KR20160006007A - An electroluminescent compound and an electroluminescent device comprising the same - Google Patents

Abstract

The present invention relates to an organic light emitting compound employed in an organic electroluminescent device. The organic light emitting compound is represented by chemical formula 1 or chemical formula 2. In addition, the organic electroluminescent device having excellent light emitting properties such as driving voltage, brightness, long lifespan, and the like is implemented when employing the organic light emitting compound as a phosphorescent host compound inside a hole transport functional layer or a light emitting layer.

Description

TECHNICAL FIELD The present invention relates to an organic electroluminescent compound and an electroluminescent device comprising the same,

BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an organic light emitting compound, and more particularly, to an organic light emitting compound which is employed as a host compound or a hole transport material in an organic electroluminescent device, and an organic electroluminescent device .

The organic electroluminescent device can not only form an element on a transparent substrate but also can operate at a low voltage of 10 V or less as compared with a plasma display panel (Plasma Display Panel) or an inorganic electroluminescence (EL) display, It has the advantage of excellent color and has three colors of green, blue, and red. It has recently become a subject of interest as a next generation display device.

However, in order for such an organic electroluminescent device to exhibit such characteristics, a hole injecting material, a hole transporting material, a light emitting material, an electron transporting material, and an electron injecting material, which are materials forming an organic layer in a device, However, until now, stable and efficient development of an organic material layer material for an organic electroluminescence device has not been sufficiently achieved. Therefore, there is a continuing demand for development of new materials having low-voltage driving, high efficiency and long life.

In particular, conventional hole transport materials include copper phthalocyanine (CuPc), MTDATA, 4,4'-bis [N- (1-naphthyl) -N- phenylamino] biphenyl (NPB), N, N, N'-bis (3-methylphenyl) - (1,1'-biphenyl) -4,4'-diamine (TPD) has been known. However, Based compound having various substituents in order to improve it, but it still has a problem that it is not enough to satisfy efficiency and long life at the same time.

Further, the most important factor for determining the luminous efficiency in an organic light emitting device is a light emitting material. However, the development of a phosphorescent material on a light-emitting mechanism is one of the ways that the luminous efficiency can be improved more theoretically. Accordingly, a variety of phosphorescent materials have been developed to date, In particular, CBP is the most widely known phosphorescent host material, and an organic light emitting device using a BALq derivative as a host is known.

However, in the case of using a material such as BAlq or CBP as a host of a phosphorescent material, the organic electroluminescent device using the phosphorescent material has a higher current efficiency than the device using the fluorescent material, There is no great advantage in terms of power efficiency, and the life of the device can not be satisfactory. Thus, development of a more stable and high-performance host material is required.

The present invention provides a novel organic electroluminescent compound which can be used for a light emitting layer, a hole injecting layer, and a hole transporting layer of an organic electroluminescent device to realize excellent luminescent characteristics, and an organic electroluminescent device including the same.

The present invention provides an organic electroluminescent compound represented by the following general formula (1) or (2) and an organic electroluminescent device including the same.

[Chemical Formula 1] (2)

The specific structures and substituents of the organic luminescent compound according to the above formula (1) or (2) will be described later.

The organic luminescent compound according to the present invention has an excellent structure flatness and a high triplet state, which enables to realize a luminescent efficiency and a longevity characteristic which are higher than those of conventional phosphorescent host compounds and hole transport compounds, The light emitting device can be used for various display devices.

1 to 5 are cross-sectional views illustrating the structure of an organic electroluminescent device according to an embodiment of the present invention.

Hereinafter, the present invention will be described more specifically.

The present invention relates to a novel organic luminescent compound represented by the following formula (1) or (2).

[Chemical Formula 1] (2)

In the above Chemical Formula 1 or Chemical Formula 2,

X ₁ to X ₁₁ are the same or different from each other, each independently from N, O, S, Te, CR 1, NR 2, CR 3 R 4, SiR 5 R 6, GeR 7 R 8, PR 9 and BR ₁₀ And R ₃ and R ₄ , R ₅ and R ₆ , R ₇ and R ₈ may be connected to each other to form a ring.

Wherein R ₁ to R ₁₀ are the same or different from each other and each independently represents hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, A substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted heterocycloalkyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, Or an unsubstituted or substituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 1 -C 30 alkylthio group, a substituted or unsubstituted C 5 -C 30 A substituted or unsubstituted alkylamine group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamine group having 5 to 30 carbon atoms, a substituted or unsubstituted aliphatic hydrocarbon group having 5 to 50 carbon atoms A substituted or unsubstituted aryl group having 5 to 50 carbon atoms, a substituted or unsubstituted aryl group having 3 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted aryl group having 5 to 50 carbon atoms, A substituted or unsubstituted C 2 -C 50 heteroaryl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted germanium group, a substituted or unsubstituted boron group , A carbonyl group, a phosphoryl group, an amino group, a thiol group, a cyano group, a hydroxyl group, a nitro group, a halogen group and an amide group.

R ₁ to R ₁₀ and substituents thereof may be bonded to each other or may be connected to adjacent substituents to form a single ring or polycyclic ring of an alicyclic or aromatic group and may form a single ring or multicyclic ring of the formed alicyclic or aromatic ring The carbon atom may be substituted with any one or more heteroatoms selected from N, S and O.

Each of R ₁ to R ₁₀ independently represents a group represented by the following formula 1 or 2:

[Structural formula 1] [Structural formula 2]

In the structural formula 1 or the structural formula 2,

L is a single bond, a substituted or unsubstituted alkylene group having 1 to 30 carbon atoms, a substituted or unsubstituted aliphatic hydrocarbon group having 2 to 30 carbon atoms A substituted or unsubstituted C2-C30 alkynylene group, a substituted or unsubstituted C3-C30 A substituted or unsubstituted C2 to C30 heteroarylene group, a substituted or unsubstituted C3 to C30 cycloalkyl, a substituted or unsubstituted C1 to C50 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, A substituted or unsubstituted C2 to C50 heteroarylene group in which at least one unsubstituted C1 to C50 arylene group and substituted or unsubstituted C3 to C30 cycloalkyl are fused together and n is 0 to 4 And when n is 2 or more, a plurality of Ls may be the same or different from each other.

A ₁ to A ₃ are the same or different and each independently represents a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted group having 5 to 50 carbon atoms A substituted or unsubstituted aryl group, a substituted or unsubstituted C2 to C50 heteroaryl group, a substituted or unsubstituted C3 to C30 cycloalkyl substituted or unsubstituted aryl group having 5 to 50 carbon atoms, And a substituted or unsubstituted C2 to C50 heteroaryl group in which one or more ring-opened cycloalkyl having 3 to 30 carbon atoms is fused.

Wherein L, A ₁ to A _3, and these substituents may be coupled or the adjacent connection with substituents each cycloaliphatic, may form a monocyclic or polycyclic ring of the aromatic group, the monocyclic or polycyclic ring of an alicyclic, aromatic so formed The carbon atom may be substituted with any one or more heteroatoms selected from N, S and O.

On the other hand, L and A ₁ to A ₃ may be more specifically selected independently from each other in the following Structural Formula 3.

[Structural Formula 3]

In the above formula 3,

Z is _{CR 1, NR 2, CR 3} R 4, SiR 5 R 6, GeR 7 R 8, PR 9, BR 10, Te, O , and is selected from S, wherein R ₁ to R ₁₀ are the Formula 1 Or the formula (2).

The L, A ₁ to A _3, and R ₁ to R ₁₀ may each be independently substituted with one or more substituents, and the one or more substituents may be selected from the group consisting of hydrogen, deuterium, substituted or unsubstituted C1- , A substituted or unsubstituted C2-C30 alkenyl group, a substituted or unsubstituted C2-C30 alkynyl group, a substituted or unsubstituted C3-C30 cycloalkyl group, a substituted or unsubstituted C2- A substituted or unsubstituted C1-C30 alkoxy group, a substituted or unsubstituted C6-C30 aryloxy group, a substituted or unsubstituted C1-C30 alkoxy group, a substituted or unsubstituted C1- A substituted or unsubstituted aryloxy group having 5 to 30 carbon atoms, a substituted or unsubstituted alkylamine group having 1 to 30 carbon atoms, a substituted or unsubstituted alkylcarbonyl group having 5 to 30 carbon atoms An arylamine group, a substituted or unsubstituted aryl group having 5 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted silyl group, a substituted or unsubstituted germanium group, A nitro group, a halogen group, a selenium group, a tellurium group, an amide group, an ether group, and an ester group among a substituted boron group, a substituted boron group, a substituted or unsubstituted aluminum group, a carbonyl group, a phosphoryl group, an amino group, a thiol group, a cyano group, Can be selected.

In the present invention, examples of the substituents will be specifically described below, but the present invention is not limited thereto.

In the present invention, the alkyl group may be linear or branched, and the number of carbon atoms is not particularly limited, but is preferably 1 to 50. Specific examples include methyl, ethyl, propyl, n-propyl, isopropyl, butyl, n-butyl, isobutyl, Ethyl, propyl, isopropyl, n-butyl, isobutyl, isobutyl, isobutyl, A tert-butyl group, a tert-butyl group, a 2-pentyl group, a 3,3-dimethylbutyl group, a 2-ethylbutyl group, a heptyl group, Ethylhexyl group, 2-propylpentyl group, n-nonyl group, 2,2-dimethylheptyl group, 1-ethyl-propyl group, 1,1-dimethyl-propyl group , Isohexyl group, 2-methylpentyl group, 4-methylhexyl group, 5-methylhexyl group and the like, but are not limited thereto.

In the present invention, the alkoxy group may be linear or branched. The number of carbon atoms of the alkoxy group is not particularly limited, but is preferably in the range of 1 to 30, which does not cause steric hindrance. Specific examples thereof include a methoxy group, an ethoxy group, an n-propoxy group, an isopropoxy group, an i-propyloxy group, a n-butoxy group, an isobutoxy group, a tert- , Neopentyloxy group, isopentyloxy group, n-hexyloxy group, 3,3-dimethylbutyloxy group, 2-ethylbutyloxy group, n-octyloxy group, n- , A benzyloxy group, a p-methylbenzyloxy group, and the like, but are not limited thereto.

In the present invention, the alkenyl group may be straight-chain or branched, and the number of carbon atoms is not particularly limited, but is preferably 2 to 40. Specific examples include a vinyl group, a 1-propenyl group, an isopropenyl group, a 1-butenyl group, a 2-butenyl group, a 3-butenyl group, a 1-pentenyl group, a 2-pentenyl group, a 3-pentenyl group, 2-phenylvinyl-1-yl group, 2,2-diphenylvinyl-1-yl group, 2-phenyl-2-yl group, But are not limited to, - (naphthyl-1-yl) vinyl-1-yl group, 2,2-bis (diphenyl-1-yl) vinyl-1-yl group, stilbenyl group, styrenyl group and the like.

In the present invention, the aryl group may be monocyclic or polycyclic, and the number of carbon atoms is not particularly limited, but is preferably 6 to 60. [ Examples of the monocyclic aryl group include a phenyl group, a biphenyl group, a terphenyl group and a stilbene group. Examples of the polycyclic aryl group include a naphthyl group, an anthracenyl group, a phenanthrenyl group, a pyrenyl group, a perylenyl group, , A chlorenyl group, a fluorenyl group, an acenaphthacenyl group, a triphenylene group, and a fluororanthrene group, but the scope of the present invention is not limited to these examples.

In the present invention, the heterocyclic group is a heterocyclic group containing O, N or S as a heteroatom, and the number of carbon atoms is not particularly limited, but is preferably 2 to 60 carbon atoms. Examples of the heterocyclic group include a thiophene group, a furane group, a furyl group, an imidazole group, a thiazole group, an oxazole group, an oxadiazole group, a triazole group, a pyridyl group, a bipyridyl group, a pyrimidyl group, A pyridazinyl group, a pyrazinopyrazinyl group, an isoquinoline group, an isoquinolinyl group, an isoquinolinyl group, an isoquinolinyl group, an isoquinolinyl group, an isoquinolyl group, , An indole group, a carbazole group, a benzoxazole group, a benzoimidazole group, a benzothiazole group, a benzocarbazole group, a benzothiophene group, a dibenzothiophene group, a benzofuranyl group, a dibenzofurancyl group, a phenanthroline group, An isothiazolyl group, an isoxazolyl group, an oxadiazolyl group, a thiadiazolyl group, a benzothiazolyl group, a phenothiazinyl group and the like, but is not limited thereto.

In the present invention, the aryl group in the aryloxy group, arylthioxy group, arylsulfoxy group and aralkylamine group is the same as the aforementioned aryl group. Specific examples of the aryloxy group include a phenoxy group, a p-tolyloxy group, an m-tolyloxy group, a 3,5-dimethyl-phenoxy group, a 2,4,6-trimethylphenoxy group, a ptert- Anthryloxy group, 2-naphthyloxy group, 2-naphthyloxy group, 4-methyl-1-naphthyloxy group, Anthryloxy group, 9-anthryloxy group, 1-phenanthryloxy group, 3-phenanthryloxy group, 9-phenanthryloxy group and the like. Examples of the arylthioxy group include phenylthioxy group, 2- A 4-tert-butylphenyloxy group, and the like. Examples of the arylsulfoxy group include benzene sulfoxy group and p-toluenesulfoxy group. However, the present invention is not limited thereto.

In the present invention, the cycloalkyl group is not particularly limited, but preferably has 3 to 60 carbon atoms, and specifically includes cyclopropyl group, cyclobutyl group, cyclopentyl group, 3-methylcyclopentyl group, 2,3-dimethylcyclopentyl group, Methylcyclohexyl group, 2,3-dimethylcyclohexyl group, 3,4,5-trimethylcyclohexyl group, 4-tert-butylcyclohexyl group, cycloheptyl group, cyclo An octyl group, and the like, but are not limited thereto.

In the present invention, examples of the halogen group include fluorine, chlorine, bromine or iodine.

In the present invention, examples of the arylamine group include a substituted or unsubstituted monoarylamine group, a substituted or unsubstituted diarylamine group, or a substituted or unsubstituted triarylamine group. The aryl group in the arylamine group may be a monocyclic aryl group or a polycyclic aryl group. The arylamine group having at least two aryl groups may contain a monocyclic aryl group, a polycyclic aryl group, or a monocyclic aryl group and a polycyclic aryl group at the same time.

Specific examples of the arylamine group include a phenylamine group, a naphthylamine group, a biphenylamine group, an anthracenylamine group, a 3-methylphenylamine group, a 4-methylnaphthylamine group, But are not limited to, an amine group, a 9-methyl-anthracenylamine group, a diphenylamine group, a phenylnaphthylamine group, a ditolylamine group, a phenyltolylamine group, a carbazole group and a triphenylamine group.

In the present invention, the silyl group is specifically exemplified by trimethylsilyl, triethylsilyl, t-butyldimethylsilyl, vinyldimethylsilyl, propyldimethylsilyl, triphenylsilyl, diphenylsilyl, But are not limited thereto.

In the present invention, the heteroaryl group in the heteroarylamine group can be selected from the examples of the above-mentioned heterocyclic group.

In the present invention, the alkyloxy group in the alkylthio group and the alkyl group in the alkylsulfoxy group are the same as the aforementioned alkyl groups. Specific examples of the alkyloxy group include a methylthio group, an ethylthio group, a tert-butylthio group, a hexylthio group and an octylthio group. Examples of the alkylsulfoxy group include a mesyl group, an ethylsulfoxy group, a propylsulfoxy group, But are not limited thereto.

In the present invention, the "substituted or unsubstituted" means a group selected from the group consisting of deuterium, halogen, nitrile, nitro, hydroxy, alkyl, cycloalkyl, , An arylsulfoxy group, an alkenyl group, a silyl group, a boron group, an alkylamine group, an aralkylamine group, an arylamine group, an aryl group, a fluorenyl group, a carbazole group and at least one of N, O and S atoms Substituted or unsubstituted with at least one substituent in the heterocyclic group.

In the present invention, the substituted arylene group means a phenyl group, a biphenyl group, a naphthalene group, a fluorenyl group, a pyrenyl group, a phenanthrenyl group, a perylene group, a tetracenyl group. Anthracenyl group and the like are substituted with other substituents.

