RU2186780C2 - Производное 8-азабицикло [3.2.1]окт-2-ена, способы его получения, фармацевтическая композиция - Google Patents
Производное 8-азабицикло [3.2.1]окт-2-ена, способы его получения, фармацевтическая композиция Download PDFInfo
- Publication number
- RU2186780C2 RU2186780C2 RU99128075/04A RU99128075A RU2186780C2 RU 2186780 C2 RU2186780 C2 RU 2186780C2 RU 99128075/04 A RU99128075/04 A RU 99128075/04A RU 99128075 A RU99128075 A RU 99128075A RU 2186780 C2 RU2186780 C2 RU 2186780C2
- Authority
- RU
- Russia
- Prior art keywords
- azabicyclo
- oct
- ene
- methyl
- thienyl
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 51
- SURHOQQBDZIWSO-UHFFFAOYSA-N 8-azabicyclo[3.2.1]oct-3-ene Chemical class N1C2CCC1C=CC2 SURHOQQBDZIWSO-UHFFFAOYSA-N 0.000 title claims abstract description 11
- 239000008194 pharmaceutical composition Substances 0.000 title claims description 14
- 230000015572 biosynthetic process Effects 0.000 title abstract description 5
- 238000003786 synthesis reaction Methods 0.000 title abstract description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 100
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 28
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 25
- 125000001544 thienyl group Chemical group 0.000 claims abstract description 24
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 15
- 230000000694 effects Effects 0.000 claims abstract description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 12
- 125000001424 substituent group Chemical group 0.000 claims abstract description 12
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 10
- 125000001072 heteroaryl group Chemical group 0.000 claims abstract description 9
- 125000004076 pyridyl group Chemical group 0.000 claims abstract description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 5
- 125000001624 naphthyl group Chemical group 0.000 claims abstract description 4
- 125000002541 furyl group Chemical group 0.000 claims abstract 5
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000001164 benzothiazolyl group Chemical group S1C(=NC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims abstract 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims abstract 2
- 125000002971 oxazolyl group Chemical group 0.000 claims abstract 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims abstract 2
- 125000000335 thiazolyl group Chemical group 0.000 claims abstract 2
- -1 amino, nitro, phenyl Chemical group 0.000 claims description 82
- 239000000203 mixture Substances 0.000 claims description 79
- 150000003839 salts Chemical class 0.000 claims description 26
- 125000003342 alkenyl group Chemical group 0.000 claims description 13
- 125000000304 alkynyl group Chemical group 0.000 claims description 13
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 12
- 125000004104 aryloxy group Chemical group 0.000 claims description 11
- 150000002367 halogens Chemical group 0.000 claims description 11
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 claims description 10
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims description 10
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 9
- 125000005309 thioalkoxy group Chemical group 0.000 claims description 9
