JP2008513432A5 - - Google Patents
Download PDFInfo
- Publication number
- JP2008513432A5 JP2008513432A5 JP2007531865A JP2007531865A JP2008513432A5 JP 2008513432 A5 JP2008513432 A5 JP 2008513432A5 JP 2007531865 A JP2007531865 A JP 2007531865A JP 2007531865 A JP2007531865 A JP 2007531865A JP 2008513432 A5 JP2008513432 A5 JP 2008513432A5
- Authority
- JP
- Japan
- Prior art keywords
- alkyl
- membered
- independently
- heteroaryl
- aryl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 125000000217 alkyl group Chemical group 0.000 claims 72
- 125000003118 aryl group Chemical group 0.000 claims 21
- 125000001072 heteroaryl group Chemical group 0.000 claims 20
- 229910052736 halogen Inorganic materials 0.000 claims 18
- 150000002367 halogens Chemical class 0.000 claims 18
- 125000003545 alkoxy group Chemical group 0.000 claims 14
- 150000001875 compounds Chemical class 0.000 claims 14
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 11
- 229910052799 carbon Inorganic materials 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 7
- 125000000753 cycloalkyl group Chemical group 0.000 claims 6
- 229910052757 nitrogen Inorganic materials 0.000 claims 6
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 5
- 239000008194 pharmaceutical composition Substances 0.000 claims 5
- 125000004432 carbon atom Chemical group C* 0.000 claims 4
- 210000003169 central nervous system Anatomy 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 4
- 125000004434 sulfur atom Chemical group 0.000 claims 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 3
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 3
- 125000003342 alkenyl group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 238000006467 substitution reaction Methods 0.000 claims 3
- 229910052717 sulfur Inorganic materials 0.000 claims 3
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 claims 2
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 claims 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 2
- 230000000626 neurodegenerative effect Effects 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 125000001424 substituent group Chemical group 0.000 claims 2
- 125000005309 thioalkoxy group Chemical group 0.000 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims 1
- 125000006713 (C5-C10) cycloalkyl group Chemical group 0.000 claims 1
- FRMYSVHRJOISJO-JYFHCDHNSA-N 1-butyl-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-3-propanoylindole-6-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C(C(=O)CC)=CN(C2=C1)CCCC)[C@H](O)CNC)C1=CC(F)=CC(F)=C1 FRMYSVHRJOISJO-JYFHCDHNSA-N 0.000 claims 1
- FIYMAZBOTNEQAR-LOSJGSFVSA-N 1-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-5-(1,3-oxazol-2-yl)-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound C=1C(C(=O)N(CCC)CCC)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNC)=CC=1C1=NC=CO1 FIYMAZBOTNEQAR-LOSJGSFVSA-N 0.000 claims 1
- DRZGHWGSHCNSOU-LOSJGSFVSA-N 1-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-5-ethynyl-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C#C)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNC)=C1 DRZGHWGSHCNSOU-LOSJGSFVSA-N 0.000 claims 1
- DEONCYDJRZCKNY-BJKOFHAPSA-N 1-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-5-methyl-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(C)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNC)=C1 DEONCYDJRZCKNY-BJKOFHAPSA-N 0.000 claims 1
- 125000006288 3,5-difluorobenzyl group Chemical group [H]C1=C(F)C([H])=C(C([H])=C1F)C([H])([H])* 0.000 claims 1
- SXHOHKJVKUSWCK-UKILVPOCSA-N 3-acetyl-1-butyl-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]indole-6-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C(C(C)=O)=CN(C2=C1)CCCC)[C@H](O)CNC)C1=CC(F)=CC(F)=C1 SXHOHKJVKUSWCK-UKILVPOCSA-N 0.000 claims 1
