WO2009025478A1 - Indole and indazole compounds as an inhibitor of cellular necrosis - Google Patents

Indole and indazole compounds as an inhibitor of cellular necrosis Download PDF

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Publication number
WO2009025478A1
WO2009025478A1 PCT/KR2008/004784 KR2008004784W WO2009025478A1 WO 2009025478 A1 WO2009025478 A1 WO 2009025478A1 KR 2008004784 W KR2008004784 W KR 2008004784W WO 2009025478 A1 WO2009025478 A1 WO 2009025478A1
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WO
WIPO (PCT)
Prior art keywords
indol
phenyl
amine
methyl
chloro
Prior art date
Application number
PCT/KR2008/004784
Other languages
French (fr)
Inventor
Soon Ha Kim
Hyoung Jin Kim
Sun Young Koo
Chul Woong Chung
Sung Bae Lee
Heui Sul Park
Seung Hyun Yoon
Hyo Shin Kwak
Dong Ook Seo
Eok Park
Original Assignee
Lg Life Sciences Ltd.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Lg Life Sciences Ltd. filed Critical Lg Life Sciences Ltd.
Priority to DK08793298.4T priority Critical patent/DK2178870T3/en
Priority to CN2008801030261A priority patent/CN101784543B/en
Priority to US12/671,038 priority patent/US8436038B2/en
Priority to BRPI0814958A priority patent/BRPI0814958B8/en
Priority to ES08793298.4T priority patent/ES2691068T3/en
Priority to MX2010000985A priority patent/MX368368B/en
Priority to SI200831995T priority patent/SI2178870T1/en
Priority to EP08793298.4A priority patent/EP2178870B1/en
Priority to JP2010521775A priority patent/JP5517935B2/en
Publication of WO2009025478A1 publication Critical patent/WO2009025478A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04—Indoles; Hydrogenated indoles
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/404—Indoles, e.g. pindolol
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    • A61K31/415—1,2-Diazoles
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Definitions

  • the present invention relates to indole or indazole compounds of formula (1), pharmaceutically acceptable salts or isomers thereof, and method and composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases comprising the same as an active ingredient.
  • PCD programmed cell death
  • necrosis has been known as an uncontrolled cell death for a long time, but a recent research (Proskurykakov SY et al. 2002, Biochemistry) reported the necrosis as an active/controlled cell death.
  • Typical diseases caused by necrosis include ischemic (e.g. myocardial infarction, stroke, renal infarction), neurodegenerative, and inflammatory diseases. Since it is believed that Necrosis is an uncontrolled, accidental cell death under morbid circumstances, researches on the functional mechanism, molecular targets, signal transduction systems, etc. thereof have rarely been conducted. Thus, there arises a compelling need to discover and develop the necrosis-inhibiting substances for the treatment of ischemic, neurodegenerative, and inflammatory diseases which are caused by necrosis, and to elucidate the biological, pathological causes of necrosis.
  • the indole derivatives according to the present invention have very useful structures from a medical viewpoint and many publications have reported the research results with reference to these structures. Among the research results, the following are the most representative of all: the patent WO2006/112549 reported some indole derivatives having the activity for the glucokinase, the patent WO95/07276 reported those useful as anti-tumor agents and as inhibitors against the production of cardiovascular system, and the patent WO2004/018428 reported those useful as antibiotics.
  • the present inventors have extensively studied under the above mentioned technical background to develop new compounds that exhibit an effect of prevention or treatment and amelioration for cellular necrosis and necrosis-associated diseases, particularly useful for the prevention or treatment of hepatic diseases.
  • the indole or indazole derivatives of formula (1) as explained below show a superior effect for the prevention and treatment of cellular necrosis and necrosis-associated diseases, whereby completed the present invention.
  • the present invention provides indole or indazole compounds of the following formula (1): in which n denotes a number of 1 to 3, m denotes 0 or 1, A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
  • X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C,
  • R 1 represent hydrogen, alkyl, -(CH 2 ) r NR 7 R 8 , or -(CH 2 ) r CO 2 H, wherein r denotes a number of 1 to 5, and R 7 and R 8 independently of one another represent hydrogen, alkyl or alkylcarbonyl, or may together form an optionally alkyl-substituted alkylene chain wherein optionally one methylene is replaced by N atom,
  • R 2 represents hydrogen, halogen, cyano, nitro, hydroxy, alkyl, alkoxy or trialkylsilyl, represents -(CH 2 ) P CO 2 R 7 , -(CH 2 ) P OR 7 , -(CH 2 ) P NR 7 R 8 , -NHR 10 , - N(H)S(O) 2 R 7 , -NHC(O)R 10 , -(CH 2 ) P S(O) 2 R 7 or (CH 2 ) p -heterocycle-R 10 , wherein p denotes a number of 0 to 3, R 7 and R 8 are as defined above, R 10 represents hydrogen, oxo, alkylsulfonyl, alkylcarbonyl, alkyloxycarbonyl, alkylaminocarbonyl, alkoxy, alkyl or heterocycle,
  • R J represents hydrogen, cyano, halogen, alkyl or phenyl, or represents - (CH 2 ) n -heterocycle or -(CH 2 ) n -aryl, wherein n denotes a number of 0 to 3,
  • R 4 represents -YR i l l , wherein Y represents a direct bond or -(CR 7 ⁇ R> 8 ⁇ ) P Y'-, wherein p denotes a number of 0 to 3, R 7 and R 8 are defined as above, Y' is selected from the group consisting of -O-, -S-, -NR 12 -, -NR 12 C(O)-, -C(O)-, -C(O)O-, - C(O)NR 12 -, -S(O) q -, and -S(O) q NR 12 -, wherein R 12 represents hydrogen, alkyl, aryl or heteroaryl, q denotes a number of 0 to 2, R 11 is selected from the group consisting of hydrogen, cyano, halogen, hydroxy, thiol, carboxy, alkyl and -(CH 2 ) t B-R 13 , wherein t denotes a number of
  • R 5 represents hydrogen, alkyl, cycloalkyl, heterocycle or heterocyclylalkyl
  • R 6 represents -(CR 7 R 8 ) P -Z-D-W-R 14 , wherein Z represents a direct bond, or is selected from the group consisting of -C(O)-, -C(O)O-, -C(O)NR 12 -, and -S(OV, y denotes a number of 1 or 2
  • D represents a direct bond, or represents cycloalkyl, heteroaryl or heterocycle
  • W represents a direct bond, or represents -NR 7 -, -C(O)-, - C(O)O-, -C(O)NR 12 -, -S(OV, -S(O) 7 NR 12 - or -NR 12 S(0) y -
  • R 14 represents hydrogen, hydroxy, alkyl, alkoxy, heterocycle, heteroaryl, aryl or aralkyl
  • alkyl' means an aliphatic hydrocarbon radical.
  • Alkyl may be saturated alkyl that does not comprise alkenyl or alkynyl moiety, or unsaturated alkyl that comprises at least one alkenyl or alkynyl moiety.
  • Alkenyl means a group containing at least one carbon- carbon double bond
  • alkynyl means a group containing at least one carbon-carbon triple bond.
  • Alkyl may be branched or straight-chain when used alone or in a composite form such as alkoxy.
  • Alkyl group may have 1 to 20 carbon atoms unless otherwise defined. Alkyl group may be a medium sized alkyl having 1 to 10 carbon atoms. Otherwise, alkyl group may be a lower alkyl having 1 to 6 carbon atoms. Typical examples thereof include, but not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, hexyl, ethenyl, propenyl, butenyl, etc.
  • Ci-C 4 -alkyl has 1 to 4 carbon atoms in the alkyl chain, and is selected from the group consisting of methyl, ethyl, propyl, isopropyl, n-butyl, iso-butyl, sec-butyl and t-butyl.
  • alkoxy means an alkyloxy having 1 to 10 carbon atoms unless otherwise defined.
  • 'cycloalkyl' means a saturated aliphatic 3-10 membered cycle unless otherwise defined. Typical examples thereof include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
  • aryl' include at least one ring having covalent 7T electron system, for example, monocyclic or fused polycyclic (i.e., cycles that share the adjacent carbon atom pairs) groups.
  • aryl means an aromatic 4-10 membered, preferably 6-10 membered, monocyclic or multicyclic ring including phenyl, naphthyl, etc., unless otherwise defined.
  • heteroaryl means an aromatic 3 ⁇ 10 membered, preferably 4-8 membered, more preferably 5-6 membered cycle that has 1 to 3 hetero atoms selected from N, O and S, and may be fused with benzo or C 3 -C 8 cycloalkyl, unless otherwise defined.
  • the monocyclic heteroaryl includes, but not limited to, thiazole, oxazole, thiophene, furan, pyrrole, imidazole, isoxazole, isothiazole, pyrazole, triazole, triazine, thiadiazole, tetrazole, oxadiazole, pyridine, pyridazine, pyrimidine, pyrazine and the like.
  • the bicyclic heteroaryl includes, but not limited to, indole, indoline, benzothiophene, benzofuran, benzimidazole, benzoxazole, benzisoxazole, benzthiazole, benzthiadiazole, benztriazole, quinoline, isoquinoline, purine, puropyridine and the like.
  • heterocycle means a 3-10 membered, preferably 4-8 membered, more preferably 5-6 membered cycle that has 1 to 3 hetero atoms selected from N, O and S, may be fused with benzo or C 3 -C 8 cycloalkyl, and is saturated or contains 1 or 2 double bonds, unless otherwise defined.
  • the heterocycle includes, but not limited to, pyrroline, pyrrolidine, imidazoline, imidazolidine, pyrazoline, pyrazolidine, pyran, piperidine, morpholine, thiomorpholine, piperazine, hydrofuran and the like.
  • A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
  • X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C
  • R 1 represents hydrogen, Q-Q-alkyl or -(CH 2 ) r NR 7 R 8 , wherein r denotes a number of 2 to 3, and R and R independently of one another represent hydrogen or C 1 - C 3 -alkyl, or may together form C 2 -C 6 -alkylene chain which is optionally substituted by Q-Q-alkyl and optionally one methylene is replaced by N atom,
  • R 2 represents hydrogen, halogen, C r C 6 -alkyl, -(CH 2 ) P CO 2 R 7 , -(CH 2 ) P OR 7 , -(CH 2 ) P NR 7 R 8 , -NHR 10 , -N(H)S(O) 2 R 7 , -NHC(O)R 10 , -(CH 2 ) P S(O) 2 R 7 or -(CH 2 ) P - heterocycle-R 10 , p denotes a number of 0 to 3,
  • R 10 represents hydrogen, oxo, CrC ⁇ -alkylsulfonyl, CrC ⁇ -alkylcarbonyl, Q-C ⁇ -alkyloxycarbonyl, Ci-C 6 -alkylaminocarbonyl, Ci-C 6 -alkoxy, Q-C ⁇ -alkyl or hydroxy-Q-Ce-alkyl, or represents 5-6 membered heterocycle which has 1 or 2 nitrogen atoms as the hetero atom, and is optionally substituted by Ci-C 3 -alkyl,
  • R 3 represents hydrogen, halogen or Ci-C 6 -alkyl, represents phenyl optionally substituted by Ci-C 6 -alkoxy, or represents heterocyclyl-d-Cs-alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
  • R 4 represents -YR 11 , wherein Y represents a direct bond or -(CR 7 R 8 ) P Y'-, wherein Y' is selected from the group consisting of -O-, -C(O)-, -C(O)O-, -NHC(O)-, - NR 12 -, -C(O)NR 12 -, -S(0) q -, and -S(O) q NR 12 -, R 12 represents hydrogen or Ci-C 3 -alkyl, q denotes a number of O to 2, R 11 is selected from the group consisting of hydrogen, halogen, hydroxy, thiol, carboxy, Ci-C 6 -alkyl, hydroxy-Ci-C 6 -alkyl and -(CH 2 ) t B-R 13 , t denotes a number of O to 3, B represents C 6 -Ci 0 -aryl, represents 5-6 membered heterocycle having 1 or 2
  • R 5 represents hydrogen, Ci-C 6 -alkyl, C 3 -C 6 -cycloalkyl, heterocycle or heterocyclyl-Ci-C ⁇ -alkyl, wherein the heterocycle is a 3-8 membered ring which has 1 to 3 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
  • R 6 represents -(CR 7 R ⁇ p -Z-D-W-R 14 ,
  • Z represents a direct bond, or is selected from the group consisting of -
  • W represents a direct bond, or represents -NR 7 -. -C(O)-, -C(O)O-, -
  • R 14 represents hydrogen, hydroxy, Ci-C 6 -alkyl, hydroxy-Ci-C 6 -alkyl, carboxy-Ci-C ⁇ -alkyl, C ⁇ -Qo-aryl or C 6 -Ci 0 -ar-Ci-C 6 -alkyl, represents 5-6 membered heterocycle which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by d-C 6 -alkyl, or
  • R 5 and R 6 together represent C 2 -C 6 -alkylene chain.
  • X is C or N, and the structure for each case may be depicted by the following formula (Ia) or (Ib).
  • the substituent A more preferably represents phenyl, pyridine or 1,4-pyrazine.
  • the substituent R 1 more preferably represents hydrogen, Ci-C ⁇ -alkyl or (Ii(C 1 - C 3 -alkyl)amino-C 2 -C 3 -alkyl, and most preferably represents hydrogen, methyl or (dimethylamino)ethyl.
  • the substituent R 2 more preferably represents hydrogen, amino, halogen, C 1 -C 3 - alkyl, carboxy, carboxy-Q-Q-alkyl, Ci-C 3 -alkoxycarbonyl, Ci-C 3 -alkoxycarbonyl-Ci- C 3 -alkyl, hydroxy-Ci-C 3 -alkyl, Ci-C 3 -alkoxy, -(CH 2 ) P NR 7 R 8 , -NHR 10 , -N(H)S(O) 2 R 7 , - NHC(O)R 10 or -(CH 2 ) p -heterocycle-R 10 , wherein p, R 7 , R 8 and R 10 are as defined in the above preferable scope.
  • R 2 is selected from the group consisting of hydrogen, methyl, methoxy, fluoro, -NH 2 , -NHAc, -NHSO 2 Me, -NHBOC, -NH(I- methyl-piperidine), l-oxo-2-hydroxy-ethyl, dimethylaminomethyl, hydroxymethyl, hydroxyethyl, carboxy, carboxymethyl, carboxyethyl, -CH 2 -(2-oxo)piperazine, -CH 2 - piperazine, -CH 2 -morpholine, -CH 2 -[I, l-dioxo-thiomorpholin-4-yl], and -CH 2 -[4- acetyl-piperazin- 1 -yl] .
  • the substituent R 3 more preferably represents hydrogen, methyl or bromo, represents phenyl optionally substituted by Ci-C 3 -alkoxy, or represents heterocyclyl-Q- C 3 -alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups.
  • R 3 is selected from the group consisting of hydrogen, methyl, bromo, phenyl, 4-MeO- phenyl, -CH 2 -(2-oxo-piperazin-4-yl), and -CH 2 -(morpholin-4-yl).
  • the substituent R 4 more preferably represents -YR 11 , wherein Y is selected from the group consisting of a direct bond, -0-, -C(O)-, -NH-, -CONH-, -SO 2 NH-, -NHC(O)-, -CH 2 CONH-, -CH 2 C(O)-, and -CH 2 SO 2 -. Most preferably, Y is selected from the group consisting of a direct bond, -0-, -C(O)-, -CH 2 C(O)- and -NHC(O)-.
  • R 11 is selected from the group consisting of hydrogen, halogen, hydroxy, Q-Co-alkyl and -(CH 2 ) t B-R 13 , wherein t, B and R 13 are as defined in the above preferable scope.
  • R is selected from the group consisting of hydrogen, methyl, ethyl, phenyl, fluoro, chloro, hydroxy, 2-carboxy-pyrrolidin-l-yl, pyrrolidin-1-yl, 4-acetic acid-l,3-thiazolin-2-yl, -CH 2 -(I, l-dioxo-thiomo ⁇ holin-4-yl), and -CH 2 -(2- oxopiperazin-4-yl).
  • the substituent R 5 more preferably represents hydrogen, Ci-C 6 -alkyl, C 3 -C 6 - cycloalkyl, heterocycle or heterocyclyl-Ci-C 6 -alkyl, wherein the heterocycle is a 5-6 membered ring which has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups.
  • R 5 is selected from the group consisting of hydrogen, methyl, cyclopentyl, tetrahydropyran-4-yl and CH 2 - (tetrahydropyran-4-yl) .
  • the substituent R 6 more preferably represents -(CR 7 R 8 ) P -Z-D-W-R 14 , wherein Z represents a direct bond, or represents -C(O)-, -C(O)O-, -C(O)NH- or -S(O) 2 -.
  • D is more preferably selected from the group consisting of cyclopentyl, cyclohexyl, pyrrolidine, tetrahydropyran, tetrahydrofuran and piperidine.
  • W more preferably represents a direct bond, or represents -SO 2 -, -CO-, -C(O)O- or -CONR 12 -, wherein R 12 is as defined in the above preferable scope.
  • W is selected from the group consisting of -SO 2 -, -CO-, -C(O)O-, -CON(Me)-, and -CONH-.
  • R 14 more preferably represents hydrogen, hydroxy, Ci-C 6 -alkyl, hydroxy-Q-C ⁇ -alkyl, C 6 -C 10 -aryl or C 6 -Cio-ar-C; ⁇ -C 3 -alkyl, represents 5-6 membered heterocycle which has O or S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 or 2 hetero atoms selected from N, O and S, and is optionally substituted by Q-Cralkyl.
  • R is selected from the group consisting of hydrogen, hydroxy, methyl, ethyl, isobutyl, hydroxymethyl, hydroxyethyl, phenyl, benzyl, thiophene, tetrahydrofuran, tetrahydropyran, 1,1-dioxo-tetrahydro-thiopyran, furan, pyridine and 5-methyl-pyridine.
  • R 5 and R 6 together with the N atom to which they are attached may more preferably form piperidine.
  • the compounds of formula (1) according to the present invention can also form a pharmaceutically acceptable salt.
  • a pharmaceutically acceptable salt includes non-toxic acid addition salt containing pharmaceutically acceptable anion, for example, a salt with inorganic acids such as sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, hydrobromic acid, hydriodic acid, etc.; a salt with organic carboxylic acids such as tartaric acid, formic acid, citric acid, acetic acid, trichloroacetic acid, trifluoroacetic acid, gluconic acid, benzoic acid, lactic acid, fumaric acid, maleic acid, salicylic acid, etc.; or a salt with sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, naphthalenesulfonic acid, etc.
  • inorganic acids such as sulfuric acid, hydroch
  • the compounds of formula (I) can also form a pharmaceutically acceptable base addition salt, for example, a salt with alkali metals or alkaline earth metals such as lithium, sodium, potassium, calcium, magnesium, etc.; a salt with amino acids such as lysine, arginine, guanidine, etc.; or an organic salt with dicyclohexylamine, N-methyl- D-glucamine, tris(hydroxymethyl)methylamine, diethanolamine, choline, triethylamine, etc.
  • the compounds of formula (I) of the present invention may be converted to their salts according to any of the conventional methods, and the salt formation can be easily carried out by a skilled artisan based on the structure of formula (1) without additional explanations thereon.
  • the term 'isomer' in the present specification means those having the same chemical or molecular formula as, but optically or sterically different from, the compounds of formula (1), or salts thereof.
  • the compounds of formula (1) of the present invention may have an asymmetric carbon center(s) in the structure, and so may exist in the form of optical isomer (R or S isomer), racemate, mixture of diastereomers, or individual diastereomer, etc. When the compounds have a double bond, they may exist in the form of geometric isomer (trans or cis isomer). All the isomers and their mixtures are also covered by the present invention.
  • the compounds of formula (1) include pharmaceutically acceptable salts and isomers thereof, unless otherwise explained.
  • the salts and isomers should be construed to be covered by the present invention.
  • the present specification briefly expresses them as the compounds of formula (1).
  • Typical compounds among the compounds of formula (1) are those selected from the following:
  • the present invention also provides processes for preparing the compounds of formula (1).
  • the processes for preparing the compounds of formula (1) are illustrated by exemplary reaction schemes for the purpose of better understanding.
  • the compounds of formula (1) may be prepared via various routes according to their structures, and such processes should be construed to fall under the scope of the present invention.
  • the compounds of formula ( 1 ) may be prepared by optionally combining various synthetic methods which are described in the present specification or disclosed in the prior arts.
  • the processes for preparing the compounds of formula (1) cover even such processes, and are not limited to those explained below.
  • the compounds of formula (1) may be prepared according to the following
  • Reaction Scheme (1) by reducing the nitro group of the compound (2) to produce the amine compound (3), and by carrying out a reductive amination reaction or coupling reaction in the presence of a base on the compound (3) with compound (4) or compound (5).
  • Reaction Scheme 1 Reaction Scheme 1
  • R represents (R ) n -A-
  • E represents a leaving group or linker, preferably may be chloro, bromo or iodo, a form of mixed anhydride, isocyanate or isothiocyanate.
  • the reduction may be conducted using an acid catalyst and a metal, or a metallic catalyst in the presence of hydrogen gas.
  • Iron, zinc, lithium, sodium, or tin (usually, tin chloride) may be used as the metal, and inorganic acid such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.; organic carboxylic acid such as acetic acid, trifluoroacetic acid, etc.; or ammonium chloride, etc. may be used as the acid catalyst.
  • inorganic acid such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.
  • organic carboxylic acid such as acetic acid, trifluoroacetic acid, etc.
  • ammonium chloride, etc. may be used as the acid catalyst.
  • palladium, nickel, platinum, ruthenium, rhodium etc. may be mentioned as the metallic catalyst, where the conventional hydrogen gas pressure ranges 1-3 atm.
  • R 6 in the formula (4) includes a carbonyl group, where the carbonyl group means an aldehyde or a ketone.
  • the reductive amination (RA) reaction may use sodium triacetoxyborohydride (NaBH(OAc) 3 ) or sodium cyanoborohydride (NaBH 3 CN), etc.
  • the coupling reaction may be carried out by reacting the compound (3) with the compound (5) using a base such as Et 3 N, EtN(iPr) 2 , DBU, N-methyl-morpholine, methyl-pyrrolidine, K 2 CO 3 , etc.
  • a base such as Et 3 N, EtN(iPr) 2 , DBU, N-methyl-morpholine, methyl-pyrrolidine, K 2 CO 3 , etc.
  • indole compound wherein X is C
  • those having a simple substituent (7-nitro-indole, 2,3-dimethyl-7-nitro-indole, etc.) may be commercially available, and most of them may be synthesized by cyclizing the acetylene intermediate such as the compound (8) in the following Reaction Scheme (2). Further, the compound (8) may be obtained via a coupling reaction of halobenzene compound (6) with acetylene compound (7).
  • R 2 and R 4 are as defined above, and Q represents iodo or bromo.
  • the compound (2-1) may be prepared by a cyclization reaction of the acetylene compound (8) in the presence of a base selected from KOBu 1 , K 2 CO 3 , DBU, etc. or a metallic catalyst selected from CuI, Pd(II), etc.
  • the preparation of acetylene compound (8) may be carried out by adding a base in the presence of a metallic catalyst, where Pd(II), Cu(I), etc. are used as the metallic catalyst, and Et 3 N, Et 2 N(iPr), DBU, N-methyl-morpholine, methyl-pyrrolidine, K 2 CO 3 , etc. are used as the base.
  • the acetylene compound (7) is usually commercially available, or may be prepared by a coupling reaction of acetylene in the presence of Pd(II) or Cu(I) and a base according to an art-known method [Synthesis, 2004 59-61; Bioorganic & Medicinal Chemistry, 13,2005, 197-209; Journal of Organic Chemistry, 71, 2006, 167-175].
  • the acetylene being used is trimethylsilylacetylene or 2-methyl-3-butyn-2- ol
  • the base being used is diethylamine, triethylamine, diisopropylethylamine, etc.
  • the halobenzene compound (6) may be obtained from a nitroaniline compound (13) using iodine or bromine as depicted in the following Reaction Scheme (3).
  • R and Q are as defined above.
  • the nitroaniline compound (13) is commercially available, or may be prepared via acetylation, nitration and deacetylation from commercially available nitro compound
  • aniline compound (12) that is not easy to obtain commercially can be prepared from the nitro compound (11).
  • the nitro compound (11) can also be commercially available, or prepared from 4-fluoro- nitrobenzene compound (9).
  • the compound (10) of formula R 4 -H means commercially available alcohols and amines.
  • the halogenating material for preparing the compound (6) may be selected from iodine, bromine, iodomonobromide and iodomonochloride, which may be used along with a silver ion such as silver nitrate (AgNO 3 ), silver carbonate (AgCO 3 ), silver sulfate (Ag 2 SO 4 ), etc.
  • a silver ion such as silver nitrate (AgNO 3 ), silver carbonate (AgCO 3 ), silver sulfate (Ag 2 SO 4 ), etc.
  • acetylation and nitration reactions are used for obtaining the compound (13) from the compound (12).
  • the nitration reaction may be carried out using undiluted nitric acid under a low temperature (-15 to 0 ° C), or various solvents such as dichloroethane or dichloromethane may be used together.
  • the reduction reaction of nitro group may also be carried out in the same manner as the process for preparing the compound (3) in Reaction Scheme (1) above.
  • the indole compound may be obtained by directly reacting the trifluoroacetyl- substituted compound (6-1) with the acetylene compound (7).
  • the indole compound (2-2) may be obtained from the nitroaniline compound (13) according to Fisher indole synthesis, as depicted in the following Reaction Scheme (5).
  • R 2 , R 3 and R 4 are as defined above.
  • the compound (14) is commercially available, or may be prepared by modifying the amine group of the compound (13) to hydrazine group according to the art-known method [Journal of the America Chemical Society, 198(48), 15374-75, 2006].
  • Hydrazine may be formed by reacting amine group with NaNO 2 in the presence of hydrochloric acid to introduce nitro group, and by reducing the nitro group using SnCl 2 , where the reaction is made using hydrochloric acid solution having a concentration of 1 to 12N, preferably 4 to 8N.
  • the hydrazone compound (15) may be prepared via condensation of the hydrazine compound (14) with the ketone compound in the presence of a base.
  • a base metal hydroxides such as sodium hydroxide, lithium hydroxide, etc., metal carbonates such as sodium bicarbonate, potassium carbonate, etc., metal acetates such as sodium acetate, etc., organic bases such as triethylamine, pyridine, etc., preferably sodium acetate, sodium bicarbonate, etc. may be mentioned.
  • the preparation of the compound (2-2) through a cyclization may be carried out in the presence of an acid catalyst, where the acid may be polyphosphoric acid, hydrochloric acid, p-toluenesulfonic acid, sulfuric acid, acetic acid, etc., preferably polyphosphoric acid.
  • the acid may be polyphosphoric acid, hydrochloric acid, p-toluenesulfonic acid, sulfuric acid, acetic acid, etc., preferably polyphosphoric acid.
  • Polyphosphoric acid may be used either alone or in the state of being mixed with aromatic hydrocarbons such as benzene, toluene, etc.
  • the reaction temperature ranges between 25 and 150 ° C
  • the reaction time ranges usually between 5 min and 60 h, preferably 5 min and 12 h.
  • the compound (2-3) having a substituent at 3-position of the indole ring may be prepared via a cyclization of the TMS-substituted acetylene compound (18) together with the compound (6), as depicted in the following Reaction Scheme (6).
  • the compounds (16), (17) and (20) are commercially available, and the compound (19) may be obtained by a conventional tosylation reaction from an alcohol or phenol.
  • Preparations of the TMS compound (18) or the compound (21) are the same as the process for preparing the compound (2-1) in Reaction Scheme (2) above.
  • the compound (2-3) may be obtained by removing TMS group, where TBNF (tetrabutylammoniumfluoride) and a base can be used.
  • the compound (2-4) wherein 3 -position of the indole ring is substituted may be prepared by introducing formyl group to the indole compound (22) to give the aldehyde compound (23), and by carrying out reductive amination reaction.
  • R 4 is as defined above, and
  • R 3 represents heterocycle containing amine.
  • Formylation reaction may be carried out using DMF in the presence of a base, where as the base, n-butyllithium, t-butyllithium, LDA (lithiumdiisopropylamine), KHMDS (potassiumhexamethyldisilane), etc. can be mentioned.
  • Reductive amination reaction may be carried out in the same manner as the process for preparing the compound (1) in Reaction Scheme (1) above.
  • the indazole compound (27) or (33) may be prepared as depicted in the following Reaction Scheme (8).
  • the indazole ring itself can be easily obtained by heating the nitroaniline compound in the presence of acetic acid according to the conventional manner.
  • the compound (33) wherein 3-position of the indazole ring is substituted may be obtained via a substitution reaction using the iodo compound.
  • mixtures are conventionally separated by column chromatography.
  • a final product it can be separated after completion of reaction by recrystallization or normal or reverse-phased HPLC (Waters, Delta Pack, 300x50 mml.D., Cl 8 5 ⁇ m, 100A).
  • HPLC Waters, Delta Pack, 300x50 mml.D., Cl 8 5 ⁇ m, 100A.
  • the product is purified through recrystallization or HPLC, the compound may be obtained in the form of a salt with trifluoroacetic acid.
  • ion exchange resin can be used.
  • the compounds according to the present invention may be obtained by various processes, and such processes for preparing the compounds of formula (1) should be construed to fall under the scope of the present invention.
  • the present invention further provides a composition for the prevention or treatment of necrosis and associated diseases, which comprises therapeutically effective amount of the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as an active ingredient together with pharmaceutically acceptable carriers or diluents.
  • the present invention further provides a method for the prevention or treatment of necrosis and associated diseases using the above described composition.
  • Necrosis and associated diseases which can be treated and/or prevented according to the present invention include acute/chronic hepatic disease (e.g. hepatitis, hepatic fibrosis, hepatocirrhosis), neurodegenerative disease (e.g.
  • diabetes dementia, Parkinson's disease, Huntington's disease
  • ischemic cardiac disease reperfusion injury, ischemic stroke or ischemic injury
  • pancreatitis bacterial/viral sepsis
  • diabetes mellitus or diabetic complications diabetic vascular disease
  • pancreatic cell destroying substances and mediated by virus, hyperglycemia, fatty acid, diet, toxin, streptozotocin and the like]
  • necrotizing procolitis cystic fibrosis, rheumatoid arthritis, degenerative arthritis, nephropathy, bacterial infection, viral infection (e.g.
