," J. Ivest Dermatol., V.60, pp. 263-69, 1973), Iauryl amine oxide (Johnson et. al., US 4,411,893), azone (Rajadhyaksha, US 4,405,616 and 3,989,816) and decylmethyl sulfoxide (Sekura, D. L. and Scala, J., "The Percutaneous Absorption of Alkylmethyl Sulfides," Pharmacology of the Skin, Advances In Biolocy of Skin, (Appleton-Century Craft) V. 12, pp. 257-69, 1972). It has been observed that increasing the polarity of the head group in amphoteric molecules increases their penetration-enhancing properties but at the expense of increasing their skin irritating properties (Cooper, E. R. and Berner, B., "Interaction of Surfactants with Epidermal Tissues: Physiochemical Aspects," Surfactant Science Series, V. 16, Reiger, M. M. ed. (Marcel Dekker, Inc.) pp. 195-210,1987).
A second class of chemieal enhancers are generally referred to as co-solvents. These materials are absorbed topically relatively easily, and, by a variety of mechanisms, achieve permeation enhancement for some drugs. Ethanol (Gale et. al., U.S. Pat. No. 4,615,699 and Campbell et. al., U.S. Pat. Nos. 4,460,372 and 4,379,454), dimethyl sulfoxide (US 3,740,420 and 3,743,727, and US 4,575,515), and glycerine derivatives (US 4,322,433) are a few examples of compounds which have shown an ability to enhance the absorption of various compounds.
The pharmaceutical compositions of the invention can also be intended for administration with aerosolized formulation to target areas of a patient's respiratory tract.
Devices and methodologies for delivering aerosolized bursts of a formulation of a drug is disclosed in US 5,906,202. Formulations are preferably solutions, e.g. aqueous solutions, ethanoic solutions, aqueous/ethanoic solutions, saline solutions, colloidal suspensions and microcrystalline suspensions. For example aerosolized particles comprise the active ingredient mentioned above and a carrier, (e.g., a pharmaceutical^ active respiratory drug and carrier) which are formed upon forcing the formulation
through a nozzle which nozzle is preferably in the form of a flexible porous membrane. The particles have a size which is sufficiently small such that when the particles are formed they remain suspended in the air for a sufficient amount of time such that the patient can inhale the particles into the patient's lungs. The invention encompasses the systems described in US 5,556,611:
- liquid gas systems (a liquefied gas is used as propellent gas (e.g. low-boiling FCHC or propane, butane) in a pressure container,
- suspension aerosol (the active substance particles are suspended in solid form in the liquid propellent phase),
- pressurized gas system (a compressed gas such as nitrogen, carbon dioxide, dinitrogen monoxide, air is used.
Thus, according to the invention the pharmaceutical preparation is made in that the active substance is dissolved or dispersed in a suitable nontoxic medium and said solution or dispersion atomized to an aerosol, i.e. distributed extremely finely in a carrier gas. This is technically possible for example in the form of aerosol propellent gas packs, pump aerosols or other devices known per se for liquid misting and solid atomizing which in particular permit an exact individual dosage.
Therefore, the invention is also directed to aerosol devices comprising the compound as defined above and such a formulation, preferably with metered dose valves.
The pharmaceutical compositions of the invention can also be intended for intranasal administration.
In this regard, pharmaceutically acceptable carriers for administering the compound to the nasal mucosal surfaces will be readily appreciated by the ordinaiy artisan. These carriers are described in the Remington's Pharmaceutical Sciences" 16th edition, 1980, Ed. By Arthur Osol, the disclosure of which is incorporated herein by reference.
The selection of appropriate carriers depends upon the particular type of administration that is contemplated. For administration via the upper respiratory tract, the composition can be formulated into a solution, e.g., water or isotonic saline, buffered or unbuffered, or as a suspension, for intranasal administration as drops or as a spray. Preferably, such solutions or suspensions are isotonic relative to nasal secretions and of about the same pH, ranging e.g., from about pH 4.0 to about pH 7.4 or, from pH 6.0 to pH 7.0. Buffers should be physiologically compatible and include, simply by way of example, phosphate buffers. For example, a representative nasal decongestant is described as being buffered to a pH of about 6.2 (Remington's, Id. at page 1445). Of course, the ordinary artisan can readily determine a suitable saline content and pH for an innocuous aqueous carrier for nasal and/or upper respiratory administration.
Common intranasal carriers include nasal gels, creams, pastes or ointments with a viscosity of, e.g., from about 10 to about 3000 cps, or from about 2500 to 6500 cps, or greater, may also be used to provide a more sustained contact with the nasal mucosal surfaces. Such carrier viscous formulations may be based upon, simply by way of example, alkylcelluloses and/or other biocompatible carriers of high viscosity well known to the art (see e.g., Remington's, cited supra. A preferred alkylcellulose is, e.g., methylcellulose in a concentration ranging from about 5 to about 1000 or more mg per 100 ml of carrier. A more preferred concentration of methyl cellulose is, simply by way of example, from about 25 to about mg per 100 ml of carrier.
Other ingredients, such as art known preservatives, colorants, lubricating or viscous mineral or vegetable oils, perfumes, natural or synthetic plant extracts such as aromatic oils, and humectants and viscosity enhancers such as, e.g., glycerol, can also be included to provide additional viscosity, moisture retention and a pleasant texture and odor for the formulation. For nasal administration of solutions or suspensions according to the
invention, various devices are available in the art for the generation of drops, droplets and sprays.
A premeasured unit dosage dispenser including a dropper or spray device containing a solution or suspension for delivery as drops or as a spray is prepared containing one or more doses of the drug to be administered and is another object of the invention. The invention also includes a kit containing one or more unit dehydrated doses of the compound, together with any required salts and/or buffer agents, preservatives, colorants and the like, ready for preparation of a solution or suspension by the addition of a suitable amount of water.
Another aspect of the invention is directed to the use of said compound to manufacture a medicament. In other words, the invention embraces a method for treating a disease related to unregulated c-kit transduction comprising administering an effective amount of a compound as defined above to a mammal in need of such treatment.
More particularly, the invention is aimed at a method for treating a disease selected from autoimmune diseases, allergic diseases, bone loss, cancers such as leukemia and GIST, tumor angiogenesis, inflammatory diseases, inflammatory bowel diseases (EBD), interstitial cystitis, mastocytosis, infections diseases, metabolic disorders, fibrosis, diabetes and CNS disorders comprising administering an effective amount a compound depicted above to a mammal in need of such treatment.
The above described compounds are useful for manufacturing a medicament for the treatment of diseases related to unregulated c-kit transduction, including, but not limited to:
- neoplastic diseases such as mastocytosis, canine mastocytoma, human gastrointestinal stromal tumor ("GIST"), small cell lung cancer, non-small cell
lung cancer, acute myelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, chronic myelogenous leukemia, colorectal carcinomas, gastric carcinomas, gastrointestinal stromal tumors, testicular cancers, glioblastomas, solid tumors and astrocytomas.
- tumor angiogenesis.
- metabolic diseases such as diabetes mellitus and its chronic complications; obesity; diabete type II; hyperlipidemias and dyslipidemias; atherosclerosis; hypertension; and cardiovascular disease.
- allergic diseases such as asthma, allergic rhinitis, allergic sinusitis, anaphylactic syndrome, urticaria, angioedema, atopic dermatitis, allergic contact dermatitis, erythema nodosum, erythema multiforme, cutaneous necrotizing venulitis and insect bite skin inflammation and blood sucking parasitic infestation.
- interstitial cystitis.
- bone loss (osteoporosis).
inflammatory diseases such as rheumatoid arthritis, conjunctivitis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions.
- autoimmune diseases such as multiple sclerosis, psoriasis, intestine inflammatory disease, ulcerative colitis, Crohn's disease, rheumatoid arthritis and polyarthritis, local and systemic scleroderma, systemic lupus erythematosus, discoid lupus erythematosus, cutaneous lupus, dermatomyositis, polymyositis, Sjogren's syndrome, nodular panarteritis, autoimmune enteropathy, as well as proliferative glomerulonephritis.
- graft-versus-host disease or graft rejection in any organ transplantation including kidney, pancreas, liver, heart, lung, and bone marrow.
- Other autoimmune diseases embraced by the invention active chronic hepatitis and chronic fatigue syndrome.
- subepidermal blistering disorders such as pemphigus.
- Vasculitis.
- melanocyte dysfunction associated diseases such as hypermelanosis resulting from melanocyte dysfunction and including lentigines, solar and senile lentigo, Dubreuilh melanosis, moles as well as malignant melanomas. In this regard, the invention embraces the use of the compounds defined above to manufacture a medicament or a cosmetic composition for whitening human skin.
- CNS disorders such as psychiatric disorders, migraine, pain, memory loss and nerve cells degeneracy. More particularly, the method according to the invention is useful for the treatment of the following disorders: Depression including dysthymic disorder, cyclothymic disorder, bipolar depression, severe or "melancholic" depression, atypical depression, refractory depression, seasonal depression, anorexia, bulimia, premenstrual syndrome, post-menopause syndrome, other syndromes such as mental slowing and loss of concentration, pessimistic worry, agitation, self-deprecation, decreased libido, pain including, acute pain, postoperative pain, chronic pain, nociceptive pain, cancer pain, neuropathic pain, psychogenic pain syndromes, anxiety disorders including anxiety associated with hyperventilation and cardiac arrhythmias, phobic disorders, obsessive-compulsive disorder, posttraumatic stress disorder, acute stress disorder, generalized anxiety disorder, psychiatric emergencies such as panic attacks, including psychosis, delusional disorders, conversion disorders, phobias, mania, delirium, dissociative episodes including dissociative amnesia, dissociative fugue and dissociative identity disorder, depersonalization, catatonia, seizures, severe psychiatric emergencies including suicidal behaviour, self-neglect, violent or aggressive behaviour, trauma, borderline personality, and acute psychosis, schizophrenia including paranoid schizophrenia, disorganized schizophrenia, catatonic schizophrenia, and undifferentiated schizophrenia,
- neurodegenerative diseases including Alzheimer's disease , Parkinson's disease, Huntington's disease, the prion diseases, Motor Neurone Disease (MND), and Amyotrophic Lateral Sclerosis (ALS).
- substance use disorders as referred herein include but are not limited to drug addiction, drug abuse, drug habituation, drug dependence, withdrawal syndrome and overdose.
- Cerebral ischemia
- Fibrosis
- Duchenne muscular dystrophy
Regarding mastocytosis, the invention contemplates the use of the compounds as defined above for treating the different categories which can be classified as follows: The category I is composed by two sub-categories (IA and IB). Category IA is made by diseases in which mast cell infiltration is strictly localized to the skin. This category represents the most frequent form of the disease and includes : i) urticaria pigmentosa, the most common form of cutaneous mastocytosis, particularly encountered in children, ii) diffuse cutaneous mastocytosis, iii) solitary mastocytoma and iv) some rare subtypes^ like bullous, erythrodermic and telangiectatic mastocytosis. These forms are characterized by their excellent prognosis with spontaneous remissions in children and a very indolent course in adults. Long term survival of this form of disease is generally comparable to that of the normal population and the translation into another form of mastocytosis is rare. Category IB is represented by indolent systemic disease (SM) with or without cutaneous involvement. These forms are much more usual in adults than in children. The course of the disease is often indolent, but sometimes signs of aggressive or malignant mastocytosis can occur, leading to progressive impaired organ function.
The category II includes mastocytosis with an associated hematological disorder, such as a myeloproliferative or myelodysplastic syndrome, or acute leukemia. These malignant mastocytosis does not usually involve the skin. The progression of the disease
depends generally on the type of associated hematological disorder that conditiones the prognosis.
The category HI is represented by aggressive systemic mastocytosis in which massive infiltration of multiple organs by abnormal mast cells is common. In patients who pursue this kind of aggressive clinical course, peripheral blood features suggestive of a myeloproliferative disorder are more prominent. The progression of the disease can be very rapid, similar to acute leukemia, or some patients can show a longer survival time.
Finally, the category IV of mastocytosis includes the mast cell leukemia, characterized by the presence of circulating mast cells and mast cell progenitors representing more than 10% of the white blood cells. This entity represents probably the rarest type of leukemia in humans, and has a very poor prognosis, similar to the rapidly progressing variant of malignant mastocytosis. Mast cell leukemia can occur either de novo or as the terminal phase of urticaria pigmentosa or systemic mastocytosis.
The invention also contemplates the method as depicted for the treatment of recurrent bacterial infections, resurging infections after asymptomatic periods such as bacterial cystitis. More particularly, the invention can be practiced for treating FimH expressing bacteria infections such as Gram-negative enterobacteria including E. coli, Klebsiella pneumoniae, Seiratia marcescens, Citrobactorfreudii and Salmonella typhimurium. In this method for treating bacterial infection, separate, sequential or concomitant administration of at least one antibiotic selected bacitracin, the cephalosporins, the penicillins, the aminoglycosides, the tetracyclines, the streptomycins and the macrolide antibiotics such as erythromycin; the fluoroquinolones, actinomycin, the sulfonamides and trimethoprim, is of interest.
In one preferred embodiment, the invention is directed to a method for treating neoplastic diseases such as mastocytosis, canine mastocytoma, human gastrointestinal stromal tumor ("GIST"), small cell lung cancer, non-small cell lung cancer, acute myelocytic leukemia, acute lymphocytic leukemia, myelodysplastic syndrome, chronic myelogenous leukemia, colorectal carcinomas, gastric carcinomas, gastrointestinal stromal tumors, testicular cancers, glioblastomas, and astrocytomas comprising administering a compound as defined herein to a human or mammal, especially dogs and cats, in need of such treatment.
In one other preferred embodiment, the invention is directed to a method for treating allergic diseases such as asthma, allergic rhinitis, allergic sinusitis, anaphylactic syndrome, urticaria, angioedema, atopic dermatitis, allergic contact dermatitis, erythema nodosum, erythema multiforme, cutaneous necrotizing venulitis and insect bite skin inflammation and blood sucking parasitic infestation comprising administering a compound as defined herein to a human or mammal, especially dogs and cats, in need of such treatment.
In still another preferred embodiment, the invention is directed to a method for treating inflammatory diseases such as rheumatoid arthritis, conjunctivitis, rheumatoid spondylitis, osteoarthritis, gouty arthritis and other arthritic conditions comprising administering a compound as defined herein to a human in need of such treatment.
In still another preferred embodiment, the invention is directed to a method for treating autoimmune diseases such as multiple sclerosis, psoriasis, intestine inflammatory disease, ulcerative colitis, Crohn's disease, rheumatoid arthritis and polyarthritis, local and systemic scleroderma, systemic lupus erythematosus, discoid lupus erythematosus, cutaneous lupus, dermatomyositis, polymyositis, Sjogren's syndrome, nodular panarteritis, autoimmune enteropathy, as well as proliferative glomerulonephritis
comprising administering a compound as defined herein to a human in need of such treatment.
hi still another preferred embodiment, the invention is directed to a method for treating graft-versus-host disease or graft rejection in any organ transplantation including kidney, pancreas, liver, heart, lung, and bone marrow comprising administering a compound as defined herein to a human in need of such treatment.
Example 1: in vitro TK inhibition assays
• Procedure
Experiments were performed using purified intracellular domain of c-kit expressed in baculovirus. Estimation of the kinase activity was assessed by the phosphorylation of tyrosine containing target peptide estimated by established ELISA assay.
• Experimental results on tested compounds
Result in Table 1 shows the potent inhibitory action of the catalytic activity of c-kit with an IC50 Table 1:

