Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
  • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
  • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
  • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
  • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D213/81—Amides; Imides
  • C07D213/82—Amides; Imides in position 3
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
  • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
  • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings

Definitions

• the present invention relates to nicotinamide derivatives, the compositions containing them and their therapeutic application, especially as anti-cancer agents.
• the invention also relates to the process for the preparation of these compounds as well as to some of the intermediate products.
• A denotes a carbocycle or heterocycle.
• R 2 may especially be an aryl or alkyl group.
• Z represents a phenyl or indanyl group and not a pyridinyl group.
• R 13 may be a 2- or 3-pyridinyl group
• R 4 and R 5 represent a hydrogen atom, an alkyl group , alkoxy, OH, -CF 3 or -CN.
• a and B may each be 1, 3- or 1,4-paraphenylene or 2,4- or 2,5-thienylene
• V is alkylene or NR 2 CO or NR 2 SO 2
• U is alkylene group or a single bond.
• Ring A may be substituted, more particularly with alkoxy groups or with a halogen atom.
• These compounds all include the -CHR 2 COOR 1 motif that does not include the compounds of the invention.
• the compounds of the invention are characterized by the presence on the ZZ 'ring of substituents A and COR 2 which is not described in WO 00/35864.
• a halogen atom a fluorine, chlorine, bromine or iodine atom
• An alkyl group a saturated aliphatic hydrocarbon group comprising from 1 to 6 carbon atoms (advantageously from 1 to 4 carbon atoms) linear or, when the alkyl chain comprises at least 3 carbon atoms, branched or cyclic. Mention may be made, for example, of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, methylcyclopropyl, pentyl, 2,2-dimethylpropyl, hexyl, cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl groups. ;
• An alkoxy group a -O-alkyl group, wherein the alkyl group is as defined above;
• a heteroatom a nitrogen, oxygen or sulfur atom
• a cycloalkyl group a cyclic alkyl group comprising between 3 and 8 carbon atoms, all the carbon atoms being involved in the cyclic structure.
• An aryl group a monocyclic aromatic group, for example a phenyl group
• a heteroaryl group a monocyclic aromatic group comprising one or more heteroatoms engaged in the cyclic structure.
• pyridine group By way of examples, mention may be made of the pyridine group; "A heterocycloalkyl group: a cycloalkyl group as defined above, further comprising from 1 to 4 heteroatoms engaged in the ring structure.
• tetrahydrofuranyl azetidinyl, pyrrolidinyl, piperidinyl, N-alkyl-piperidinyl, morpholinyl, piperazinyl, azepanyl, thiomorpholinyl, 1-oxo-thiomorpholinyl, 1,1-dioxothiomorpholinyl groups.
• the present invention relates to a compound of formula (I):
• A represents a group -NR 1 R 1 ! or (C r C 6 ) alkoxy
• Ri and RS are such that: (i) R 1 represents: a hydrogen atom;
• aryl group optionally substituted with one or more halogen atom (s); a heteroaryl group;
• a (CrC 6 ) alkyl group optionally substituted with: one or more hydroxyl groups or (C 1 -C 6) alkyl groups, preferably (C 1 -C 4 ) alkoxy groups, an aryl group; (C 3 -C 6 ) cycloalkyl, a heteroaryl group, a heterocycloalkyl group or a group -NR 3 R b in which R a and R b represent, independently of one another, a hydrogen atom or a or (C 1 -C 4 ) alkyl, or together with the nitrogen atom to which they are attached form a heterocycloalkyl group optionally comprising another nitrogen atom; hydrogen or a group (CrC ⁇ Jalkyl, or
• R 2 represents a group -QR 4 ;
• Q represents an oxygen atom or the group -NH-.
• R 4 represents:
• A may represent a group -NRiR 1 'in which: (i) R 1 may be:
• aryl group optionally substituted by one or more halogen atom (s) (preferably a fluorine atom).
• s halogen atom
• the aryl group may be the phenyl group;
• a heteroaryl group such as, for example, the 3- or 4-pyridinyl group
• a (C 3 -C 6 ) cycloalkyl group such as for example the cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl group