  • HIV HIV
  • multiple sclerosis leukemia, lymphoma, neonatal respiratory distress syndrome, asphyxia, tuberculosis, endometriosis, angiasthenia, psoriasis, chilblain, steroid treatment complications, gangrene, pressure sores, hemoglobinuria, burns, hyperthermia, Crohn's disease, celiac disease, compartment syndrome, spiral cord injury, glomerulonephritis, muscular dystrophy, metabolic inherited disease, mycoplasmal disease, anthrax, Andersen's disease, congenital mitochondrial disease, phenylketonuria, placental infarction, syphilis, aseptic necrosis etc.
  • necrosis and associated diseases caused by drugs and toxic substances are selected from the group consisting of the necrosis associated with alcoholism, the exposure to, and/or administration and/or self-administration of, cocaine, drugs (e.g., paracetamol), antibiotics, anti-cancer agent, adriamycin, puromycin, bleomycin, NSAID, cyclosporine, chemical toxins (e.g., carbon tetrachloride, cyanide, methanol, ethylene glycol), poison gas, agrochemicals, heavy metals (e.g., lead, mercury, cadmium), or injury due to the exposure to radioactivity/UV and associated necrosis thereof.
  • drugs e.g., paracetamol
  • antibiotics e.g., anti-cancer agent
  • adriamycin e.g., puromycin, bleomycin, NSAID
  • cyclosporine e.g., chemical toxins (e.g., carbon tet
  • the composition according to the present invention exhibits not only the effects for hepatoprotection and hepatic functional improvement, but also shows the prophylactic and therapeutic effects on the chronic hepatic disease such as fatty liver, hepatic fibrosis, hepatocirrhosis, etc. and acute/chronic hepatic disease such as hepatitis, etc. caused by virus or drugs. Consequently, complications of hepatic disease including, but not limited to, portal hypertention also may be prevented or treated.
  • the medical composition according to the present invention is also effective for the treatment or prevention of the hepatic disease selected from liver transplantation, alcoholic or non-alcoholic fatty liver, hepatic fibrosis, hepatocirrhoisis and hepatitis caused by virus or drugs, and is effective for alcoholic acute/chronic hepatic disease.
  • the hepatic disease selected from liver transplantation, alcoholic or non-alcoholic fatty liver, hepatic fibrosis, hepatocirrhoisis and hepatitis caused by virus or drugs, and is effective for alcoholic acute/chronic hepatic disease.
  • composition according to the present invention is effective for the treatment or prevention of fatty acid-induced fatty liver or acute/chronic hepatic disease derived from fatty liver.
  • treatment means the interrupting or delaying the progress of the disease when applied to the subject showing the onset of disease symptoms
  • prevention means the interrupting or delaying the sign of the onset of disease when applied to the subject that does not show, but is at risk of, the onset of disease symptoms.
  • composition may comprise pharmaceutically acceptable carriers, diluents, excipients, or their combinations, if needed, together with the compounds of the present invention.
  • Pharmaceutical composition facilitates the administration of the compound into a living organism.
  • carrier means a substance which facilitates the incorporation of the compound into the cells or tissues.
  • DMSO dimethylsulfoxide
  • diluent is defined as a substance that is diluted in water which dissolves the compound, as well as stabilizes the biologically active form of the subject compound.
  • the salts dissolved in buffer solution are utilized as diluents in the art.
  • buffer solution is phosphate buffered saline which mimics the salt form of human solution. Buffer diluents rarely alter the biological activities of the compound, as the buffer salts can control the pH of solution at low concentration.
  • pharmaceutically acceptable means the property that does not impair the biological activities and physical properties of the compound.
  • the compounds of the present invention can be formulated as various pharmaceutical dosage forms according to the desired purpose.
  • active ingredient specifically, the compounds of formula (1), pharmaceutically acceptable salt or isomer thereof is mixed together with various pharmaceutically acceptable carriers which can be selected according to the formulation to be prepared.
  • the pharmaceutical composition of the present invention can be formulated as injectable preparation, oral preparation, etc., according to the desired purpose.
  • the compounds of the present invention can be formulated by the methods known in the art, which utilize pharmaceutical carriers and excipients known in the art, and be incorporated into the containers of unit dose form or mult-dose form.
  • the form of the preparation can be solutions, suspensions or emulsions in oily or aqueous media, and contain typical dispersing agents, suspending agents or stabilizers. Further, for example, it can be a form of dry powder which is intended to be reconstructed by dissolving in sterile, pyrogen-free water prior to use.
  • the compounds of the present invention also can be formulated into suppository forms utilizing typical suppository base such as cocoa butter or other glycerides.
  • solid dosage forms for oral administration capsules, tablets, pills, powder and granule can be prepared, and capsules and tablets are especially useful. Preferably, tablets and pills are prepared as enteric coated forms.
  • Solid dosage forms can be prepared by mixing the compounds of the present invention together with carriers such as one or more inert diluents such as sucrose, lactose, starch, etc., lubricants such as magnesium stearate, disintegrant, binder, etc.
  • carriers such as one or more inert diluents such as sucrose, lactose, starch, etc.
  • lubricants such as magnesium stearate, disintegrant, binder, etc.
  • the compounds of the present invention or the pharmaceutical compositions containing the same can also be administered in combination with other active agents including cytoprotective agents with various action mechanisms of different types, especially the existing agents utilized for hepatoprotection, hepatic functional improvement, and prevention or treatment of hepatic disease - hepatocyte regeneration promoters, hepatic functional adjuvants, anti-viral agents, immunosuppressants, fibrosis inhibitors, etc.
  • the compounds of the present invention or the pharmaceutical compositions containing the same can be co-administered with prophylactic or therapeutic agents for any drug-derived necrosis and associated diseases.
  • drugs include the drugs for any disease group such as antibiotics, anti-cancer agents, anti-viral agents, anti- infectives, anti-inflammatory agents, anti-coagulants, lipid-improving agents, cell death inhibitors, anti-hypertensive agents, anti-diabetic/anti-obesity agents, therapeutic agents for cardiovascular disease, therapeutic agents for neurodegenerative disease, anti-aging agents, therapeutic agents for metabolic disease, etc.
  • drugs for any disease group such as antibiotics, anti-cancer agents, anti-viral agents, anti- infectives, anti-inflammatory agents, anti-coagulants, lipid-improving agents, cell death inhibitors, anti-hypertensive agents, anti-diabetic/anti-obesity agents, therapeutic agents for cardiovascular disease, therapeutic agents for neurodegenerative disease, anti-aging agents, therapeutic agents for metabolic disease, etc.
  • the compounds of the present invention or the pharmaceutical compositions containing the same can be used for the prevention of the cell injury and subsequent necrosis and associated diseases derived by various causes such as toxins, and these causes include reactive oxygen species (ROS), heavy metals, alcohol, food, supplement, radiation, diet, etc.
  • ROS reactive oxygen species
  • the dosage of the compounds of formula (1) depends on the prescription of a physician, taking into account such factors as body weight, sex, age, condition of health, and diet of the patient, specific nature of the disease, administration time of the agent, administration method, mixing ratio of agents, and severity of the disease, etc.
  • dosage needed for the treatment of an adult is typically from about 1.0 mg to 2,000 mg per day, depending on the intensity and frequency of the administration.
  • total dosage typically from about 1.0 mg to 300 mg per day will be sufficient when separately administered in a single dosage, but for some patients a higher daily dosage may be desirable.
  • the present invention further provides a method of preparing the composition for the prevention or treatment of necrosis and associated diseases, which comprises the step of mixing the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as an active ingredient together with pharmaceutically acceptable carriers or diluents.
  • M means molar concentration
  • N means normal concentration
  • DIPEA diisopropylethylamine
  • DMAP 4-dimethylaminopyridine
  • HBTU 2-( 1 H-benzotriazol- 1 -yl)- 1 , 1 ,3 ,3-tetramethyluronium hexafluorophosphate
  • i-Pr isopropyl
  • i-Pen isopentyl
  • KHMDS potassium bis(trimethylsilyl) amide
  • TEA triethylamine
  • TFA trifluoroacetic acid
  • THF tetrahydrofuran
  • THP tetrahydropyran
  • TMS trimethylsilyl TBNF: tetrabutylammoniumfluoride
  • N-(4-phenoxy-phenyl)-acetamide (1.00 g, 4.03 mmol) prepared in Step A was dissolved in fuming nitric acid (2 mL), and the mixture was stirred for 2 h at -15 ° C .
  • reaction mixture was poured into 100 mL of ice water, which was then extracted with ethyl acetate.
  • the extracted organic solution was dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.67 g, 2.33 mmol).
  • Step C 2-Nitro-4-phenoxv-phenylamine N-(2-nitro-4-phenoxy-phenyl)acetamide (0.67 g, 2.33 mmol) prepared in Step B was dissolved in methanol (5 niL), 6.0N sodium hydroxide (1.5 mL) was added thereto, and the mixture was stirred for 18 h at room temperature. After completion of the reaction, 6.0N aqueous hydrochloric acid solution (1.3 mL) and ammonium chloride solution (100 mL) were added thereto.
  • Step B N-r(4-methyl-2-nitro-phenylVN'-[l-(pyridin-2-vD-ethylidenelhvdrazine hydrochloride
  • Step B 5-Methyl-7-nitro-2-phenyl-lH-indole 4-Methyl-2-nitro-6-(phenylacetylene)-phenylamine (4.5 g, 17.8 mmol) prepared in Step A was dissolved in tetrahydrofuran (120 mL) and N-methyl-pyrrolidinone (30 mL). Potassium t-butoxide (4 g, 35.7 mmol) was added, and the mixture was stirred for 3 h at room temperature. After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.0 g, Yield 22%).
  • Step B 5-Chloro-7-nitro-3-(2-oxo-piperazin-4-yDmethyl-2-phenyl-lH-indole
  • 5-Chloro-3-formyl-7-nitro-2-phenyl-lH-indole (0.5 g, 1.66 mmol) prepared in Step A was dissolved in dichloroethane (20 mL).
  • Acetic acid (0.10 g, 1.66 mmol)
  • 2- oxopiperazine 0.3 g, 3.32 mmol
  • sodium triacetoxyborohydride (0.71g, 3.32 mmol
  • reaction mixture was diluted with water, extracted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.55g, Yield 86%).
  • 2,4-Dimethylaniline (8.0 g, 66.0 mmol) was dissolved in acetic anhydride (50 mL), and nitric acid (5 mL) was slowly added in drops thereto at 0 ° C . After stirring for 30 min, the mixture was diluted with ice water (200 mL). Cone, hydrochloric acid (10 mL) was added in drops thereto, and the resulting mixture was stirred under reflux for 4 h. After the reaction mixture was cooled to room temperature, the solvent was removed under reduced pressure. The residue was diluted with aqueous ammonium hydroxide solution. The resulting orange solid was filtered and dried to give the title compound (10.6 g, Yield 97%).
  • Step B 3-Iodo-7-nitro-l-(4-methoxybenzyl)-lH-indazole 3-Iodo-7-nitro-lH-indazole (2.50 g, 8.65 mmol) prepared in Step A was dissolved in acetone (50 niL). Potassium hydroxide (0.73 g, 12.97 mmol) and 4- methoxybenzylchloride (1.63 g, 10.38 mmol) were added in drops thereto at 0 ° C, and the mixture was stirred for 2 h.
  • reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (3.2 g, Yield 91%).
  • Step A l-BOC-5-methyl-7-nitro-2-phenyl-indole
  • Step B l-BOC-3-bromo-5-bromomethyl-7-nitro-2 -phenyl-indole l-BOC-5-methyl-7-nitro-2-phenyl-indole (3.5 g, 10 mmol) prepared in Step A was dissolved in carbon tetrachloride (30 mL). N-bromosuccinimide (NBS, 2.3g, 13 mmol) and benzoyl peroxide (100 mg) were added thereto, and the mixture was stirred under reflux for 4 h at 80 ° C . After filtration, the solid moiety was removed. Water was added, and the mixture was extracted with DCM.
  • N-bromosuccinimide N-bromosuccinimide
  • benzoyl peroxide 100 mg
  • Step C 4-r(l-BOC-3-bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyll-piperazin- 2-one l-BOC-3-bromo-5-bromomethyl-7-nitro-2-phenyl-indole prepared in Step B (1.0 g, 2 mmol) was dissolved in DCM (10 mL). Et 3 N (560 uL, 4 mmol) was added,
  • Step D [(3-Bromo-7-mtro-2-phenyl-lH-indol-5-vDmethyl]-piperazin-2-one 4-[(l-BOC-3-bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyl]-piperazin-2-one
  • Preparation 48 4-r(3-Bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyll- morpholine l-BOC-3-bromo-5-bromomethyl-7-nitro-2-phenyl-indole prepared in Step B of Preparation 47 and morpholine were reacted according to the same procedures as Steps C and D of Preparation 47 to give the title compound.
  • Mass [M+H] 416
  • Step A 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole 5-Methyl-7-nitro-2-(pyridin-2-yl)-lH-indole (6.9 g, 27.3 mmol) prepared in
  • Preparation 8 was dissolved in a solvent mixture of tetrahydrofuran (130 mL), methanol (1 mL) and water (130 mL), and NH 4 Cl (14.6 g, 27.3 mmol) was added thereto.
  • the reaction mixture was warmed to 60 ° C, iron powder (15.2 g, 273 mmol) was added thereto, and the mixture was stirred for 30 min.
  • the reaction mixture was filtered through a cellite to remove the solid. Certain amount of the solvent was removed under reduced pressure from the resulting solution, which was then extracted with EtOAc. The extracted organic material was dried over MgSO 4 , and the solvent was removed under reduced pressure to give the title compound (5.0 g, Yield 40%).
  • Step B Cyclopentyl- [5-methyl-2-(p yridin-2- ylV 1 H-indol-7- yl] -amine
  • Example 2 Cvclopentyl-[5-methyl-2-phenyl-lH-indol-7-yl]-amine 5-Methyl-7-nitro-2-phenyl-lH-indole prepared in Preparation 24 was reacted according to the same procedures as Steps A and B of Example 1 to give the title compound.
  • 1H-NMR 500MHz, DMSO-d 6 ); ⁇ 10.91(brs, IH), 7.75(m, 2H), 7.65(m, IH),
  • Step A ⁇ ,4-Dioxa-r4.51dec-8-yl)-r5-memyl-2-f ⁇ yridin-2-ylHH-indol-7- yl)amine
  • Step B d-Cvclohexanon-4-ylVr5-methyl-2-(pyridin-2-ylVlH-indol-7-yll-amine
  • Example 21 4-[(5-Chloro-2-phenyl-lH-mdol-7-vDamino]-cyclohexan-l-one 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 was reacted according to the same procedure as Example 20 to give the title compound.
  • Example 23 l-Etfayl-3-r5-methyl-2-fpyridin-2-ylVlH-indol-7-yl1-urea 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and ethylisocyanate were reacted according to the same procedure as Example 22 to give the title compound.
  • Example 24 l-Phenyl-3-r5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-urea 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and phenylisocyanate were reacted according to the same procedure as Example 22 to give the title compound.
  • 1H-NMR 400MHz, CDCl 3 /MeOH-d 4 ); ⁇ 8.52(d, IH), 7.79(d, IH), 7.73(m,
  • Example 25 Thiophene-2-sulfonic acid (2-pyridin-2-yl-lH-indol-7-ylVamide 2-Pyridin-2-yl-7-nitro-lH-indole prepared in Preparation 9 and 2- thiophenesulfonylchloride were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.
  • Example 26 Thiophene-2-sulfonic acid r5-methyl-2-(pyridin-2-yl)-lH-indol-7- yl] -amide 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and 2-thiophenesulfonylchloride were reacted according to the same procedure as Example 22 to give the title compound.
  • Step A 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid ethyl ester
  • 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid (14.1 g, 50 mmol) prepared in Preparation 30 was dissolved in ethanol (40 mL). Cone, sulfuric acid (10 mL) was added thereto, and the mixture was stirred for 2 h at 50 ° C . After completion of the reaction, IN NaOH was added to the reaction mixture, which was then extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was recrystallized from EtOAc and hexane to give the title compound (14.1 g, Yield 95%).
  • Step B 7-(Cvclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester
  • 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid ethyl ester prepared in Step A and cyclopentanone were reacted according to the same procedure as Example 1 to give the title compound.
  • Step B Cyclopentyl-fS-hydroxymethyl ⁇ -phenyl-lH-indol ⁇ -yll-amine 5-Hydroxymethyl-2-phenyl-7-nitro-lH-indole prepared in Step A was reacted according to the same procedure as Example 1 to give the title compound.
  • Example 30 7-(CvclopentvDamino-2-phenyl-lH-indole-5-carboxylic acid 7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester (5 g, 14.3 mmol) prepared in Example 28 was added to a solvent mixture of MeOH (20 niL) and water (20 mL). NaOH (1.3 g, 33.8 mmol) was added thereto, and the mixture was stirred for 4 h at room temperature. After completion of the reaction, MeOH was removed under reduced pressure, and IN HCl was added to the residue. The resulting mixture was extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was recrystallized from EtOAc and n-Hex to give the title compound.
  • Example 33 2-[7-(Cvclopentyl)amino-2-phenyl-lH-indol-5-yllacetic acid 2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]acetic acid ethyl ester prepared in Example 31 was reacted according to the same procedure as Example 30 to give the title compound.
  • Step B 5 -( 1,1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-7-nitro- 1 H-indole 5-Iodomethyl-2-phenyl-7-nitro-lH-indole (850 mg, 2.5 mmol) prepared in Step
  • Step C (Tetrahydrop yran-4- vD- F2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4- ypmethyl- 1 H-indol-7- yl] amine
  • Examples 40 to 78 The compounds prepared in Preparations 24 to 40, 43, 44 and 47 and commercially available ketone or aldehyde were reacted according to a method selected from Examples 26 to 37 to synthesize the Example Compounds in the following table.
  • Example 79 (Tetrahvdropyran-4-vD-(5-chloro-3-phenyl-lH-indol-7-yl)-aniine S-Chloro-V-nitro-S-phenyl-lH-indole prepared in Preparation 41 and tetrahydropyran-4-one were reacted according to the same procedure as Example 1 to give the title compound.
  • Example 80 Cyclopentyl-(5-chloro-3-phenyl-lH-indol-7-yl)-amine 5-Chloro-7-nitro-3-phenyl-lH-indole prepared in Preparation 41 and cyclopentanone were reacted according to the same procedure as Example 1 to give the title compound.
  • Example 82 Cvclopentyl-[2-(4-aminophenylV5-chloro-lH-indol-7-yll-amine Cyclopentyl-[2-(4-BOC-aminophenyl)-5-chloro-lH-indol-7-yl]-amine (430 mg, 1 mmol) prepared in Example 78 was added to DCM (5 mL).
  • Example 85 C yclopentyl- ⁇ 5 -( 1 , 1 -dioxo-thiomorpholin-4- vDmethyl-2- [4- (acetyl)aminophenyl "
  • Examples 86 to 89 7-Amino-5-(l,l-dioxo-thiomorpholin-4-yl)methyl-2-[4-(acetyl)aminophenyl]- lH-indole prepared as an intermediate in the process of Example 85 and commercially available ketone or aldehyde were reacted according to the same procedure as Step B of Example 1 to synthesize the Example Compounds in the following table.
  • Example 90 (5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine Step A: l-BOC-(5-methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine 7-Amino-5-methyl-2-phenyl-lH-indole prepared in Example 2 and 1-BOC- piperidinone were reacted according to the same procedure as Preparation 23 to give the title compound.
  • Step B (5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine l-BOC-(5-methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine prepared in Step A was reacted according to the same procedure as Example 82 to give the title compound.
  • Example 93 (5-Chloro-2-phenyl-lH-indol-7-ylVpiperidin-4-yl-amine 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and l-BOC-4- piperidinone were reacted according to the same procedure as Step B of Example 1 to give the title compound.
  • Example 94 4-(5 -Chloro-2-phenyl- 1 H-indol-7-yr)amino-piperidin- 1 - yl- carboxylic acid phenylamide
  • Step A l-r4-(5-Chloro-2-phenyl-lH-indol-7-yDamino-piperidin-l-yl1-2-BOC- amino-ethanone
  • Step B 1 - [4-(5-Chloro-2-phenyl- 1 H-indol-7-yl)amino-piperidin- 1 -yl] -2-amino- ethanone l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]-2-BOC-amino- ethanone prepared in Step A was reacted according to the same procedure as Example 82 to give the title compound.
  • Step C l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yll-2- dimethylamino-ethanone l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]-2-amino-ethanone prepared in Step B and formaldehyde were reacted according to the same procedure as Step B of Example 1 to give the title compound.
  • Example 97 (5-( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl- 1 H-indol-7- yl)-( 1 -methanesulfonyl-piperidin-4-yl)-amine
  • Step A (5-Fluoro-2-phenyl-lH-indol-7-vD-piperidin-4-yl-amine 5-Fluoro-7-nitro-2-phenyl-lH-indole prepared in Preparation 25 and 1-BOC- piperidinone were reacted according to the same procedure as Example 90 to give the title compound.
  • Step B (5-Fluoro-2-phenyl- 1 H-indol-7-yD-[ 1 -(U -dioxo-tetrahvdrothiopyran-4- yl s )-piperidin-4- yl] -amine
  • Example 102 4-(5-Chloro-2-phenyl-lH-indol-7-vDamino-cyclohexane-l- carboxylic acid
  • Example 103 4-(5-Methyl-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 - carboxylic acid
  • Example 104 4-(5 -Chloro-2-phenyl- 1 H-indol-7- vDamino-cyclohexane- 1 - carboxylic acid amide
  • Example 102 4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-cyclohexane-l-carboxylic acid prepared in Example 102 and NH 4 Cl were reacted according to the same procedure as Example 92 to give the title compound.
  • Example 102 4-(5-Chloro-2 -phenyl- lH-indol-7-yl)amino-cyclohexane-l-carboxylic acid prepared in Example 102 and methylamine (HCl salt) were reacted according to the same procedure as Example 92 to give the title compound.
  • Example 107 2-(5-Fluoro-2-phenyl-lH-mdol-7-yl)amino-acetic acid 2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester prepared in
  • Example 106 was reacted according to the same procedure as Example 30 to give the title compound.
  • Example 108 (5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester prepared in Example 108 was reacted according to the same procedure as Example 30 to give the title compound.
  • Example 110 2-[(5-Phenoxy-2-phenyl-lH-indol-7-vDamino]-propionic acid methyl ester
  • Example 111 2-(5-Phenoxy-2-phenyl-lH-indol-7-vDamino-propionic acid 2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-propionic acid methyl ester prepared in Example 110 was reacted according to the same procedure as Example 30 to give the title compound.
  • Example 112 2-(5-Chloro-2-phenyl-lH-mdol-7-vDamino-propionic acid 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and methyl 2- bromopropionic acid ester were reacted according to the same procedures as Examples 22 and 30 sequentially to give the title compound.
  • Example 114 (5-Chloro-2-phenyl-lH-indol-7-yl)-5-methyl-pyridin-2-yl-amme 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and 2-bromo-5- methyl-pyridine were reacted according to the same procedure as Example 113 to give the title compound.
  • Step A (RV4-(4-methoxy-benzylsulfanylV3-
  • Step B 2-r(R)-2-(7-nitro-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4-yll- acetic acid methyl ester
  • Step C 2-r(RV2-(7-cvclopentylamino-2-phenyl-lH-indol-5-ylV4.5-dihvdro- thiazol-4-yl] -acetic acid
  • Example 122 2-r(RV2-(2-phenyl-7-(tetrahvdropyran-4-yl ' )methvlamino- 1 H- indol-5-yl)-4,5-dihydro-thiazol-4-yl]-acetic acid
  • Step A 3-(5-Chloro-7-amino-lH-indol-2-yl)benzoic acid methyl ester 3-(5-Chloro-7-nitro-lH-indol-2-yl)benzoic acid prepared in Preparation 32 was reacted according to the same procedure as Example 28 to give the title compound.
  • Step B 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methylester
  • Example 124 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester prepared in Example 123 was reacted according to the same procedure as Example 30 to give the title compound.
  • Example 10 prepared in Example 123 was reacted according to the same procedure as Example 32 to give the title compound.
  • Example 150 l-(4-r3-(5-Chloro-7-tetrahvdropyran-4-ylamino-lH-indol-2-ylV benzyl]-piperazin- 1 -vU -ethanone
  • Example 151 ⁇ 5-Chloro-2-[3-(2-oxo-piperazin-4-vDethylphenyll-lH-indol-7- yl ⁇ -(tetrahydropyran-4-yl)-amine
  • Example 152 ⁇ 5 -Chloro-2- [3-C 1 , 1 -dioxo-thiomo ⁇ holin-4- yl)ethvbhenyl "
  • the substances used to derive hepatocyte death include CCl 4 , ActD, H 2 O 2 , doxorubicin, anti-Fas Ab/Actinomycin D, acetaminophen, EtOH, CdCl 2 , palmitate, stearate, cyclophosphamide, terfenadine, diclofenac, simvastatin, and adefovir.
  • Primary hepatocytes were isolated using the method of Seglen PO (Experimental Cell Research 74(1972) p ⁇ 450-454).
  • hepatocytes were isolated according to the two-step collagenase perfusion method, and dead cells were removed by low speed (500 rpm) centrifugation for 10 min using percoll gradient (Kreamer BL etc, In Vitro Cellular & Developmental Biology 22(1986) pp201-211). During this step, the viability of cells was maintained 90% or above. The cells were suspended in HepatoZYME media (Gibco BRL), and the number of cells was counted. 1.5X10 4 cells in 100 ⁇ Jt were placed into the collagen-coated 96- well plate (BD biocoat), and adhered on the bottom for 3 - 4 h.
  • hepatocyte protective effect In order to assess the hepatocyte protective effect, above adhered cells were pretreated with the Example compounds for 30 min. At this time, the concentration of the Example compounds were serially diluted by 2-fold or 3-fold over 5 steps starting from 30 uM, 10 uM or 1 uM depending on the experiments, and the final concentration of DMSO was adjusted to 0.2%. 30 min after the treatment by compounds, cells were treated by the substances deriving hepatocyte death or hepatotoxic drugs at the concentrations indicated in Table 1. After 24 - 48 h, the viability of cells was determined to estimate the hepatocyte protective effects. The viability of cells was determined using WST-I (MK-400, Takeda) method by the absorbance at 440 nm. Hepatocyte protective effects of the Example compounds were represented by "EC 50 " which was calculated from measured values. "EC 50 " herein means the concentration of the compound at which 50% of maximum protective effect is observed in the experiment.
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • Table 1 shows the treatment concentrations of various substances deriving hepatotoxity and the hepatocyte protective effect of the compound of Example 41.
  • Table 2 shows the cell protective effects of the Example compounds against a substance which results in hepatotoxicity, doxorubicin.
  • Hepatocytes were isolated according to the same procedure as Experimental
  • Example 1 suspended in DMEM (Gibco + 10% FBS + IX antibiotics) media, and distributed to the plate. After 24 h from the distribution of hepatocytes, the compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which the cells were pretreated for 30 min. Cells were treated with tBHP at the final concentration of 300 uM, and the protective effects were determined after 1 h. As in Experimental Example 1, after the treatment with WST-I (Takeda, lOuL) for 1.5 h, EC 50 values were calculated by absorbance measurements at 440 nm using SpectraMax (Molecular Device).
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • Linni5F pancreatic cells
  • SRB Sulforhodamine B Protein
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • the compounds of Examples 56, 106, and 107 as representative compounds showed excellent activities in the present experiment, and their EC 50 values were 0.1 uM or less.
  • H9C2 cells were distributed in the amount of 1.5X10 4 cells/well, and incubated for 24 h.
  • the Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 45 min.
  • Cells were treated with tBHP at the final concentration of 400 uM, and incubated for 2 h.
  • Protective effect of each compound was determined using the same SRB method as in Linm5F of above mentioned 2).
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • EC 50 of the compound of Example 86 was 0.5 uM.
  • the compounds of Examples 39, 74, 86, 97 and 117 showed excellent activities in the present experiment, and their EC 50 values were 0.2 uM or less.
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • EC 50 of the compound of Example 56 was 0.66 uM.
  • chondrocytes were isolated from 2 hind legs of 16 week-old SD rats (body weight: 450 - 460 g). Isolation method is as follows. Cartilage isolated from the knee regions of rat hind legs was transferred to a 100 pi plate containing PBS (+1X antibiotics). PBS was maintained 4 ° C in an ice-bath. PBS was exchanged with fresh one, and centrifuged at 1000 rpm. After removal of PBS, 3 mL of IX trypsin (Gibco) at the temperature of 37 ° C was added and followed by the treatment for 15 min. Supernatant was discarded after centrifugation, and washed again with PBS.
  • PBS +1X antibiotics
  • EC 50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
  • the compounds of Examples 56 and 63 showed excellent activities in the present experiment, and their EC 50 values were 0.1 uM or less.
  • SK-N-MC Protective effect when tBHP was treated on brain cells
  • 2X10 4 brain cells were distributed into the 96-well plate using DMEM media (Gibco, 10% FBS), and incubated for 24 h.
  • the Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 1 h.
  • EC 50 of the Example compound is 30 uM or less, more preferably,
  • the novel compounds according to the present invention not only exhibit the effects for hepatoprotection and hepatic functional improvement, but also can be useful for the prevention and treatment of the chronic hepatic diseases such as fatty liver, hepatic fibrosis, hepatocirrhosis, etc. and acute/chronic hepatic diseases such as hepatitis, etc. caused by virus or drugs.
  • the compounds of the present invention also exhibit the necrosis inhibitory efficacy in the cells from pancreas, kidney, brain, cartilage, and heart.
  • the compounds of the present invention can be useful in the prevention and treatment of necrosis and associated diseases.

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Abstract

The present invention relates to indole or indazole compounds, pharmaceutically acceptable salts or isomers thereof which are useful for the prevention or treatment of cellular necrosis and necrosis-associated diseases. The present invention also relates to a method and a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, comprising said indole or indazole compounds as an active ingredient.

Description

[SPECIFICATION] [Title of Invention]
INDOLE AND INDAZOLE COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSIS
[Technical Field]
The present invention relates to indole or indazole compounds of formula (1), pharmaceutically acceptable salts or isomers thereof, and method and composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases comprising the same as an active ingredient.
