KR101825065B1 - Pharmaceutical composition for inducing the degradation of ALK protein and pharmaceutical composition for use in preventing or treating cancer containing the same as an active ingredient - Google Patents

Abstract

The present invention relates to a method for producing a drug that induces the degradation of ALK protein and a pharmaceutical composition for preventing or treating cancer comprising the same as an active ingredient. The compound represented by formula (1) according to the present invention comprises an inverse lymphoma kinase (ALK) Inhibit or decompose cancer cells, and thus are useful for the prevention and treatment of diseases associated with inverse-forming lymphoma kinase (ALK), for example, cancer.

Description

[0001] The present invention relates to a pharmaceutical composition for inducing the degradation of ALK protein and a pharmaceutical composition for preventing or treating cancer containing the same as an active ingredient. an active ingredient}

The present invention relates to a method for producing a drug that induces degradation of ALK protein and a pharmaceutical composition for preventing or treating cancers containing the same as an effective ingredient.

A recent research team at Yale University (Craig Crews) is developing a Proteolysis Targeting Chimera (PROTAC) technology and is working on applying it to various diseases. The above-described technique is under study for developing an anticancer agent using a PROTAC substance by linking an inhibitor or a binding agent binding to a specific protein and a ligand characteristic binding to E3 ubiquitin ligase with various kinds of linkers. Yale University team has produced polypeptides that bind to VHL (von Hippel-Lindau) E3 ubiquitin ligase for several years and have recently developed organic low-molecular materials through optimization studies of low-affinity polypeptides, and have combined with ERRa inhibitors ERRa-PROTAC substance significantly reduced ERRa protein in animal models.

In addition, a team at Harvard University (Bradner) succeeded in developing a substance that is effective in treating leukemia using a CRBN E3 ubiquitin ligase-bound thalidomide and a BRD4 inhibitor, the JQ1 compound.

Since the anticancer target therapeutic agent directly acts on the cancer-causing target, the side effect is less than that of the conventional cytotoxic therapeutic agent and the therapeutic effect is excellent. However, in order to inhibit the signal transmission of the target, a high inhibitory power to the target is required, In order to show the therapeutic effect, it is disadvantageous to administer a large amount of treatment for a long time. In addition, resistance to drugs rapidly develops, and drug resistance occurs within one year after administration, thereby lowering the effect of the drug. Therefore, there is a continuing need to develop new targets and develop therapeutic agents. On the other hand, since the proteolysis-inducing agent decomposes the protein causing the disease, resistance to the drug is low, and if the target protein can only bind to the target protein, the target protein can be degraded sufficiently, Is becoming popular as a technology that can be applied to undruggable targets.

Recently, anaplastic lymphoma kinase (ALK) has been found in several cancer cell tumors of the human body and has been studied as a target of target therapy. The carcinogenesis process of reversed lymphoma kinase (ALK) It is known to be due to the observed fusion gene of ALK-NPM (Nucleophosmin, nucleophosphin). When the inverse lymphoma kinase (ALK) is activated by the gene fusion, the tyrosine kinase behaves abnormally, and cancer is induced therefrom. In other words, an abnormally activated inverse lymphoma kinase (ALK) induces cell proliferation, prevents apoptosis, which is one of the ways of cell death, and prevents cell death, rearranges the cell skeleton, Transform the shape.

Cancer geneation of inverse lymphoma kinase (ALK) as described above is accomplished by interaction with a downstream molecule which is a target substance of inverse lymphoma kinase (ALK). Sub molecules are substances that mediate intracellular signal transduction. Inverse lymphoma kinase (ALK) is linked to other tyrosine kinases that are normal or cancer-genetically modified to interact or activate a variety of other pathways. In particular, the inverse Lymphoma kinase (ALK) gene in lung cancer cells is fused with EML4 (Echinoderm Microtubule-Associated Protein-Like 4) gene to produce active tyrosine kinase, EML4-ALK, It has been known that cancer mutations in EML4-reverse forming lymphoma kinase (ALK) are dependent on enzyme activity, and in addition, about 26% of the 491 neuroblastoma specimens have been reported for amplification of the inverse-forming lymphoma kinase (ALK) gene have. In addition, the inverse lymphoma kinase (ALK) gene can be used to detect a large number of B cells, such as large B-cell lymphoma, systemic albinism, inflammatory myoblastic sarcoma, esophageal squamous cell carcinoma, non-small cell lung carcinoma, rhabdomyosarcoma, myoblastoma, melanoma, In the rare disease of inflammatory myeloid fibroblastoma, several types of inverse lymphoma kinase (ALK) fusion proteins have been found to be expressed in hematopoietic cell tumors, suggesting that these fusion proteins are deeply involved in the development of tumors .

Thus, therapeutic agents targeting ALK-NPM for the treatment of cancer are being developed by blocking the activation pathway of inverse lymphoma kinase (ALK). Recently, Pfizer was developed as a selective inhibitor of cancer cell tumorigenic mutation. As a small molecule tyrosine kinase inhibitor, clitorotinib is an inhibitor of reversed-type lymphoma kinase (ALK) and is effective in the treatment of non-small cell lung cancer And has been approved as a new drug by the FDA in 2011. In addition, Novartis's LDK-378 (ceritinib) compound has been approved and clinical trials of a number of inverse-forming lymphoma kinase (ALK) inhibitors are underway. However, crytotinib showed drug resistance and various mutations within one year of administration. In LDK378, the activity of some resistant proteins is inhibited, but the activity of some mutant proteins including G1202R is weak.

Accordingly, the present inventors have developed a novel ALK-PROTAC substance by linking an ALK inhibitor, LDK378, with a VHL ligand or a CRBN ligand (thalidomide) through various linkers to decompose adipogenic lymphoma kinase (ALK) And can be useful as a preventive or therapeutic agent for cancer, and the present invention has been completed.

WO 2013/106643 A2

It is an object of the present invention to provide a compound useful as an active ingredient of a pharmaceutical composition for the prevention or treatment of an inverse lymphoma kinase (ALK) -related disease.

Another object of the present invention is to provide a process for producing the above compound.

It is still another object of the present invention to provide a pharmaceutical composition for preventing or treating a reversed-type lymphoma kinase (ALK) -related disease containing the above-mentioned compound as an active ingredient.

Another aspect of the present invention is to provide a pharmaceutical composition for preventing or treating cancer containing the above-mentioned compound as an active ingredient.

Another object of the present invention is to provide a health functional food for preventing or ameliorating an inverse-forming lymphoma kinase (ALK) -related disease containing the above-mentioned compound as an active ingredient.

In order to achieve the above object,

The present invention provides a compound represented by the following general formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof:

[Chemical Formula 1]

In Formula 1,

Linker is a linker having 3 to 20 linkages selected from the group consisting of - (CH ₂ ) -, - (C═O) -, -NH- and -O-,

The linking group can not be linked to -O- in succession; And

A is

or

to be.

The present invention also relates to a process for producing a compound represented by the formula (1)

A-H and a compound represented by Linker-X to prepare a compound represented by A-Linker-X (Step 1);

(Step 2) of preparing a compound represented by A-Linker-Y represented by A-Linker-X prepared in the step 1; And

Reacting a compound represented by A-Linker-Y prepared in Step 2 and a compound represented by Formula (2) to prepare a compound represented by Formula (1) (Step 3) Lt; RTI ID = 0.0 >

[Reaction Scheme 1]

In the above Reaction Scheme 1,

Linker, and A are the same as defined in Formula 1 above; And

If X and Y is X is -CO ₂ -tBu, Y is a -CO ₂ H, when X is Cl or Br, Y is I.

Further, the present invention provides a pharmaceutical composition for preventing or treating a reverse-forming lymphoma kinase (ALK) -related disease comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient .

The present invention also provides a pharmaceutical composition for preventing or treating cancer comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient.

Furthermore, the present invention provides a health functional food for preventing or ameliorating an adverse affliction lymphoma kinase (ALK) -related disease comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient .

The compound represented by the formula (1) according to the present invention can inhibit or degrade inverse lymphoma kinase (ALK), and thus has a useful effect for the prevention and treatment of a disease associated with inverse lymphoma kinase (ALK), for example, cancer.

FIG. 1 is a graph showing the change in tumor volume after administering the compound of Example 3 of the present invention (three times a day, 50 mg / kg, for a total of 14 days) to H3122 xenograft SCID mice.

Hereinafter, the present invention will be described in detail.

The following description is provided to assist the understanding of the invention, and the present invention is not limited to the following description.

The present invention provides a compound represented by the following general formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof:

[Chemical Formula 1]

In Formula 1,

Linker is a linker having 3 to 20 linkages selected from the group consisting of - (CH ₂ ) -, - (C═O) -, -NH- and -O-,

The linking group can not be linked to -O- in succession; And

A is

or

to be.

Preferably,

The linker,

However,

Wherein a and i are independently 0 or 1 and can not be 0 at the same time;

B is an integer from 0 to 20;

Wherein c is 0 or 1;

D is an integer of 0-3;

E is 0 or 1;

F is an integer from 1 to 10;

G is 0 or 1;

H is an integer of 0-3;

J and k are independently an integer of 0-5.

More preferably,

The linker,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

or

to be.

Preferable examples of the compound represented by the formula (1) according to the present invention include the following compounds.

(1) 5- (4- (4- (5-chloro-4- (2- (isopropylsulfonyl) phenylamino) pyrimidin- 4-ylamino) butyl) -5- (4-fluoropyridin-2-yl) Oxopentanamide;

(2S, 4R) -1 - ((R) -2- (tert-butyl) -17- ) Pyrimidin-2-ylamino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -4,13,17-trioxo-6,9-dioxa-3,12- 1-oyl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(3) Synthesis of (2S, 4R) -1 - ((R) -2- (5- (4- (4- Methylphenyl) piperidin-l-yl) -5-oxopentanamido) -3,3-dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(4) Synthesis of 5- (4- (4- ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-ioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) pentanamide;

(5) Preparation of 5- (4- (4 - ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- amides;

(6) Synthesis of 2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) -2-oxoethoxy) -N- (2- (2,6- dioxopiperidin- 4-yl) acetamide;

(7) Synthesis of (2R, 4R) -1 - ((R) -2- (5- (4- (4- Methylphenyl) piperidin-1-yl) pentanamido) -3,3-dimethylbutanoyl) -4-hydroxy-N- (4 - (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(8) 7- (4- (4- ((2- (Isopropylsulfonyl) phenyl) amino) pyrimidin-2- yl) amino) -5-isopropoxy- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1, 3- diolisoisoindol- amides;

(9) Synthesis of (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) ethoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(10) Synthesis of (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1- yl) butoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(11) Synthesis of (2S, 4R) -1 - ((R) -2- (7- (4- (4- Methylphenyl) piperidin-l-yl) -7-oxoheptanamido) -3,3-dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(12) 2- (2- (2- (2- (isopropylsulfonyl) phenyl) amino) pyrimidin-2-yl) amino Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) - 1,3-dioxoisoindolin-4-yl) acetamide;

(13) Synthesis of 2- (4- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin- 1 -yl) butoxy) -N- (2- (2,6- dioxopiperidin-3-yl) -1,3-dioxoisoindolin- ) Acetamide;

(14) 2- (2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxo 4-yl) acetamide;

(15) 2- (2- (4- (4 - ((5-Chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) ethoxy) -N- (2- (2,6-dioxopiperidin- ) Acetamide;

(16) Synthesis of (2S, 4R) -1 - ((R) -1- (4- (4- -Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -14,14- dimethyl- 11-oxo-3,6,9- trioxa-12- azapentadecanecarbo Yl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(17) Synthesis of 6- (4- (4 - ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) hexanamide;

(18) Synthesis of (2R, 4S) -1 - ((S) -2- (6- (4- (4- Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -6- oxohexanamido) -3,3- dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(19) Synthesis of (2R, 4S) -1 - ((S) -2- (2- (3- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) propoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;

(20) 2- (3- (4- (4- ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) propoxy) -N- (2- (2,6-dioxopiperidin- ) Acetamide; And

(21) Synthesis of (2R, 4S) -1 - ((R) -2- (2- (5- (4- (4- ) Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) pentyl) oxy) acetamido) -3,3- -Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide.