• (CrC 6) alkyl optionally substituted by: one or more group (s) -OH or (C 1 -C 6 JaIcOXy 1 preferably (C r C 4) alkoxy: for example methoxy, o aryl for example, phenyl group, a (C 3 -C 6 ) cycloalkyl group: for example the cyclopropyl group, a heteroaryl group: for example the pyridinyl group, in particular 2-, 3- or 4-pyridinyl group; heterocycloalkyl: for example the 2-tetrahydrofuryl group; a -NR a R b group in which R 3 and R b represent, independently of one another, a hydrogen atom or a (C 1 -C 6 ) alkyl group, preferably (C 1 -
• R 3 and R b may be two groups (C r C 6 ) alkyl, for example two methyl groups.
• the heterocycloalkyl formed by R a and R b can for example be the
• R 1 from one of those described in Table I.
• R * ! represents a hydrogen atom or a (C ⁇ CeJalkyle.
• R 1 from any of those described in Table I. It may also choose a combination R 1 ⁇ 1 from one of those described in Table I.
• R 1 and R'i together with the nitrogen atom to which they are attached form a group heterocycloalkyl, for example pyrrolidinyl ( N -), piperidinyl ) or
• A may also represent a group (C 1 -C 6) alkyl, for example the ethoxy group.
• heteroaryl group such as, for example, the pyridinyl group, in particular 2-, 3- or 4-pyridinyl;
• a (C 3 -C 6 ) cycloalkyl group such as for example the cyclopropyl or cyclopentyl group; a (C 1 -C 6 ) alkyl group, optionally substituted by: one or more -OH or (C 1 -C 6 ) alkoxy groups, preferably (C 1 -C 4 ) alkoxy groups, for example methoxy; a heteroaryl group: for example the pyridinyl group, in particular 2-, 3- or 4-pyridinyl; a heterocycloalkyl group: for example the morpholinyl, pyrrolidinyl, piperazinyl or piperidinyl group, more particularly by the 4-piperidinyl group; ), eg. 4-N-methyl-piperidinyl
• the heterocycloalkyl group formed by R c and R d may be for example the pyrrolidinyl group
• the heterocycloalkyl group formed by R 0 and R d may be optionally substituted by one or more substituents, which are identical to or different from each other when there are several of them, chosen from: -OH; (C 1 -C 4 ) alkoxy: for example methoxy; (C 1 -C 4) Alkyl: for example methyl, halogen atom: for example fluorine atom, thus substituted heterocycloalkyl
• R 3 is in position 5 or 6 on the pyridine ring (the L group being in position 3 on this ring) as shown below: position 6 position 5
• R 3 is even more preferentially in the 6- position.
• R 3 represents an atom hydrogen or 5- or 6-NH 2 .
• R 3 represents the -OH group in position 2 or 6 (see compound No. 123), the pyridine ring also exists in the 2-pyridone form: case of the -OH group in position 6
• L may be one of those described in Table I.
• R 1 and R 1 ! independently of one another represent a hydrogen atom or a (C 1 -C 6 ) alkyl group
• Q is -NH-; - R 4 represents a hydrogen atom or a group ⁇ C r C 6 ) alkyl.
• R 1 represents a group (C 1 -C 6 ) alkyl and R 1 represents a hydrogen atom or R 1 and R 1 represent two groups (C 1 -C 6 alkyl).
• R 1 and RS represent, independently of one another, a hydrogen atom or a (C 1 -C 6 alkyl) group
• R 4 represents a group (CrC ⁇ ) alkyl substituted with one or more -OH or (C 1 -C 6) alkyl groups, preferably (C 1 -C 4) alkyl groups, and the group -NR 0 R d in which R 0 and R d independently of one another represent a hydrogen atom or a group (C r C 6 ) alkyl or together with the nitrogen atom to which they are attached a heterocycloalkyl group selected from: pyrrolidinyl, piperidinyl, piperazinyl or N- (C 1 -C 4 ) alkylpiperazinyl, azepanyl, morpholinyl, thiomorpholinyl, 1-oxothythomorpholinyl, 1,1-dioxothiomorpholinyl, 3- or 4-hydroxy-piperidinyl, 4,4'-difluoro piperidinyl, 4-methoxy-piperidinyl, 2-methyl-pyrroli
• R 1 represents a group (CrC 6 ) alkyl substituted with: o one or more group (s) -OH or (CrC 6 ) alkoxy, preferably (CrC 4 ) alkoxy; a group -NR a R b in which R 3 and R b represent, independently of one another, a hydrogen atom or a (C 1 -C 6 ) alkyl group, preferably (C 1 -
• C 4 alkyl or together with the nitrogen atom to which they are attached form a heterocycloalkyl group selected from: pyrrolidinyl, piperazinyl, piperidinyl or N-fCVC-Oalkyl-piperidinyl;
• R 4 represents a group (C r C 6 ) alkyl.
• R a and R b may be identical and both represent a hydrogen atom or a (C 1 -C 6 ) alkyl group or may be different and represent a hydrogen atom and a (C 1 -C 6 ) alkyl group.
• R 1 represents a group (CrC 6 ) alkyl substituted by a phenyl group or 2-, 3- or 4-pyridinyl;
• Q is -NH-; - R 4 represents a group (CrC ⁇ Jalkyl.
