Tricyclic compounds and pharmaceutical uses thereof

Abstract

To provide a compound acting as a serotonin receptor antagonist, and its pharmaceutical use for diseases associated with serotonin activation.SOLUTION: Provided is a compound which is a tricyclic derivative represented by the following chemical formula, a pharmaceutically acceptable salt thereof, or a stereoisomer thereof. Specific examples thereof include 8-chloro-11 - (1 - (methylsulfonyl) piperidin-4-ylidene) - 611 - dihydro - 5H - benzo [5,6] cyclohepta [1, 2-b] pyridine. These compounds have an excellent inhibitory action on serotonin activity, and can be used for the prophylaxis or treatment of metabolic diseases and the like associated with serotonin activation by a pharmaceutical composition comprising the same.SELECTED DRAWING: None

Description

[Technical Field]

[0001] The present invention relates to a tricyclic compound that acts as a serotonin receptor antagonist and its pharmaceutical use for metabolic diseases, etc. More specifically, the present invention relates to a tricyclic compound that acts as a serotonin 2A receptor antagonist and its pharmaceutical use for the treatment of obesity, fatty liver, steatohepatitis, etc. [Background technology]

[0002] Obesity is the accumulation of excess body fat in the body. It is caused by the accumulation of excess energy in the form of body fat when calories burned are less than calories consumed. Causes of obesity include poor eating habits, excessive food intake, lack of exercise, genetic factors, or psychological factors. Obesity can manifest as shortness of breath and joint pain, as well as cardiovascular disease, high blood pressure, sleep apnea, dyslipidemia, hyperinsulinemia, and osteoarthritis.

[0003] The goal of obesity treatment is to prevent and treat obesity-related complications. The most basic treatment for obesity is lifestyle changes, and in the case of drug treatment, appetite suppressants are mainly used. However, these appetite suppressants act on the central nervous system and have side effects such as psychiatric disorders such as depression.

[0004] Appetite suppressants regulate serotonin (5-HT) in the central nervous system, a neurotransmitter that regulates mood, sleep, and appetite. Serotonin acts not only on the central nervous system but also on peripheral tissues, and it has been reported to play an important role in regulating the metabolism of peripheral tissues. Because serotonin cannot cross the blood-brain barrier, serotonin in the central nervous system and serotonin in peripheral tissues are thought to be independent systems.

[0005] It is known that inhibition of serotonin synthesis in peripheral tissues reduces lipogenesis in white fat cells and burns energy by generating heat in brown fat cells (Oh C et al., Nature Communication 6, 6794, 2015).

[0006] On the other hand, fatty liver is a disease caused by an increase in the fat content of the liver due to the accumulation of large amounts of fat in liver cells. Fatty liver is broadly divided into alcoholic fatty liver and non-alcoholic fatty liver. Excessive alcohol consumption causes fat to accumulate in liver cells, and alcohol metabolites damage liver cells. However, non-alcoholic fatty liver is a disease in which fat accumulates in the liver even when a person does not drink alcohol or drinks only small amounts.

[0007] Fatty liver includes various forms of liver disease, ranging from simple fatty liver, in which only fat accumulates and hepatocytes are not damaged, to steatohepatitis, in which hepatocyte damage persists, and cirrhosis, accompanied by ascites and jaundice. Fatty liver is caused by the accumulation of triglycerides in hepatocytes, and the size of the accumulated triglyceride blisters increases over time. Such fatty blisters increase the inflammatory response and induce hepatitis or liver fibrosis.

[0008] Treatments for fatty liver include weight loss through diet and exercise, and in the case of drug treatment, diabetes medications that improve insulin resistance are used for short-term treatment. However, these medications are used for short-term treatment, and their long-term therapeutic effects have not been reported. Furthermore, commercially available lipid-improving or hepatoprotective agents are intended only for maintenance, not treatment.

[0009] Recent studies have shown that treatment of mice with liver injury with serotonin receptor antagonists inhibits proliferation and increases the rate of apoptosis in injured liver cells (Ruddell et al., The American Journal of Pathology, 169(3), 861-876, September 2006). Furthermore, treatment with serotonin receptor inhibitors, ketanserin and sarpogrelate, reduces cell viability and induces apoptosis in LX-2 cells after liver injury (Kim et al., Liver International, 33(4), 535-543, 2013). Furthermore, liver-specific knockout mice of serotonin receptor 2A (HTR2A) showed improved hepatic steatosis, reduced inflammation, and decreased expression of fibrosis-related genes (Choi et al., Nature Communications, 9, 4824, 2018). [Prior art documents] [Non-patent literature]

[0010] [Non-Patent Document 1] Oh C et al., Nature Communications, 6, 6794, 2015 [Non-patent document 2] Ruddell et al., The American Journal of Pathology, 169(3), 861-876, 2006 September [Non-patent document 3] Kim et al., Liver International, 33(4), 535-543, 2013 [Non-patent document 4] Choi et al., Nature Communications, 9, 4824, 2018 Summary of the Invention [Problem to be solved by the invention]

[0011] For the treatment of obesity, it is important to inhibit the synthesis of serotonin present in the peripheral nervous system. Therefore, the present inventors attempted to find obesity-related serotonin receptors in peripheral tissues, and as a result, in the obese state, serotonin 2A (5-HT 2A Furthermore, knocking out the serotonin 2A receptor was shown to reduce body weight and improve fatty liver, steatohepatitis, and liver fibrosis.

[0012] It is therefore an object of the present invention to provide compounds that act as serotonin receptor antagonists and their pharmaceutical use for diseases associated with serotonin activation. [Means for solving the problem]

[0013] Thus, the present invention provides compounds that are tricyclic derivatives represented by Chemical Formula 1, or pharmaceutically acceptable salts, stereoisomers, or prodrugs thereof.

[0014] Furthermore, the present invention provides pharmaceutical compositions for preventing or treating diseases associated with serotonin activation, and pharmaceutical compositions comprising the compounds of the present invention as an active ingredient. [Effects of the Invention]

[0015] The tricyclic derivatives or pharmaceutically acceptable salts, stereoisomers, or prodrugs thereof according to the present invention can exhibit excellent antagonistic activity against serotonin receptors, particularly serotonin 2A receptors.

[0016] Therefore, the compounds according to the present invention can be effectively used for the prevention or treatment of diseases associated with serotonin activation, for example, metabolic diseases such as obesity, fatty liver and steatohepatitis. DETAILED DESCRIPTION OF THE INVENTION

[0017] The present invention will be described in detail below.

[0018] As used herein, the term "halogen" means F, Cl, Br, or I, unless otherwise specified.

[0019] The term "alkyl" means, unless otherwise specified, a straight or branched chain saturated hydrocarbon group. For example, "C 1-10 "Alkyl" means an alkyl having a backbone of 1 to 10 carbon atoms. Specifically, C 1-10 Alkyl can be methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, i-pentyl, t-pentyl, sec-pentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, and the like.

[0020] The term "alkoxy" means a straight or branched chain alkyl-oxy group, unless otherwise specified. For example, "C 1-6 The term "alkoxy" refers to an alkyloxy having a skeleton of 1 to 6 carbon atoms. 1-6 Alkoxy includes methoxy, ethoxy, n-propoxy, i-propoxy, n-butoxy, i-butoxy, t-butoxy, n-pentoxy, i-pentoxy, t-pentoxy, sec-pentoxy, neopentoxy, hexyloxy, and the like.

[0021] The term "haloalkyl" or "haloalkoxy" means an alkyl or alkoxy substituted with one or more halogens. Specifically, the haloalkyl or haloalkoxy can be an alkyl or alkoxy substituted with one or more of the same or different halogens.

[0022] The term "cycloalkyl" means a saturated monocyclic or polycyclic group containing only carbon atoms in the ring. For example, a cycloalkyl is a monocyclic group and can have from 3 to 7 carbon atoms.

