AR037465A1 - Compuesto derivado de 5-sulfanil-4h-1,2,4-triazol, composicion farmaceutica que lo comprende y proceso para su preparacion en fase liquida - Google Patents
Compuesto derivado de 5-sulfanil-4h-1,2,4-triazol, composicion farmaceutica que lo comprende y proceso para su preparacion en fase liquidaInfo
- Publication number
- AR037465A1 AR037465A1 ARP020104601A ARP020104601A AR037465A1 AR 037465 A1 AR037465 A1 AR 037465A1 AR P020104601 A ARP020104601 A AR P020104601A AR P020104601 A ARP020104601 A AR P020104601A AR 037465 A1 AR037465 A1 AR 037465A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- aryl
- amino
- heteroaryl
- optionally substituted
- Prior art date
Links
- 239000007791 liquid phase Substances 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- 239000002131 composite material Substances 0.000 title 1
- 125000003118 aryl group Chemical group 0.000 abstract 10
- -1 aralkyl radical Chemical group 0.000 abstract 6
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 5
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 5
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 4
- 125000001475 halogen functional group Chemical group 0.000 abstract 4
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 4
- 125000001424 substituent group Chemical group 0.000 abstract 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 108050001286 Somatostatin Receptor Proteins 0.000 abstract 2
- 102000011096 Somatostatin receptor Human genes 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 201000010099 disease Diseases 0.000 abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- AFBBKYQYNPNMAT-UHFFFAOYSA-N 1h-1,2,4-triazol-1-ium-3-thiolate Chemical compound SC=1N=CNN=1 AFBBKYQYNPNMAT-UHFFFAOYSA-N 0.000 abstract 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 abstract 1
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 235000005985 organic acids Nutrition 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Compuesto derivado de 5-sulfanil-4H-1,2,4-triazol que responde a la fórmula general (1) en forma racémica, enantiomérica o cualquier combinación de dichas formas, en donde: uno de los radicales R1, R2 ó R3 representa un radical de fórmula -(CH2)n-[Q]p-(CH2)m-NXY ó -(CH2)n-W en donde W representa un heterocicloalquilo que contiene al menos un átomo de nitrógeno; Q representa -O-, -S-, -C(O)-NH-, -C(Zq)(Zq')-, arilo ó cicloalquilo C3-7; Zq y Zq' representan, independientemente, el átomo de hidrógeno, arilo opcionalmente sustituido por arilo, cicloalquil C3-7-alquilo, arilalquilo, -C(O)O-R ó -C(O)-NH-R'; R representa un alquilo C1-6, arilo ó aralquilo radical, arilo y aralquilo que es opcionalmente sustituido por uno o más sustituyentes idénticos o diferentes seleccionados entre: alcoxi C1-6, hidroxi, halo, nitro ciano, amino, alquilamino C1-6 y di(alquil C1-6)amino; R' representa un alquilo C1-6, arilo, aralquilo, heteroarilo o heteroaril-alquilo radical, estando los radicales arilo, aralquilo, heteroarilo y heteroaril-alquilo opcionalmente sustituido por uno o más sustituyentes idénticos o diferentes seleccionados entre: alcoxi C1-6, hidroxi, halo, nitro ciano, amino, alquilamino C1-6, di(alquil C1-6) amino; X e Y representan, independientemente, el átomo de hidrógeno, alquilo C1-6, alcoxi C1-6-carbonilo ó un heteroaril-alquilo, ó X e Y forman junto con el átomo de nitrógeno al cual están unidos, un heterocicloalquilo opcionalmente sustituido por un alquilo C1-6; p representa 0 ó 1; n y m representan, independientemente, un entero entre 0 y 6; y los otros dos radicales representan, independientemente, un radical de fórmula -(CH2)n'[Q']p'[C(X')(Y')]m'Z' en donde: Q' representa -O-, -S-, -C(O)-, -NH-, -CH=CH-, -C:::C-; ó X', Y' y