MX350891B - Proceso para la preparacion de (2z,5z)-5-(3-cloro-4-((r)-2,3-dihid roxipropoxi) bencilideno)-2-(propilimino)-3-(o-tolil) tiazolidin-4-ona y el intermediario usado en dicho proceso. - Google Patents
Proceso para la preparacion de (2z,5z)-5-(3-cloro-4-((r)-2,3-dihid roxipropoxi) bencilideno)-2-(propilimino)-3-(o-tolil) tiazolidin-4-ona y el intermediario usado en dicho proceso.Info
- Publication number
- MX350891B MX350891B MX2015002127A MX2015002127A MX350891B MX 350891 B MX350891 B MX 350891B MX 2015002127 A MX2015002127 A MX 2015002127A MX 2015002127 A MX2015002127 A MX 2015002127A MX 350891 B MX350891 B MX 350891B
- Authority
- MX
- Mexico
- Prior art keywords
- chloro
- propylimino
- tolyl
- preparation
- benzylidene
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/70—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form
- C07C45/71—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction with functional groups containing oxygen only in singly bound form being hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
- C07D277/54—Nitrogen and either oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/64—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/77—Preparation of chelates of aldehydes or ketones
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/78—Separation; Purification; Stabilisation; Use of additives
- C07C45/81—Separation; Purification; Stabilisation; Use of additives by change in the physical state, e.g. crystallisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/52—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings
- C07C47/575—Compounds having —CHO groups bound to carbon atoms of six—membered aromatic rings containing ether groups, groups, groups, or groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/13—Crystalline forms, e.g. polymorphs
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Crystallography & Structural Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
La presente invención se refiere a un nuevo proceso para la preparación de (2Z,5Z)-5-(3-cloro-4-((R)-2,3-dihidroxipropoxi)benc ilideno)-2-(propilimino)-3-(o-tolil)tiazolidin-4-ona y al nuevo intermediario (R)-3-cloro-4-(2,3-dihidroxipropoxi)-benzaldehído usado en este proceso. (2Z,5Z)-5-(3-cloro-4-((R)-2,3-dihidroxiprop oxi)bencilideno)-2-(propilimino)-3-(o-tolil)tiazolidin-4-ona se describe en el documento WO 2005/054215 que actúa como un agente inmunosupresivo. La presente invención además también se relaciona con un nuevo proceso para la preparación de (R)-3-cloro-4-(2,3-dihidroxipropoxi)-benzaldehído.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP12180920 | 2012-08-17 | ||
PCT/IB2013/056662 WO2014027330A1 (en) | 2012-08-17 | 2013-08-15 | Process for the preparation of|(2z,5z)-5-(3-chloro-4-((r)-2,3-dihydroxypropoxy)benzylidene)-2-(propylimino)-3-|(o-tolyl)thiazolidin-4-one and intermediate used in said process |
Publications (2)
Publication Number | Publication Date |
---|---|
MX2015002127A MX2015002127A (es) | 2015-05-11 |
MX350891B true MX350891B (es) | 2017-09-22 |
Family
ID=46940231
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX2015002127A MX350891B (es) | 2012-08-17 | 2013-08-15 | Proceso para la preparacion de (2z,5z)-5-(3-cloro-4-((r)-2,3-dihid roxipropoxi) bencilideno)-2-(propilimino)-3-(o-tolil) tiazolidin-4-ona y el intermediario usado en dicho proceso. |
Country Status (20)
Country | Link |
---|---|
US (1) | US9340518B2 (es) |
EP (1) | EP2885266B1 (es) |