[0023] In one aspect, the present invention provides a compound of formula 1: [ka] (chemical formula 1) [In the formula, X is H, halogen, C 1-6 Alkyl, or C 1-6 is alkoxy; R is H, C 1-10 Alkyl, -A, -L 1 -R 1 , -L 1 -A, -L 1 -L 2 -A or -L 1 -L 2 -L 3 -A; L 1 is -(CH2) n -, -C(=O)-, -C(=O)-O-, -CH(-OH)-CH2-, -S(=O)2-, or -C(=S)-NH-; L 2 is -O-, -C(=O)-, -CH(-OH)-, -CH2-CH(-NH2)-, [ka] and; L 3 is -C(=O)-, -(CH2) n - or -(CH2) n -O-; n is an integer from 1 to 6; A is, [ka] and R 1 and R 2 are each independently H, halogen, -OH, haloC 1-6 Alkyl, C 1-6 Alkoxy, HaloC 1-6 Alkoxy, -CN, -COOH, C 1-6 Alkyl, aryl, C 3-6Cycloalkyl, amino, -NH-C(=O)-C 1-6 Alkyl, -NH-C(=O)-C 1-6 Alkoxy, -C(=O)-C 1-6 Alkoxy, or [ka] ] or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof.

[0024] In Chemical Formula 1, the substitution position of the X group can be the 7th, 8th, 9th, or 10th carbon in 5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridine.

[0025] Examples of various substitution positions for the X group include the following formulae 1-1 to 1-4. [ka]

[0026] According to one embodiment, in Formula 1, R is H, C 1-10 Alkyl or -L 1 -R 1 and;L 1 is -(CH2) n -, -C(=O)-, -C(=O)-O-, -S(=O)2-, or -C(=S)-NH-; n is an integer of 1 to 6; R 1 is -OH, or C 1-3 It is alkyl.

[0027] According to another embodiment, in Formula 1, R is -A, -L 1 -A, -L 1 -L 2 -A or -L 1 -L 2 -L 3 -A;L 1 is -(CH2) n -, or -C(=O)-; L 2is -O-, or [ka] and;L 3 is -C(=O)-; n is an integer from 1 to 6; A is [ka] and R 1 and R 2 are each independently H, -Cl, or C 1-3 It is alkyl.

[0028] According to yet another embodiment, in Formula 1, R is -L 1 -R 1 , -L 1 -L 2 -A or -L 1 -L 2 -L 3 -A;L 1 is -(CH2) n -And;L 2 is -CH(-OH)-, or [ka] and;L 3 is -(CH2) n -; n is an integer from 1 to 6; A is [ka] and R 1 and R 2 are both H.

[0029] According to yet another embodiment, in Formula 1, R is -L 1 -L 2 -A or -L 1 -L 2 -L 3 -A;L 1 is -(CH2) n -, or -C(=O)-; L 2is -O-, -CH(-OH)-, or [ka] and;L 3 is -C(=O)- or -(CH2) n -O-; each n is an integer from 1 to 6; A is [ka] and R 1 and R 2 are each independently H or C 1-3 It is alkyl.

[0030] According to yet another embodiment, in Formula 1, R is -A, -L 1 -A, -L 1 -L 2 -A or -L 1 -L 2 -L 3 -A;L 1 is -(CH2) n - or -C(=O);L 2 is -O-, -C(=O)-, -CH(-OH)-, -CH2-CH(-NH2)-, or [ka] and;L 3 is -C(=O)- or -(CH2) n -; n is an integer from 1 to 6; A is [ka] and R 1 and R 2 are each independently H, -F, -Cl, -Br, -OH, -CF3, -CN, -COOH, or C 1-3 It is alkyl.

[0031] According to yet another embodiment, in Formula 1, R is -L 1 -L2 -A or -L 1 -L 2 -L 3 -A;L 1 is -(CH2) n -And;L 2 is -O- or -CH(-OH)-; L 3 is -(CH2) n -O-; A is [ka] and R 1 and R 2 are independently H, F, and C 1-6 Alkyl, C 1-6 Alkoxy, -CF3, Allyl, -COOH, C 3-6 Cycloalkyl, amino, -C(=O)-C 1-6 Alkoxy, or [ka] is.

[0032] According to one particular embodiment, the tricyclic derivative is of formula 1a: [ka] (Formula 1a) [In the formula, X is H, halogen, C 1-6 Alkyl, or C 1-6 is alkoxy; and R 1 and R 2 are each independently H, halogen, -OH, or C 1-6 Alkyl, HaloC 1-6 Alkyl, or C 1-6 It is alkoxy. It can be expressed as:

[0033] According to another particular embodiment, the tricyclic derivative is of formula 1b: [ka] (Formula 1b) [In the formula, X is H, halogen, C 1-6 Alkyl, or C 1-6 is alkoxy; and R 1 and R 2 are each independently H, halogen, -OH, or C 1-6 Alkyl, HaloC 1-6 Alkyl, or C 1-6 It is alkoxy. It can be expressed as:

[0034] According to yet another particular embodiment, the tricyclic derivative is of formula 1c: [ka] (Chemical formula 1c) [In the formula, X is H, halogen, C 1-6 Alkyl, or C 1-6 is alkoxy; A is, [ka] and R 1 and R 2 are each independently H, halogen, -OH, or C 1-6 Alkyl, HaloC 1-6 Alkyl, or C 1-6 It is alkoxy. It can be expressed as:

[0035] The compounds of the present invention include pharmaceutically acceptable salts of the tricyclic derivatives represented by Chemical Formula 1.

[0036] A pharmaceutically acceptable salt should have low toxicity to humans and should not adversely affect the biological activity and physicochemical properties of the parent compound. For example, a pharmaceutically acceptable salt can be an acid addition salt formed using a pharmaceutically acceptable free acid.

[0037] The free acid may be an inorganic acid or an organic acid, where the inorganic acid may be hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, perchloric acid, bromic acid, etc., and the organic acid may be acetic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, fumaric acid, maleic acid, malonic acid, phthalic acid, succinic acid, lactic acid, citric acid, gluconic acid, tartaric acid, salicylic acid, malic acid, oxalic acid, benzoic acid, embonic acid, aspartic acid, glutamic acid, etc.

[0038] The acid addition salts can be prepared by conventional methods, for example, by dissolving the compound of Formula 1 in an excess of aqueous acidic solution and precipitating the salt using a water-miscible organic solvent, such as methanol, ethanol, acetone, or acetonitrile.

[0039] The pharmaceutically acceptable salt may be an alkali metal salt (such as a sodium salt) or an alkaline earth metal salt (such as a potassium salt). The alkali metal salt or alkaline earth metal salt can be obtained, for example, by dissolving the compound represented by Chemical Formula 1 in a solution of an excess amount of alkali metal hydroxide or alkaline earth metal hydroxide, filtering off the insoluble compound salt, and evaporating the filtrate to dryness.

[0040] Furthermore, the compounds of the present invention may have chiral carbon centers and therefore may exist in the form of R or S isomers, racemates, individual enantiomers or mixtures thereof, or individual diastereomers or mixtures thereof, and all such stereoisomers and mixtures thereof may be included within the scope of the present invention.

[0041] Furthermore, the compounds of the present invention may include prodrugs of the compounds represented by Formula 1. A prodrug may refer to a functional derivative of the compound and is easily convertible to the compound in vivo. A prodrug may be administered more easily than the compound in some situations and is therefore useful in some cases. Unlike the compound, a prodrug is bioavailable, for example, by oral administration. A prodrug may also have improved solubility in pharmaceutical compositions compared to the compound. A prodrug can also be converted to the corresponding drug by various mechanisms, such as enzymatic processes or metabolic hydrolysis. An example of a prodrug is a compound in which the amino group of the compound is protected with a protecting group such as t-butyloxycarbonyl (Boc).

