AR079015A1 - Acidos 3-fenilpropionicos sustituidos, metodo de preparacion y uso de los mismos - Google Patents
Acidos 3-fenilpropionicos sustituidos, metodo de preparacion y uso de los mismosInfo
- Publication number
- AR079015A1 AR079015A1 ARP100103934A ARP100103934A AR079015A1 AR 079015 A1 AR079015 A1 AR 079015A1 AR P100103934 A ARP100103934 A AR P100103934A AR P100103934 A ARP100103934 A AR P100103934A AR 079015 A1 AR079015 A1 AR 079015A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- formula
- represents hydrogen
- trifluoromethyl
- fluorine
- Prior art date
Links
- 239000002253 acid Substances 0.000 title abstract 3
- 238000000034 method Methods 0.000 title abstract 3
- 150000007513 acids Chemical class 0.000 title 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 8
- 239000001257 hydrogen Substances 0.000 abstract 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 7
- 229910052731 fluorine Inorganic materials 0.000 abstract 7
- 239000011737 fluorine Chemical group 0.000 abstract 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 6
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 4
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 239000012453 solvate Substances 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 3
- 125000004432 carbon atom Chemical group C* 0.000 abstract 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 3
- 229910052801 chlorine Inorganic materials 0.000 abstract 3
- 239000000460 chlorine Chemical group 0.000 abstract 3
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 abstract 3
- 125000006002 1,1-difluoroethyl group Chemical group 0.000 abstract 2
- 125000004206 2,2,2-trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- -1 cyano, methyl Chemical group 0.000 abstract 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- 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 abstract 1
- 206010002383 Angina Pectoris Diseases 0.000 abstract 1
- 206010003210 Arteriosclerosis Diseases 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 206010019280 Heart failures Diseases 0.000 abstract 1
- 206010020772 Hypertension Diseases 0.000 abstract 1
- 208000001435 Thromboembolism Diseases 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 230000004075 alteration Effects 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 208000011775 arteriosclerosis disease Diseases 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 150000002148 esters Chemical group 0.000 abstract 1
- 238000007327 hydrogenolysis reaction Methods 0.000 abstract 1
- 239000012442 inert solvent Substances 0.000 abstract 1
- 208000028867 ischemia Diseases 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 230000004089 microcirculation Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 208000002815 pulmonary hypertension Diseases 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 238000003797 solvolysis reaction Methods 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 208000019553 vascular disease Diseases 0.000 abstract 1
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- A61K31/195—Carboxylic acids, e.g. valproic acid having an amino group
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| DE102008018675A1 (de) | 2008-04-14 | 2009-10-15 | Bayer Schering Pharma Aktiengesellschaft | Oxo-heterocyclisch substituierte Carbonsäure-Derivate und ihre Verwendung |
| DE102009012314A1 (de) * | 2009-03-09 | 2010-09-16 | Bayer Schering Pharma Aktiengesellschaft | Oxo-heterocyclisch substituierte Alkylcarbonsäuren und ihre Verwendung |