[Background Art]
Most researches associated with cell death have been concentrated on apoptosis of cells, also known as programmed cell death (PCD). With the discovery of the enzyme caspase, a number of pharmaceutical companies have promoted the development of drugs utilizing caspase inhibitors during the past 10 years. However, the current status is that there have hardly been any of these drugs approved by FDA. This is because the apoptosis of cells is a cell death which occurs under physiological circumstances and such a cell death may be probably due to the defense mechanism for maintaining homeostasis in the body. In contrast, necrosis is a cell death which mainly occurs under morbid circumstances, and in most cases it is characterized by accompanying the inflammatory response. Necrosis has been known as an uncontrolled cell death for a long time, but a recent research (Proskurykakov SY et al. 2002, Biochemistry) reported the necrosis as an active/controlled cell death. Typical diseases caused by necrosis include ischemic (e.g. myocardial infarction, stroke, renal infarction), neurodegenerative, and inflammatory diseases. Since it is believed that Necrosis is an uncontrolled, accidental cell death under morbid circumstances, researches on the functional mechanism, molecular targets, signal transduction systems, etc. thereof have rarely been conducted. Thus, there arises a compelling need to discover and develop the necrosis-inhibiting substances for the treatment of ischemic, neurodegenerative, and inflammatory diseases which are caused by necrosis, and to elucidate the biological, pathological causes of necrosis.
The indole derivatives according to the present invention have very useful structures from a medical viewpoint and many publications have reported the research results with reference to these structures. Among the research results, the following are the most representative of all: the patent WO2006/112549 reported some indole derivatives having the activity for the glucokinase, the patent WO95/07276 reported those useful as anti-tumor agents and as inhibitors against the production of cardiovascular system, and the patent WO2004/018428 reported those useful as antibiotics.
[Detailed Description of the Invention] [Technical Subject to be Solved]
Thus, the present inventors have extensively studied under the above mentioned technical background to develop new compounds that exhibit an effect of prevention or treatment and amelioration for cellular necrosis and necrosis-associated diseases, particularly useful for the prevention or treatment of hepatic diseases. As a result thereof, they confirmed that the indole or indazole derivatives of formula (1) as explained below show a superior effect for the prevention and treatment of cellular necrosis and necrosis-associated diseases, whereby completed the present invention.
Therefore, it is an object of the present invention to provide new indole or indazole derivatives of formula (1).
It is another object of the present invention to provide a composition for the prevention or treatment of cellular necrosis and necrosis-associated diseases, in particular, for hepatoprotection, hepatic functional improvement, and prevention or treatment of acute/chronic hepatic diseases, which comprises as an active ingredient the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof together with a pharmaceutically acceptable carrier or diluent, and process for preparing the same.
It is still another object of the present invention to provide a method for the prevention or treatment of cellular necrosis and associated diseases, in particular, for hepatoprotection, hepatic functional improvement, and prevention or treatment of acute/chronic hepatic diseases using said composition.
[Means for Solving the Technical Subject]
To accomplish the above objects, the present invention provides indole or indazole compounds of the following formula (1):
Figure imgf000005_0001
in which n denotes a number of 1 to 3, m denotes 0 or 1, A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C,
R1 represent hydrogen, alkyl, -(CH2)rNR7R8, or -(CH2)rCO2H, wherein r denotes a number of 1 to 5, and R7 and R8 independently of one another represent hydrogen, alkyl or alkylcarbonyl, or may together form an optionally alkyl-substituted alkylene chain wherein optionally one methylene is replaced by N atom,
R2 represents hydrogen, halogen, cyano, nitro, hydroxy, alkyl, alkoxy or trialkylsilyl, represents -(CH2)PCO2R7, -(CH2)POR7, -(CH2)PNR7R8, -NHR10, - N(H)S(O)2R7, -NHC(O)R10, -(CH2)PS(O)2R7 or (CH2)p-heterocycle-R10, wherein p denotes a number of 0 to 3, R7 and R8 are as defined above, R10 represents hydrogen, oxo, alkylsulfonyl, alkylcarbonyl, alkyloxycarbonyl, alkylaminocarbonyl, alkoxy, alkyl or heterocycle,
RJ represents hydrogen, cyano, halogen, alkyl or phenyl, or represents - (CH2)n-heterocycle or -(CH2)n-aryl, wherein n denotes a number of 0 to 3,
R4 represents -YR i l l , wherein Y represents a direct bond or -(CR 7τ R> 8\ )PY'-, wherein p denotes a number of 0 to 3, R7 and R8 are defined as above, Y' is selected from the group consisting of -O-, -S-, -NR12-, -NR12C(O)-, -C(O)-, -C(O)O-, - C(O)NR12-, -S(O)q-, and -S(O)qNR12-, wherein R12 represents hydrogen, alkyl, aryl or heteroaryl, q denotes a number of 0 to 2, R11 is selected from the group consisting of hydrogen, cyano, halogen, hydroxy, thiol, carboxy, alkyl and -(CH2)tB-R13, wherein t denotes a number of 0 to 3, B represents heterocycle, heteroaryl or aryl, R13 represents hydrogen, cyano, halogen, hydroxy, oxo, thiol, carboxy, carboxyalkyl, alkylcarbonyloxy, alkyl, alkoxy, alkylthio, alkylcarbonyl or alkylsulfonyl,
R5 represents hydrogen, alkyl, cycloalkyl, heterocycle or heterocyclylalkyl, R6 represents -(CR7R8)P-Z-D-W-R14, wherein Z represents a direct bond, or is selected from the group consisting of -C(O)-, -C(O)O-, -C(O)NR12-, and -S(OV, y denotes a number of 1 or 2, D represents a direct bond, or represents cycloalkyl, heteroaryl or heterocycle, W represents a direct bond, or represents -NR7-, -C(O)-, - C(O)O-, -C(O)NR12-, -S(OV, -S(O)7NR12- or -NR12S(0)y-, wherein R14 represents hydrogen, hydroxy, alkyl, alkoxy, heterocycle, heteroaryl, aryl or aralkyl, R5 and R6 together represent alkylene chain, where alkyl, alkoxy, aryl, cycloalkyl, heterocycle and heteroaryl may be optionally substituted, and the substituents are one or more selected from the group consisting of hydroxy, halogen, nitrile, amino, alkylamino, dialkylamino, carboxy, alkyl, alkoxy, carboxyalkyl, alkylcarbonyloxy, alkylthio, alkyloxycarbonyl, alkylaminocarbonyl, arylalkoxy and oxo, and pharmaceutically acceptable salts or isomers thereof.
In the above definitions for the compounds of formula (1), the term 'alkyl' means an aliphatic hydrocarbon radical. Alkyl may be saturated alkyl that does not comprise alkenyl or alkynyl moiety, or unsaturated alkyl that comprises at least one alkenyl or alkynyl moiety. "Alkenyl" means a group containing at least one carbon- carbon double bond, and "alkynyl" means a group containing at least one carbon-carbon triple bond. Alkyl may be branched or straight-chain when used alone or in a composite form such as alkoxy.
Alkyl group may have 1 to 20 carbon atoms unless otherwise defined. Alkyl group may be a medium sized alkyl having 1 to 10 carbon atoms. Otherwise, alkyl group may be a lower alkyl having 1 to 6 carbon atoms. Typical examples thereof include, but not limited to, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, hexyl, ethenyl, propenyl, butenyl, etc. For example, Ci-C4-alkyl has 1 to 4 carbon atoms in the alkyl chain, and is selected from the group consisting of methyl, ethyl, propyl, isopropyl, n-butyl, iso-butyl, sec-butyl and t-butyl.
The term 'alkoxy' means an alkyloxy having 1 to 10 carbon atoms unless otherwise defined.
The term 'cycloalkyl' means a saturated aliphatic 3-10 membered cycle unless otherwise defined. Typical examples thereof include, but not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
The term 'aryl' include at least one ring having covalent 7T electron system, for example, monocyclic or fused polycyclic (i.e., cycles that share the adjacent carbon atom pairs) groups. In the present specification, aryl means an aromatic 4-10 membered, preferably 6-10 membered, monocyclic or multicyclic ring including phenyl, naphthyl, etc., unless otherwise defined.
The term 'heteroaryl' means an aromatic 3~10 membered, preferably 4-8 membered, more preferably 5-6 membered cycle that has 1 to 3 hetero atoms selected from N, O and S, and may be fused with benzo or C3-C8 cycloalkyl, unless otherwise defined. The monocyclic heteroaryl includes, but not limited to, thiazole, oxazole, thiophene, furan, pyrrole, imidazole, isoxazole, isothiazole, pyrazole, triazole, triazine, thiadiazole, tetrazole, oxadiazole, pyridine, pyridazine, pyrimidine, pyrazine and the like. The bicyclic heteroaryl includes, but not limited to, indole, indoline, benzothiophene, benzofuran, benzimidazole, benzoxazole, benzisoxazole, benzthiazole, benzthiadiazole, benztriazole, quinoline, isoquinoline, purine, puropyridine and the like.
The term 'heterocycle' means a 3-10 membered, preferably 4-8 membered, more preferably 5-6 membered cycle that has 1 to 3 hetero atoms selected from N, O and S, may be fused with benzo or C3-C8 cycloalkyl, and is saturated or contains 1 or 2 double bonds, unless otherwise defined. The heterocycle includes, but not limited to, pyrroline, pyrrolidine, imidazoline, imidazolidine, pyrazoline, pyrazolidine, pyran, piperidine, morpholine, thiomorpholine, piperazine, hydrofuran and the like.
Other terms and abbreviations in the present specification may be understood to have the meaning conventionally used in this field by a skilled artisan, unless otherwise defined. Preferred compounds among the compounds of formula (1) above are those wherein n denotes a number of 1 to 3, m denotes 0 or 1,
A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C, R1 represents hydrogen, Q-Q-alkyl or -(CH2)rNR7R8, wherein r denotes a number of 2 to 3, and R and R independently of one another represent hydrogen or C1- C3-alkyl, or may together form C2-C6-alkylene chain which is optionally substituted by Q-Q-alkyl and optionally one methylene is replaced by N atom,
R2 represents hydrogen, halogen, CrC6-alkyl, -(CH2)PCO2R7, -(CH2)POR7, -(CH2)PNR7R8, -NHR10, -N(H)S(O)2R7, -NHC(O)R10, -(CH2)PS(O)2R7 or -(CH2)P- heterocycle-R10, p denotes a number of 0 to 3,
R10 represents hydrogen, oxo, CrCδ-alkylsulfonyl, CrCό-alkylcarbonyl, Q-Cό-alkyloxycarbonyl, Ci-C6-alkylaminocarbonyl, Ci-C6-alkoxy, Q-Cό-alkyl or hydroxy-Q-Ce-alkyl, or represents 5-6 membered heterocycle which has 1 or 2 nitrogen atoms as the hetero atom, and is optionally substituted by Ci-C3-alkyl,
R3 represents hydrogen, halogen or Ci-C6-alkyl, represents phenyl optionally substituted by Ci-C6-alkoxy, or represents heterocyclyl-d-Cs-alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
R4 represents -YR11, wherein Y represents a direct bond or -(CR7R8)PY'-, wherein Y' is selected from the group consisting of -O-, -C(O)-, -C(O)O-, -NHC(O)-, - NR12-, -C(O)NR12-, -S(0)q-, and -S(O)qNR12-, R12 represents hydrogen or Ci-C3-alkyl, q denotes a number of O to 2, R11 is selected from the group consisting of hydrogen, halogen, hydroxy, thiol, carboxy, Ci-C6-alkyl, hydroxy-Ci-C6-alkyl and -(CH2)tB-R13, t denotes a number of O to 3, B represents C6-Ci0-aryl, represents 5-6 membered heterocycle having 1 or 2 hetero atoms selected from N, O and S, or represents 5-6 membered heteroaryl having 1 or 2 N atoms, R13 represents hydrogen, halogen, hydroxy, oxo, thiol, carboxy, carboxy-Ci-Cό-alkyl, Ci-Cβ-alkylcarbonyloxy, Q-Q-alkyl, Cj-C6- alkoxy, Q-Ce-alkylthio, Ci-C6-halogenoalkyl, Ci-C6-alkylcarbonyl or Ci-C6- alkylsulfonyl,
R5 represents hydrogen, Ci-C6-alkyl, C3-C6-cycloalkyl, heterocycle or heterocyclyl-Ci-Cβ-alkyl, wherein the heterocycle is a 3-8 membered ring which has 1 to 3 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
R6 represents -(CR7R^p-Z-D-W-R14,
Z represents a direct bond, or is selected from the group consisting of -
C(O)-, -C(O)O-, -C(O)NR12-, and -S(O)r, wherein y denotes a number of 1 to 2, D represents C4-C6-cycloalkyl, or represents 5-6 membered heterocycle which has 1 or 2 hetero atoms selected from N, O and S, and optionally contains an oxo group,
W represents a direct bond, or represents -NR7-. -C(O)-, -C(O)O-, -
C(O)NR12-, -S(OV, -S(O)yNR12- or -NR12S(O)y-, R14 represents hydrogen, hydroxy, Ci-C6-alkyl, hydroxy-Ci-C6-alkyl, carboxy-Ci-Cό-alkyl, Cό-Qo-aryl or C6-Ci0-ar-Ci-C6-alkyl, represents 5-6 membered heterocycle which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by d-C6-alkyl, or
R5 and R6 together represent C2-C6-alkylene chain.
In the compounds of formula (1) according to the present invention, X is C or N, and the structure for each case may be depicted by the following formula (Ia) or (Ib).
Figure imgf000011_0001
Figure imgf000011_0002
In the compounds of formula (1) of the present invention, the substituent A more preferably represents phenyl, pyridine or 1,4-pyrazine. The substituent R1 more preferably represents hydrogen, Ci-Cό-alkyl or (Ii(C1- C3-alkyl)amino-C2-C3-alkyl, and most preferably represents hydrogen, methyl or (dimethylamino)ethyl.
The substituent R2 more preferably represents hydrogen, amino, halogen, C1-C3- alkyl, carboxy, carboxy-Q-Q-alkyl, Ci-C3-alkoxycarbonyl, Ci-C3-alkoxycarbonyl-Ci- C3-alkyl, hydroxy-Ci-C3-alkyl, Ci-C3-alkoxy, -(CH2)PNR7R8, -NHR10, -N(H)S(O)2R7, - NHC(O)R10 or -(CH2)p-heterocycle-R10, wherein p, R7, R8 and R10 are as defined in the above preferable scope. Most preferably, R2 is selected from the group consisting of hydrogen, methyl, methoxy, fluoro, -NH2, -NHAc, -NHSO2Me, -NHBOC, -NH(I- methyl-piperidine), l-oxo-2-hydroxy-ethyl, dimethylaminomethyl, hydroxymethyl, hydroxyethyl, carboxy, carboxymethyl, carboxyethyl, -CH2-(2-oxo)piperazine, -CH2- piperazine, -CH2-morpholine, -CH2-[I, l-dioxo-thiomorpholin-4-yl], and -CH2-[4- acetyl-piperazin- 1 -yl] .
The substituent R3 more preferably represents hydrogen, methyl or bromo, represents phenyl optionally substituted by Ci-C3-alkoxy, or represents heterocyclyl-Q- C3-alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups. Most preferably, R3 is selected from the group consisting of hydrogen, methyl, bromo, phenyl, 4-MeO- phenyl, -CH2-(2-oxo-piperazin-4-yl), and -CH2-(morpholin-4-yl).
The substituent R4 more preferably represents -YR11, wherein Y is selected from the group consisting of a direct bond, -0-, -C(O)-, -NH-, -CONH-, -SO2NH-, -NHC(O)-, -CH2CONH-, -CH2C(O)-, and -CH2SO2-. Most preferably, Y is selected from the group consisting of a direct bond, -0-, -C(O)-, -CH2C(O)- and -NHC(O)-. Further, R11 is selected from the group consisting of hydrogen, halogen, hydroxy, Q-Co-alkyl and -(CH2)tB-R13, wherein t, B and R13 are as defined in the above preferable scope. Most preferably, R is selected from the group consisting of hydrogen, methyl, ethyl, phenyl, fluoro, chloro, hydroxy, 2-carboxy-pyrrolidin-l-yl, pyrrolidin-1-yl, 4-acetic acid-l,3-thiazolin-2-yl, -CH2-(I, l-dioxo-thiomoφholin-4-yl), and -CH2-(2- oxopiperazin-4-yl).
The substituent R5 more preferably represents hydrogen, Ci-C6-alkyl, C3-C6- cycloalkyl, heterocycle or heterocyclyl-Ci-C6-alkyl, wherein the heterocycle is a 5-6 membered ring which has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups. Most preferably, R5 is selected from the group consisting of hydrogen, methyl, cyclopentyl, tetrahydropyran-4-yl and CH2- (tetrahydropyran-4-yl) .
The substituent R6 more preferably represents -(CR7R8)P-Z-D-W-R14, wherein Z represents a direct bond, or represents -C(O)-, -C(O)O-, -C(O)NH- or -S(O)2-. D is more preferably selected from the group consisting of cyclopentyl, cyclohexyl, pyrrolidine, tetrahydropyran, tetrahydrofuran and piperidine. W more preferably represents a direct bond, or represents -SO2-, -CO-, -C(O)O- or -CONR12-, wherein R12 is as defined in the above preferable scope. Most preferably, W is selected from the group consisting of -SO2-, -CO-, -C(O)O-, -CON(Me)-, and -CONH-. R14 more preferably represents hydrogen, hydroxy, Ci-C6-alkyl, hydroxy-Q-Cό-alkyl, C6-C10-aryl or C6-Cio-ar-C;ι-C3-alkyl, represents 5-6 membered heterocycle which has O or S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 or 2 hetero atoms selected from N, O and S, and is optionally substituted by Q-Cralkyl. Most preferably, R is selected from the group consisting of hydrogen, hydroxy, methyl, ethyl, isobutyl, hydroxymethyl, hydroxyethyl, phenyl, benzyl, thiophene, tetrahydrofuran, tetrahydropyran, 1,1-dioxo-tetrahydro-thiopyran, furan, pyridine and 5-methyl-pyridine.
Furthermore, R5 and R6 together with the N atom to which they are attached may more preferably form piperidine.
The compounds of formula (1) according to the present invention can also form a pharmaceutically acceptable salt. Such a "pharmaceutically acceptable salt" includes non-toxic acid addition salt containing pharmaceutically acceptable anion, for example, a salt with inorganic acids such as sulfuric acid, hydrochloric acid, nitric acid, phosphoric acid, hydrobromic acid, hydriodic acid, etc.; a salt with organic carboxylic acids such as tartaric acid, formic acid, citric acid, acetic acid, trichloroacetic acid, trifluoroacetic acid, gluconic acid, benzoic acid, lactic acid, fumaric acid, maleic acid, salicylic acid, etc.; or a salt with sulfonic acids such as methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, p-toluenesulfonic acid, naphthalenesulfonic acid, etc. The compounds of formula (I) can also form a pharmaceutically acceptable base addition salt, for example, a salt with alkali metals or alkaline earth metals such as lithium, sodium, potassium, calcium, magnesium, etc.; a salt with amino acids such as lysine, arginine, guanidine, etc.; or an organic salt with dicyclohexylamine, N-methyl- D-glucamine, tris(hydroxymethyl)methylamine, diethanolamine, choline, triethylamine, etc. The compounds of formula (I) of the present invention may be converted to their salts according to any of the conventional methods, and the salt formation can be easily carried out by a skilled artisan based on the structure of formula (1) without additional explanations thereon.
The term 'isomer' in the present specification means those having the same chemical or molecular formula as, but optically or sterically different from, the compounds of formula (1), or salts thereof. The compounds of formula (1) of the present invention may have an asymmetric carbon center(s) in the structure, and so may exist in the form of optical isomer (R or S isomer), racemate, mixture of diastereomers, or individual diastereomer, etc. When the compounds have a double bond, they may exist in the form of geometric isomer (trans or cis isomer). All the isomers and their mixtures are also covered by the present invention.
Hereinafter, the compounds of formula (1) include pharmaceutically acceptable salts and isomers thereof, unless otherwise explained. The salts and isomers should be construed to be covered by the present invention. For the sake of convenience, the present specification briefly expresses them as the compounds of formula (1).
Typical compounds among the compounds of formula (1) are those selected from the following:
Cyclopentyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl- [5 -methyl-2 -phenyl- 1 H-indol-7-yl] -amine; 5-Chloro-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
(Tetrahydropyran-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[2-(pyrazin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[5-methyl-2-(pyrazin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[2-(pyridin-2-yl)-lH-indol-7-yl] -amine;
(Tetrahydropyran-4-yl)- [2-(pyridin-2-yl)- 1 H-indol-7-yl] -amine;
Cyclopentyl-[5-phenoxy-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[5-ethoxy-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclohexyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; l-[4-[(5-Methyl-2-(pyridin-2-yl)-lH-indol-7-yl)amino]piperidin-l-yl]ethanone;
(l-Methylpiperidin-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
(l-Benzylpyrrolidin-3-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentylmethyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
5-Methyl-(7-piperidin-l-yl)amino-2-(pyridin-2-yl)-lH-indole; Dimethyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[l,5-dimethyl-2-(pyridin-2-yl)-indol-7-yl]-amine;
Cyclopentyl-[5-methyl-2-(6-methylpyridin-2-yl)-lH-indol-7-yl]-amine;
(l-Cyclohexanon-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
4- [(5-Chloro-2-phenyl- 1 H-indol-7-yl)amino] -cyclohexan- 1 -one; N-(5-Methyl-2-(pyridin-2-yl)-lH-indol-7-yl)-benzamide; l-Ethyl-3-[5-methyl-2-(ρyridin-2-yl)-lH-indol-7-yl]-urea; l-Phenyl-3-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-urea;
Thiophene-2-sulfonic acid (2-pyridin-2-yl-lH-indol-7-yl)-amide;
Thiophene-2-sulfonic acid [5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amide; Cyclopentyl-methyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester;
Cyclopentyl-[5-hydroxymethyl-2-phenyl-lH-indol-7-yl]-amine;
7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid; 2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]-acetic acid ethyl ester;
2-[7-(Cyclopentylamino)-2-phenyl-lH-indol-5-yl]ethanol;
2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]acetic acid;
2-[2-Phenyl-7-(tetrahydropyran-4-yl)amino-lH-indol-5-yl]-acetic acid;
2- [2-Phenyl-7-( 1 , 1 -dioxo-tetrahydro-thiopyran-4-yl)amino- 1 H-indol-5-yl] - acetic acid;
(Tetrahydropyran-4-yl)- [2-phenyl-5-( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl- 1 H- indol-7-yl]amine;
(Tetrahydropyran-4-yl)-[2-phenyl-5-(2-oxo-piperazin-4-yl)methyl-lH-indol-7- yl] amine; Cyclopentyl-[2-(3-fluoro)phenyl-5-(2-oxo-piperazin-4-yl)methyl-lH-indol-7- yl] amine;
(Tetrahydropyran-4-yl)-[2-(4-methoxy)phenyl-5-(l,l-dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine;
Cyclopentyl-[3,5-dimethyl-2-phenyl-lH-indol-7-yl]-amine; (Tetrahydropyran-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine;
Cyclopentylmethyl-(5 -methyl-2-phenyl- 1 H-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine;
(l-Methylpiperidin-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine;
1 -[-4-[(5-Methyl-2-phenyl- lH-indol-7-yl)amino]piperidin- 1 -yl]ethanone; Cyclopentyl-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; Cyclohexyl-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (Tetrahydropyran-4-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; Cyclopentylmethyl-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (Tetrahydropyran-4-ylmethyl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine;
(l-Benzylpyrrolidin-3-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; ( 1 -Methylpiperidin-4-yl)-(5 -chloro-2-phenyl- 1 H-indol-7-yl)-amine; (l,4-Dioxaspiro[4.5]decan-8-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; 2-[(5-Chloro-2-phenyl- 1 H-indol-7-yl)amino]propan- 1 ,3-diol; (Tetrahydropyran-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-methyl-amine;
(Tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -(1,1 -dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine;
Di(tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine; Di(tetrahydropyran-4-yl)- [2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl-
1 H-indol-7-yl] amine;
(l-Methyl-piperidinemethyl-4-yl)-[5-fluoro-2-phenyl-lH-indol-7-yl]amine; 2-[4-[(5-Fluoro-2-phenyl-lH-indol-7-yl)amino]piperidin-l-yl]ethanol; [l-(Tetrahydropyran-4-yl)piperidin-4-yl]-(5-fluoro-2-phenyl-lH-indol-7- yl)amine;
(Tetrahydropyran-4-yl)-(5-phenoxy-2-phenyl-lH-indol-7-yl)-amine; (Tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -(2-oxo-piperazin-4-yl)methyl- 1 H- indol-7-yl] amine;
(Tetrahydropyran-4-yl)-[5-chloro-l-(2-diethylaminoethyl)-2-phenyl-lH-indol- 7-yl] amine;
Dimethyl-(5-chloro-l-methyl-2-phenyl-lH-indol-7-yl)amine;
(Tetrahydropyran-4-yl)-(5 -chloro- 1 -methyl-2 -phenyl- 1 H-indol-7-yl)- methylamine; (Tetrahydropyran-4-yl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine;
Cyclopentyl-(5-chloro-3-phenyl-lH-indol-7-yl)-amine;
(Tetrahydropyran-4-ylmethyl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine;
Cyclopentyl-(5 -chloro-3 -(morpholin-4-yl)methyl-2-phenyl- 1 H-indol-7-yl)- amine; (Tetrahydropyran-4-yl)-(5 -chloro-3-(morpholin-4-yl)methyl-2 -phenyl- 1 H- indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-lH- indol-7-yl)-amine;
Cyclopentyl-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-lH-indol-7- yl)-amine;
(Tetrahydropyran-4-ylmethyl)-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2- phenyl-lH-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(3-bromo-5-(l , 1 -dioxo-thiomorpholin-4-yl)methyl-2- phenyl- 1 H-indol-7-yl)-amine; Cyclopentyl-(3 -bromo-5-( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl-2 -phenyl- 1 H- indol-7-yl)-amine;
(Tetrahydropyran-4-ylmethyl)-(3-bromo-5-(l,l-dioxo-thiomorpholin-4- yl)methyl-2-phenyl- 1 H-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5 -(1,1 -dioxo-thiomorpholin-4-yl)methyl-2-(3 - fluorophenyl)- lH-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine;
(3-Methylbutyl)-[5-(l , 1 -dioxo-thiomorpholin-4-yl)methyl-2-(4- methoxyphenyl)- 1 H-indol-7-yl]-amine; t-Butyl N-[4-[5-chloro-7-(cyclopentylamino)-lH-indol-2-yl]phenyl]carbamate;
Cyclopentyl-[2-(4-aminophenyl)-5 -chloro- 1 H-indol-7-yl] -amine;
Cyclopentyl-{5-chloro-2-[4-(l-methyl-piperidin-4-yl)aminophenyl]-lH-indol- 7-yl} -amine;
N-[4-(5-chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]- methanesulfonamide;
Cyclopentyl- {5-(l , 1 -dioxo-thiomorpholin-4-yl)methyl-2-[4- (acetyl)aminophenyl] - 1 H-indol-7-yl} -amine;
Dicyclopentyl-{5-(l,l-dioxo-thiomorpholin-4-yl)-2-[4-(acetyl)aminophenyl]- lH-indol-7-yl} -amine; (Tetrahydropyran-4-yl)methyl-{5-(l,l-dioxo-thiomorpholin-4-yl)-2-[4-
(acetyl)aminophenyl]-lH-indol-7-yl}-amine;
Di(tetrahydropyran-4-yl)methyl-{5-(l,l-dioxo-thiomorpholin-4-yl)-2-[4- (acetyl)aminophenyl] - 1 H-indol-7-yl} -amine;
(Tetrahydropyran-4-yl)- { 5-( 1 , 1 -dioxo-thiomorpholin-4-yl)-2- [4- (acetyl)aminophenyl] - 1 H-indol-7-yl} -amine;
(5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine;
[ 1 -(Methanesulfonyl)piperidin-4-yl]-(5-methyl-2-phenyl- 1 H-indol-7-yl)-amine;
2-Hydroxy- 1 -[4-(5 -methyl-2-phenyl- 1 H-indol-7-yl)amino-piperidin- 1 -yl] - ethanone; (5-Chloro-2-phenyl- 1 H-indol-7-yl)-piperidin-4-yl-amine;
4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl-carboxylic acid phenylamide; l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]-2- dimethylamino-ethanone;
[5-(l,l-Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-lH-indol-7-yl]-(piperidin- 4-yl)methyl-amine;
(5-( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2 -phenyl- 1 H-indol-7-yl)-( 1 - methanesulfonyl-piperidin-4-yl)-amine; {4-[5-(l,l-Dioxo-thiomoφholin-4-yl)methyl-2-phenyl-lH-indol-7-yl]amino- piperidin- 1 -yl} -(tetrahydrofuran-2-yl)-methanone;
(5-Fluoro-2-phenyl-lH-indol-7-yl)-[l-(l,l-dioxo-tetrahydrothiopyran-4-yl)- piperidin-4-yl]-amine;
N-(5-Chloro-2-phenyl-lH-indol-7-yl)-N',N'-dimethyl-cyclohexane-l,4- diamine;
N-(5-Chloro-2-phenyl-lH-indol-7-yl)-N'-methyl-cyclohexane-l,4-di amine;
4-(5 -Chloro-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 -carboxylic acid;
4-(5-Methyl-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 -carboxylic acid;
4-(5 -Chloro-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 -carboxylic acid amide;
4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-cyclohexanecarboxylic acid methylamide;
(2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester;
2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid; 2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester;
2-[(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino]-acetic acid;
2- [(5 -Phenoxy-2-phenyl-lH-indol-7-yl)amino] -propionic acid methyl ester;
2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-propionic acid; 2-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-propionic acid;
(5-Chloro-2-phenyl-lH-indol-7-yl)-pyridin-2-yl-amine;
(5-Chloro-2-phenyl-lH-indol-7-yl)-5-methyl-pyridin-2-yl-amine;
(5-Chloro-3-phenyl-lH-indol-7-yl)-(5-methyl-pyridin-2-yl)-amine;
(2S)-l-(7-cyclopentylamino-2-phenyl-lH-indole-5-carbonyl)-pyrrolidine-2- carboxylic acid methyl ester;
(2S)-l-(7-cyclopentylamino-2-phenyl-lH-indole-5-carbonyl)-pyrrolidine-2- carboxylic acid;
(2S)-I- [2-phenyl-7-(tetrahydropyran-4-yl)amino- 1 H-indole-5-carbonyl] - pyrrolidine-2-carboxylic acid; 2-(7-Cyclopentylamino-2-phenyl- lH-indol-5-yl]- 1 -pyrrolidin- 1 -yl-ethanone;
Cyclopentyl-[2-phenyl-5-(2-pyrrolidin-l-yl-ethyl)-lH-indol-7-yl]-amine;
2-[(R)-2-(7-cyclopentylamino-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4- yl] -acetic acid;
2-[(R)-2-(2-phenyl-7-(tetrahydropyran-4-yl)methylamino-lH-indol-5-yl)-4,5- dihydro-thiazol-4-yl]-acetic acid;
3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester;
3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid;
[3-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-methanol;
{3-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]-phenyl}-methanol; 2-{3-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]-phenyl}- acetic acid;
2-[3-(5-Chloro-7-cyclopentylamino-l-H-indol-2-yl)-phenyl]-acetic acid;
2- {3-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]-phenyl} -acetic acid;
2-{3-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]-phenyl}- acetic acid methyl ester;
2-[3-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-acetic acid methyl ester; 2-{3-[5-Chloro-7-(tetrahydropyran-4-yl)amino)-lH-indol-2-yl]-phenyl}-acetic acid methyl ester;
[2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl] -methanol;
2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid;
2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid methyl ester; [4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-methanol;
2- {4-[5-Chloro-7-(tetrahydropyran-4-yl)amino- 1 H-indol-2-yl]phenyl} -ethanol;
4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid;
2-{4-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]phenyl}- acetic acid; 2-[4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)phenyl]-acetic acid;
2-{4-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]phenyl}-acetic acid;
4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)benzoic acid methyl ester;
4-(7-Cyclopentylamino-5 -methyl- lH-indol-2-yl)benzoic acid methyl ester; 2-{4-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]phenyl}- acetic acid methyl ester;
2-[4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)phenyl]acetic acid methyl ester; 2-{4-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]phenyl}-acetic acid methyl ester;
[5 -Chloro-2-(3 -dimethylaminoethylphenyl)- 1 H-indol-7-yl] -(tetrahydropyran-4- yl)-amine;
[5 -Chloro-2-(3 -moφholin-4-ylmethylphenyl)- 1 H-indol-7-yl] -(tetrahydropyran- 4-yl)-amine;
[5-Chloro-2-(3-pyrrolidin-4-ylmethylphenyl)-lH-indol-7-yl]-(tetrahydropyran- 4-yl)-amine;
1 - {4- [3-(5 -Chloro-7-tetrahydropyran-4-ylamino- 1 H-indol-2-yl)-benzyl] - piperazin- 1 -yl} -ethanone; {5-Chloro-2-[3-(2-oxo-piperazin-4-yl)ethylphenyl]-lH-indol-7-yl}-
(tetrahydropyran-4-yl)-amine;
{5-Chloro-2-[3-(l,l-dioxo-thiomoφholin-4-yl)ethylphenyl]-lH-indol-7-yl}- (tetrahydropyran-4-yl)-amine;
Cyclopentyl-(lH-indazol-7-yl)-amine; (Tetrahydropyran-4-yl)-(lH-indazol-7-yl)-amine;
Cyclopentyl-(5-methyl- 1 H-indazol-7-yl)-amine;
(5-Methyl-lH-indazol-7-yl)-(tetrahydropyran-4-yl)-amine;
Cyclopentyl-[3-(4-methoxyphenyl)- 1 H-indazol-7-yl)-amine;
[3-(4-Methoxyphenyl)-lH-indazol-7-yl)]-(tetrahydropyran-4-yl)-amine; [3-(4-Methoxyphenyl)-lH-indazol-7-yl)-(tetrahydropyran-4-ylmethyl)-amine;
(Tetrahydropyran-4-yl)-[5-(l , 1 -dioxo-thiomorpholin-4-yl)methyl-3-phenyl-2- trimethylsilyl-lH-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-[5-(l,l-dioxo-thiomorpholin-4-yl)methyl-3-phenyl-lH- indol-7-yl)-amine; and
(Tetrahydropyran-4-yl)-[3-bromo-5-(morpholin-4-yl)methyl-2-phenyl-lH-indol- 7-yl]-amine.