The compound represented by the formula (1) of the present invention can be used in the form of a pharmaceutically acceptable salt, and as the salt, an acid addition salt formed by a pharmaceutically acceptable free acid is useful. Acid addition salts include those derived from inorganic acids such as hydrochloric acid, nitric acid, phosphoric acid, sulfuric acid, hydrobromic acid, hydroiodic acid, nitrous acid, phosphorous acid and the like, aliphatic mono- and dicarboxylates, phenyl-substituted alkanoates, Derived from organic acids such as acetic acid, benzoic acid, citric acid, lactic acid, maleic acid, gluconic acid, methanesulfonic acid, 4-toluenesulfonic acid, tartaric acid, fumaric acid and the like. Examples of such pharmaceutically innocuous salts include, but are not limited to, sulfate, pyrosulfate, bisulfate, sulfite, bisulfite, nitrate, phosphate, monohydrogenphosphate, dihydrogenphosphate, metaphosphate, pyrophosphate chloride, bromide, But are not limited to, but are not limited to, but are not limited to, but are not limited to, but are not limited to, halides, halides, halides, halides, halides, halides, But are not limited to, lactose, sebacate, fumarate, maleate, butyne-1,4-dioate, hexane-1,6-dioate, benzoate, chlorobenzoate, methylbenzoate, dinitrobenzoate, Methoxybenzoate, phthalate, terephthalate, benzene sulfonate, toluene sulfonate, chloro Such as benzenesulfonate, benzenesulfonate, xylenesulfonate, phenylacetate, phenylpropionate, phenylbutyrate, citrate, lactate,? -Hydroxybutyrate, glycolate, maleate, tartrate, methanesulfonate, propanesulfonate, naphthalene- 1-sulfonate, naphthalene-2-sulfonate, mandelate and the like.

The acid addition salt according to the present invention can be prepared by a conventional method, for example, by dissolving the derivative of Chemical Formula 1 in an organic solvent such as methanol, ethanol, acetone, dichloromethane, acetonitrile and the like, Followed by filtration and drying, or by distillation of the solvent and excess acid under reduced pressure, followed by drying and crystallization in an organic solvent.

In addition, bases can be used to make pharmaceutically acceptable metal salts. The alkali metal or alkaline earth metal salt is obtained, for example, by dissolving the compound in an excess amount of an alkali metal hydroxide or an alkaline earth metal hydroxide solution, filtering the insoluble compound salt, and evaporating and drying the filtrate. At this time, it is preferable for the metal salt to produce sodium, potassium or calcium salt. In addition, the corresponding salt is obtained by reacting an alkali metal or alkaline earth metal salt with a suitable salt (such as silver nitrate).

Furthermore, the present invention encompasses the compounds represented by the formula (1) and pharmaceutically acceptable salts thereof as well as solvates, optical isomers and hydrates thereof which can be prepared therefrom.

The present invention also relates to a process for producing a compound represented by the formula (1)

A-H and a compound represented by Linker-X to prepare a compound represented by A-Linker-X (Step 1);

(Step 2) of preparing a compound represented by A-Linker-Y represented by A-Linker-X prepared in the step 1; And

Reacting a compound represented by A-Linker-Y prepared in Step 2 and a compound represented by Formula (2) to prepare a compound represented by Formula (1) (Step 3) Lt; RTI ID = 0.0 >

[Reaction Scheme 1]

In the above Reaction Scheme 1,

Linker, and A are the same as defined in Formula 1 above; And

If X and Y is X is -CO ₂ -tBu, Y is a -CO ₂ H, when X is Cl or Br, Y is I.

Hereinafter, the process for preparing the compound represented by the formula (1) according to the present invention will be described in detail.

In the process for preparing a compound represented by the formula (1) according to the present invention, the above step 1 is a step of reacting a compound represented by AH with a compound represented by Linker-X to prepare a compound represented by A-Linker-X to be.

At this time, this step may be considered as a step of introducing a linker, and is not particularly limited as long as it is a method for introducing a linker that can be used in the field. For example, a method using a protecting group, There is a method of introducing the data. As a more specific example, the method described in the production method of the compound of the example of the present invention may be used, and the method may be modified or applied.

In addition, H ₂ O, ethanol, tetrahydrofuran (THF), dichloromethane, toluene, acetonitrile, dimethylformamide and the like can be used as the solvent in the above step, and dichloromethane can be preferably used.

The reaction temperature in the above step is not particularly limited, but it is preferably carried out at a boiling point of the solvent at 20-90 ° C, and the reaction time is not particularly limited, but it is preferable to carry out the reaction for 0.5-20 hours.

In the process for preparing the compound represented by the formula (1) according to the present invention, the step (2) is a step of preparing the compound represented by A-Linker-Y prepared in the above step 1 as A-Linker-Y .

At this time, the above step is a step of removing the protecting group and a step of replacing Cl or Br at the terminal with I. As a more specific example, the method described in the production method of the compound of the example of the present invention may be used, and the method may be modified or applied.

In the process for preparing the compound represented by the formula (1) according to the present invention, the step 3 is a step of reacting the compound represented by A-Linker-Y prepared in the above step 2 with the compound represented by the formula (2) Is prepared.

At this time, the above step is a step of linking the compound represented by the formula (2) with the A-Linker prepared in step 2, which can bind to and inhibit the inverse lymphoma kinase (ALK).

The compound represented by Formula 2 may be applied to the method of the present invention as long as it is a compound capable of binding or inhibiting reverse forming lymphoma kinase (ALK), and the compound represented by A of the present invention and the linker And can inhibit or degrade inverse lymphoma kinase (ALK). Herein, the compound represented by A has a characteristic of forming a bond with an enzyme capable of degrading the inverse Lymphoma kinase and inducing the degradation of LPS kinase.

The compound represented by A, as shown in Formula 1 of the present invention,

or

And those skilled in the art can similarly apply modifications or applications.

In addition, H ₂ O, ethanol, tetrahydrofuran (THF), dichloromethane, toluene, acetonitrile, dimethylformamide and the like can be used as the solvent in the above step, and dichloromethane can be preferably used.

The reaction temperature in the above step is not particularly limited, but it is preferably carried out at a boiling point of the solvent at 20-90 ° C, and the reaction time is not particularly limited, but it is preferable to carry out the reaction for 0.5-20 hours.

In the method for preparing a compound represented by the general formula (1) according to the present invention, the steps 1 to 3 may be carried out mutually or may be carried out by a method in which a linker is divided and introduced.

For example, the preparation method represented by the above-mentioned Scheme 1 can be carried out by introducing a linker to a compound represented by AH and then reacting with a compound represented by the formula 2 to prepare a compound represented by the formula 1, For example, a linker may be first introduced into the compound represented by Formula 2, a linker may be introduced into the compound represented by A, and then the compound represented by Formula 1 may be prepared.

More precisely, the method of preparing the compound represented by the following Example 1 can be exemplified, and can be carried out as shown in the following Reaction Scheme 2.

[Reaction Scheme 2]

Referring to Reaction Scheme 2,

The compound of Example 1,

Introducing a linker into the compound represented by Formula 2 and the compound represented by A, respectively, (Step 1) and

It is confirmed that the respective compounds prepared in the step 1 are reacted with each other to prepare the compound of Example 1 (step 2).

As described above, the process for preparing the compound represented by the formula (1) according to the present invention can be carried out according to the reaction scheme 1 or the scheme 2, and the process can be carried out by modifying or modifying the process.

Further, the present invention provides a pharmaceutical composition for preventing or treating an inverse-forming lymphoma kinase (ALK) -related disease comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient .

Herein, inverse lymphoma kinase (ALK) -related diseases include, but are not limited to, all diseases that can be expressed from inverted lymphoma kinase (ALK). In particular, examples of degenerative lymphoma kinase (ALK) -related diseases include cancers, which, when they are derived from inverted lymphoma kinase (ALK) in association with cell proliferation of cancer cells, include compounds of the present invention, optical isomers thereof, Acceptable salts inhibit or degrade inverse lymphoma kinase (ALK) and may be useful in the prevention or treatment of diseases referred to as inverse lymphoma kinase (ALK) -related diseases.

The present invention also provides a pharmaceutical composition for preventing or treating cancer comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient.

Herein, the compound may be characterized by inhibiting or decomposing the inverse lymphoma kinase (ALK) to prevent or treat cancer. The cancer may be, for example, colon cancer, liver cancer, stomach cancer, breast cancer, colon cancer, Pancreatic cancer, pancreatic cancer, head or neck cancer, uterine cancer, ovarian cancer, rectal cancer, esophageal cancer, small intestine cancer, perianal cancer, colon cancer, fallopian tube carcinoma, endometrial carcinoma, cervical cancer, vaginal carcinoma, vulvar carcinoma, Kidney cancer, ureter cancer, kidney cell carcinoma, renal pelvic carcinoma, central nervous system tumor, and leukemia.

Further, the present invention provides a health functional food for preventing or ameliorating an inverse-forming lymphoma kinase (ALK) -related disease comprising the compound represented by the formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient .

Herein, the inverse lymphoma-related kinase (ALK) -related disease includes, for example, colon cancer, liver cancer, stomach cancer, breast cancer, colon cancer, bone cancer, pancreatic cancer, head or neck cancer, uterine cancer, ovarian cancer, rectal cancer, Cancer, colon cancer, fallopian tube carcinoma, endometrial carcinoma, cervical cancer, vaginal carcinoma, vulvar carcinoma, Hodgkin's disease, prostate cancer, bladder cancer, renal cancer, ureter cancer, renal cell carcinoma, renal pelvic carcinoma, central nervous system tumor and leukemia One or more selected from the group consisting of

The compound of formula (I) according to the present invention may be administered orally or parenterally in a variety of formulations at the time of clinical administration. In the case of formulation, the compound of the present invention may be used as a filler, an extender, a binder, a wetting agent, a disintegrant, Diluents or excipients.