- RPJDXMAIYKVRML-UHFFFAOYSA-N 3-(1-benzofuran-2-yl)-8-methyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C1=CC=C2OC(C3=CC4CCC(C3)N4C)=CC2=C1 RPJDXMAIYKVRML-UHFFFAOYSA-N 0.000 claims description 7
- 125000003682 3-furyl group Chemical group O1C([H])=C([*])C([H])=C1[H] 0.000 claims description 7
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 5
- 125000002619 bicyclic group Chemical class 0.000 claims description 5
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- 125000002941 2-furyl group Chemical group O1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- RORUEWFPGKJEPN-UHFFFAOYSA-N 3-(1-benzofuran-2-yl)-8-ethyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C1=CC=C2OC(C3=CC4CCC(C3)N4CC)=CC2=C1 RORUEWFPGKJEPN-UHFFFAOYSA-N 0.000 claims description 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 4
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
- ACDNBQIGAKRKBQ-UHFFFAOYSA-N 1-(8-methyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)ethanone Chemical compound C1C(C(C)=O)=CC2CCC1N2C ACDNBQIGAKRKBQ-UHFFFAOYSA-N 0.000 claims description 3
- CBIVWNSFZSWGPL-UHFFFAOYSA-N 2-(8-methyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1,3-benzothiazole Chemical compound C1=CC=C2SC(C3=CC4CCC(C3)N4C)=NC2=C1 CBIVWNSFZSWGPL-UHFFFAOYSA-N 0.000 claims description 3
- JNTUJVNMCQZBLW-UHFFFAOYSA-N 2-(8-methyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)-1,3-thiazole Chemical compound CN1C(C2)CCC1C=C2C1=NC=CS1 JNTUJVNMCQZBLW-UHFFFAOYSA-N 0.000 claims description 3
- DOXXUIIBFXZGDL-UHFFFAOYSA-N 3-(1-benzofuran-3-yl)-8-methyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C1=CC=C2C(C3=CC4CCC(C3)N4C)=COC2=C1 DOXXUIIBFXZGDL-UHFFFAOYSA-N 0.000 claims description 3
- VCTUNRRIDDKDLD-UHFFFAOYSA-N 3-(1-benzothiophen-2-yl)-8-methyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C1=CC=C2SC(C3=CC4CCC(C3)N4C)=CC2=C1 VCTUNRRIDDKDLD-UHFFFAOYSA-N 0.000 claims description 3
- CTIFCRVFVGUGEB-UHFFFAOYSA-N 3-(8-methyl-8-azabicyclo[3.2.1]oct-3-en-3-yl)quinoline Chemical compound C1=CC=CC2=CC(C3=CC4CCC(C3)N4C)=CN=C21 CTIFCRVFVGUGEB-UHFFFAOYSA-N 0.000 claims description 3
- ANCYAZAGAVYFFY-UHFFFAOYSA-N 3-(furan-2-yl)-8-methyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound CN1C(C2)CCC1C=C2C1=CC=CO1 ANCYAZAGAVYFFY-UHFFFAOYSA-N 0.000 claims description 3
- WKIDQHCAQKRASI-UHFFFAOYSA-N 3-[3-(furan-3-yl)thiophen-2-yl]-8-methyl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound CN1C(C2)CCC1C=C2C=1SC=CC=1C=1C=COC=1 WKIDQHCAQKRASI-UHFFFAOYSA-N 0.000 claims description 3
- GVAIGIAEFMORID-UHFFFAOYSA-N 8-benzyl-3-pyridin-3-yl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C=1C=CC=CC=1CN1C(C2)CCC1C=C2C1=CC=CN=C1 GVAIGIAEFMORID-UHFFFAOYSA-N 0.000 claims description 3
- UYJMAFZVUPEINB-UHFFFAOYSA-N 8-methyl-3-naphthalen-2-yl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound C1=CC=CC2=CC(C3=CC4CCC(C3)N4C)=CC=C21 UYJMAFZVUPEINB-UHFFFAOYSA-N 0.000 claims description 3
- OZAJXVSFXYHSBL-UHFFFAOYSA-N 8-methyl-3-pyridin-3-yl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound CN1C(C2)CCC1C=C2C1=CC=CN=C1 OZAJXVSFXYHSBL-UHFFFAOYSA-N 0.000 claims description 3
- UWEJCTMVDPCGSY-UHFFFAOYSA-N 8-methyl-3-thiophen-2-yl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound CN1C(C2)CCC1C=C2C1=CC=CS1 UWEJCTMVDPCGSY-UHFFFAOYSA-N 0.000 claims description 3