[0042] Furthermore, the compounds of the present invention may include hydrates or solvates of the compounds represented by Chemical Formula 1. The hydrates or solvates can be prepared using known methods and are preferably non-toxic and water-soluble. In particular, the hydrates or solvates may be those having 1 to 5 molecules of water or alcohol solvent (particularly, ethanol, etc.) bound thereto.

[0043] According to certain embodiments, specific examples of compounds of the present invention are as follows: 1) Ethyl 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carboxylate; 2) 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine dihydrochloride; 3) 8-chloro-11-(1-(methylsulfonyl)piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 4) 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-N-isopropylpiperidine-1-carbothioamide; 5) 1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-one; 6) (R)-3-amino-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-(2,4,5-trifluorophenyl)butan-1-one dihydrochloride; 7) (S)-2-amino-3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carbonyl)phenyl)propionic acid dihydrochloride; 8) (S)-1-(2-amino-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-oxobutyl)-5,5-difluoropiperidin-2-one dihydrochloride; 9) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 10) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 11) 2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethan-1-one; 12) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)quinazoline-2,4(1H,3H)-dione; 13) 8-chloro-11-(1-methylpiperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 14) (S)-2-amino-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 15) 2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethan-1-ol; 16) Ethyl (S)-2-((t-butoxycarbonyl)amino)-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propanoate; 17) (S)-2-((t-butoxycarbonyl)amino)-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid; 18) 7-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)-3,4-dihydroquinolin-2(1H)-one; 19) 2-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)hexahydro-1H-isoindole-1,3(2H)-dione; 20) (S)-2-Amino-3-(3-chloro-4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 21) (S)-2-amino-3-(3-chloro-4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride; 22) (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride; 23) (2S,4S)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)pyrrolidine-2-carboxylic acid trihydrochloride; 24) 1-(4-bromophenyl)-2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-one; 25) (4R,7S)-2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 26) 2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; 27) 1-(4-bromophenyl)-2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-ol; 28) (2S,4R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)pyrrolidine-2-carboxylic acid; 29) (S)-2-Amino-3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)phenyl)propionic acid dihydrochloride; 30) (4R,7S)-2-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 31) Ethyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 32) 4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butan-1-ol; 33) 3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)-1H-indole-5-carbonitrile; 34) t-Butyl ((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamate; 35) (2R,3S)-3-amino-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-phenylbutan-2-ol; 36) trans-methyl 2-(-4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetate; 37) 2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropyl)hexahydro-1H-isoindole-1,3(2H)-dione; 38) (4R,7S)-2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 39) 6-chloro-5-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)indolin-2-one; 40) trans-methyl 2-(-4-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)cyclohexyl)acetate; 41) trans-2-(4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetic acid; 42) trans-2-(4-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)cyclohexyl)acetic acid; 43) (S)-2-((t-butoxycarbonyl)amino)-3-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)propionic acid; 44) (S)-2-amino-3-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)propionic acid trihydrochloride; 45) trans-2-(4-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)cyclohexyl)acetic acid; 46) N-((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)-2-phenyl-5-(trifluoromethyl)oxazole-4-carboxamide; 47) (4R,7S)-2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 48) 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 49) Isopropyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 50) Neopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 51) Cyclopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 52) 4-((3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-9-yl)oxy)-4-oxobutanoic acid; 53) 2-((1R,4R)-4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetic acid; 54) 4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)-4''-(trifluoromethoxy)-[1,1':3',1''-terphenyl]-5'-carboxylic acid; 55) (2S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)propionic acid trihydrochloride; 56) 3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)benzyl)-1-(4-fluorobenzyl)-1-(1-methylpiperidin-4-yl)urea; 57) N-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)acetamide; 58) t-Butyl (4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)carbamate; 59) N-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)-2-(4-fluorophenyl)acetamide; 60) 1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-(2-(3-methoxyphenethyl)phenoxy)propan-2-ol; 61) 1-(2-allylphenoxy)-3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propan-2-ol; 62) (E)-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-(2-(3-methoxystyryl)phenoxy)propan-2-ol; 63) 9-Hydroxy-3-(2-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 64) 9-Hydroxy-2-methyl-3-(2-(4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 65) 3-(2-(4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 66) (S)-2-Amino-3-(4-(4-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 67) (S)-2-Amino-3-(4-(4-(4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 68) (S)-2-Amino-3-(4-(4-(4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 69) (4R,7S)-2-((trans-2-((4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 70) (4R,7S)-2-((trans-2-((4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 71) (4R,7S)-2-((trans-2-((4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 72) 2-((trans-2-((4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; 73) 2-((trans-2-((4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; and 74) 2-((trans-2-((4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione.

[0044] In another aspect, the present invention provides the use of a compound that is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, as a serotonin receptor antagonist (particularly a serotonin 2A receptor antagonist).

[0045] Furthermore, the present invention provides the use of a compound that is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, for the prevention or treatment of a disease associated with serotonin activation.

[0046] As used herein, "prevention" refers to the effect of suppressing or delaying the onset, spread, and recurrence of a metabolic or abnormal proliferative disease by administering a pharmaceutical composition, and "treatment" refers to the effect of improving or beneficially altering the symptoms of the aforementioned disease by administering a pharmaceutical composition.

[0047] The present invention further provides use of a compound which is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, for the manufacture of a medicament for preventing or treating a disease associated with serotonin activation.The present invention further provides use of a compound which is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, for the manufacture of a medicament for inhibiting the activity of serotonin.

[0048] The present invention further provides a method for preventing or treating a disease associated with serotonin activation, comprising administering a compound which is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, to a subject in need thereof. The present invention also provides a method for inhibiting the activity of serotonin, comprising administering a compound which is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, to a subject in need thereof. Here, "subject in need thereof" refers to any animal that has or may develop a disease associated with serotonin activation, including humans, monkeys, cows, horses, sheep, pigs, chickens, turkeys, quail, cats, dogs, mice, rats, and rabbits.

[0049] Furthermore, "administration" means providing a predetermined substance to a subject in need thereof in an appropriate manner, and the administration route of the compound of the present invention can be any common route as long as the compound can reach the target tissue.

[0050] In yet another aspect, the present invention provides a pharmaceutical composition for inhibiting the activity of serotonin, comprising, as an active ingredient, a compound that is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof.

[0051] In yet another aspect, the present invention provides a pharmaceutical composition for preventing or treating a disease associated with serotonin activation, comprising, as an active ingredient, a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof.

[0052] The serotonin receptors inhibited by the compounds or pharmaceutical compositions of the present invention are, in particular, serotonin 2A (5-HT 2A ) receptors.

[0053] Furthermore, the disease associated with serotonin activation and prevented or treated in the present invention may be a metabolic disease or cancer.

[0054] The metabolic disease may be selected from the group consisting of obesity, diabetes, hyperlipidemia, arteriosclerosis, fatty liver, steatohepatitis, fibrosis, and hypertension, where fatty liver and steatohepatitis include alcoholic fatty liver disease, nonalcoholic fatty liver disease (NAFLD), and nonalcoholic steatohepatitis (NASH).

[0055] Additionally, the cancer may be selected from the group consisting of colon cancer, breast cancer, and ovarian cancer.

[0056] The pharmaceutical composition of the present invention may contain, as an active ingredient, a compound which is a tricyclic derivative represented by Chemical Formula 1, or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof, in an amount of 0.1 to 90% by weight, specifically 0.1 to 75% by weight, more specifically 1 to 50% by weight, based on the total weight of the composition.

[0057] In addition to the compounds of the present invention, the compositions of the present invention may further contain common non-toxic pharmaceutically acceptable additives that are mixed as active ingredients in conventional formulations. For example, pharmaceutical compositions may further contain pharmaceutically acceptable carriers, diluents, or excipients.

