RU2500680C2 - Новые замещенные пиридин-2-оны и пиридазин-3-оны - Google Patents
Новые замещенные пиридин-2-оны и пиридазин-3-оны Download PDFInfo
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- RU2500680C2 RU2500680C2 RU2011101774/04A RU2011101774A RU2500680C2 RU 2500680 C2 RU2500680 C2 RU 2500680C2 RU 2011101774/04 A RU2011101774/04 A RU 2011101774/04A RU 2011101774 A RU2011101774 A RU 2011101774A RU 2500680 C2 RU2500680 C2 RU 2500680C2
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- lower alkyl
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- heterocycloalkyl
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- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 title abstract 2
- UBQKCCHYAOITMY-UHFFFAOYSA-N pyridin-2-ol Chemical class OC1=CC=CC=N1 UBQKCCHYAOITMY-UHFFFAOYSA-N 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims abstract 13
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims abstract 8
- 150000001875 compounds Chemical class 0.000 claims abstract 7
- 125000005842 heteroatom Chemical group 0.000 claims abstract 4
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract 2
- 230000002401 inhibitory effect Effects 0.000 claims abstract 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 102000001253 Protein Kinase Human genes 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 239000003085 diluting agent Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 239000000546 pharmaceutical excipient Substances 0.000 claims 1
- 108060006633 protein kinase Proteins 0.000 claims 1
- 125000004076 pyridyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000006413 ring segment Chemical group 0.000 abstract 2
- 230000000694 effects Effects 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
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Abstract
Изобретение относится к новым производным пиридин-2-онов и пиридазин-3-онов, обладающим ингибирующей активностью в отношении Btk-киназы. В формулах I-IV:
R обозначает -R1-R2-R3 или -R2-R3; R1 обозначает гетероарил, содержащий в кольце 6 атомов, включая один гетероатом N; R2 обозначает -C(=O), -C(=O)N(R2'), где R2' обозначает H; R3 обозначает R4; где R4 - низший алкил, гетероциклоалкил, (низший алкил)гетероциклоалкил или гетероциклоалкил(низший алкил), где гетероциклоалкил содержит в кольце 6 атомов, включая два гетероатома, выбранных из N и O; и где R4 может быть замещен одним или более заместителем, выбранным из низшего алкила, оксогруппы и низшей алкоксигруппы; X обозначает CH или N; Y1 обозначает низший алкил; n и m равны 0; значения радикалов Y2, Y4 приведены в формуле изобретения. Изобретение также относится к фармацевтической композиции, содержащей указанные соединения. 2 н. и 4 з.п. ф-лы, 2 табл., 42 пр.
Description
Claims (6)
1. Соединение формулы I, II, III или IV:
в которой:
R обозначает -R1-R2-R3 или -R2-R3; где
R1 обозначает гетероарил, содержащий в кольце 6 атомов, включая один гетероатом N;
R2 обозначает -C(=O), -C(=O)N(R2'), где R2' обозначает H;
R3 обозначает R4; где R4 обозначает низший алкил, гетероциклоалкил, (низший алкил)гетероциклоалкил или гетероциклоалкил(низший алкил), где гетероциклоалкил содержит в кольце 6 атомов, включая два гетероатома, выбранных из N и O; и где R4 может быть замещен одним или более заместителем, выбранным из низшего алкила, оксогруппы и низшей алкоксигруппы;
X обозначает СН или N;
Y1 обозначает низший алкил;
Y2 обозначает Y2b; где Y2b обозначает низший алкил, необязательно замещенный одним Y2b'; и Y2b' обозначает гидроксигруппу;
n равен 0;
m равен 0;
Y4 обозначает Y4a, Y4b, Y4c или Y4d; где
Y4a обозначает галоген;
Y4b обозначает низший алкил, необязательно содержащий один заместитель, выбранный из гидроксигруппы;
Y4c обозначает низший циклоалкил; и
Y4d обозначает аминогруппу, необязательно замещенную одним или более низшим алкилом;
или его фармацевтически приемлемая соль.
в которой:
R обозначает -R1-R2-R3 или -R2-R3; где
R1 обозначает гетероарил, содержащий в кольце 6 атомов, включая один гетероатом N;
R2 обозначает -C(=O), -C(=O)N(R2'), где R2' обозначает H;
R3 обозначает R4; где R4 обозначает низший алкил, гетероциклоалкил, (низший алкил)гетероциклоалкил или гетероциклоалкил(низший алкил), где гетероциклоалкил содержит в кольце 6 атомов, включая два гетероатома, выбранных из N и O; и где R4 может быть замещен одним или более заместителем, выбранным из низшего алкила, оксогруппы и низшей алкоксигруппы;
X обозначает СН или N;
Y1 обозначает низший алкил;
Y2 обозначает Y2b; где Y2b обозначает низший алкил, необязательно замещенный одним Y2b'; и Y2b' обозначает гидроксигруппу;
n равен 0;
m равен 0;
Y4 обозначает Y4a, Y4b, Y4c или Y4d; где
Y4a обозначает галоген;
Y4b обозначает низший алкил, необязательно содержащий один заместитель, выбранный из гидроксигруппы;
Y4c обозначает низший циклоалкил; и
Y4d обозначает аминогруппу, необязательно замещенную одним или более низшим алкилом;
или его фармацевтически приемлемая соль.
2. Соединение по п.1, в котором Y1 обозначает метил.
3. Соединение по п.1, в котором X обозначает CH.
4. Соединение по п.1, в котором Y2 обозначает метил или гидроксиметил.
5. Соединение по п.1, в котором R обозначает -R1-R2-R3; где R1 обозначает пиридил; R2 обозначает -C(=O); R3 обозначает R4; и R4 обозначает морфолин или пиперазин.
6. Фармацевтическая композиция, обладающая ингибирующей активностью в отношении Btk-киназы, включающая соединение по любому из пп.1-5 в терапевтически эффективном количестве в смеси по меньшей мере с одним фармацевтически приемлемым носителем, инертным наполнителем или разбавителем.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US7527708P | 2008-06-24 | 2008-06-24 | |
| US61/075,277 | 2008-06-24 | ||
| PCT/EP2009/057320 WO2009156284A1 (en) | 2008-06-24 | 2009-06-15 | Novel substituted pyridin-2-ones and pyridazin-3-ones |
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| Publication Number | Publication Date |
|---|---|
| RU2011101774A RU2011101774A (ru) | 2012-07-27 |
| RU2500680C2 true RU2500680C2 (ru) | 2013-12-10 |
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| RU2011101774/04A RU2500680C2 (ru) | 2008-06-24 | 2009-06-15 | Новые замещенные пиридин-2-оны и пиридазин-3-оны |
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| EP (1) | EP2297142B1 (ru) |
| JP (1) | JP5536049B2 (ru) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW200900396A (en) * | 2007-04-10 | 2009-01-01 | Kudos Pharm Ltd | Phthalazinone derivatives |
| AU2009265813B2 (en) * | 2008-07-02 | 2014-04-10 | F. Hoffmann-La Roche Ag | Novel phenylpyrazinones as kinase inhibitors |
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