• Ri represents a (C 3 -C 6 ) cycloalkyl group
• Q is -NH-; - R 4 represents a group (CrC 6 ) alkyl or a (C 3 -C 6 ) cycloalkyl group.
• R 1 may be cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl.
• R 4 may be cyclopropyl or cyclopentyl.
• R 1 represents a phenyl or 3- or 4-pyridinyl group
• RY represents a hydrogen atom
• R 4 represents a (C 1 -C 6 ) alkyl group.
• R 1 represents a phenyl group optionally substituted by one or more halogen atom (s);
• Q is -NH-;
• R 4 represents a (C 1 -C 6) alkyl group optionally substituted with the group -NR c R d in which R c and R d together with the nitrogen atom to which they are attached form a heterocycloalkyl group chosen from the group pyrrolidinyl or piperidinyl.
• R 1 and R ' 1 represent, independently of one another, a hydrogen atom or a (C 1 -C 6 ) alkyl group
• R 4 represents a group (C r C 6 ) alkyl substituted by the 2-, 3 or 4-pyridinyl group.
• R 1 , R 1 , R 4 are as defined above, in particular according to one of the combinations 1 to 8.
• the compounds of the invention may exist in the form of bases or addition salts with acids. Such addition salts are also part of the invention. These salts are advantageously prepared with pharmaceutically acceptable acids, but the salts of other acids that are useful, for example, for the purification or the isolation of the compounds also form part of the invention.
• the compounds according to the invention may also exist in the form of hydrates or solvates, namely in the form of combinations or combinations with one or more molecules of water or with a solvent. Such hydrates and solvates are also part of the invention.
• the compounds may have one or more asymmetric carbon atoms. They can therefore exist as enantiomers or diastereoisomers. These enantiomers, diastereoisomers, as well as their mixtures are part of the invention.
• the invention provides the process for preparing compounds of to the invention as well as some of the reaction intermediates.
• a Suzuki type coupling of P 3 and P 6 is carried out .
• HaI represents a halogen atom (chlorine, bromine, iodine).
• the coupling is carried out in the presence of a palladium complex (in the oxidation state (O) or (N)) such as for example Pd (PPh 3 J 4 , PdCl 2 (PPh 3 J 2 , Pd (OAc) 2 , PdCl 2 (dppf) or bis (di-tert-butyl (4-dimethylaminophenyl) phosphine) dichloropalladium (II)
• the most frequently used complexes are palladium (O) complexes, the coupling being favored in the presence of of a base, which can be for example K 2 CO 3 , NaHCO 3 , and 3 N, K 3 PO 4 , Ba (OH) 2 , NaOH, KF, CsF, Cs 2 CO 3 ...
• the coupling can be in a mixture of an ethereal solvent and an alcohol, for example a dimethoxyethane / ethanol mixture, it can also be a toluene / water mixture (see ex.19), the temperature can be between 50.degree. and 100 ° C. More details on the Suzuki coupling, the operating conditions as well as the palladium complexes usable in: N.Miyaura and A.Suzuki, Chem. Rev. (1995), 95, 2457-2483; A.Suzuki in "Metal-catalyzed cross-coupling reactions"; Diederich, F .; Stang, PJ. Eds. Wiley-VCH: Weinhein, Germany, 1998, Chapter 2, 49-97; Littke, A. and Fu, G., Angew. Chem. Int., Ed. (1999), 38, 3387-3388.
• K and K ' represent a hydrogen atom, an alkyl or aryl group, optionally linked together to form together with the boron atom and the two oxygen atoms a 5 to 7-membered ring.
• one of the following groups can be used:
• P 2 is obtained from P 1 acid by monosubstitution in position 2 with an amine of formula R 1 R 1 T NH.
• P 1 is a 2,6-dihalogenonicotinic acid, for example 2,6-dichloronicotinic acid, which is commercially available (see Example 1).
• the reaction can take place at room temperature and in a protic solvent such as an alcohol or water.
• P 2 is obtained from 2,4-dihydroxy-pyrimidine-5-carboxylic acid (see ex.11). .
• P 3 is prepared by amidification by reacting P 2 with an excess of R 4 NH 2 amine. It is advantageous to use an acid activator ("coupling agent”) such as, for example, benzotriazol-1-yloxytris (dimethylamino) -phosphonium hexafluorophosphate (or BOP, CAS:
• an acid activator such as, for example, benzotriazol-1-yloxytris (dimethylamino) -phosphonium hexafluorophosphate (or BOP, CAS:
• reaction is preferably carried out in the presence of a base (such as triethylamine) at room temperature, in a solvent such as tetrahydrofuran (THF) or dimethylformamide (DMF).