| DE102009046115A1 (de) | 2009-10-28 | 2011-09-08 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 3-Phenylpropansäuren und ihre Verwendung |
| EP2549875B1 (en) | 2010-03-25 | 2015-05-13 | Merck Sharp & Dohme Corp. | Soluble guanylate cyclase activators |
| MA34330B1 (fr) | 2010-05-27 | 2013-06-01 | Merck Sharp & Dohme | Activateurs de guanylate cyclase soluble |
| EP2632551B1 (en) | 2010-10-28 | 2016-07-06 | Merck Sharp & Dohme Corp. | Soluble guanylate cyclase activators |
| ES2544532T3 (es) | 2010-12-07 | 2015-09-01 | Bayer Intellectual Property Gmbh | Ácidos 1-bencilcicloalquilcarboxílicos sustituidos y su uso |
| DE102011007272A1 (de) * | 2011-04-13 | 2012-10-18 | Bayer Pharma Aktiengesellschaft | Verzweigte 3-Phenylpropionsäure-Derivate und ihre Verwendung |
| NZ631569A (en) * | 2012-02-28 | 2016-10-28 | Piramal Entpr Ltd | Phenyl alkanoic acid derivatives as gpr agonists |
| DE102012208530A1 (de) | 2012-05-22 | 2013-11-28 | Bayer Pharma AG | Substituierte Piperidinoacetamide und ihre Verwendung |
| TWI594975B (zh) * | 2013-04-24 | 2017-08-11 | 第一三共股份有限公司 | 二羧酸化合物 |
| TW201625584A (zh) | 2014-07-02 | 2016-07-16 | 諾華公司 | 茚滿及吲哚啉衍生物及其作為可溶性鳥苷酸環化酶活化劑之用途 |
| TW201625601A (zh) | 2014-07-02 | 2016-07-16 | 諾華公司 | 噻吩-2-基-吡啶-2-基-1h-吡唑-4-羧酸衍生物及其作為可溶性鳥苷酸環化酶活化劑之用途 |
| TW201625586A (zh) | 2014-07-02 | 2016-07-16 | 諾華公司 | 環己烯-1-基-吡啶-2-基-1h-吡唑-4-羧酸衍生物及其作為可溶性鳥苷酸環化酶活化劑之用途 |
| US20170327457A1 (en) | 2014-09-09 | 2017-11-16 | Bristol-Myers Squibb Company | Phenyl-(aza)cycloalkyl carboxylic acid gpr120 modulators |
| JP6742316B2 (ja) * | 2014-09-09 | 2020-08-19 | ベーリンガー インゲルハイム インターナショナル トレイディング (シャンハイ) カンパニー リミテッド | スピロ[2.5]オクタン−5,7−ジオンおよびスピロ[3.5]ノナン−6,8−ジオンの調製のための新規なプロセス |
| CA2962724C (en) | 2014-09-26 | 2019-11-19 | Daiichi Sankyo Company, Limited | Salt of dicarboxylic acid compound |
| WO2016058881A2 (en) | 2014-10-14 | 2016-04-21 | Syngenta Participations Ag | Process for the preparation of halo-substituted benzenes |
| EP3233802A1 (en) * | 2014-12-18 | 2017-10-25 | Bayer Pharma Aktiengesellschaft | Substituted pyridyl-cycloalkyl-carboxylic acids, compositions containing them and medical uses thereof |
| MX2017014057A (es) | 2015-05-06 | 2018-04-10 | Bayer Pharma AG | El uso de estimuladores sgc, activadores gc, solos y combinaciones con inhibidores pde5 para el tratamiento de ulceras digitales (du) concomitante con esclerosis sistemica (ssc). |
| SI3325013T2 (sl) | 2015-07-23 | 2023-11-30 | Bayer Pharma Aktiengesellschaft | Stimulatorji/aktivatorji topne gvanilat ciklaze v kombinaciji z zaviralcem NEP in/ali antagonistom angiotenzina II in njihova uporaba |
| EP3525778A1 (de) | 2016-10-11 | 2019-08-21 | Bayer Pharma Aktiengesellschaft | Kombination enthaltend sgc aktivatoren und mineralocorticoid-rezeptor-antagonisten |
| CN106565637A (zh) * | 2016-11-04 | 2017-04-19 | 天津雅奥科技发展有限公司 | 一种3‑氧杂环丁烷乙酸的合成方法 |
| WO2019081456A1 (en) | 2017-10-24 | 2019-05-02 | Bayer Aktiengesellschaft | USE OF SGC ACTIVATORS AND STIMULATORS COMPRISING A BETA2 SUBUNIT |
| SG11202004577VA (en) * | 2017-12-01 | 2020-06-29 | Bayer Pharma AG | Method for producing (3s)-3-(4-chlor-3-{[(2s,3r)-2-(4-chlorphenyl)-4,4,4-trifluor-3-methylbutanoyl]amino}phenyl)-3-cyclo-propylpropanoic acid and the crystalline form thereof for use as a pharmaceutical ingredient |
| EP3498298A1 (en) | 2017-12-15 | 2019-06-19 | Bayer AG | The use of sgc stimulators and sgc activators alone or in combination with pde5 inhibitors for the treatment of bone disorders including osteogenesis imperfecta (oi) |