- RGCGZUCJMJYZMV-AHKZPQOWSA-N 3-acetyl-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-1-hexylindole-6-carboxamide Chemical compound C([C@H](NC(=O)C1=CC=C2C(C(C)=O)=CN(C2=C1)CCCCCC)[C@H](O)CNC)C1=CC(F)=CC(F)=C1 RGCGZUCJMJYZMV-AHKZPQOWSA-N 0.000 claims 1
- WLXXVMAHARAHFI-XZOQPEGZSA-N 5-bromo-1-n-[(2s,3r)-1-(3,5-difluorophenyl)-3-hydroxy-4-(methylamino)butan-2-yl]-3-n,3-n-dipropylbenzene-1,3-dicarboxamide Chemical compound CCCN(CCC)C(=O)C1=CC(Br)=CC(C(=O)N[C@@H](CC=2C=C(F)C=C(F)C=2)[C@H](O)CNC)=C1 WLXXVMAHARAHFI-XZOQPEGZSA-N 0.000 claims 1
- KPJDOBLKTXEADO-UHFFFAOYSA-N 6-methylpyridine-2,4-dicarboxylic acid Chemical compound CC1=CC(C(O)=O)=CC(C(O)=O)=N1 KPJDOBLKTXEADO-UHFFFAOYSA-N 0.000 claims 1
- 208000024827 Alzheimer disease Diseases 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims 1
- -1 homomorpholinyl Chemical group 0.000 claims 1
- RCCPEORTSYDPMB-UHFFFAOYSA-N hydroxy benzenecarboximidothioate Chemical compound OSC(=N)C1=CC=CC=C1 RCCPEORTSYDPMB-UHFFFAOYSA-N 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000003386 piperidinyl group Chemical group 0.000 claims 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000001422 pyrrolinyl group Chemical group 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 claims 1
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US61177704P | 2004-09-21 | 2004-09-21 | |
| PCT/IB2005/002877 WO2006032999A1 (en) | 2004-09-21 | 2005-09-09 | N-methyl hydroxyethylamine useful in treating cns conditions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2008513432A JP2008513432A (ja) | 2008-05-01 |
| JP2008513432A5 true JP2008513432A5 (enExample) | 2008-10-16 |
Family
ID=35559297
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2007531865A Withdrawn JP2008513432A (ja) | 2004-09-21 | 2005-09-09 | Ｃｎｓ状態の治療に有用なｎ−メチルヒドロキシエチルアミン |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US20080132552A1 (enExample) |
| EP (1) | EP1794114A1 (enExample) |
| JP (1) | JP2008513432A (enExample) |
| BR (1) | BRPI0515528A (enExample) |
| CA (1) | CA2581023A1 (enExample) |
| MX (1) | MX2007002459A (enExample) |
| WO (1) | WO2006032999A1 (enExample) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8791135B2 (en) * | 2008-07-01 | 2014-07-29 | Purdue Research Foundation | Nonpeptide HIV-1 protease inhibitors |
| US8993572B2 (en) | 2010-04-22 | 2015-03-31 | Intra-Cellular Therapies, Inc. | Pyrido[3′,4′:4,5]pyrrolo[1,2,3-de]quinoxalines derivatives and [1,4]oxazino[2,3,4-hi]pyrido[4,3-b]indole derivatives |
| CN102344402B (zh) * | 2010-07-30 | 2015-01-07 | 中国人民解放军军事医学科学院毒物药物研究所 | 苯并氮杂环羟乙基胺类化合物、其制备方法和用途 |
| WO2013155504A1 (en) * | 2012-04-14 | 2013-10-17 | Intra-Cellular Therapies, Inc. | Novel methods |
| WO2014145192A1 (en) | 2013-03-15 | 2014-09-18 | Intra-Cellular Therapies, Inc. | Organic compounds |
| IL321987A (en) | 2013-12-03 | 2025-09-01 | Intra Cellular Therapies Inc | A long-acting injectable preparation containing polymeric microspheres of modified compressed gamma-carboline heterocyclic compounds or a sustained-release pharmaceutical preparation containing these compounds for use in the treatment of bipolar I and/or bipolar II disorders |
| AU2015240526A1 (en) | 2014-04-04 | 2016-11-24 | Intra-Cellular Therapies, Inc. | Organic compounds |
| MX388258B (es) | 2014-04-04 | 2025-03-19 | Intra Cellular Therapies Inc | Gamma-carbolinas fusionadas con heterociclos sustituidas con deuterio. |
| PT3407888T (pt) | 2016-01-26 | 2021-03-19 | Intra Cellular Therapies Inc | Compostos de piridopirroloquinoxalina, suas composições e utilizações |
| JP6686168B2 (ja) | 2016-03-25 | 2020-04-22 | イントラ−セルラー・セラピーズ・インコーポレイテッドＩｎｔｒａ−Ｃｅｌｌｕｌａｒ Ｔｈｅｒａｐｉｅｓ， Ｉｎｃ． | 有機化合物 |
| JP2019510039A (ja) | 2016-03-28 | 2019-04-11 | イントラ−セルラー・セラピーズ・インコーポレイテッドＩｎｔｒａ−Ｃｅｌｌｕｌａｒ Ｔｈｅｒａｐｉｅｓ， Ｉｎｃ． | 新規組成物および方法 |