The present invention also provides processes for preparing the compounds of formula (1). Hereinafter, the processes for preparing the compounds of formula (1) are illustrated by exemplary reaction schemes for the purpose of better understanding.
However, a skilled artisan in the field to which the present invention pertains may prepare the compounds of formula (1) via various routes according to their structures, and such processes should be construed to fall under the scope of the present invention. In other words, the compounds of formula ( 1 ) may be prepared by optionally combining various synthetic methods which are described in the present specification or disclosed in the prior arts. The processes for preparing the compounds of formula (1) cover even such processes, and are not limited to those explained below.
First, the compounds of formula (1) may be prepared according to the following
Reaction Scheme (1) by reducing the nitro group of the compound (2) to produce the amine compound (3), and by carrying out a reductive amination reaction or coupling reaction in the presence of a base on the compound (3) with compound (4) or compound (5). Reaction Scheme 1
(Carbonyl) R6— H
Figure imgf000026_0001
R5— E 5
in the above Reaction Scheme (1), m, X, R1, R3, R4 and R6 are as defined above,
R represents (R )n-A-, and
E represents a leaving group or linker, preferably may be chloro, bromo or iodo, a form of mixed anhydride, isocyanate or isothiocyanate.
In Reaction Scheme (1), the reduction may be conducted using an acid catalyst and a metal, or a metallic catalyst in the presence of hydrogen gas. Iron, zinc, lithium, sodium, or tin (usually, tin chloride) may be used as the metal, and inorganic acid such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, etc.; organic carboxylic acid such as acetic acid, trifluoroacetic acid, etc.; or ammonium chloride, etc. may be used as the acid catalyst. Also in the reduction reaction using a metallic catalyst in the presence of hydrogen gas, palladium, nickel, platinum, ruthenium, rhodium etc. may be mentioned as the metallic catalyst, where the conventional hydrogen gas pressure ranges 1-3 atm. R6 in the formula (4) includes a carbonyl group, where the carbonyl group means an aldehyde or a ketone. The reductive amination (RA) reaction may use sodium triacetoxyborohydride (NaBH(OAc)3) or sodium cyanoborohydride (NaBH3CN), etc.
The coupling reaction may be carried out by reacting the compound (3) with the compound (5) using a base such as Et3N, EtN(iPr)2, DBU, N-methyl-morpholine, methyl-pyrrolidine, K2CO3, etc.
In the case of an indole compound wherein X is C, those having a simple substituent (7-nitro-indole, 2,3-dimethyl-7-nitro-indole, etc.) may be commercially available, and most of them may be synthesized by cyclizing the acetylene intermediate such as the compound (8) in the following Reaction Scheme (2). Further, the compound (8) may be obtained via a coupling reaction of halobenzene compound (6) with acetylene compound (7).
Reaction Scheme 2
Figure imgf000027_0001
2-1
in the above Reaction Scheme (2), R2 and R4 are as defined above, and Q represents iodo or bromo. The compound (2-1) may be prepared by a cyclization reaction of the acetylene compound (8) in the presence of a base selected from KOBu1, K2CO3, DBU, etc. or a metallic catalyst selected from CuI, Pd(II), etc.
The preparation of acetylene compound (8) may be carried out by adding a base in the presence of a metallic catalyst, where Pd(II), Cu(I), etc. are used as the metallic catalyst, and Et3N, Et2N(iPr), DBU, N-methyl-morpholine, methyl-pyrrolidine, K2CO3, etc. are used as the base.
The acetylene compound (7) is usually commercially available, or may be prepared by a coupling reaction of acetylene in the presence of Pd(II) or Cu(I) and a base according to an art-known method [Synthesis, 2004 59-61; Bioorganic & Medicinal Chemistry, 13,2005, 197-209; Journal of Organic Chemistry, 71, 2006, 167-175]. The acetylene being used is trimethylsilylacetylene or 2-methyl-3-butyn-2- ol, and the base being used is diethylamine, triethylamine, diisopropylethylamine, etc.
The halobenzene compound (6) may be obtained from a nitroaniline compound (13) using iodine or bromine as depicted in the following Reaction Scheme (3).
Reaction Scheme 3 R4— H Substitution Reduction
Figure imgf000029_0001
Figure imgf000029_0003
Figure imgf000029_0002
12
10 11
i) Acetylation ii) Nitration iii) Deacetylation
Figure imgf000029_0004
13 in the above Reaction Scheme (3), R and Q are as defined above.
The nitroaniline compound (13) is commercially available, or may be prepared via acetylation, nitration and deacetylation from commercially available nitro compound
(11) or aniline compound (12). The aniline compound (12) that is not easy to obtain commercially can be prepared from the nitro compound (11). Likewise, the nitro compound (11) can also be commercially available, or prepared from 4-fluoro- nitrobenzene compound (9). In the Reaction Scheme (3), the compound (10) of formula R4-H means commercially available alcohols and amines.
The halogenating material for preparing the compound (6) may be selected from iodine, bromine, iodomonobromide and iodomonochloride, which may be used along with a silver ion such as silver nitrate (AgNO3), silver carbonate (AgCO3), silver sulfate (Ag2SO4), etc.
Conventional acetylation and nitration reactions are used for obtaining the compound (13) from the compound (12). The nitration reaction may be carried out using undiluted nitric acid under a low temperature (-15 to 0°C), or various solvents such as dichloroethane or dichloromethane may be used together. The reduction reaction of nitro group may also be carried out in the same manner as the process for preparing the compound (3) in Reaction Scheme (1) above.
As depicted in the following Reaction Scheme (4), the indole compound may be obtained by directly reacting the trifluoroacetyl- substituted compound (6-1) with the acetylene compound (7).
Reaction Scheme 4
Figure imgf000030_0001
In the meantime, the indole compound (2-2) may be obtained from the nitroaniline compound (13) according to Fisher indole synthesis, as depicted in the following Reaction Scheme (5).
Reaction Scheme 5 Condensation
Figure imgf000031_0002
Figure imgf000031_0001
13 14 15
Cyclization
Figure imgf000031_0003
2-2 in the above Reaction Scheme (5), R2 , R3 and R4 are as defined above.
The compound (14) is commercially available, or may be prepared by modifying the amine group of the compound (13) to hydrazine group according to the art-known method [Journal of the America Chemical Society, 198(48), 15374-75, 2006].
Hydrazine may be formed by reacting amine group with NaNO2 in the presence of hydrochloric acid to introduce nitro group, and by reducing the nitro group using SnCl2, where the reaction is made using hydrochloric acid solution having a concentration of 1 to 12N, preferably 4 to 8N.
The hydrazone compound (15) may be prepared via condensation of the hydrazine compound (14) with the ketone compound in the presence of a base. As the base, metal hydroxides such as sodium hydroxide, lithium hydroxide, etc., metal carbonates such as sodium bicarbonate, potassium carbonate, etc., metal acetates such as sodium acetate, etc., organic bases such as triethylamine, pyridine, etc., preferably sodium acetate, sodium bicarbonate, etc. may be mentioned. The preparation of the compound (2-2) through a cyclization may be carried out in the presence of an acid catalyst, where the acid may be polyphosphoric acid, hydrochloric acid, p-toluenesulfonic acid, sulfuric acid, acetic acid, etc., preferably polyphosphoric acid. Polyphosphoric acid may be used either alone or in the state of being mixed with aromatic hydrocarbons such as benzene, toluene, etc. The reaction temperature ranges between 25 and 150 °C , and the reaction time ranges usually between 5 min and 60 h, preferably 5 min and 12 h.
The compound (2-3) having a substituent at 3-position of the indole ring may be prepared via a cyclization of the TMS-substituted acetylene compound (18) together with the compound (6), as depicted in the following Reaction Scheme (6).
Reaction Scheme 6
R3 — ^ + TMS — Cl
Figure imgf000032_0001
Coupling R3— OTf + ≡ — TMS
19 20 in the above Reaction Scheme (6), R >3 and i τ R)4 a . re as defined above.
The compounds (16), (17) and (20) are commercially available, and the compound (19) may be obtained by a conventional tosylation reaction from an alcohol or phenol. Preparations of the TMS compound (18) or the compound (21) are the same as the process for preparing the compound (2-1) in Reaction Scheme (2) above. The compound (2-3) may be obtained by removing TMS group, where TBNF (tetrabutylammoniumfluoride) and a base can be used.
The compound (2-4) wherein 3 -position of the indole ring is substituted may be prepared by introducing formyl group to the indole compound (22) to give the aldehyde compound (23), and by carrying out reductive amination reaction.
Reaction Scheme 7
Figure imgf000033_0001
in the above Reaction Scheme (7),
R4 is as defined above, and
R3 represents heterocycle containing amine.
Formylation reaction may be carried out using DMF in the presence of a base, where as the base, n-butyllithium, t-butyllithium, LDA (lithiumdiisopropylamine), KHMDS (potassiumhexamethyldisilane), etc. can be mentioned. Reductive amination reaction may be carried out in the same manner as the process for preparing the compound (1) in Reaction Scheme (1) above. The indazole compound (27) or (33) may be prepared as depicted in the following Reaction Scheme (8). First, the indazole ring itself can be easily obtained by heating the nitroaniline compound in the presence of acetic acid according to the conventional manner. The compound (33) wherein 3-position of the indazole ring is substituted may be obtained via a substitution reaction using the iodo compound.
Reaction Scheme 8
Figure imgf000034_0001
The compounds whose preparation methods are not specifically explained in the present specification are known per se, or those that can be prepared from a known compound according to a known process or a similar process thereto.
In the processes according to the present invention, mixtures are conventionally separated by column chromatography. In the case of a final product, it can be separated after completion of reaction by recrystallization or normal or reverse-phased HPLC (Waters, Delta Pack, 300x50 mml.D., Cl 8 5μm, 100A). When the product is purified through recrystallization or HPLC, the compound may be obtained in the form of a salt with trifluoroacetic acid. When a salt with hydrochloric acid is desirable, ion exchange resin can be used.
As explained above, the compounds according to the present invention, starting materials, intermediates, etc. for the preparation thereof may be obtained by various processes, and such processes for preparing the compounds of formula (1) should be construed to fall under the scope of the present invention.
[Effect]
The present invention further provides a composition for the prevention or treatment of necrosis and associated diseases, which comprises therapeutically effective amount of the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as an active ingredient together with pharmaceutically acceptable carriers or diluents.
The present invention further provides a method for the prevention or treatment of necrosis and associated diseases using the above described composition.
Necrosis and associated diseases which can be treated and/or prevented according to the present invention include acute/chronic hepatic disease (e.g. hepatitis, hepatic fibrosis, hepatocirrhosis), neurodegenerative disease (e.g. dementia, Parkinson's disease, Huntington's disease), ischemic cardiac disease, reperfusion injury, ischemic stroke or ischemic injury, pancreatitis, bacterial/viral sepsis, diabetes mellitus or diabetic complications, diabetic vascular disease [in particular, these diabetes are caused by pancreatic cell destroying substances, and mediated by virus, hyperglycemia, fatty acid, diet, toxin, streptozotocin and the like], necrotizing procolitis, cystic fibrosis, rheumatoid arthritis, degenerative arthritis, nephropathy, bacterial infection, viral infection (e.g. HIV), multiple sclerosis, leukemia, lymphoma, neonatal respiratory distress syndrome, asphyxia, tuberculosis, endometriosis, angiasthenia, psoriasis, chilblain, steroid treatment complications, gangrene, pressure sores, hemoglobinuria, burns, hyperthermia, Crohn's disease, celiac disease, compartment syndrome, spiral cord injury, glomerulonephritis, muscular dystrophy, metabolic inherited disease, mycoplasmal disease, anthrax, Andersen's disease, congenital mitochondrial disease, phenylketonuria, placental infarction, syphilis, aseptic necrosis etc. In addition, necrosis and associated diseases caused by drugs and toxic substances are selected from the group consisting of the necrosis associated with alcoholism, the exposure to, and/or administration and/or self-administration of, cocaine, drugs (e.g., paracetamol), antibiotics, anti-cancer agent, adriamycin, puromycin, bleomycin, NSAID, cyclosporine, chemical toxins (e.g., carbon tetrachloride, cyanide, methanol, ethylene glycol), poison gas, agrochemicals, heavy metals (e.g., lead, mercury, cadmium), or injury due to the exposure to radioactivity/UV and associated necrosis thereof.
In particular, the composition according to the present invention exhibits not only the effects for hepatoprotection and hepatic functional improvement, but also shows the prophylactic and therapeutic effects on the chronic hepatic disease such as fatty liver, hepatic fibrosis, hepatocirrhosis, etc. and acute/chronic hepatic disease such as hepatitis, etc. caused by virus or drugs. Consequently, complications of hepatic disease including, but not limited to, portal hypertention also may be prevented or treated. More particularly, the medical composition according to the present invention is also effective for the treatment or prevention of the hepatic disease selected from liver transplantation, alcoholic or non-alcoholic fatty liver, hepatic fibrosis, hepatocirrhoisis and hepatitis caused by virus or drugs, and is effective for alcoholic acute/chronic hepatic disease.
Further, the composition according to the present invention is effective for the treatment or prevention of fatty acid-induced fatty liver or acute/chronic hepatic disease derived from fatty liver.
As used herein, "treatment" means the interrupting or delaying the progress of the disease when applied to the subject showing the onset of disease symptoms , and
"prevention" means the interrupting or delaying the sign of the onset of disease when applied to the subject that does not show, but is at risk of, the onset of disease symptoms.
The above-mentioned "pharmaceutical composition" may comprise pharmaceutically acceptable carriers, diluents, excipients, or their combinations, if needed, together with the compounds of the present invention. Pharmaceutical composition facilitates the administration of the compound into a living organism. There exist a number of techniques to administer the compound, and they include, but not limited to, oral, injectable, aerosol, parenteral and topical administration. As used herein, "carrier" means a substance which facilitates the incorporation of the compound into the cells or tissues. For example, dimethylsulfoxide (DMSO) is a typical carrier which is used to facilitate the introduction of various organic compounds into the cells or tissues of living organisms.
As used herein, "diluent" is defined as a substance that is diluted in water which dissolves the compound, as well as stabilizes the biologically active form of the subject compound. The salts dissolved in buffer solution are utilized as diluents in the art. Typically used buffer solution is phosphate buffered saline which mimics the salt form of human solution. Buffer diluents rarely alter the biological activities of the compound, as the buffer salts can control the pH of solution at low concentration.
As used herein, "pharmaceutically acceptable" means the property that does not impair the biological activities and physical properties of the compound.
The compounds of the present invention can be formulated as various pharmaceutical dosage forms according to the desired purpose. For the preparation of the pharmaceutical composition of the present invention, active ingredient, specifically, the compounds of formula (1), pharmaceutically acceptable salt or isomer thereof is mixed together with various pharmaceutically acceptable carriers which can be selected according to the formulation to be prepared. For example, the pharmaceutical composition of the present invention can be formulated as injectable preparation, oral preparation, etc., according to the desired purpose. The compounds of the present invention can be formulated by the methods known in the art, which utilize pharmaceutical carriers and excipients known in the art, and be incorporated into the containers of unit dose form or mult-dose form. The form of the preparation can be solutions, suspensions or emulsions in oily or aqueous media, and contain typical dispersing agents, suspending agents or stabilizers. Further, for example, it can be a form of dry powder which is intended to be reconstructed by dissolving in sterile, pyrogen-free water prior to use. The compounds of the present invention also can be formulated into suppository forms utilizing typical suppository base such as cocoa butter or other glycerides. As solid dosage forms for oral administration, capsules, tablets, pills, powder and granule can be prepared, and capsules and tablets are especially useful. Preferably, tablets and pills are prepared as enteric coated forms. Solid dosage forms can be prepared by mixing the compounds of the present invention together with carriers such as one or more inert diluents such as sucrose, lactose, starch, etc., lubricants such as magnesium stearate, disintegrant, binder, etc.
If needed, the compounds of the present invention or the pharmaceutical compositions containing the same can also be administered in combination with other active agents including cytoprotective agents with various action mechanisms of different types, especially the existing agents utilized for hepatoprotection, hepatic functional improvement, and prevention or treatment of hepatic disease - hepatocyte regeneration promoters, hepatic functional adjuvants, anti-viral agents, immunosuppressants, fibrosis inhibitors, etc. The compounds of the present invention or the pharmaceutical compositions containing the same can be co-administered with prophylactic or therapeutic agents for any drug-derived necrosis and associated diseases. These drugs include the drugs for any disease group such as antibiotics, anti-cancer agents, anti-viral agents, anti- infectives, anti-inflammatory agents, anti-coagulants, lipid-improving agents, cell death inhibitors, anti-hypertensive agents, anti-diabetic/anti-obesity agents, therapeutic agents for cardiovascular disease, therapeutic agents for neurodegenerative disease, anti-aging agents, therapeutic agents for metabolic disease, etc.
The compounds of the present invention or the pharmaceutical compositions containing the same can be used for the prevention of the cell injury and subsequent necrosis and associated diseases derived by various causes such as toxins, and these causes include reactive oxygen species (ROS), heavy metals, alcohol, food, supplement, radiation, diet, etc.
The dosage of the compounds of formula (1) depends on the prescription of a physician, taking into account such factors as body weight, sex, age, condition of health, and diet of the patient, specific nature of the disease, administration time of the agent, administration method, mixing ratio of agents, and severity of the disease, etc. However, dosage needed for the treatment of an adult is typically from about 1.0 mg to 2,000 mg per day, depending on the intensity and frequency of the administration. When administered to an adult via intramuscular or intravenous routes, total dosage typically from about 1.0 mg to 300 mg per day will be sufficient when separately administered in a single dosage, but for some patients a higher daily dosage may be desirable.
The present invention further provides a method of preparing the composition for the prevention or treatment of necrosis and associated diseases, which comprises the step of mixing the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as an active ingredient together with pharmaceutically acceptable carriers or diluents.
[Best Mode for Carrying Out the Invention]
The present invention will be more specifically explained by the following preparations and examples. However, it should be understand that they are intended to illustrate the present invention but not in any manner to limit the scope of the present invention. In the following preparations and examples, M means molar concentration, and N means normal concentration.
The following Preparations explain more in detail preparations of intermediates that are required for syntheses of Example compounds. The abbreviations used in the following Preparations and Examples are as follows. Ac: acetyl
BOC: t-butoxycarbonyl
Bu: butyl
Bn: benzyl c-Pen: cyclopentyl c-Hex: cyclohexyl
DME: dimethoxyethane
DCM: dichloromethane
DIPEA: diisopropylethylamine DMAP: 4-dimethylaminopyridine
DMF: N,N-dimethylformamide
EDC: l-(3-dimethylaminopropyl)-3-ethylcarbodiimide, hydrochloride
Et: ethyl
Hex: n-hexane HOBT: hydroxybenzotriazole
HBTU: 2-( 1 H-benzotriazol- 1 -yl)- 1 , 1 ,3 ,3-tetramethyluronium hexafluorophosphate i-Pr: isopropyl i-Pen: isopentyl KHMDS : potassium bis(trimethylsilyl) amide
LDA: lithium diisopropylamine
Me: methyl
Ph: phenyl
Pid: piperidine Piz: piperazine
Pyd: pyrrolidine
Pro: proline
PMB: paramethoxybenzyl
TEA: triethylamine TFA: trifluoroacetic acid THF: tetrahydrofuran THP: tetrahydropyran TMS: trimethylsilyl TBNF: tetrabutylammoniumfluoride
Preparation 1 : 2-Nitro-4-phenoxy-phenylamine
Step A: N-(4-phenoxy-phenyl)-acetamide
Commercial available 4-phenoxy-aniline (4.16 g, 20.8 mmol) was dissolved in dichloromethane (100 mL), and triethylamine (3.05 g, 31.1 mmol) and acetic anhydride
(2.22 g, 20.8 mmol) were added in drops. The mixture was stirred for 1 h at 0°C to room temperature. After completion of the reaction, the mixture was filtered using dichloromethane and crystallized to give the title compound (4.50 g, 18.6 mmol)
Step B: N-(2-nitro-4-phenoxy-phenvDacetamide
N-(4-phenoxy-phenyl)-acetamide (1.00 g, 4.03 mmol) prepared in Step A was dissolved in fuming nitric acid (2 mL), and the mixture was stirred for 2 h at -15 °C .
After completion of the reaction, the reaction mixture was poured into 100 mL of ice water, which was then extracted with ethyl acetate. The extracted organic solution was dried over anhydrous magnesium sulfate, the solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.67 g, 2.33 mmol).
Step C: 2-Nitro-4-phenoxv-phenylamine N-(2-nitro-4-phenoxy-phenyl)acetamide (0.67 g, 2.33 mmol) prepared in Step B was dissolved in methanol (5 niL), 6.0N sodium hydroxide (1.5 mL) was added thereto, and the mixture was stirred for 18 h at room temperature. After completion of the reaction, 6.0N aqueous hydrochloric acid solution (1.3 mL) and ammonium chloride solution (100 mL) were added thereto. The reaction mixture was extracted with ethyl acetate, dried over magnesium sulfate, and recrystallized from dichloromethane and hexane to give the title compound (521 mg, 2.12 mmol). Mass [M+H] = 230
Preparations 2 to 7:
Commercially available anilines were reacted according to the same procedure as Preparation 1 to synthesize the Preparation Compounds in the following table.
Figure imgf000044_0001
Figure imgf000044_0002
Preparation 8: 5-Methγl-2-(pyridin-2-yl)-7-nitro-lH-indole Step A: (2-Nitro-4-methyl-phenyl)-hydrazine hydrochloride The commercially available 4-methyl-2-nitro-phenylamine (40 g, 0.23 mol) was dissolved in 12N-hydrochloric acid (100 mL), to which sodium nitrite (16 g, 0.23 mol) dissolved in water (50 mL) was slowly added in drops at 0°C . The reaction mixture was stirred for 30 min at 0°C . After lowering the temperature of the reaction mixture to 0°C , tin (II) chloride (132 g, 0.70 mol) dissolved in 100 mL of 12N-hydrochloric acid was slowly added in drops thereto. The reaction mixture was stirred for 3 h at 0°C to room temperature. The resulting yellow solid was filtered, washed with a small amount of 6N-HC1, and dried to give the title compound (30 g, Yield 63%).
1H-NMR (400HMz, DMSOd6); δ 9.21(s, IH), 7.98(d, J=2.4Hz, IH), 7.66 (d, J=9.6Hz, IH), 7.55(dd, J=2.4, 9.6Hz, IH), 4.74(br s, 2H)
Step B: N-r(4-methyl-2-nitro-phenylVN'-[l-(pyridin-2-vD-ethylidenelhvdrazine hydrochloride
(2-Nitro-4-methyl-phenyl)-hydrazine hydrochloride (30 g, 0.14 mol) prepared in Step A and pyridinemethylketone (14.4 mL, 0.16 mol) were dissolved in methanol (300 mL), and sodium acetate (14.2 g, 0.17 mol) was added thereto. The reaction mixture was stirred for 8 h at room temperature. The resulting yellow solid was filtered, washed with water and methanol, and dried to give the title compound (30 g, Yield 82%).
Step C: 5-Memyl-2-(pyridin-2-ylV7-nitro-lH-indole
To N-[(4-methyl-2-nitro-phenyl)-N'-[l-(pyridin-2-yl)-ethylidene]hydrazine hydrochloride (13 g, 46 mmol) prepared in Step B was added polyphosphoric acid (100 mL), which was then heated for 4 h at 100°C. After completion of the reaction, water was added to the reaction mixture, and the water insoluble solid was collected. This solid was washed with water and dried to give the title compound (6.0 g, Yield 49%). Mass [M+H] = 253
Preparations 9 to 15:
Commercially available nitroanilines, the compound prepared in Preparation 3, pyridine, pyrazineketone, etc. were reacted according to the same procedure as Preparation 8 to synthesize the Preparation Compounds in the following table.
Figure imgf000046_0001
Figure imgf000046_0002
Preparation 16: 2-Bromo-6-nitro-4-phenoxy-phenylamine
2-Nitro-4-phenoxy-phenylamine (2.3 g, 10 mmol) prepared in Preparation 1 was dissolved in DCM (30 mL), Br2 (720 ul, 35%) was added thereto at 0°C, and the mixture was stirred for 2 h. After completion of the reaction, saturated aqueous sodium thiosulfate solution was added. The resulting mixture was extracted with EtOAc, and dried over MgSO4. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (2.84 g, Yield 92%).
Mass [M+H] = 309
Preparation 17: 2-Amino-5-methyl-3-nitro-phenyliodide
Commercially available 4-methyl-2-nitro-phenylamine (20 g, 131.5 mmol) was dissolved in ethanol (300 mL), silver nitrate (27 g, 157.7 mmol) and iodine (40 g, 157.7 mmol) were added thereto, and the mixture was stirred for 8 h at room temperature. After completion of the reaction, the reaction mixture was filtered through a cellite, washed with 100 mL of ethyl acetate, and concentrated. Water was added to the residue, which was then extracted with ethyl acetate, washed with saturated sodium chloride solution, and dried over anhydrous magnesium sulfate to give the title compound (29 g, Yield 69%). 1H-NM (500MHz, CDCl3); δ 7.94(s, IH), 7.75(s, IH), 6.48(br s, 2H), 2.23(s,
3H)
Preparations 18 to 22:
Commercially available nitroanilines and the compounds prepared in Preparations 1 to 7 were reacted according to the same procedure as Preparation 17 to synthesize the Preparation Compounds in the following table.