Z' representan, independientemente un átomo de hidrógeno, alquilo C1-6, alcoxi C1-6, alcoxi C1-6-carbonilo, ciano, amino, alquilamino C1-6, di(alquil C1-6) amino, cicloalquilo C3-7, heterocicloalquilo, arilo o heteroarilo, ó un radical de fórmulas (2), (3), (4), (5); r = 1, 2 ó 3, estando los radicales cicloalquilo C3-7, heterocicloalquilo, arilo y heteroarilo opcionalmente sustituidos por uno o más sustituyentes idénticos o diferentes seleccionados entre: -(CH2)q'-X''-Y'', hidroxi, halo, nitro, ciano, amino, alquilamino C1-6 y di(alquil C1-6) amino; X'' representa -O-, -S-, -C(O)-, -C(O)-O-, -SO2- ó una unión covalente; Y'' representa un radical alquilo C1-6 opcionalmente sustituido por uno o más radicales halo idénticos o diferentes; o radical arilo o heteroarilo opcionalmente sustituido por uno o más sustituyentes idénticos o diferentes seleccionados entre: alcoxi C1-6, hidroxi, halo, nitro ciano, amino, alquilamino C1-6 y di(alquil c1-6) amino; p' representa 0 ó 1; y n', m' y q' representan, independientemente, un entero entre 0 y 6; con exclusión de los compuestos en los cuales i) R1 representa -(CH2)2-W y W morfolino o piperazinilo; R2 fenilo, m-clorofenilo ó 4-piridilo, y R3 hidrógeno; ii) R1 representa -(CH2)2-W y W pirrolidinilo, R2 p-clorofenilo y R3 hidrógeno; o sus sales de adición con ácidos minerales u orgánicos aceptables para uso farmacéutico. Estos productos tienen una buena afinidad por determinados subtipos de receptores de somatostatina, son particularmente útiles para tratar estados patológicos o enfermedades en las cuales participan uno (o más) receptores de somatostatina. También se revelan composiciones farmacéuticas que contienen dichos productos y el proceso para su preparación en fase líquida.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0115342A FR2832710B1 (fr) | 2001-11-28 | 2001-11-28 | Derives de 5-sulfanyl-4h-1,2,4-triazoles et leur utilisation en tant que medicaments |
| FR0207697 | 2002-06-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR037465A1 true AR037465A1 (es) | 2004-11-10 |
Family
ID=26213278
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP020104601A AR037465A1 (es) | 2001-11-28 | 2002-11-28 | Compuesto derivado de 5-sulfanil-4h-1,2,4-triazol, composicion farmaceutica que lo comprende y proceso para su preparacion en fase liquida |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US20050154039A1 (es) |
| EP (1) | EP1465880B1 (es) |
| JP (1) | JP2005513035A (es) |
| KR (1) | KR100961332B1 (es) |
| CN (1) | CN100462359C (es) |
| AR (1) | AR037465A1 (es) |
| AT (1) | ATE438630T1 (es) |
| AU (1) | AU2002361345B8 (es) |
| BR (1) | BR0214553A (es) |
| CA (1) | CA2468184A1 (es) |
| CZ (1) | CZ2004760A3 (es) |
| DE (1) | DE60233265D1 (es) |
| ES (1) | ES2330927T3 (es) |
| HU (1) | HUP0402489A3 (es) |
| MX (1) | MXPA04005099A (es) |
| MY (1) | MY133406A (es) |
| NO (1) | NO20042635L (es) |
| NZ (1) | NZ533397A (es) |
| PL (1) | PL370140A1 (es) |
| RU (1) | RU2367655C2 (es) |
| TW (1) | TWI283670B (es) |
| WO (1) | WO2003045926A1 (es) |
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| TWI297335B (en) | 2001-07-10 | 2008-06-01 | Synta Pharmaceuticals Corp | Taxol enhancer compounds |
| TWI332943B (en) * | 2001-07-10 | 2010-11-11 | Synta Pharmaceuticals Corp | Taxol enhancer compounds |
| TWI252847B (en) * | 2001-07-10 | 2006-04-11 | Synta Pharmaceuticals Corp | Synthesis of taxol enhancers |
| TWI330079B (en) * | 2003-01-15 | 2010-09-11 | Synta Pharmaceuticals Corp | Treatment for cancers |
| ES2430373T3 (es) * | 2004-06-23 | 2013-11-20 | Synta Pharmaceuticals Corp. | Sales de bis(tio-hidrazida amida) para tratamiento de cánceres |
| EP2298748B1 (en) | 2004-11-18 | 2016-07-20 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate HSP90 activity |