(Table Removed)
Example 2 : ex vivo TK inhibition assays • Procedures
C-Kit WT and mutated C-Kit (JM) assay
Proliferation assays
Cells were washed two times in PBS before plating at 5 x 104 cells per well of 96-well plates in triplicate and stimulated either with hematopoietic growth factors (HGF) or without. After 2 days of culture, 37 Bq (1.78 Tbq/mmol) of [3H] thymidine (Amersham Life Science, UK) was added for 6 hours. Cells were harvested and filtered through glass fiber filters and [3H] thymidine incorporation was measured in a scintillation counter. For proliferation assay, all drugs were prepared as 20mM stock solutions in DMSO and conserved at -80°C. Fresh dilutions in PBS were made before each experiment. DMSO dissolved drugs were added at the beginning of the culture. Control cultures were done with corresponding DMSO dilutions. Results are represented in percentage by taking the proliferation without inhibitor as 100%. Cells
Ba/F3 murine kit and human kit, Ba/F3 mkitA27 (juxtamembrane deletion) are derived from the murine IL-3 dependent Ba/F3 proB lymphoid cells. The FMA3 and P815 cell lines are mastocytoma cells expressing endogenous mutated forms of Kit, i.e., frame deletion in the murine juxtamembrane coding region of the receptor-codons 573 to 579. The human leukaemic MC line HMC-1 expresses mutations JM-V560G; hnmunoprecipitation assays and western blotting analysis
For each assay, 5.106 Ba/F3 cells and Ba/F3-derived cells with various c-kit mutations were lysed and immune-precipitated as described (Beslu et ah, 1996), excepted that cells were stimulated with 250 ng / ml of rmKL. Cell lysates were immunoprecipitated with a rabbit immunserum anti murine KIT, directed against the KIT cytoplasmic domain (Rottapel et al., 1991). Western blot was hybridized either with the 4G10 anti-phosphotyrosine antibody (UBI) or with the rabbit immunserum anti-murine KIT or with different antibodies (described in antibodies paragraph). The membrane was then incubated either with HRP-conjugated goat anti mouse IgG antibody or with HRP-
conjugated goat anti rabbit IgG antibody (Iramunotech), Proteins of interest were then visualized by incubation with ECL reagent (Amersham).
• Experimental results
The experimental results for various compounds according to the invention using above-described protocols are set forth at Table 2:
Table 2:

(Table Removed)
Example 3 : in vivo activity • Procedures
GIST cells: Ba/F3 cells were transfected by c-kit gene having A27 mutation (GIST model). Ba/F3 expressing the mutated c-kit gene readily proliferate in the absence of IL3 or SCF and are tumorigenic in nude mice. Protocol:
Mice were irradiated at J-l (5Gy) Tumor cells (106) were subcutaneously grafted at Jo Tumor size were daily measured from J14 Number of survival mice were daily estimated In this experimental model, the tumor size at J14 is about 20 mm3
Treated mice received per os twice a day a dose of 100 mg/kg of one compound of formula II-3 during 5 days (from 326 to J30).
o Rhumatoid Arthritis The mice were pretreated with the compound of formula II-3 (2 x, 12.5 mg/kg) for two days (day-2, day -1) before induction of arthritis. Arthritis was induced by ip injection of 150-µl serums at days 0 and 2. The treatment with the compound (2x, 12.5 mg/kg) was continued for 14 days. The control mice were injected with, 1% PBS before the induction of arthritis and during the course of the disease. Ankle thickness and arthritis score was evaluated for 15 days. Arthritis Score: Sum of scores of each limb (0 no disease; 1 mild swelling of paw or of just a few digits; 2 clear joint inflammation; 3 severe joint inflammation) maximum score=12. Table 3A and Table 3B show the number of mice used in this study. Two sets of experiments were done with different number of mice, one with 4 mices the other with 8 mices. Table 3 A