In the present invention, the substituted heteroarylene group includes a pyridyl group, a thiophenyl group, a triazine group, a quinoline group, a phenanthroline group, an imidazole group, a thiazole group, an oxazole group, a carbazole group and condensed heterocyclic groups, Such as a benzoquinoline group, a benzimidazole group, a benzoxazole group, a benzothiazole group, a benzzcarbazole group, a dibenzothiophenyl group, a dibenzofurane group and the like are substituted with other substituents.

The organic luminescent compound according to the present invention represented by Formula 1 or Formula 2 may be used as an organic material layer of an organic electroluminescent device due to its structural specificity, and more specifically, a hole transport material .

Particularly, specific examples of the organic luminescent compound which can be employed in the hole transporting functional layer represented by the formula (1) or (2) according to the present invention include, but are not limited to, the following compounds.

The organic luminescent compound according to the present invention represented by the above formula (1) or (2) can be used as an organic material layer of an organic electroluminescent device due to its structural specificity, and more specifically, have.

Specific examples of the organic luminescent compound that can be employed as the phosphorescent host compound of the luminescent layer represented by the formula (1) or (2) according to the present invention include, but are not limited to, the following compounds.

An organic luminescent compound having the intrinsic characteristics of the substituent introduced by introducing various substituents into the core structure having the above structure can be synthesized. For example, by introducing a substituent used in a hole injecting layer material, a hole transporting layer material, a light emitting layer material, and an electron transporting layer material used in manufacturing an organic electroluminescent device into the structure, a material meeting the requirements of each organic material layer is manufactured .

In particular, as described above, the organic luminescent compound represented by the formula (1) or (2) according to the present invention has an excellent flat structure and a high triplet state It is possible to realize an organic electroluminescent device exhibiting excellent characteristics in terms of efficiency, drive voltage, lifetime, etc. in the organic material layer of the organic electroluminescent device.

The compound of the present invention can be applied to a device according to a conventional method of manufacturing an organic electroluminescent device.

The organic electroluminescent device according to one embodiment of the present invention may have a structure including a first electrode, a second electrode and an organic material layer disposed therebetween, and the organic electroluminescent compound according to the present invention may be used for an organic material layer And can be manufactured using conventional device manufacturing methods and materials.

The organic material layer of the organic electroluminescent device according to the present invention may have a single layer structure, but may have a multilayer structure in which two or more organic material layers are stacked. For example, a structure including a hole injecting layer, a hole transporting layer, a light emitting layer, an electron transporting layer, and an electron injecting layer. However, it is not limited to this and may include a smaller number of organic layers.

Therefore, in the organic electroluminescent device of the present invention, the organic material layer may be a hole injecting layer, a hole transporting layer, an electron transporting layer, an electron injecting layer, a layer simultaneously injecting and transporting holes, a layer simultaneously performing electron injection and electron transporting, One or more layers may be included, and at least one of the layers may include a compound represented by the formula (1) or (2).

In particular, the organic luminescent compound according to the present invention may be contained in the hole transporting functional layer or the luminescent layer, and may be included as a host material in the luminescent layer.

When the compound represented by Formula 1 or Formula 2 is included as a host material in the light emitting layer, the light emitting layer may include at least one phosphorescent dopant, and when the light emitting layer includes a host and a dopant, The content of the dopant may be selected in the range of about 0.01 to about 20 parts by weight, based on 100 parts by weight of the host.

According to an embodiment of the present invention, the light emitting layer may further contain at least one dopant compound selected from the following [structural formulas 4] to [structural formula 10] in the host compound represented by the general formula [1] have.

[Structural Formula 4]

[Structural Formula 5]

[Structural Formula 6]

[Structural Formula 7]

[Structural formula 8]

[Structural formula 8]

[Structural Formula 10]

In the organic compound layer having such a multi-layer structure, the compound represented by the formula (1) or (2) may be used as a light emitting layer, a layer that simultaneously transports holes and holes, a layer that simultaneously transports holes and emits light, And the like.

For example, the structure of an organic electronic device according to the present invention is illustrated in Figs.

1 shows an organic electronic device in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5, an electron transporting layer 6 and a cathode 7 are sequentially laminated on a substrate 1 Structure is illustrated. In such a structure, the compound represented by Formula 1 or Formula 2 may be included in the hole injection layer 3, the hole transport layer 4, the light emitting layer 5, or the electron transport layer 6.

2 shows the structure of an organic electronic device in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5 and a cathode 7 are sequentially laminated on a substrate 1. In such a structure, the compound represented by Formula 1 or Formula 2 may be included in the hole injecting layer 3, the hole transporting layer 4, or the electron transporting layer 6.

3 illustrates the structure of an organic electronic device in which an anode 2, a hole transporting layer 4, a light emitting layer 5, an electron transporting layer 6, and a cathode 7 are sequentially stacked on a substrate 1. In such a structure, the compound represented by the formula (1) or (2) may be included in the hole transport layer (4), the light emitting layer (5), or the electron transport layer (6).

4 illustrates the structure of an organic electronic device in which an anode 2, a light emitting layer 5, an electron transport layer 6, and a cathode 7 are sequentially laminated on a substrate 1. In FIG. In such a structure, the compound represented by the formula (1) or (2) may be included in the light emitting layer (5) or the electron transport layer (6).

5 illustrates the structure of an organic electronic device in which an anode 2, a light-emitting layer 5, and a cathode 7 are sequentially stacked on a substrate 1. As shown in Fig. In such a structure, the compound represented by the formula (1) or (2) can be included in the luminescent layer (5).

For example, the structure of an organic electronic device according to the present invention is illustrated in Figs.

1 shows an organic electroluminescent device 1 in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5, an electron transporting layer 6 and a cathode 7 are sequentially laminated on a substrate 1 Are illustrated. In such a structure, the compound represented by Formula 1 or Formula 2 may be included in the hole injection layer 3, the hole transport layer 4, the light emitting layer 5, or the electron transport layer 6.

2 shows a structure of an organic electroluminescent device in which an anode 2, a hole injecting layer 3, a hole transporting layer 4, a light emitting layer 5 and a cathode 7 are sequentially laminated on a substrate 1 . In such a structure, the compound represented by Formula 1 or Formula 2 may be included in the hole injecting layer 3, the hole transporting layer 4, or the electron transporting layer 6.

3 illustrates the structure of an organic electroluminescent device in which an anode 2, a hole transport layer 4, a light emitting layer 5, an electron transport layer 6, and a cathode 7 are sequentially laminated on a substrate 1. In such a structure, the compound represented by the formula (1) or (2) may be included in the hole transport layer (4), the light emitting layer (5), or the electron transport layer (6).

4 shows the structure of an organic electroluminescent device in which an anode 2, a light emitting layer 5, an electron transport layer 6 and a cathode 7 are sequentially laminated on a substrate 1. [ In such a structure, the compound represented by the formula (1) or (2) may be included in the light emitting layer (5) or the electron transport layer (6).

5 illustrates the structure of an organic electroluminescent device in which an anode 2, a light-emitting layer 5, and a cathode 7 are sequentially laminated on a substrate 1. As shown in FIG. In such a structure, the compound represented by the formula (1) or (2) can be included in the luminescent layer (5).

For example, the organic electroluminescent device according to the present invention can be manufactured by using a physical vapor deposition (PVD) method such as sputtering or e-beam evaporation to form a metal oxide or a conductive metal oxide on the substrate, An anode is formed by depositing an alloy on the anode, and an organic material layer including a hole injecting layer, a hole transporting layer, a light emitting layer, and an electron transporting layer is formed on the anode, and then a substance usable as a cathode is deposited thereon.

In addition to such a method, an organic electroluminescent device may be formed by sequentially depositing a cathode material, an organic material layer, and a cathode material on a substrate. The organic material layer may have a multi-layer structure including a hole injection layer, a hole transport layer, a light emitting layer, and an electron transport layer, but is not limited thereto and may have a single layer structure. In addition, the organic material layer may be formed using a variety of polymer materials by a solvent process such as a spin coating process, a dip coating process, a doctor blading process, a screen printing process, an inkjet printing process or a thermal transfer process, Layer.

As the anode material, a material having a large work function is preferably used so that hole injection can be smoothly conducted into the organic material layer. Specific examples of the cathode material that can be used in the present invention include metals such as vanadium, chromium, copper, zinc and gold or alloys thereof, zinc oxide, indium oxide, indium tin oxide (ITO), indium zinc oxide (IZO) metal oxides, ZnO: Al or SnO _2: a combination of a metal and an oxide such as Sb, poly (3-methylthiophene), poly [3,4- (ethylene-1,2-dioxy) thiophene] (PEDT) , Conductive polymers such as polypyrrole and polyaniline, but are not limited thereto.

The negative electrode material is preferably a material having a small work function to facilitate electron injection into the organic material layer. Specific examples of the negative electrode material include a metal such as magnesium, calcium, sodium, potassium, titanium, indium, yttrium, lithium, gadolinium, aluminum, silver, tin and lead or an alloy thereof, a multilayer such as LiF / Al or LiO ₂ / Structural materials, and the like, but are not limited thereto.

As the hole injecting material, it is preferable that the highest occupied molecular orbital (HOMO) of the hole injecting material be between the work function of the anode material and the HOMO of the surrounding organic layer. Specific examples of the hole injecting material include metal porphyrine, oligothiophene, arylamine-based organic materials, hexanitrile hexaazatriphenylene, quinacridone-based organic materials, perylene-based organic materials, Anthraquinone, polyaniline and a polythiophene-based conductive polymer, but are not limited thereto.

As the hole transporting material, a material capable of transporting holes from the anode or the hole injection layer to the light emitting layer and having high mobility to holes is suitable. Specific examples include arylamine-based organic materials, conductive polymers, and block copolymers having a conjugated portion and a non-conjugated portion together, but are not limited thereto.

The light emitting material is preferably a material capable of emitting light in the visible light region by transporting and combining holes and electrons from the hole transporting layer and the electron transporting layer, respectively, and having a high quantum efficiency for fluorescence or phosphorescence. Specific examples include 8-hydroxy-quinoline aluminum complex (Alq ₃ ), carbazol-based compounds, dimerized styryl compounds, BAlq, 10-hydroxybenzoquinoline-metal compounds, benzoxazole, benzthiazole and A benzimidazole-based compound, a poly (p-phenylene vinylene) (PPV) -based polymer, a spiro compound, polyfluorene, rubrene, and the like.

As the electron transporting material, a material capable of transferring electrons from the cathode well into the light emitting layer, which is highly mobile, is suitable. Specific examples thereof include, but are not limited to, an Al complex of 8-hydroxyquinoline, a complex containing Alq ₃ , an organic radical compound, and a hydroxyflavone-metal complex.

The organic electroluminescent device according to the present invention may be a front emission type, a back emission type, or a both-sided emission type, depending on the material used.

In addition, the organic electroluminescent compound according to the present invention can act on a principle similar to that applied to an organic electroluminescent device in an organic electronic device including an organic solar cell, an organophotoreceptor, an organic transistor and the like.

Hereinafter, preferred embodiments of the present invention will be described in order to facilitate understanding of the present invention. However, the following examples are intended to illustrate the invention and are not intended to limit the scope of the invention.

Example  1: Synthesis of compound 1

(One) Manufacturing example  1: Synthesis of intermediate A

Methyl 2-bromobenzoate (2.6 g, 0.012 mol) was added to 3-bromo-5-chloro-1,1-dimethyl-1H-isoindole (2.6 g, 0.010 mol) and dissolved in a 60 mL ehter. After dropping 2.5 M BuLi (0.01 mL, 0.0005 mol), the mixture was stirred for 1 hour. The mixture was slowly warmed to room temperature and stirred for 4 hours. After completion of the reaction, the reaction mixture was extracted with 100 mL of water, and the organic layer was dried under reduced pressure. This was recrystallized from EtOH: Acetone to give intermediate A (1.3 g, 41%) (m / z = 313).

(2) Manufacturing example  2: Synthesis of intermediate A-1

Intermediate A (3.1 g, 0.010 mol) was dissolved in a 30 mL ehter, cooled to -78 ° C, and 2.5 M BuLi (0.01 mL, 0.0005 mol) was dropwise added thereto, followed by stirring for 1 hour. The mixture was slowly warmed to room temperature and stirred for 4 hours. After completion of the reaction, the reaction mixture was extracted with 100 mL of water, and the organic layer was dried under reduced pressure. This was recrystallized from EtOH: Acetone to give intermediate A-1 (2.0 g, 63%) (m / z = 313).

(3) Manufacturing example  3: Synthesis of intermediate A-2

Intermediate A-1 (3.1 g, 0.010 mol) was dissolved in 50 mL of concentrated H ₃ PO ₄ and stirred for 5 hours. It was extracted with 100 mL of water and 100 mL of Ethyl Acetate, and the organic layer was dried under reduced pressure. This was recrystallized from 100 mL of EtOH to give intermediate A-2 (2.1 g, 72%) (m / z = 295).

(4) Manufacturing example  4: Synthesis of intermediate 1-1

Bis (pinacolato) dibron (2.5 g, 0.012 mol) was added to N- (biphenyl-4-yl) -N- (4- bromophenyl) -9,9-dimethyl-9H- 100 mL of 1,4-dioxane was added to PdCl ₂ (dppf) (0.4 g, 0.0005 mol) and potassium acetate (2.7 g, 0.020 mol), and the mixture was reacted at 95 ° C for 24 hours with stirring. After completion of the reaction, the reaction mixture was cooled, separated into H ₂ O: MC and subjected to column purification (n-hexane: MC) to obtain 4.0 g (m / z = 563) of intermediate 1-1.

(5) Manufacturing example  5: Synthesis of Compound 1

To a solution of Intermediate 1-1 (6.8 g, 0.012 mol), Pd (pph ₃ ) ₄ (0.6 g, 0.0005 mol) and potassium carbonate (2.8 g, 0.020 mol) in THF 100 mL, and the mixture was reacted at 65 ° C for 18 hours with stirring. After completion of the reaction, the reaction mixture was cooled, separated into H ₂ O: MC and subjected to column purification (n-hexane: MC) to obtain 4.9 g (yield 70%) of <Compound 1>.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.990 / d, 7.87 / d, 7.69 / d, 7.62 / d, 7.61 / m, 7.55 / d, 7.41 / m, 7.38 / m, 7.28 / m D, 6.75 / s, 6.58 / d) 2H (7.52 / d, 1.61 / s) 3H (7.51 /

LC / MS: m / z = 697 [(M + 1) ^&lt; ^{+ &}

Example  2: Synthesis of compound 2

(One) Manufacturing example  1: Synthesis of intermediate 2-1

dibromo-2,5-dimethylbenzene (2.6 g, 0.010 mol), Pd (dba) ₂ (0.09 mol) and bis (9,9- 0.5 g, 0.0005 mol) and sodium-tert-butoxide (1.9 g, 0.020 mol) were added 100 mL of Tol and reacted at 95 ° C for 4 hours with stirring. After completion of the reaction, the reaction product was cooled, and the product was separated into H ₂ O: MC and subjected to column purification (n-hexane: MC) to obtain 4.5 g (m / z = 585)

(2) Manufacturing example  2: Synthesis of intermediate 2-2

<Intermediate 2-2> 4.3 g (0.012 mol) of bis (pinacolato) dibron was added to Intermediate 2-1 (5.9 g, 0.010 mol) g (yield: 72%). (m / z = 591)

(3) Manufacturing example  3: Synthesis of Compound 2

Synthesis was conducted in the same manner as in Example 1 (4), except that Intermediate 2-2 (7.1 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.90 / d, 7.69 / d, 7.61 / m, 7.54 / d, 7.51 / m, 7.42 / d, 7.23 / d, 6.49 / s, 2.59 / s , 2.12 / s) 2H (7.87 d, 7.62 d, 7.55 d, 7.38 m, 7.28 m, 6.75 d, 6.58 d,

LC / MS: m / z = 766 [(M + 1) ^&lt; ^{+ &}

Example  3: Synthesis of compound 3

(One) Manufacturing example  1: Intermediate 3-1 Synthesis

2,6-dibromonaphthalene (2.9 g, 0.010 mol) was added to N- (biphenyl-4-yl) -9,9-dimethyl-9H-fluoren- Synthesis was conducted in the same manner as in Example (1) to obtain 4.4 g (yield 77%) of Intermediate 3-1 (m / z = 566)