- DJNFHLLQBYEIJO-UHFFFAOYSA-N 8-methyl-3-thiophen-3-yl-8-azabicyclo[3.2.1]oct-3-ene Chemical compound CN1C(C2)CCC1C=C2C=1C=CSC=1 DJNFHLLQBYEIJO-UHFFFAOYSA-N 0.000 claims description 3
- 229940075993 receptor modulator Drugs 0.000 claims description 3
- 125000001766 1,2,4-oxadiazol-3-yl group Chemical group [H]C1=NC(*)=NO1 0.000 claims description 2
- 125000004505 1,2,4-oxadiazol-5-yl group Chemical group O1N=CN=C1* 0.000 claims description 2
- 125000004516 1,2,4-thiadiazol-5-yl group Chemical group S1N=CN=C1* 0.000 claims description 2
- 125000004508 1,2,5-oxadiazol-4-yl group Chemical group O1N=CC(=N1)* 0.000 claims description 2
- 125000004518 1,2,5-thiadiazol-3-yl group Chemical group S1N=C(C=N1)* 0.000 claims description 2
- 125000004519 1,2,5-thiadiazol-4-yl group Chemical group S1N=CC(=N1)* 0.000 claims description 2
- 125000001462 1-pyrrolyl group Chemical group [*]N1C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
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| Publication number | Priority date | Publication date | Assignee | Title |
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| RU2350961C2 (ru) * | 2003-02-21 | 2009-03-27 | Ипсен Лимитед | Количественное определение токсина ботулизма |
| RU2376984C2 (ru) * | 2005-02-21 | 2009-12-27 | Лтс Ломанн Терапи-Зюстеме Аг | Способ комбинированного лечения и применимые для этого сочетания лекарственных средств |
| RU2420284C2 (ru) * | 2006-06-12 | 2011-06-10 | Пфайзер Продактс Инк. | Антагонист ccr5 для усиления иммуновосстановительной терапии и лечения оппортунистической инфекции у пациентов с вич |
| RU2469035C2 (ru) * | 2007-07-20 | 2012-12-10 | Тереванс, Инк. | СПОСОБ ПОЛУЧЕНИЯ ПРОМЕЖУТОЧНОГО ПРОДУКТА ДЛЯ СИНТЕЗА АНТАГОНИСТОВ мю-РЕЦЕПТОРА ОПИОИДОВ |
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| US6218383B1 (en) * | 1998-08-07 | 2001-04-17 | Targacept, Inc. | Pharmaceutical compositions for the prevention and treatment of central nervous system disorders |
| ATE259804T1 (de) * | 1998-11-27 | 2004-03-15 | Neurosearch As | 8-azabicyclo(3.2.1)okt-2-en- und -oktanderivate |
| US6953855B2 (en) | 1998-12-11 | 2005-10-11 | Targacept, Inc. | 3-substituted-2(arylalkyl)-1-azabicycloalkanes and methods of use thereof |
| US6432975B1 (en) * | 1998-12-11 | 2002-08-13 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
| AU2278700A (en) | 1999-01-28 | 2000-08-18 | Neurosearch A/S | Novel azabicyclo derivatives and their use |
| US7265115B2 (en) | 1999-01-29 | 2007-09-04 | Abbott Laboratories | Diazabicyclic CNS active agents |
| ES2305373T3 (es) * | 1999-01-29 | 2008-11-01 | Abbott Laboratories | Derivados diazabiciclicos como ligandos del receptor nicotinico de la acetilcolina. |
| NZ513575A (en) | 1999-05-04 | 2003-07-25 | Neurosearch As | Heteroaryl diazabicycloalkanes useful for treating or preventing a disease or a disorder responsive to the activity of nAChR modulators |
| US6890935B2 (en) | 1999-11-01 | 2005-05-10 | Targacept, Inc. | Pharmaceutical compositions and methods for use |
| MY145722A (en) * | 2000-04-27 | 2012-03-30 | Abbott Lab | Diazabicyclic central nervous system active agents |
| NZ522793A (en) | 2000-07-04 | 2005-02-25 | Neurosearch As | Aryl and heteroaryl diazabicycloalkanes, their preparation and use |