Figure imgf000047_0001
Figure imgf000048_0001
Preparation 23: p-(BOC-amino)-phenyl-acetylene p-Aminophenyl-acetylene (1.17g, 10 mmol) was added to DCM (30 mL), and Et3N (2.8 mL, 20 mmol) was added thereto. (BOC)2O (2.3 g, 10 mmol) was added, and the mixture was stirred for 2 h at room temperature. After completion of the reaction, IN HCl was added, which was then extracted with EtOAc and dried over anhydrous magnesium sulfate. After filtration, the solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound. Mass [M+H] = 117
Preparation 24: 5-Methyl-7-nitro-2-phenyl-lH-indole Step A: 4-Methyl-2-nitro-6-(phenylacetyleneVphenylamine 2-Amino-5-methyl-3-nitro-phenyliodide (7 g, 25.2 mmol) prepared in Preparation 17 and phenylacetylene (3.3 mL, 30.22 mmol) were dissolved in tetrahydrofuran (100 mL). Triethylamine (11 mL, 75.5 mmol), dichloro(bistriphenylphosphine)palladium (II) (1.8 g, 2.52 mmol) and cupper (I) iodide (0.48 g, 2.52 mmol) were added thereto, and the mixture was stirred for 8 h at room temperature. After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (4.5 g, Yield 71%).
1H-NMR (400HMz, CDCl3); δ 7.93(s, IH), 7.53(m, 2H), 7.46(s, IH), 7.39(m, 3H), 6.62(br s, 2H), 2.26(s, 3H)
Step B: 5-Methyl-7-nitro-2-phenyl-lH-indole 4-Methyl-2-nitro-6-(phenylacetylene)-phenylamine (4.5 g, 17.8 mmol) prepared in Step A was dissolved in tetrahydrofuran (120 mL) and N-methyl-pyrrolidinone (30 mL). Potassium t-butoxide (4 g, 35.7 mmol) was added, and the mixture was stirred for 3 h at room temperature. After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.0 g, Yield 22%).
1H-NMR (400HMz, CDCl3); δ 11.53(br s, IH), 8.02(d, J-7.6Hz, IH), 7.94(s, IH), 7.87(s, IH), 7.50(m, 2H), 7.41(m, IH), 7.09(m, J=2.0Hz, IH), 2.49(s, 3H)
Preparations 25 to 40:
The compounds prepared in Preparations 16, 18 to 22, commercially available acetylene compounds, and the compound prepared in Preparation 23 were reacted according to the same procedure as Preparation 24 to synthesize the Preparation Compounds in the following table.
Figure imgf000050_0001
Figure imgf000050_0002
Preparation 41: 5-Chloro-3-phenyl-7-nitro-lH-indole
Step A: 5-Chloro-7-nitro-3-phenyl-2-trimethylsilyl-lH-indole
2-Amino-5-chloro-3-nitro-phenyliodide (1.5 g, 4.90 mmol) prepared in Preparation 19 and l-phenyl-2-trimethylsilylacetylene (4.3 g, 24.50 mmol) were dissolved in DMF (50 rnL). Palladium acetate (0.11 g, 0.5 mmol), lithium chloride (0.21 g, 4.90 mmol) and triethylamine (2.48 g, 24.50 mmol) were added thereto, and the mixture was stirred under heating for 3 h to 100°C . After completion of the reaction, water was added to the reaction mixture, which was then extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.05 g, Yield 87%). 1H-NMR (400HMz, CDCl3); δ 9.78(br s, IH), 8.15(s, IH), 7.78(s, IH),
7.38~7.48(m, 5H), 0.26(s, 9H)
Step B: 5-Chloro-3-phenyl-7-nitro-lH-indole
5-Chloro-7-nitro-3-phenyl-2-trimethylsilyl-lH-indole (1.5 g, 4.35 mmol) prepared in Step A was dissolved in tetrahydrofuran (30 mL), and tetrabutylammonium fluoride IM solution (5.2 mL, 5.2 mmol) was added in drops thereto at 0°C . After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.2 g, Yield 100%)ifr T1^-*}!^ 1}.
1H-NMR (400HMz, CDCl3); δ 10.03(br s, IH), 8.24(d, J=8Hz, 2H), 7.62(m, 3H), 7.55(m, 2H), 7.43(m, IH) Preparation 42: [3-Phenyl-7-nitro-lH-indol-5-yl]-carboxylic acid 3-Iodo-4-amino-5-nitro-l-benzoic acid ethyl ester prepared in Preparation 20 was reacted according to the same procedure as Steps A and B of Preparation 41 to give the title compound. 1H-NMR (400HMz, CDCl3); δ 9.94(br s, IH), 8.86(s,lH), 8.52(s, IH), 7.48(m,
5H), 4.42(q, 2H), 1.43(t, 3H), 0.27(s, 9H)
Preparation 43 : 5-Chloro-7-nitro-3-(2-oxo-piperazm-4-yl)methyl-2-phenyl-lH- indole Step A: 5-Chloro-3-formyl-7-nitro-2-ρhenyl-lH-mdole
7-Nitro-5-chloro-2-phenyl-lH-indole (1.Og, 3.67 mmol) prepared in Preparation 26 was dissolved in dichloromethane (20 niL). Phosphoryloxychloride (0.84g, 5.50 mmol) and DMF (0.80g, 11.01 mmol) were added in drops thereto at 0°C, and the mixture was stirred for 6 h at room temperature. After completion of the reaction, the reaction was quenched by saturated aqueous sodium hydrogen carbonate solution. The reaction mixture was extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.5g, Yield 45%). 1H-NMR (400HMz, DMSO-d6); δ 9.89(s, IH), 8.46(s,lH), 7.93(s, IH), 7.81(d,
J=9.2Hz, 2H), 7.53(m, 3H)
Step B: 5-Chloro-7-nitro-3-(2-oxo-piperazin-4-yDmethyl-2-phenyl-lH-indole 5-Chloro-3-formyl-7-nitro-2-phenyl-lH-indole (0.5 g, 1.66 mmol) prepared in Step A was dissolved in dichloroethane (20 mL). Acetic acid (0.10 g, 1.66 mmol), 2- oxopiperazine (0.3 g, 3.32 mmol) and sodium triacetoxyborohydride (0.71g, 3.32 mmol) were added in drops thereto, and the mixture was stirred for 4 h at room temperature. After completion of the reaction, the reaction mixture was diluted with water, extracted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.55g, Yield 86%).
1H-NMR (400HMz, DMSO-d6); δ 9.89(s, IH), 8.46(s,lH), 7.93(s, IH), 7.81(d, J=9.2Hz, 2H), 7.53(m, 3H)
Preparation 44: 5-Chloro-3-(morpholin-4-yl)methyl-7-nitro-2-phenyl-lH-indole 5-Chloro-3-formyl-7-nitro-2-phenyl-lH-indole prepared in Step A of
Preparation 43 and morpholine were reacted according to the same procedure as Step B of Preparation 43 to give the title compound.
1H-NMR (400HMz, CDCl3); δ 9.86(br s, IH), 8.23(s,lH), 8.14(s, IH), 7.77(d,
J=12Hz, 2H), 7.47~7.56(m, 3H), 3.70(m, 4H + 2H), 2.49(m, 4H)
Preparation 45: 5-Methyl-7-nitro-lH-indazole Step A: 4,6-Dimethyl-2-nitro-phenylamine
2,4-Dimethylaniline (8.0 g, 66.0 mmol) was dissolved in acetic anhydride (50 mL), and nitric acid (5 mL) was slowly added in drops thereto at 0 °C . After stirring for 30 min, the mixture was diluted with ice water (200 mL). Cone, hydrochloric acid (10 mL) was added in drops thereto, and the resulting mixture was stirred under reflux for 4 h. After the reaction mixture was cooled to room temperature, the solvent was removed under reduced pressure. The residue was diluted with aqueous ammonium hydroxide solution. The resulting orange solid was filtered and dried to give the title compound (10.6 g, Yield 97%).
Step B: 5-Methyl-7-nitro-lH-indazole
4,6-Dimethyl-2-nitro-phenylamine (10.6 g, 64.08 mmol) prepared in Step A was dissolved in acetic acid (150 mL). Sodium nitrite (5.3 g, 76.90 mmol) was added in drops thereto, and the mixture was stirred for 12 h. After completion of the reaction, the reaction mixture was diluted with ammonium hydroxide, extracted with dichloromethane, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (1.0 g, Yield 9%). 1H-NMR (400HMz,CDCl3); δ 11.29(br s, IH), 8.18(d,J=8Hz, 2H), 7.93(s, IH),
2.58(s, 3H)
Preparation 46: 3-(4-Methoxy-phenyl-l-ylV7-nitro-lH-indazole Step A: 3-Iodo-7-nitro-lH-indazole 7-Nitroindazole (1.60 g, 9.80 mmol) was dissolved in DMF (100 mL), and potassium hydroxide (2.20 g, 39.20 mmol) and iodine (4.98 g, 19.61 mmol) were added in drops thereto. After stirring for 2 h, the reaction mixture was diluted with 10% aqueous sodium bisulfite solution. The resulting solid was collected and dried to give the title compound (2.50 g, Yield 88%). 1H-NMR (400HMz, CDCl3); δ 11.49(br s, IH), 8.45(d, J=8Hz, IH), 7.94(d, J=8Hz, IH), 7.41(t, IH)
Step B: 3-Iodo-7-nitro-l-(4-methoxybenzyl)-lH-indazole 3-Iodo-7-nitro-lH-indazole (2.50 g, 8.65 mmol) prepared in Step A was dissolved in acetone (50 niL). Potassium hydroxide (0.73 g, 12.97 mmol) and 4- methoxybenzylchloride (1.63 g, 10.38 mmol) were added in drops thereto at 0°C, and the mixture was stirred for 2 h. After completion of the reaction, the reaction mixture was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (3.2 g, Yield 91%).
1H-NMR (400HMz, CDCl3); δ 8.08(d, J=8Hz, IH), 7.83(d, J=8Hz, IH), 7.28(m, IH), 6.97(d, J=8Hz, IH), 6.75(d, J=8Hz, IH), 5.83(s, 2H), 3.72(s, 3H)
Step C: 3-(4-Methoxy-phenyl-l-vD-7-nitro-lH-indazole
3-Iodo-7-nitro-l-(4-methoxybenzyl)-lH-indazole (1.50 g, 3.67 mmol) prepared in Step B was dissolved in dimethoxyethane (20 mL). Sodium carbonate (1.17 g, 11.01 mmol), 4-methoxyphenylboronic acid (0.84 g, 5.50 mmol) and tetrakis(triphenylphosphine)palladium (0) (0.43 g, 0.37 mmol) were added in drops thereto, and the mixture was stirred under reflux for 2 h. After the reaction solution was cooled, it was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was dissolved in trifluoroacetic acid (20 mL). After the mixture was stirred under reflux for 5 h, the solvent was removed under reduced pressure. The residue was diluted with water, extracted with ethyl acetate, washed with saturated aqueous sodium chloride solution, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (0.85 g, Yield 86%).
1H-NMR (400HMz, CDCl3); δ 11.33(br s, IH), 8.39(t, 2H), 7.90(d, J=8Hz, 2H), 7.36(t, IH), 7.08(d, J=8Hz, 2H), 3.91(s, 3H)
Preparation 47: 4-[(3-Bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyl"|-piperazin-
2-one
Step A: l-BOC-5-methyl-7-nitro-2-phenyl-indole
5-Methyl-7-nitro-2-phenyl-lH-indole prepared in Preparation 24, (BOC)2O and DMAP were reacted according to the same procedure as Preparation 23 to give the title compound.
Step B: l-BOC-3-bromo-5-bromomethyl-7-nitro-2 -phenyl-indole l-BOC-5-methyl-7-nitro-2-phenyl-indole (3.5 g, 10 mmol) prepared in Step A was dissolved in carbon tetrachloride (30 mL). N-bromosuccinimide (NBS, 2.3g, 13 mmol) and benzoyl peroxide (100 mg) were added thereto, and the mixture was stirred under reflux for 4 h at 80°C . After filtration, the solid moiety was removed. Water was added, and the mixture was extracted with DCM. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (2.3 g, Yield 46 %). Step C: 4-r(l-BOC-3-bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyll-piperazin- 2-one l-BOC-3-bromo-5-bromomethyl-7-nitro-2-phenyl-indole prepared in Step B (1.0 g, 2 mmol) was dissolved in DCM (10 mL). Et3N (560 uL, 4 mmol) was added,
2-oxo-piperazine (300 mg, 3 mmol) was added, and the mixture was stirred for 12 h at room temperature. After completion of the reaction, saturated aqueous NH4Cl solution was added, and the reaction mixture was extracted with DCM. After drying, the solvent was removed under reduced pressure. The residue was purified by column chromatography to give the title compound (825 mg, Yield 78 %).
Step D: [(3-Bromo-7-mtro-2-phenyl-lH-indol-5-vDmethyl]-piperazin-2-one 4-[(l-BOC-3-bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyl]-piperazin-2-one
(825 mg, 1.6 mmol) prepared in Step C was dissolved in diethylester (5 mL). HCl (4 M dioxane solution, 5 mL) was added, and the mixture was stirred for 2 h at room temperature. After completion of the reaction, the solvent was removed under reduced pressure. The residue was dried, and used in the next reaction. Mass [M+H] = 429
Preparation 48: 4-r(3-Bromo-7-nitro-2-phenyl-lH-indol-5-yl)methyll- morpholine l-BOC-3-bromo-5-bromomethyl-7-nitro-2-phenyl-indole prepared in Step B of Preparation 47 and morpholine were reacted according to the same procedures as Steps C and D of Preparation 47 to give the title compound. Mass [M+H] = 416
Example 1 : Cvclopentyl-r5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine
Step A: 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole 5-Methyl-7-nitro-2-(pyridin-2-yl)-lH-indole (6.9 g, 27.3 mmol) prepared in
Preparation 8 was dissolved in a solvent mixture of tetrahydrofuran (130 mL), methanol (1 mL) and water (130 mL), and NH4Cl (14.6 g, 27.3 mmol) was added thereto. The reaction mixture was warmed to 60 °C, iron powder (15.2 g, 273 mmol) was added thereto, and the mixture was stirred for 30 min. After completion of the reaction, the reaction mixture was filtered through a cellite to remove the solid. Certain amount of the solvent was removed under reduced pressure from the resulting solution, which was then extracted with EtOAc. The extracted organic material was dried over MgSO4, and the solvent was removed under reduced pressure to give the title compound (5.0 g, Yield 40%).
Step B : Cyclopentyl- [5-methyl-2-(p yridin-2- ylV 1 H-indol-7- yl] -amine
7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole (5 g, 22.4 mmol) prepared in Step A and cyclopentanone (1.88 g, 22.4 mmol) were added to dichloroethane (50 mL). NaBH(OAc)3 (9.5 g, 44.8 mmol) was added thereto, and the mixture was stirred for 12 h at room temperature. After completion of the reaction, the reaction mixture was diluted with saturated aqueous NaHCO3 solution, and extracted with dichloromethane and EtOAc. The extracted organic material was washed with water and aqueous NaCl solution, and dried over MgSO4. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (eluent EtOAc/n-Hex = 1/5) to give the title compound (3.77 g, Yield 58%).
1H-NMR (400HMz, CDCl3); δ 9.73(br s, IH), 8.53(d, J=4.8Hz, IH), 7.78(d,
J=8.0Hz, IH), 7.70(m, IH), 7.13(m, IH), 6.91(d, J=2.0Hz, IH), 6.87(s, IH), 6.32(s, IH),
3.91(m, IH), 3.60(br s, IH), 2.41(s, 3H), 2.00(m, 2H), 1.65(m, 4H), 1.51(m, 2H)
Example 2: Cvclopentyl-[5-methyl-2-phenyl-lH-indol-7-yl]-amine 5-Methyl-7-nitro-2-phenyl-lH-indole prepared in Preparation 24 was reacted according to the same procedures as Steps A and B of Example 1 to give the title compound. 1H-NMR (500MHz, DMSO-d6); δ 10.91(brs, IH), 7.75(m, 2H), 7.65(m, IH),
7.41(m, 2H), 7.26(m, IH), 6.64(s, IH), 6.53(s, IH), 6.02(s, IH), 5.20(m, IH), 3.57(m,
2H), 3.51(m, 5H), 3.14(m, 2H), 2.29(m, 4H), 2.24(s, 3H), 1.87(m, 2H), 1.78(m, 2H),
1.68(m, 2H), 1.53(m, 2H)
Example 3: [5-Chloro-2-phenyl-lH-indol-7-yl]-amine
5-Chloro-7-nitro-2-phenyl-lH-indole prepared in Preparation 26 was reacted according to the same procedure as Step A of Example 1 to give the title compound.
1H-NMR (500MHz, DMSOd6); δ 10.96(brs, IH), 7.76(d, 2H), 7.46(t, 2H), 7.30(t, IH), 6.75(s, IH), 6.72(s, IH), 6.19(s, IH), 5.13(s, 2H)
Example 4: (Tetrahydropyran-4- ylV [5 -methyl-2-(p yridin-2-vD- 1 H-indol-7- yll - amine
7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and 4-oxo-tetrahydropyran were reacted according to the same procedure as Step B of Example 1 to give the title compound (25 mg, Yield 36%).
1H-NMR (400HMz, CDCl3); δ 10.65(br s, IH), 8.49(d, J=4.8Hz, IH), 7.81(d, J=8.0Hz, IH) 7.72(m, IH), 7.13(m, IH), 6.92(d, J=2.0Hz, IH), 6.88(s, IH), 6.27(s, IH), 3.92(m, IH), 3.49(m, 3H), 2.39(s, 3H), 1.95(m, 2H), 1.30(m, 2H)
Examples 5 to 19:
The compounds prepared in Preparations 8 to 15 and commercially available ketone or aldehyde were reacted according to the same procedure as Example 1 to synthesize the Example Compounds in the following table.
Figure imgf000060_0001
Figure imgf000060_0002
Figure imgf000061_0001
Figure imgf000062_0001
Figure imgf000063_0001
Example 20: (l-Cvclohexanon-4-ylVr5-methyl-2-(pyridin-2-ylVlH-indol-7-yll- amine
Step A: α,4-Dioxa-r4.51dec-8-yl)-r5-memyl-2-fρyridin-2-ylHH-indol-7- yl)amine
7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and 1 ,4-cyclohexanedione monoethylene acetal were reacted according to the same procedure as Step B of Example 1 to give the title compound.
Step B: d-Cvclohexanon-4-ylVr5-methyl-2-(pyridin-2-ylVlH-indol-7-yll-amine
(l,4-Dioxa-[4.5]dec-8-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl)amine (30 mg, 0.13 mmol) prepared in Step A was dissolved in acetone (10 mL) and water (5 niL).
IN hydrochloric acid solution (1 mL) was added thereto, and the mixture was stirred for
8 h at 80 °C . After completion of the reaction, saturated aqueous NaHCO3 solution was added. The reaction mixture was extracted with EtOAc, and dried over anhydrous
MgSO4. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (eluent EtOAc/n-Hex = 1/5) to give the title compound (10 mg, Yield 23%).
1H-NMR (400HMz, CDCl3); δ 10.72(br s, IH), 8.48(d, J=4.4Hz, IH), 7.81(d, J=8.0Hz, IH), 7.73(m, IH), 7.13(m, IH), 6.92(d, J=2.0Hz, IH), 6.91(s, IH), 6.32(s, IH), 3.78(m, IH) 2.41(s, 3H), 2.35(m, 4H), 2.20(m, 2H), 1.52(m, 2H)
Example 21 : 4-[(5-Chloro-2-phenyl-lH-mdol-7-vDamino]-cyclohexan-l-one 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 was reacted according to the same procedure as Example 20 to give the title compound. 1H-NMR (500MHz, DMSO-d6); δ 11.09(s, IH), 7.76(d, J=6.7 Hz, 2H), 7.45(t,
J=7.3 Hz, 2H), 7.30(t, J=7.3 Hz, IH), 6.79(d J=I.25 Hz, IH), 6.74(d, J=I.8 Hz, IH),
6.32(d, J=1.85 Hz, IH), 5.66(m, IH), 3.92(m, IH), 2.55(m, 2H), 2.38-2.21(m, 4H),
1.72(m, 2H)
Example 22: N-(5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl)-benzamide
7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole (45 mg, 0.20 mmol) prepared in Step A of Example 1 was dissolved in dichloromethane (10 mL). Et3N (0.56 mL, 0.4 mmol) and benzoyl chloride (0.03 mL, 0.22 mmol) were added thereto, and the mixture was stirred for 2 h at room temperature. After completion of the reaction, the reaction mixture was diluted with water, extracted with EtOAc, and dried over anhydrous MgSO4. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (eluent EtOAc/n-Hex = 1/5) to give the title compound (18 mg, Yield 27%).
1H-NMR (500HMz, CDCl3); δ 10.98(br s, IH), 8.61(s, IH), 8.50(d, J=4.9Hz, IH), 7.90(d, J=7.4Hz, 2H), 7.77(d, J=8.0Hz, IH), 7.69(m, IH), 7.50(m, IH)5 7.43(m, 2H), 7.31(s, IH), 7.26(s, IH), 7.14(m, IH), 6.95(d, J=I.8Hz, IH), 2.41(s, 3H)
Example 23 : l-Etfayl-3-r5-methyl-2-fpyridin-2-ylVlH-indol-7-yl1-urea 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and ethylisocyanate were reacted according to the same procedure as Example 22 to give the title compound.
1H-NMR (400MHz, MeOH-d4); δ 8.53(d, IH), 7.77(d, IH), 7.72(m, IH), 7.21(s, IH), 7.17(m, IH), 7.02(s, IH), 6.95(s, IH), 3.27(q, 2H), 2.41(s, 3H), 1.14(t, 3H)
Example 24: l-Phenyl-3-r5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-urea 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and phenylisocyanate were reacted according to the same procedure as Example 22 to give the title compound. 1H-NMR (400MHz, CDCl3 /MeOH-d4); δ 8.52(d, IH), 7.79(d, IH), 7.73(m,
IH), 7.45(d, 2H), 7.30(t, 2H), 7.21(s, IH), 7.18(m, IH), 7.13(s, IH), 7.04(m, IH), 6.96(s, IH), 2.42(s, 3H)
Example 25: Thiophene-2-sulfonic acid (2-pyridin-2-yl-lH-indol-7-ylVamide 2-Pyridin-2-yl-7-nitro-lH-indole prepared in Preparation 9 and 2- thiophenesulfonylchloride were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.
1H-NMR (400MHz, CDCl3); δ 10.25(br s, IH), 7.71(d, IH)5 7.66(m, IH), 7.60(br s, IH), 7.47(d, IH), 7.43~7.40(m, 2H), 7.13(m, IH), 6.97(d, IH), 6.94~6.86(m, 2H), 6.74(d, IH)
Example 26: Thiophene-2-sulfonic acid r5-methyl-2-(pyridin-2-yl)-lH-indol-7- yl] -amide 7-Amino-5-methyl-2-(pyridin-2-yl)-lH-indole prepared in Step A of Example 1 and 2-thiophenesulfonylchloride were reacted according to the same procedure as Example 22 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 9.13(br s, IH), 8.5 l(d, IH), 7.81(m, 2H), 7.68(m, 3H), 7.48(s, IH), 7.10(m, 2H), 6.88(d, IH), 6.69(s, IH), 2.36(s, 3H)
Example 27: Cyclopentyl-methyl-[5-methyl-2-(pyridin-2-ylVlH-indol-7-yl]- amine
Cyclopentyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine prepared in Example 1 and formaldehyde were reacted according to the same procedure as Step B of Example 1 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 9.53(br s, IH), 8.63(d, IH), 7.80(m, IH), 7.73(m, IH), 7.79(m, 2H), 6.96(s, IH), 6.81(s, IH), 3.73(m, IH), 2.84(s, 3H), 2.47(s, 3H), 1.91~1.21(m, 8H)
Example 28: 7-(CvclopentvDammo-2-phenyl-lH-indole-5-carboxylic acid ethyl ester
Step A: 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid ethyl ester 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid (14.1 g, 50 mmol) prepared in Preparation 30 was dissolved in ethanol (40 mL). Cone, sulfuric acid (10 mL) was added thereto, and the mixture was stirred for 2 h at 50 °C . After completion of the reaction, IN NaOH was added to the reaction mixture, which was then extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was recrystallized from EtOAc and hexane to give the title compound (14.1 g, Yield 95%).
Step B: 7-(Cvclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester 2-Phenyl-7-nitro-lH-indole-5-carboxylic acid ethyl ester prepared in Step A and cyclopentanone were reacted according to the same procedure as Example 1 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 9.47(brs, IH), 7.90(s, IH), 7.67(m, 2H), 7.34(m,
2H), 7.24(m, IH), 7.18(s, IH), 6.83(s, IH), 4.41(q, 2H), 3.87(m, IH), 1.95(m, 2H),
1.62(m, 2H), 1.49(m, 4H), 1.39(t, 3H)
Example 29: Cyclopentyl-[5-hvdroxymethyl-2-phenyl-lH-indol-7-yl1-amine
Step A: 5-Hvdroxymethyl-2-phenyl-7-nitro-lH-indole
2-Phenyl-7-nitro-lH-indole-5-carboxylic acid ethyl ester (10 g, 29 mmol) prepared in Step A of Example 28 was dissolved in methanol (100 mL), and LiBH4 (IM THF solution, 4 mL) was added thereto at 0"C . After warming to room temperature, the mixture was stirred for 3 h. A small amount of water was added to quench the reaction. Methanol was removed under reduced pressure. IN HCl was added to the residue, which was then extracted with EtOAc, dried, and used in the next reaction without further purification. Step B: Cyclopentyl-fS-hydroxymethyl^-phenyl-lH-indol^-yll-amine 5-Hydroxymethyl-2-phenyl-7-nitro-lH-indole prepared in Step A was reacted according to the same procedure as Example 1 to give the title compound.
1H-NMR (400MHz, MeOH-d4); δ 7.88(s, IH), 7.75(m, 2H), 7.42(m, 2H), 7.30(m, IH), 7.16(s, IH), 6.85(s, IH), 4.03(m, IH), 2.13(m, 2H), 1.77(m, 2H), 1.66(m,
4H)
Example 30: 7-(CvclopentvDamino-2-phenyl-lH-indole-5-carboxylic acid 7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester (5 g, 14.3 mmol) prepared in Example 28 was added to a solvent mixture of MeOH (20 niL) and water (20 mL). NaOH (1.3 g, 33.8 mmol) was added thereto, and the mixture was stirred for 4 h at room temperature. After completion of the reaction, MeOH was removed under reduced pressure, and IN HCl was added to the residue. The resulting mixture was extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was recrystallized from EtOAc and n-Hex to give the title compound.
1H-NMR (400MHz, MeOH-d4); δ 7.88(s, IH), 7.75(m, 2H), 7.42(m, 2H), 7.30(m, IH), 7.16(s, IH), 6.85(s, IH), 4.03(m, IH), 2.13(m, 2H), 1.77(m, 2H), 1.66(m, 4H)
Example 31: 2-[~7-(CyclopentvDamino-2-phenyl-lH-indol-5-yl"|-acetic acid ethyl ester
2-(2-Phenyl-7-nitro-lH-indol-5-yl)acetic acid prepared in Preparation 29 was reacted according to the same procedure as Example 28 to give the title compound. 1H-NMR (400MHz, CDCl3); δ 8.12(brs, IH), 7.67(m, 2H), 7.42(m, 2H), 7.30(m, IH), 6.99(s, IH), 6.74(s, IH), 6.46(s, IH), 4.16(q, 2H), 3.93(m, IH), 3.66(s, 2H), 2.10(m, 2H), 1.77(m, 2H), 1.66(m, 2H), 1.59(t, 3H), 1.26(t, 3H)
Example 32: 2-[7-(CvclopentylaminoV2-phenyl-lH-indol-5-yl]ethanol
2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]acetic acid ethyl ester prepared in Example 31 and cyclopentanone were reacted according to the same procedure as Example 29 to give the title compound (257 mg, Yield 80%).
1H-NMR (400MHz, CDCl3+Me0H-d4); δ 7.71(m, 2H), 7.40(m, 2H), 7.28(m, IH), 6.89(s, IH), 6.72(s, IH), 6.32(s, IH), 3.97(m, IH), 3.87(m, 2H), 3.43(m, IH), 2.91(m, 2H), 2.09(m, 2H), 1.77(m, 2H), 1.62(m, 4H)
Example 33: 2-[7-(Cvclopentyl)amino-2-phenyl-lH-indol-5-yllacetic acid 2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]acetic acid ethyl ester prepared in Example 31 was reacted according to the same procedure as Example 30 to give the title compound.
1H-NMR (400MHz, CDCl3+Me0H-d4); δ 11.31(s, IH), 7.81(m, 2H), 7.37(m,
2H), 7.25(m, IH), 7.05(s, IH), 6.65(s, IH), 3.89(m, IH), 1.88(m, 7H), 1.41(m, 3H)
Example 34: 2-[2-Phenyl-7-(tetrahvdropyran-4-yl)amino-lH-indol-5-yl"|-acetic acid
2-(2-Phenyl-7-amino-lH-indol-5-yl)-acetic acid ethyl ester prepared as an intermediate in the process of Example 31 and 4-oxo-tetrahydropyran were reacted according to the same procedures as Step B of Example 1 and Example 30 to give the title compound.
1H-NMR (400MHz, DMSOd6, Na salt); δ 10.88(br s, IH), 7.81(d, J=8Hz, 2H), 7.43(m, 2H), 7.28(m, IH), 6.67)s, IH), 6.62(s, IH), 6.29(s, IH), 5.23(m, IH), 3.92(d, J=8Hz, 2H), 3.67(m, IH), 3.47(m, 2H), 3.14(s, 2H), 2.06(m, 2H), 1.48(m, 2H)
Example 35 : 2- \ 2-Phenyl-7-( 1 , 1 -dioxo-tetrahydro-thiopyran-4- vDamino- 1 H- indol-5-yll-acetic acid
2-(2-Phenyl-7-amino-lH-indol-5-yl)acetic acid ethyl ester prepared as an intermediate in the process of Example 31 and l,l-dioxo-tetrahydro-thiopyran-4-one were reacted according to the same procedures as Step B of Example 1 and Example 30 to give the title compound.