• a base such as triethylamine
• THF tetrahydrofuran
• DMF dimethylformamide
• the reaction is conducted in the presence of triphosgene. It is also preferably conducted in the presence of a base such as for example triethylamine and at a temperature between -5 ° C. and room temperature in an ethereal solvent such as THF.
• A- (4,4,5,5-tetramethyl- [1,3,2] dioxaborolan-2-yl) -phenylamine has frequently been used for P 5 .
• Example 8.1 presents an illustrative procedure for this reaction.
• P 4 can be either commercial or prepared according to methods known to those skilled in the art.
• 2-amino-5-aminomethylpyridine can also be prepared according to EP 0607804.
• 2-amino-5-aminomethylpyridine and 6-amino-3-aminomethyl-5-methylpyridine can be prepared according to preparations D and F of EP 1050534.
• 2-Fluoro-5-aminomethylpyridine (CAS No. 205744 -17-8) can be prepared according to Chinese Journal of Chemistry 2006, 24 (4), 521-526.
• 5-Aminomethyl-2- (dimethylamino) pyridine (CAS No. 354824-17-2) is commercially available or can be prepared according to Journal of Agricultural and Food Chemistry 2008, 56 (1), 204-212.
• 3-Fluoro-5-aminomethylpyridine (CAS No. 23586-96-1) and 2-fluoro-3-aminomethylpyridine can be prepared according to WO 2005066126 (preparations 46 and 47).
• 2-Amino-3-methyl-5-aminomethylpyridine (CAS No.
• Esterification is known to those skilled in the art and consists in reacting the acid function of P 2 or P 8 with the alcohol function of R 4 OH in the presence of a strong acid as a catalyst (Practical Organic Chemistry AI Vogel 3rd ed. page 382) or of an acid activator such as EDCI.
• P 10 can be either commercial or prepared according to methods known to those skilled in the art.
• trans-3- (3-pyridyl) acrylic acid is marketed by Sigma-Aldrich.
• P 10 can also be prepared according to J.Org.Chem. 1998, 63, 8785-8789 from the ⁇ - corresponding formylpyridine.
• P 12 can be either commercial or prepared according to methods known to those skilled in the art. For example, 3- (3-pyridinyl) propanoic acid is marketed by Sigma-Aldrich. P 12 can also be prepared by hydrogenation of P 10 (Journal of Medicinal Chemistry 1993, 36 (22), 3293-9).
• P 13 can be obtained according to Scheme 6.
• the amidation by R 4 NH 2 can be carried out in presence of an acid activator such as, for example, N, N'-carbonyl diimidazole (CDI) (see: R. Paul, GW Anderson (1960).) N.N'-Carbonyldiimidazole, a New Peptide Forming Reagent ', Journal of the American Chemical Society 82: 4596-4600).
• the reaction may be conducted in a solvent such as THF. We can take inspiration from the conditions of ex.10.1.
• the next step is performed in the presence of the alcoholate R ⁇ O ".
• the reaction may be carried out in THF at a temperature of about 70 0 C. It will be guided by conditions ex.10.2 .
• a protecting group to protect one or more chemical function (s), including a primary or secondary amine function.
• PG protecting group
• R c and R d both represent a hydrogen atom
• the amidification of Scheme 2 is carried out using for R 4 NH 2 the compound 2 HN- (C r )
• the function (s) is / are then obtained (s) by a deprotection step (final or intermediate) whose conditions depend on the nature of the function (s) protected (s) and protective group used.
• the deprotection step is carried out in an acid medium using, for example, HCl or triflic acid. This gives the corresponding salt (hydrochloride or triflate) if appropriate; see compounds No. 5, 32, 94, 104, 119.
• Another method of obtaining salts is to contact the compound in its base form with the acid.
• the starting compounds and the reagents when their method of preparation is not described, are commercially available or described in the literature, or they can be prepared according to methods described therein or which are known to those skilled in the art. Those skilled in the art may also be inspired by the operating conditions given in the examples which are described below.
• the invention relates to a pharmaceutical composition comprising a compound as defined above in combination with a pharmaceutically acceptable excipient.
• the excipient is selected from the usual excipients known to those skilled in the art according to the pharmaceutical form and the desired mode of administration.
• the mode of administration can be, for example, orally or intravenously.