(Table Removed)
Table 3 B

(Table Removed)
Histology
At the end of the experiment the hind limbs were collected. The skin of the limb was
removed and the limbs were subsequently fixed in 2% Para formaldehyde,
• Experimental results
GIST Treated mice (with one compound of formula II-3) displays significant decrease of tumor size at J30 and J33 compared to control.
When administrated per os, one tested compound of the formula II-3 displays a significant antitumor activity against tumors cells expressing c-kit A27.
RA A compound of the formula H-3 has demonstrated significant activity in the in vivo mouse model of arthritis. Results are shown on figures 1,2, 3,4.
Figure legends
Figure 1: Effect of the compound in serum transfer experiments, Protocol , ip daily
treatment with the compound ( 2x 12.5 mg/kg) and on days -2 and -1, set of experiment
with 4 mices (T: treated, C: control)
Figure 2: Effect of the compound in serum transfer experiments, Protocol , ip daily
treatment with the compound ( 2x 12.5 mg/kg) and on days -2 and -1, set of experiment
with 4 mices (T: treated, C: control)
Figure 3: Effect of the compound in serum transfer experiments, Protocol , ip daily treatment with the compound ( 2x 12.5 mg/kg) and on days -2 and -1, set of experiment with 8 mices (T: treated, C: control)
Figure 4: Effect of the compound in serum transfer experiments, Protocol , ip daily treatment with the compound ( 2x 12.5 mg/kg) and on days -2 and -1, set of experiment with 8 mices (T: treated, C: control)