[0058] The additives used in the composition of the present invention can include, for example, sweeteners, binders, solvents, solubilizers, wetting agents, emulsifiers, isotonicity agents, absorbents, disintegrants, antioxidants, preservatives, lubricants, fillers, and flavorings.For example, additives can include lactose, dextrose, sucrose, mannitol, sorbitol, cellulose, glycine, silica, talc, stearic acid, stearin, magnesium stearate, magnesium aluminosilicate, starch, gelatin, tragacanth gum, alginic acid, sodium alginate, methylcellulose, sodium carboxymethylcellulose, agar, water, ethanol, polyethylene glycol, polyvinylpyrrolidone, sodium chloride, calcium chloride, orange essence, strawberry essence, vanilla flavor, etc.

[0059] The compositions of the present invention can be formulated in a variety of dosage forms for oral administration (e.g., tablets, pills, powders, capsules, syrups, or emulsions) or parenteral administration (e.g., intramuscular, intravenous, or subcutaneous injection).

[0060] Preferably, the composition of the present invention can be formulated as a preparation for oral administration, and excipients used in such a preparation include cellulose, calcium silicate, corn starch, lactose, sucrose, dextrose, calcium phosphate, stearic acid, magnesium stearate, calcium stearate, gelatin, talc, surfactants, suspending agents, emulsifiers, diluents, etc.

[0061] Specifically, solid preparations for oral administration include tablets, pills, powdered medicines, granules, capsules, etc., and such solid preparations can be prepared by mixing the composition with at least one excipient, for example, starch, calcium carbonate, sucrose, lactose, gelatin, etc. Furthermore, in addition to simple excipients, lubricants such as magnesium stearate and talc can be used.

[0062] Liquid preparations for oral administration include, for example, suspensions, oral liquids, emulsions, and syrups, and may contain various excipients such as wetting agents, sweeteners, cooling agents, preservatives, and the like in addition to water and liquid paraffin, which are commonly used simple diluents.

[0063] Parenteral formulations include sterile aqueous solutions, non-aqueous solvents, suspensions, emulsions, lyophilized preparations, and suppositories. Non-aqueous solvents and suspensions include propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable esters such as ethyl oleate. Suppository bases include witepsol, macrogol, Tween 61, cocoa butter, laurinum, and glycerogelatin. Injectables may contain additives from related technologies, such as solubilizers, isotonicity agents, suspending agents, emulsifiers, stabilizers, and preservatives.

[0064] The compounds or compositions of the invention can be administered to a patient in a therapeutically or pharmaceutically effective amount.

[0065] As used herein, a "therapeutically effective amount" or "pharmaceutically effective amount" refers to an amount of a compound or composition effective in preventing or treating a target disease, sufficient to treat the disease at a reasonable benefit / risk ratio applicable to any medical treatment, but not causing side effects. The level of the effective amount can be determined according to factors such as the patient's health condition, the type and severity of the disease, the activity of the drug, sensitivity to the drug, the method of administration, the time of administration, the route of administration, the excretion rate, the duration of treatment, co-administered or co-used drugs, and other factors well known in the medical field.

[0066] The compounds or compositions of the present invention can be administered as individual therapeutic agents or in combination with other therapeutic agents, can be administered simultaneously or sequentially with therapeutic agents in the related art, and can be administered in single or multiple doses. Taking all of the above factors into consideration, it is important to administer an amount that can achieve the maximum effect with the minimum amount without causing side effects, and such an amount can be easily determined by one skilled in the art.

[0067] Specifically, the effective amount of the compound in the composition of the present invention varies depending on the age, sex, and weight of the patient, and generally ranges from 0.1 to 1,000 mg, preferably 5 to 200 mg, per kg of body weight, and can be administered daily or every other day, or in 1 to 3 divided doses per day. However, the amount can be increased or decreased depending on the route of administration, severity of the disease, sex, weight, age, etc., and therefore the scope of the present invention is not limited thereto.

[0068] Preferably, the compounds or compositions of the present invention can be administered for tumor treatment in combination with chemotherapy, radiotherapy, immunotherapy, hormone therapy, bone marrow transplantation, stem cell replacement therapy, other biological therapy, surgical intervention, or a combination thereof.For example, the compounds or compositions of the present invention can be used as adjuvant therapy together with other long-term progressive treatment strategies, or can be used to maintain the condition of severely ill patients undergoing tumor regression or chemoprevention therapy.

[0069] Preferably, the pharmaceutical composition of the present invention may further comprise one or more active ingredients, and the additional active ingredients may be antiproliferative compounds, such as aromatase inhibitors, antiestrogens, topoisomerase I inhibitors, topoisomerase II inhibitors, microtubule active compounds, alkylating compounds, histone deacetylase inhibitors, compounds that induce cell differentiation processes, cyclooxygenase inhibitors, MMP inhibitors, mTOR inhibitors, antitumor antimetabolites, platinum compounds, compounds that target / reduce protein or lipid kinase activity, antiangiogenic compounds, compounds that target, reduce, or inhibit protein or lipid phosphatase activity, gonadorelin agonists, antiandrogens, Examples include, but are not limited to, methionine aminopeptidase inhibitors, bisphosphonates, biological response modifiers, antiproliferative antibodies, heparanase inhibitors, Ras oncogenic isotype inhibitors, telomerase inhibitors, proteasome inhibitors, compounds used in the treatment of hematologic malignancies, compounds that target, reduce, or inhibit Flt-3 activity, Hsp90 inhibitors, kinesin spindle protein inhibitors, MEK inhibitors, leucovorin, EDG binders, anti-leukemia compounds, ribonucleotide reductase inhibitors, S-adenosylmethionine decarboxylase inhibitors, hemostatic steroids, corticosteroids, other chemotherapeutic compounds, or photosensitizing compounds. [Example]

[0070] Aspects of the invention The present invention will be described in more detail below with reference to the following examples, which are provided only to better understand the present invention and are not intended to limit the scope of the present invention.

[0071] Example 2: Preparation of 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine dihydrochloride [ka] Loratadine (10 g, 26.117 mmol) was added to 100 mL of concentrated hydrochloric acid solution, and the resulting mixture was refluxed with stirring for 12 hours. The excess hydrochloric acid solution was then evaporated to give the title compound (9.5 g, 95% yield). 1 H NMR (300 MHz, DMSO-d6): δ 9.43 (bs, 3H), 8.67 (d, J=5.49 Hz, 1H), 8.39 (d, J=7.63 Hz, 1H), 7.93-7.81 (m, 1H), 7.47-7.39 (m, 1H), 7.34 (d, J=8.24 Hz, 1H), 7.20 (d, J=7.93 Hz, 1H), 3.20-2.30 (m, 12H).