(2) Manufacturing example  2: Intermediate 3-2 Synthesis

Intermediate 3-2 was prepared according to the same procedure as in Example 1 (4), except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 3-1 (5.7 g, 0.010 mol) g (yield: 72%). (m / z = 613)

(3) Manufacturing example  3: Synthesis of compound 3

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 4-2 (7.4 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.90 / d, 7.87 / d, 7.84 / d, 7.74 / s, 7.64 / d, 7.63 / d, 7.61 / m, 7.55 / d, 7.54 / d 7.51 / m, 7.49 / d, 7.46 / s, 7.38 / m, 7.28 / m, 7.23 / d, 6.75 / , 1.61 / s) 4H (7.69 / d, 1.72 / s)

LC / MS: m / z = 747 [(M + 1) ^&lt; ^{+ &}

Example  4: Synthesis of compound 4

(One) Manufacturing example  1: Synthesis of Intermediate 4-1

Intermediate 4-1 was synthesized by the same method as in Example 2 (1) except that 1,3,5-tribromobenzene (3.1 g, 0.010 mol) was added to dip-tolylamine (2.0 g, 0.010 mol) 4.2 g (yield 77%) was obtained. (M / z = 547)

(2) Manufacturing example  2: Synthesis of intermediate 4-2

Intermediate 4-2 was synthesized as in Intermediate 4-1 (5.5 g, 0.010 mol) by the same procedure as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) g (yield: 72%). (m / z = 595)

(3) Manufacturing example  3: Synthesis of Compound 4

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 4-2 (7.1 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.90 / d, 7.69 / d, 7.61 / m, 7.54 / d, 7.51 / m, 7.23 / d, 5.73 / s) 2H (6.25 / s, 1.72 / s, 1.61 / s) 4H (2.34 / s) 8H (6.98 / d, 6.51 / d)

LC / MS: m / z = 728 [(M + 1) ^&lt; ^{+ &}

Example  5: Synthesis of compound 5

(One) Manufacturing example  1: Synthesis of intermediate 5-1

4-chloro-2,5-dimethylbenzene (1.8 g, 0.012 mol) was added to 4-tert-butylphenylboronic acid (1.8 g, 0.010 mol) in the same manner as in Example 1- To obtain 1.6 g (yield 72%) of Intermediate 5-1 (m / z = 272)

(2) Manufacturing example  2: Synthesis of Intermediate 5-2

Synthesis was carried out in the same manner as in Example 2 (1) except that 9,9-dimethyl-9H-fluoren-2-amine (2.1 g, 0.010 mol) was added to Intermediate 5-1 (2.7 g, 0.010 mol) 3.4 g (yield 77%) of Intermediate 5-2 (m / z = 445) was obtained.

(3) Manufacturing example  3: Synthesis of intermediate 5-3

<Intermediate 5-3> 4.6 g (0.010 mol) of 1,4-dibromobenzene was added to Intermediate 5-2 (4.4 g, 0.010 mol) g (yield: 77%). (m / z = 600)

(4) Manufacturing example  4: Synthesis of intermediate 5-4

<Intermediate 2-2> 4.7 g (0.012 mol) of bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 5-3 (6.0 g, 0.010 mol) g (yield: 72%). (m / z = 647)

(5) Manufacturing example  5: Synthesis of Compound 5

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 4-2 (7.8 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 70%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.90 / d, 7.87 / d, 7.69 / d, 7.62 / d, 7.61 / m, 7.55 / d, 7.51 / m, 7.42 / s, 7.38 / m , 7.28 / m, 7.23 / d, 6.75 / s, 6.58 / d, 6.49 / s, 2.59 / s, 2.12 /

LC / MS: m / z = 782 [(M + 1) ^&lt; ^{+ &}

Example  6: Synthesis of Compound 6

(One) Manufacturing example  1: Synthesis of intermediate 6-1

Boronic acid (1.4 g, 0.012 mol) was added to 1-bromo-3-chloronaphthalene (2.4 g, 0.010 mol) and the intermediate <6-1 > 1.7 g (yield 72%). (M / z = 238)

(2) Manufacturing example  2: Synthesis of intermediate 6-2

Intermediate 6-2 was synthesized in the same manner as in Example 2 (1) except that 4-bromoaniline (1.7 g, 0.010 mol) was added to Intermediate 6-1 (2.4 g, 0.010 mol) Yield: 77%). (M / z = 329)

(3) Manufacturing example  3: Synthesis of intermediate 6-3

<Intermediate 2-2> 2.9 (3 g, 0.012 mol) was synthesized in the same manner as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 6-2 g (yield 70%). (m / z = 421)

(4) Manufacturing example  4: Synthesis of intermediate 6-4

Intermediate 6 (4.2 g, 0.010 mol) was reacted with 4-bromo-N, N-diphenylaniline (32.6 g, 0.008 mol) in the same manner as in Example 1- -4> 3.9 g (yield: 74%). (M / z = 664)

(5) Manufacturing example  5: Synthesis of Compound 6

Synthesis was conducted in the same manner as in Example 1-Preparation Example (5), except that Intermediate 4-2 (8.0 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.43 / d, 7.90 / d, 7.85 / d, 7.69 / d, 7.61 / m, 7.51 / m, 7.46 / m, 7.41 / m, 7.32 / m D, 6.99 / s, 6.76 / s) 2H (7.79 / d, 7.51 / m, 6.81 / , 6.63 / d, 6.38 / d)

LC / MS: m / z = 799 [(M + 1) ^&lt; ^{+ &}

Example  7: Synthesis of Compound 7

(One) Manufacturing example  1: Synthesis of Intermediate 7-1

(1.3 g, 0.008 mol) was added to Intermediate 6-3 (6.6 g, 0.010 mol) in the same manner as in Example 2-Preparation Example (1) %). (M / z = 497)

(2) Manufacturing example  2: Synthesis of Compound 7

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 7-1 (6.0 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.43 / d, 7.90 / d, 7.85 / d, 7.69 / d, 7.61 / m, 7.51 / m, 7.46 / m, 7.41 / m, 7.32 / m 7.51 / m, 7.20 / m, 6.69 / d, 6.63 / d, 1.72 / s, 1.61 / s) 3H (7.54 / d)

LC / MS: m / z = 631 [(M + 1) ^&lt; ^{+ &}

Example  8: Compound 8 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 8-1

Synthesis was conducted in the same manner as in Example 2 (1) except that 2-bromo-9,9-dimethyl-9H-fluorene (2.2 g, 0.008 mol) was added to Intermediate 6-3 (6.6 g, 0.010 mol) 3.8 g (yield: 77%) of Intermediate 8-1 (m / z = 613) was obtained.

(2) Manufacturing example  2: Synthesis of Compound 8

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 8-1 (7.4 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.43 / d, 7.90 / d, 7.87 / d, 7.85 / d, 7.69 / d, 7.62 / d, 7.61 / m, 7.55 / d, 7.51 / m , 7.46 / m, 7.41 / m, 7.38 / m, 7.32 / m, 7.28 / m, 7.23 / d, 6.99 / s, 6.76 / s, 6.75 / s, 6.58 / , 6.69 / d, 1.61 / s) 3H (7.54 / d) 4H (1.72 / s)

LC / MS: m / z = 747 [(M + 1) ^&lt; ^{+ &}

Example  9: Synthesis of Compound 9

(One) Manufacturing example  1: Synthesis of intermediate B

2-bromobenzoate (2.6 g, 0.012 mol) was added to 3,7-dibromo-5-chloro-1,1-dimethyl-1H-isoindole (3.4 g, 0.010 mol) (M / z = 392) (1.8 g, yield 46%). &Lt;

(2) Manufacturing example  2: Synthesis of intermediate B-1

Synthesis was conducted in the same manner as in Example 1 (2), except that Intermediate B (3.9 g, 0.010 mol) was added to obtain 2.6 g (yield 66%) of Intermediate B-1. M / z = 392 )

(3) Manufacturing example  3: Synthesis of intermediate B-2

2.5 g (yield 66%) of <Intermediate B-2> was obtained by the same method as employed in the preparation example (3) of Example 1, except that Intermediate B-1 (3.9 g, 0.010 mol) = 374)

(4) Manufacturing example  4: Synthesis of intermediate 9-1

Synthesis was conducted in the same manner as in Example 1 (5), except that 4- (diphenylamino) phenylboronic acid (3.5 g, 0.012 mol) was added to Intermediate B-2 (3.7 g, 0.010 mol) > 3.9 g (yield 72%). (M / z = 539)

(5) Manufacturing example  5: Synthesis of Compound 9

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 6-3 (6.0 g, 0.012 mol) was added to Intermediate 9-1 (5.4 g, 0.010 mol) 73%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.43 / d, 7.90 / d, 7.85 / d, 7.61 / m, 7.54 / d, 7.51 / m, 7.46 / m, 7.41 / m, 7.32 / m M, 6.99 / s, 6.76 / s, 6.55 / s) 2H (7.79 / d, 7.54 / d, 7.51 / , 6.63 (d)

LC / MS: m / z = 799 [(M + 1) ^&lt; ^{+ &}

Example  10: Compound 10 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 10-1

(3.1 g, 0.010 mol) was added to dip-tolylamine (2.0 g, 0.010 mol) in the same manner as in Example 2 (1) (Yield: 77%) of the title compound (m / z = 431)

(2) Manufacturing example  2: Synthesis of intermediate 10-2

2-amine (2.1 g, 0.010 mol) was added to 4-bromo-4'-methylbiphenyl (2.5 g, 0.010 mol) Synthesis was conducted in the same manner to obtain 3.0 g (yield 80%) of Intermediate 10-2 (m / z = 375)

(3) Manufacturing example  3: Synthesis of intermediate 10-3

Intermediate 10-3 was synthesized in the same manner as in Example 2 (1) except that Intermediate 10-2 (3.8 g, 0.010 mol) was added to Intermediate 10-1 (4.3 g, 0.010 mol) (Yield: 77%). (M / z = 725)

(4) Manufacturing example  4: Synthesis of intermediate 10-4

<Intermediate 2-2> 5.4 (4 g, 0.012 mol) was obtained by the same method as in Example 1 (4), except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 10-3 g (yield: 70%). (m / z = 772)

(5) Manufacturing example  5: Synthesis of Compound 10

Synthesis was conducted in the same manner as in Example 1-Preparation Example (5), except that Intermediate 4-2 (9.3 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 75%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.90 / d, 7.87 / d, 7.69 / d, 7.62 / s, 7.61 / m, 7.55 / d, 7.51 / m, 7.38 / m, 7.28 / m , 7.23 / d, 6.75 / s, 6.58 / d, 5.73 / s) 2H (7.33 / d, 7.29 / d, 6.69 / d, 6.25 / s, 1.61 / s) (6.98 / d, 6.51 / d, 1.72 / s)

LC / MS: m / z = 907 [(M + 1) ^&lt; ^{+ &}

Example  11: Compound 11 Synthesis

(1) Production example 1: Synthesis of intermediate 11-1

2-amine (2.9 g, 0.010 mol) was added to 1,4-dibromobenzene (2.4 g, 0.010 mol) in the same manner as in Example 2 (1) To obtain 2.8 g (yield: 77%) of Intermediate 11-1 (m / z = 364)

(2) Manufacturing example  2: Synthesis of intermediate 11-2

Intermediate 11-2 was synthesized by the same method as in Example 1 (5), except that phenyl boronic aicd (1.4 g, 0.012 mol) was added to 1-bromo-5-chloronaphthalene (2.4 g, 0.010 mol) 1.7 g (yield 72%) of the title compound was obtained (m / z = 238)

(3) Manufacturing example  3: Synthesis of intermediate 11-3

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 11-1 (3.6 g, 0.010 mol) was added to Intermediate 11-2 (2.5 g, 0.010 mol) (Yield: 77%). (M / z = 566)

(4) Manufacturing example  4: Synthesis of intermediate 11-4

Synthesis was conducted in the same manner as in Example 1 (4), except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 11-3 (5.7 g, 0.010 mol) g (yield: 72%). (m / z = 613)

(5) Manufacturing example  5: Synthesis of Compound 11

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 11-4 (7.4 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 73%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.40 / d, 8.04 / d, 8.03 / d, 7.90 / d, 7.87 / d, 7.69 / d, 7.62 / d, 7.61 / m, 7.60 / m 7.51 / m, 7.28 / m, 7.23 / d, 6.98 / d, 6.75 / s, 6.58 / d) 2H (7.79 / d, 7.51 / m, 7.38 / ) 3H (7.54 / d) 4H (1.72 / s)

LC / MS: m / z = 747 [(M + 1) ^&lt; ^{+ &}

Example  12: Compound 12 Synthesis

(1) Production Example 1: Synthesis of Intermediate C

(2-bromo-5-chloro-1,1-dimethyl-1H-isoindole (2.6 g, (M / z = 319) (Intermediate C) (1.3 g, yield 41%).

(2) Manufacturing example  2: Synthesis of intermediate C-1

2.0 g (yield 62%) of Intermediate C-1 was obtained in the same manner as in Example 1 (2) except that Intermediate C (3.2 g, 0.010 mol) was added. M / z = 319 )

(3) Manufacturing example  3: Synthesis of intermediate C-2

2.0 g (yield 66%) of <Intermediate C-2> was obtained by the same method as in Example 1- (3), except that Intermediate C-1 (3.3 g, 0.010 mol) = 301)

(4) Manufacturing example  4: Synthesis of Compound 12

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 1-1 (6.8 g, 0.012 mol) was added to Intermediate C-2 (3.0 g, 0.010 mol) 62%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.87 / d, 7.69 / d, 7.62 / d, 7.55 / d, 7.41 / m, 7.38 / m, 7.28 / m, 7.21 / m, 6.75 / s D) 2H (7.52 / d, 7.51 / m, 1.72 / s, 1.53 / s, 1.50 / s, 1.40 / s, 1.30 / s)

LC / MS: m / z = 703 [(M + 1) ^&lt; ^{+ &}

Example  13: Compound 13 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 13-1

Intermediate 13-1 was synthesized in the same manner as in Example 2 (1) except that 4-bromobiphenyl (2.4 g, 0.010 mol) was added to Intermediate 6-3 (4.2 g, 0.010 mol) Yield: 67%). (M / z = 578)

(2) Manufacturing example  2: Synthesis of Compound 13

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 4-2 (6.9 g, 0.012 mol) was added to Intermediate A-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.43 / d, 7.90 / d, 7.85 / d, 7.69 / d, 7.61 / m, 7.51 / m, 7.46 / m, 7.41 / m, 7.32 / m D, 7.53 / d, 6.99 / s, 6.76 / s) 2H (7.79 / d, 7.51 /

LC / MS: m / z = 712 [(M + 1) ^&lt; ^{+ &}

Example  14: Compound 14 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate D

(2-tert-butylphenyl) magnesium bromide (2.8 g, 0.012 mol) was added to 3-methoxyisobenzofuran-1 (3H) -one (1.6 g, 0.010 mol) and the resulting solution was dissolved in 50 mL of THF. M BuLi (0.01 mL, 0.0005 mol) was added dropwise and stirred for 1 hour. The mixture was slowly warmed to room temperature and stirred for 4 hours. After completion of the reaction, the reaction mixture was extracted with 100 mL of water, and the organic layer was dried under reduced pressure. This was recrystallized from EtOH: Acetone to give Intermediate D (1.0 g, 41%). (M / z = 246)

(2) Manufacturing example  2: Synthesis of intermediate D-1

Potassium fluoride (2.3 g, 0.040 mol) was added to Intermediate D (2.5 g, 0.010 mol), 50 mL of THF / H ₂ O was added at a ratio of 5: 2 and the mixture was stirred at 25 ° C for 1 hour. After cooling, the mixture was separated into H ₂ O: MC and column-purified (n-hexane: MC) to obtain 1.3 g (yield: 51%) of Intermediate D-1. (m / z = 260)

(3) Manufacturing example  3: Synthesis of intermediate D-2

100 mL of DMF was added to N-bromosuccinimide (1.8 g, 0.010 mol) in Intermediate D-1 (2.6 g, 0.010 mol) and the mixture was reacted at 20 ° C for 8 hours with stirring. After completion of the reaction H ₂ 0: column purification after phase separation with ethyl acetate (n-Hexane: MC) to the intermediate D-2 to yield 1.6 g (48%) (m / z = 339).