• the invention relates to a medicament which comprises a compound as defined above and the use of a compound as defined above for the manufacture of a medicament. It can be useful for treating a pathological condition, especially cancer. This drug may find use in therapy, particularly in the treatment or prevention of diseases caused or exacerbated by the proliferation of cells and in particular tumor cells.
• the drug (as well as a compound according to the invention) can be administered in combination with one (or more) anticancer agents, in particular chosen from: "chemotherapy agents such as alkylating agents, platinum derivatives, antibiotic agents, antimicrotubule agents, taxoids, anthracyclines, group I and II topoisomerase inhibitors, fluoropyrimidines, cytidine analogues, adenosine analogs, enzymes, as well as estrogenic and androgenic hormones; • antivascular or anti-angiogenic agents.
• chemotherapy agents such as alkylating agents, platinum derivatives, antibiotic agents, antimicrotubule agents, taxoids, anthracyclines, group I and II topoisomerase inhibitors, fluoropyrimidines, cytidine analogues, adenosine analogs, enzymes, as well as estrogenic and androgenic hormones; • antivascular or anti-angiogenic agents.
• a treatment with radiation.
• This treatment can be administered simultaneously, separately or sequentially.
• the treatment will be adapted by the practitioner according to the patient and the tumor to be treated.
• the invention also relates to a method of treatment of pathologies indicated above which comprises administering to a patient an effective dose of a compound of the invention or a pharmaceutically acceptable salt or hydrates or solvates.
• the following examples illustrate the preparation of certain compounds according to the invention. These examples are not limiting and only illustrate the present invention.
• the numbers of the compounds exemplified refer to those given in the table below, which illustrates the chemical structures and the physical properties of some compounds according to the invention.
• the compounds were analyzed by HPLC-UV-MS coupling (liquid chromatography, ultraviolet (UV) detection and mass detection).
• the device used consists of an Agilent chromatographic chain equipped with an Agilent diode array detector and a ZQ Waters single quadrupole mass spectrometer or a Quattro-MicroWaters triple quadrupole mass spectrometer.
• the liquid chromatography / mass spectrometry (LC / MS) spectra were recorded in electrospray (ESI) positive mode, in order to observe the ions resulting from the protonation of analyzed compounds (MH + ) or the formation of adducts with other cations such as Na + , K + , etc.
• the ionization parameters are as follows: cone voltage: 20 V; capillary voltage: 3 kV; source temperature: 120 ° C. desolvation temperature: 450 ° C; gas desolvation: N 2 to 450 Uh.
• HPLC conditions are chosen from one of the following methods:
• Example 11 4-Ethylamino-2- [4- (3-pyridin-3-ylmethyl-ureido) -phenyl] -pyrimidine-5-carboxylic acid (2-piperidin-1-yl-ethyl) -amide (compound no. 80) 11.1. 2,4-dichloro-pyrimidine-5-carbonyl chloride
• Example 12 6- ⁇ 4- [3- (6-amino-pyridin-3-ylmethyl) -ureido] -phenyl ⁇ -2-ethylamino-N- (2-piperidin-1-yl-ethyl) -nicotinamide (compound No. 81) 12.1. 6-Chloro-2-ethylamino-N- (2-piperidin-1-yl-ethyl) -nicotinamide
• Example 14 2- (Cyclopropylmethylamino) -N-methyl-6- [4- (3-pyridin-3-ylmethyl-ureido) phenyl] -nicotinamide (Compound No. 48)
• Example 17 2- (2-Methoxy-ethylamino) -N-methyl-6- [4- (3-pyridin-3-ylmethyl-ureido) - phenyl] -nicotinamide (compound 51)
• Example 19 4 '- [3- (6-Amino-pyridin-3-ylmethyl) -ureido] -3-ethylamino-biphenyl-4-carboxylic acid (2-piperidin-1-yl-ethyl) -amide (compound no.
• the medium is stirred for 30 min at room temperature and under argon, and then 0.034 g (0.05 mmol) of bis (di-tert-butyl (4-dimethylaminophenyl) phosphine) dichloropalladium (II) are added.
• the reaction medium is stirred under reflux and under argon for 5 h.
• the solvent is evaporated under reduced pressure.
• the residue is taken up in dichloromethane, washed successively with water and saturated NaCl solution and the organic phase is dried over sodium sulphate.
• nBu n-butyl
• tBu tert-butyl
• iPr isopropyl for R3: 6-NH 2 means -NH 2 at the 6-position on the pyridine ring as indicated; 2-F means -F in position 5 on the pyridine ring