Solid formulations for oral administration include tablets, pills, powders, granules, capsules, troches, and the like, which may contain one or more excipients such as starch, calcium carbonate, Sucrose, lactose, gelatin or the like. In addition to simple excipients, lubricants such as magnesium stearate talc are also used. Liquid preparations for oral administration include suspensions, solutions, emulsions or syrups. Various excipients such as wetting agents, sweeteners, fragrances, preservatives and the like are included in addition to commonly used simple diluents such as water and liquid paraffin. .

Formulations for parenteral administration include sterilized aqueous solutions, non-aqueous solutions, suspensions, emulsions, freeze-dried preparations, suppositories, and the like. Examples of the non-aqueous solvent and suspending agent include propylene glycol, polyethylene glycol, vegetable oil such as olive oil, injectable ester such as ethyl oleate, and the like. As a base for suppositories, witepsol, macrogol, tween 61, cacao paper, laurin, glycerol, gelatin and the like can be used.

The effective dose of the compound of the present invention on the human body may vary depending on the age, weight, sex, dosage form, health condition and disease severity of the patient, and is generally about 0.001-100 mg / kg / 0.0 > mg / kg / day. ≪ / RTI > It is generally from 0.07 to 7000 mg / day, preferably from 0.7 to 2500 mg / day, based on adult patients weighing 70 kg, and may be administered once a day It may be divided into several doses.

The compounds according to the present invention were found to have ALK protein inhibitory activity, degradative activity, and cancer growth inhibitory activity.

First, was a result of performing the ALK protein inhibitory activity evaluation test of the compounds according to the invention, ALK inhibitory activity IC ₅₀ values of Examples 1 to 16 The compounds according to the present invention appeared to nanomolar concentrations of 10 to 150, which , The compounds of the present invention were found to excellently inhibit the ALK protein.

In addition, the compounds of Examples 1 to 16 according to the present invention were able to degrade ALK protein at a concentration of 300 nM, and in particular, the compounds of Examples 3, 4, 10 and 11 showed a decomposition activity of more than 50% at a concentration of 300 nM.

Therefore, the compound of the present invention can excellently degrade the ALK protein at a concentration of nano-mol units, and thus it can be effectively used for the prevention and treatment of ALK-related diseases.

Further, as a result of conducting an experiment to evaluate the cancer growth inhibitory activity of the compounds according to the present invention, it was found that the SCID mouse administered with the compound of Example 3 according to the present invention had a tumor size It can be confirmed that it is maintained or decreased. Therefore, the compound according to the present invention was confirmed to have cancer growth inhibitory activity as confirmed in Experimental Example 3, and it was judged that the compound could be useful for prevention and treatment of cancer as a pharmaceutical composition containing the compound.

Hereinafter, the present invention will be described in detail with reference to Examples and Experimental Examples.

However, the following examples and experimental examples are illustrative of the present invention, and the present invention is not limited thereto.

< Example  2-ylamino) -5-isopropoxy-2-methylphenyl) piperidine &lt; / RTI &gt; 1-yl) -N- (4- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-ylamino) butyl) Preparation of pentanamide

Step 1: tert -Butyl 4- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-ylamino) butylcarbamate &lt; / RTI &gt;

1,3-dione (20 mg, 0.072 mmol) was dissolved in dimethylformamide (0.5 mL), and the mixture was stirred at &lt; RTI ID = 0.0 &gt; (14 uL, 0.072 mmol) and diisopropylethylamine (21 uL, 0.144 mmol) were mixed and heated at 90 占 폚 for 12 hours. After the reaction was completed, the temperature was lowered to room temperature, diluted with ethyl acetate, and washed with water and brine. The residue of the organic layer was dried over anhydrous magnesium sulfate, filtered and concentrated, and then purified to obtain the desired compound (51%, green gel).

^{1 H NMR (300 MHz, CDCl} 3) δ 8.26 (s, 1H), 7.50 (t, J = 7.8 Hz, 1H), 7.11 (d, J = 7.1 Hz, 1H), 6.90 (d, J = 8.5 Hz (M, 1H), 3.62 (q, J = 6.3 Hz, 2H), 3.26-3.15 (m, 2H), 2.95-2.69 (m, 3H), 2.22-2.11 (m, 1H), 1.77-1.57 (m, 4H), 1.46 (s, 9H). LC / MS (ESI) m / z 445 [M + H] &lt; ^{+ &}

step 2: 4 -(4- Aminobutylamino ) -2- (2,6- Dioxopiperidine -3 days) Isoindoline -1,3-dione hydrochloride

The compound (81 mg, 0.182 mmol) prepared in the above step 1 was dissolved in dichloromethane (1 mL), 1,4-dioxane solution (4 mL) containing 4 N hydrochloric acid was added, and the mixture was stirred at room temperature . After the reaction was completed, the reaction solution was concentrated under reduced pressure to obtain the target compound, and the obtained compound was used in the next step without further purification.

step 3: 5 - (4- (4- (5- Chloro -4- (2- ( Isopropylsulfonyl ) Phenylamino ) Pyrimidin-2-ylamino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -5-oxopentanoic acid

5-Chloro -N ² - (2- isopropoxy-5-methyl-4- (piperidin-4-yl) phenyl) -N ⁴ - (2- (isopropylsulfonyl) phenyl) pyrimidine -2 , 4-diamine (LDK378, 0.5 g, 0.9 mmol) and glutaric anhydride (0.112 g, 9.85 mmol) were dissolved in dichloromethane (5 mL), tetraethylamine (0.151 mL, 1.08 mmol) (N, N-dimethylamino) pyridine was added, and the mixture was stirred at room temperature for 6 hours. After completion of the reaction, the reaction product was diluted with dichloromethane and then washed with water, saturated ammonium chloride aqueous solution and brine. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure to give the desired compound (0.5 g, white solid).

^{1 H NMR (300 MHz, CDCl} 3) δ 9.56 (s, 1H), 8.59 (d, J = 8.3 Hz, 1H), 8.16 (s, 1H), 7.98 (d, J = 7.3 Hz, 1H), 7.95 (d, J = 8.0, 1.4 Hz, IH), 7.74 (s, IH), 7.69-7.54 (m, IH), 7.32-7.23 (M, 1H), 2.92 (t, &lt; RTI ID = 0.0 &gt; 2H), 1.85 (s, 2H, J = 12.1 Hz, 1 H), 2.67 (t, J = 11.8 Hz, 1H), 2.58-2.44 ), 1.70-1.52 (m, 2H), 1.42-1.27 (m, 12H); LC / MS (ESI) m / z 672.2 [M + H] &lt; ^{+ &}

Step 4: Preparation of 5- (4- (4- (5-chloro-4- (2- (isopropylsulfonyl) phenylamino) pyrimidin- 4-ylamino) butyl) -5- (4-fluoropyridin-2-yl) Preparation of oxopentanamide

The compound (20 mg, 0.031 mmol) obtained in the above step 3 was dissolved in dichloromethane (1 mL), and the compound (11.8 mg, 0.031 mmol), benzotriazol-1-yloxy) tri Pyrrolidinophosphonium hexafluorophosphate (16.1 mg, 0.031 mmol) and triethylamine (11 uL, 0.078 mmol) were added thereto, followed by stirring at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

LC / MS (ESI) m / z 998.2 [M + H] &lt; ^{+ &}

< Example  (2S, 4R) -1 - ((R) -2- (tert-butyl) -17- Ylamino) -5-isopropoxy-2-methylphenyl) piperidin-1-yl) -4,13,17-trioxo-6,9-dioxa-3,12-diaza Preparation of 4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1: tert - (2- (2- (4- (4-methylthiazol-5-yl) benzylcarbamoyl) Pyrrolidin-1-yl) -3,3-dimethyl-1-oxobutan-2-ylamino) -2-oxoethoxy) ethoxy) ethylcarbamate

(2R, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4- (0.42 g, 1.187 mmol) was dissolved in N, N-dimethylformamide (5 mL), and 2,2-dimethyl-4-oxo-3,8,11-trioxa- 5-aziridecane-13-oxacic acid (0.275 mg, 1.187 mmol), 1- [bis (dimethylamino) methylene] -1H-1,2,3-triazolo [4,5- b] pyridinium 3- (0.496 g, 1.3 mmol) and diethylisopropylethylamine (0.83 mL, 4.75 mmol) were added thereto, followed by stirring at room temperature. The reaction is terminated, the reaction is diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and purified to give the desired compound (0.54 g, yellow oil).

LC / MS (ESI) m / z 676 [M + H] &lt; ^{+ &}

Step 2: (2S, 4R) -1 - ((R) -2- (2- (2- (2-Aminoethoxy) ethoxy) acetamido) -3,3- Preparation of hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide hydrochloride

The compound (0.54 g, 0.799 mmol) prepared in the above Step 1 was dissolved in dichloromethane (5 mL), 1,4-dioxane (4 mL) containing 4 N hydrochloric acid was added, and the mixture was stirred at room temperature. The reaction was terminated and the reaction product was concentrated under reduced pressure to give the desired compound.

LC / MS (ESI) m / z 612 [M + H] &lt; ^{+ &}

Step 3: (2S, 4R) -1 - ((R) -2- (tert- ) Pyrimidin-2-ylamino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -4,13,17-trioxo-6,9-dioxa-3,12- Preparation of 4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

2-ylamino) -5-isopropoxy-2-methylphenyl) piperidine-l- 5-oxopentanoic acid (10 mg) was dissolved in dichloromethane (1 mL), and the compound (8 mg), benzotriazol-1-yloxy) tripyrrolidino Phosphonium hexafluorophosphate (7.4 mg) and diisopropylethylamine (9.1 uL) were added thereto, followed by stirring at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the desired compound (12 mg, white solid).

LC / MS (ESI) m / z 1231 [M + H-15] &lt; ^{+ &}

< Example  3> Preparation of (2S, 4R) -1 - ((R) -2- (5- (4- (4- Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -5-oxopentanamido) -3,3- dimethylbutanoyl) -4-hydroxy-N - (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Amino) -5-isopropoxy-2-methylphenyl) - &lt; / RTI & Amino-3, &lt; RTI ID = 0.0 &gt; 3- (2- Benzyl) pyrrolidine-2-carboxamide hydrochloride (7 mg), benzotriazol-1-yloxy (7.4 mg) and diisopropylethylamine (9.1 uL) were added to the solution, and the mixture was stirred at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound (14 mg, white solid).

LC / MS (ESI) m / z 1084.0 [M + H] &lt; ^{+ &}

< Example  Amino] pyrimidin-2-yl) amino) -5-isopropoxy-2- (isopropylsulfonyl) Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) pentanamide

step 1: 5 - Broo -N- (2- (2,6- Moving Sphypperidin Yl) -1,3- Dioxoisoindoline -4-yl) pentanamide &lt; / RTI &gt;

1,3-dione (0.1 g, 0.37 mmol) was dissolved in tetrahydrofuran (2 mL), and 5-bromo Pentanyl chloride (0.049 mL, 0.37 mL) was added and the mixture was heated to reflux for 4 hours. The reaction was terminated, and the reaction product was concentrated under reduced pressure and purified by separation and purification.

