Cyclic azine derivatives, processes for producing these, and organic electroluminescent element containing these as component

Patent metadata

Field	Value
Publication number	US-9624193-B2
Application number	US-201514809999-A
Country	US
Kind code	B2
Filing date	Jul 27, 2015
Priority date	Aug 21, 2009
Publication date	Apr 18, 2017
Grant date	Apr 18, 2017

Abstract

A cyclic azine compound represented by general formula (1):

wherein each Ar 1 represents an aromatic group, which is unsubstituted or substituted by a C 1-4 alkyl group, a phenyl group or a pyridyl group; and A represents a group selected from those which are represented by general formulae (2) to (5), described in the description. The cyclic azine compound is useful for an organic compound layer of fluorescent or phosphorescent EL device.

First claim

What is claimed is:

1. A cyclic azine compound represented by the formula (1):

wherein, in the formula (1), each Ar 1 represents phenyl group, p-tolyl group, m-tolyl group, o-tolyl group, 2,6-dimethylphenyl group, 4-tert-butylphenyl group, 4-biphenylyl group, 3-biphenylyl group, 2-biphenylyl group, 3-(3-pyridyl)phenyl group, 4-(3-pyridyl)phenyl group, 3-(4-pyridyl)phenyl group, or 4-(4-pyridyl)phenyl group; and
A represents a group selected from the group consisting of those which are represented by the following formulae (2) to (4):

wherein, in the formula (2), each Ar 2 represents a substituted phenyl group or a condensed aromatic hydrocarbon group not having a 16 group element, provided that a 1,3,5-trimethylphenyl group is excluded from Ar 2 ;

wherein, in the formula (3), Ar 3 represents a phenyl group, a pyridyl group or a pyrimidyl group; Ar 4 represents an anthryl group which is unsubstituted or substituted by an alkyl group having 1 to 4 carbon atoms or a phenyl group, a phenanthryl group which is unsubstituted or substituted by an alkyl group having 1 to 4 carbon atoms or a phenyl group, a fluorenyl group which is unsubstituted or substituted by an alkyl group having 1 to 4 carbon atoms or a phenyl group, a benzofluorenyl group which is unsubstituted or substituted by an alkyl group having 1 to 4 carbon atoms or a phenyl group, an unsubstituted pyrenyl group, an unsubstituted triphenylenyl group; X represents a phenylene group or a pyridylene group; p represents an integer of 0 to 2 provided that, when p is 2, the two Xs may be the same or different; and Z 1 represents a carbon atom;

wherein, in the formula (4), each Ar 5 represents a pyridyl group, and each Ar 6 represent a phenyl group or a pyridyl group; Z 2 represents a carbon atom and each Z 3 represents a carbon atom or a nitrogen atom.

2. The cyclic azine compound according to claim 1 , wherein each Ar 2 in the formula (2) represents a phenyl group substituted by an alkyl group having 1 to 4 carbon atoms, a phenyl group substituted by a halogen atom, a phenyl group substituted by an unsubstituted or substituted phenyl group, a phenyl group substituted by an unsubstituted or substituted pyrimidinyl group, a phenyl group substituted by an unsubstituted or substituted thiazolyl group, a phenyl group substituted by a pyridyl group, or a phenyl group substituted by a phenanthrolinyl group.

3. The cyclic azine compound according to claim 1 , wherein each Ar 2 in the formula (2) represents a quinolyl group.

4. The cyclic azine compound according to claim 1 , wherein Ar 4 in the formula (3) represents an anthryl group which is unsubstituted or substituted by a phenyl group, a phenanthryl group which is unsubstituted or substituted by a phenyl group, a fluorenyl group which is unsubstituted or substituted by a phenyl group, a benzofluorenyl group which is unsubstituted or substituted by a phenyl group, an unsubstituted pyrenyl group, or an unsubstituted triphenylenyl group.

5. The cyclic azine compound according to claim 1 , wherein Ar 4 in the formula (3) represents an unsubstituted anthryl group, a unsubstituted phenanthryl group, a unsubstituted fluorenyl group, a unsubstituted benzofluorenyl group, an unsubstituted pyrenyl group, or an unsubstituted triphenylenyl group.