| WO2006113695A1 (en) * | 2005-04-15 | 2006-10-26 | Synta Pharmaceuticals Corp. | Combination cancer therapy with bis(thiohydrazide) amide compounds |
| CA2618628C (en) * | 2005-08-18 | 2014-11-18 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
| EP2034995A2 (en) * | 2006-05-25 | 2009-03-18 | Synta Pharmaceuticals Corporation | Method for treating proliferative disorders associated with protooncogene products |
| WO2007139960A2 (en) * | 2006-05-25 | 2007-12-06 | Synta Pharmaceuticals Corp. | Compounds that modulate hsp90 activity and methods for identifying same |
| WO2007139955A2 (en) * | 2006-05-25 | 2007-12-06 | Synta Pharmaceuticals Corp. | Triazole compounds that modulate hsp90 activity |
| RU2475478C2 (ru) | 2006-08-21 | 2013-02-20 | Синта Фармасьютиклз Корп. | Соединения для лечения пролиферативных расстройств |
| EP2076254A2 (en) * | 2006-08-31 | 2009-07-08 | Synta Pharmaceuticals Corporation | Combination with bis(thiohydrazide amides) for treating cancer |
| CA2684147A1 (en) * | 2007-05-15 | 2008-11-27 | Boehringer Ingelheim International Gmbh | Urotensin ii receptor antagonists |
| KR100980328B1 (ko) * | 2007-12-14 | 2010-09-06 | 한국생명공학연구원 | 단백질 포스파타제의 활성을 억제하는트리아졸릴-티오-에타논 유도체 또는 이의 약학적으로 허용가능한 염을 유효성분으로 함유하는 암 예방 및 치료용조성물 |
| AU2009230127B2 (en) | 2008-03-26 | 2011-12-22 | Daiichi Sankyo Company, Limited | Novel tetrahydroisoquinoline derivative |
| CN101684103B (zh) * | 2008-09-22 | 2011-04-06 | 天津药物研究院 | 1,2,4-三唑结构的化合物、其制备方法和用途 |
| CN102395567A (zh) * | 2009-02-12 | 2012-03-28 | 埃克塞利希斯股份有限公司 | 在治疗糖尿病和肥胖症中用作的tgr5激动剂的三唑和咪唑衍生物 |
| US9205086B2 (en) | 2010-04-19 | 2015-12-08 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of a Hsp90 inhibitory compounds and a EGFR inhibitor |
| EP2773345A1 (en) | 2011-11-02 | 2014-09-10 | Synta Pharmaceuticals Corp. | Cancer therapy using a combination of hsp90 inhibitors with topoisomerase i inhibitors |
| US20140286902A1 (en) | 2011-11-02 | 2014-09-25 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with platinum-containing agents |
| CA2854188A1 (en) | 2011-11-14 | 2013-05-23 | Synta Pharmaceuticals Corp. | Combination therapy of hsp90 inhibitors with braf inhibitors |
| EP2828249B1 (en) * | 2012-03-23 | 2018-10-10 | The Regents of The University of California | Premature-termination-codons readthrough compounds |
| CN103755652B (zh) * | 2013-12-20 | 2015-08-05 | 陕西理工学院 | 一种磺酰胺类化合物及其应用 |
| CN104370844A (zh) * | 2014-10-29 | 2015-02-25 | 广西师范大学 | 3-硫酮-5-巯基甲基-1,2,4-三唑的合成方法 |
| CN106831529A (zh) * | 2016-12-11 | 2017-06-13 | 湖南华腾制药有限公司 | 一种三氟甲基吲哚衍生物的制备方法 |
| MX2019009419A (es) | 2017-02-08 | 2019-10-02 | Ono Pharmaceutical Co | Compuesto que tiene actividad agonista del receptor de somatostatina y uso farmaceutico del mismo. |
| EP3634406B1 (en) * | 2017-05-12 | 2023-09-06 | Board of Trustees of The Southern Illinois University on behalf of Southern Illinois University Edwardsville | 3,4,5-trisubstituted-1,2,4-triazoles and 3,4,5-trisubstituted-3-thio-1,2,4-triazoles and uses thereof |
| US11912687B2 (en) | 2017-05-12 | 2024-02-27 | Board of Trustees of the Southern Illinois University | 3,4,5-trisubstituted-1,2,4-triazoles and 3,4,5-trisubstituted-3-thio-1,2,4-triazoles and uses thereof |
| CN109666022B (zh) * | 2017-10-17 | 2021-06-15 | 中国科学院上海药物研究所 | 三氮唑衍生物及其制备方法和用途 |
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| EP0409332A3 (en) * | 1989-07-19 | 1991-08-07 | Merck & Co. Inc. | Substituted triazoles as angiotensin ii antagonists |
| US5177095A (en) * | 1990-02-13 | 1993-01-05 | Merck & Co., Inc. | Triazole angiotensin II antagonists incorporating a substituted benzyl element |
| GB2263635A (en) * | 1992-01-28 | 1993-08-04 | Merck & Co Inc | Substitiuted triazoles as neurotensin antagonists |