^{1 H NMR (300 MHz, DMSO} ) δ 11.16 (s, 1H), 9.73 (s, 1H), 8.46 (d, J = 8.4 Hz, 1H), 5.15 (m, 1H), 3.58 (t, J = 6.5 1H), 1.97-1.82 (m, 2H), 1.82-1.67 (m, 2H), 3.02-2.80 (m, 2H), 2.69-2.54 (m, 3H), 2.14-1.99

Step 2: Preparation of 5- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-1-yl) -N- (2- (2,6-ioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) pentanamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 20 mg, 0.036 mmol) was dissolved in N, N-dimethylformamide (2 mL) and 5-bromo-N- (2- Dioxoisoindolin-4-yl) pentanamide (15.6 mg, 0.036 mmol) and diisopropylethylamine (16 uL, 0.09 mmol) were added thereto, followed by stirring at 90 占 폚. The reaction product was concentrated under reduced pressure and purified to obtain the target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 9.52 (s, 1H), 9.45 (s, 1H), 8.82 (d, J = 8.5 Hz, 1H), 8.60 (d, J = 8.4 Hz, 1H), 8.53 (s, IH), 8.18 (s, IH), 8.02 (s, IH), 8.01-7.92 (m, IH), 7.74 (t, J = 7.9 Hz, IH), 7.67-7.49 2H), 3.32-3.24 (m, 1H), 4.60 (brs, 1H), 3.32-3.25 (m, 2H), 2.89-2.71 (m, 4H), 2.63-2.53 (m, 3H), 2.26-2.14 J = 6.0 Hz, 6H), 1.33 (d, J = 6.8 Hz, 6H).

< Example  Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2- (4-fluoro- Methylphenyl) piperidin-1-yl) -N- (2- (2,6-ioxopiperidin-3- yl) -1,3-dioxoisoindolin-4-yl) -5-oxopentanamide Manufacturing

step 1: 5 - ((2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-yl) amino) -5-oxopentanoic acid

1,3-dione (0.1 g, 0.37 mmol) was dissolved in acetic acid (2 mL), and dihydro-2H-pyran -2,3 (3H) -dione (0.23 g) and potassium acetate (0.108 g, 1.1 mmol) were added thereto, followed by stirring at 90 ° C for 2 hours. The reaction was terminated and the reaction was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, purified by separation, and the objective compound was prepared.

^{1 H NMR (300 MHz, DMSO} ) δ 11.14 (s, 1H), 9.72 (s, 1H), 8.44 (d, J = 8.4 Hz, 1H), 7.90 - 7.78 (m, 1H), 7.62 (d, J = 7.2 Hz, 1H), 5.15 (dd, J = 12.8, 5.4 Hz, 1H), 2.98-2.83 (m, 1H), 2.67-2.53 , 2.24 (t, J = 7.4 Hz, 2H), 2.13-2.00 (m, 1H), 1.92-1.76 (m, 2H), 1.76-1.63 (m, 1H).

Step 2: Preparation of 5- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- Preparation of amide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 14.4 mg, 0.026 mmol) was dissolved in dichloromethane (2 mL), and 5 - ((2- (2,6-dioxopiperidin- (10 mg, 0.031 mmol), diisopropyl (2-pyridyl) benzylamine, and diisopropylethylamine Ethylamine (6.7 uL, 0.039 mmol) was added thereto, followed by stirring at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 9.53 (s, 1H), 9.46 (s, 1H), 8.83 (d, J = 8.5 Hz, 1H), 8.73 (s, 1H), 8.59 (d, J = 1H), 7.66-7.59 (m, 2H), 7.72 (t, J = 7.9 Hz, 1H), 7.54 (d, J = 7.3 Hz, 1H), 7.27 (t, J = 7.5 Hz, 1H), 6.71 ), 4.60-4.52 (m, 1H), 4.04 (d, J = 13.2 Hz, 1H), 3.33-3.23 2H), 2.87-2.74 (m, 2H), 2.70-2.60 (m, 3H), 2.54 (t, J = 7.1 Hz, 2H) (t, J = 14.1 Hz, 2H), 1.65-1.52 (m, 2H), 1.40-1.35 (m, 6H), 1.33 (d, J = 6.8 Hz, 6H). LC / MS (ESI) m / z 927 [M + H] &lt; ^{+ &}

< Example  6) Preparation of 2- (2- (4- (4 - ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -2-methylphenyl) piperidin-1-yl) -2-oxoethoxy) -N- (2- (2,6-dioxopiperidin- 4-yl) acetamide

step 1: 2 - (2 - ((2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline 4-yl) amino) -2-oxoethoxy) acetic acid

1,3-dione (0.1 g, 0.37 mmol) was dissolved in acetic acid (2 mL), 1,4-dioxane -2,6-dione (0.21 g, 1.83 mmol) and potassium acetate (0.108 g, 1.1 mmol), followed by stirring at 90 ° for 12 hours. The reaction was terminated and the reaction was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and purified by separation and purification to give the desired compound (55 mg, ivory solid).

^{1 H NMR (300 MHz, DMSO} ) δ 11.14 (s, 2H), 10.61 (s, 2H), 8.68 (d, J = 8.4 Hz, 2H), 7.87 (t, J = 7.9 Hz, 2H), 7.63 ( 4H), 3.17 (s, 2H), 3.00-2.79 (m, 2H), 5.16 (dd, J = , 3H), 2.70-2.52 (m, 4H), 2.17-2.01 (m, 2H).

Step 2: Preparation of 2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) -2-oxoethoxy) -N- (2- (2,6- iodopyrimidin- Yl) acetamide &lt; / RTI &gt;

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 20 mg, 0.036 mmol) was dissolved in dichloromethane (2 mL) to give 2- (2 - ((2,6-dioxopiperidin- (16 mg, 0.043 mmol), di (tert-butyldimethylsilyloxy) ethoxy) acetic acid (14 mg, 0.036 mmol), benzotriazol- Isopropylethylamine (9.4 uL, 0.054 mmol) was added thereto, followed by stirring at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 10.45 (s, 1H), 9.54 (s, 1H), 8.84 (d, J = 7.2 Hz, 1H), 8.60 (d, J = 8.3 Hz, 1H), 8.46 J = 7.7 Hz, 1H), 7.72 (d, J = 7.2 Hz, 1H), 7.64 (t, J = (D, J = 12.2 Hz, 1H), 7.58 (s, 2H), 7.28-7.21 1H), 4.62-4.54 (m, 1H), 4.47 (q, J = 14.2 Hz, 2H), 4.40-4.29 2H), 2.19 (s, 3H), 2.18-2.12 (m, 1H), 2.19-2.28 (m, 1.91-1.73 (m, 2H), 1.73-1.52 (m, 2H), 1.45-1.31 (m, 12H). LC / MS (ESI) m / z 927 [M + H] &lt; ^{+ &}

< Example  (7-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidine Methylphenyl) piperidin-1-yl) pentanamido) -3,3-dimethylbutanoyl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1: ( 2S, 4R ) -1 - ((R) -2- (5- Bromopentanamide ) -3,3- Dimethylbutane oil ) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

(2R, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4- 2-carboxamide hydrochloride was dissolved in dichloromethane, 5-bromo pentane oil chloride and diisopropylethylamine were added, and the mixture was stirred at room temperature. The reaction was terminated. The reaction mixture was diluted with dichloromethane, washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and purified by separation and purification.

^{1 H NMR (300 MHz, CDCl} 3) δ 8.68 (s, 1H), 7.39-7.29 (m, 4H), 6.11 (d, J = 8.7 Hz, 1H), 4.73 (t, J = 8.0 Hz, 1H) , 4.61-4.48 (m, 3H), 4.35-4.30 (m, 1H), 4.08 (d, J = 11 Hz, 1H), 3.71-3.64 (t, J = 6.5 Hz, 2H), 3.15-3.10 (m, 3H), 3.01 (s, 2H), 2.16-2.09 (m, 1H), 1.84-1.71 (m, 8H), 0.93 (s, 9H)

Step 2: (2R, 4R) -1 - ((R) -2- (5- (4- (4- Methylphenyl) piperidin-1-yl) pentanamido) -3,3-dimethylbutanoyl) -4-hydroxy-N- (4 - (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; (2S, 4R) -1 - ((R) -2- (5-bromopentanamido) - diamine (LDK378, 20 mg, 0.036 mmol) was dissolved in N, N- dimethylformamide Pyrrolidine-2-carboxamide (21 mg, 0.036 mmol), iodobutyric acid (2-amino-3-methylbenzyloxy) Sodium (5.4 mg, 0.036 mmol) and diisopropylethylamine (9.4 uL, 0.054 mmol) were added and stirred at 60 &lt; 0 &gt; C. The reaction mixture was concentrated under reduced pressure to remove N, N-dimethylformamide, diluted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure, followed by purification to obtain the target compound. LC / MS (ESI) m / z 1070 [M + H] &lt; ^{+ &}

< Example  Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2- (isopropylsulfonyl) Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-diolisoisoindolin-4-yl) -7-oxoheptanamide Manufacturing

Step 1: tert -Butyl 7 - ((2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-yl) amino) -7-oxoheptanoate

7-oxoheptanoic acid (0.174 g, 0.636 mmol) was dissolved in dichloromethane (1 mL), oxalyl chloride (0.381 mL, 4.45 mmol) and a drop of DMF were added, Lt; / RTI &gt; for 1 hour. The reaction mixture was concentrated under reduced pressure, and the residue was dissolved in tetrahydrofuran (3 mL). To the residue was added 4-amino-2- (2,6-dioxopiperidin-3-yl) isoindoline- mmol) was added and the mixture was heated to reflux. When the reaction was complete, it was diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified separately to give the desired compound (0.174 g).

^{1 H NMR (500 MHz, CDCl} 3) δ 9.43 (s, 1H), 8.86 (d, J = 8.5 Hz, 1H), 8.06 (s, 1H), 7.74 (t, J = 7.9 Hz, 1H), 7.57 (d, J = 7.3 Hz, 1H), 4.98 (dd, J = 12.4, 5.3 Hz, 1H), 2.96 2H), 1.72-1.63 (m, 2H), 1.51-1.40 (m, 2H), 2.26 (t, J = 7.4 Hz, 2H), 2.24-2.16 (m, 11 H).

step 2: 7 - ((2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-yl) amino) -7-oxoheptanoic acid

amino) -7-oxoheptanoate (0.174 g) was added to a solution of tert-butyl 7 - [(2- (2,6-dioxopiperidin- Was dissolved in 20% trifluoroacetic acid / dichloromethane solution (5 mL) and stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure to obtain the target compound, which was used in the next reaction without purification.