Landscapes

• Organic Chemistry (AREA)
• Chemical & Material Sciences (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Medicinal Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• General Chemical & Material Sciences (AREA)
• Pharmacology & Pharmacy (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Animal Behavior & Ethology (AREA)
• General Health & Medical Sciences (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Pyridine Compounds (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)

Applications Claiming Priority (2)

Publications (1)

Family

ID=39356668

Family Applications (1)

Country Status (19)

Families Citing this family (25)

Family Cites Families (6)

• 2007
  • 2007-09-28 FR FR0706799A patent/FR2921657A1/fr not_active Withdrawn
• 2008
  • 2008-09-24 TW TW097136703A patent/TW200918056A/zh unknown
  • 2008-09-26 KR KR1020107006595A patent/KR20100065165A/ko not_active Application Discontinuation
  • 2008-09-26 UY UY31367A patent/UY31367A1/es not_active Application Discontinuation
  • 2008-09-26 JP JP2010526335A patent/JP2010540504A/ja not_active Withdrawn
  • 2008-09-26 RU RU2010116765/04A patent/RU2010116765A/ru not_active Application Discontinuation
  • 2008-09-26 MX MX2010003445A patent/MX2010003445A/es not_active Application Discontinuation
  • 2008-09-26 CN CN200880109332A patent/CN101808996A/zh active Pending
  • 2008-09-26 PE PE2008001687A patent/PE20091033A1/es not_active Application Discontinuation
  • 2008-09-26 AR ARP080104193A patent/AR066171A1/es unknown
  • 2008-09-26 PA PA20088797301A patent/PA8797301A1/es unknown
  • 2008-09-26 WO PCT/FR2008/001338 patent/WO2009074749A2/fr active Application Filing
  • 2008-09-26 CA CA2700559A patent/CA2700559A1/fr not_active Abandoned
  • 2008-09-26 CL CL2008002893A patent/CL2008002893A1/es unknown
  • 2008-09-26 EP EP08859496A patent/EP2205566A2/fr not_active Withdrawn
  • 2008-09-26 AU AU2008334457A patent/AU2008334457A1/en not_active Abandoned
  • 2008-09-26 BR BRPI0817973-5A patent/BRPI0817973A2/pt not_active IP Right Cessation
• 2010
  • 2010-03-22 IL IL204663A patent/IL204663A0/en unknown
  • 2010-03-26 US US12/732,749 patent/US20100222319A1/en not_active Abandoned

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events