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| DE4425144A1 (de) * | 1994-07-15 | 1996-01-18 | Basf Ag | Triazolverbindungen und deren Verwendung |
| US6080772A (en) * | 1995-06-07 | 2000-06-27 | Sugen, Inc. | Thiazole compounds and methods of modulating signal transduction |
| DE19600934A1 (de) * | 1996-01-12 | 1997-07-17 | Basf Ag | Substituierte Aza- und Diazacycloheptan- und Cyclooctanverbindungen und deren Verwendung |
| WO1998056376A1 (en) * | 1997-06-13 | 1998-12-17 | Sugen, Inc. | Novel heteroaryl compounds for the modulation of protein tyrosine enzyme related cellular signal transduction |
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| FR2802206B1 (fr) * | 1999-12-14 | 2005-04-22 | Sod Conseils Rech Applic | Derives de 4-aminopiperidine et leur utilisation en tant que medicament |
| MXPA02011373A (es) * | 2000-05-19 | 2003-06-26 | Yamanouchi Pharma Co Ltd | Derivados de triazol. |
-
2002
- 2002-11-27 TW TW091134432A patent/TWI283670B/zh active
- 2002-11-27 AT AT02796876T patent/ATE438630T1/de not_active IP Right Cessation
- 2002-11-27 DE DE60233265T patent/DE60233265D1/de not_active Expired - Lifetime
- 2002-11-27 BR BR0214553-7A patent/BR0214553A/pt not_active IP Right Cessation
- 2002-11-27 PL PL02370140A patent/PL370140A1/xx not_active Application Discontinuation
- 2002-11-27 MX MXPA04005099A patent/MXPA04005099A/es active IP Right Grant
- 2002-11-27 KR KR1020047008002A patent/KR100961332B1/ko not_active Expired - Fee Related
- 2002-11-27 NZ NZ533397A patent/NZ533397A/en not_active IP Right Cessation
- 2002-11-27 AU AU2002361345A patent/AU2002361345B8/en not_active Ceased
- 2002-11-27 CZ CZ2004760A patent/CZ2004760A3/cs unknown
- 2002-11-27 US US10/496,820 patent/US20050154039A1/en not_active Abandoned
- 2002-11-27 CN CNB028276248A patent/CN100462359C/zh not_active Expired - Fee Related
- 2002-11-27 CA CA002468184A patent/CA2468184A1/fr not_active Abandoned
- 2002-11-27 JP JP2003547378A patent/JP2005513035A/ja active Pending
- 2002-11-27 MY MYPI20024450A patent/MY133406A/en unknown
- 2002-11-27 WO PCT/FR2002/004055 patent/WO2003045926A1/fr not_active Ceased
- 2002-11-27 ES ES02796876T patent/ES2330927T3/es not_active Expired - Lifetime
- 2002-11-27 EP EP02796876A patent/EP1465880B1/fr not_active Expired - Lifetime
- 2002-11-27 HU HU0402489A patent/HUP0402489A3/hu unknown
- 2002-11-27 RU RU2004119406/04A patent/RU2367655C2/ru not_active IP Right Cessation
- 2002-11-28 AR ARP020104601A patent/AR037465A1/es unknown
-
2004
- 2004-06-23 NO NO20042635A patent/NO20042635L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| ES2330927T3 (es) | 2009-12-17 |
| ATE438630T1 (de) | 2009-08-15 |
| DE60233265D1 (de) | 2009-09-17 |
| EP1465880B1 (fr) | 2009-08-05 |
| CN1617859A (zh) | 2005-05-18 |
| JP2005513035A (ja) | 2005-05-12 |
| NO20042635L (no) | 2004-06-23 |
| TW200300760A (en) | 2003-06-16 |
| AU2002361345B2 (en) | 2008-06-05 |
| RU2004119406A (ru) | 2005-05-10 |
| HUP0402489A2 (hu) | 2005-05-30 |
| PL370140A1 (en) | 2005-05-16 |
| CN100462359C (zh) | 2009-02-18 |
| HK1070361A1 (zh) | 2005-06-17 |
| NZ533397A (en) | 2005-12-23 |
| WO2003045926A1 (fr) | 2003-06-05 |
| MY133406A (en) | 2007-11-30 |
| US20050154039A1 (en) | 2005-07-14 |
| CA2468184A1 (fr) | 2003-06-05 |
| AU2002361345B8 (en) | 2008-06-26 |
| EP1465880A1 (fr) | 2004-10-13 |
| CZ2004760A3 (cs) | 2005-01-12 |
| TWI283670B (en) | 2007-07-11 |
| HUP0402489A3 (en) | 2009-09-28 |
| RU2367655C2 (ru) | 2009-09-20 |
| KR100961332B1 (ko) | 2010-06-04 |
| MXPA04005099A (es) | 2004-08-19 |
| BR0214553A (pt) | 2004-10-13 |
| AU2002361345A1 (en) | 2003-06-10 |
| KR20040062969A (ko) | 2004-07-09 |
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