Step 3: Preparation of 7- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1, 3- diolisoisoindol- Preparation of amide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 20 mg, 0.0358 mmol) was dissolved in dichloromethane (2 mL), and 7 - ((2- (2,6-dioxopiperidin- 4-yl) amino) -7-oxoheptanoic acid (14.9 mg, 0.0358 mmol), benzotriazol-1-yloxy) tripyrrolidinophosphonium hexafluorophosphate (16.4 mg, 0.043 mmol) Ethylamine (9.4 uL, 0.054 mmol) was added thereto, followed by stirring at room temperature. When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 9.53 (s, 1H), 9.44 (s, 1H), 8.83 (d, J = 8.5 Hz, 1H), 8.70 (d, J = 7.0 Hz, 1H), 8.59 (d, J = 8.3 Hz, 1H), 8.18 (s, 1H), 8.02 1H), 7.58 (d, J = 7.3 Hz, 1H), 7.58 (d, J = 7.3 Hz, 1H) (M, 1H), 4.84 (d, J = 13.1 Hz, 1H), 4.59-4.49 J = 7.5 Hz, 2H), 2.42 (m, 2H), 2.85-2.73 (m, 2H), 2.70-2.60 2H), 1.65-1.44 (m, 4H), 1.41-1.35 (m, 6H), 2.27-2.15 1.33 (d, J = 6.8 Hz, 6H).

< Example  (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- ) Pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) ethoxy) acetamido) -3,3- -N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1: ( 2S, 4R ) -1 - ((R) -2- (2- (2- Chloroethoxy ) Acetamido ) -3,3- Dimethyl part Carbonyl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-

(2R, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4- 2-carboxamide hydrochloride (0.3 g, 0.697 mmol) was dissolved in dichloromethane (5 mL), and 2- (2-chloroethoxy) acetic acid (0.095 g, 0.697 mmol) Amino) methylene] -1H-1,2,3-triazolo [4,5-b] pyridinium 3-oxide hexafluorophosphate (0.291 g, 0.767 mmol), diisopropylethylamine mmol) was added thereto, followed by stirring at room temperature. The reaction was terminated, and the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and purified to give the desired compound (0.113 g).

¹ H NMR (300 MHz, CDCl ₃ )? 8.68 (s, 1H), 7.42-7.32 (m, 5H), 4.74 (t, J = 8.0 Hz, 1H), 4.61-4.46 2H), 3.67 (m, 2H), 3.67 (t, J = 5.1 Hz, 2H), 3.29 (s, 2H) (S, 3H), 3.01 (s, IH), 2.14-2.04 (m, IH), 1.87-1.79

step 2: N - (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoindoline -4-yl) -2- (4-iodobutoxy) acetamide

(2S, 4R) -1 - ((R) -2- (2- (2-Chloroethoxy) acetamido) -3,3- dimethylbutanoyl) -4-hydroxy- (0.1 g, 0.181 mmol) was dissolved in acetone (3 mL), sodium iodide (0.272 g, 1.81 mmol) was added to the solution, And heated to reflux for 18 hours. The reaction was concentrated, diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to give the desired compound (0.082 g, yellow oil).

¹ H NMR (300 MHz, CDCl ₃ )? 8.70 (s, 1 H), 7.39-7.33 (m, 5H), 7.25-7.22 2H), 4.46 (d, J = 8.4 Hz, 1H), 4.36-4.30 (m, (m, 3H), 3.64-3.59 (m, IH), 3.30 (t, J = 6.2 Hz, 2H), 2.63 (s, 2H), 2.52 s, 9H).

Step 3: (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) ethoxy) acetamido) -3,3- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 20 mg, 0.036 mmol) was dissolved in N, N-dimethylformamide (2 mL) to give N- (2- (2,6-dioxopiperidin- (23 mg, 0.036 mmol) and diisopropylethylamine (13 uL, 0.072 mmol) were added to the solution, and the mixture was stirred at room temperature. The reaction mixture was concentrated under reduced pressure to remove N, N-dimethylformamide, diluted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure, followed by purification to obtain the target compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 9.50 (s, 1H), 8.66 (s, 1H), 8.58 (t, J = 8.5 Hz, 1H), 8.15 (s, 1H), 8.01 (s, 1H) , 7.93 (d, J = 7.5 Hz, 1H), 7.61 (t, J = 7.5 Hz, 1H), 7.53 (s, 1H), 7.34-7.31 (m, 5H), 7.15-7.12 (M, 3H), 4.47 (d, J = 8.5 Hz, 1H), 4.76 (t, J = 2H), 3.63-3.60 (m, 2H), 3.29-7.30 (m, 2H) (S, 3H), 2.51 (s, 3H), 2.15 (s, 3H), 0.96 (s, 9H); LC / MS (ESI) m / z 1073.1 [M + H] &lt; ⁺ &gt;

< Example  (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- ) Pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) butoxy) acetamido) -3,3-dimethylbutaneoyl) -4- -N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1: ( 2S, 4R ) -1 - ((R) -2- (2- (2- Chlorobutoxy ) Acetamido ) -3,3- Dimethyl part Carbonyl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-

(2R, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4- 2-carboxamide hydrochloride (0.1 g, 0.232 mmol) was dissolved in dichloromethane (5 mL), and 2- (4-chlorobutoxy) acetic acid (0.051 g, 0.279 mmol) Amino) methylene] -1H-1,2,3-triazolo [4,5-b] pyridinium 3-oxide hexafluorophosphate (0.115 g, 0.302 mmol), diisopropylethylamine (0.061 mL, 348 mmol) was added thereto, followed by stirring at room temperature. The reaction is terminated, the reaction is diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and purified to give the desired compound (0.1 g, colorless gel).

LC / MS (ESI) m / z 579.2 [M + H] &lt; ^{+ &}

Step 2: ( 2R, 4R ) -4-hydroxy-1 - ((R) -2- (2- (4- Butoxy ) Acetamido ) -3,3-dimethylbutanoyl) -N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

(2S, 4R) -1 - ((R) -2- (2- (2-chlorobutoxy) acetamido) -3,3- dimethylbutanoyl) -4-hydroxy- (0.1 g, 0.167 mmol) was dissolved in acetone (5 mL), sodium iodide (0.251 g, 1.67 mmol) was added, and 18 Lt; / RTI &gt; for one hour. The reaction was concentrated, diluted with ethyl acetate and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to give the desired compound (0.048 g, yellow oil).

Step 3: (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) ethoxy) acetamido) -3,3- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; (2R, 4R) -4-hydroxy-1 - ((R) -2- (2- (4- (2-pyridyl) (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide (24 mg , 0.036 mmol) and diisopropylethylamine (13 uL, 0.072 mmol) were added, followed by stirring at room temperature. The reaction mixture was concentrated under reduced pressure to remove N, N-dimethylformamide, diluted with ethyl acetate, and washed with brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure, followed by purification to obtain the desired compound (10 mg, ivory gel).

LC / MS (ESI) m / z 1100.3 [M + H] &lt; ^{+ &}

< Example  (2S, 4R) -1 - ((R) -2- (7- (4- (4- Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -7-oxoheptanamido) -3,3- dimethylbutanoyl) -4-hydroxy-N - (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1  : tert - ((4- (4-methylthiazol-5-yl) benzyl) carbamoyl) pyrrolidine- Yl) -3,3-dimethyl-1-oxobutan-2-yl) amino) -7-oxoheptanoate

(2R, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4- 7- (tert-butoxy) -7-oxoheptanoic acid (0.065 g, 0.279 mmol), 1- (2-chlorophenyl) 4,5-b] pyridinium 3-oxide hexafluorophosphate (0.115 g, 0.302 mmol), diisopropylethylamine ( 0.061 mL, 348 mmol), and the mixture was stirred at room temperature. The reaction was terminated, and the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and then purified to yield the desired compound (0.162 g, colorless gel).

step 2: 7 - (((R) -1 - (( 2R, 4R ) -4-hydroxy-2 - ((4- (4- Methyl thiazole -5 days) benzyl ) Car 3-dimethyl-1-oxobutan-2-yl) amino) -7-oxoheptanoic acid

((R) -1- ((2R, 4R) -4-hydroxy-2 - ((4- (4-methylthiazol- 5- yl) benzyl) carbamoyl) pyrrolidine -1,3-dimethyl-1-oxobutan-2-yl) amino) -7-oxoheptanoate (0.16 g, 0.232 mmol) was dissolved in 20% trifluoroacetic acid / dichloromethane ), And the mixture was stirred at room temperature. The reaction mixture was concentrated under reduced pressure and purified to obtain the target compound (0.135 g, white solid).

Step 3: (2S, 4R) -1 - ((R) -2- (7- (4- (4- Methylphenyl) piperidin-l-yl) -7-oxoheptanamido) -3,3-dimethylbutanoyl) -4-hydroxy- Preparation of N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; (4-hydroxy-2 - ((4- (4-fluorophenyl) -4- (4-fluorophenyl) 3-dimethyl-l-oxobutan-2-yl) amino) -7-oxoheptanoic acid (24 mg, Triphenylphosphonium hexafluorophosphate (16.3 mg, 0.043 mmol) and diisopropylethylamine (7 uL, 0.054 mmol) were added at room temperature Lt; / RTI &gt; When the reaction was complete, the reaction was diluted with dichloromethane and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate and then filtered, concentrated under reduced pressure, and purified to give the desired compound (20 mg, white solid).

LC / MS (ESI) m / z 1113.3 [M + H] &lt; ^{+ &}

< Example  Amino) pyrimidin-2-yl) amino) - &lt; / RTI &gt; Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1 , 3-dioxoisoindolin-4-yl) acetamide

Step 1: N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline Yl) -2- (2- (2- (2-iodoethoxy) ethoxy) ethoxy) acetamide

ethoxy) acetate (0.2 g, 0.899 mmol) was dissolved in 20% trifluoroacetic acid / dichloromethane solution (1 mL) After that, the mixture was stirred at room temperature for 1 hour. The reaction mixture was concentrated, dissolved in tetrahydrofuran (2 mL), thionyl chloride (0.162 mL, 2.24 mmol) was added, and the mixture was heated to reflux at 60 ° C for 1 hour. The reaction mixture was concentrated and then dissolved in tetrahydrofuran (2 mL). To the mixture was added 4-amino-2- (2,6-dioxopiperidin-3-yl) isoindoline- mmol) and the mixture was refluxed at 80 ° C for 12 hours. After completion of the reaction, the solid material was removed by filtration, the filtrate was diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 10.47 (s, 1H), 8.87 (d, J = 8.4 Hz, 1H), 8.45 (s, 1H), 7.73 (t, J = 8.0 Hz, 1H), 7.58 (dd, J = 7.2 Hz, 0.6 Hz, 1H), 4.97 (dd, J = 12.3 Hz, 5.4 Hz, 1H), 4.22 (s, 2H), 3.84-3.79 , 2H), 2.96-2.74 (m, 3H), 2.19-2.13 (m, 1H)

Step 2: Preparation of 2- (2- (2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) - 1,3-dioxoisoindolin-4-yl) acetamide

Phenyl) -N4- (2- (isopropylsulfonyl) phenyl) pyrimidine-2,4 &lt; RTI ID = 0.0 &gt; -Diamine (LDK378, 20 mg, 0.036 mmol) was dissolved in N, N-dimethylformamide (2 mL) to give N- (2- (2,6-dioxopiperidin- 2- (2- (2-iodoethoxy) ethoxy) ethoxy) acetamide (41 mg, 0.072 mmol) and diisopropylethylamine (13 uL, 0.072 mmol), which was stirred at 90 &lt; 0 &gt; C. The reaction mixture was concentrated under reduced pressure to remove N, N-dimethylformamide, diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure, followed by purification to obtain the target compound.