JP (2) | JP6322630B2 (es) |
KR (1) | KR101731739B1 (es) |
CN (1) | CN104540800B (es) |
CA (1) | CA2895172C (es) |
CY (1) | CY1123300T1 (es) |
DK (1) | DK2885266T3 (es) |
ES (1) | ES2795105T3 (es) |
HR (1) | HRP20200883T1 (es) |
HU (1) | HUE050733T2 (es) |
IL (1) | IL237198A (es) |
LT (1) | LT2885266T (es) |
MX (1) | MX350891B (es) |
PL (1) | PL2885266T3 (es) |
PT (1) | PT2885266T (es) |
RS (1) | RS60408B1 (es) |
SI (1) | SI2885266T1 (es) |
TW (1) | TWI606036B (es) |
WO (1) | WO2014027330A1 (es) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2617628T5 (es) | 2008-03-17 | 2020-06-01 | Actelion Pharmaceuticals Ltd | Régimen de dosificación para un agonista selectivo del receptor de S1P1 |
JP6322630B2 (ja) * | 2012-08-17 | 2018-05-09 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | (2Z,5Z)−5−(3−クロロ−4−((R)−2,3−ジヒドロキシプロポキシ)ベンジリデン)−2−(プロピルイミノ)−3−(o−トリル)チアゾリジン−4−オンの製造方法及び前記方法において使用される中間体 |
MA41139A (fr) | 2014-12-11 | 2017-10-17 | Actelion Pharmaceuticals Ltd | Combinaison pharmaceutique comportant un agoniste sélectif du récepteur sip1 |
MY188764A (en) | 2014-12-11 | 2021-12-30 | Actelion Pharmaceuticals Ltd | Dosing regimen for a selective s1p1 receptor agonist |
CA3009713A1 (en) * | 2015-12-25 | 2017-06-29 | Crystal Pharmatech Co., Ltd. | Crystalline forms of ponesimod and preparation method thereof |
JOP20190207A1 (ar) | 2017-03-14 | 2019-09-10 | Actelion Pharmaceuticals Ltd | تركيبة صيدلانية تشتمل على بونيسيمود |
US11220488B2 (en) | 2017-09-19 | 2022-01-11 | Teva Pharmaceuticals International Gmbh | Crystalline polymorph of Ponesimod |
US11186556B1 (en) | 2018-10-16 | 2021-11-30 | Celgene Corporation | Salts of a thiazolidinone compound, solid forms, compositions and methods of use thereof |
US11014940B1 (en) | 2018-10-16 | 2021-05-25 | Celgene Corporation | Thiazolidinone and oxazolidinone compounds and formulations |
US11013723B1 (en) | 2018-10-16 | 2021-05-25 | Celgene Corporation | Solid forms of a thiazolidinone compound, compositions and methods of use thereof |
US11014897B1 (en) | 2018-10-16 | 2021-05-25 | Celgene Corporation | Solid forms comprising a thiazolidinone compound, compositions and methods of use thereof |
KR102365655B1 (ko) | 2018-11-29 | 2022-02-22 | 원광대학교 산학협력단 | 콩 발효 추출물을 유효성분으로 포함하는 피부 주름 예방 또는 개선용 조성물 |
AU2020372647A1 (en) | 2019-10-31 | 2022-06-16 | Idorsia Pharmaceuticals Ltd | Combination of a CXCR7 antagonist with an S1P1 receptor modulator |
WO2023022896A1 (en) | 2021-08-17 | 2023-02-23 | Teva Czech Industries S.R.O | Polymorphs of ponesimod |
EP4212156A1 (en) | 2022-01-13 | 2023-07-19 | Abivax | Combination of 8-chloro-n-(4-(trifluoromethoxy)phenyl)quinolin-2-amine and its derivatives with a s1p receptor modulator |
WO2023152691A1 (en) * | 2022-02-10 | 2023-08-17 | Metrochem Api Pvt Ltd | Process for the preparation of ponesimod and its intermediates thereof |
Family Cites Families (47)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3077402A (en) | 1954-12-06 | 1963-02-12 | Polaroid Corp | Photographic color processes, products, and compositions |
NL270002A (es) | 1960-10-08 | |||
GB1001479A (en) | 1962-10-10 | 1965-08-18 | Angeli Inst Spa | Glycerol ethers |
OA03835A (fr) | 1970-07-17 | 1971-12-24 | Rhone Poulenc Sa | Nouveaux dérivés de la thiazolidine, leur préparation et les compositions qui les contiennent. |
DE69123738T2 (de) | 1990-04-27 | 1997-07-03 | Orion Yhtymae Oy | Pharmakologisch aktive catecholderivate |
TW221689B (es) | 1991-08-27 | 1994-03-11 | Otsuka Pharma Co Ltd | |
