Heterocyclic modulators of lipid synthesis
US-2024400552-A1 · Dec 5, 2024 · US
US2022352472A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2022352472-A1 |
| Application number | US-201917269190-A |
| Country | US |
| Kind code | A1 |
| Filing date | Aug 30, 2019 |
| Priority date | Aug 31, 2018 |
| Publication date | Nov 3, 2022 |
| Grant date | — |
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A cyclic compound represented by Chemical Formula 1, and an organic light emitting device comprising the same, and the compound used as a material of an organic material layer in the organic light emitting device and providing improved efficiency, low driving voltage and improved lifetime characteristics of the organic light emitting device.
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1 . A compound represented by Chemical Formula 1: in Chemical Formula 1, Q 1 and Q 2 are each independently a C 6-30 aromatic ring; n is an integer of 1 to 3, a and b are each independently an integer of 0 to 3, X is a single bond; CR 3 R 4 ; SiR 5 R 6 ; NR 7 ; O; S; SO 2 ; or a substituent represented by Chemical Formula 2, R 1 to R 7 are each independently hydrogen; deuterium; a substituted or unsubstituted C 1-60 alkyl; a substituted or unsubstituted C 1-60 alkoxy; a substituted or unsubstituted C 6-60 aryl; or a substituted or unsubstituted C 5-60 heteroaryl containing at least one heteroatom selected from the group consisting of N, O and S, or adjacent groups of R 1 to R 7 are bonded to each other to form a ring, L is a single bond; a substituted or unsubstituted C 6-60 arylene; or a substituted or unsubstituted C 2-60 heteroarylene containing at least one heteroatom selected from the group consisting of N, O and S, and Ar is a substituted or unsubstituted C 6-60 aryl; or a substituted or unsubstituted C 2-60 heteroaryl containing at least one heteroatom selected from the group consisting of N, O and S; or a di(C 6-60 aryl)phosphine oxide group. 2 . The compound of claim 1 , wherein Q 1 and Q 2 are each independently a benzene or naphthalene ring. 3 . The compound of claim 1 , wherein X is a single bond; C(CH 3 ) 2 ; C(phenyl) 2 ; N(phenyl); O; S; SO 2 ; or a substituent represented by Chemical Formula 2: 4 . The compound of claim 1 , wherein n is 1. 5 . The compound of claim 1 , wherein both a and b are 0. 6 . The compound of claim 1 , wherein L is a single bond; phenylene; biphenyldiyl; naphthalenediyl; furandiyl; thiophenediyl; or pyridindiyl. 7 . The compound of claim 1 , wherein Ar is a phenyl substituted with cyano; —P(O)(phenyl) 2 ; or any one selected from the group consisting of the following: wherein, L 1 and L 2 are each independently a single bond; a substituted or unsubstituted C 6-60 arylene; or a substituted or unsubstituted C 2-60 heteroarylene containing at least one heteroatom selected from the group consisting of N, O, and S, X is each independently N or C(R 8 ), provided that at least one of X is N, Ar 1 and Ar 2 are each independently hydrogen; a substituted or unsubstituted C 6-60 aryl; or a substituted or unsubstituted C 2-60 heteroaryl containing at least one heteroatom selected from the group consisting of N, O, and S, and R 8 is hydrogen; deuterium; a substituted or unsubstituted C 1-60 alkyl; a substituted or unsubstituted C 1-60 alkoxy; a substituted or unsubstituted C 6-60 aryl; a substituted or unsubstituted C 5-60 heteroaryl containing at least one heteroatom selected from the group consisting of N, O and S. 8 . The compound of claim 7 , wherein L 1 and L 2 are each independently a single bond; phenylene; biphenyldiyl; or naphthalenediyl. 9 . The compound of claim 7 , wherein Ar 1 and Ar 2 are each independently hydrogen; phenyl; phenyl substituted with cyano; biphenylene; terphenylene; naphthyl; phenanthrenyl; 9,10-dimethylphenanthrenyl; triphenylenyl; pyridinyl; dimethylfluorenyl; dibenzofuranyl; dibenzothiophenyl; carbazolyl; benzocarbazolyl; phenalenyl; quinolinyl; fluoranthenyl; phenoxazinyl; phenothiazinyl; 10-phenylphenazinyl; or 9,9-dimethylacridinyl. 10 . The compound of claim 1 , wherein Ar is any one selected from the group consisting of the following: wherein, X′ is N or CH, provided that at least one of X′ is N. 11 . The compound of claim 1 , wherein the compound represented by Chemical Formula 1 is any one selected from the group consisting of the following:
containing organic luminescent materials · CPC title
containing three or more hetero rings · CPC title
linked by a carbon chain containing aromatic rings · CPC title
with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached to ring carbon atoms of the hetero ring · CPC title
Ortho-condensed systems · CPC title
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