_{^{1 H NMR (CDCl 3, 500}} MHz) δ 10.66 (s, 1H), 9.49 (s, 1H), 8.83 (d, J = 8.5 Hz, 1H), 8.58 (d, J = 8.0 Hz, 1H), 8.15 (s, 1H), 7.98 (s, 1H), 7.93 (d, J = 7.5 Hz, 1H), 7.72 (d, J = 7.5 Hz, 1H), 7.54 (s, 1H), 7.25 (d, J = 8.0 Hz, 1H), 6.81 J = 15 Hz, 1H), 3.85-3.68 (m, 8H), 3.29-3.24 (m, 1H), 3.19-3.17 2H), 2.14 (s, 3H), 2.05 (m, 2H), 2.88-2.79 (m, 2H), 2.73-2.66 (s, 1H), 2.01 (d, J = 11.5 Hz, 1H), 1.75-1.73 (m, 3H), 1.35 (t, J = 6.0 Hz, 6H), 1.32

< Example  Amino) pyrimidin-2-yl) amino) -5-isopropoxy-3- (4- (4- Yl) butoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- Preparation of acetamide

step 1: 2 -(4- Chlorobutoxy ) -N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline Yl) acetamide &lt; / RTI &gt;

(0.5 g, 3 mmol) was dissolved in tetrahydrofuran (5 mL), and thionyl chloride (0.544 mL, 7.5 mmol) was added. The mixture was heated at 60 ° C. for 1 hour Lt; / RTI &gt; The reaction mixture was concentrated and then dissolved in tetrahydrofuran (5 mL), and then 4-amino-2- (2,6-dioxopiperidin-3-yl) isoindoline- 1 mmol) was added and the mixture was refluxed at 80 ° C for 12 hours. After completion of the reaction, the solid material was removed by filtration, the filtrate was diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound.

LC / MS (ESI) m / z 422 [M + H] &lt; ^{+ &}

step 2: 2 -(4- Iodobutoxy ) -N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxo Isoindolin-4-yl) acetamide

The compound (0.2 g, 0.474 mmol) prepared in the above Step 1 was dissolved in acetone (10 mL), sodium iodide (0.71 g, 4.74 mmol) was added, and the mixture was heated under reflux for 18 hours. The reaction was concentrated, diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the desired compound.

¹ H NMR (300 MHz, CDCl ₃ )? 8.70 (s, 1 H), 7.39-7.33 (m, 5H), 7.25-7.22 2H), 4.46 (d, J = 8.4 Hz, 1H), 4.36-4.30 (m, (m, 3H), 3.64-3.59 (m, IH), 3.30 (t, J = 6.2 Hz, 2H), 2.63 (s, 2H), 2.52 s, 9H)

Step 3: Preparation of 2- (4- (4- (4-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin- 1 -yl) butoxy) -N- (2- (2,6- dioxopiperidin-3-yl) -1,3-dioxoisoindolin- ) Preparation of acetamide

5-Chloro -N ² - (2- isopropoxy-5-methyl-4- (piperidin-4-yl) phenyl) -N ⁴ - (2- (isopropylsulfonyl) phenyl) pyrimidine -2 (20 mg, 0.036 mmol) was dissolved in N, N-dimethylformamide (2 mL), and the compound (24 mg, 0.036 mmol) prepared in Step 2 and diisopropylethylamine (13 uL , 0.072 mmol), and the mixture was stirred at room temperature. The reaction mixture was concentrated under reduced pressure to remove N, N-dimethylformamide, diluted with ethyl acetate, and washed with water and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and distilled under reduced pressure, followed by purification to obtain the desired compound.

^{1 H NMR (500 MHz, CDCl} 3) δ 10.56 (s, 1H), 9.52 (s, 1H), 8.87 (d, J = 8.5 Hz, 1H), 8.60 (d, J = 8.3 Hz, 1H), 8.17 (s, 1H), 8.02 (s, 1H), 7.94 (dd, J = 8.0,1.5 Hz, 1H), 7.78-7.69 2H), 7.29-7.24 (m, 1H), 6.85 (s, IH), 5.02 (s, IH), 4.58 ), 3.47-3.21 (m, 2H), 2.94-2.62 (m, 5H), 2.26-2.11 (m, 4H), 1.95-1.76 ), 1.33 (d, J = 6.9 Hz, 6H). LC / MS (ESI) m / z 943.2 [M + H] &lt; ^{+ &}

< Example  Amino) pyrimidin-2-yl) amino) -5- (2- (2- (4- (4- Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoine Yl) acetamide &lt; / RTI &gt;

Step 1: tert Butyl 2- (2- (2- Chloroethoxy ) Ethoxy ) &Lt; / RTI &gt; acetate

After dissolving 2- (2-chloroethoxy) ethan-1-ol (1.0 eq.) And tert-butyl 2-bromoacetate (1.2 eq.) In tetrahydrofuran, potassium tert- butoxide (1.5 eq. ) Was added and stirred at room temperature. After completion of the reaction, the reaction mixture was washed with ethyl acetate and water, and the organic layer was extracted and washed with water and brine. Water was removed with anhydrous magnesium sulfate, and the mixture was concentrated under reduced pressure, followed by separation and purification to obtain tert-butyl 2- (2-chloroethoxy) acetate.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 4.04 (s, 1H), 3.79 - 3.75 (m, 2H), 3.74 - 3.68 (m, 8H), 3.66 - 3.62 (m, 2H), 1.49 (s, 9H )

step 2: 2 - (2- (2- Chloroethoxy ) Ethoxy ) Preparation of acetic acid

To the 20% trifluoroacetic acid / dichloromethane solution was added the compound prepared in the above step 1 and stirred at room temperature. After completion of the reaction, the mixture was concentrated to give 2- (2- (2-chloroethoxy) ethoxy) acetic acid.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 11.14 (s, 1H), 4.24 (s, 2H), 3.82 - 3.74 (m, 6H), 3.65 (t, J = 5.7 Hz, 2H)

step 3: 2 - (2- (2- Chloroethoxy ) Ethoxy ) -N- (2- (2,6- Dioxopiperidine 3-yl) -1,3-dioxoisoindolin-4-yl) acetamide

The compound (3.0 eq.) Prepared in the above step 2 was dissolved in tetrahydrofuran, thionyl chloride (7.5 eq.) Was added, and the mixture was stirred at 60 ° C. After the reaction was terminated, the mixture was concentrated and dissolved in tetrahydrofuran, followed by the addition of formalidomide (1.0 eq.) And stirring at 60 ° C. After completion of the reaction, the mixture was concentrated and separated and purified to obtain the desired compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 10.47 (s, 1H), 8.87 (d, J = 8.4 Hz, 1H), 8.45 (s, 1H), 7.73 (t, J = 8.0 Hz, 1H), 7.58 (dd, J = 7.2 Hz, 0.6 Hz, 1H), 4.97 (dd, J = 12.3 Hz, 5.4 Hz, 1H), 4.22 (s, 2H), 3.84-3.79 , 2H), 2.96-2.74 (m, 3H), 2.19-2.13 (m, 1H)

Step 4: Preparation of N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-yl) -2- (2- (2-iodoethoxy) ethoxy) acetamide

The compound (1.0 eq.) Prepared in the above step 3 was dissolved in acetone, sodium iodide (10.0 eq.) Was added, and the mixture was stirred at 80 ° C. After completion of the reaction, the mixture was concentrated to give N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- Iodoethoxy) ethoxy) acetamide was obtained.

¹ H NMR (CDCl ₃ , 300 MHz)? 10.47 (s, 1H), 8.87 (d, J = 8.4 Hz, 1H), 8.37 1H), 3.29 (t, J = 1.5 Hz, 2H), 3.74-3.96 (m, J = 7.1 Hz, 1H), 2.95-2.74 (m, 3H), 2.19-2.13 (m, 1H)

Step 5: 2- (2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxo 4-yl) acetamide &lt; / RTI &gt;

The compound (1.0 eq.) And LDK378 (1.0 eq.) Prepared in the above step 4 were dissolved in dimethylformamide, diisopropylethylamine (2.5 eq.) Was added, and the mixture was stirred at 90 ° C. After the reaction was completed, the mixture was concentrated, separated and purified to obtain the desired compound.

_{^{1 H NMR (CDCl 3, 500}} MHz) δ 10.66 (s, 1H), 9.49 (s, 1H), 8.83 (d, J = 8.5 Hz, 1H), 8.58 (d, J = 8.0 Hz, 1H), 8.15 (s, 1H), 7.98 (s, 1H), 7.93 (d, J = 7.5 Hz, 1H), 7.72 (d, J = 7.5 Hz, 1H), 7.54 (s, 1H), 7.25 (d, J = 8.0 Hz, 1H), 6.81 J = 15 Hz, 1H), 3.85-3.68 (m, 8H), 3.29-3.24 (m, 1H), 3.19-3.17 2H), 2.14 (s, 3H), 2.05 (m, 2H), 2.88-2.79 (m, 2H), 2.73-2.66 (s, 1H), 2.01 (d, J = 11.5 Hz, 1H), 1.75-1.73 (m, 3H), 1.35 (t, J = 6.0 Hz, 6H), 1.32

< Example  Amino) pyrimidin-2-yl) amino) -5-isopropoxy-3- (2- (4- (4- Yl) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- Preparation of acetamide

Step 1: tert -Butyl 2- (2- Chloroethoxy ) &Lt; / RTI &gt; acetate

The procedure of Step 1 of Example 14 was repeated except that 2-chloroethanol was used instead of 2- (2-chloroethoxy) ethan-1-ol used in Step 1 of Example 14 to obtain the desired compound .

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 4.04 (s, 1H), 3.79 - 3.75 (m, 2H), 3.74 - 3.68 (m, 8H), 3.66 - 3.62 (m, 2H), 1.49 (s, 9H )

step 2: 2 -(2- Chloroethoxy ) Preparation of acetic acid

Using the compound prepared in the above Step 1, the procedure of Step 2 of Example 14 was repeated to produce the target compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 11.11 (s, 1H), 4.26 (s, 2H), 3.87 (t, J = 5.5 Hz, 2H), 3.69 (t, J = 5.5 Hz, 2H)

step 3: 2 -(2- Chloroethoxy ) -N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxo 4-yl) acetamide &lt; / RTI &gt;

Using the compound prepared in the above Step 2, the procedure of Step 3 of Example 14 was repeated to produce the target compound.