| EP3787610A1 (en) | 2018-04-30 | 2021-03-10 | Bayer Aktiengesellschaft | The use of sgc activators and sgc stimulators for the treatment of cognitive impairment |
| CN112384213A (zh) | 2018-05-15 | 2021-02-19 | 拜耳公司 | 用于治疗与神经纤维敏化有关的疾病的1,3-噻唑-2-基取代的苯甲酰胺 |
| US11508483B2 (en) | 2018-05-30 | 2022-11-22 | Adverio Pharma Gmbh | Method of identifying a subgroup of patients suffering from dcSSc which benefits from a treatment with sGC stimulators and sGC activators in a higher degree than a control group |
| US10905667B2 (en) | 2018-07-24 | 2021-02-02 | Bayer Pharma Aktiengesellschaft | Orally administrable modified-release pharmaceutical dosage form |
| US20220128561A1 (en) | 2019-01-17 | 2022-04-28 | Bayer Aktiengesellschaft | Methods to determine whether a subject is suitable of being treated with an agonist of soluble gyanylyl cyclase (sgc) |
| WO2020164008A1 (en) | 2019-02-13 | 2020-08-20 | Bayer Aktiengesellschaft | Process for the preparation of porous microparticles |
| CN113866282A (zh) * | 2020-06-30 | 2021-12-31 | 天津药业研究院股份有限公司 | 3-卤代-7-(4-溴苯甲酰基)-1氢-吲哚中异构体杂质的分离检测方法及应用 |
| WO2022237797A1 (zh) * | 2021-05-14 | 2022-11-17 | 南京明德新药研发有限公司 | 烷基羧酸化合物及其应用 |
| CN117460713A (zh) * | 2021-07-15 | 2024-01-26 | 江苏恒瑞医药股份有限公司 | 3-苯基丙酸类化合物、其制备方法及其在医药上的应用 |
| WO2023155873A1 (zh) * | 2022-02-18 | 2023-08-24 | 江苏恒瑞医药股份有限公司 | 羧酸类化合物、其制备方法及其在医药上的应用 |
| EP4536205A1 (en) | 2022-06-09 | 2025-04-16 | Bayer Aktiengesellschaft | Soluble guanylate cyclase activators for use in the treatment of heart failure with preserved ejection fraction in women |
| WO2024099361A1 (zh) * | 2022-11-08 | 2024-05-16 | 南京明德新药研发有限公司 | 一种烷基羧酸类化合物的晶型及其应用 |
| CN115850102A (zh) * | 2022-12-29 | 2023-03-28 | 浙江工业大学 | 一种奥司他韦的制备方法 |
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| DE102009012314A1 (de) * | 2009-03-09 | 2010-09-16 | Bayer Schering Pharma Aktiengesellschaft | Oxo-heterocyclisch substituierte Alkylcarbonsäuren und ihre Verwendung |
| DE102009046115A1 (de) | 2009-10-28 | 2011-09-08 | Bayer Schering Pharma Aktiengesellschaft | Substituierte 3-Phenylpropansäuren und ihre Verwendung |
| ES2544532T3 (es) | 2010-12-07 | 2015-09-01 | Bayer Intellectual Property Gmbh | Ácidos 1-bencilcicloalquilcarboxílicos sustituidos y su uso |
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| EP2493845B1 (de) | 2013-12-25 |
| TW201127373A (en) | 2011-08-16 |
| PT2493845E (pt) | 2014-02-24 |
| BR112012010057A2 (pt) | 2019-09-24 |
| TWI487519B (zh) | 2015-06-11 |
| CA2777152C (en) | 2017-09-19 |
| IL218989A (en) | 2015-10-29 |
| US20140142069A1 (en) | 2014-05-22 |
| PL2493845T3 (pl) | 2014-05-30 |
| US20110130445A1 (en) | 2011-06-02 |
| JP2013509369A (ja) | 2013-03-14 |
| WO2011051165A1 (de) | 2011-05-05 |
| IL218989A0 (en) | 2012-06-28 |
| HK1177195A1 (en) | 2013-08-16 |
| MX2012004951A (es) | 2012-06-13 |
| AU2010311678B2 (en) | 2015-09-03 |
| JP5801312B2 (ja) | 2015-10-28 |
| CN102712577B (zh) | 2014-10-15 |
| CA2777152A1 (en) | 2011-05-05 |
| DK2493845T3 (en) | 2014-03-24 |
| UY32970A (es) | 2011-05-31 |
| EP2493845A1 (de) | 2012-09-05 |
| CN102712577A (zh) | 2012-10-03 |
| RU2553263C2 (ru) | 2015-06-10 |
| ES2446970T3 (es) | 2014-03-11 |
| US9018414B2 (en) | 2015-04-28 |
| RU2012121577A (ru) | 2013-12-10 |
| AU2010311678A1 (en) | 2012-05-17 |
| ZA201202465B (en) | 2013-08-28 |
| HRP20140270T1 (hr) | 2014-04-25 |
| KR20120101411A (ko) | 2012-09-13 |
| DE102009046115A1 (de) | 2011-09-08 |
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