(4) Manufacturing example  4: Synthesis of Compound 14

Intermediate 1-1 (6.8 g, 0.012 mol) was added to Intermediate D-2 (3.4 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- (5) 70%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.87 / d, 7.62 / d, 7.55 / d, 7.42 / d, 7.41 / m, 7.38 / m, 7.36 / m, 7.30 / d, 7.28 / m 7.52 / d, 7.51 / m, 7.25 / d, 7.12 / d, 6.69 / d, 6.63 / d), 7.27 /

LC / MS: m / z = 696 [(M + 1) ^&lt; ^{+ &}

Example  15: Compound 15 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate E

(2-tert-butyl-3-chlorophenyl) magnesium bromide (3.2 g, 0.012 mol) was added to 3-methoxyisobenzofuran-1 (3H) (M / z = 280) of Intermediate E < 1.1 g (yield 40%).

(2) Manufacturing example  2: Synthesis of intermediate E-1

Intermediate E (2.8 g, 0.010 mol) was synthesized in the same manner as in Example 1- (5) to give 2.1 g (m / z = 294) of Intermediate E-1.

(3) Manufacturing example  3: Synthesis of intermediate E-2

Intermediate E-2 was synthesized in the same manner as in Example 14 (3) except that N-bromosuccinimide (1.8 g, 0.010 mol) was added to Intermediate E-1 (2.9 g, 0.010 mol) Yield: 41%). m / z = 373)

(4) Manufacturing example  4: Synthesis of intermediate 15-1

Intermediate 15-1 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate E-2 (3.7 g, 0.010 mol) Yield: 72%). (M / z = 370)

(5) Manufacturing example  5: Synthesis of compound 15

Synthesis was conducted in the same manner as in Example 1 (5) to obtain Intermediate 1-1 (6.8 g, 0.012 mol) and Intermediate 15-1 (3.7 g, 0.010 mol) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.87 / d, 7.62 / s, 7.55 / d, 7.48 / d, 7.42 / d, 7.41 / m, 7.38 / m, 7.30 / d, 7.30 / m D, 7.58 / d, 7.51 / m, 7.19 / m, 6.95 / d) 4H (7.54 / d, 6.69 / d, 7.28 / m, 7.27 / m, 7.22 / / d) 6H (1.72 / s)

LC / MS: m / z = 773 [(M + 1) ^&lt; ^{+ &}

Example  16: Compound 16 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 16-1

(3.1 g, 0.010 mol) was added to dip-tolylamine (2.0 g, 0.010 mol) in the same manner as in Example 2 (1) 16-1> 4.8 g (yield: 87%). (M / z = 547)

(2) Manufacturing example  2: Synthesis of intermediate 16-2

<Intermediate 16-2> 4.3 (5 g, 0.010 mol) was synthesized in the same manner as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) g (yield: 72%). (m / z = 594)

(3) Manufacturing example  3: Synthesis of Compound 16

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 16-1 (7.1 g, 0.012 mol) and Intermediate 15-1 (3.7 g, 0.010 mol) 67%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.48 / d, 7.42 / d, 7.30 / m, 7.30 / d, 7.27 / m, 7.22 / m, 7.18 / d, 5.73 / s) 2H (7.19 d, 6.25 / s) 4H (2.34 / s, 1.72 / s) 8H (6.98 / d, 6.51 / d)

LC / MS: m / z = 804 [(M + 1) ^&lt; ^{+ &}

Example  17: Compound 17 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate F

Methyl 2-bromo-6-chlorobenzoate (2.7 g, 0.012 mol) was added to 3-bromo-1,1-dimethyl-1H- pyrrolo [ (M / z = 314) (1.2 g, yield 37%) was obtained by the same method as in Preparation Example (2)

(2) Manufacturing example  2: Synthesis of intermediate F-1

(M / z = 314 (M < + &gt;) was obtained by the procedure of Intermediate F (3.1 g, 0.010 mol) )

(3) Manufacturing example  3: Synthesis of intermediate F-2

2.0 g (yield 66%) of Intermediate F-2 was obtained in the same manner as in Example 1 (3), except that Intermediate F-1 (3.1 g, 0.010 mol) = 296)

(4) Manufacturing example  4: Synthesis of intermediate 17-1

(Pinacolato) dibron (3.0 g, 0.012 mol) was added to 2- (4-bromophenyl) -4,6-diphenyl-1,3,5-triazine (3.9 g, 0.010 mol) (M / z = 435) was obtained (3.1 g, yield 72%).

(5) Manufacturing example  5: Synthesis of Compound 17

The compound 17-1 (5.2 g, 0.012 mol) was added to Intermediate F-2 (3.0 g, 0.010 mol) and the compound was obtained in the same manner as in Example 1- (5) 69%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.68 / d, 7.77 / d, 7.71 / d, 7.49 / d, 7.40 / m) 2H (7.85 / d, 7.41 / m, 7.25 / d) 4H (8.28 / d, 7.51 / m, 1.72 / s)

LC / MS: m / z = 570 [(M + 1) ^&lt; ^{+ &}

Example  18: Compound 18 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate G

(3.0 g, 0.012 mol) was added to 3-bromo-1,1-dimethyl-1H-isoindole (2.2 g, 0.010 mol) and methyl 2-bromo-6-chlorobenzoate Synthesis was conducted in the same manner to obtain 1.2 g (yield 37%) of Intermediate G (m / z = 313)

(2) Manufacturing example  2: Synthesis of intermediate G-1

2.0 g (yield 66%) of Intermediate G-1 was obtained by the same procedure as in Example 1 (2) except that Intermediate G (3.1 g, 0.010 mol) was added. M / z = 313 )

(3) Manufacturing example  3: Synthesis of intermediate G-2

Intermediate G-2 (1.8 g, yield 60%) was obtained by the same method as in Example 1 (3), except that Intermediate G-1 (3.3 g, 0.010 mol) = 296)

(4) Manufacturing example  4: Synthesis of Intermediate 18-1

(3.3 g, 0.012 mol) of triphenylen-2-ylboronic acid was added to 1,4-dibromo-2,5-dimethylbenzene (2.6 g, 0.010 mol) in the same manner as in Example 1- 3.0 g (yield: 72%) of Intermediate 18-1 (m / z = 411) was obtained.

(5) Manufacturing example  5: Synthesis of intermediate 18-2

Intermediate 18-2 was synthesized as in Intermediate 18-2 (4.1 g, 0.010 mol) by the same procedure as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) g (yield: 72%). (m / z = 458)

(6) Manufacturing example  6: Synthesis of compound 18

The compound 18 was synthesized in the same manner as in Example 1 (5), except that Intermediate 18-2 (5.5 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 67%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d, 7.95 / d, 7.86 / d, 7.57 / m, 7.36 / m) 2H (8.93 / d, 8.12 (dl / d, 7.88 / m, 7.82 / m, 7.73 / s, 7.17 / d, 2.59 / s)

LC / MS: m / z = 592 [(M + 1) ^&lt; ^{+ &}

Example  19: Compound 19 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 19-1

Intermediate 19-1 (3.1 g, 0.008 mol) was added to 9-carbazol-3-ylboronic acid (2.1 g, 0.010 mol) in the same manner as in Example 1- 1> 3.2 g (yield: 72%). (M / z = 442)

(2) Manufacturing example  2: Synthesis of Compound 19

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 19-1 (5.3 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 75%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.95 / d, 7.94 / d, 7.87 / d, 7.86 / d, 7.77 / d, 7.69 / d, 7.57 / m, 7.36 / m , 7.33 / m, 7.25 / m) 2H (7.41 / m, 7.17 / d) 4H (8.28 / d, 7.51 /

LC / MS: m / z = 658 [(M + 1) ^&lt; ^{+ &}

Example  20: Compound 20 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 20-1

100 mL of 1,2-dichlorobenzene was added to triphenylphosphine (4.5 g, 0.017 mol) in 2-bromo-2'-nitrobiphenyl (5.0 g, 0.017 mol) and reacted at 180 ° C for 24 hours with stirring. After completion of the reaction, the reaction mixture was cooled, and the product was separated into H ₂ O: MC and subjected to column purification (n-hexane: MC) to obtain 4.2 g (m / z = 246)

(2) Manufacturing example  2: Synthesis of intermediate 20-2

The intermediate 20-1 (3.0 g, 0.012 mol) was dissolved in 30 mL of anhydrous THF, and then 5.9 mL of n-BuLi (2.5 M) was slowly added dropwise at -78 ° C. After maintaining for 1 hour, triisopropyl borate (3.4 g, 0.018 mol) was added and stirred at room temperature for 24 hours. After completion of the reaction, 1N HCl was added and the mixture was stirred for 1 hour. After separation into EA: H ₂ O, the product was recrystallized with n-hexane to obtain 1.8 g (yield 70%) of Intermediate 20-2 )

(3) Manufacturing example  3: Synthesis of intermediate 20-3

<Intermediate 20-3> 2.0 (0.19 g, 0.008 mol) was synthesized in the same manner as in Example 1 (5) except that 1,4-dibromobenzene (1.9 g, 0.008 mol) was added to Intermediate 20-2 g (yield: 77%). (m / z = 322)

(4) Manufacturing example  4: Synthesis of intermediate 20-4

Intermediate 20-4 was synthesized by the same procedure as in Example 1 (4) (2.9 g, 0.012 mol) with bis (pinacolato) dibron (3.0 g, 0.012 mol) g (yield 78%). (m / z = 369)

(5) Manufacturing example  5: Synthesis of intermediate 20-5

To the intermediate 20-4 (4.4 g, 0.012 mol) was added 2-bromo-4,6-diphenyl-1,3,5-triazine (3.1 g, 0.010 mol) (M / z = 600) (yield: 72%) was obtained by the same method as Intermediate 20-5 (Intermediate 20-5)

(6) Manufacturing example  6: Synthesis of Compound 20

The compound 20 was synthesized in the same manner as in Example 1 (5), except that Intermediate 20-5 (7.2 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 73%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.95 / d, 7.94 / d, 7.86 / d, 7.79 / d, 7.59 / d, 7.57 / m, 7.43 / m, 7.36 / m , 7.33 / m, 7.25 / m) 2H (7.41 / m, 7.17 / d) 4H (8.28 / d, 7.51 / m, 7.25 / d, 1.72 /

LC / MS: m / z = 734 [(M + 1) ^&lt; ^{+ &}

Example  21: Compound 21 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 21-1

Intermediate 21-1 (2.7 g, Yield 77%) was synthesized in the same manner as in Example 2 (1) except that bromobenzene (1.3 g, 0.008 mol) was added to Intermediate 20-4 (3.7 g, 0.010 mol) %). (M / z = 445)

(2) Manufacturing example  2: Synthesis of Compound 21

Intermediate 21-1 (5.3 g, 0.012 mol) was added to Intermediate G-2 (3.1 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- 74%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.95 / d, 7.94 / d, 7.86 / d, 7.79 / d, 7.59 / d, 7.57 / m, 7.45 / m, 7.43 / m , 7.36 / m, 7.33 / m, 7.25 / m) 2H (7.58 / m, 7.50 / d, 7.17 / d)

LC / MS: m / z = 579 [(M + 1) ^&lt; ^{+ &}

Example  22: Compound 22 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 22-1

Intermediate 20-1 (2.5 g, 0.010 mol) was added to Intermediate 20-2 (2.9 g, 0.010 mol) and the same reaction procedure as in Preparation Example (1) (Yield: 77%). (M / z = 458)

(2) Manufacturing example  2: Synthesis of Intermediate 22-2

Intermediate 22-2 (4.1 g, Yield 77%) was obtained by synthesizing bromobenzene (1.6 g, 0.010 mol) in Intermediate 22-1 (4.6 g, 0.010 mol) %). (M / z = 534)

(3) Manufacturing example  3: Synthesis of Compound 22

The compound 22-2 (6.4 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) and the compound was obtained in the same manner as in Example 1- (5) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.95 / d, 7.86 / d, 7.79 / d, 7.63 / d, 7.59 / d, 7.57 / m, 7.45 / m, 7.43 / m, 7.37 / m D, 7,34 / d, 7.58 / m, 7.50 / d, 7.33 / m, 7.25 / m, 7.17 / d)

LC / MS: m / z = 668 [(M + 1) ^&lt; ^{+ &}

Example  23: Compound 23 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 23-1

(Pinacolato) dibron (3.0 g, 0.012 mol) was added to 3,6-dibromo-9-phenyl-9H-carbazole (4.0 g, 0.010 mol) in the same manner as in Example 1- To obtain 3.5 g (yield 70%) of Intermediate 23-1 (m / z = 495)

(2) Manufacturing example  2: Synthesis of Compound 23

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 4-2 (5.9 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 68%). (M / z = 000)

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.18 / d, 8.00 / d, 7.87 / d, 7.69 / d, 7.45 / m) 2H (7.95 / d, 7.86 / d, 7.77 / s, 7.58 7.57 / m, 7.50 / d, 7.36 / m) 4H (7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 762 [(M + 1) ^&lt; ^{+ &}

Example  24: Compound 24 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 24

To the intermediate G-2 (3.0 g, 0.010 mol) was added 4- (dibenzo [b, d] thiophen-4-yl) phenylboronic acid (3.6 g, 0.012 mol) Synthesis was conducted in the same manner to obtain 3.7 g (yield 72%) of <Compound 24>.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.95 / d, 7.86 / d, 7.58 / m, 7.57 / m, 7.52 / m , 7.50 / m, 7.36 / m) 2H (7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 520 [(M + 1) ^&lt; ^{+ &}

Example  25: Compound 25 Synthesis

(One) Manufacturing example  1: Synthesis of Compound (25)

To the intermediate G-2 (3.0 g, 0.010 mol) was added 4- (2-phenyl-1H-benzo [d] imidazol-1-yl) phenylboronic acid (3.8 g, 0.012 mol) ) To obtain 3.9 g (yield 74%) of <Compound 25>.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.56 / d, 7.95 / d, 7.86 / d, 7.59 / d, 7.57 / m, 7.41 / m, 7.36 / m) 2H (8.28 / d, 7.79 / d, 7.68 / d, 7.51 / m, 7.22 / m, 7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 530 [(M + 1) ^&lt; ^{+ &}

Example  26: Compound 26 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 26-1

2-phenyl-1H-benzo [d] imidazole (1.9 g, 0.010 mol) was added to 3-bromo-9H-carbazole (2.5 g, 0.010 mol) To obtain 3.0 g (yield 84%) of Intermediate 26-1 (m / z = 359)

(2) Manufacturing example  2: Synthesis of Compound 26

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 26-1 (3.6 g, 0.010 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 77%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.56 / d, 8.55 / d, 7.94 / d, 7.63 / s, 7.59 / d, 7.50 / d, 7.50 / s, 7.41 / m, 7.36 / m D, 7.31 / d, 7.25 / m) 2H (8.28 / d, 7.51 / m, 7.90 / d, 7.22 / m, 7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 619 [(M + 1) ^&lt; ^{+ &}

Example  27: Compound 27 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 27-1

Synthesis was conducted in the same manner as in Example 2 (1) except that 9H-carbazole (1.7 g, 0.010 mol) was added to 1,3,5-tribromobenzene (3.1 g, 0.010 mol) 27-1> (yield: 85%). (M / z = 487)

(2) Manufacturing example  2: Synthesis of intermediate 27-2

Intermediate 27-2 was synthesized by the same method as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 27-1 (4.9 g, 0.010 mol) g (yield 75%). (m / z = 534)

(3) Manufacturing example  3: Synthesis of Compound 27

Synthesis was conducted in the same manner as in Example 1 (5) to obtain Intermediate 27-2 (6.4 g, 0.012 mol) and Intermediate 27 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.95 / d, 7.86 / d, 7.57 / m, 7.20 / s) 2H (8.55 / d, 8.12 / d, 8.09 / s, 7.94 / d, 7.63 7.25 / m, 7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 668 [(M + 1) ^&lt; ^{+ &}

Example  28: Compound 28 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 28-1