_{^{1 H NMR (CDCl 3, 500}} MHz) δ 10.46 (s, 1H), 8.86 (d, J = 8.5 Hz, 1H), 8.01 (s, 1H), 7.74 (t, J = 7.7 Hz, 1H), 7.59 (d, J = 7.5 Hz, 1H), 4.97 (dd, J = 12.5 Hz, 5.5 Hz, 1H), 4.23 (s, 2H), 3.95-3.92 , 2H), 2.96-2.73 (m, 3H), 2.20-2.15 (m, 1H)

Step 4: Preparation of N- (2- (2,6- Dioxopiperidine Yl) -1,3- Dioxoisoindoline -4-yl) -2- (2-iodoethoxy) acetamide

Using the compound prepared in the above Step 3, the procedure of Step 4 of Example 14 was repeated to produce the target compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 10.45 (s, 1H), 8.85 (d, J = 8.1 Hz, 1H), 8.08 (s, 1H), 7.74 (t, J = 7.9 Hz, 1H), 7.59 (dd, J = 7.2 Hz, 0.6 Hz, 1H), 4.97 (dd, J = 12.3 Hz, 5.4 Hz, 1H), 4.20 t, J = 6.9 Hz, 2H), 2.97-2.75 (m, 3H), 2.20-2.15

Step 5: Preparation of 2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) ethoxy) -N- (2- (2,6-dioxopiperidin- ) Preparation of acetamide

Using the compound prepared in the above Step 4, the procedure of Step 5 of Example 14 was repeated to produce the target compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 10.47 (s, 1H), 9.50 (s, 1H), 8.88 (d, J = 5.1 Hz, 1H), 8.59 (d, J = 5.1 Hz, 1H), 8.15 (s, 1H), 8.07 (s, 1H), 8.00 (s, 1H), 7.93 (dd, J = 4.8 Hz, J = 0.6 Hz, 1H) J = 4.5 Hz, 1H), 7.81 (s, 1H), 7.94 (d, J = 1H, J = 7.2 Hz, J = 3.0 Hz, 1H), 4.54-4.52 (m, 1H), 4.20 (s, 2H), 3.83 (s, 2H), 3.29-3.24 2H), 2.15-2.00 (m, 1H), 2.11-2.13 (m, 1H), 2.91-2.69 1H), 1.76 (s, 4H), 1.63 (s, 1H), 1.35 (d, J = 3.6 Hz, 6H)

< Example  (2S, 4R) -1 - ((R) -1- (4- (4 - ((5- Yl) -14,14-dimethyl-11-oxo-3,6,9-trioxa-12-aza-pentadecane carbonyl ) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Step 1: tert -Butyl 2- (2- (2- (2- Chloroethoxy ) Ethoxy ) Ethoxy ) &Lt; / RTI &gt; acetate

(1 g, 5.42 mmol) and tert-butyl bromoacetate (0.8 mL, 5.42 mmol) were dissolved in tetrahydrofuran (10 mL) and KOtBu ( 0.638 g, 5.69 mmol) at 0 ° C, and the mixture was stirred at room temperature. When the reaction was complete, it was extracted with water and ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated, and purified to obtain the desired compound.

¹ H NMR (300 MHz, CDCl ₃ )? 4.04 (s, 1H), 3.83-3.58 (m, 5H), 1.49 (s, 4H).

Step 2: tert Amino) pyrimidin-2-yl) amino) - &lt; / RTI &gt; -5-isopropoxy-2-methylphenyl) piperidin-1-yl) ethoxy) ethoxy) ethoxy) acetate

(27 mg, 0.09 mmol), Cs ₂ CO ₃ (59 mg, 0.18 mmol) and potassium iodide (3 mg, 0.018 mmol) were dissolved in DMF (1 mL ), And the mixture was stirred at room temperature. The reaction product was extracted with water and ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated, and purified to obtain the desired compound.

^{1 H NMR (300 MHz, CDCl} 3) δ 9.50 (s, 1H), 8.59 (d, J = 8.4 Hz, 1H), 8.00 (s, 1H), 8.05 - 7.98 (m, 1H), 7.94 (d, J = 7.7 Hz, 1H), 7.63 (t, J = 7.7 Hz, 1H), 7.55 (s, 1H), 7.26 (m, 1H), 3.14 (d, J = 11.1 Hz, 2H), 2.69 (t, J = 5.8 Hz, , 2H), 2.28-2.10 (m, 5H), 1.91-1.72 (m, 2H), 1.48 (s, 9H), 1.35 (m, 13H).

Step 3: tert Amino) pyrimidin-2-yl) amino) - &lt; / RTI &gt; -5-isopropoxy-2-methylphenyl) piperidin-1-yl) ethoxy) ethoxy) ethoxy) acetic acid hydrochloride

The compound (37 mg, 0.090 mmol) prepared in step 2 was dissolved in dichloromethane (1 mL), 4N hydrochloric acid / dioxane (1 mL) was added thereto, and the mixture was stirred at room temperature for 6 hours. The reaction was concentrated under reduced pressure and used in the next step without purification.

Step 4: (2S, 4R) -1 - ((R) -1- (4- (4- -Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -14,14- dimethyl- 11-oxo-3,6,9- trioxa-12- azapentadecanecarbo Preparation of 4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

(10 mg, 13 mmol) and (2S, 4R) -1 - ((R) -2-amino-3,3-dimethylbutane oil) -4-hydroxy- -Carboxamide hydrochloride (6 mg, 13 mmol), HATU (7.4 mg, 19.5 mmol), diisopropylethylamine (9.1 uL, 52 mmol) was dissolved in dichloromethane (1 mL), and the mixture was stirred at room temperature. The reaction mixture was extracted with water and dichloromethane. The organic layer was dried over anhydrous magnesium sulfate, filtered, concentrated under reduced pressure, and purified to obtain the target compound. LC / MS (ESI) m / z 1190.7 [M + H-15] &lt; ^{+ &}

< Example  Amino] pyrimidin-2-yl) amino) -5-isopropoxy-2- (isopropylsulfonyl) Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) hexanamide

The objective compound was prepared in a manner similar to Example 4, except that 5-bromohexanoic acid was used in place of the 5-bromophenic acid oil used in Step 1 of Example 4 above.

_{^{1 H NMR (CDCl 3, 300MHz}} ) δ 9.49 (s, 1H), 9.43 (s, 1H), 8.83 (d, J = 8.4 Hz, 1H), 8.58 (d, J = 8.4 Hz, 1H), 8.15 ( J = 7.9 Hz, 1H), 7.00 (d, J = 7.8 Hz, 1H) 6.96 (br, 1H), 4.96 (dd, J = 12.0, 6.0 Hz, 1H), 4.60-4.50 (m, 2H), 2.96-2.70 (m, 5H), 2.49 (t, J = 7.3 Hz, 3H), 2.23-2.13 (m, J = 6.0 Hz, 6H), 1.32 (d, J = 6.9 Hz, 6H), 2.15 (s, 3H), 1.86-1.61 (m, 9H), 1.52-1.39

< Example  (2R, 4S) -1 - ((S) -2- (6- (4- (4- Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -6-oxohexanamido) -3,3- dimethylbutanoyl) -4-hydroxy-N - (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

Amino) pyrimidin-2-yl) amino) -5-isopropoxycarbonylamino-5- (4- (4- -4 - ((2- (isopropylsulfonyl) piperidin-1-yl) -5-oxopentanoic acid in place of 6- (4- Phenylphenyl) amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -6-oxohexanoic acid was used in place of To give the desired compound.

_{^{1 H NMR (CDCl 3, 300}} MHz) δ 9.51 (s, 1H), 8.67 (s, 1H), 8.58 (d, J = 8.7 Hz, 1H), 8.16 (s, 1H), 8.03 (s, 1H) , 7.93 (dd, J = 8.1,1.5 Hz, 1H), 7.65-7.59 (m, 1H), 7.54 (s, 1H), 7.39-7.22 (m, 5H), 7.29-7.33 (m, merged with CHCl3, 1H), 6.68 (d, J = 0.9 Hz, 1H), 6.45 (dd, J = 15.0,7.8 Hz, (Dd, J = 15.3, 5.4 Hz, 1H), 4.11 (d, J = 10.2 Hz, 1H), 3.96 2H), 3.51-3.44 (m, 1H), 3.31-3.22 (m, 1H), 3.11 (t, J = 12.9 Hz, 1H), 2.92-2.84 1H), 1.81 (t, J = 11.3 Hz, 2H), 1.68-1.66 (m, 1H), 2.52 (s, 3H), 2.37-2.22 (D, J = 5.7, 2.1 Hz, 6H), 1.32 (d, J = 6.9 Hz, 6H), 1.25 (s, 1H), 0.94 )

< Example  (2S, 4S) -1 - ((S) -2- (2- (3- (4- (4- 1-yl) propoxy) acetamido) -3,3-dimethylbutaneoyl) -4-hydroxypyrrolidin- -N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

The procedure of Example 10 was repeated except for using 2- (5-chloropropoxy) acetic acid instead of 2- (4-chlorobutoxy) acetic acid used in Step 1 of Example 10 to obtain the desired compound .

LC / MS (ESI) m / z 1113.3 [M + H] &lt; + &

< Example  Amino] pyrimidin-2-yl) amino) -5-isopropoxy-3- (4- (4- Yl) propoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- Preparation of acetamide

The procedure of Example 13 was repeated except for using 2- (5-chloropropoxy) acetic acid instead of 2- (4-chlorobutoxy) acetic acid used in Step 1 of Example 13 to obtain the desired compound .

LC / MS (ESI) m / z 1113.3 [M + H] &lt; ^{+ &}

< Example  (2R, 4S) -1 - ((R) -2- (2 - ((5- (4- (4- (2- (isopropylsulfonyl) phenyl) Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) pentyl) oxy) acetamido) -3,3- Preparation of hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide

The procedure of Example 10 was repeated except for using 2- (5-chloropentoxy) acetic acid instead of 2- (4-chlorobutoxy) acetic acid used in Step 1 of Example 10 to obtain the desired compound .

LC / MS (ESI) m / z 1114 [M + H] &lt; ^{+ &}

Example constitutional formula One

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18

19

20

21

< Experimental Example  1> ALK  Evaluation of protein inhibitory activity

To evaluate the ALK protein inhibitory activity of the compounds according to the present invention, the following experiment was conducted.

