Heterocyclic modulators of lipid synthesis
US-2024400552-A1 · Dec 5, 2024 · US
US2016118601A1 · US · A1
| Field | Value |
|---|---|
| Publication number | US-2016118601-A1 |
| Application number | US-201514804898-A |
| Country | US |
| Kind code | A1 |
| Filing date | Jul 21, 2015 |
| Priority date | Oct 23, 2014 |
| Publication date | Apr 28, 2016 |
| Grant date | — |
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A condensed cyclic compound represented by Formulae 1A or 1B: wherein in Formulae 1A and 1B, groups and variables are the same as described in the specification.
Opening claim text (preview).
What is claimed is: 1 . A condensed cyclic compound represented by Formulae 1A or 1B: wherein in Formulae 1A and 1B, X 1 is N or C(R 1 ), X 2 is N or C(R 2 ), X 3 is N or C(R 3 ), X 4 is N or C(R 4 ), X 5 is N or C(R 5 ), X 6 is N or C(R 6 ), X 7 is N or C(R 7 ), X 8 is N or C(R 8 ), X 11 is N or C(R 11 ), X 12 is N or C(R 12 ), X 13 is N or C(R 13 ), X 14 is N or C(R 14 ), X 15 is N, C or C(R 15 ), X 16 is N, C or C(R 16 ), X 17 is N, C, or C(R 17 ), and X 18 is N, C, or C(R 18 ), and when X 15 is C, X 15 is connected with *-(L 2 ) a2 -*′, when X 16 is C, X 16 is connected with *-(L 2 ) a2 -*′, when X 17 is C, X 17 is connected with *-(L 2 ) a2 -*′, and when X 18 is C, X 18 is connected with *-(L 2 ) a2 -*′, X 21 is selected from O, S, Se, C(R 21 )(R 22 ), Si(R 21 )(R 22 ), and N(R 23 ), X 22 is selected from O, S, Se, C(R 24 )(R 25 ), Si(R 24 )(R 25 ), and N(R 26 ), X 23 is selected from O, S, Se, C(R 27 )(R 28 ), Si(R 27 )(R 28 ), and N(R 29 ), L 1 and L 2 are each independently selected from a phenylene group, a pyridinylene group, a fluorenylene group, a dibenzofuranylene group, and a dibenzothiophenylene group; a phenylene group, a pyridinylene group, a fluorenylene group, a dibenzofuranylene group, and a dibenzothiophenylene group, each substituted with at least one of a deuterium, —F, —Cl, —Br, —I, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 20 alkyl group, a C 1 -C 20 alkoxy group, a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and —Si(Q 1 )(Q 2 )(Q 3 ); and —Si(R 41 )(R 42 )—, —O—, —S—, and —Se—, wherein a1 and a2 are each independently an integer selected from 0 to 5, and when a1 is 2 or more, 2 or more groups L 1 are identical to or different from each other, and when a2 is 2 or more, 2 or more groups L 2 are identical to or different from each other, R 1 to R 8 , R 11 to R 18 , and R 31 to R 34 are each independently selected from a hydrogen, a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 20 alkyl group, and a C 1 -C 20 alkoxy group; a C 1 -C 20 alkyl group and a C 1 -C 20 alkoxy group, each substituted with at least one of a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, and a phosphoric acid group or a salt thereof; a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group; a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, each substituted with at least one of a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 20 alkyl group, a C 1 -C 20 alkoxy group, a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, a dibenzothiophenyl group, and —Si(Q 11 )(Q 12 )(Q 13 ); and —Si(Q 21 )(Q 22 )(Q 23 ), and b1 and b3 are each independently 1, 2, or 3, and b2 and b4 are each independently 1, 2, 3, or 4, and when b1 is 2 or more, 2 or more groups R 31 are identical to or different from each other, when b2 is 2 or more, 2 or more groups R 32 are identical to or different from each other, when b3 is 2 or more, 2 or more groups R 33 are identical to or different from each other, and when b4 is 2 or more, 2 or more groups R 34 are identical to or different from each other, in Formula 1A, i) at least one of X 3 and X 7 is C(CN), ii) at least one of groups R 31 (s) in the number of b1 and groups R 32 in the number of b2 is a cyano group, or iii) at least one of X 3 and X 7 is C(CN) and at least one of groups R 31 in the number of b1 and groups R 32 in the number of b2 is a cyano group, in Formula 1B, i) at least one of X 13 and X 17 is C(CN), ii) at least one of groups R 33 in the number of b3 and groups R 34 in the number of b4 is a cyano group, or iii)) at least one X 13 and X 17 is C(CN) and at least one of groups R 33 in the number of b3 and groups R 34 in the number of b4 is a cyano group, In Formula 1B, when X 22 is N(R 26 ) and X 23 is N(R 29 ), a2 is not 0, R 21 to R 29 , R 41 , R 42 , Q 1 to Q 3 , Q 11 to Q 13 , and Q 21 to Q 23 are each independently selected from a C 1 -C 20 alkyl group and a C 1 -C 20 alkoxy group; a C 1 -C 20 alkyl group and a C 1 -C 20 alkoxy group, each substituted with at least one of a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, and a phosphoric acid group or a salt thereof; a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group; and a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, each substituted with at least one of a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a salt thereof, a C 1 -C 20 alkyl group, a C 1 -C 20 alkoxy group, a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group. 2 . The condensed cyclic compound of claim 1 , wherein in Formulae 1A, X 1 is C(R 1 ), X 2 is C(R 2 ), X 3 is C(R 3 ), X 4 is C(R 4 ), X 5 is C(R 5 ), X 6 is C(R 6 ), X 7 is C(R 7 ), X 8 is C(R 8 ), X 11 is C(R 11 ), X 12 is C(R 12 ), X 13 is C(R 13 ), and X 14 is C(R 14 ). 3 . The condensed cyclic compound of claim 1 , wherein R 1 , R 2 , R 4 , R 5 , R 6 , and R 8 in Formula 1A are not a cyano group, and R 11 , R 12 , and R 14 in Formula 1B are not a cyano group. 4 . The condensed cyclic compound of claim 1 , wherein in Formula 1B, X 21 is selected from O, S, C(R 21 )(R 22 ), and N(R 23 ), X 22 is selected from O, S, C(R 24 )(R 25 ), and N(R 26 ), X 23 is selected from O, S, C(R 27 )(R 28 ), and N(R 29 ), R 21 , R 22 , R 24 , R 25 , R 27 , and R 28 are each independently selected from a C 1 -C 20 alkyl group and a C 1 -C 20 alkoxy group; a C 1 -C 20 alkyl group and a C 1 -C 20 alkoxy group, each substituted with at least one of a deuterium, —F, and a cyano group; a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group; and a phenyl group, a pyridinyl group, a fluorenyl group, a dibenzofuranyl group, and a dibenzothiophenyl group, each substituted with at least one of a deuterium, —F, a hydroxyl group, a cyano group, a nitro group, an amino group, an amidino group, a hydrazine group, a hydrazone group, a carboxylic acid group or a salt thereof, a sulfonic acid group or a salt thereof, a phosphoric acid group or a s
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