CN1037842C (zh) | 1993-02-26 | 1998-03-25 | 大制药株式会社 | 取代的噻唑烷衍生物及其药物组合物和用途 |
KR960022486A (ko) | 1994-12-29 | 1996-07-18 | 김준웅 | 신규 티아졸리딘-4-온 유도체 |
US6353006B1 (en) | 1999-01-14 | 2002-03-05 | Bayer Corporation | Substituted 2-arylimino heterocycles and compositions containing them, for use as progesterone receptor binding agents |
ATE393150T1 (de) | 1999-09-14 | 2008-05-15 | Shionogi & Co | 2-imino-1,3-thiazin-derivate |
DK1142885T3 (da) | 1999-11-12 | 2007-02-26 | Fujimoto Brothers Co Ltd | 2-(N-cyanoimino)thiazolidin-4-on-derivater |
US20050019825A9 (en) | 2002-03-15 | 2005-01-27 | Qing Dong | Common ligand mimics: pseudothiohydantoins |
CA2493843C (en) | 2002-07-10 | 2012-04-17 | Applied Research Systems Ars Holding N.V. | Azolidinone-vinyl fused-benzene derivatives |
GB0217152D0 (en) | 2002-07-24 | 2002-09-04 | Novartis Ag | Organic compounds |
AU2003261434A1 (en) | 2002-08-12 | 2004-02-25 | Bristol-Myers Squibb Company | Iminothiazolidinones as inhibitors of hcv replication |
NZ539873A (en) | 2002-11-22 | 2008-09-26 | Smithkline Beecham Corp | Novel chemical compounds, thiazolidin-4-one, thiazol-4-one |
US20040167192A1 (en) | 2003-01-16 | 2004-08-26 | David Solow-Cordero | Methods of treating conditions associated with an Edg-7 receptor |
JP2007510136A (ja) | 2003-10-06 | 2007-04-19 | ソルヴィーアス アクチェンゲゼルシャフト | 分子状固体の結晶形態を並行検出する方法 |
USRE43833E1 (en) | 2003-11-21 | 2012-11-27 | Actelion Pharmaceuticals Ltd. | Thiazolidin-4-one derivatives |
ES2352555T3 (es) | 2003-11-21 | 2011-02-21 | Actelion Pharmaceuticals Ltd. | Derivados de 5-(benc-(z)-iliden)tiazolidin-4-ona como agentes inmunosupresores. |
EP1718642A4 (en) | 2004-02-25 | 2010-11-24 | Glaxosmithkline Llc | NEW CHEMICAL COMPOUNDS |
WO2005123677A1 (en) | 2004-06-16 | 2005-12-29 | Actelion Pharmaceuticals Ltd | 4-carbonyl substituted 1,1,2-trimethyl-1a,4,5,5a-tetrahydro-1h-4-aza-cyclopropa'a!pentalene derivatives as agonists for the g-protein-coupled receptor s1p1/edg1 and immunosuppressive agents |
WO2006010379A1 (en) | 2004-07-29 | 2006-02-02 | Actelion Pharmaceuticals Ltd. | Novel thiophene derivatives as immunosuppressive agents |
RU2478384C2 (ru) | 2004-11-29 | 2013-04-10 | Новартис Аг | Курс лечения с использованием агониста рецептора s1p |
WO2006094233A1 (en) | 2005-03-03 | 2006-09-08 | Sirtris Pharmaceuticals, Inc. | N,n'-dicyclic isothiourea sirtuin modulators |
AU2006226020A1 (en) | 2005-03-23 | 2006-09-28 | Actelion Pharmaceuticals Ltd. | Novel thiophene derivatives as sphingosine-l-phosphate-1 receptor agonists |
CN101180050B (zh) | 2005-03-23 | 2011-07-27 | 埃科特莱茵药品有限公司 | 作为鞘氨醇-1-磷酸盐-1受体激动剂的新颖噻吩衍生物 |
ES2365747T3 (es) | 2005-03-23 | 2011-10-10 | Actelion Pharmaceuticals Ltd. | Derivados de benzo[c]tiofeno hidrogenados como inmunomoduladores. |
JP2008546758A (ja) * | 2005-06-24 | 2008-12-25 | アクテリオン ファーマシューティカルズ リミテッド | 新規チオフェン誘導体 |
AR057894A1 (es) | 2005-11-23 | 2007-12-26 | Actelion Pharmaceuticals Ltd | Derivados de tiofeno |
TWI404706B (zh) | 2006-01-11 | 2013-08-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
ATE447568T1 (de) | 2006-01-24 | 2009-11-15 | Actelion Pharmaceuticals Ltd | Neue pyrinderivate |
US7879821B2 (en) | 2006-01-26 | 2011-02-01 | University Of Medicine And Dentistry Of New Jersey | Method for modulating inflammatory responses by altering plasma lipid levels |
TWI408139B (zh) | 2006-09-07 | 2013-09-11 | Actelion Pharmaceuticals Ltd | 新穎噻吩衍生物 |
JP5253401B2 (ja) | 2006-09-07 | 2013-07-31 | アクテリオン ファーマシューティカルズ リミテッド | 免疫調節薬としてのピリジン−4−イル誘導体 |