We Claim:
1- A compound 2-(3-aminoaryl)amino-4-aryl-thiazoles of formula I :
(Formula Removed)
Wherein R1 is:
a) a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, CL, Br and F, and bearing a pendant basic nitrogen functionality;
b) an aryl substituted by an alkyl or aryl group substituted with an heteroatom, notably a halogen selected from I, CI, Br and F and / or bearing a pendant basic nitrogen functionality;
c) a -CO-NH-R, - CO-R", -CO-OR or a -CO-NRR' group, wherein R and R' are
independently chosen from H or an aryl, heteroaryl, alkyl and cycloalkyl group, R" is
chosen from an aryl, heteroaryl, and cyclo alkyl group,
optionally substituted with at least one heteroatom, notably a halogen selected from
I, Cl, Br and F, or bearing a pendant basic nitrogen functionality;
R2 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R3 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
R4 is hydrogen, halogen or a linear branched alkyl group containing from 1 to 10
carbon atoms, trifluoromethyl or alkoxy;
iv) H, a halogen selected from I, F, Cl or Br; NH2, N02 or S02-R, wherein R is a linear or branched alkyl group containing one or more group such as 1 to 10 carbon atoms, and optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, and / or bearing a pendant basic nitrogen functionality.
2. A compound as claimed in claim 1 selected from:
• 4-DiethylaminomeAyl-N-[4-methyl-3-(4-pvridin-3-yI-thiazol-2-yIamino)-
phenyl]-benzamide,
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-morpholin-4-ylmethyl-benzamide,
• 4-DipropylaminomethyI-N-[4-methyl-3^4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-benzamide,
• N-[4-Methyl-3-(4-pyridin-3-yI-4-thiazol-2-ylamino)-phenyl]-4-piperidin-l-ylmethyl-benzamide,
• 3-Iodo-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-y!amino)-phenyl]-benzamide,
• 4-Hydroxymethyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide,
• 4-Amino-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-benzamide,
• 2-Iodo-N-[4-nethyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-benzaraide,
• 4-Iodo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide,
• 4-(3-{4-[4-Methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenylcarbamoyl]-phenyI}-ureido)-benzoic acid ethyl ester,
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl3-4-[3-(4-trifluoromethyl-phenyl)-ureido]-benzamide,
4-[3-(4-Bromo-phenyl)-ureido]-N-[4-methyl-3-{4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide,
{4-[4-MethyI-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenylcarbamoyl]--ben2yI}-
carbamic acid tert-buryl ester,
4-Hydroxy-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-benzam
4-[(Diisopropylamino)-methyl]-N-[4-methyl-3-(4-pyridin-3-yI-thiazoi-2-
ylamino)-phenyl]-benzamide,
N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-yIambo)-phenyl]-4-(3-thiophen-2-yl-
ureido)-benzamide,
4-[3-(3,5-Dimethyl-isoxazol-4-yl)-ureido]-N-[4-me1hyl-3-(4-pyridin-3-yl-tbiazol-
2-yIamino)-phenyI]-benzarmde,
4-[3-(4-Methoxy-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide,
4-[3-(4-Difluoromethoxy-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-
2-ylamino)-phenyl]-benzamide,
Thiophene-2-sulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylarnino)-
phenylcarbamoyl]-phenyl ester,
4-Iodo-benzenesulfonic acid 4-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-
phenylcarbamoyl]-phenyI ester,
N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-pyrrolidin-l-
ylmethyl-ben2amide,
3-Methyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzarnide,
N-[4-Methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-3-trifluorornethyl-
benzamide,
4-[3-(2,4-Dirnethoxy-phenyl)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylamino)-phenyl]-benzamide,
N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-[3-(4-
trifluoromethyl-phenyl)-ureidomethyl]-benzamide,
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-pfaenyl]-4-[3-(3,4,5-trimethoxy-phenyl)-ureido]-benzamide,
• 4-[3-(2-Iodo-phenyl)-ureido]-N-[4-methyl-3-(4-pyriidin-3-y]-thiazol-2-ylamino)-phenyl]-benzamide,
• 4-[3-(4-Fluoro-phenyI)-ureido]-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-yIamino)-phenyl]-benzamide,
• 2-FIuoro-benzenesulfonic acid 4-[4-methyI-3-(4-pyridin-3-yl-thiazol-2-ylatnino)-phenylcarbamoyl]-phenyl ester,
• 3-F!uoro-benzenesulfonic acid 4-[4-methyI-3-(4-pyridin-3-yI-thiazol-2-ylamino)-
phcnylcarbamoyl]-phenyl ester,
• 4-(4-Mcthyl-piperazin-l-ylmethyl)-N-[3-(4-pyridin-3-yl-thiazoI-2-ylamino)-
phenyl]-benzamide
• N-[4-Methyl-3-(4-phenyl-thiazol-2-ylamino)-phenyl]-4-(4-methyl-piperazin-l-
ylmethyl)-benzamide
• N-[3-([2,4']Bithiazolyl-2-ylamino)-4-methyl-phenyl}-4,4-methylrpiperazin-l -
ylmethyl)-benzamide
• 4-(4-Methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyrazin-2-yl-thiazol-2-
ylam ino)-phenyI]-benzamide
• N-[4-Chloro-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-4-(4-methyl-piperazin-
1 -ylmethyl)-benzamide
• N-{3-[4-(4-Methoxy-phenyl)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-
piperazin-1 -ylmethyl)-benzamide
• 4-(4-Methyl-piperazin-l-ylmethyl)-N-{4-methyI-3-[4-(3-trifluoromethyl-phenyl)-
thiazol-2-ylamino]-phenyl}-benzamide
• N-{3-[4-(2,5-Dimethyl-phenyI)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyI-
piperazin-1 -ylmethyl)-benzam ide
• N-{3-[4-(4-ChIoro-phenyl)-thiazol-2-yIamino]-4-methyl-phenyI}-4-(4-methyI-
piperazin-1-yhnethyl)-benzamide
• 3-Bromo-4-methyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
• 4-Fluoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
• 3,5-Dibromo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-
piperidin-1-ylmethyl-benzamide
• N-{3-[4-(3-Fluoro-phenyl)-thiazoI-2-yIamino]-4-methyI-phenyl}-4-(4-methyl-
piperazin-1 -ylmethyl)-benzamide
• N-{3-[4-(3-Methoxy-phenyI)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-piperazm-l-ylmethyl)-benzamide
• N-{3-[4-(2-Fluoro-phenyl)4hiazol-2-ylamino]-4-methyI-phenyl}-4-(4-methyl-piperazin-1 -ylmethyl)-benzamide
• 4-(4-Methyl-piperazin-l-yImethyl)-N-[4-methyl-3-(4-pyridin-2-yl-thiazol-2-ylamino)-phenyl]-benzamide
• 4-Cyano-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide

• 4-Fluoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-benzamide
• l-(2-Fluoro-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-
urea
• 1-(2-Chloro-phenyl)-3-[4-methyI-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-
urea
• l-(3-FIuoro-phenyl)-3-[4-methyI-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-
urea
• 1 -[4-Methyl-3-(4-pyridiii-3-yI-thiazol-2-ylamino)-phenyl3-3-p-tolyI-urea
• 3-Bromo-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-benzamide
• N-[4-Methyl-3-(4-pyridh-3-yl-thiazoI-2-ylamino)-phenyl]-4-(thi6phene-2-
sulfonylamino)-benzamide
• 3-Fluoro-N-[4-methyl-3-4-pyridin-3-yl-thiazoI-2-ylamino)-phenyI]-benzamide
• N-[4-Methyl-3-(4-pyridm-3-yl-tbiazol-2-ylamino)-phenyl]-4-pyridin-4-yl-
benzamide
• 4-DimethyIamino-N-[4-methyl-3,4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
• 2-Fluoro-5-methyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-
benzamide
• 4-tert-Butyl-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
• 4-Isopropoxy-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylmethyl)-phenyl]-
benzamide
• Benzo[l,3]dioxoIe-5-carboxylic acid [4-methyl-3-(4-pyridin-3-yI-tbiazoI-2-
ylmethyl)-phenyl]-amide
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyI]-3-(2-morpholin-4-yl-
ethoxy)-benzamide
• N-[4-Methyl-3-(4-pyridm-3-yl-thiazol-2-ylmethyl)-phenyl]-4-pyridin-4-yl-
benzamide
• 3-Cyano-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-benzamide
• 2-Fluoro-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-
trifluoromethyl-benzamide
• 4-Aminomethyl-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-yIamino)-phenyl]-
benzamide
• 3-Methoxy-N-[4-methyl-3-(4-pyridin-3-yI-thiazoI-2-ylinetihyl)-phenyl]-benzamide
• 4-(4-Methyl-piperazin-l-yl)-N-[4-methyI-3-(4-pyridin-3-yl-thiazol-2-ylmetby
phenyl]-benzamide
• Biphenyl-3-carboxylic acid [4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-
phenyl]-amide
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-isonicotinamide
• 2,6-Dichloro-N-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-
isonicotinamide
• 3,5-Dibromo-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-melhyl-3-(4-pyridin-3-yl-
thiazol-2-ylamino)-phenyI]-benzamide
• 3-Fluoro-4(4-metliyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-
thiazol-2-ylamino)-phenyl]-benzamide
• 4-(4-Methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-
ylmethyl)-phenyl]-3-trifluoromethyI-benzamide
• 2,3,5,6-Tetrafluoro-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-
3-yl-thiazol-2-ylamino)-phenyl]-benzamide
• N-{3-[4-(4-Fluoro-phenyl)-thiazol-2-ylamino]-4-methyl-phenyl}-4-(4-methyl-
piperazin-l-ylmethyl)-benzamide
• 3-Bromo-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-niethyl-3-(4-pyridin-3-yl-
thiazoI-2-ylamino)-phenyl]-benzamide
• 3-Chloro-4-(4-methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-3-yl-
thiazol-2-ylamino)-phenyl]-benzamide
• 4-(4-Methyl-piperazin-l-ylmethyl)-N-[4-methyl-3-(4-pyridin-4-yl-thiazol-2-
ylamino)-phenyl]-benzamide
• N-{3-[4-(4-Cyano-phenyl)-thiazol-2-ylammo]-4-methyl-phenyl}-4-(4-methyl-
piperazin-1-ylmethyl)-benzamide
• 4-[l-(4-Methyl-piperazin-l-yl)-ethyl]-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylmethyl)-phenyl]-benzamide
• 4-( 1 -Methoxy-ethyl)-N-[4-methyI-3-(4-pyridin-3-yI-thiazol-2-ylmethyl)-phenyI]-
benzamide
• N-{4-Methyl-3-[4-(5-methyI-pyridin-3-yI)-thiazol-2-ylamino]-phenyI}-4-(4-
methyl-piperazin-1 -ylmethyl)-benzamide
• 3-iodo-4-(4-methyl-piperazin-1 -ylmelhyl)-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-
2-ylmethyl)-phenyI]-ben2aniide
• 3,5-Dibrorao-N-[4-methy]-3-(4-pyridin-3-yl-thiazol-2-y]amino)-phenyl]-4-[(3-
morpholin-4-yl-propylamino)-methyl]-benzamide
• 3-Dimethylamino-N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phehyl]-
benzamide
• 3-(4-Methyl-piperazin-l-yl)-N-[4-methyl-3-(4-pyridin-3-yl4hiazol-2-ylamino)-
phenylj-benzamide
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-3-morpholin-4-yl-
benzamide
• Cyclohexanecarboxylic acid [4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylmethyl)-
phenyl]-amide
• 5-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenylcarbamoyI]-pentanoic
acid ethyl ester
• 1-Methyl-cyclohexanecarboxylic acid [4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylmethyl)-phenyfj-amide
• 4-tert-Butyl-cyclohexanecarboxylic acid [4-methyl-3-(4-pyridm-3-yl-thiazol-2-
ylamino)-phenyl]-amide
• N-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-4-morpaholine-4-yl-
butyramide
• [4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-carbamic acid isobutyl
ester
• 2-(2-methyll-5-tert-butoxycarbonylamino)phenyl-4-(3-pyridyl)-thiazole
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a
4. A compound as claimed in claim 1 of the following formula:
linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality.
I. A compound as claimed in claim 1 of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group optionally substituted with a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality; a sulfonyl or a -S02-R group where in R is H, an alkyl, cycloalkyl, aryl or heteroaryl optionally substituted with an heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H, an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably selected from I, C1, Br and F, or bearing a pendant basic nitrogen functionality.
5. A compound as claimed in claim 1 of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, CI, Br and F, or bearing a pendant basic nitrogen functionality; a cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or an alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality;
a sulfonyl or a -S02-R group wherein R is H or an alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, Cl, Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H or an aryl heteroaryl, alkyl and cycloalkyl group optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality.
6. A compound as claimed in claim 1 of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom, notably a halogen selected from I, Cl, Br and F, or bearing a pendant basic nitrogen functionality;
a cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality; or an alkyl, cycloalkyl, aryl or heteroaryl group substituted by a alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, CI, Br and F or bearing a pendant basic nitrogen functionality; a sulfonyl or a -S02-R group wherein R is H or an alkyl, cycloalkyl, aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, CI, Br and F or bearing a pendant basic nitrogen functionality; or a -CO-R or a -CO-NRR' group, wherein R and R' are independently chosen from H or an aryl heteroaryl, alkyl and cycloalkyl group optionally substituted with at least one heteroatom or bearing a pendant basic nitrogen functionality.
7. A compound as claimed in claim 1 of the following formula:
(Formula Removed)
wherein R is H or an organic group that can be selected for example from a linear or branched alkyl group containing from 1 to 10 carbon atoms optionally substituted with at least one heteroatom (for example an halogen) or bearing a pendant basic nitrogen functionality; a cycloalkyl, an aryl or heteroaryl group optionally substituted with at least one heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality; or a cycloalkyl, an aryl or heteroaryl group substituted by an alkyl, a cycloalkyl, an aryl or heteroaryl group optionally substituted with an heteroatom, notably a halogen selected from I, C1, Br and F or bearing a pendant basic nitrogen functionality.
(Formula Removed)
wherein X is R or NRR' and wherein R and R' are independently chosen from an aryl, an heteroaryl and a cycloalkyl group optionally substituted with at least one heteroatom, such as for example a halogen chosen from F, I, CI and Br and optionally bearing a pendant basic nitrogen functionality; or an aryl, an heteroaryl, an alkyl and a cycloalkyl group substituted with an aryl, an heteroaryl, an alkyl and a cycloalkyl group optionally substituted with at least one heteroatom, such as for example a halogen chosen from F, I, CI and Br and optionally bearing a pendant basic nitrogen functionality,
R2 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl or alkoxy;
R3 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl or alkoxy;
R4 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl or alkoxy;
R5 is hydrogen, halogen or a linear or branched alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl or alkoxy; R6 is one of the following:
(i) an aryl group such as phenyl or a substituted variant thereof bearing any combination, at any one ring position, of one or more substituents such as halogen, alkyl groups containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy;
(ii) a heteroaryl group such as a 2, 3, or 4-pyridyl group, which may additionally bear any combination of one or more substituents such as halogen, alkyl groups containing from 1 to 10 carbon atoms, trifluoromethyl and alkoxy; (iii) a five-membered ring aromatic heterocyclic group such as for example 2-thienyl, 3-thienyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, which may additionally
bear any combination of one or more substituents such as halogen, an alkyl group containing from 1 to 10 carbon atoms, trifluoromethyl, and alkoxy.
9. A compound as claimed in claim 8 selected from:
• l-(4-Methoxy-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-
2 -ylamino) -phenyl] -urea,
• l-(4-Bromo-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-urea,
• l-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-y]amino)-phenyl]-3-(4-trifluoromethyl-phenyl)-urea,
• l-(4-FIuoro-phenyl)-3-[4-methyl-3-{4-pyridin-3-yl-thiazol-2-ylammo)-phenyl]-urea,
• l-[4-Methyl-3-(4-pyridin-3-yI-thiazoI-2-ylamino)-phenyI]-3-(3,4,5-trimethoxy-phenyl)-urea,
• 4-{3-[4-Methyl-3-(4-pyridin-3-yI-thiazol-2-yIamino)-phenyl]-ureido}-benzoic acid ethyl ester,
• l-[4-Methyl-3-(4-pyridin-3-yl-thiazol-2-ylainino)-phenyl]-3-thiophen-2-yl-urea,
• 1 -Cyclohexyl-1 -{N-Cyclohexyl-formamide)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea,
• l-(2,4-Dimethoxy-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea,
• l-(2-Iodo-phenyI)-l-(N-(2-Iodo-phenyl)-fonnamide)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-yIamino)-phenyl]-urea,