Synthesis was carried out in the same manner as in Example 1 (5), except that 4-bromodibenzo [b, d] thiophene (2.1 g, 0.008 mol) was added to Intermediate 20-4 (3.7 g, 0.010 mol) -1> 2.4 g (yield 72%). (M / z = 425)

(2) Manufacturing example  2: Synthesis of compound 28

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 28-1 (4.3 g, 0.010 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 77%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.94 / d, 7.79 / d, 7.59 / d, 7.58 / m D, 7.17 / d, 1.72 / s, 1.61 / s), 4H (7.25 / d), 7.52 / m, 7.50 / d, 7.50 / d, 7.43 / m, 7.33 /

LC / MS: m / z = 685 [(M + 1) ^&lt; ^{+ &}

Example  29: Compound 29 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 29-1

2-ylboronic acid (2.5 g, 0.012 mol) was added to 9- (4-bromophenyl) -9H-carbazole (3.2 g, 0.010 mol) in the same manner as in Example 1- To obtain 2.9 g (yield 72%) of Intermediate 29-1 (m / z = 408)

(2) Manufacturing example  2: Synthesis of Compound 29

The compound 29 was synthesized in the same manner as in Example 2 (1) except that Intermediate 29-1 (4.1 g, 0.010 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 82%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.91 / m) 2H (8.55 / d, 8.12 / d, 7.94 / d, 7.63 / d, 7.50 / m, 7.33 / m, 7.29 / m, 7.25 / m, 7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 668 [(M + 1) ^&lt; ^{+ &}

Example  30: Compound 30 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 30-1

Phenylboronic acid (1.4 g, 0.012 mol) was added to 4,6-dibromo-2,5-dichloropyrimidine (3.1 g, 0.010 mol) and the title compound was synthesized in the same manner as in Example 1- 30-1> 2.2 g (yield 72%). (M / z = 301)

(2) Manufacturing example  2: Synthesis of intermediate 30-2

(3.3 g, 0.012 mol) of 4,6-diphenyl-1,3,5-triazin-2-ylboronic acid was added to Intermediate 30-1 (3.0 g, 0.010 mol) (M / z = 498) (3.6 g, yield: 72%). &Lt;

(3) Manufacturing example  3: Synthesis of intermediate 30-3

<Intermediate 30-3> 4.2 (0.2 g, 0.012 mol) was added to the intermediate 30-2 (5.0 g, 0.010 mol) and bis (pinacolato) dibron g (yield: 72%). (m / z = 589)

(4) Manufacturing example  4: Synthesis of compound 30

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 30-3 (7.1 g, 0.012 mol) and Intermediate G-2 (3.0 g, 0.010 mol) 62%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.95 / d, 7.86 / d, 7.57 / m, 7.36 / m) 2H (7.17 / d, 1.72 / s, 1.61 / s) 4H (8.28 / d , 7.79 / d, 7.41 / m) 8H (7.51 / m)

LC / MS: m / z = 723 [(M + 1) ^&lt; ^{+ &}

Example  31: Compound 31 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 31-1

The procedure of Example 2 was repeated except that 1,4-dibromobenzene (2.4 g, 0.010 mol) was added to 2- (4-bromophenyl) -1H-benzo [d] imidazole (2.7 g, 0.010 mol) (M / z = 428) of Intermediate 31-1 (yield: 77%).

(2) Manufacturing example  2: Synthesis of intermediate 31-2

<Intermediate 31-2> 3.8 (0.1 g, 0.012 mol) was synthesized in the same manner as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 31-1 g (yield: 72%). (m / z = 522)

(3) Manufacturing example  3: Synthesis of Compound 31

The compound 31 was synthesized in the same manner as in Example 1 (5), except that Intermediate 31-2 (6.3 g, 0.012 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) 66%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.56 / d, 7.59 / d) 2H (7.95 / d, 7.86 / d, 7.85 / d, 7.79 / d, 7.68 / d, 7.57 / m, 7.36 / m, 7.25 / d, 7.22 / m) 4H (7.17 / d, 1.72 / s, 1.61 / s)

LC / MS: m / z = 790 [(M + 1) ^&lt; ^{+ &}

Example  32: Compound 32 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate H

To a solution of methyl 4-bromo-2-chloronicotinate (3.0 g, 0.012 mol) in 3-bromo-1,1-dimethyl-1H-isoindole (2.2 g, 0.010 mol) (M / z = 314) (Intermediate H) (1.2 g, yield 39%).

(2) Manufacturing example  2: Synthesis of Intermediate H-1

Intermediate H-1 (1.6 g, yield 51%) was obtained by the same method as in Example 1- (2), except that Intermediate H (3.1 g, 0.010 mol) was added. M / z = 314 )

(3) Manufacturing example  3: Synthesis of intermediate H-2

Intermediate H-2 (1.5 g, yield 52%) was obtained by the same method as in Example 1 (3), except that Intermediate H-1 (3.1 g, 0.010 mol) = 296)

(4) Manufacturing example  4: Synthesis of Compound 32

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 17-1 (5.2 g, 0.012 mol) was added to Intermediate H-2 (3.0 g, 0.010 mol) 65%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.60 / d, 7.36 / m, 7.21 / d) 2H (8.81 / d, 7.88 / d, 7.41 / m, 7.17 / d, 1.72 / s, 1.30 / s) 4H (8.28 / d, 7.51 / m)

LC / MS: m / z = 570 [(M + 1) ^&lt; ^{+ &}

Example  33: Compound 33 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate I

(2-tert-butyl-3-chlorophenyl) magnesium bromide (3.2 g, 0.012 mol) was added to 3-methoxyisobenzofuran-1 (3H) (M / z = 280) (Intermediate I) (1.1 g, yield 40%).

(2) Manufacturing example  2: Synthesis of Intermediate I-1

Intermediate I (2.8 g, 0.010 mol) was synthesized in the same manner as in Example 1- (5) to give 1.9 g (63% yield) of Intermediate I-1 (m / z = 294)

(3) Manufacturing example  3: Synthesis of intermediate I-2

Intermediate I-2 was synthesized in the same manner as in Example 14- (3) except that N-bromosuccinimide (1.8 g, 0.010 mol) was added to Intermediate I-1 (2.9 g, 0.010 mol) Yield: 34%). (M / z = 373)

(4) Manufacturing example  4: Synthesis of intermediate 33-1

Intermediate 33-1 was prepared by the same method as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate I-2 (3.7 g, 0.010 mol) Yield: 72%). (M / z = 370)

(5) Manufacturing example  5: Synthesis of Compound 33

Intermediate 19-1 (5.3 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) and the compound was synthesized by the same method as in Example 1 (5) to give 4.8 g 66%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.87 / d, 7.77 / s, 7.69 / d, 7.56 / d, 7.38 / d, 7.36 / m, 7.30 / m , 7.25 / m) 2H (7.41 / m, 7.33 / m, 7.19 / m, 7.12 / d, 6.95 / d, 1.72 / s, 1.69 / s)

LC / MS: m / z = 733 [(M + 1) ^&lt; ^{+ &}

Example  34: Compound 34 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 34

The compound 27-2 (6.4 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1 (5) 70%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.56 / d, 7.38 / d, 7.36 / m, 7.34 / m, 7.31 / m, 7.20 / s) 2H (8.55 / d, 8.12 / d, 8.09 7.9 / d, 7.63 / d, 7.50 / m, 7.33 / m, 7.30 / m, 7.29 / m, 7.19 / m, 7.12 / d, 6.95 / d, 1.72 / s,

LC / MS: m / z = 743 [(M + 1) ^&lt; ^{+ &}

Example  35: Compound 35 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 35-1

Dibromobenzene (1.9 g, 0.008 mol) was added to 9-carbazol-3-ylboronic acid (2.1 g, 0.010 mol) -1> 1.8 g (yield: 71%). (M / z = 322)

(2) Manufacturing example  2: Synthesis of intermediate 35-2

To the intermediate 35-1 (3.2 g, 0.010 mol) was added 9,9-dimethyl-9H-fluoren-2-ylboronic acid (2.9 g, 0.012 mol) To obtain 3.1 g (yield 72%) of Intermediate 35-2 (m / z = 435)

(3) Manufacturing example  3: Synthesis of Compound 35

Synthesis was conducted in the same manner as in Example 2 (1) except that Intermediate 35-2 (4.4 g, 0.010 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 78%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.93 / d, 7.69 / d, 7.66 / m, 7.63 / d, 7.55 / d, 7.42 / d, 7.38 / m , 7.36 / m, 7.33 / m, 7.30 / m, 7.28 / m, 7.25 / m, 7.11 / d) 2H (7.87 d, 7.77 s, 7.19 m, 7.12 d, 6.95 d, ) 4H (7.25 / d, 1.72 / s)

LC / MS: m / z = 771 [(M + 1) ^&lt; ^{+ &}

Example  36: Compound 36 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 36

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 30-3 (6.4 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 67%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.56 / d, 7.38 / d, 7.36 / m, 7.33 / m, 7.30 / m) 2H (7.19 / m, 7.12 / d, 6.95 / d, 1.72 / s, 1.69 / s) 4H (8.28 / d, 7.79 / d, 7.41 / m) 8H (7.51 /

LC / MS: m / z = 798 [(M + 1) ^&lt; ^{+ &}

Example  37: Compound 37 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 37-1

(1.6 g, 0.010 mol) was added to 2-bromo-3,10-dihydroimidazo [4,5-a] carbazole (2.9 g, 0.010 mol) in the same manner as in Example 2- To obtain 2.8 g (yield: 77%) of Intermediate 37-1 (m / z = 362)

(2) Manufacturing example  2: Synthesis of intermediate 37-2

2.6 g (Intermediate 37-2) was synthesized in the same manner as in Example 1 (5) except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 37-1 (3.6 g, 0.010 mol) Yield: 72%). (M / z = 359)

(3) Manufacturing example  3: Synthesis of intermediate 37-3

Intermediate 37-3> 4.1 (4-fluorobenzene) was synthesized in the same manner as in Example 2 (1) except that 1,4-dibromobenzene (2.4 g, 0.010 mol) g (yield: 80%). (m / z = 514)

(4) Manufacturing example  4: Synthesis of intermediate 37-4

Intermediate 37-4 was synthesized in the same manner as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 37-3 (5.1 g, 0.010 mol) g (yield: 72%). (m / z = 561)

(5) Manufacturing example  5: Synthesis of Compound 37

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 37-4 (6.7 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 65%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.22 / d, 7.94 / d, 7.85 / d, 7.58 / m, 7.56 / d, 7.45 / m, 7.41 / m, 7.38 / d D, 7.75 / d, 7.50 / d, 7.33 / m, 7.12 / d, 6.95 / d, 1.72 / , 1.69 / s) 3H (7.19 / m)

LC / MS: m / z = 770 [(M + 1) ^&lt; ^{+ &}

Example  38: Compound 38 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 38-1

2- (4-bromophenyl) triphenylene (3.8 g, 0.010 mol) was added to 5-bromo-2-phenyl-1H-benzo [d] imidazole (2.7 g, 0.010 mol) (M / z = 575) (yield: 81%) was obtained by the same method as in the synthesis of Intermediate 38-1 (Intermediate 38-1)

(2) Manufacturing example  2: Synthesis of Intermediate 38-2

Intermediate 38-2 &gt; 4.5 (4.5 g, 0.010 mol) was synthesized in the same manner as in Example 1- (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) g (yield: 72%). (m / z = 622)

(3) Manufacturing example  3: Synthesis of Compound 38

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 38-1 (7.5 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.07 / d, 8.04 / d, 7.92 / s, 7.56 / d, 7.41 / m, 7.38 / d, 7.36 / m M, 7,30 / m, 7,12 / d, 8,12 / d, 7.88 / m, 7.82 / , 1.72 / s, 1.69 / s)

LC / MS: m / z = 832 [(M + 1) ^&lt; ^{+ &}

Example  39: Compound 39 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 39

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 20-5 (7.2 g, 0.012 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 62%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1h (8.55 / d, 7.94 / d, 7.79 / d, 7.59 / d, 7.56 / d, 7.43 / m, 7.38 / d, 7.36 / m, 7.30 / m , 7.25 / m) 2H (7.41 / m, 7.33 / m, 7.19 / m, 7.12 / d, 6.95 / d, 1.72 / s,

LC / MS: m / z = 810 [(M + 1) ^&lt; ^{+ &}

Example  40: Compound 40 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 40

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 28-1 (4.3 g, 0.010 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 80%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.94 / d, 7.79 / d, 7.66 / m, 7.59 / d M, 7,12 / m, 7.52 / m, 7.50 / m, 7.43 / m, 7.42 / d, 7.36 / m, 7.33 / , 6.95 / d, 1.72 / s, 1.69 / s) 4H (7.25 / d)

LC / MS: m / z = 761 [(M + 1) ^&lt; ^{+ &}

Example  41: Compound 41 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 41-1

Intermediate 20-1 (2.0 g, 0.008 mol) was added to Intermediate 20-2 (2.1 g, 0.010 mol), and 2.4 g of Intermediate 41-1 was synthesized in the same manner as in Example 1- (Yield: 72%). (M / z = 332)

(2) Manufacturing example  2: Synthesis of intermediate 41-2

Intermediate 41-2 (3.4 g, Yield 83%) was synthesized in the same manner as in Example 2 (1) except that bromobenzene (1.6 g, 0.010 mol) was added to Intermediate 41-1 (3.3 g, 0.010 mol) %). (M / z = 408)

(3) Manufacturing example  3: Synthesis of Compound 41

Synthesis was conducted in the same manner as in Example 2 (1) except that Intermediate 41-2 (4.1 g, 0.010 mol) was added to Intermediate 33-1 (3.7 g, 0.010 mol) 77%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.12 / d, 8.10 / d, 7.94 / d, 7.90 / d, 7.79 / d, 7.66 / m, 7.63 / d, 7.59 / d M, 7.46 / m, 7.42 / d, 7.39 / m, 7.36 / m, 7.33 / m, 7.30 / m, 7.29 / m, 7.25 / m, , 7.50 / d, 7.19 / m, 7.12 / d, 6.95 / d, 1.72 / s, 1.69 / s)

LC / MS: m / z = 743 [(M + 1) ^&lt; ^{+ &}

Example  42: Compound 42 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate J

To a solution of methyl 4-bromo-2-chloronicotinate (3.0 g, 0.012 mol) in 3-bromo-1,1-dimethyl-1H-isoindole (2.2 g, 0.010 mol) (M / z = 314) (Intermediate J) (1.3 g, yield 40%).