6. The cyclic azine compound according to claim 1 , wherein Ar 3 in the formula (3) represents a phenyl group or a pyridyl group.

7. A process for preparing a cyclic azine compound represented by the formula (1a):

wherein, in the formula (1a), each Ar 1 represents phenyl group, p-tolyl group, m-tolyl group, o-tolyl group, 2,6-dimethylphenyl group, 4-tert-butylphenyl group, 4-biphenylyl group, 3-biphenylyl group, 2-biphenylyl group, 3-(3-pyridyl)phenyl group, 4-(3-pyridyl)phenyl group, 3-(4-pyridyl)phenyl group, or 4-(4-pyridyl)phenyl group, and each Ar 2 represents a substituted phenyl group or a condensed aromatic hydrocarbon group not having a 16 group element, provided that a 1,3,5-trimethylphenyl group is excluded from Ar 2 ;
characterized by coupling a compound represented by the formula (6) with a compound represented by the formula (7) in the presence of a palladium catalyst and in the presence or absence of a base;

wherein, in the formula (6), each Ar 1 is the same as defined above; and each Y 1 represents a chlorine, bromine or iodine atom;
Ar 2 -M  (7)

wherein, in the formula (7), Ar 2 is the same as defined above; and M represents a metal group or a hetero atom group.

8. A process for preparing a cyclic azine compound represented by the formula (1a):

wherein, in the formula (1a), each Ar 1 represents phenyl group, p-tolyl group, m-tolyl group, o-tolyl group, 2,6-dimethylphenyl group, 4-tert-butylphenyl group, 4-biphenylyl group, 3-biphenylyl group, 2-biphenylyl group, 3-(3-pyridyl)phenyl group, 4-(3-pyridyl)phenyl group, 3-(4-pyridyl)phenyl group, or 4-(4-pyridyl)phenyl group, and each Ar 2 represents a substituted phenyl group or a condensed aromatic hydrocarbon group not having a 16 group element, provided that a 1,3,5-trimethylphenyl group is excluded from Ar 2 ;
characterized by coupling a compound represented by the formula (8) with a compound represented by the formula (9) in the presence of a palladium catalyst and a base;

wherein, in the formula (8), each Ar 1 is the same as defined above; each R 1 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or a phenyl group; and groups R 1 in the two —B(OR 1 ) groups may be the same or different, and two groups R 1 in each of the two —B(OR 1 ) groups may form a ring together with the oxygen atoms and the boron atom;
Ar 2 —Y 1   (9)

wherein, in the formula (9), Ar 2 is the same as defined above; and Y 1 represents a chlorine, bromine or iodine atom.

9. The process for preparing a cyclic azine compound according to claim 7 , wherein the palladium catalyst has a tertiary phosphine as a ligand.

10. The process for preparing a cyclic azine compound according to claim 7 , wherein the metal group or the hetero atom group, represented by M in the formulae (7) and (11), is a group represented by the following formula:
—B(OR 1 ) 2 or —ZnR 2

wherein R 1 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or a phenyl group; two groups R 1 in the group —B(OR 1 ) 2 may be the same or different and the two groups R 1 in the group —B(OR 1 ) 2 may form a ring together with the oxygen atoms and the boron atom; and R 2 represents a halogen atom.

11. An organic electroluminescent device comprising as a constituent a cyclic azine compound represented by the formula (1):

wherein, in the formula (1), each Ar 1 is the same

Assignees

• Tosoh Corp
• Sagami Chemical Res Inst

Inventors

• Aihara Hidenori
• Ogata Akitoshi
• Hisamatsu Yousuke
• Tanaka Tsuyoshi
• Arai Nobumichi
• Abe Mayumi
• Miyashita Yuichi
• Iida Takashi
• Uchida Naoki

Classifications

• C07D251/24

  to three ring carbon atoms · CPC title

• C07D471/04

  Ortho-condensed systems · CPC title

• C09K2211/1037

  with sulfur · CPC title

• C09K11/06

  containing organic luminescent materials · CPC title

• C07D417/14

  containing three or more hetero rings · CPC title