| EP3525763B1 (en) | 2016-10-12 | 2025-03-05 | Intra-Cellular Therapies, Inc. | Amorphous solid dispersions |
| WO2018126140A1 (en) | 2016-12-29 | 2018-07-05 | Intra-Cellular Therapies, Inc. | Organic compounds |
| US10906906B2 (en) | 2016-12-29 | 2021-02-02 | Intra-Cellular Therapies, Inc. | Organic compounds |
| CN116327770B (zh) | 2017-03-24 | 2025-10-31 | 细胞内治疗公司 | 新组合物和方法 |
| IL272252B2 (en) | 2017-07-26 | 2024-03-01 | Intra Cellular Therapies Inc | Derivatives of substituted heterocycle fused gamma-carbolines, pharmaceutical compositions comnprising them and their use in treatment |
| BR112020001666A2 (pt) | 2017-07-26 | 2020-07-21 | Intra-Cellular Therapies, Inc. | compostos orgânicos |
| MX2020009928A (es) | 2018-03-23 | 2021-01-08 | Intra Cellular Therapies Inc | Compuestos organicos. |
| MX2020013335A (es) | 2018-06-08 | 2021-05-27 | Intra Cellular Therapies Inc | Metodos novedosos. |
| EP3843729A4 (en) | 2018-08-29 | 2022-06-01 | Intra-Cellular Therapies, Inc. | NEW COMPOSITIONS AND METHODS |
| EP3843738A4 (en) | 2018-08-31 | 2022-06-01 | Intra-Cellular Therapies, Inc. | NEW METHODS |
| US10695345B2 (en) | 2018-08-31 | 2020-06-30 | Intra-Cellular Therapies, Inc. | Pharmaceutical capsule compositions comprising lumateperone mono-tosylate |
| JP7673040B2 (ja) | 2019-07-07 | 2025-05-08 | イントラ－セルラー・セラピーズ・インコーポレイテッド | 新規方法 |
| US12414948B2 (en) | 2022-05-18 | 2025-09-16 | Intra-Cellular Therapies, Inc. | Methods |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE302751T1 (de) | 2000-06-30 | 2005-09-15 | Elan Pharm Inc | Verbindungen zur behandlung der alzheimerischen krankheit |
| AU2002320490B2 (en) | 2001-07-11 | 2008-10-02 | Elan Pharmaceuticals, Inc. | N-(3-amino-2-hydroxy-propyl) substituted alkylamide compounds |
| GB0228410D0 (en) | 2002-12-05 | 2003-01-08 | Glaxo Group Ltd | Novel Compounds |
-
2005
- 2005-09-09 WO PCT/IB2005/002877 patent/WO2006032999A1/en not_active Ceased
- 2005-09-09 MX MX2007002459A patent/MX2007002459A/es unknown
- 2005-09-09 JP JP2007531865A patent/JP2008513432A/ja not_active Withdrawn
- 2005-09-09 BR BRPI0515528-2A patent/BRPI0515528A/pt not_active IP Right Cessation
- 2005-09-09 CA CA002581023A patent/CA2581023A1/en not_active Abandoned
- 2005-09-09 EP EP05783711A patent/EP1794114A1/en not_active Withdrawn
- 2005-09-21 US US11/231,483 patent/US20080132552A1/en not_active Abandoned
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JP2008513432A5 (enExample) | ||
| JP2008523069A5 (enExample) | ||
| JP2011037841A5 (enExample) | ||
| NO20073667L (no) | [4-(heteroaryl) piperazin-1-yl]-(2,5-substituert-fenyl)metanonderivater som glycintransportor 1(GLYT-1)- inhibitorer for behandling av neurologiske og neuropsykiatriske lidelser | |
| CY1116119T1 (el) | Παραγωγα ισοξαζολο-πυριδινης | |
| JP2010504286A5 (enExample) | ||
| MX2009008465A (es) | Nuevas 2-aminooxazolinas como ligandos de taar1. | |
| JP2010256891A5 (enExample) | ||
| CY1114932T1 (el) | Αντιπαρασιτικοι παραγοντες | |
| JP2009519903A5 (enExample) | ||
| JP2005517643A5 (enExample) | ||
| RU2010113358A (ru) | Гуанидинсодержащие соединения, применимые в качестве антагонистов мускариновых рецепторов | |
| JP2008518900A5 (enExample) | ||
| JP2013515037A5 (enExample) | ||
| JPWO2022138968A5 (enExample) | ||
| JP2007532582A5 (enExample) | ||
| BRPI0409471A (pt) | processo para a preparação de 2-cianopirrolidinas n-substituìdas | |
| JP2007538042A5 (enExample) | ||
| WO2007147770A3 (en) | Substituted phenyl methanone derivatives | |
| JP2004527639A5 (enExample) | ||
| JP2009508952A5 (enExample) | ||
| EA200401077A1 (ru) | 2-оксазоламины и их применение в качестве антагонистов рецептора 5-ht2b | |
| JP2005517707A5 (enExample) | ||
| JP2008116785A5 (enExample) | ||
| JP2006316032A5 (enExample) |