(2) Manufacturing example  2: Synthesis of intermediate J-1

2.1 g (yield 66%) of Intermediate J-1 was obtained in the same manner as in Example 1 (2) except that Intermediate J (3.1 g, 0.010 mol) was added. M / z = 314 )

(3) Manufacturing example  3: Synthesis of intermediate J-2

2.0 g (yield 66%) of <Intermediate J-2> was obtained by the same method as employed in the preparation example (3) of Example 1, with the intermediate J-1 (3.1 g, 0.010 mol) = 297)

(4) Manufacturing example  4: Synthesis of Compound 42

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 17-1 (5.2 g, 0.012 mol) was added to Intermediate J-2 (3.0 g, 0.010 mol) 74%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.60 / d, 7.36 / m, 7.21 / d) 2H (8.81 / d, 7.88 / d, 7.41 / m, 7.17 / d, 1.72 / s, 1.30 / s) 4H (8.28 / d, 7.51 / m)

LC / MS: m / z = 570 [(M + 1) ^&lt; ^{+ &}

Example  43: Compound 43 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 43-1

Synthesis was conducted in the same manner as in Example 1 (4), except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to 2- (4-bromophenyl) triphenylene (3.8 g, 0.010 mol) -1> 3.1 g (yield 72%). (M / z = 430)

(2) Manufacturing example  2: Synthesis of Compound 43

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 43-1 (5.2 g, 0.012 mol) was added to Intermediate J-2 (3.0 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.60 / d, 8.18 / d, 8.04 / d, 7.36 / m, 7.21 / d) 2H (8.93 / d, 8.81 / d, 8.12 / d, 7.88 / m, 7.88 / d, 7.82 / m, 7.17 / d, 1.72 / s, 1.30 / s)

LC / MS: m / z = 565 [(M + 1) ^&lt; ^{+ &}

Example  44: Compound 44 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate K

Methyl 3-bromopicolinate (2.6 g, 0.012 mol) was added to 3-bromo-7-chloro-1,1-dimethyl-1H pyrrolo [3,4- (M / z = 316) (Intermediate K) (1.4 g, yield 43%) was synthesized in the same manner as in Preparation Example (2)

(2) Manufacturing example  2: Synthesis of Intermediate K-1

2.1 g (yield 66%) of Intermediate K-1 was obtained in the same manner as in Example 1 (2), except that Intermediate K (3.2 g, 0.010 mol) was added. M / z = 316 )

(3) Manufacturing example  3: Synthesis of Intermediate K-2

1.4 g (yield: 48%) of Intermediate K-2 was obtained by the same method as in Example 1 (3), except that Intermediate K-1 (3.2 g, 0.010 mol) = 297)

(4) Manufacturing example  4: Synthesis of Compound 44

The same procedure as in Example 1 (5) was repeated except that 4- (dibenzo [b, d] thiophen-4-yl) phenylboronic acid (3.7 g, 0.012 mol) was added to Intermediate K-2 (3.0 g, 0.010 mol) Synthesis was conducted in the same manner to obtain 3.6 g (yield 69%) of <Compound 44>.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.09 / s, 8.68 / d, 8.41 / d, 8.20 / d, 8.17 / d, 7.98 / d, 7.58 / m, 7.52 / d, 7.50 / m , 7.49 / m) 2H (1.72 / s, 1.30 / s) 4H (7.25 / d)

LC / MS: m / z = 522 [(M + 1) ^&lt; ^{+ &}

Example  45: Compound 45 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 45-1

3.1 g (yield: 77%) of Intermediate 45-1 was synthesized in the same manner as in Example 2 (1) except that bromobenzene (1.6 g, 0.010 mol) was added to Intermediate 35-1 (3.2 g, 0.010 mol) %). (M / z = 398)

(2) Manufacturing example  2: Synthesis of intermediate 45-2

Intermediate 45-2> 3.3 g (0.012 mol) of bis (pinacolato) dibron was added to Intermediate 45-1 (4.0 g, 0.010 mol) g (yield: 74%). (m / z = 445)

(3) Manufacturing example  3: Synthesis of Compound 45

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 45-2 (5.3 g, 0.012 mol) was added to Intermediate K-2 (3.0 g, 0.010 mol) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.09 / s, 8.68 / d, 8.55 / d, 8.17 / d, 7.94 / d, 7.87 / d, 7.77 / s, 7.69 / d, 7.49 / m , 7.45 / m, 7.33 / m, 7.25 / m) 2H (7.58 / m, 7.50 /

LC / MS: m / z = 581 [(M + 1) ^&lt; ^{+ &}

Example  46: Compound 46 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate L

Methyl 3-bromopicolinate (2.6 g, 0.012 mol) was added to 5-bromo-3-chloro-7,7-dimethyl-7H-pyrrolo [3,4- (M / z = 316) (Intermediate L) was obtained (1.3 g, 41% yield) in the same manner as in Preparation Example (2)

(2) Manufacturing example  2: Synthesis of intermediate L-1

Intermediate L-1 (1.6 g, yield 51%) was obtained by introducing intermediate L (3.2 g, 0.010 mol) in the same manner as in Example 1- (2) to give m / z = 316 )

(3) Manufacturing example  3: Synthesis of intermediate L-2

2.0 g (yield 66%) of <Intermediate L-2> was obtained by the same method as in Example 1- (3), except that Intermediate L-1 (3.2 g, 0.010 mol) = 297)

(4) Manufacturing example  4: Synthesis of Compound 46

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 17-1 (5.2 g, 0.012 mol) was added to Intermediate L-2 (3.0 g, 0.010 mol) 63%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.09 / s, 8.68 / d, 8.17 / d, 7.49 / m) 2H (7.85 / d, 7.41 / m, 7.25 / d, 1.72 / s, 1.30 / s) 4H (8.28 / d, 7.51 / m)

LC / MS: m / z = 571 [(M + 1) ^&lt; ^{+ &}

Example  47: Compound 47 Synthesis

(One) Manufacturing example  1: Synthesis of compound 47

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 43-1 (5.2 g, 0.012 mol) was added to Intermediate L-2 (3.0 g, 0.010 mol) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 9.09 / s, 8.68 / d, 8.18 / d, 8.17 / d, 8.04 / d, 7.49 / m) 2H (8.93 / d, 8.12 / d, 7.88 / m, 7.82 / m, 1.72 / s, 1.30 / s)

LC / MS: m / z = 566 [(M + 1) ^&lt; ^{+ &}

Example  48: Compound 48 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 48-1

2-bromo-6-chlorophenol (2.5 g, 0.012 mol) was added to 3,4-dibromo-1,1-dimethyl-1H-isoindole (3.0 g, 0.010 mol) (M / z = 269) (yield: 41%). &Lt;

(2) Manufacturing example  2: Synthesis of Compound 48

(Dibenzo [b, d] thiophen-4-yl) phenylboronic acid (3.7 g, 0.012 mol) was added to Intermediate 48-1 (2.7 g, 0.010 mol) Synthesis was conducted in the same manner to obtain 3.6 g (yield 73%) of <Compound 48>.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.45 / d, 8.41 / d, 8.20 / d, 7.99 / d, 7.98 / d, 7.90 / d, 7.58 / m, 7.52 / m, 7.50 / m , 7.47 / m, 7.40 / m, 7.21 / d, 7.07 / d) 2H (1.61 / s)

LC / MS: m / z = 494 [(M + 1) ^&lt; ^{+ &}

Example  49: Compound 49 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 49

(3.5 g, 0.012 mol) was added to Intermediate 48-1 (2.7 g, 0.010 mol) and the compound 45 was synthesized in the same manner as in Example 1 (5) 64%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.99 / d, 7.94 / d, 7.90 / d, 7.87 / d, 7.77 / s, 7.69 / s, 7.47 / m, 7.45 / m M, 7.50 / d, 1.61 / s) 4H (7.25 / d)

LC / MS: m / z = 553 [(M + 1) ^&lt; ^{+ &}

Example  50: Compound 50 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate N

(2-bromo-6-chlorobenzoate (3.0 g, 0.012 mol) was added to 2,3-dibromo-1H-indole (2.7 g, 0.010 mol) To obtain 1.6 g (yield 41%) of Intermediate N. (m / z = 364)

(2) Manufacturing example  2: Synthesis of intermediate N-1

2.1 g (yield 658%) of Intermediate N-1 was obtained in the same manner as in Example 1 (2) except that Intermediate N (3.6 g, 0.010 mol) )

(3) Manufacturing example  3: Synthesis of intermediate N-2

Intermediate N-2 (2.1 g, yield 62%) was obtained by the same method as in Example 1 (3), except that Intermediate N-1 (3.6 g, 0.010 mol) = 346)

(4) Manufacturing example  4: Synthesis of intermediate 50-1

Intermediate 50-1> 3.2 g (Yield 77%) was obtained by synthesizing the same method as that of Preparation Example (1) of Example 2, with the introduction of bromobenzene (1.6 g, 0.010 mol) into Intermediate N-2 (3.5 g, 0.010 mol) %). (M / z = 422)

(5) Manufacturing example  5: Synthesis of intermediate 50-2

Intermediate 50-2 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 50-1 (4.2 g, 0.010 mol) Yield: 72%). (M / z = 419)

(6) Manufacturing example  6: Synthesis of Compound 50

5.0 g (yield: 5.0 g, 0.012 mol) was obtained from Intermediate 50-2 (4.2 g, 0.010 mol) by the same procedure as in Example 1- 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.53 / d, 7.45 / m, 7.39 / m, 7.34 / m, 7.00 / d) 2H (7.85 / d, 7.79 / d, 7.67 / d, 7.58 m, 7.50 / d, 7.25 / d, 1.72 / s) 3H (7.41 / m) 4H (8.28 / d)

LC / MS: m / z = 693 [(M + 1) ^&lt; ^{+ &}

Example  51: Compound 51 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate 51-1

2-bromo-6-chlorophenol (2.1 g, 0.010 mol) was added to 2,3,4-tribromo-1H-indole (3.5 g, 0.010 mol) in the same manner as in Example 2- 2.1 g (yield 65%) of Intermediate 51-1 (m / z = 320)

(2) Manufacturing example  2: Synthesis of intermediate 51-2

Intermediate 51-2 (3.0 g, yield 77%) was synthesized in the same manner as in Example 2 (1) except that bromobenzene (1.6 g, 0.010 mol) was added to Intermediate 51-1 (3.2 g, 0.010 mol) %). (M / z = 396)

(3) Manufacturing example  3: Synthesis of Intermediate 51-3

Intermediate 51-3 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 51-2 (4.0 g, 0.010 mol) Yield: 72%). (M / z = 393)

(4) Manufacturing example  4: Synthesis of Compound 51

The compound 43-1 (5.2 g, 0.012 mol) was added to Intermediate 51-3 (3.9 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1 (5) 74%). (M / z = < RTI ID = 0.0 > 000)

M, 7.38 / m, 7.29 / m, 6.88 / d (1 H-NMR (200 MHz, CDCl ₃ ) ), 2H (8.93 d, 8.12 d, 7.88 m, 7.82 m, 7.79 d, 7.71 d, 7.58 m, 7.51 m, 7.50 d)

LC / MS: m / z = 662 [(M + 1) ^&lt; ^{+ &}

Example  52: Synthesis of compound 52

(One) Manufacturing example  1: Synthesis of Intermediate 52-1

2-bromo-6-chlorobenzenethiol (2.2 g, 0.010 mol) was added to 2,3,4-tribromo-1H-indole (3.5 g, 0.010 mol) in the same manner as in Example 2- To obtain 1.8 g (yield 55%) of Intermediate 52-1 (m / z = 336)

(2) Manufacturing example  2: Synthesis of intermediate 52-2

Intermediate 52-2 (3.2 g, Yield 77%) was synthesized by the same method as in Example 2 (1), except that bromobenzene (1.6 g, 0.010 mol) was added to Intermediate 52-1 (3.4 g, 0.010 mol) %). (M / z = 412)

(3) Manufacturing example  3: Synthesis of intermediate 52-3

Intermediate 52-3 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 52-2 (4.1 g, 0.010 mol) Yield: 72%). (M / z = 409)

(4) Manufacturing example  4: Synthesis of Compound 52

(5.2 g, 0.012 mol) was added to Intermediate 52-3 (4.1 g, 0.010 mol) in the same manner as in Example 1-Preparation Example (5) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.45 / d, 7.45 / m, 7.41 / m, 7.31 / m, 7.22 / m, 7.10 / d) 2H (7.85 / d, 7.79 / d, 7.58 7.55 / d, 7.51 / m, 7.50 / d, 7.41 / m, 7.25 / d) 4H (8.28 / d, 7.51 /

LC / MS: m / z = 683 [(M + 1) ^&lt; ^{+ &}

Example  53: Compound 53 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 53

The compound 43-1 (5.2 g, 0.012 mol) was added to Intermediate 52-3 (4.1 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- (5) to give 4.9 g 73%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d, 7.45 / d, 7.45 / m, 7.41 / m, 7.31 / m, 7.22 / m, 7.10 / d ), 2H (8.93 / d, 8.12 / d, 7.88 / m, 7.82 / m, 7.79 / d, 7.58 / m, 7.55 / d, 7.51 / m, 7.50 /

LC / MS: m / z = 678 [(M + 1) ^&lt; ^{+ &}

Example  54: Compound 54 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 54-1

2.4 g (yield: 58%) of Intermediate 54-1 was synthesized in the same manner as in Example 2 (1) except that bromobenzene (3.2 g, 0.020 mol) was added to Intermediate G-2 (3.0 g, 0.010 mol) %). (M / z = 419)

(2) Manufacturing example  2: Synthesis of compound 54

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 43-1 (5.2 g, 0.012 mol) and Intermediate 54-1 (4.2 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d, 7.95 / d, 7.86 / d, 7.57 / m, 7.32 / m, 7.16 / d, 7.10 / d 7H (7.33 / m, 7.25 / d, 7.23 / d) 2H (8.93 d, 8.12 d, 7.88 m, 7.82 m, 7.26 m,

LC / MS: m / z = 688 [(M + 1) ^&lt; ^{+ &}

Example  55: Compound 55 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate O-1

(2-bromo-5-chlorobenzoate (3.0 g, 0.012 mol) was added to 3-bromo-1,1-dimethyl-1H- isoindolepyridine (2.2 g, 0.010 mol) (M / z = 313) (Intermediate O-1) (1.3 g, yield 41%).

(2) Manufacturing example  2: Synthesis of Intermediate O-2

Intermediate O-2 (1.8 g, yield: 56%) was obtained in the same manner as in Example 1 (2) except that Intermediate O-1 (3.1 g, 0.010 mol) = 313)

(3) Manufacturing example  3: Synthesis of Intermediate O-3

Intermediate O-3 (1.9 g, yield 66%) was obtained in the same manner as in Example 1- (3) except that Intermediate O-2 (3.1 g, 0.010 mol) = 295)

(4) Manufacturing example  4: Synthesis of intermediate 55-1

2.4 g (yield: 57%) of Intermediate 55-1 was synthesized in the same manner as in Example 2 (1) except that bromobenzene (3.3 g, 0.020 mol) was added to Intermediate O-3 (3.0 g, 0.010 mol) %). (M / z = 419)

(5) Manufacturing example  5: Synthesis of Compound 55

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 17-1 (5.2 g, 0.012 mol) was added to Intermediate 55-1 (4.2 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.03 / d, 7.92 / d, 7.69 / d, 7.32 / d, 7.16 / d) 2H (7.85 / d, 7.41 / m, 7.26 / m, 7.25 / d, 1.61 / s) 4H (8.28 / d, 7.51 / m, 7.33 / m, 7.11 / d)

LC / MS: m / z = 693 [(M + 1) ^&lt; ^{+ &}

Example  56: Compound 56 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 56-1

(2.4 g, 0.020 mol) was added to Intermediate D-2 (3.4 g, 0.010 mol) in the same manner as in Example 2-Preparation Example (1) %). (M / z = 463)

(2) Manufacturing example  2: Synthesis of compound 56

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 43-1 (5.2 g, 0.012 mol) and Intermediate 56-3 (4.6 g, 0.010 mol) 70%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d) 2H (8.93 / d, 8.12 / d, 7.88 / m, 7.82 / m, 7.64 / d, 7.56 / d, 1.69 / s) 4H (7.26 / m) 6H (7.33 / m, 7.11 / d)

LC / MS: m / z = 687 [(M + 1) ^&lt; ^{+ &}

Example  57: Compound 57 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate M

0.8 g (Yield: 31%) of Intermediate M was synthesized in the same manner as in Example 1-Preparation Example (2) after dropping MeLi into methyl 2-benzyl-6-chlorobenzoate (2.6 g, 0.010 mol) (M / z = 260).

(2) Manufacturing example  2: Synthesis of intermediate M-1

1.5 g (yield 60%) of <Intermediate M-1> was obtained by the same method as in Example 1-Preparation Example (3), except that Intermediate M (2.6 g, 0.010 mol) )

(3) Manufacturing example  3: Synthesis of intermediate M-2

Intermediate M-1 (2.4 g, 0.010 mol) in _{KMnO 4 (3.2 g, 0.0020 mol} ) MC into the 60 mL was reacted by stirring at 25 ℃ 48 sigan H ₂ 0 cooled after the completion of the reaction to: separation layer EA Post-column purification (n-hexane: EA) gave 1.8 g (71% yield) of intermediate M-2. (m / z = 256)

(4) Manufacturing example  4: Synthesis of intermediate M-3

(1.1 g, 0.010 mol), Potassium carbonate (2.8 g, 0.020 mol), Copper (0.1 g, 0.0020 mol) and iodine copper (1.1 g, 0.006 mol) were added to Intermediate M-2 (2.6 g, 0.010 mol) dissolved in 70 mL of n-butyl ether, and reacted under nitrogen for 48 hours with stirring. After completion of the reaction, the reaction mixture was cooled to room temperature, and subjected to column purification (n-hexane: EA) after separation of H ₂ O: MC layer to obtain 2.4 g (m / z = 349)

(5) Manufacturing example  5: Synthesis of intermediate 57-1

Intermediate 57-1 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate M-3 (3.5 g, 0.010 mol) Yield: 74%). (M / z = 344)

(6) Manufacturing example  6: Synthesis of Compound 57

Benzofuro [2,3-a] carbazole (2.6 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) in the same manner as in Example 1- Compound 57> 4.6 g (yield: 72%) was obtained.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.09 / d, 7.66 / d, 7.53 / d, 7.52 / m, 7.51 / m, 7.48 / d, 7.46 / d, 7.41 / m D, 7.89 / d, 7.67 / d, 7.51 / m, 1.72 / s (7.39 / m, 7.38 / m, 7.33 / m, 7.30 / m, 7.25 / m, 7.22 / )

LC / MS: m / z = 642 [(M + 1) ^&lt; ^{+ &}

Example  58: Compound 58 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 58-1

(1.6 g, 0.010 mol) was added to 11,12-dihydroindolo [2,3-a] carbazole (2.6 g, 0.010 mol) (M / z = 332) of 2.6 g (yield: 77%) was obtained.