[0072] Example 9 Preparation of 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one [ka]

[0073] Step 1: Preparation of 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Loratadine (2 g, 5.2 mmol) was dissolved in 10 mL of concentrated hydrochloric acid solution and refluxed for 12 hours. After evaporating the hydrochloric acid solution, water was added to the mixture. The pH was adjusted to 8 using ammonium hydroxide, and the mixture was extracted with dichloromethane and then washed with water and brine. The combined organic layer was dried over anhydrous sodium sulfate and then concentrated to give the title compound as a white solid (1.5 g, 92% yield). 1H NMR (400 MHz, DMSO-d6): δ 8.32 (d, J=4.58 Hz, 1H), 7.56 (d, J=7.63 Hz, 1H), 7.28 (s, 1H), 7.23-7.15 (m, 2H), 7.06 (dd, J=8.24, 1.53 Hz, 1H), 3.46-3.21 (m, 3H), 2.93-2.75 (m, 4H), 2.65-2.53 (m, 1H), 2.34-2.04 (m, 4H); LCMS [M+H] 311.1

[0074] Step 2: Preparation of 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one The compound obtained in Step 1 of Example 9 (120 mg, 0.313 mmol) was dissolved in 2 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (99.43 mg, 0.938 mmol), potassium iodide (51.91 mg, 0.313 mmol), and 3-(2-chloroethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one (77.74 mg, 0.344 mmol), and the resulting mixture was heated to 80 °C. After the reaction was completed, the mixture was extracted twice with brine and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and then concentrated. The residue was purified by silica gel column chromatography to give the title compound (140 mg, 89% yield). 1 H NMR (300 MHz, MeOD): δ 8.49 (dd, J=4.88, 1.22 Hz, 1H), 7.87 (d, J=7.63 Hz, 1H), 7.50-7.44 (m, 1H), 7.38 (d, J=2.14 Hz, 1H), 7.35-7.23 (m, 2H), 4.92-4.78 (m, 2H), 3.65-3.28 (m, 9H), 2.96-2.43 (m, 16H)

[0075] Example 10: Preparation of 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one [ka]

[0076] Step 1: Preparation of 3-(2-chloroethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one In a 10 L reaction vessel connected to a gas sparger and a thermostat, 3-(2-chloroethyl)-9-hydroxy-2-methyl-4H-pyrido[1,2-a]pyrimidin-4-one hydrochloride (400 g, 1.45 mol) was dissolved in methanol (4,800 mL) and the resulting mixture was stirred. After filling the reaction vessel with nitrogen gas, 10% Pd / C / RD-854 (80 g) was added. The resulting solution was heated to 55 °C and stirred for 2 hours while slowly introducing hydrogen gas. After the reaction was complete, the mixture was cooled to room temperature and filtered through Celite under nitrogen to remove the Pd / C. The residue was washed with methanol (2 × 400 mL) and then concentrated. Water (1,480 mL) was added to the resulting mixture, and the resulting mixture was heated at 80-85 °C for 15 minutes. The mixture was cooled to room temperature, and potassium acetate (285.4 g, 2.9077 mol) dissolved in 300 mL of water was slowly added over 1 hour. The solution was stirred at room temperature for 1 hour, cooled to 8-12 °C for 2 hours, and then stirred. The resulting crystals were filtered and washed with 400 mL of water containing ethylenediaminetetraacetic acid disodium salt dihydrate (2 g), followed by water (400 mL) and isopropyl alcohol (200 mL) to obtain a solid. The solid was dried under vacuum to give the title compound as a white solid (266 g, 75% yield). 1H NMR (400 MHz, DMSO-d6): δ 5.71 (s, 1H), 4.48-4.41 (m, 1H), 3.96-3.84 (m, 1H), 3.78-3.62 (m, 3H), 2.95-2.85 (m, 2H), 2.28 (s, 3H), 2.06-1.74 (m, 4H); LCMS [M+H] 243.1

[0077] Step 2: Preparation of 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Loratadine (2 g, 5.2 mmol) was dissolved in 10 mL of concentrated hydrochloric acid solution, and the resulting mixture was refluxed for 12 hours. After evaporating the hydrochloric acid solution, water was added to the mixture. The pH was adjusted to 8 using ammonium hydroxide, and the mixture was extracted with dichloromethane and then washed with water and brine. The combined organic layer was dried over anhydrous sodium sulfate and then concentrated to give the title compound as a white solid (1.5 g, 92% yield). 1 H NMR (400 MHz, DMSO-d6): δ 8.32 (d, J=4.58 Hz, 1H), 7.56 (d, J=7.63 Hz, 1H), 7.28 (s, 1H), 7.23-7.15 (m, 2H), 7.06 (dd, J=8.24, 1.53 Hz, 1H), 3.46-3.21 (m, 3H), 2.93-2.75 (m, 4H), 2.65-2.53 (m, 1H), 2.34-2.04 (m, 4H); LCMS [M+H] 311.1

[0078] Step 3: Preparation of 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one The compound obtained in Step 2 of Example 10 (500 mg, 1.609 mmol) was dissolved in 4 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (511.49 mg, 4.826 mmol), potassium iodide (267.04 mg, 1.0609 mmol), and the compound obtained in Step 1 of Example 10 (390.41 mg, 1.609 mmol), successively. The mixture was heated to 80°C. After completion of the reaction, the mixture was extracted twice with ethyl acetate and brine. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (745 mg, 90% yield). 1 H NMR (400 MHz, DMSO-d6): δ 8.30 (d, J=4.58 Hz, 1H), 7.53 (d, J=7.63 Hz, 1H), 7.26 (s, 1H), 7.21-7.12 (m, 2H), 7.04 (d, J=7.93 Hz, 1H), 5.63 (d, J=4.27 Hz, 1H), 4.43-4.34 (m, 1H), 3.89-3.78 (m, 1H), 3.67-3.55 (m, 1H), 3.29 (s, 3H), 3.35-3.20 (m, 2H), 2.86-2.42 (m, 6H), 2.40-2.04 (m, 10H), 1.98-1.68 (m, 2H); LCMS [M+H] 517.2

[0079] Example 22: Preparation of (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride [ka]

[0080] Step 1: Preparation of ethyl(t-butoxycarbonyl)-L-tyrosine [ka] L-tyrosine (100 g, 0.552 mol) was dissolved in 800 mL of ethanol, and then thionyl chloride (100.1 mL, 1.38 mol) was slowly added while stirring. The mixture was stirred at 0°C for 1 hour and then refluxed overnight. After the reaction was complete, the mixture was concentrated to remove volatiles, yielding ethyl L-tyrosinate hydrochloride. Ethyl L-tyrosinate hydrochloride was added to 100 mL of methanol and 800 mL of dichloromethane, and the mixture was stirred at room temperature. Then, triethylamine (154 mL, 1.1 mol) and di-t-butyl dicarbonate (120.5 g, 0.552 mol) dissolved in 200 mL of dichloromethane were sequentially added to the reaction solution at 0°C. The mixture was stirred at room temperature overnight, and the solid was then removed by filtration. The mixture was extracted with water, and the organic layer was treated with sodium sulfate and then concentrated to give the title compound (136 g, yield 80%) as a white solid.

[0081] Step 2: Preparation of ethyl (S)-3-(4-(3-bromopropoxy)phenyl)-2-((t-butoxycarbonyl)amino)propanoate [ka] Ethyl (t-butoxycarbonyl)-L-tyrosinate (2 g, 6.645 mmol), calcium carbonate (902.39 mg, 6.53 mmol), and 1,3-dibromopropane (3.92 g, 19.39 mmol) were dissolved in 20 mL of N,N-dimethylformamide, and the resulting mixture was stirred at 100 °C for 7 hours. After the mixture was cooled to room temperature, 200 mL of water was added, followed by extraction with ethyl acetate and washing with brine. The organic layer was treated with sodium sulfate, and the filtrate was concentrated and then purified by silica gel column chromatography to give the title compound (1.1 g, 40% yield).

[0082] Step 3: Preparation of ethyl (S)-2-((t-butoxycarbonyl)amino)-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate [ka] 8-Chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine (200 mg, 0.521 mmol) was dissolved in 4 mL of N,N-dimethylformamide and the resulting mixture was stirred. Sodium carbonate (209.91 mg, 1.98 mmol) and ethyl (S)-3-(4-(3-bromopropoxy)phenyl)-2-((t-butoxycarbonyl)amino)propanoate (246.69 mg, 0.573 mmol) were added sequentially to the reaction solution. The mixture was then heated to 80°C and stirred for 3 hours. After the reaction was complete, the mixture was extracted with brine and ethyl acetate. The organic layer was treated with sodium sulfate, and the filtrate was concentrated and purified by silica gel column chromatography to give the title compound (310 mg, 90% yield).