1H-NMR (400MHz, DMSOd6, Na salt); δ 10.90(s, IH), 7.80(d, J=8Hz, 2H), 7.43(t, 2H), 7.29(m, IH), 6.69(q, 2H), 6.28(s, IH), 5.35(m, IH), 3.81(m, IH), 3.31(m, 2H), 3.20(m, 2H), 3.16(s, 2H), 2.33(m, 2H), 2.02(m, 2H)
Example 36: (Tetrahydropyran-4-ylV[2-phenyl-5-(l J-dioxo-thiomoφholm^- yDmethyl- 1 H-indol-7- yl] amine
Step A: 5-Iodomethyl-2-phenyl-7-nitro-lH-indole
5-Hydroxymethyl-2-phenyl-7-nitro-lH-indole (804 mg, 3 mmol) prepared in Step A of Example 29 was dissolved in THF (10 mL), and imidazole (408 mg, 6 mmol) and triphenylphosphine (1.52 g, 6 mmol) were added thereto. Iodine (453 mg, 3.9 mmol) was added to the mixture, which was then stirred for 2 h. After completion of the reaction, the reaction mixture was filtered through a cellite, and the product was used in the next reaction without further purification. Step B : 5 -( 1,1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-7-nitro- 1 H-indole 5-Iodomethyl-2-phenyl-7-nitro-lH-indole (850 mg, 2.5 mmol) prepared in Step
A was dissolved in THF (10 mL). 1,1-Dioxo-thiomorpholine (405 mg, 2.25 mmol) was added thereto, and the mixture was stirred for 2 h. After completion of the reaction, the reaction mixture was diluted with water, extracted with EtOAc, dried over anhydrous magnesium sulfate, and filtered. The residue was recrystallized from DCM and hexane to give the title compound (625 mg, Yield 65%).
Step C : (Tetrahydrop yran-4- vD- F2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4- ypmethyl- 1 H-indol-7- yl] amine
5-(l,l-Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-7-nitro-lH-indole prepared in Step B and tetrahydropyran-4-one were reacted according to the same procedure as
Example 1 to give the title compound. 1H-NMR (500MHz, CDCl3); δ 8.38(br s, IH), 7.69(d, J=7.3 Hz, IH), 7.44(t,
J=7.3 Hz, 2H), 7.32(t, J=7.3 Hz, IH), 7.00(s, IH), 6.75(d, J=I.85 Hz, IH), 6.47(d,
J=I.85 Hz, IH), 4.07(m, 2H), 3.65(m, 3H), 3.57(m, 2H), 3.02(m, 8H), 2.12(m, 2H),
1.61(m, 2H)
Example 37: (Tetrahvdropyran-4-ylVr2-phenyl-5-(2-oxo-piperazin-4-yl)methyl-
1 H-indol-7- yl] amine
5 -Hydroxymethyl-2-phenyl-7-nitro-l H-indole prepared in Step A of Example 29, 2-oxopiperazine and 4-oxo-tetrahydropyran were sequentially reacted according to the same procedure as Example 36 to give the title compound. 1H-NMR (500MHz, CDCl3); δ 8.96(br s, IH), 7.67(d, J=7.3 Hz5 IH), 7.41 (t, J=7.3 Hz, 2H), 7.29(t, J=7.3 Hz, IH), 6.98(s, IH), 6.73(d, J=1.85 Hz, IH), 6.44(d, J=I.85 Hz, IH), 6.07(brs, IH), 4.00(m, 2H), 3.61(m, 3H), 3.53(m, 2H), 3.33(m, 2H), 3.21(m, 2H), 2.66(m, 2H), 1.51(m, 2H)
Example 38: Cvclopentyl-[2-("3-fluoro)phenyl-5-(2-oxo-piperazin-4-vDmethyl- 1 H-indol-7-yll amine
2-(3-Fluorophenyl)-7-nitro-lH-indole-5-carboxylic acid prepared in Preparation 39 was reacted according to the same procedures as Step A of Example 28, Examples 32 and 36 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 8.46(s, IH), 7.50(d, IH), 7.42(m, 2H), 7.06(t, IH), 7.02(s, IH), 6.80(d, IH), 6.54(s, IH), 4.03(m, IH), 3.72(s, 2H), 3.07(m, 8H), 2.16(m, 2H), 1.85(m, 2H), 1.74(m, 2H), 1.67(m, 2H)
Example 39: (Tetrahvdropyran-4-ylH2-(4-methoxy)phenyl-5-(l,l-dioxo- thiomorpholm-4-vDmethyl- 1 H-indol-7- yll amine
2-(4-Methoxy-phenyl)-7-nitro-lH-indole-5-carboxylic acid prepared in
Preparation 40 was reacted according to the same procedures as Step A of Example 28,
Examples 32 and 36 to give the title compound. 1H-NMR (500MHz, DMSO-d6); δ 10.79(s, IH), 7.67(d, 2H), 7.01(d, 2H), 6.68(s,
IH), 6.57(s, IH), 6.24(d, IH), 5.26(d, IH), 3.90(m, 2H), 3.77(s, 3H), 3.61(m, IH),
3.58(s, 2H), 3.46(t, 2H), 3.04(m, 4H), 2.83(m, 4H), 2.01(d, 2H), 1.43(m, 2H)
Examples 40 to 78: The compounds prepared in Preparations 24 to 40, 43, 44 and 47 and commercially available ketone or aldehyde were reacted according to a method selected from Examples 26 to 37 to synthesize the Example Compounds in the following table.
Figure imgf000073_0001
Figure imgf000073_0002
Figure imgf000074_0001
Figure imgf000075_0001
Figure imgf000076_0001
Figure imgf000077_0001
Figure imgf000078_0001
Figure imgf000079_0001
Figure imgf000080_0001
Example 79 : (Tetrahvdropyran-4-vD-(5-chloro-3-phenyl-lH-indol-7-yl)-aniine S-Chloro-V-nitro-S-phenyl-lH-indole prepared in Preparation 41 and tetrahydropyran-4-one were reacted according to the same procedure as Example 1 to give the title compound. 1H-NMR (400MHz, CDCl3); δ 8.10(br s, IH), 7.61(d, J=8Hz, 2H), 7.43(t, 2H),
7.38(s, IH), 7.3 l(m, 2H), 6.56(s, IH), 4.05(m, 2H), 3.65(m, IH), 3.62(t, 2H), 2.15(d,
J=12Hz, 2H), 1.62(m, 5H)
Example 80 : Cyclopentyl-(5-chloro-3-phenyl-lH-indol-7-yl)-amine 5-Chloro-7-nitro-3-phenyl-lH-indole prepared in Preparation 41 and cyclopentanone were reacted according to the same procedure as Example 1 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 8.06(br s, IH), 7.58(d, J=8Hz, 2H), 7.39(t, 2H), 7.33(s, IH), 7.26(m, IH), 7.17(s, IH), 6.51(s, IH), 3.91(m, IH), 2.08(m, 2H), 1.74(m, 2H), 1.66(m, 2H), .54(m, 2H)
Example 81 : (Tetrahydropyran-4-yl')methyl-('5-chloro-3-phenyl-lH-indol-7-yl)- amine
5-Chloro-7-nitro-3-phenyl-lH-indole prepared in Preparation 41 and tetrahydropyran-4-carboxyaldehyde were reacted according to the same procedure as Example 1 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 8.08(br s, IH), 7.61(d, J=8Hz, 2H), 7.44(t, 2H), 7.37(s, IH), 7.29(m, 2H), 6.52(s, IH), 4.04(dd, 2H), 3.44(t, 2H), 3.19(d, J=4Hz, 2H), 1.97(m, IH), 1.79(d, J- 12Hz, 2H), 1.41(m, 2H) Example 82: Cvclopentyl-[2-(4-aminophenylV5-chloro-lH-indol-7-yll-amine Cyclopentyl-[2-(4-BOC-aminophenyl)-5-chloro-lH-indol-7-yl]-amine (430 mg, 1 mmol) prepared in Example 78 was added to DCM (5 mL). TFA (5 niL) was added thereto, and the mixture was stirred for 2 h. After completion of the reaction, TFA was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound (310 mg, Yield 95 %).
1H-NMR (400MHz, DMSO-d6); δ 10.76(br s, IH), 7.47(d, IH), 6.70(d, IH), 6.63(d, IH), 6.43(d, IH), 6.11(d, IH), 5.61(d, IH), 5.30(br s, 2H), 3.68(m, IH), 2.03(m, 2H), 1.74-1.52(m, 6H)
Example 83j Cvclopentyl-(5-chloro-2-r4-(l-methyl-piperidin-4- vDaminophenyll-lH-indol-7-vU-amine
Cyclopentyl- [2-(4-aminophenyl)-5-chloro- 1 H-indol-7-yl] -amine prepared in Example 82 and l-methyl-piperidin-4-one were reacted according to the same procedure as Step B of Example 1 to give the title compound.
1H-NMR (400MHz, MeOH-d4/CDCl3); δ 7.5 l(d, 2H), 6.89(d, IH), 6.62(d, 2H), 6.49(s, IH), 6.33(d, IH), 3.91(m, IH), 3.37(m, IH), 3.04(m, 2H), 2.49~2.39(m, 4H), 2.08(m, 2H), 1.78~1.64(m, 6H)
Example 84: N-[4-(5-chloro-7-cvclopentylamino-lH-indol-2-yl')-phenyll- methanesulfonamide
Cyclopentyl- [2-(4-aminophenyl)-5-chloro-l H-indol-7-yl] -amine prepared in Example 82 and methanesulfonylchloride were reacted according to the same procedure as Example 22 to give the title compound.
1H-NMR (500MHz, MeOH-d4/CDCl3); δ 7.63(d, 2H), 7.26(d, 2H), 6.93(s, IH), 6.59(s, IH), 6.36(s, IH), 3.86(m, IH), 2.96(s, 3H), 2.06(m, 2H), 1.74~1.58(m, 6H)
Example 85 : C yclopentyl- { 5 -( 1 , 1 -dioxo-thiomorpholin-4- vDmethyl-2- [4- (acetyl)aminophenyl"|-lH-indol-7-yl} -amine
2-(4-BOC-amino-phenyl)-7-nitro-lH-indole-5-carboxylic acid prepared in Preparation 40 was reacted according to the same procedures as Example 28, Step A of Example 29 and Example 36 sequentially to give the title compound.
1H-NMR (400MHz, MeOH-d4/CDCl3); δ 9.08 (s, IH), 7.48 (d, J= 8Hz,2H), 7.39 (dd, Jl = 8Hz, J2 = 4Hz, 2H), 6.89 (s, IH), 6.60 (d, J=4 Hz, IH), 3.96 (m, IH), 3.67 (s, 2H), 3.00 (m, 8H), 2.18(s, 3H), 2.06 (m, 2H), 1.26 ~ 1.77(m, 6H)
Examples 86 to 89: 7-Amino-5-(l,l-dioxo-thiomorpholin-4-yl)methyl-2-[4-(acetyl)aminophenyl]- lH-indole prepared as an intermediate in the process of Example 85 and commercially available ketone or aldehyde were reacted according to the same procedure as Step B of Example 1 to synthesize the Example Compounds in the following table.
Figure imgf000083_0001
Figure imgf000083_0002
Figure imgf000084_0001
Example 90: (5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine Step A: l-BOC-(5-methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine 7-Amino-5-methyl-2-phenyl-lH-indole prepared in Example 2 and 1-BOC- piperidinone were reacted according to the same procedure as Preparation 23 to give the title compound.
Step B: (5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine l-BOC-(5-methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine prepared in Step A was reacted according to the same procedure as Example 82 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.33(brs, IH), 8.68(m, 2H), 7.83(m, 2H), 7.41(m, 2H), 7.26(m, IH), 6.72(m, 2H), 6.29(s, IH), 3.74(m, IH), 3.47(m, 2H), 3.01(m, 2H), 2.28(s, 3H), 2.13(m, 2H), 1.77(m, 2H)
Example 91 : [l-(Methanesulfonyl)piperidin-4-yll-(5-methyl-2-phenyl-lH-indol- 7-yl)-amine
(5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine prepared in Example 90 and methanesulfonylchloride were reacted according to the same procedure as Example 22 to give the title compound.
1H-NMR (500MHz, DMSOd6); δ 10.79(brs, IH), 7.74(m, 2H), 7.42(m, 2H), 7.26(m, IH), 6.66(s, IH), 6.57(s, IH), 6.1 l(s, IH), 5.27(m, IH), 3.57(m, 2H), 3.13(m, IH), 2.93(m, IH), 2.87(s, 3H), 2.25(s, 3H), 2.14(m, 2H), 1.46(m, 2H)
Example 92: 2-Hvdroxy-l-[4-(5-methyl-2-phenyl-lH-indol-7-yl)amino- piperidin- 1 - yl] -ethanone
(5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine (305 mg, 1 mmol) prepared in Example 90 was dissolved in DMF (5 mL). Hydroxyacetic acid (76 mg, 1 mmol), EDC (232 mg, 1.3 mmol), HOBT (229 mg, 1.5 mmol) and Et3N (280 uL, 2 mmol) were added thereto, and the mixture was stirred for 4 h at room temperature.
After completion of the reaction, saturated aqueous NaHCO3 solution was added to the reaction mixture, which was then extracted with EtOAc, washed with saturated aqueous
NaCl solution and IN HCl, dried over anhydrous magnesium sulfate, and filtered. The solvent was removed under reduced pressure, and the residue was purified by column chromatography to give the title compound.
1H-NMR (500MHz, MEOH-d4); δ 7.72(m, 2H), 7.38(m, 2H), 7.23(m, IH),
6.71(2, IH), 6.63(s, IH), 6.30(s, IH), 4.40(m, IH), 4.23(m, 2H), 3.74(m, 2H), 3.24(m,
IH), 3.02(m, IH), 2.33(s, 3H), 2.19(m, 2H), 1.45(m, 2H)
Example 93 : (5-Chloro-2-phenyl-lH-indol-7-ylVpiperidin-4-yl-amine 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and l-BOC-4- piperidinone were reacted according to the same procedure as Step B of Example 1 to give the title compound. 1H-NMR (500MHz, DMSO-d6); δ 11.57(s, IH), 8.66(brs, 2H), 7.87(d, J=6.7 Hz,
2H), 7.42(t, J=7.3 Hz, 2H), 7.28(t, J=7.3 Hz, IH), 6.75(m, 2H), 6.26(m, IH), 3.76(m,
IH), 3.36(m, 2H), 3.05(m, 2H), 2.12(m, 2H), 1.70(m, 2H)
Example 94 : 4-(5 -Chloro-2-phenyl- 1 H-indol-7-yr)amino-piperidin- 1 - yl- carboxylic acid phenylamide
(5-Chloro-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine prepared in Example 93 and phenylisocyanate were reacted according to the same procedure as Example 22 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.05(s, IH), 8.53(s, IH), 7.76(d, J=7.3 Hz, 2H), 7.44(m, 4H), 7.30(t, J=7.3 Hz, IH), 7.20(t, J=7.3 Hz, 2H), 6.91(t, J=7.3 Hz, IH), 6.77(d, J=I.85 Hz, IH), 6.73(d, J=I.85 Hz, IH), 6.29(d, J=I.85 Hz, IH), 5.62(m, IH), 4.08(m, 2H), 3.65(m, IH), 3.04(m, 2H), 2.05(m, 2H), 1.36(m, 2H)
Example 95: l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yll-2- dimethylamino-ethanone
Step A: l-r4-(5-Chloro-2-phenyl-lH-indol-7-yDamino-piperidin-l-yl1-2-BOC- amino-ethanone
(5 -Chloro-2 -phenyl- lH-indol-7-yl)-piperidin-4-yl-amine prepared in Example 93 and N-BOC-GIy-OH were reacted according to the same procedure as Example 92 to give the title compound.
Step B : 1 - [4-(5-Chloro-2-phenyl- 1 H-indol-7-yl)amino-piperidin- 1 -yl] -2-amino- ethanone l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]-2-BOC-amino- ethanone prepared in Step A was reacted according to the same procedure as Example 82 to give the title compound.
Step C: l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yll-2- dimethylamino-ethanone l-[4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]-2-amino-ethanone prepared in Step B and formaldehyde were reacted according to the same procedure as Step B of Example 1 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.97(s, IH), 9.54(brs, IH), 7.95(d, J=6.7 Hz, 2H), 7.40(t, J=7.3 Hz, 2H), 7.26(t, J=7.3 Hz, IH), 6.74(m, 2H), 6.25(m, IH), 4.41- 4.22(m, 3H), 3.69(m, 2H), 3.22(m, IH), 3.02(m, IH), 2.79(m, 6H), 2.03(m, 2H), 1.51(m, 2H)
Example 96: [5-(L 1 -Dioxo-miomorpholin-4- vDmethyl-2 -phenyl- lH-indol-7- yl] -(piperidin-4- yPmethyl-amine
5-( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-7-nitro- 1 H-indole prepared in Step B of Example 36 and l-BOC-piperidine-4-carboxyaldehyde were reacted according to the same procedures as Examples 1 and 90 sequentially to give the title compound.
1H-NMR (400MHz, DMSO-d6;2TFA salt); δ 11.10(s, IH), 8.57(m, IH), 8.28(m, IH), 7.82(d, 2H), 7.50(t, 2H), 7.34(t, IH), 6.90(s, IH), 6.84(s, IH), 6.35(s, IH), 3.52(m, 2H), 3.39(m, 8H), 3.18(m, 4H), 2.90(m, 2H), 2.02(m, 3H), 1.42(m, 2H)
Example 97 : (5-( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl- 1 H-indol-7- yl)-( 1 -methanesulfonyl-piperidin-4-yl)-amine
(5-(l,l-Dioxo-thiomoφholin-4-yl)methyl-2-phenyl-lH-indol-7-yl)-(piperidin-4- yl)methyl-amine prepared in Example 96 and methanesulfonylchloride were reacted according to the same procedure as Example 22 to give the title compound. 1H-NMR (500MHz, DMSOd6); δ 10.92(s, IH), 7.76(d, 2H), 7.43(t, 2H), 7.27(t,
IH), 6.72(m, 2H), 6.26(s, IH), 5.35(d, IH), 3.57(m, 5H), 3.05(m, 4H), 2.95(t, 2H),
2.88(s, 3H), 2.84(m, 4H), 2.14(d, 2H), 1.47(m, 2H)
Example 98 : (4-[5-(I Λ -Dioxo-thiomorpholin-4-yl)methyl-2-phenvl- 1 H-indol-7- yl1ammo-piperidin-l-yl|-(tetrahvdrofuran-2-vD-methanone
(5-(l,l-Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-lH-indol-7-yl)-(piperidin-4- yl)methyl-amine prepared in Example 96 and tetrahydrofuran-2-carboxylic acid were reacted according to the same procedure as Example 92 to give the title compound. 1H-NMR (500MHz, DMSOd6); δ 10.87(s, IH), 7.75(d, 2H), 7.43(t, 2H), 7.27(t,
IH), 6.72(s, 2H), 6.29(s, IH), 5.30(d, IH), 4.27(d, IH), 3.95(d, IH), 3.86(m, IH), 3.68(m, 4H), 3.59(s, 2H), 3.37(m, IH), 3.27(m, IH), 3.06(m, 4H), 2.92(m, IH), 2.84(m, 4H), 2.02(m, 4H), 1.29(m, 2H)
Example 99j (5-Fluoro-2-phenyl- lH-indol-7-yl)-r 1 -(1.1 -dioxo- tetrahydrothiopyran-4-yl')-piperidin-4-yl1-amine
Step A: (5-Fluoro-2-phenyl-lH-indol-7-vD-piperidin-4-yl-amine 5-Fluoro-7-nitro-2-phenyl-lH-indole prepared in Preparation 25 and 1-BOC- piperidinone were reacted according to the same procedure as Example 90 to give the title compound.
Step B : (5-Fluoro-2-phenyl- 1 H-indol-7-yD-[ 1 -(U -dioxo-tetrahvdrothiopyran-4- yls)-piperidin-4- yl] -amine
(5-Fluoro-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine prepared in Step A and 1,1-dioxo-tetrahydro-thiopyranone were reacted according to the same procedure as Step B of Example 1 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 7.66(d, 2H), 7.44(t, 2H), 7.33(t, IH), 6.74(d, IH), 6.72(d, IH), 6.26(d, IH), 3.39(m, IH), 3.22(m, 2H), 2.92(m, 4H), 2.57(t, IH), 2.33(m, 4H), 2.28(m, 4H), 1.53(m, 2H) Example 100: N-(5-chloro-2-phenyl-lH-indol-7-ylVN\N'-dimethyl- cyclohexane- 1 ,4-diamine
7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and A- dimethylaminohexanone were reacted according to the same procedure as Step B of Example 1 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.05(s, IH), 7.75(d, 1=6.1 Hz, 2H), 7.44(t, J=7.3 Hz, 2H), 7.29(t, J=7.3 Hz, IH), 6.73(m, 2H), 6.17(m, IH), 5.52(m, IH), 4.55(m, IH), 3.46(m, IH), 3.29(m, 6H), 2.05(m, 2H), 1.86(m, 2H), 1.33(m, 2H), 1.23(m, 2H)
Example 101 : N-(5-chloro-2-phenyl-lH-indol-7-yl)-N'-methyl-cvclohexane- 1 ,4-diamine
During the process of Example 100, the monoalkylated title compound was obtained. 1H-NMR (500MHz, DMSO-d6); δ 11.05(s, IH), 7.75(d, J=6.7 Hz, 2H), 7.44(t,
J=7.3 Hz, 2H), 7.30(t, J=7.3 Hz, IH), 6.73(m, 2H), 6.17(m, IH), 5.51(m, IH), 4.55(m, IH), 3.45(m, IH), 3.28(m, 3H), 3.13(m, IH), 2.05(m, 2H), 1.86(m, 2H), 1.33(m, 2H), 1.23(m, 2H)
Example 102: 4-(5-Chloro-2-phenyl-lH-indol-7-vDamino-cyclohexane-l- carboxylic acid
7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and 4-oxo- cyclohexane-1-carboxylic acid methyl ester were reacted according to the same procedures as Step B of Example 1 and Example 30 sequentially to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.08(m, IH), 7.76(d, J=6.7 Hz, 2H), 7.44(t, J=7.3 Hz, 2H), 7.30(t, J=7.3 Hz, IH), 6.74(d J=I.25 Hz, IH), 6.72(d, J=I.8 Hz, IH), 6.18(m, IH), 5.55(m, IH), 3.50(m, IH), 3.34(m, IH), 2.1 l(m, IH), 1.95(m, 2H), 1.81(m, IH), 1.65(m, IH), 1.53(m, 2H), 1.23(m, IH)
Example 103 : 4-(5-Methyl-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 - carboxylic acid
5-Methyl-7-nitro-2-phenyl-lH-indole prepared in Preparation 24 and 4-oxo- cyclohexyl-1 -carboxylic acid were reacted according to the same procedures as Examples 1 and 30 sequentially to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 10.81(brs, IH), 7.74(m, 2H), 7.42(m, 2H), 7.25(m, IH), 6.64(d, J=2.45Hz, IH), 6.53(s, IH), 6.05(s, IH), 5.17(m, IH), 3.50(m, 2H), 2.24(s, 3H), 1.95(m, IH), 1.81(m, 2H), 1.64(m, 2H), 1.57(m, 2H)
Example 104 : 4-(5 -Chloro-2-phenyl- 1 H-indol-7- vDamino-cyclohexane- 1 - carboxylic acid amide
4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-cyclohexane-l-carboxylic acid prepared in Example 102 and NH4Cl were reacted according to the same procedure as Example 92 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.20(s, IH), 7.76(d, J=6.7 Hz, 2H), 7.44(t, J=7.3 Hz, 2H), 7.29(t, J=7.3 Hz, IH), 7.21(brs, IH), 6.73(m, 3H), 6.14(m, IH), 5.55(m, IH), 3.54(m, IH), 2.26(m, IH), 1.87(m, 2H), 1.72(m, 4H), 1.59(m, 2H) Example 105: 4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino- cyclohexanecarboxylic acid methylamide
4-(5-Chloro-2 -phenyl- lH-indol-7-yl)amino-cyclohexane-l-carboxylic acid prepared in Example 102 and methylamine (HCl salt) were reacted according to the same procedure as Example 92 to give the title compound.
1H-NMR (500MHz, DMSO-d6); δ 11.26(s, IH), 7.77(d, J=6.7 Hz, 2H), 7.66(m, IH), 7.44(t, J=7.3 Hz, 2H), 7.30(t, J=7.3 Hz, IH), 6.76(d J=I.25 Hz, IH), 6.72(d, J=I.8 Hz, IH), 6.15(m, IH), 3.57(m, IH), 2.55(m, 3H), 2.24(m, IH), 1.88(m, 2H), 1.80- 1.65(m, 4H), 1.57(m, 2H)
Example 106: 2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester
7-Nitro-5-fluoro-2-phenyl-lH-indole prepared in Preparation 27 and methyl bromoacetate were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.
1H-NMR (400MHz, CDCl3); δ 7.56(d, 2H), 7.41(t, 2H), 7.34(t, IH), 6.80(d, IH), 6.71(s, IH), 6.19(d, IH), 4.09(s, 2H), 3.85(s, 3H)
Example 107: 2-(5-Fluoro-2-phenyl-lH-mdol-7-yl)amino-acetic acid 2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester prepared in
Example 106 was reacted according to the same procedure as Example 30 to give the title compound.
1H-NMR (400MHz, DMSO-d6); δ 7.9 l(d, 2H), 7.41 (t, 2H), 7.26(t, IH), 6.73(s, IH), 6.41(d, IH), 5.78(d, IH), 6.17(br s, IH), 3.48(s, 2H) Example 108: 2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester
7-Nitro-5~phenoxy-2-phenyl-lH-indole prepared in Preparation 27 and methyl bromoacetate were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.
1H-NMR (400MHz, DMSO-d6); δ 8.46(brs, IH), 7.66(d, 2H), 7.44(t, 2H), 7.35~7.28(m, 3H), 7.09~6.99(m, 3H), 6.80 (d, J=2.0Hz, IH), 6.73(d, J=2.0 Hz, IH), 6.24(d, J=2.0Hz, IH), 5.38(m, IH), 4.47(brs, IH), 4.04(s, 2H), 3.82(s, 3H).
Example 109 : 2-r(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino"l-acetic acid
(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester prepared in Example 108 was reacted according to the same procedure as Example 30 to give the title compound. 1H-NMR (500MHz, MeOH-d4); δ 7.76(d, J=7.3 Hz, 2H), 7.39(t, J=7.3 Hz, 2H),
7.25(m, 3H), 6.96(t, J=7.3 Hz, IH), 6.90(d, J=7.3 Hz, 2H), 6.68(m, IH), 6.53(d, J=I.85 Hz, IH), 6.00(d, J=I.85 Hz, IH), 3.96(s, 2H)
Example 110: 2-[(5-Phenoxy-2-phenyl-lH-indol-7-vDamino]-propionic acid methyl ester
2-Phenyl-5-phenoxy-7-nitro-lH-indole prepared in Preparation 27 and methyl 2- bromopropionic acid ester were reacted according to the same procedures as Step A of Example 1 and Example 22 sequentially to give the title compound.
1H-NMR (500MHz, MeOH-d4); δ 8.56(brs, IH), 7.66(d, 2H), 7.43(t, 2H), 7.32~7.26(m, 3H), 7.09~6.61(m, 3H), 6.77(d, J=I.8Hz, IH), 6.71(d, J=I.8Hz, IH), 6.23(d, J=I.8Hz, IH), 5.33(m, IH), 4.23(q, IH), 3.73(s, 3H) 1.53(d, 3H).
Example 111: 2-(5-Phenoxy-2-phenyl-lH-indol-7-vDamino-propionic acid 2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-propionic acid methyl ester prepared in Example 110 was reacted according to the same procedure as Example 30 to give the title compound.
1H-NMR (500MHz, MeOH-d4); δ 7.76(d, J=7.3 Hz, 2H), 7.40(t, J=7.3 Hz, 2H), 7.24(m, 3H), 6.94(t, J=7.3 Hz, IH), 6.89(d, J=7.3 Hz, 2H), 6.68(m, IH), 6.52(d, J=I.85 Hz, IH), 4.57(m, IH), 1.55(m, 3H)
Example 112: 2-(5-Chloro-2-phenyl-lH-mdol-7-vDamino-propionic acid 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and methyl 2- bromopropionic acid ester were reacted according to the same procedures as Examples 22 and 30 sequentially to give the title compound.
1H-NMR (400MHz, CDCl3); δ 8.62(br s, IH), 7.55(d, J=8Hz, 2H), 7.38(t, 2H),
7.30(t, IH), 7.00(s, IH), 6.60(s, IH), 6.3 l(s, IH), 4.47(br s, IH), 4.27(m, IH), 1.58(d, J-
8Hz, 3H)
Example 113: (5-Chloro-2-phenyl-lH-indol-7-yl)-pyridin-2-yl-amine
7-Amino-5-chloro-2-phenyl-lH-indole (200 mg, 0.82 mmol) prepared in Example 3 was dissolved in toluene (30 mL). 2-Bromopyridine (182 mg, 1.15 mmol), Pd2(dba)3, Xantphos (42 mg, 0.07 mmol) and Na2CO3 were added thereto. The mixture was degassed, and stirred for 12 h at 100 °C . After completion of the reaction, the reaction mixture was filtered through a cellite. The solvent was removed under reduced pressure, and the residue was purified by column chromatography (eluent: EtOAc/n-Hex = 1/3) to give the title compound (25 mg, Yield 13 %).
1H-NMR (400MHz, CDCl3); δ 8.06(m, IH), 7.68(d, J=7.2Hz, 2H), 7.50(t, IH), 7.37(m, 3H), 7.29(d, J=8Hz, IH), 6.90(d, J=2Hz, IH), 6.74(m, 3H)
Example 114: (5-Chloro-2-phenyl-lH-indol-7-yl)-5-methyl-pyridin-2-yl-amme 7-Amino-5-chloro-2-phenyl-lH-indole prepared in Example 3 and 2-bromo-5- methyl-pyridine were reacted according to the same procedure as Example 113 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 10.64(s, IH), 7.75(d, J=8Hz, 2H), 7.47(m, 4H),
7.36(m, IH), 6.91(s, IH), 6.80(s, IH), 6.67(d, J=8Hz, IH), 6.59(d, J=8Hz, IH), 2.47(s,
3H)
Example 115: (5-Chloro-3-phenyl-lH-mdol-7-vD-(5-methyl-pyridin-2-ylV amine
5-Chloro-3-phenyl-7-nitro-lH-indole prepared in Preparation 41 was reacted according to the same procedures as Step A of Example 1 and Example 113 to give the title compound.