(2) Manufacturing example  2: Synthesis of compound 58

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 58-1 (3.3 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 78%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.12 / d, 8.09 / d, 7.57 / d, 7.52 / d, 7.46 / m, 7.45 / m, 7.42 / d, 7.41 / m, 7.39 / m M, 7.00 / s) 2H (8.55 / d, 8.10 / d, 7.94 / d, 7.67 / d, 7.58 / m, 7.51 / m, 7.50 / d, 7.33 / m, 7.25 / )

LC / MS: m / z = 717 [(M + 1) ^&lt; ^{+ &}

Example  59: Compound 59 Synthesis

(One) Manufacturing example  1: Synthesis of compound 59

The compound 17-1 (5.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was synthesized by the same method as in Example 1- (5) to give 4.7 g 76%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.48 / d, 7.39 / m, 7.30 / m, 7.00 / d) 2H (8.10 / d, 7.85 / d, 7.67 / d, 7.51 / m, 7.25 / d, 1.72 / s) 3H (7.41 / m) 4H (8.28 / d, 7.51 /

LC / MS: m / z = 618 [(M + 1) ^&lt; ^{+ &}

Example  60: Compound 60 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 60-1

2-bromo-6-chlorophenol (2.1 g, 0.010 mol) was added to 2,3,4-tribromobenzofuran (3.5 g, 0.010 mol) in the same manner as in Example 2- 60-1> 1.8 g (yield: 55%). (M / z = 321)

(2) Manufacturing example  2: Synthesis of intermediate 60-2

Synthesis was conducted in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 60-1 (3.2 g, 0.010 mol) Yield: 76%). (M / z = 318)

(3) Manufacturing example  3: Synthesis of Compound 60

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 43-1 (5.2 g, 0.012 mol) was added to Intermediate 60-2 (3.2 g, 0.010 mol) 69%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d, 7.41 / m, 7.38 / d, 7.34 / m, 7.29 / m, 7.13 / d) 2H (8.93 d, 8.10 / d, 7.88 / m, 7.82 / m, 7.71 / d, 7.51 /

LC / MS: m / z = 587 [(M + 1) ^&lt; ^{+ &}

Example  61: Compound 61 Synthesis

(One) Manufacturing example  1: Synthesis of Intermediate K

MeLi was dropped on methyl 2-chloro-6- (pyridin-3-ylmethyl) benzoate (5.2 g, 0.020 mol) and then synthesized in the same manner as in Example 1- g (yield: 29%). (m / z = 261)

(2) Manufacturing example  2: Synthesis of Intermediate K-1

1.5 g (yield 60%) of Intermediate K-1 was obtained in the same manner as in Example 1 (3), except that Intermediate K (2.6 g, 0.010 mol) )

(3) Manufacturing example  3: Synthesis of Intermediate K-2

Intermediate K-1 (2.4 g, 0.010 mol) in _{KMnO 4 (3.2 g, 0.0020 mol} ) MC into the 60 mL was reacted by stirring at 25 ℃ 48 sigan H ₂ 0 cooled after the completion of the reaction to: separation layer EA Post-column purification (n-hexane: EA) gave 1.7 g (yield 68%) of intermediate K-2. (m / z = 256)

(4) Manufacturing example  4: Synthesis of intermediate K-3

(1.1 g, 0.010 mol), Potassium carbonate (2.8 g, 0.020 mol), Copper (0.1 g, 0.0020 mol) and iodine copper (1.1 g, 0.006 mol) were added to Intermediate K-2 dissolved in 70 mL of n-butyl ether, and reacted under nitrogen for 48 hours with stirring. After completion of the reaction, the reaction mixture was cooled to room temperature, and subjected to column separation (n-hexane: EA) after separation of H ₂ O: MC layer to obtain 2.2 g (m / z = 351)

(5) Manufacturing example  5: Synthesis of intermediate 61-1

2.4 g of Intermediate 61-1 was synthesized in the same manner as in Example 1 (5) except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate K-3 (3.5 g, 0.010 mol) Yield: 70%). (M / z = 345)

(6) Manufacturing example  6: Synthesis of Compound 61

The compound 43-1 (5.2 g, 0.012 mol) was added to Intermediate 61-1 (3.5 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1 (5) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.43 / d, 8.18 / d, 8.04 / d, 7.41 / m, 7.39 / m, 7.18 / d) 2H (8.93 / d, 8.12 d, 7.88 / m, 7.82 / m, 7.67 / d, 7.51 / m, 1.72 / s)

LC / MS: m / z = 614 [(M + 1) ^&lt; ^{+ &}

Example  62: Compound 62 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate K-4

(1.1 g, 0.010 mol), Potassium carbonate (2.8 g, 0.020 mol), Copper (0.1 g, 0.0020 mol) and iodine copper (1.1 g, 0.006 mol) were added to Intermediate K-2 dissolved in 70 mL of n-butyl ether, and reacted under nitrogen for 48 hours with stirring. After completion of the reaction, the reaction mixture was cooled to room temperature, and subjected to column purification (n-hexane: EA) after separation of H ₂ O: MC layer to obtain 2.1 g (m / z = 351)

(2) Manufacturing example  2: Synthesis of intermediate 62-1

Intermediate 62-1 was synthesized in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate K-4 (3.5 g, 0.010 mol) Yield: 72%). (M / z = 345)

(3) Manufacturing example  3: Synthesis of Compound 62

Intermediate 43-1 (5.2 g, 0.012 mol) was added to Intermediate K-4 (3.5 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- 75%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.39 / d, 8.18 / d, 8.04 / d, 7.89 / d, 7.73 / d, 7.54 / d, 7.41 / m) 2H (8.93 m), 7.41 / m, 1.72 / s), 4H (7.25 / d)

LC / MS: m / z = 614 [(M + 1) ^&lt; ^{+ &}

Example  63: Compound 63 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 63-1

2-bromo-4,6-diphenyl-1,3,5-triazine (2.6 g, 0.008 mol) was added to Intermediate 20-2 (2.1 g, 0.010 mol) (M / z = 524) (Intermediate 63-1) was obtained (yield: 77%).

(2) Manufacturing example  2: Synthesis of Compound 63

The compound 63-1 (6.3 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was used in the same manner as in Example 1 (5) 62%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.79 / d, 7.59 / d, 7.48 / d, 7.43 / m, 7.39 / m, 7.33 / m, 7.30 / m (7.21 / m, 7.00 / d) 2H (8.10 / d, 7.67 / d, 1.72 / s)

LC / MS: m / z = 707 [(M + 1) ^&lt; ^{+ &}

Example  64: Compound 64 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 64

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 20-5 (7.2 g, 0.010 mol) and Intermediate 57-1 (3.4 g, 0.010 mol) 76%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.59 / d, 7.48 / d, 7.43 / m, 7.39 / m, 7.33 / m, 7.30 / m, 7.25 / m M) 2H (8.28 / d, 8.10 / d, 7.67 / d, 1.72 / s) 3H (7.79 / d, 7.41 /

LC / MS: m / z = 782 [(M + 1) ^&lt; ^{+ &}

Example  65: Synthesis of compound 65

(One) Manufacturing example  1: Synthesis of Compound 65

Intermediate 22-2 (6.4 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.79 / d, 7.63 / d, 7.59 / d, 7.48 / d, 7.43 / m, 7.39 / m, 7.37 / m, 7.30 / m, 7.23 / d M, 7.50 / d, 7.00 / d) 2H (8.55 / d, 8.10 d, 7.94 d, 7.67 d, 7.58 m, 7.51 m, 7.50 d, 7.41 m, 7.33 m, 7.25 m, )

LC / MS: m / z = 717 [(M + 1) ^&lt; ^{+ &}

Example  66: Compound 66 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 66

Intermediate 49-2 (2.6 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound obtained in Synthesis Example (5) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.87 / d, 7.77 / s, 7.69 / d, 7.48 / d, 7.45 / m, 7.41 / m, 7.39 / m D, 7.50 / d, 7.50 / d, 1.72 / s) 4H (7.25 / d)

LC / MS: m / z = 628 [(M + 1) ^&lt; ^{+ &}

Example  67: Compound 67 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 67

(Dibenzo [b, d] thiophen-4-yl) phenylboronic acid (3.6 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) Synthesis was conducted in the same manner to obtain 3.3 g (yield 58%) of Compound 67.

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.58 / m, 7.52 / m, 7.50 / m, 7.48 / d, 7.41 / m M), 7.30 / m, 7.00 / d) 2H (8.10 / d, 7.67 / d, 7.51 /

LC / MS: m / z = 569 [(M + 1) ^&lt; ^{+ &}

Example  68: Compound 68 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 68

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 17-1 (5.2 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 61%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.48 / d, 7.39 / m, 7.30 / m, 7.00 / d) 2H (8.10 / d, 7.85 / d, 7.67 / d, 7.25 / d, 1.72 / s) 3H (7.41 / m) 4H (8.28 / d) 6H (7.51 / m)

LC / MS: m / z = 618 [(M + 1) ^&lt; ^{+ &}

Example  69: Compound 69 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 69

Intermediate 26-1 (3.6 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound obtained in Preparation Example (5) 65%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.56 / d, 8.55 / d, 7.94 / d, 7.71 / d, 7.63 / d, 7.59 / d, 7.50 / s, 7.48 / d, 7.31 / d M, 7,30 / m, 7.25 / m, 7.22 / d, 7.00 / d) 2H (8.28 / d, 8.10 / d, 7.41 / m, 7.33 /

LC / MS: m / z = 668 [(M + 1) ^&lt; ^{+ &}

Example  70: Compound 70 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 70

Synthesis was conducted in the same manner as in Example 1-Preparation Example (5), except that Intermediate 27-2 (6.4 g, 0.011 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 62%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.48 / d, 7.41 / m, 7.39 / m, 7.30 / m, 7.20 / s, 7.00 / d) 2H (8.55 / d, 8.12 / d, 8.10 7.51 / m, 7.50 / m, 7.33 / m, 7.29 / m, 7.25 / m, 1.72 / s)

LC / MS: m / z = 717 [(M + 1) ^&lt; ^{+ &}

Example  71: Compound 71 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 71

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 28-1 (4.3 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 76%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.94 / d, 7.79 / d, 7.71 / d, 7.59 / d 7.51 / m, 7.50 / m, 7.48 / d, 7.43 / m, 7.41 / m, 7.30 / m, 7.25 / m, 7.22 / d, 7.00 / , 7.33 / m, 1.72 / s) 4H (7.25 / d)

LC / MS: m / z = 734 [(M + 1) ^&lt; ^{+ &}

Example  72: Compound 72 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 72-1

3-ylboronic acid (2.8 g, 0.024 mol) was added to 1,3-dibromo-2,5-dichlorobenzene (3.0 g, 0.010 mol) 2.2 g (yield 72%) of Intermediate 72-1 (m / z = 301) was obtained.

(2) Manufacturing example  2: Synthesis of intermediate 72-2

(4.2 g, 0.012 mol) of 4,6-diphenyl-1,3,5-triazin-2-ylboronic acid was added to the intermediate 72-1 (3.0 g, 0.010 mol) (M / z = 498) (Intermediate 72-2) in an amount of 3.0 g (yield: 61%).

(3) Manufacturing example  3: Synthesis of intermediate 72-3

Intermediate 2-2> 3.5 g (0.012 mol) of bis (pinacolato) dibron was added to Intermediate 72-2 (5.0 g, 0.010 mol) g (yield: 60%). (m / z = 590)

(4) Manufacturing example  4: Synthesis of Compound 72

Synthesis was conducted in the same manner as in Example 1 (5) to give Intermediate 72-3 (7.1 g, 0.012 mol) and Intermediate 57-1 (3.4 g, 0.010 mol) 57%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.48 / d, 7.39 / m, 7.30 / m, 7.00 / d) 2H (9.24 / s, 8.70 / d, 8.42 / d, 8.10 / d, 7.72 / s, 7.67 / d, 7.57 / m, 1.72 / s) 3H (7.41 / m) 4H (8.28 / d)

LC / MS: m / z = 785 [(M + 1) ^&lt; ^{+ &}

Example  73: Compound 73 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 73-1

2-bromo-4,6-diphenyl-1,3,5-triazine (3.1 g, 0.010 mol) was added to 2-bromo-3,10-dihydroimidazo [4,5- (M / z = 517) was obtained in the same manner as in Example 2 (1), and 3.7 g (yield: 71%) of Intermediate 73-1 was obtained.

(2) Manufacturing example  2: Synthesis of Intermediate 73-2

Synthesis was conducted in the same manner as in Example 1 (5), except that phenyl boronic acid (1.4 g, 0.012 mol) was added to Intermediate 73-1 (5.2 g, 0.010 mol) Yield: 72%). (M / z = 514)

(3) Manufacturing example  3: Synthesis of Intermediate 73-3

Intermediate 73-3> 5.2 (4-fluorobenzyl) was synthesized in the same manner as in Example 2 (1) except that 1,4-dibromobenzene (2.4 g, 0.010 mol) g (yield: 77%). (m / z = 670)

(4) Manufacturing example  4: Synthesis of Intermediate 73-4

<Intermediate 73-4> 4.5 (4-aminophenoxy)] was synthesized in the same manner as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 73-3 g (yield: 63%). (m / z = 716)

(5) Manufacturing example  5: Synthesis of Compound 73

Intermediate 73-4 (8.6 g, 0.012 mol) was added to intermediate 57-1 (3.4 g, 0.010 mol) and 6.7 g (yield: 74%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.22 / d, 7.94 / d, 7.85 / d, 7.48 / d, 7.39 / m, 7.33 / m, 7.30 / m, 7.25 / m M) 2H (8.10 / d, 7.79 / d, 7.68 / d, 7.67 / d, 1.72 / s)

LC / MS: m / z = 900 [(M + 1) ^&lt; ^{+ &}

Example  74: Compound 74 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 74

(7.5 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) in the same manner as in Example 1- (5) 67%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.07 / d, 8.04 / d, 7.92 / d, 7.48 / d, 7.39 / m, 7.30 / m, 7.00 / d ) 2H (8.93 d, 8.12 d, 8.10 d, 7.88 m, 7.82 m, 7.79 d, 7.68 d, 7.67 d, 7.41 m, 1.72 s) (7.51 / m)

LC / MS: m / z = 805 [(M + 1) ^&lt; ^{+ &}

Example  75: Compound 75 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 75-1

(3-bromophenyl) -9H-carbazole (2.6 g, 0.008 mol) was added to 9H-carbazol-3-ylboronic acid (2.1 g, 0.010 mol) To obtain 3.5 g (yield 77%) of Intermediate 75-1 (m / z = 452).

(2) Manufacturing example  2: Synthesis of Compound 75

Intermediate 75-1 (4.5 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- (5) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (7.87 / d, 7.77 / s, 7.69 / d, 7.39 / m, 7.30 / m, 7.00 / d) 2H (8.55 / d, 8.12 / d, 8.10 7.50 / d, 7.50 / m, 7.33 / m, 7.29 / m, 7.25 / m, 1.72 / s)

LC / MS: m / z = 717 [(M + 1) ^&lt; ^{+ &}

Example  76: Compound 76 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 76

The compound 77-1 (5.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- (5) 77%).