[0083] Step 4: Preparation of (S)-2-((t-butoxycarbonyl)amino)-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid [ka] The compound obtained in Step 3 of Example 22 (310 mg, 0.469 mmol) was dissolved in 80 mL of a tetrahydrofuran / water (3:1) solution, and then sodium hydroxide (93.9 mg, 2.34 mmol) was added. The mixture was then stirred at room temperature for 24 hours. After the reaction was completed, the tetrahydrofuran was evaporated, and the pH was adjusted to 4 using 1N hydrochloric acid solution. 50 mL of water was added, followed by extraction with ethyl acetate (3 x 100 mL). The organic layer was washed with brine, then treated with sodium sulfate, and the filtrate was concentrated. The concentrated mixture was purified by silica gel column chromatography to give the title compound (260 mg, 87% yield).

[0084] Step 5: Preparation of (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride [ka] ((S)-2-((t-butoxycarbonyl)amino)-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid was dissolved in 10 mL of ethyl acetate, and 10 mL of a 4.0 M solution of 1,4-dioxin in hydrochloric acid was added. The mixture was then stirred for 12 hours. The mixture was concentrated and then filtered to give the title compound (180 mg, yield 77%) as a white solid. 1H NMR (300 MHz, DMSO-d6): δ 11.40 (s, 1H), 8.63-8.55 (m, 1H), 8.45 (bs, 3H), 8.24-8.11 (m, 1H), 7.79-7.63 (m, 1H), 7.42 (dd, J=9.00, 2.14 Hz, 1H), 7.32 (d, J=8.24 Hz, 1H), 7.29-7.11 (m, 3H), 6.90 (dd, J=18.92, 8.54 Hz, 2H), 4.12-3.98 (m, 3H), 3.53-3.41 (m, 2H), 3.36-2.76 (m, 8H), 2.67-2.35 (m, 6H), 2.31-2.11 (m, 2H).

[0085] Example 25 Preparation of (4R,7S)-2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione [ka]

[0086] Step 1: Preparation of ((1R,2R)-cyclohexane-1,2-diyl)bis(methylene)dimethanesulfonate [ka] Methanesulfonyl chloride (1.2 mL, 15.257 mmol) and triethylamine (2.5 mL, 17.337 mmol) were added to 50 mL of dichloromethane containing ((1R,2R)-cyclohexane-1,2-diyl)dimethanol (1 g, 6.935 mmol) at 0°C to 5°C. The temperature was slowly raised to room temperature, and the reaction solution was stirred for 2 hours. 50 mL of dichloromethane was added to the resulting mixture, which was then extracted with water. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (1.8 g, 86% yield).

[0087] Step 2: Preparation of ((1R,2R)-2-(((4R,7S)-1,3-dioxooctahydro-2H-4,7-methanolisoindol-2-yl)methyl)cyclohexyl)methyl methanesulfonate [ka] The compound obtained in Step 1 of Example 25 (545 mg, 1.81 mmol) and (4R,7S)-hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione (300 mg, 1.816 mmol) were dissolved in 20 mL of acetone, and potassium carbonate (376.45 mg, 2.724 mmol) was added. The resulting mixture was refluxed for 12 hours. The resulting mixture was concentrated, and the residue was purified by silica gel column chromatography to give the title compound (520 mg, 78% yield).

[0088] Step 3: Preparation of (4R,7S)-2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione [ka] The compound obtained in Step 2 of Example 10 (200 mg, 0.521 mmol) was dissolved in 2 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (165.72 mg, 1.564 mmol) and the compound obtained in Step 2 of Example 25 (211.84 mg, 0.573 mmol), and the resulting mixture was stirred at 80°C for 3 hours. After the reaction was completed, the mixture was extracted twice with brine and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and then concentrated. The residue was purified by silica gel column chromatography to give the title compound (250 mg, 82% yield). 1 H NMR (300 MHz, CDCl3): δ 8.47-8.32 (m, 1H), 7.42 (d, J=7.93 Hz, 1H), 7.24-7.02 (m, 4H), 4.01-3.11 (m, 4H), 2.93-0.93 (m, 32H)

[0089] Example 26: Preparation of 2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione [ka]

[0090] Step 1: Preparation of ((1R,2R)-2-((1,3-dioxooctahydro-2H-isoindol-2-yl)methyl)cyclohexyl)methyl methanesulfonate [ka] The compound obtained in Step 1 of Example 25 (588.25 mg, 1.958 mmol) and hexahydro-1H-isoindole-1,3(2H)-dione (300 mg, 1.958 mmol) were dissolved in 20 mL of acetone, and potassium carbonate (405.94 mg, 2.937 mmol) was added. The mixture was refluxed for 12 hours. The mixture was concentrated, and the residue was purified by silica gel column chromatography to give the title compound (550 mg, 79% yield).

[0091] Step 2: Preparation of 2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione [ka] The compound obtained in Step 2 of Example 10 (200 mg, 0.521 mmol) was dissolved in 2 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (165.72 mg, 1.564 mmol) and the compound obtained in Step 1 of Example 26 (204.96 mg, 0.573 mmol), and the resulting mixture was heated to 80°C for 3 hours. After the reaction was completed, the mixture was extracted twice with brine and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (260 mg, 87% yield). 1 H NMR (300 MHz, CDCl3): δ 8.44-8.34 (m, 1H), 7.41 (d, J=7.93 Hz, 1H), 7.23-7.03 (m, 4H), 3.48-3.12 (m, 2H), 2.92-0.94 (m, 34H).

[0092] Example 31: Preparation of ethyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride [ka] The compound obtained in Step 3 of Example 22 (900 mg, 1.36 mmol) was dissolved in 20 mL of ethyl acetate, and then 15 mL of a 4.0 M solution of hydrochloric acid in 1,4-dioxin was added. The resulting mixture was stirred for 12 hours. The mixture was then concentrated and filtered to give the title compound (810 mg, 88% yield) as a white solid. 1 H NMR (300 MHz, DMSO-d6): δ 8.66-8.47 (m, 4H), 8.24-8.08 (m, 1H), 7.78-7.60 (m, 1H), 7.39 (d, J=11.29 Hz, 1H), 7.29 (d, J=8.24 Hz, 1H), 7.17-7.07 (m, 3H), 6.93-6.79 (m, 2H), 4.21-3.94 (m, 5H), 3.49-3.37 (m, 2H), 3.30-2.08 (m, 18H), 1.13 (t, J=7.02 Hz, 3H).

[0093] Example 48: Preparation of 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine [ka] The compound obtained in Example 2 (5 g) was dissolved in water, and then aqueous ammonia was added to adjust the pH to 8. The mixture was then extracted with ethyl acetate (3 × 100 mL). The organic layer was washed with brine and treated with sodium sulfate, and the filtrate was concentrated to obtain the title compound. LC-MS (m / z): 311.1270 (M+H)

[0094] Example 51: Preparation of cyclopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride [ka]

[0095] Step 1: Preparation of cyclopentyl (S)-3-(4-(3-bromopropoxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoate [ka] Triphenylphosphine (563 g, 2.146 mmol) and 3-bromopropan-1-ol (298 mg, 2.146 mmol) were added to cyclopentyl (tert-butoxycarbonyl)-L-tyrosinate (500 mg, 1.431 mmol) dissolved in 100 mL of tetrahydrofuran. The mixture was cooled to 0 °C, and then diisopropyl azodicarboxylate (DIAD, 0.4 mL, 2.146 mmol) was slowly added. The temperature of the mixture was slowly raised to room temperature, and the mixture was stirred for 24 hours. The resulting mixture was evaporated and then extracted with water and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (560 mg, 83% yield).