• l-(3,5-Dimethyl-isoxazoI-4-yl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea,
• l-(24odo-phenyl)-3-[4-methyl-3-(4-pyridin-3-yI-thiazol-2-ylamino)-phenyl]-urea,
• l-(4-Difluoromethoxy-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazoI-2-ylamino)-phenyl]-urea,
• and 1 -(4-Dimethylamino-phenyl)-3-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-phenyl]-urea.
10. A compound as claimed in claim 8, wherein X is a substituted alkyl, aryl or heteroaryl group bearing a pendant basic nitrogen functionality represented for example by the structures a to f shown below, wherein the wavy line corresponds to the point of attachment to core structure of formula II:
(Formula Removed)
11. A compound as claimed in claim 8, wherein X is group d and R6 is a 3-pyridyl group.
12. A compound as claimed in claim 8, wherein X is group d and R4 is a methyl group.
13. A compound as claimed in claim 8, wherein X is group d and R2 and/or R3 and/or R5 is H.
14. A. compound as claimed in claim 1 or 8, wherein R6 is a 3-pyridyl group and R4 is a methyl group.
15. A compound as claimed in claim 1 or 8, wherein R6 is a 3-pyridyl group and R2 and/or R3 and/or R5 is H.
16. A compound as claimed in claim 1 or 8, wherein R2 and/or R3 and/or R5 is H and R4 is a methyl group.
17. A compound as claimed in claim 1 or 8, wherein R2 and/or R3 and/or R5 is
H, R4 is a methyl group and R6 is a 3-pyridyl group.
18. A compound as claimed in claim 8, which is:
4- (4-methyl -piperazin -1- ylmethyl) -N-[4-methyl-3-(4-pyridin-3-yl-thiazol-2-
ylamino) -phenyl] -benzamide,
4-(4-methyl- piperazin- l-yl)-N- [4-methyl-3-(4-pyridin-3-yl-thiazol-2-ylamino)-
phenyl] - benzamide,
4-(4-Methyl-piperazin-l -ylmethyl)-N-[4-methyl-3-(4-pyridin-4-yl-thiazol-2-
ylamino)-phenyl]-benzamide, or
N- {3 -[4-(4-cyano-phenyl)-thiazol-2-ylamino]} -4-methyl-phenyl-4-(4-methyl-
piperazin-1 -ylmethyl)-benzamide.
19. Tablets, pills, dragees, capsules, liquids, gels, syrups, slurries and
suspensions whenever comprising the compound as claimed in any of the
preceding claims.