LC / MS: m / z = 618 [(M + 1) ^&lt; ^{+ &}

Example  77: Compound 77 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 77-1

3.1 g (yield: 71%) of Intermediate 77-1 was synthesized in the same manner as in Example 2 (1) except that bromobenzene (1.6 g, 0.010 mol) was added to Intermediate 20-4 (3.7 g, 0.010 mol) %). (M / z = 445)

(2) Manufacturing example  2: Synthesis of Compound 77

Intermediate 77-1 (5.3 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound obtained in Synthesis Example (5) 71%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.79 / d, 7.59 / d, 7.48 / d, 7.45 / m, 7.43 / m, 7.41 / m, 7.39 / m (7.10 / d, 7.67 / d, 7.58 / m, 7.51 / m, 7.50 / d, 1.72 / s)

LC / MS: m / z = 628 [(M + 1) ^&lt; ^{+ &}

Example  78: Compound 78 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 78

Intermediate 43-1 (5.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) and the compound was synthesized in the same manner as in Example 1- (5) 66%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.18 / d, 8.04 / d, 7.48 / d, 7.41 / m, 7.39 / m, 7.30 / m, 7.00 / d) 2H (8.93 d, 8.10 / d, 7.88 / m, 7.82 / m, 7.67 / d, 7.51 / m, 1.72 / s)

LC / MS: m / z = 626 [(M + 1) ^&lt; ^{+ &}

Example  79: Compound 79 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 79-1

2-bromo-4,6-diphenyl-1,3,5-triazine (3.1 g, 0.010 mol) was added to 9H-carbazol-2-ylboronic acid (2.1 g, 0.010 mol) ) (3.4 g, Yield: 77%) (m / z = 442).

(2) Manufacturing example  2: Synthesis of intermediate 79-2

Intermediate 79-2> 3.2 (4-aminopyridine) was synthesized by the same method as in Example 1 (5), except that 1,4-dibromobenzene (1.9 g, 0.008 mol) g (yield: 72%). (m / z = 553)

(3) Manufacturing example  3: Synthesis of intermediate 79-3

Intermediate 79-3 was synthesized by the same method as in Example 1 (4) except that bis (pinacolato) dibron (3.0 g, 0.012 mol) was added to Intermediate 79-2 (5.5 g, 0.010 mol) g (yield: 72%). (m / z = 600)

(4) Manufacturing example  4: Synthesis of Compound 79

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 79-3 (7.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 70%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.18 / d, 7.94 / d, 7.79 / d, 7.62 / d, 7.48 / d, 7.39 / m, 7.33 / m, 7.30 / m (7.21 / m, 7.00 / d) 2H (8.10 / d, 7.67 / d, 1.72 / s)

LC / MS: m / z = 783 [(M + 1) ^&lt; ^{+ &}

Example  80: Compound 80 Synthesis

(One) Manufacturing example  1: Synthesis of Compound 80

Synthesis was conducted in the same manner as in Example 1 (5), except that Intermediate 20-5 (7.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 72%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 7.94 / d, 7.79 / d, 7.59 / d, 7.48 / d, 7.43 / m, 7.39 / m, 7.33 / m, 7.30 / m (7.21 / m, 7.00 / d) 2H (8.10 / d, 7.67 / d, 1.72 / s)

LC / MS: m / z = 796 [(M + 1) ^&lt; ^{+ &}

Example  81: Synthesis of compound 81

(One) Manufacturing example  1: Synthesis of Compound 81

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 28-1 (4.3 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 77%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.45 / d, 8.41 / d, 8.20 / d, 7.98 / d, 7.94 / d, 7.79 / d, 7.71 / d, 7.59 / d 7.51 / m, 7.50 / m, 7.48 / d, 7.43 / m, 7.41 / m, 7.30 / m, 7.25 / m, 7.22 / , 1.72 / s) 4H (7.25 / d)

LC / MS: m / z = 734 [(M + 1) ^&lt; ^{+ &}

Example  82: Compound 82 Synthesis

(One) Manufacturing example  1: Synthesis of Compound (82)

Synthesis was conducted in the same manner as in Example 2 (1) except that Intermediate 41-2 (4.1 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 80%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.55 / d, 8.12 / d, 8.10 / d, 7.94 / d, 7.90 / d, 7.79 / d, 7.71 / d, 7.63 / d, 7.59 / d 7.50 / m, 7.43 / m, 7.41 / m, 7.39 / m, 7.29 / m, 7.22 / d) 2H (8.10 / d, 7.58 / m, 7.51 / , 1.72 / s)

LC / MS: m / z = 717 [(M + 1) ^&lt; ^{+ &}

Example  83: Synthesis of compound 83

(One) Manufacturing example  1: Synthesis of Compound 83

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 26-1 (3.6 g, 0.010 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 73%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (8.56 / d, 8.55 / d, 7.94 / d, 7.71 / d, 7.63 / d, 7.59 / d, 7.50 / s, 7.48 / d, 7.31 / d M, 7,30 / m, 7.25 / m, 7.22 / d, 7.00 / d) 2H (8.28 / d, 8.10 / d, 7.41 / m, 7.33 /

LC / MS: m / z = 668 [(M + 1) ^&lt; ^{+ &}

Example  84: Compound 84 Synthesis

(One) Manufacturing example  1: Synthesis of intermediate 84-1

2-bromotriphenylene (3.1 g, 0.010 mol) was added to 9-carbazol-3-ylboronic acid (2.1 g, 0.010 mol) > 3.1 g (yield: 72%). (M / z = 437)

(2) Manufacturing example  2: Synthesis of Compound 84

Synthesis was conducted in the same manner as in Example 2 (1), except that Intermediate 84-1 (5.2 g, 0.012 mol) was added to Intermediate 57-1 (3.4 g, 0.010 mol) 63%).

_{H-NMR (200MHz, CDCl 3} ): δ ppm, 1H (9.15 / s, 8.55 / d, 8.18 / d, 8.04 / d, 7.94 / d, 7.87 / d, 7.77 / s, 7.69 / d, 7.48 / d D, 8.10 / d, 7.88 / m, 7.82 / m, 7.67 / d, 7.31 / , 7.51 / m, 1.72 / s)

LC / MS: m / z = 702 [(M + 1) ^&lt; ^{+ &}

device Example  1: Compound 1 With hole transport material  So Organic electroluminescent device  Produce

<Compound 1> was deposited on ITO-coated glass substrate to form a hole transporting layer of 120 nm, followed by deposition of Ir (ppy) ₃ as a dopant at a deposition rate of 0.009 nm / sec and using CBP as a host The deposition rate was 0.1 nm / sec, and Ir (ppy) ₃ was doped to a deposition rate ratio of 9% to form a light emitting layer with a thickness of 30 nm on the hole transport layer.

Balq was deposited thereon to a thickness of 10 nm to form a hole blocking layer for preventing holes from moving to the electron transporting layer through the light emitting layer, and Alq ₃ was deposited thereon to form an electron transporting layer of 40 nm. Lithium fluoride To form a 1 nm electron injection layer. Aluminum was deposited on the electron injection layer to form a 120 nm negative electrode, thereby fabricating an organic electroluminescent device.

At this time, the deposition rate of each material was set to 0.1 nm / sec for CBP, compound 1, Alq ₃ , Balq, 0.01 nm / sec for lithium fluoride, and 0.5 nm / sec for aluminum, which are organic materials.

device Example  2 to 15

An organic electroluminescent device of each of the device embodiments 2 to 15 was fabricated in the same manner as in the device example 1, except that the compound described in [Table 1] was used in place of the compound 1 described above.

device Comparative Example  One

The organic light emitting diode device for Comparative Example 1 was fabricated in the same manner except that NPB, which is generally used as a hole transport material, was used instead of the compound 1 produced by the invention in the device structure of the above embodiment.

device Example  16: Compound 16 The light-  As a host material Organic electroluminescence Manufacturing

NPB was deposited on a glass substrate coated with ITO to form a hole transport layer having a thickness of 120 nm, followed by deposition of Ir (ppy) ₃ as a dopant at a deposition rate of 0.009 nm / sec. The deposition rate was 0.1 nm / sec, and Ir (ppy) ₃ was doped to a deposition rate ratio of 9% to form a light emitting layer with a thickness of 30 nm on the hole transport layer.

Balq was deposited thereon to a thickness of 10 nm to form a hole blocking layer for preventing holes from moving to the electron transporting layer through the light emitting layer, and Alq ₃ was deposited thereon to form an electron transporting layer of 40 nm. Lithium fluoride To form a 1 nm electron injection layer. Aluminum was deposited on the electron injection layer to form a 120 nm negative electrode, thereby fabricating an organic electroluminescent device.

At this time, the deposition rate of each material was set to 0.1 nm / sec for compound 16, NPB, Alq ₃ , Balq, 0.01 nm / sec for lithium fluoride, and 0.5 nm / sec for aluminum.

device Example  17 to 84

An organic electroluminescent device of each of the device embodiments 17 to 84 was fabricated in the same manner as in the device example 16, except that the compound described in [Table 2] was used instead of the compound 16.

device Comparative Example  2

The organic light emitting diode device for Comparative Example 2 was fabricated in the same manner except that CBP, which is generally used as a phosphorescent host material, was used instead of the compound 16 produced by the invention in the device structure of the embodiment.

The structures of Ir (ppy) ₃ , CBP and NPB used in the above are as follows.

Hereinafter, the characteristics of the organic electroluminescent device manufactured according to the device embodiments 1 to 84 and the device comparison examples 1 and 2 are compared, and the results are shown in Table 1 and Table 2, respectively.

[Table 1]

[Table 2]

Measurement of driving voltage and luminous efficiency

After fixing the organic light emitting device (substrate size: 25 × 25 mm 2 / deposition area: 2 × 2 mm 2) made in the above to the IVL measurement set (CS-2000 + jig + IVL program), the current was increased by 1 mA / (Cd / m 2), a driving voltage (V), a current density (A / m 2) and a luminous efficiency (cd / A) 1] and [Table 2].

As shown in the above Tables 1 and 2, when the compound for an organic electroluminescence device according to the present invention is used as a host material and a hole transporting material of the light emitting layer of an organic electroluminescence device, the conventional CBP (host material) The driving voltage is lowered and the luminous efficiency is increased as compared with the case of using NPB (hole transporting material).

Claims (10)

An organic light-emitting compound represented by the following Chemical Formula 1 or Chemical Formula 2:
[Chemical Formula 1] &lt; EMI ID =

In the above Chemical Formula 1 or Chemical Formula 2,
X ₁ to X ₁₁ are the same or different from each other, each independently from N, O, S, Te, CR 1, NR 2, CR 3 R 4, SiR 5 R 6, GeR 7 R 8, PR 9 and BR ₁₀ R ₃ and R ₄ , R ₅ and R ₆ , R ₇ and R ₈ may be linked to each other to form a ring,
Wherein R ₁ to R ₁₀ are the same or different from each other and each independently represents hydrogen, deuterium, a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 30 carbon atoms, A substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted heterocycloalkyl group having 2 to 30 carbon atoms, a substituted or unsubstituted cycloalkenyl group having 5 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, Or an unsubstituted or substituted C 1 -C 30 alkoxy group, a substituted or unsubstituted C 6 -C 30 aryloxy group, a substituted or unsubstituted C 1 -C 30 alkylthio group, a substituted or unsubstituted C 5 -C 30 A substituted or unsubstituted alkylamine group having 1 to 30 carbon atoms, a substituted or unsubstituted arylamine group having 5 to 30 carbon atoms, a substituted or unsubstituted aliphatic hydrocarbon group having 5 to 50 carbon atoms A substituted or unsubstituted aryl group having 5 to 50 carbon atoms, a substituted or unsubstituted aryl group having 3 to 50 carbon atoms, a substituted or unsubstituted heteroaryl group having 3 to 50 carbon atoms, a substituted or unsubstituted aryl group having 5 to 50 carbon atoms, A substituted or unsubstituted C 2 -C 50 heteroaryl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted germanium group, a substituted or unsubstituted boron group , A carbonyl group, a phosphoryl group, an amino group, a thiol group, a cyano group, a hydroxy group, a nitro group, a halogen group and an amide group,
The R ₁ to R ₁₀ and substituents thereof may be bonded to each other or may be connected with adjacent substituents to form a monocyclic or polycyclic ring of an alicyclic or aromatic group and the carbon atom of the formed alicyclic or aromatic monocyclic or polycyclic ring may be a N, S and O. The term &quot; heteroaryl &quot; The method according to claim 1,
Wherein each of R ₁ to R ₁₀ independently represents an organic luminescent compound represented by the following formula 1 or 2:
[Structural formula 1] [Structural formula 2]

In the structural formula 1 or the structural formula 2,
L is a single bond, a substituted or unsubstituted alkylene group having 1 to 30 carbon atoms, a substituted or unsubstituted aliphatic hydrocarbon group having 2 to 30 carbon atoms A substituted or unsubstituted C2-C30 alkynylene group, a substituted or unsubstituted C3-C30 A substituted or unsubstituted C2 to C30 heteroarylene group, a substituted or unsubstituted C3 to C30 cycloalkyl, a substituted or unsubstituted C1 to C50 arylene group, a substituted or unsubstituted C2 to C30 heteroarylene group, A substituted or unsubstituted C2 to C50 heteroarylene group in which at least one unsubstituted or substituted unsubstituted arylene group having 5 to 50 carbon atoms and a substituted or unsubstituted C3 to C30 cycloalkyl is fused,
n is an integer of 0 to 4, and when n is 2 or more, plural Ls are the same or different from each other,
A ₁ to A ₃ are the same or different and each independently represents a substituted or unsubstituted alkyl group having 1 to 30 carbon atoms, a substituted or unsubstituted cycloalkyl group having 3 to 30 carbon atoms, a substituted or unsubstituted group having 5 to 50 carbon atoms A substituted or unsubstituted aryl group, a substituted or unsubstituted C2 to C50 heteroaryl group, a substituted or unsubstituted C3 to C30 cycloalkyl substituted or unsubstituted aryl group having 5 to 50 carbon atoms, A substituted or unsubstituted C2 to C50 heteroaryl group in which one or more ring-opened cycloalkyls having 3 to 30 carbon atoms is fused,
Wherein L, A ₁ to A _3, and these substituents may be coupled or the adjacent connection with substituents each cycloaliphatic, may form a monocyclic or polycyclic ring of the aromatic group, the monocyclic or polycyclic ring of an alicyclic, aromatic so formed The carbon atom may be substituted with any one or more heteroatoms selected from N, S and O. 3. The method of claim 2,
Wherein L and A ₁ to A ₃ are each independently selected from the following structural formula 3:
[Structural Formula 3]

In the above formula 3,
Z is _{CR 1, NR 2, CR 3} R 4, SiR 5 R 6, GeR 7 R 8, PR 9, BR 10, Te, O , and is selected from S, wherein R ₁ to R ₁₀ are the Formula 1 Or the formula (2). The method according to claim 1,
[Formula 1] or [Formula 2] is selected from the following [Compound 1] to [Compound 752]:

1. An organic electroluminescent device comprising a first electrode, a second electrode, and at least one organic material layer disposed between the first electrode and the second electrode,
Wherein at least one of the organic material layers comprises an organic light emitting compound represented by Formula 1 or Formula 2 according to Claim 1. 6. The method of claim 5,
Wherein the organic material layer includes at least one of a hole injecting layer, a hole transporting layer, a hole injecting and transporting layer, an electron transporting layer, an electron injecting layer, a layer simultaneously performing electron transport and electron injection, and a light emitting layer, Wherein at least one layer comprises an organic light-emitting compound represented by the above Chemical Formula (1) or (2). The method according to claim 6,
Wherein the light emitting layer comprises an organic light emitting compound represented by the formula (1) or (2). 8. The method of claim 7,
The organic electroluminescent compound represented by Formula 1 or Formula 2 is used as a host compound in the light emitting layer, and the light emitting layer further includes at least one dopant compound. The method according to claim 6,
Wherein the hole transporting layer or the layer simultaneously injecting holes and transporting holes comprises an organic light emitting compound represented by the formula (1) or (2). 6. The method of claim 5,
Wherein at least one of the organic light emitting layers emitting red, green or blue light is further included in the organic material layer to emit white light.

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