[0096] Step 2: Preparation of cyclopentyl (S)-2-((tert-butoxycarbonyl)amino)-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate [ka] The compound obtained in Step 2 of Example 10 (170 mg, 0.443 mmol) was dissolved in 2 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (141 mg, 1.329 mmol) and the compound obtained in Step 1 of Example 51 (219 mg, 0.465 mmol), and the resulting mixture was heated to 80°C for 3 hours. After the reaction was completed, the mixture was extracted twice with brine and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (270 mg, 87% yield).

[0097] Step 3: Preparation of cyclopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride [ka] The compound obtained in Step 2 of Example 51 (270 mg, 0.386 mmol) was dissolved in ethyl acetate (20 mL), and then a 4 M solution of 1,4-dioxin in hydrochloric acid was added and the resulting mixture was stirred. The mixture was evaporated and then filtered to give the title compound (220 mg, 80% yield). 1 H NMR (300 MHz, DMSO-d6): δ 8.66-8.52 (m, 4H), 8.22 (s, 1H), 7.76 (s, 1H), 7.43 (dd, J=11.14, 2.14 Hz, 1H), 7.33 (dd, J=8.24, 2.14 Hz, 1H), 7.29-7.09 (m, 3H), 6.90 (dd, J=18.62, 8.54 Hz, 2H), 5.11-5.0 (m, 1H), 4.18-3.95 (m, 3H), 3.54-3.37 (m, 2H), 3.33-2.71 (m, 8H), 2.68-2.32 (m, 6H), 2.31-2.08 (m, 2H), 1.83-1.65 (m, 2H), 1.63-1.31 (m, 6H)

[0098] Example 63: Preparation of 9-hydroxy-3-(2-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one [ka]

[0099] Step 1: Preparation of 8-methoxy-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine Ethyl 4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carboxylate (150 mg, 0.396 mmol) was dissolved in 1 mL of concentrated hydrochloric acid solution and refluxed for 12 hours. After evaporating the hydrochloric acid solution, water was added. The pH was adjusted to 8 with ammonium hydroxide, followed by extraction with dichloromethane. The combined organic layers were washed with water and brine, dried over anhydrous sodium sulfate, and concentrated to give the title compound (110 g, 90% yield).

[0100] Step 2: Preparation of 9-hydroxy-3-(2-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one The compound obtained in Step 1 of Example 63 (100 mg, 0.326 mmol) was dissolved in 2 mL of N,N-dimethylformamide, followed by the addition of sodium carbonate (103.77 mg, 0.979 mmol), potassium iodide (54.18 mg, 0.326 mmol), and the compound obtained in Step 1 of Example 10 (79.21 mg, 0.326 mmol), and the resulting mixture was heated to 80 °C. After the reaction was completed, the mixture was extracted twice with brine and ethyl acetate. The combined organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified by silica gel column chromatography to give the title compound (140 mg, 84% yield). LCMS [M+H] 513.2

[0101] The example compounds shown in Table 1 below were synthesized via the synthetic route described above and routes similar to the synthetic route.

[0102] [Table 1] [Table 2] [Table 3] [Table 4] [Table 5] [Table 6] [Table 7] [Table 8] [Table 9] Table 10 Table 11 Table 12 Table 13 Table 14 Table 15 Table 16 Table 17 Table 18 Table 19 Table 20 Table 21 Table 22 Table 23 [Table 24] [Table 25]

[0103] Experimental example: Measurement of inhibitory activity against serotonin 2A receptors Serotonin 2A (5-HT 2A The inhibitory activity of the compounds synthesized in the examples against the α- and β-glucan receptor was measured in vitro. The results are shown in Table 2 below.

[0104] [Table 26]

[0105] As shown in Table 2, the inhibitory activity of the compounds of the examples against the serotonin 2A receptor was confirmed. Therefore, the compounds of the present invention can be useful for the prevention or treatment of diseases associated with serotonin activation, such as metabolic diseases such as obesity, fatty liver, and steatohepatitis.

Claims

1. Chemical formula 1: 【Chemistry 1】 (Chemical formula 1) [In the formula, X is H, halogen, C １－６ Alkyl, or C １－６ is alkoxy; R is H, C １－１０ Alkyl, -A, -L １ -R １ , -L １ -A, -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ is -(CH ２ ) ｎ -, -C(=O)-, -C(=O)-O-, -CH(-OH)-CH ２ -, -S(=O) ２ - or -C(=S)-NH-; L ２ は、-O-、-C(=O)-、-CH(-OH)-、-CH ２ -CH(-NH ２ )-、 【Chemistry 2】 and L ３ is -C(=O)-, -(CH ２ ) ｎ - or -(CH ２ ) ｎ -O-; n is an integer from 1 to 6; A is, 【Transformation 3】 and and, R １ and R ２ are each independently H, halogen, —OH, haloC １－６ Alkyl, C １－６ Alkoxy, HaloC １－６ Alkoxy, -CN, -COOH, C １－６ Alkyl, aryl, C ３－６ Cycloalkyl, amino, —NH—C(═O)—C １－６ Alkyl, —NH—C(═O)—C １－６ Alkoxy, —C(═O)—C １－６ Alkoxy, or 【Chemistry 4】 It is.] or a pharmaceutically acceptable salt, stereoisomer, or prodrug thereof.

2. R is H, C １－１０ Alkyl or -L １ -R １ and L １ But -(CH ２ ) ｎ -, -C(=O)-, -C(=O)-O-, -S(=O) ２ - or -C(=S)-NH-; n is an integer from 1 to 6; and R １ is —OH, or C １－３ is alkyl, The compound of claim 1.

3. R is -A, -L １ -A, -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ But -(CH ２ ) ｎ - or -C(=O)-; L ２ is -O-, or 【Transformation 5】 and L ３ is —C(═O)—; n is an integer from 1 to 6; A is, 【Transformation 6】 and and, R １ and R ２ are each independently H, —Cl, or C １－３ is alkyl, The compound of claim 1.

4. R is -L １ -R １ , -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ But -(CH ２ ) ｎ - and; L ２ is —CH(—OH)—, or 【Transformation 7】 and L ３ But -(CH ２ ) ｎ - and; n is an integer from 1 to 6; A is, 【Transformation 8】 and and, R １ and R ２ But both are H. The compound of claim 1.

5. R is -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ But -(CH ２ ) ｎ - or -C(=O)-; L ２ is —O—, —CH(—OH)—, or 【Chemistry 9】 and L ３ is -C(=O)- or -(CH ２ ) ｎ -O-; n is an integer from 1 to 6; A is, 【Chemistry 10】 and and, R １ and R ２ are each independently H or C １－３ is alkyl, The compound of claim 1.

6. R is -A, -L １ -A, -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ But -(CH ２ ) ｎ - or -C(=O); L ２ is -O-, -C(=O)-, -CH(-OH)-, -CH ２ -CH(-NH ２ )-,or, 【Chemistry 11】 and L ３ is -C(=O)- or -(CH ２ ) ｎ - and; n is an integer from 1 to 6; A is, 【Chemistry 12】 and and, R １ and R ２ are each independently H, —F, —Cl, —Br, —OH, or —CF ３ , —CN, —COOH, or C １－３ is alkyl, The compound of claim 1.

7. R is -L １ -L ２ -A or -L １ -L ２ -L ３ -A; L １ But -(CH ２ ) ｎ - and; L ２ is —O— or —CH(—OH)—; L ３ But -(CH ２ ) ｎ -O-; A is, 【Chemistry 13】 and and, R １ and R ２ are independently H, F, C １－６ Alkyl, C １－６ Alkoxy, —CF ３ , Allyl, -COOH, C ３－６ Cycloalkyl, amino, —C(═O)—C １－６ Alkoxy, or 【Chemistry 14】 That is, The compound of claim 1.