Example 116: (2S)-I -(7-cyclopentylamino-2 -phenyl- 1 H-indole-5 -carbonyl)- pyrrolidine-2-carboxylic acid methylester
7-Cyclopentylamino-2-phenyl-l H-indole-5 -carboxylic acid prepared in Example 30 and (2S)-Pro-OMe were reacted according to the same procedure as Example 92 to give the title compound.
1H-NMR (500MHz, CDCl3); δ 9.76(brs, IH), 7.67(d, 2H), 7.37(t, 2H), 7.26~7.22(m, 2H), 6.72(d, IH), 6.59(d, IH), 4.68(m, IH), 3.81(m, 3H), 3.65(s, 3H), 2.31(m, IH), 2.01(m, 3H), 1.81(m, 3H), 1.56(m, 2H), 1.43(m, 2H), 1.33(m, 2H)
Example 117: (2S)-l-(7-cvclopentylamino-2-phenyl-lH-indole-5-carbonyl)- pyrrolidine-2-carboxylic acid
(2S)-l-(7-cyclopentylamino-2-phenyl-lH-indole-5-carbonyl)-pyπOlidine-2- carboxylic acid methylester prepared in Example 116 was reacted according to the same procedure as Example 30 to give the title compound.
1H-NMR (500MHz, MeOH-d4); δ 7.75(d, J=7.3 Hz, 2H), 7.39(t, J=7.3 Hz, 2H), 7.26(t, J=7.3 Hz, IH), 7.15(m, IH), 6.78(m, IH), 6.55(m, IH), 4.58(m, IH), 3.97(m, IH), 3.69(m, 2H), 2.37(m, IH), 2.08(m, 2H), 1.98(m, 2H), 1.82(m, 3H), 1.65(m, 4H)
Example 118: (2S)-l-[2-phenyl-7-(tetrahydropyran-4-yl)amino-lH-indole-5- carbonyll -pyrrolidme-2-carboxylic acid
2-Phenyl-7-nitro-lH-indole-5-carboxylic acid prepared in Preparation 28, (2S)-
Pro-OMe and tetrahydropyran-4-one were reacted according to the same procedures as
Examples 92, 1 and 30 sequentially to give the title compound. 1H-NMR (500MHz, MeOH-d4); δ 7.75(d, J=7.3 Hz, 2H), 7.39(t, J=7.3 Hz, 2H),
7.27(t, J=7.3 Hz, IH), 7.17(m, IH), 6.79(m, IH), 6.62(m, IH), 4.56(m, IH), 4.00(m,
2H), 3.71(m, 2H), 3.66-3.55(m, 3H), 2.36(m, IH), 2.12(m, 2H), 1.99(m, 2H), 1.84(m,
IH), 1.55(m, 2H) Example 119: 2-(7-Cvclopentylamino-2-phenyl-lH-indol-5-yll-l-pyrrolidin-l- yl-ethanone
2- [7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl] -acetic acid prepared in Example 33 and pyrrolidine were reacted according to the same procedure as Example 92 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 9.92(br s, IH), 7.69(d, IH), 7.32(t, IH), 7.20(t, IH), 6.80(s, IH), 6.63(d, IH), 6.22(d, IH), 3.69(s, 2H), 3.59(m, IH), 3.46(m, 4H), 1.91(m, 4H), 1.77(m, 2H), 1.63(m, 2H), 1.43(m, 4H)
Example 120: Cvclopentyl-r2-phenyl-5-(2-pyrrolidin-l-yl-ethyl)-lH-indol-7- yll -amine
2-[7-Cyclopentylamino-2-phenyl-lH-indol-5-yl]-ethanol prepared in Example
32 and pyrrolidine were reacted according to the same procedures as Steps A and B of
Example 36 to give the title compound. 1H-NMR (500MHz, MeOH-d4); δ 7.75(d, J=7.3 Hz, 2H), 7.38(t, J=7.3 Hz, 2H),
7.24(t, J=7.3 Hz, IH), 6.76(m, IH), 6.67(m, IH), 3.98(m, IH), 3.07(m, 2H), 2.92(m,
6H), 2.08(m, 2H), 1.91(m, 4H), 1.80(m, 2H), 1.66(m, 4H)
Example 121 : 2-r(RV2-(7-cvclopentylammo-2-phenyl-lH-indol-5-ylV4,5- dihydro-thiazol-4- yl] -acetic acid
Step A: (RV4-(4-methoxy-benzylsulfanylV3-|"('7-nitro-2-phenyl-lH-indole-5- carbonylVarnino] -butyric acid methyl ester
2-Phenyl-7-nitro-lH-indole-5-carboxylic acid prepared in Preparation 28 and (R)-3-amino-4-(4-methoxy-benzylsulfanyl)-butyric acid methyl ester hydrochloride prepared in Preparation 47 were reacted according to the same procedure as Example 92 to give the title compound.
Step B: 2-r(R)-2-(7-nitro-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4-yll- acetic acid methyl ester
(R)-4-(4-methoxy-benzylsulfanyl)-3-[(7-nitro-2-phenyl-lH-indole-5-carbonyl)- amino] -butyric acid methyl ester (533 mg, 1 mmol) prepared in Step A was dissolved in DCM (10 mL). Phosphorus pentachloride (406 mg, 2 mmol) was added thereto, and the mixture was stirred for 5 h at room temperature. The reaction was quenched by saturated aqueous sodium bicarbonate solution. The reaction mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure. The residue was purified by column chromatography to give the title compound (240 mg, Yield 60%).
Step C: 2-r(RV2-(7-cvclopentylamino-2-phenyl-lH-indol-5-ylV4.5-dihvdro- thiazol-4-yl] -acetic acid
2-[(R)-2-(7-nitro-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4-yl]-acetic acid methyl ester prepared in Step B and cyclopentanone were reacted according to the same procedures as Examples 1 and 30 to give the title compound. 1H-NMR (400MHz, DMSOd6); δ 11.81(s, IH), 7.92(m, 2H), 7.60(m, 2H),
7.50(m, 2H), 7.34(m, IH), 6.83(m, IH), 4.99(m, IH), 3.95(m, IH), 3.70(m, 2H), 2.87(m,
IH), 2.71(m, IH), 2.08(m, 2H), 1.77(m, 2H), 1.64(m, 4H)
Example 122 : 2-r(RV2-(2-phenyl-7-(tetrahvdropyran-4-yl')methvlamino- 1 H- indol-5-yl)-4,5-dihydro-thiazol-4-yl]-acetic acid
2-[(R)-2-(7-nitro-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4-yl]-acetic acid methyl ester prepared in Step B of Example 121 and tetrahydropyran-4-one were reacted according to the same procedures as Examples 1 and 30 sequentially to give the title compound.
1H-NMR (400MHz, DMSOd6); δ 11.79(m, IH), 7.91(m, 2H), 7.51(m, 2H), 7.39(m, 2H), 7.01(m, IH), 6.80(m, IH), 4.96(m, IH), 3.93(m, 2H), 3.33(m, 3H), 3.15(m, 2H), 2.87(m, 2H), 2.75(m, IH), 1.95(m, IH), 1.79(m, 2H), 1.36(m, 2H)
Example 123: 3-(7-Cvclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester
Step A: 3-(5-Chloro-7-amino-lH-indol-2-yl)benzoic acid methyl ester 3-(5-Chloro-7-nitro-lH-indol-2-yl)benzoic acid prepared in Preparation 32 was reacted according to the same procedure as Example 28 to give the title compound.
Step B: 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methylester
3-(5-Chloro-7-amino-lH-indol-2-yl)benzoic acid methyl ester prepared in Step A was reacted according to the same procedure as Example 1 to give the title compound. 1H-NMR (400MHz, CDCl3); δ 8.78(br s, IH), 8.3 l(s, IH), 7.94(m, IH), 7.85(m,
IH), 7.46(t, IH), 7.03(s, IH), 6.76(s, IH), 6.47(s, IH), 3.93(m, 4H), 2.16~1.63(m, 3H)
Example 124: 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester prepared in Example 123 was reacted according to the same procedure as Example 30 to give the title compound.
1H-NMR (400MHz, DMSO-d6); δ 13.20(br s, IH), 11.21(br s, IH), 8.37(s, IH), 8.06(d, IH), 7.91(d, IH), 7.60(t, IH), 6.85(d, IH), 6.82(d, IH), 6.20(d, IH), 5.80(br s, IH), 3.88(m, IH), 2.51~1.58(m, 8H)
Example 125: [3 -(5 -Chloro-7-cvclopentylamino- 1 H-indol-2- ylVphenyl] - methanol
3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester
10 prepared in Example 123 was reacted according to the same procedure as Example 32 to give the title compound.
Examples 126 to 146:
Indole derivatives prepared in Preparations 31 to 37 were reacted according to a
15 method selected from Examples 123 to 125 to synthesize the Example Compounds in the following table.
Figure imgf000100_0001
Example R2 R4 R6 1H-NMR
126 m-CH20H Cl THP-4-yl (400MHz, DMSOd6); δ 11.08(s, IH), 7.76(s, IH),
7.67(d, J=8Hz, IH), 7.43(t, IH), 7.27(d, J=8Hz, IH),
6.81(s, IH), 6.75(s, IH), 6.29(s, IH), 5. 74(br s, IH),
Figure imgf000101_0001
Figure imgf000102_0001
Figure imgf000103_0001
Figure imgf000104_0001
Example 147: [5-Chloro-2-(3-dimemylaminomethylphenyl)-lH-indol-7-yll- (tetrahvdropyran~4-yl')-amine
[3-(5-Chloro-7-(tetrahydropyran-4-yl)-phenyl)]-methanol prepared in Example 126 and dimethylamine (HCl salt) were reacted according to the same procedure as Example 36 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 10.77(br s, IH), 7.95(br s, IH), 7.75(d, J=8Hz, IH), 7.37(t, IH), 7.06(m, IH), 6.94(s, IH), 6.71(s, IH), 6.36(s, IH), 4.05(d, J=12Hz, 2H), 3.85(m, IH), 3.84(s, 2H), 3.66(m, 4H), 3.56(t, 2H), 2.74(m, 4H), 2.1 l(m, 2H), 2.08(s, 3H), 1.62(m, 2H)
Example 148 : r5-Chloro-2-(3-morpholin-4-ylmethylρhenyl)-lH-indol-7-yll- (tetrahvdropyran-4-yl)-amine
[3-(5-Chloro-7-(tetrahydropyran-4-yl)-phenyl)]-methanol prepared in Example 126 and morpholine were reacted according to the same procedure as Example 36 to give the title compound.
1H-NMR (400MHz, DMSO-d6); δ 11.12(s, IH), 7.77(m, 2H), 7.43(t, IH), 7.28(d, J=8Hz, IH), 6.80(s, IH), 6.76(s, IH), 6.31(s, IH), 5.73(d, J=8Hz, IH), 3.94(d, J=12Hz, 2H), 3.64(m, IH), 3.59(m, 4H), 3.53(s, 2H), 3.48(m, 2H), 2.39(m, 4H), 2.02(d, J=12Hz, 2H), 1.48(m, 2H)
Example 149 : [5 -Chloro-2-(3-p yrrolidin-4- ylmethylphenyl)- 1 H-indol-7-vH - (tetrahvdropyran-4-yiyamine
[3-(5-Chloro-7-(tetrahydropyran-4-yl)-phenyl)]-methanol prepared in Example 126 and 1-BOC-piperazine were reacted according to the same procedures as Examples 36 and 82 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 11.18(s, IH), 8.26(s, IH), 7.82(d, J=8Hz, IH), 7.37(t, IH), 7.02(d, J=8Hz, IH), 6.91(s, IH), 6.71(s, IH), 6.33(s, IH), 5.65(m, IH), 4.15(m, 2H), 4.09(s, 2H), 3.63(m, 2H), 3.56(t, 2H), 2.14(m, 4H), 2.09(m, 2H), 1.79(m, 2H)
Example 150: l-(4-r3-(5-Chloro-7-tetrahvdropyran-4-ylamino-lH-indol-2-ylV benzyl]-piperazin- 1 -vU -ethanone
[3-(5-Chloro-7-(tetrahydropyran-4-yl)-phenyl)]-methanol prepared in Example 126 and 1-acetyl-piperazine were reacted according to the same procedure as Example 36 to give the title compound.
1H-NMR (400MHz, CDCl3); δ 10.77(br, IH), 7.95(s, IH), 7.74(d, J=8Hz, IH), 7.59(t, IH), 7.06(d, J=8Hz, IH), 6.94(s, IH), 6.71(s, IH), 6.36(s, IH), 4.06(d, 2H), 4.03(m, IH), 3.82(s, 2H), 3.66(m, 4H), 3.53(t, 2H), 2.74 (m, 4H), 2.08(s, 3H), 2.04 ~ 2.11 (m, 2H), 1.64(m, 2H).
Example 151: {5-Chloro-2-[3-(2-oxo-piperazin-4-vDethylphenyll-lH-indol-7- yl} -(tetrahydropyran-4-yl)-amine
2- [3-(7-Tetrahydropyran-4-ylamino-5 -chloro- 1 H-indol-2-yl)-phenyl] -acetic acid methyl ester prepared in Example 132 and 2-oxo-piperazine were reacted according to the same procedures as Example 32 and Steps A and B of Example 36 sequentially to give the title compound.
1H-NMR (400MHz, DMSOd6); δ 11.04(s, IH), 7.71(d, J=8Hz, 2H), 7.35(d, J=8Hz, 2H), 6.79(s, IH), 6.72(s, IH), 6.28(s, IH), 5.62(d, J=8Hz, IH), 3.93(d, J=12Hz, 2H), 3.65(m, IH), 3.50(t, 2H)5 3.15(s, 2H), 3.00(s, 2H), 2.79(m, 2H), 2.63(m, 4H), 2.03(m, 2H), 1.47(m, 2H)
Example 152: {5 -Chloro-2- [3-C 1 , 1 -dioxo-thiomoφholin-4- yl)ethvbhenyl"| - 1 H- indol-7-yll-(tetrahydropyran-4-yl)-amine
2-[3-(7-Tetrahydropyran-4-ylamino-5-chloro-lH-indol-2-yl)-phenyl]-acetic acid methyl ester prepared in Example 132 and 1,1-dioxo-thiomorpholine were reacted according to the same procedures as Example 32 and Steps A and B of Example 36 sequentially to give the title compound.
10 1H-NMR (400MHz, DMSOd6); θ 7.70(d, 2H), 7.34(d, 2H), 6.79(s, IH), 6.72(s, IH), 6.28(s, IH), 3.91(d, 2H), 3.65(m, IH), 3.53(t, 2H), 3.16(d, 4H), 3.00(d, 4H), 2.77(br s, 4H), 2.02(d, 2H), 1.45(d, 2H)
Examples 153 to 161:
15 Indole and indazole derivatives prepared in Preparations 44, 48 and 49 were reacted according to the same procedure as Example 1 to synthesize the Example Compounds in the following table.
Figure imgf000107_0001
Figure imgf000107_0002
Figure imgf000108_0001
Figure imgf000109_0001
Example 162: (Tetrahydropyran-4-vD-[3-bromo-5-(morpholin-4-vDmethyl-2- phenyl- 1 H-indol-7-yl] -amine
4-[3-Bromo-2-phenyl-7-nitro-lH-indol-5-yl]-morpholine prepared in Preparation 48 and tetrahydropyran-4-one were reacted according to the same procedure as Example 1 to give the title compound.
1H-NMR (500MHz, CDCl3); δ 8.12(br, IH), 7.81(d, J=7.3 Hz, 2HO, 7.49(t, J=7.3Hz, 2H), 7.40(t, J=7.3Hz, IH), 7.02(s, IH), 6.64(s, IH), 4.04(m, 2H), 3.73~3.66(m, 5H), 3.60~3.54(m, 4H), 2.47(m, 4H), 2.10(m, 2H), 1.56(m, 2H)
Experimental Example 1: Measurements and analysis of the Example compounds for the hepatocyte protective effect against the substances deriving hepatocyte toxicity.
Various endogenous/exogenous attacks on the cells trigger the mechanisms of cell death which is broadly classified into two types, i.e. apoptosis or necrosis. Using these cell death mechanisms, in the present experimental example, primary hepatocytes isolated from rats were treated with drugs which were clinically shown to result in serious side-effects of hepatocyte toxicity or various chemicals which derive cell death, and the compounds synthesized in the Examples were estimated for their hepatocyte protective effects, after 24 - 48 h. The substances used to derive hepatocyte death include CCl4, ActD, H2O2, doxorubicin, anti-Fas Ab/Actinomycin D, acetaminophen, EtOH, CdCl2, palmitate, stearate, cyclophosphamide, terfenadine, diclofenac, simvastatin, and adefovir. Primary hepatocytes were isolated using the method of Seglen PO (Experimental Cell Research 74(1972) pρ450-454). Briefly, hepatocytes were isolated according to the two-step collagenase perfusion method, and dead cells were removed by low speed (500 rpm) centrifugation for 10 min using percoll gradient (Kreamer BL etc, In Vitro Cellular & Developmental Biology 22(1986) pp201-211). During this step, the viability of cells was maintained 90% or above. The cells were suspended in HepatoZYME media (Gibco BRL), and the number of cells was counted. 1.5X104 cells in 100 μJt were placed into the collagen-coated 96- well plate (BD biocoat), and adhered on the bottom for 3 - 4 h. In order to assess the hepatocyte protective effect, above adhered cells were pretreated with the Example compounds for 30 min. At this time, the concentration of the Example compounds were serially diluted by 2-fold or 3-fold over 5 steps starting from 30 uM, 10 uM or 1 uM depending on the experiments, and the final concentration of DMSO was adjusted to 0.2%. 30 min after the treatment by compounds, cells were treated by the substances deriving hepatocyte death or hepatotoxic drugs at the concentrations indicated in Table 1. After 24 - 48 h, the viability of cells was determined to estimate the hepatocyte protective effects. The viability of cells was determined using WST-I (MK-400, Takeda) method by the absorbance at 440 nm. Hepatocyte protective effects of the Example compounds were represented by "EC50" which was calculated from measured values. "EC50" herein means the concentration of the compound at which 50% of maximum protective effect is observed in the experiment.
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
Table 1 shows the treatment concentrations of various substances deriving hepatotoxity and the hepatocyte protective effect of the compound of Example 41. Table 2 shows the cell protective effects of the Example compounds against a substance which results in hepatotoxicity, doxorubicin.
Table 1 Protective effect of the compound of Example 41 against the substances deriving hepatotoxicity
Figure imgf000112_0001
Table 2 Cell protective effects against doxorubicin in hepatocytes
Figure imgf000112_0002
Figure imgf000113_0001
Figure imgf000114_0001
Experimental Example 2: Protective effects when tBHP ("tert-Butyl Hydroxy Peroxide; t-BuOOH) was treated on hepatocytes and other cells derived from various tissues 1) Protective effect when tBHP was treated on primary hepatocytes
Hepatocytes were isolated according to the same procedure as Experimental
Example 1, suspended in DMEM (Gibco + 10% FBS + IX antibiotics) media, and distributed to the plate. After 24 h from the distribution of hepatocytes, the compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which the cells were pretreated for 30 min. Cells were treated with tBHP at the final concentration of 300 uM, and the protective effects were determined after 1 h. As in Experimental Example 1, after the treatment with WST-I (Takeda, lOuL) for 1.5 h, EC50 values were calculated by absorbance measurements at 440 nm using SpectraMax (Molecular Device).
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less.
2) Protective effect when tBHP was treated on pancreatic cells (Linm5F) In order to determine the protective effect on pancreatic cells, Linni5F cells, a sort of the beta cells, were distributed into the 96-well plate in the amount of 2X104 cells/well, and incubated for 24 h. The Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 1 h. Cells were treated with tBHP at the final concentration of 400 uM, and further incubated for 5 h. Protective effects were determined using SRB (Sulforhodamine B Protein) method in which total amount of cellular protein is stained. Briefly, cells were incubated for 5 h, 50 uL of 4% formaldehyde solution was added to each well to fix the cells, and stored for about 30 min at room temperature. After discarding the media, each well was washed with distilled water 2 - 3 times, and the plate was dried in an oven at 50 °C . 50 uL of SRB solution was added to each well, and placed for about 30 min at room temperature. After removing SRB solution, the plate was washed with 1% acetic acid solution 2 - 3 times. After drying the plate in an oven at 50 °C , 100 uL of 10 mM Tris was added to elute SRB which was staining the intracellular protein. Absorbance was measured at 590 nm and 650 nm using SpectrMax, and the absorbance at 650 nm was subtracted from the absorbance at 590 nm to calculate EC50 value.
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less. The compounds of Examples 56, 106, and 107 as representative compounds showed excellent activities in the present experiment, and their EC50 values were 0.1 uM or less.
3) Protective effect when tBHP was treated on cardiac cells (H9C2, white rat cardiomyocyte)
In order to assess the protective effect on cardiac cells, H9C2 cells were distributed in the amount of 1.5X104 cells/well, and incubated for 24 h. The Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 45 min. Cells were treated with tBHP at the final concentration of 400 uM, and incubated for 2 h. Protective effect of each compound was determined using the same SRB method as in Linm5F of above mentioned 2).
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less. As representative compounds, for example, EC50 of the compound of Example 86 was 0.5 uM. Also, the compounds of Examples 39, 74, 86, 97 and 117 showed excellent activities in the present experiment, and their EC50 values were 0.2 uM or less. 4) Protective effect when tBHP was treated on kidney cells (LLC-PKl)
In order to determine the protective effect on kidney cells, 4X104 cells were distributed into each well, and incubated for 24 h. Cells were treated with the Example compounds at the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, and incubated for 30 min. Cells were treated with 400 uM tBHP, and further incubated for 6 h. Protective effect of each compound was determined using the same SRB method as in Linm5F of above mentioned 2).
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less. Representatively, EC50 of the compound of Example 56 was 0.66 uM.
5) Protective effect when tBHP was treated on chondrocytes
In order to determine the protective effect on chondrocytes, chondrocytes were isolated from 2 hind legs of 16 week-old SD rats (body weight: 450 - 460 g). Isolation method is as follows. Cartilage isolated from the knee regions of rat hind legs was transferred to a 100 pi plate containing PBS (+1X antibiotics). PBS was maintained 4°C in an ice-bath. PBS was exchanged with fresh one, and centrifuged at 1000 rpm. After removal of PBS, 3 mL of IX trypsin (Gibco) at the temperature of 37 °C was added and followed by the treatment for 15 min. Supernatant was discarded after centrifugation, and washed again with PBS. Supernatant was discarded after centrifugation. After the addition of 0.2% collagenase (Worthington, type II) thereto, the cells were isolated by the overnight incubation in a rotating 37 "C incubator. Filtered cell solution was centrifuged, and the supernatant was discarded. Following the washing with PBS, cells were suspended in 10 niL of DMEM/F-12 (Gibco, 10% FBS). 2X104 cells were distributed to each well, and incubated for 24 h. The Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 1 h. Cells were treated with tBHP at the final concentration of 500 uM, and incubated for 3 h. Protective effect of each compound was determined using the same SRB staining method as in Linm5F of above mentioned 2).
Preferably, EC50 of the Example compound is 30 uM or less, more preferably, 10 uM or less, and especially preferably, 1.0 uM or less. Representatively, the compounds of Examples 56 and 63 showed excellent activities in the present experiment, and their EC50 values were 0.1 uM or less.
6) Protective effect when tBHP was treated on brain cells (SK-N-MC) In order to assess the protective effect on brain cells, 2X104 brain cells were distributed into the 96-well plate using DMEM media (Gibco, 10% FBS), and incubated for 24 h. The Example compounds were serially diluted by 3-fold to the final concentration of 30, 10, 3, 1, 0.3, 0.1 uM, by which each well was treated for 1 h.
Cells were treated with tBHP at the final concentration of 400 uM, and incubated for 6 h. 50 uL of media was taken from each well to proceed with LDH assay (Promega). In
LDH assay, 50 uL of media was mixed with 50 uL of assay solution. After the reaction for 30 min at room temperature, absorbance was measured at 490 nm using
SpectraMax (Molecular Device). Preferably, EC50 of the Example compound is 30 uM or less, more preferably,
10 uM or less, and especially preferably, 1.0 uM or less. Representatively, EC50 value of the compound of Example 115 was 0.26 uM. Also, the compounds of Examples 37,
55 and 63 showed excellent activities in the present experiment, and their EC50 values were 0.1 uM or less.
[Industrial Applicability]
As is demonstrated in above results, the novel compounds according to the present invention not only exhibit the effects for hepatoprotection and hepatic functional improvement, but also can be useful for the prevention and treatment of the chronic hepatic diseases such as fatty liver, hepatic fibrosis, hepatocirrhosis, etc. and acute/chronic hepatic diseases such as hepatitis, etc. caused by virus or drugs. The compounds of the present invention also exhibit the necrosis inhibitory efficacy in the cells from pancreas, kidney, brain, cartilage, and heart.
Thus, the compounds of the present invention can be useful in the prevention and treatment of necrosis and associated diseases.
It will be within the ability of those skilled in the art, to conduct various applications and modifications without departing from the scope of the present invention.

Claims

[CLAIMS] [Claim 1 ]
Indole or indazole compounds of the following formula (1):
Figure imgf000120_0001
in which n denotes a number of 1 to 3, m denotes 0 or 1,
A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C,
R1 represent hydrogen, alkyl, -(CH2)rNR7R8, or -(CH2)rCO2H, wherein r denotes a number of 1 to 5, and R7 and R8 independently of one another represent hydrogen, alkyl or alkylcarbonyl, or may together form an optionally alkyl-substituted alkylene chain wherein optionally one methylene is replaced by N atom,
R2 represents hydrogen, halogen, cyano, nitro, hydroxy, alkyl, alkoxy or trialkylsilyl, represents -(CH2)PCO2R7, -(CH2)POR7, -(CH2)PNR7R8, -NHR10, - N(H)S(O)2R7, -NHC(O)R10, -(CH2)PS(O)2R7 or (CH2)p-heterocycle-R10, wherein p denotes a number of 0 to 3, R7 and R8 are as defined above, R10 represents hydrogen, oxo, alkylsulfonyl, alkylcarbonyl, alkyloxycarbonyl, alkylaminocarbonyl, alkoxy, alkyl or heterocycle, R3 represents hydrogen, cyano, halogen, alkyl or phenyl, or represents -
(CH2)n-heterocycle or -(CH2)n-aryl, wherein n denotes a number of 0 to 3,
R4 represents -YR11, wherein Y represents a direct bond or -(CR7R8)PY'-, wherein p denotes a number of 0 to 3, R and R are as defined above, Y' is selected from the group consisting of -O-, -S-, -NR12-, -NR12C(O)-, -C(O)-, -C(O)O-, -
C(O)NR12-, -S(O)0 and -S(0)qNR12-, wherein R12 represents hydrogen, alkyl, aryl or heteroaryl, q denotes a number of 0 to 2, R is selected from the group consisting of hydrogen, cyano, halogen, hydroxy, thiol, carboxy, alkyl and -(CH2)tB-R13, wherein t denotes a number of 0 to 3, B represents heterocycle, heteroaryl or aryl, R13 represents hydrogen, cyano, halogen, hydroxy, oxo, thiol, carboxy, carboxyalkyl, alkylcarbonyloxy, alkyl, alkoxy, alkylthio, alkylcarbonyl or alkylsulfonyl,
R5 represents hydrogen, alkyl, cycloalkyl, heterocycle or heterocyclylalkyl,
R6 represents -(CR7R8)P-Z-D-W-R14, wherein Z represents a direct bond, or is selected from the group consisting of -C(O)-, -C(O)O-, -C(O)NR12-, and -S(0)y-, y denotes a number of 1 or 2, D represents a direct bond, or represents cycloalkyl, heteroaryl or heterocycle, W represents a direct bond, or represents -NR7-. -C(O)-, -
C(O)O-, -C(O)NR12-, -S(0)y-, -S(0)yNR12- or -NR12S(0)r, wherein R14 represents hydrogen, hydroxy, alkyl, alkoxy, heterocycle, heteroaryl, aryl or aralkyl,
R5 and R6 together represent alkylene chain, where alkyl, alkoxy, aryl, cycloalkyl, heterocycle and heteroaryl may be optionally substituted, and the substituents are one or more selected from the group consisting of hydroxy, halogen, nitrile, amino, alkylamino, dialkylamino, carboxy, alkyl, alkoxy, carboxyalkyl, alkylcarbonyloxy, alkylthio, alkyloxycarbonyl, alkylaminocarbonyl, arylalkoxy and oxo, and pharmaceutically acceptable salts or isomers thereof. [Claim 2]
The compounds according to Claim 1 wherein n denotes a number of 1 to 3, m denotes 0 or 1,
A represents a direct bond, represents phenyl, or represents 6 membered heteroaryl having 1 to 2 nitrogen atoms,
X represents C or N, with the proviso that m is 0 when X is N, and m is 1 when X is C,
1 7 S R represents hydrogen, Q-Cό-alkyl or -(CH2)rNR R , wherein r denotes a number of 2 to 3, and R7 and R8 independently of one another represent hydrogen or C1- C3-alkyl, or may together form C2-C6-alkylene chain which is optionally substituted by Ci-C6-alkyl and optionally one methylene is replaced by N atom,
R2 represents hydrogen, halogen, Ci-C6-alkyl, -(CH2)PCO2R7, -(CH2)POR7, -(CH2)PNR7R8, -NHR10, -N(H)S(O)2R7, -NHC(O)R10, -(CH2)PS(O)2R7 or -(CH2)P- heterocycle-R10, p denotes a number of 0 to 3,
R10 represents hydrogen, oxo, Q-Cό-alkylsulfonyl, Q-Cό-alkylcarbonyl, CrQ-alkyloxycarbonyl, CrCό-alkylaminocarbonyl, Q-Cό-alkoxy, d-Q-alkyl or hydroxy-d-Cό-alkyl, or represents 5-6 membered heterocycle which has 1 or 2 nitrogen atoms as the hetero atom, and is optionally substituted by d-C3-alkyl,
R3 represents hydrogen, halogen or Ci-C6-alkyl, represents phenyl optionally substituted by Ci-C6-alkoxy, or represents heterocyclyl-Cj-Cs-alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
R4 represents -YR11, wherein Y represents a direct bond or -(CR7R8)PY'-, wherein Y' is selected from the group consisting of -O-, -C(O)-, -C(O)O-, -NHC(O)-, - NR12-, -C(O)NR12-, -S(O),-, and -S(O)qNR12-, R12 represents hydrogen or Ci-C3-alkyl, q denotes a number of O to 2, R11 is selected from the group consisting of hydrogen, halogen, hydroxy, thiol, carboxy, d-Cβ-alkyl, hydroxy-d-C6-alkyl and -(CH2)tB-R13, t denotes a number of O to 3, B represents C6-C10-aryl, represents 5~6 membered heterocycle having 1 or 2 hetero atoms selected from N, O and S, or represents 5-6 membered heteroaryl having 1 or 2 N atoms, R13 represents hydrogen, halogen, hydroxy, oxo, thiol, carboxy, carboxy-d-C6-alkyl, d-Cό-alkylcarbonyloxy, d-C6-alkyl, C1-C6- alkoxy, d-C6-alkylthio, d-C6-halogenoalkyl, d-C6-alkylcarbonyl or C1-C6- alkylsulfonyl,
R5 represents hydrogen, d-C6-alkyl, C3-C6-cycloalkyl, heterocycle or heterocyclyl-d-Ce-alkyl, wherein the heterocycle is a 3-8 membered ring which has 1 to 3 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups,
R6 represents -(CR7R8)P-Z-D-W-R14,
Z represents a direct bond, or is selected from the group consisting of -
C(O)-, -C(O)O-, -C(O)NR12-, and -S(0)y-, wherein y denotes a number of 1 to 2, D represents C4-C6-cycloalkyl, or represents 5-6 membered heterocycle which has 1 or 2 hetero atoms selected from N, O and S, and optionally contains an oxo group,
W represents a direct bond, or represents -NR7-. -C(O)-, -C(O)O-, -
C(O)NR12-, -S(O)y, -S(0)yNR12- or -NR12S(O)y-, R14 represents hydrogen, hydroxy, Ci-C6-alkyl, hydroxy-Ci-C6-alkyl, carboxy-Ci-Cό-alkyl, Cδ-Cio-aryl or C6-Ci0-ar-Ci-C6-alkyl, represents 5-6 membered heterocycle which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 to 3 hetero atoms selected from N, O and S, and is optionally substituted by C!-C6-alkyl, or
R5 and R6 together represent C2-C6-alkylene chain.