Specifically, in order to measure the inhibitory activity against inverse lymphoma kinase (ALK), the compounds prepared in Examples 1 to 21 were added to a Grayer 96 well round bottom plate at a concentration of 1230 [mu] M, and inverse lymphoma kinase (ALK) Enzyme (1 ml) and biotin-conjugated peptide substrate (2 ml) were mixed for 15 minutes and cultured. ATP solution (5 ml) was added thereto and the kinase reaction was carried out at room temperature for 30 minutes. An anti-phosphotyrosine antibody (5 ml) with streptavidin (XL 665, 5 ml) and europium (Eu ³⁺ ) dissolved in ethylene diamine tetraacetic acid solution was added to the reaction solution The reaction was stopped and incubated for 1 hour and then analyzed using homogeneous time-resolved fluorescence (HTRF, Cisbio). And read in a wavelength range of 615/665 nm with a Wallac Envision 2103 instrument. In Table 2 below, the IC ₅₀ of the compounds prepared in Examples 1-21 were implemented using prism (version 5.01, GraphPad) software. Table 2 shows inhibitory activity when the activity of inverse lymphoma kinase (ALK) enzyme is reduced to 50% or less. IC ₅₀ of the compound is shown in Table 2 below.

Example IC ₅₀ , nM Example IC ₅₀ , nM One 95 11 140 2 140 12 34 3 110 13 70 4 18 14 29 5 69 15 46 6 100 16 16 7 32 8 110 9 89 10 29

As shown in Table 2, it can be seen that Examples 1 to 16 of the present invention can inhibit the ALK protein with a unit concentration of nM.

< Experimental Example  2> ALK  Evaluation of proteolytic activity

To evaluate the ALK proteolytic activity of the compounds according to the present invention, the following experiment was conducted.

Su-Dhl-1 cells were injected 6x105 cells into each well of a 12 well plate. The next day, the compound was treated in each well to a final concentration of 30 nM, 100 nM, 300 nM, and 1 uM. One well was treated with the same percentage of DMSO. After 16 hours of treatment, the cells were collected and cultured in TBS-N lysis buffer (20 mM Tris-Cl, pH 8.0, 150 mM NaCl, 0.5% NP-40, 1.5 mM EDTA, 0.5 mM Na3VO4, and protease inhibitor cocktail) Western blotting was performed by making seafood (cell lysate).

H3122 cells were injected 6x105 cells into each well of a 12 well plate. The next day, the compound was treated in each well to a final concentration of 30 nM, 300 nM, 3 uM, and 30 uM. One well was treated with the same percentage of DMSO. After 16 hours of treatment, the cells were collected and cultured in TBS-N lysis buffer (20 mM Tris-Cl, pH 8.0, 150 mM NaCl, 0.5% NP-40, 1.5 mM EDTA, 0.5 mM Na3VO4, and protease inhibitor cocktail) Western blotting was performed by making seafood (cell lysate).

The experimental results are shown in Table 3 below.

Example ALK degradation activity Example ALK degradation activity One + 10 ++ 2 + 11 ++ 3 ++ 12 + 4 ++ 13 + 5 + 14 + 6 + 15 + 7 + 16 + 8 + 9 +

++: decomposition (> 50%) in excess of 50% at 300 nM concentration

+: Less than 50% degradation (<50%) at 300 nM concentration

The compounds of Examples 1 to 16 according to the present invention can decompose ALK protein at a concentration of 300 nM. In particular, the compounds of Examples 3, 4, 10 and 11 exhibit a 50% Lt; RTI ID = 0.0 &gt; of &lt; / RTI &gt;

Therefore, the compound according to the present invention can excellently degrade the ALK protein at a concentration of nano-mol units, and thus can be effectively used for the prevention and treatment of ALK-related diseases.

< Experimental Example  3> In vivo  Evaluation of Cancer Growth Inhibitory Activity

In order to evaluate the cancer growth inhibitory activity of the compounds according to the present invention, the following experiment was conducted.

SCID mice using the H3122 xenograft model were divided into a control group (8 rats) and an experimental group (8 rats). In the above experimental group, the compound of Example 3 according to the present invention was intraperitoneally administered at a dose of 50 mg / kg three times a day The results are shown in FIG.

FIG. 1 is a graph showing the change in tumor volume after administering the compound of Example 3 of the present invention (three times a day, 50 mg / kg, for a total of 14 days) to H3122 xenograft SCID mice.

1, it can be confirmed that the tumor size of the experimental group administered with the compound of Example 3 according to the present invention is maintained or decreased with the passage of time.

Therefore, the compound according to the present invention has been confirmed to have cancer growth inhibitory activity as shown in Experimental Example 3, and it can be used as a pharmaceutical composition containing the same for the prevention and treatment of cancer .

Claims (10)

Claims 1. A compound represented by the following formula (1), an optical isomer thereof or a pharmaceutically acceptable salt thereof:
[Chemical Formula 1]

(In the formula 1,

Linker structure

ego,
Wherein a and i are independently 0 or 1 and can not be 0 at the same time,
B is an integer of 0-20,
C is an integer of 0 or 1,
D is an integer of 1 to 3,
E is an integer of 1,
F is an integer of 1-10,
G is an integer of 1,
Wherein h is an integer of 1 to 3,
J and k are each independently an integer of 0-5,

In the Linker structure, the total sum of - (CH ₂ ) -, - (C═O) -, -NH- and -O- is 3-20; And

A is

or

to be).
delete The method according to claim 1,
The linker,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

,

or

&Lt; / RTI &gt; or an &lt; RTI ID = 0.0 &gt; pharmaceutically &lt; / RTI &gt; acceptable salt thereof.
The method according to claim 1,
The compound represented by the formula (1) is any one selected from the group consisting of the following compounds, an optical isomer thereof or a pharmaceutically acceptable salt thereof:
(1) 5- (4- (4- (5-chloro-4- (2- (isopropylsulfonyl) phenylamino) pyrimidin- 4-ylamino) butyl) -5- (4-fluoropyridin-2-yl) Oxopentanamide;
(2S, 4R) -1 - ((R) -2- (tert-butyl) -17- ) Pyrimidin-2-ylamino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -4,13,17-trioxo-6,9-dioxa-3,12- 1-oyl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(3) Synthesis of (2S, 4R) -1 - ((R) -2- (5- (4- (4- Methylphenyl) piperidin-l-yl) -5-oxopentanamido) -3,3-dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(4) Synthesis of 5- (4- (4- ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-ioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) pentanamide;
(5) Preparation of 5- (4- (4 - ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-1-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin- amides;
(6) Synthesis of 2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) -2-oxoethoxy) -N- (2- (2,6- dioxopiperidin- 4-yl) acetamide;
(7) Synthesis of (2R, 4R) -1 - ((R) -2- (5- (4- (4- Methylphenyl) piperidin-1-yl) pentanamido) -3,3-dimethylbutanoyl) -4-hydroxy-N- (4 - (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(8) 7- (4- (4- ((2- (Isopropylsulfonyl) phenyl) amino) pyrimidin-2- yl) amino) -5-isopropoxy- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1, 3- diolisoisoindol- amides;
(9) Synthesis of (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) ethoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(10) Synthesis of (2S, 4R) -1 - ((R) -2- (2- (2- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1- yl) butoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(11) Synthesis of (2S, 4R) -1 - ((R) -2- (7- (4- (4- Methylphenyl) piperidin-l-yl) -7-oxoheptanamido) -3,3-dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(12) 2- (2- (2- (2- (isopropylsulfonyl) phenyl) amino) pyrimidin-2-yl) amino Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) - 1,3-dioxoisoindolin-4-yl) acetamide;
(13) Synthesis of 2- (4- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin- 1 -yl) butoxy) -N- (2- (2,6- dioxopiperidin-3-yl) -1,3-dioxoisoindolin- ) Acetamide;
(14) 2- (2- (2- (4- (4-fluoro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- Ethoxy) ethoxy) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxo 4-yl) acetamide;
(15) 2- (2- (4- (4 - ((5-Chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) ethoxy) -N- (2- (2,6-dioxopiperidin- ) Acetamide;
(16) Synthesis of (2S, 4R) -1 - ((R) -1- (4- (4- -Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -14,14- dimethyl- 11-oxo-3,6,9- trioxa-12- azapentadecanecarbo Yl) -4-hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(17) Synthesis of 6- (4- (4 - ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- -Methylphenyl) piperidin-l-yl) -N- (2- (2,6-dioxopiperidin-3-yl) -1,3-dioxoisoindolin-4-yl) hexanamide;
(18) Synthesis of (2R, 4S) -1 - ((S) -2- (6- (4- (4- Yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) -6- oxohexanamido) -3,3- dimethylbutanoyl) -4-hydroxy- N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(19) Synthesis of (2R, 4S) -1 - ((S) -2- (2- (3- (4- (4- Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) propoxy) acetamido) -3,3- Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide;
(20) 2- (3- (4- (4- ((5-chloro-4 - ((2- (isopropylsulfonyl) phenyl) amino) pyrimidin- 2-methylphenyl) piperidin-1-yl) propoxy) -N- (2- (2,6-dioxopiperidin- ) Acetamide; And
(21) Synthesis of (2R, 4S) -1 - ((R) -2- (2- (5- (4- (4- ) Amino) pyrimidin-2-yl) amino) -5-isopropoxy-2-methylphenyl) piperidin- 1 -yl) pentyl) oxy) acetamido) -3,3- -Hydroxy-N- (4- (4-methylthiazol-5-yl) benzyl) pyrrolidine-2-carboxamide.
As shown in Scheme 1 below,
AH and a compound represented by Linker-X to prepare a compound represented by A-Linker-X (Step 1);
(Step 2) of preparing a compound represented by A-Linker-Y represented by A-Linker-X prepared in the step 1; And
Reacting a compound represented by A-Linker-Y produced in Step 2 with a compound represented by Formula (2) to prepare a compound represented by Formula (1) (Step 3). Preparation of the indicated compounds:
[Reaction Scheme 1]

(In the above Reaction Scheme 1,
Linker, and A are as defined in Chemical Formula 1 of claim 1;
X is -CO ₂ -tBu, Cl or Br; And
Y is when X is a -CO ₂ -tBu, Y is a -CO ₂ H, when X is Cl or Br, Y is I).
delete A pharmaceutical composition for preventing or treating cancer comprising the compound represented by the general formula (1) of claim 1, an optical isomer thereof or a pharmaceutically acceptable salt thereof as an active ingredient.
8. The method of claim 7,
Wherein said compound inhibits or decomposes reverse priming lymphoma kinase (ALK) to prevent or treat cancer.
8. The method of claim 7,
Wherein the cancer is selected from the group consisting of colon cancer, liver cancer, stomach cancer, breast cancer, colon cancer, bone cancer, pancreatic cancer, head or neck cancer, uterine cancer, ovarian cancer, rectal cancer, esophageal cancer, small intestine cancer, Wherein the composition is selected from the group consisting of vaginal cancer, vulvar carcinoma, Hodgkin's disease, prostate cancer, bladder cancer, kidney cancer, ureter cancer, renal cell carcinoma, renal pelvic carcinoma central nervous system tumor and leukemia.
A health functional food for preventing or ameliorating a cancer containing the compound represented by the general formula (1) of claim 1 or an optical isomer thereof as an active ingredient.

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