8. The tricyclic derivative has the formula 1a: 【Chemistry 15】 (Chemical formula 1a) [In the formula, X is H, halogen, C １－６ Alkyl, or C １－６ is alkoxy; and R １ and R ２ are each independently H, halogen, —OH, C １－６ Alkyl, haloC １－６ Alkyl, or C １－６ It is alkoxy. The compound of claim 1, wherein

9. The tricyclic derivative is represented by formula 1b: 【Chemistry 16】 (Chemical formula 1b) [In the formula, X is H, halogen, C １－６ Alkyl, or C １－６ is alkoxy; and R １ and R ２ are each independently H, halogen, —OH, C １－６ Alkyl, haloC １－６ Alkyl, or C １－６ It is alkoxy. The compound of claim 1, wherein

10. The tricyclic derivative has the formula 1c: 【Chemistry 17】 (Chemical formula 1c) [In the formula, X is H, halogen, C １－６ Alkyl, or C １－６ is alkoxy; A is, [Chemistry 18] and and, R １ and R ２ are each independently H, halogen, —OH, C １－６ Alkyl, haloC １－６ Alkyl, or C １－６ It is alkoxy. The compound of claim 1, wherein

11. 10. The compound of claim 1, which is selected from the group consisting of: 1) Ethyl 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carboxylate; 2) 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine dihydrochloride; 3) 8-chloro-11-(1-(methylsulfonyl)piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 4) 4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)-N-isopropylpiperidine-1-carbothioamide; 5) 1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-one; 6) (R)-3-amino-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-(2,4,5-trifluorophenyl)butan-1-one dihydrochloride; 7) (S)-2-amino-3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidine-1-carbonyl)phenyl)propionic acid dihydrochloride; 8) (S)-1-(2-amino-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-oxobutyl)-5,5-difluoropiperidin-2-one dihydrochloride; 9) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 10) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 11) 2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethan-1-one; 12) 3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)quinazoline-2,4(1H,3H)-dione; 13) 8-chloro-11-(1-methylpiperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 14) (S)-2-amino-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 15) 2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-1-(6-methylimidazo[2,1-b]thiazol-5-yl)ethan-1-ol; 16) Ethyl (S)-2-((t-butoxycarbonyl)amino)-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propanoate; 17) (S)-2-((t-butoxycarbonyl)amino)-3-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid; 18) 7-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)-3,4-dihydroquinolin-2(1H)-one; 19) 2-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)hexahydro-1H-isoindole-1,3(2H)-dione; 20) (S)-2-amino-3-(3-chloro-4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 21) (S)-2-amino-3-(3-chloro-4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride; 22) (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propionic acid trihydrochloride; 23) (2S,4S)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)pyrrolidine-2-carboxylic acid trihydrochloride; 24) 1-(4-bromophenyl)-2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-one; 25) (4R,7S)-2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 26) 2-(((1S,2S)-2-((4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; 27) 1-(4-bromophenyl)-2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethan-1-ol; 28) (2S,4R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)pyrrolidine-2-carboxylic acid; 29) (S)-2-amino-3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)phenyl)propionic acid dihydrochloride; 30) (4R,7S)-2-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 31) Ethyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 32) 4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butan-1-ol; 33) 3-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butyl)-1H-indole-5-carbonitrile; 34) t-butyl ((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamate; 35) (2R,3S)-3-amino-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-4-phenylbutan-2-ol; 36) trans-methyl 2-(-4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetate; 37) 2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropyl)hexahydro-1H-isoindole-1,3(2H)-dione; 38) (4R,7S)-2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 39) 6-chloro-5-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)indolin-2-one; 40) trans-methyl 2-(-4-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)cyclohexyl)acetate; 41) trans-2-(4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetic acid; 42) trans-2-(4-(4-(4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)cyclohexyl)acetic acid; 43) (S)-2-((t-butoxycarbonyl)amino)-3-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)propionic acid; 44) (S)-2-amino-3-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)propionic acid trihydrochloride; 45) trans-2-(4-(4-(((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)carbamoyl)phenyl)cyclohexyl)acetic acid; 46) N-((2S,3R)-4-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-hydroxy-1-phenylbutan-2-yl)-2-phenyl-5-(trifluoromethyl)oxazole-4-carboxamide; 47) (4R,7S)-2-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 48) 8-chloro-11-(piperidin-4-ylidene)-6,11-dihydro-5H-benzo[5,6]cyclohepta[1,2-b]pyridine; 49) Isopropyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 50) Neopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 51) Cyclopentyl (S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)phenyl)propanoate trihydrochloride; 52) 4-((3-(2-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-4-oxo-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-9-yl)oxy)-4-oxobutanoic acid; 53) 2-((1R,4R)-4-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)cyclohexyl)acetic acid; 54) 4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)-4″-(trifluoromethoxy)-[1,1′:3′,1″-terphenyl]-5′-carboxylic acid; 55) (2S)-2-amino-3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)propionic acid trihydrochloride; 56) 3-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propoxy)benzyl)-1-(4-fluorobenzyl)-1-(1-methylpiperidin-4-yl)urea; 57) N-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)acetamide; 58) t-butyl(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)carbamate; 59) N-(4-(3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-2-hydroxypropoxy)phenyl)-2-(4-fluorophenyl)acetamide; 60) 1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-(2-(3-methoxyphenethyl)phenoxy)propan-2-ol; 61) 1-(2-allylphenoxy)-3-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)propan-2-ol; 62) (E)-1-(4-(8-chloro-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)-3-(2-(3-methoxystyryl)phenoxy)propan-2-ol; 63) 9-hydroxy-3-(2-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 64) 9-hydroxy-2-methyl-3-(2-(4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 65) 3-(2-(4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)ethyl)-9-hydroxy-2-methyl-6,7,8,9-tetrahydro-4H-pyrido[1,2-a]pyrimidin-4-one; 66) (S)-2-amino-3-(4-(4-(4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 67) (S)-2-amino-3-(4-(4-(4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 68) (S)-2-amino-3-(4-(4-(4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)butoxy)phenyl)propionic acid trihydrochloride; 69) (4R,7S)-2-((trans-2-((4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 70) (4R,7S)-2-((trans-2-((4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 71) (4R,7S)-2-((trans-2-((4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-4,7-methanoisoindole-1,3(2H)-dione; 72) 2-((trans-2-((4-(8-methoxy-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; 73) 2-((trans-2-((4-(5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione; and, 74) 2-((trans-2-((4-(8-methyl-5,6-dihydro-11H-benzo[5,6]cyclohepta[1,2-b]pyridin-11-ylidene)piperidin-1-yl)methyl)cyclohexyl)methyl)hexahydro-1H-isoindole-1,3(2H)-dione.

12. A pharmaceutical composition for preventing or treating a disease associated with serotonin activation, comprising the compound according to any one of claims 1 to 11 as an active ingredient.

13. The pharmaceutical composition according to claim 12, wherein the disease associated with serotonin activation is a metabolic disease or cancer.

14. 14. The pharmaceutical composition of claim 13, wherein the metabolic disease is selected from the group consisting of obesity, diabetes, hyperlipidemia, arteriosclerosis, fatty liver, steatohepatitis, fibrosis, and hypertension, and the cancer is selected from the group consisting of colon cancer, breast cancer, and ovarian cancer.

15. Use of a compound according to any one of claims 1 to 11 for the prevention or treatment of diseases associated with serotonin activation.

16. Use of a compound according to any one of claims 1 to 11 for the manufacture of a medicament for the prevention or treatment of a disease associated with serotonin activation.

17. Use of a compound according to any one of claims 1 to 11 as a serotonin receptor antagonist.

18. Use of a compound according to any one of claims 1 to 11 for the manufacture of a medicament for inhibiting the activity of serotonin.

19. A method for preventing or treating a disease associated with serotonin activation, comprising administering a compound according to any one of claims 1 to 11 to a subject in need thereof.

20. A method of inhibiting the activity of serotonin, comprising administering to a subject in need thereof a compound according to any one of claims 1 to 11.

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