| CN100398103C (zh) * | 2000-10-13 | 2008-07-02 | 神经研究公司 | 通过烟碱性受体激动剂和单胺能物质的联合作用治疗情感性精神障碍 |
| CA2462453C (en) * | 2001-10-02 | 2009-07-28 | Pharmacia & Upjohn Company | Azabicyclic-substituted fused-heteroaryl compounds for the treatment of disease |
| DE10164139A1 (de) | 2001-12-27 | 2003-07-10 | Bayer Ag | 2-Heteroarylcarbonsäureamide |
| CA2476681A1 (en) | 2002-02-19 | 2003-08-28 | Bruce N. Rogers | Fused bicyclic-n-bridged-heteroaromatic carboxamides for the treatment of disease |
| CN100522976C (zh) * | 2002-05-07 | 2009-08-05 | 神经研究公司 | 氮杂环乙炔基衍生物 |
| DE602004013427T2 (de) * | 2003-02-28 | 2009-06-04 | Schering Corp. | Biaryltetrahydroisochinolin-piperidine als selektive mch-rezeptor-antagonisten zur behandlung von adipositas und verwandten erkrankungen |
| KR100767854B1 (ko) | 2003-03-12 | 2007-10-17 | 화이자 프로덕츠 인크. | 피리딜옥시메틸 및 벤즈이속사졸 아자비시클릭 유도체 |
| AU2005284908B2 (en) | 2004-09-13 | 2011-12-08 | Morningside Venture Investments Limited | Biosynchronous transdermal drug delivery |
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| EP1869034A1 (en) * | 2005-04-08 | 2007-12-26 | NeuroSearch A/S | (+) - and (-) -8-alkyl-3-(trifluoralkylsulfonyloxy)-8-azabicycl (3.2.1.)oct-2-ene |
| FR2889701B1 (fr) * | 2005-08-12 | 2007-10-05 | Sanofi Aventis Sa | Derives de 5-pyridinyl-1-azabicyclo[3.2.1]octane, leur preparation en therapeutique. |
| ATE473978T1 (de) | 2005-12-06 | 2010-07-15 | Neurosearch As | Neue diazabicyclische arylderivate und medizinische verwendung dafür |
| US20070134169A1 (en) * | 2005-12-11 | 2007-06-14 | Rabinoff Michael D | Methods for smoking cessation or alcohol cessation or other addiction cessation |
| AU2007213670A1 (en) | 2006-02-10 | 2007-08-16 | Neurosearch A/S | 3,9-diazabicyclo[3.3.1]nonane derivatives and their use as monoamine neurotransmitter re-uptake inhibitors |
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| CN101379063A (zh) | 2006-02-10 | 2009-03-04 | 神经研究公司 | 3,9-二氮杂双环[3.3.1]壬烷衍生物及其作为单胺神经递质再摄取抑制剂的用途 |
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| SA08290475B1 (ar) | 2007-08-02 | 2013-06-22 | Targacept Inc | (2s، 3r)-n-(2-((3-بيردينيل)ميثيل)-1-آزا بيسيكلو[2، 2، 2]أوكت-3-يل)بنزو فيوران-2-كربوكساميد، وصور أملاحه الجديدة وطرق استخدامه |
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| US12397141B2 (en) | 2018-11-16 | 2025-08-26 | Morningside Venture Investments Limited | Thermally regulated transdermal drug delivery system |
| KR102272452B1 (ko) | 2020-12-11 | 2021-07-05 | (주)예광솔라 | 스파이럴 파일 공법 및 이에 적용되는 스파이럴 파일 |
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Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2350961C2 (ru) * | 2003-02-21 | 2009-03-27 | Ипсен Лимитед | Количественное определение токсина ботулизма |
| RU2376984C2 (ru) * | 2005-02-21 | 2009-12-27 | Лтс Ломанн Терапи-Зюстеме Аг | Способ комбинированного лечения и применимые для этого сочетания лекарственных средств |
| RU2420284C2 (ru) * | 2006-06-12 | 2011-06-10 | Пфайзер Продактс Инк. | Антагонист ccr5 для усиления иммуновосстановительной терапии и лечения оппортунистической инфекции у пациентов с вич |
| RU2469035C2 (ru) * | 2007-07-20 | 2012-12-10 | Тереванс, Инк. | СПОСОБ ПОЛУЧЕНИЯ ПРОМЕЖУТОЧНОГО ПРОДУКТА ДЛЯ СИНТЕЗА АНТАГОНИСТОВ мю-РЕЦЕПТОРА ОПИОИДОВ |
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