Documents:

365-delnp-2005-abstract.pdf

365-DELNP-2005-Claims.pdf

365-delnp-2005-complete specification (as-files).pdf

365-delnp-2005-complete specification (granted).pdf

365-delnp-2005-correspondence-others.pdf

365-delnp-2005-correspondence-po.pdf

365-DELNP-2005-Description (Complete).pdf

365-delnp-2005-form-1.pdf

365-delnp-2005-form-18.pdf

365-DELNP-2005-Form-2.pdf

365-delnp-2005-form-3.pdf

365-delnp-2005-form-5.pdf

365-delnp-2005-gpa.pdf

365-delnp-2005-pct-101.pdf

365-delnp-2005-pct-199.pdf

365-delnp-2005-pct-210.pdf

365-delnp-2005-pct-301.pdf

365-delnp-2005-pct-304.pdf

365-delnp-2005-pct-306.pdf

365-delnp-2005-pct-308.pdf

365-delnp-2005-pct-409.pdf

365-delnp-2005-pct-416.pdf

365-delnp-2005-petition-137.pdf

365-delnp-2005-petition-138.pdf


Patent Number 240219
Indian Patent Application Number 365/DELNP/2005
PG Journal Number 19/2010
Publication Date 07-May-2010
Grant Date 29-Apr-2010
Date of Filing 01-Feb-2005
Name of Patentee AB SCIENCE
Applicant Address 3, AVEUNE GEORGES V, F-75008 PARIS, FRANCE,
Inventors:
# Inventor's Name Inventor's Address
1 BRUNO GIETHLEN 39, DOMAINE DE 1'LLE, 67400 ILLKRICH, FRANCE.
2 MARCO CIUFOLINI 16 RUE DE CREQUI, 69006 LYON, FRANCE.
3 CAMILLE WERMUTH 3, RUE DE LA COTE D'AZUR, 67100 STRASBOURG, FRANCE.
4 ALAIN MOUSSY 22 BIS, PASSAGE DAUPHINE, PARIS 75006, FRANCE
PCT International Classification Number C07D 417/04
PCT International Application Number PCT/IB2003/3685
PCT International Filing date 2003-07-31
PCT Conventions:
# PCT Application Number Date of Convention Priority Country
1 60/400,064 2002-08-02 U.S.A.