[Claim 3]
The compounds according to Claim 1, which are depicted by the following formula (Ia) or (Ib).
Figure imgf000124_0001
Figure imgf000124_0002
in which n, A, R1 , R2, R3, R4, R5 and R6 are as defined in Claim 1.
[Claim 4]
The compounds according to Claim 2 wherein A represents phenyl, pyridine or 1,4-pyrazine.
[Claim 5]
The compounds according to Claim 2 wherein R1 represents hydrogen, Cj-C6- alkyl or di(d-C3-alkyl)amino-C2-C3-alkyl.
[Claim 6] The compounds according to Claim 5 wherein R1 represents hydrogen, methyl or (dimethylamino)ethyl.
[Claim 7]
The compounds according to Claim 2 wherein R2 represents hydrogen, amino, halogen, Ci-C3-alkyl, carboxy, carboxy-Ci-C3-alkyl, Ci-C3-alkoxycarbonyl, C1-C3- alkoxycarbonyl-CrCralkyl, hydroxy-Ci-C3-alkyl, CrC3-alkoxy, -(CH2)PNR7R8, - NHR10, -N(H)S(O)2R7, -NHC(O)R10 or -(CH2)p-heterocycle-R10, wherein p, R7, R8 and R10 are as defined in Claim 2.
[Claim 8]
The compounds according to Claim 7 wherein R2 is selected from the group consisting of hydrogen, methyl, methoxy, fluoro, -NH2, -NHAc, -NHSO2Me, -NHBOC, -NH( 1 -methyl-piperidine), 1 -oxo-2-hydroxy-ethyl, dimethylaminomethyl, hydroxymethyl, hydroxyethyl, carboxy, carboxymethyl, carboxyethyl, -CH2-(2- oxo)piperazine, -CH2-piperazine, -CH2-morpholine, -CH2- [1,1 -dioxo-thiomorpholin-4- yl], and -CH2-[4-acetyl-piperazin-l-yl].
[Claim 9]
The compounds according to Claim 2 wherein R3 represents hydrogen, methyl or bromo, represents phenyl optionally substituted by Ci-C3-alkoxy, or represents heterocyclyl-d-C3-alkyl wherein the heterocycle is 5-6 membered, has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups.
[Claim 10]
The compounds according to Claim 9 wherein R3 is selected from the group consisting of hydrogen, methyl, bromo, phenyl, 4-MeO-phenyl, -CH2-(2-oxo-piperazin- 4-yl), and -CH2-(morpholin-4-yl).
[Claim 11 ]
The compounds according to Claim 2 wherein Y is selected from the group consisting of a direct bond, -O-, -C(O)-, -NH-, -CONH-, -SO2NH-, -NHC(O)-, - CH2CONH-, -CH2C(O)-, and -CH2SO2-.
[Claim 12] The compounds according to Claim 11 wherein Y is selected from the group consisting of a direct bond, -0-, -C(O)-, -CH2C(O)- and -NHC(O)-.
[Claim 13]
The compounds according to Claim 2 wherein R11 is selected from the group consisting of hydrogen, halogen, hydroxy, d-C6-alkyl and -(CH2)tB-R13, wherein t, B and R13 are as defined in Claim 2.
[Claim 14]
The compounds according to Claim 13 wherein R11 is selected from the group consisting of hydrogen, methyl, ethyl, phenyl, fluoro, chloro, hydroxy, 2-carboxy- pyrrolidin-1-yl, pyrrolidin-1-yl, 4-acetic acid-l,3-thiazolin-2-yl, -CH2-(1, 1-dioxo- thiomorpholin-4-yl), and -CH2-(2-oxopiperazin-4-yl).
[Claim 15]
The compounds according to Claim 2 wherein R5 represents hydrogen, C1-C6- alkyl, C3-C6-cycloalkyl, heterocycle or heterocyclyl-Ci-C6-alkyl, wherein the heterocycle is a 5-6 membered ring which has 1 or 2 hetero atoms selected from N and O, and is optionally substituted by 1 or 2 oxo groups.
[Claim 16]
The compounds according to Claim 15 wherein R5 is selected from the group consisting of hydrogen, methyl, cyclopentyl, tetrahydropyran-4-yl and CH2- (tetrahydropyran-4-yl).
[Claim 17]
The compounds according to Claim 2 wherein Z represents a direct bond, or represents -C(O)-, -C(O)O-, -C(O)NH- or -S(O)2-.
[Claim 18] The compounds according to Claim 2 wherein D is selected from the group consisting of cyclopentyl, cyclohexyl, pyrrolidine, tetrahydropyran, tetrahydrofuran and piperidine.
[Claim 19]
The compounds according to Claim 2 wherein W represents a direct bond, or represents -SO2-, -CO-, -C(O)O- or -CONR12-, wherein R12 is as defined in Claim 2.
[Claim 20]
The compounds according to Claim 19 wherein W is selected from the group consisting Of-SO2-, -CO-, -C(O)O-, -CON(Me)-, and -CONH-.
[Claim 21 ] The compounds according to Claim 2 wherein R14 represents hydrogen, hydroxy,
Ci-C6-alkyl, hydroxy-Ci-C6-alkyl, C6-C10-aryl or Co-Cio-ar-CrCralkyl, represents 5-6 membered heterocycle which has O or S, and is optionally substituted by 1 or 2 oxo groups, or represents 5-6 membered heteroaryl which has 1 or 2 hetero atoms selected from N, O and S, and is optionally substituted by Ci-C3-alkyl.
[Claim 22]
The compounds according to Claim 21 wherein R14 is selected from the group consisting of hydrogen, hydroxy, methyl, ethyl, isobutyl, hydroxymethyl, hydroxyethyl, phenyl, benzyl, thiophene, tetrahydrofuran, tetrahydropyran, 1,1-dioxo-tetrahydro- thiopyran, furan, pyridine and 5-methyl-pyridine.
[Claim 23]
The compounds according to Claim 2 wherein R5 and R6 together with the N atom to which they are attached form piperidine.
[Claim 24] The compounds according to Claim 2, which are selected from the following:
Cyclopentyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[5-methyl-2 -phenyl- lH-indol-7-yl] -amine; 5-Chloro-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
(Tetrahydropyran-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[2-(pyrazin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[5-methyl-2-(pyrazin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[2-(pyridin-2-yl)-lH-indol-7-yl]-amine; (Tetrahydropyran-4-yl)-[2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[5-phenoxy-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentyl-[5-ethoxy-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclohexyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; l-[4-[(5-Methyl-2-(pyridin-2-yl)-lH-indol-7-yl)amino]piperidin-l-yl]ethanone; (l-Methylpiperidin-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; (l-Benzylpyrrolidin-3-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine; Cyclopentylmethyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
5-Methyl-(7-piperidin-l-yl)amino-2-(pyridin-2-yl)-lH-indole;
Dimethyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
Cyclopentyl-[ 1 ,5-dimethyl-2-(pyridin-2-yl)-indol-7-yl]-amine; Cyclopentyl-[5-methyl-2-(6-methylpyridin-2-yl)-lH-indol-7-yl]-amine;
(l-Cyclohexanon-4-yl)-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amine;
4-[(5-Chloro-2 -phenyl- 1 H-indol-7-yl)amino]-cyclohexan- 1 -one;
N-(5 -Methyl-2-(pyridin-2-yl)- 1 H-indol-7-yl)-benzamide; l-Ethyl-3-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-urea; l-Phenyl-3-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-urea;
Thiophene-2-sulfonic acid (2-pyridin-2-yl-lH-indol-7-yl)-amide;
Thiophene-2-sulfonic acid [5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-amide;
Cyclopentyl-methyl-[5-methyl-2-(pyridin-2-yl)-lH-indol-7-yl]-aniine;
7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid ethyl ester; Cyclopentyl-[5-hydroxymethyl-2-phenyl-lH-indol-7-yl]-amine;
7-(Cyclopentyl)amino-2-phenyl-lH-indole-5-carboxylic acid;
2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]-acetic acid ethyl ester;
2-[7-(Cyclopentylamino)-2-phenyl-lH-indol-5-yl]ethanol;
2-[7-(Cyclopentyl)amino-2-phenyl-lH-indol-5-yl]acetic acid; 2-[2-Phenyl-7-(tetrahydropyran-4-yl)amino-lH-indol-5-yl]-acetic acid;
2- [2-Phenyl-7-( 1 , 1 -dioxo-tetrahydro-thiopyran-4-yl)amino- 1 H-indol-5-yl] - acetic acid;
(Tetrahydropyran-4-yl)- [2-phenyl-5-( 1 , 1 -dioxo-thiomoφholin-4-yl)methyl- 1 H- indol-7-yl] amine; (Tetrahydropyran-4-yl)-[2-phenyl-5-(2-oxo-piperazin-4-yl)methyl-lH-indol-7- yl] amine;
Cyclopentyl-[2-(3-fluoro)phenyl-5-(2-oxo-piperazin-4-yl)methyl-lH-indol-7- yl] amine; (Tetrahydropyran-4-yl)-[2-(4-methoxy)phenyl-5-(l,l-dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine;
Cyclopentyl-[3,5-dimethyl-2-phenyl-lH-indol-7-yl]-amine; (Tetrahydropyran-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine; Cyclopentylmethyl-(5 -methyl-2-phenyl- 1 H-indol-7-yl)-amine; (Tetrahydropyran-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine;
(l-Methylpiperidin-4-yl)-(5-methyl-2-phenyl-lH-indol-7-yl)-amine; l-[-4-[(5-Methyl-2-phenyl-lH-mdol-7-yl)amino]piperidin-l-yl]ethanone; Cyclopentyl-(5-chloro-2-phenyl- 1 H-indol-7-yl)-amine; Cyclohexyl-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (Tetrahydropyran-4-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine;
Cyclopentylmethyl-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (Tetrahydropyran-4-ylmethyl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (l-Benzylpyrrolidm-3-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (l-Methylpiperidin-4-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine; (l,4-Dioxaspiro[4.5]decan-8-yl)-(5-chloro-2-phenyl-lH-indol-7-yl)-amine;
2-[(5-Chloro-2 -phenyl- lH-indol-7-yl)amino]propan-l,3-diol; (Tetrahydropyran-4-yl)-(5 -methyl-2-phenyl- 1 H-indol-7-yl)-methyl-amine; (Tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine ; Di(tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -( 1 , 1 -dioxo-thiomorpholin-4- yl)methyl- 1 H-indol-7-yl] amine;
Di(tetrahydropyran-4-yl)-[2-phenyl-5-(l,l-dioxo-thiomorpholin-4-yl)methyl- 1 H-indol-7-yl] amine; (l-Methyl-piperidinemethyl-4-yl)-[5-fluoro-2-phenyl-lH-indol-7-yl]amine;
2-[4-[(5-Fluoro-2-phenyl-lH-indol-7-yl)amino]piperidin-l-yl]ethanol;
[l-(Tetrahydropyran-4-yl)piperidin-4-yl]-(5-fluoro-2-phenyl-lH-indol-7- yl)amine;
(Tetrahydropyran-4-yl)-(5 -phenoxy-2 -phenyl- 1 H-indol-7-yl)-amine; (Tetrahydropyran-4-ylmethyl)- [2-phenyl-5 -(2-oxo-piperazin-4-yl)methyl- 1 H- indol-7-yl]amine;
(Tetrahydropyran-4-yl)-[5-chloro-l-(2-diethylaminoethyl)-2-phenyl-lH-indol- 7-yl] amine;
Dimethyl-(5 -chloro- 1 -methyl-2-phenyl- 1 H-indol-7-yl)amine; (Tetrahydropyran-4-yl)-(5-chloro-l-methyl-2-phenyl-lH-indol-7-yl)- methylamine;
(Tetrahydropyran-4-yl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine;
Cyclopentyl-(5-chloro-3 -phenyl- lH-indol-7-yl)-amine;
(Tetrahydropyran-4-ylmethyl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine; Cyclopentyl-(5-chloro-3-(moφholin-4-yl)methyl-2-phenyl-lH-indol-7-yl)- amine;
(Tetrahydropyran-4-yl)-(5-chloro-3-(morpholin-4-yl)methyl-2-phenyl-lH- indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-lH- indol-7-yl)-amine;
Cyclopentyl-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2-phenyl-lH-indol-7- yl)-amine;
(Tetrahydropyran-4-ylmethyl)-(5-chloro-3-(2-oxo-piperazin-4-yl)methyl-2- phenyl- lH-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(3-bromo-5-( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl-2- phenyl- 1 H-indol-7-yl)-amine;
Cyclopentyl-(3 -bromo-5-( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl-2-phenyl- 1 H- indol-7-yl)-amine; (Tetrahydropyran-4-ylmethyl)-(3 -bromo-5 -( 1 , 1 -dioxo-thiomorpholin-4- yl)methyl-2-phenyl- 1 H-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-(l,l-dioxo-thiomoφholin-4-yl)methyl-2-(3- fluorophenyl)- 1 H-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)-(5-chloro-3-phenyl-lH-indol-7-yl)-amine; (3-Methylbutyl)-[5-(l,l-dioxo-thiomoφholin-4-yl)methyl-2-(4- methoxyphenyl)- 1 H-indol-7-yl] -amine; t-Butyl N-[4-[5-chloro-7-(cyclopentylamino)-lH-indol-2-yl]phenyl]carbamate;
Cyclopentyl-[2-(4-aminophenyl)-5-chloro-lH-indol-7-yl]-amine;
Cyclopentyl- { 5-chloro-2-[4-( 1 -methyl-piperidin-4-yl)aminophenyl] - 1 H-indol- 7-yl} -amine;
N-[4-(5-chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]- methanesulfonamide;
Cyclopentyl- {5-(l,l-dioxo-thiomoφholin-4-yl)methyl-2-[4- (acetyl)aminophenyl]-lH-indol-7-yl} -amine; Dicyclopentyl- {5-(l , 1 -dioxo-thiomoφholin-4-yl)-2-[4-(acetyl)aminophenyl]- lH-indol-7-yl} -amine;
(Tetrahydropyran-4-yl)methyl- {5-(l , 1 -dioxo-thiomorpholin-4-yl)-2-[4- (acetyl)aminophenyl]-lH-indol-7-yl}-amine; Di(tetrahydropyran-4-yl)methyl- {5-(l , 1 -dioxo-thiomorpholin-4-yl)-2-[4-
(acetyl)aminophenyl]-lH-indol-7-yl}-amine;
(Tetrahydropyran-4-yl)- {5-(l ,1 -dioxo-thiomorpholin-4-yl)-2-[4- (acetyl)aminophenyl]-lH-indol-7-yl}-amine;
(5-Methyl-2-phenyl-lH-indol-7-yl)-piperidin-4-yl-amine; [1 -(Methanesulfonyl)piperidin-4-yl] -(5-methyl-2 -phenyl- 1 H-indol-7-yl)-amine;
2-Hydroxy-l-[4-(5-methyl-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl]- ethanone;
(5-Chloro-2-phenyl- 1 H-indol-7-yl)-piperidin-4-yl-amine;
4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-piperidin-l-yl-carboxylic acid phenylamide;
1 -[4-(5 -Chloro-2-phenyl- 1 H-indol-7-yl)amino-piperidin- 1 -yl] -2- dimethylamino-ethanone;
[5-(l,l-Dioxo-thiomorpholin-4-yl)methyl-2-phenyl-lH-indol-7-yl]-(piperidin- 4-yl)methyl-amine; (5-( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl- 1 H-indol-7-yl)-( 1 - methanesulfonyl-piperidin-4-yl)-amine;
{4-[5 -( 1 , 1 -Dioxo-thiomorpholin-4-yl)methyl-2-phenyl- 1 H-indol-7-yl] amino- piperidin- 1 -yl} -(tetrahydrofuran-2-yl)-methanone;
(5-Fluoro-2-phenyl- 1 H-indol-7-yl)- [ 1 -( 1 , 1 -dioxo-tetrahydrothiopyran-4-yl)- piperidin-4-yl] -amine;
N-(5-Chloro-2-phenyl-lH-indol-7-yl)-N',N'-dimethyl-cyclohexane-l,4- di amine;
N-(5-Chloro-2-phenyl-lH-indol-7-yl)-N'-methyl-cyclohexane-l,4-diamine; 4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-cyclohexane-l-carboxylic acid;
4-(5-Methyl-2 -phenyl- 1 H-indol-V-ytyamino-cyclohexane- 1 -carboxylic acid;
4-(5-Chloro-2-phenyl- 1 H-indol-7-yl)amino-cyclohexane- 1 -carboxylic acid amide;
4-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-cyclohexanecarboxylic acid methylamide;
(2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester;
2-(5-Fluoro-2-phenyl-lH-indol-7-yl)amino-acetic acid;
2-(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino-acetic acid methyl ester;
2-[(5-Phenoxy-2-phenyl- lH-indol-7-yl)amino]-acetic acid; 2-[(5-Phenoxy-2-phenyl-lH-indol-7-yl)amino]-propionic acid methyl ester;
2-(5-Phenoxy-2-phenyl- 1 H-indol-7-yl)amino-propionic acid;
2-(5-Chloro-2-phenyl-lH-indol-7-yl)amino-propionic acid;
(5-Chloro-2-phenyl-lH-indol-7-yl)-pyridin-2-yl-amine;
(5-Chloro-2-phenyl-lH-indol-7-yl)-5-methyl-pyridin-2-yl-amine; (5-Chloro-3-phenyl-lH-indol-7-yl)-(5-methyl-pyridin-2-yl)-amine;
(2S)- l-(7-cyclopentylamino-2 -phenyl- lH-indole-5 -carbonyl)-pyrrolidine-2- carboxylic acid methyl ester;
(2S)-l-(7-cyclopentylamino-2-phenyl-lH-indole-5-carbonyl)-pyrrolidine-2- carboxylic acid; (2S)-l-[2-phenyl-7-(tetrahydropyran-4-yl)amino-lH-indole-5-carbonyl]- pyrrolidine-2-carboxylic acid;
2-(7-Cyclopentylamino-2-phenyl- 1 H-indol-5 -yl] - 1 -pyrrolidin- 1 -yl-ethanone;
Cyclopentyl-[2-phenyl-5-(2-pyπOlidin-l-yl-ethyl)-lH-indol-7-yl]-amine; 2-[(R)-2-(7-cyclopentylamino-2-phenyl-lH-indol-5-yl)-4,5-dihydro-thiazol-4- yl]-acetic acid;
2-[(R)-2-(2-phenyl-7-(tetrahydropyran-4-yl)methylamino-lH-indol-5-yl)-4,5- dihydro-thiazol-4-yl]-acetic acid;
3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid methyl ester; 3-(7-Cyclopentylamino-5-chloro-lH-indol-2-yl)-benzoic acid;
[3-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-methanol;
{3-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]-phenyl}-methanol;
2-{3-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]-phenyl}- acetic acid; 2-[3-(5-Chloro-7-cyclopentylamino-l-H-indol-2-yl)-phenyl]-acetic acid;
2- {3-[5-Chloro-7-(tetrahydropyran-4-yl)amino- 1 H-indol-2-yl] -phenyl} -acetic acid;
2-{3-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]-phenyl}- acetic acid methyl ester; 2-[3-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-acetic acid methyl ester;
2-{3-[5-Chloro-7-(tetrahydropyran-4-yl)amino)-lH-indol-2-yl]-phenyl}-acetic acid methyl ester;
[2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-methanol; 2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid;
2-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid methyl ester;
[4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-phenyl]-methanol;
2- {4-[5-Chloro-7-(tetrahydropyran-4-yl)amino- 1 H-indol-2-yl]phenyl} -ethanol; 4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)-benzoic acid;
2-{4-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]phenyl}- acetic acid;
2-[4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)phenyl]-acetic acid;
2-{4-[5-Chloro-7-(tetrahydropyran-4-yl)amino-lH-indol-2-yl]phenyl}-acetic acid;
4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)benzoic acid methyl ester;
4-(7-Cyclopentylamino-5 -methyl- lH-indol-2-yl)benzoic acid methyl ester;
2-{4-[5-Chloro-7-(tetrahydropyran-4-ylmethyl)amino-lH-indol-2-yl]phenyl}- acetic acid methyl ester; 2-[4-(5-Chloro-7-cyclopentylamino-lH-indol-2-yl)phenyl]acetic acid methyl ester;
2- {4-[5-Chloro-7-(tetrahydropyran-4-yl)amino- 1 H-indol-2-yl]phenyl} -acetic acid methyl ester;
[5-Chloro-2-(3-dimethylaminoethylphenyl)-lH-indol-7-yl]-(tetrahydropyran-4- yl)-amine;
[5-Chloro-2-(3-morpholin-4-ylmethylphenyl)-lH-indol-7-yl]-(tetrahydropyran- 4-yl)-amine;
[5 -Chloro-2-(3 -pyrrolidin-4-ylmethylphenyl)- 1 H-indol-7-yl] -(tetrahydropyran- 4-yl)-amine; l-{4-[3-(5-Chloro-7-tetrahydropyran-4-ylamino-lH-indol-2-yl)-benzyl]- piperazin- 1 -yl} -ethanone;
{5-Chloro-2-[3-(2-oxo-piperazin-4-yl)ethylphenyl]-lH-indol-7-yl}- (tetrahydropyran-4-yl)-amine; {5-Chloro-2-[3-(l,l-dioxo-thiomorpholin-4-yl)ethylphenyl]-lH-indol-7-yl}-
(tetrahydropyran-4-yl)-amine;
Cyclopentyl-(lH-indazol-7-yl)-amine; (Tetrahydropyran-4-yl)-( 1 H-indazol-7-yl)-amine; Cyclopentyl-(5 -methyl- 1 H-indazol-7-yl)-amine; (5 -Methyl- 1 H-indazol-7-yl)-(tetrahydropyran-4-yl)-amine;
Cyclopentyl-[3-(4-methoxyphenyl)-lH-indazol-7-yl)-amine; [3-(4-Methoxyphenyl)-lH-indazol-7-yl)]-(tetrahydropyran-4-yl)-amine; [3-(4-Methoxyphenyl)-lH-indazol-7-yl)-(tetrahydropyran-4-ylmethyl)-amine; (Tetrahydropyran-4-yl)-[5-(l , 1 -dioxo-thiomorpholin-4-yl)methyl-3-phenyl-2- trimethylsilyl- 1 H-indol-7-yl)-amine;
(Tetrahydropyran-4-yl)- [ 5 -( 1 , 1 -dioxo-thiomorpholin-4-yl)methyl-3 -phenyl- IH- indol-7-yl)-amine; and
(Tetrahydropyran-4-yl)-[3-bromo-5-(moφholin-4-yl)methyl-2-phenyl-lH-indol- 7-yl]-amine.
[Claim 25]
A composition for the prevention or treatment of necrosis and necrosis- associated diseases, which comprises therapeutically-effective amount of the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as defined in Claim 1 as an active ingredient together with pharmaceutically acceptable carriers or diluents.
[Claim 26]
The composition of Claim 25 wherein necrosis and necrosis-associated diseases are selected from the group consisting of acute/chronic hepatic disease, neurodegenerative disease, ischemic disease, diabetes, pancreatitis, bacterial/viral sepsis, necrotizing procolitis, cystic fibrosis, rheumatoid arthritis, degenerative arthritis, nephropathy, bacterial infection, viral infection, multiple sclerosis, leukemia, lymphoma, neonatal respiratory distress syndrome, asphyxia, tuberculosis, endometriosis, angiasthenia, psoriasis, chilblain, steroid treatment complications, gangrene, pressure sores, hemoglobinuria, burns, hyperthermia, Crohn's disease, celiac disease, compartment syndrome, spiral cord injury, glomerulonephritis, muscular dystrophy, metabolic inherited disease, mycoplasmal disease, anthrax, Andersen's disease, congenital mitochondrial disease, phenylketonuria, placental infarction, syphilis, and aseptic necrosis.
[Claim 27]
The composition of Claim 25 wherein necrosis and necrosis-associated diseases are caused by drugs and toxic substances and are selected from the group consisting of the necrosis associated with alcoholism, the exposure to, or administration or self- administration of, cocaine, drugs, antibiotics, anti-cancer agent, adriamycin, puromycin, bleomycin, NSAID, cyclosporins, chemical toxins, poison gas, agrochemicals, heavy metals, or injury due to the exposure to radioactivity/UV and associated necrosis thereof.
[Claim 28]
The composition of Claim 25 which is for hepatoprotection, hepatic functional improvement, and prevention or treatment of hepatic disease.
[Claim 29]
The composition of Claim 28 wherein the hepatic disease is selected from the group consisting of liver transplantation, alcoholic or non-alcoholic fatty liver, hepatic fibrosis, hepatocirrhoisis and hepatitis caused by virus or drugs.
[Claim 30]
The composition of Claim 28 wherein the hepatic disease is alcoholic acute/ chronic hepatic disease.
[Claim 31 ]
The composition of Claim 28 wherein the hepatic disease is fatty acid-induced fatty liver or acute/chronic hepatic disease derived from fatty liver.
[Claim 32]
The composition of Claim 28 wherein the hepatic disease is mediated by reactive oxygen species (ROS).
[Claim 33] The composition of Claim 28 wherein the hepatic disease is mediated by heavy metals.
[Claim 34]
The composition of Claim 25, which is co-administered with prophylactic or therapeutic agents for drug-derived necrosis and necrosis-associated diseases.
[Claim 35]
The composition of Claim 34 wherein the prophylactic or therapeutic agents for drug-derived necrosis and necrosis-associated diseases are selected from the group consisting of antibiotics, anti-cancer agents, anti-viral agents, anti-infectives, anti- inflammatory agents, anti-coagulants, lipid-improving agents, cell death inhibitors, anti- hypertensive agents, anti-diabetic/anti-obesity agents, therapeutic agents for cardiovascular disease, therapeutic agents for neurodegenerative disease, anti-aging agents, and therapeutic agents for metabolic disease.
[Claim 36] The composition of Claim 28, which is co-administered with agents selected from the group consisting of hepatocyte regeneration promoters, hepatic functional adjuvants, anti-viral agents, immunosuppressants, and fibrosis inhibitors.
[Claim 37]
The composition of Claim 26 wherein the neurodegenerative disease is dementia, Parkinson's disease, or Huntington's disease.
[Claim 38]
The composition of Claim 26 wherein the ischemic disease is cardiac disease, reperfusion injury, ischemic stroke, or ischemic injury.
[Claim 39] The composition of Claim 26 wherein the diabetes is caused by pancreatic cell destroying substances, diabetic complications, or diabetic vascular disease. [Claim 40]
The composition of Claim 39 wherein the diabetes is mediated by virus, hyperglycemia, fatty acid, diet, toxin, or streptozotocin. [Claim 41 ]
A method of preparing a composition for the prevention or treatment of necrosis and necrosis-associated diseases, which comprises the step of mixing the compounds of formula (1), pharmaceutically acceptable salts or isomers thereof as defined in Claim 1 as an active ingredient together with pharmaceutically acceptable carriers.
PCT/KR2008/004784 2007-08-17 2008-08-18 Indole and indazole compounds as an inhibitor of cellular necrosis WO2009025478A1 (en)

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DK08793298.4T DK2178870T3 (en) 2007-08-17 2008-08-18 INDOLE AND INDAZOLIC COMPOUNDS AS AN INHIBITOR OF CELLULAR NECROSE
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US12/671,038 US8436038B2 (en) 2007-08-17 2008-08-18 Indole and indazole compounds as an inhibitor of cellular necrosis
BRPI0814958A BRPI0814958B8 (en) 2007-08-17 2008-08-18 indole compounds, e, composition
ES08793298.4T ES2691068T3 (en) 2007-08-17 2008-08-18 Indole and indazole compounds as inhibitors of cell necrosis
MX2010000985A MX368368B (en) 2007-08-17 2008-08-18 Indole and indazole compounds as an inhibitor of cellular necrosis.
SI200831995T SI2178870T1 (en) 2007-08-17 2008-08-18 Indole and indazole compounds as an inhibitor of cellular necrosis
EP08793298.4A EP2178870B1 (en) 2007-08-17 2008-08-18 Indole and indazole compounds as an inhibitor of cellular necrosis
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