NZ576059A (en) | 2006-09-08 | 2012-03-30 | Actelion Pharmaceuticals Ltd | Pyridin-3-yl derivatives as immunomodulating agents |
WO2008035239A1 (en) | 2006-09-21 | 2008-03-27 | Actelion Pharmaceuticals Ltd | Phenyl derivatives and their use as immunomodulators |
US8912340B2 (en) | 2006-11-23 | 2014-12-16 | Actelion Pharmaceuticals Ltd. | Process for the preparation of 2-imino-thiazolidin-4-one derivatives |
EP2094676B1 (en) | 2006-11-23 | 2013-04-10 | Actelion Pharmaceuticals Ltd. | New process for the preparation of 2-iminothiazolidin-4-one derivatives |
NZ580454A (en) | 2007-03-16 | 2011-05-27 | Actelion Pharmaceuticals Ltd | Amino- pyridine derivatives as s1p1 /edg1 receptor agonists |
SI2195311T1 (sl) | 2007-08-17 | 2011-07-29 | Actelion Pharmaceuticals Ltd | Derivati piridina kot modulatorji receptorja s1p1/edg1 |
ES2617628T5 (es) | 2008-03-17 | 2020-06-01 | Actelion Pharmaceuticals Ltd | Régimen de dosificación para un agonista selectivo del receptor de S1P1 |
GB0819182D0 (en) | 2008-10-20 | 2008-11-26 | Actelion Pharmaceuticals Ltd | Crystalline forms |
US20100160369A1 (en) | 2008-12-04 | 2010-06-24 | Exelixis, Inc. | S1P1 Agonists and Methods of Making And Using |
LT3409274T (lt) | 2008-12-22 | 2020-02-10 | Novartis Ag | Dozavimo schema s1p receptoriaus agonistui |
AR074825A1 (es) | 2008-12-22 | 2011-02-16 | Novartis Ag | Regimen de dosificacion de un agonista de los receptores de s1p, metodo de tratamiento y kit |
JP6322630B2 (ja) * | 2012-08-17 | 2018-05-09 | アクテリオン ファーマシューティカルズ リミテッドActelion Pharmaceuticals Ltd | (2Z,5Z)−5−(3−クロロ−4−((R)−2,3−ジヒドロキシプロポキシ)ベンジリデン)−2−(プロピルイミノ)−3−(o−トリル)チアゾリジン−4−オンの製造方法及び前記方法において使用される中間体 |
-
2013
- 2013-08-15 JP JP2015527061A patent/JP6322630B2/ja active Active
- 2013-08-15 PT PT137793782T patent/PT2885266T/pt unknown
- 2013-08-15 HU HUE13779378A patent/HUE050733T2/hu unknown
- 2013-08-15 MX MX2015002127A patent/MX350891B/es active IP Right Grant
- 2013-08-15 DK DK13779378.2T patent/DK2885266T3/da active
- 2013-08-15 EP EP13779378.2A patent/EP2885266B1/en active Active
- 2013-08-15 PL PL13779378T patent/PL2885266T3/pl unknown
- 2013-08-15 ES ES13779378T patent/ES2795105T3/es active Active
- 2013-08-15 WO PCT/IB2013/056662 patent/WO2014027330A1/en active Application Filing
- 2013-08-15 RS RS20200642A patent/RS60408B1/sr unknown
- 2013-08-15 KR KR1020157006474A patent/KR101731739B1/ko active IP Right Grant
- 2013-08-15 US US14/422,167 patent/US9340518B2/en active Active
- 2013-08-15 CN CN201380042658.2A patent/CN104540800B/zh active Active
- 2013-08-15 CA CA2895172A patent/CA2895172C/en active Active
- 2013-08-15 SI SI201331742T patent/SI2885266T1/sl unknown
- 2013-08-15 LT LTEP13779378.2T patent/LT2885266T/lt unknown
- 2013-08-16 TW TW102129570A patent/TWI606036B/zh active
-
2015
- 2015-02-12 IL IL237198A patent/IL237198A/en active IP Right Grant
-
2017
- 2017-04-13 JP JP2017079804A patent/JP6424250B2/ja active Active
-
2020
- 2020-06-02 HR HRP20200883TT patent/HRP20200883T1/hr unknown
- 2020-06-11 CY CY20201100532T patent/CY1123300T1/el unknown
Also Published As
Publication number | Publication date |
---|---|
PT2885266T (pt) | 2020-05-29 |
MX2015002127A (es) | 2015-05-11 |
IL237198A0 (en) | 2015-04-30 |
CA2895172A1 (en) | 2014-02-20 |
ES2795105T3 (es) | 2020-11-20 |
TWI606036B (zh) | 2017-11-21 |
HRP20200883T1 (hr) | 2020-09-04 |
TW201408634A (zh) | 2014-03-01 |
JP2015530373A (ja) | 2015-10-15 |
CA2895172C (en) | 2020-08-18 |
LT2885266T (lt) | 2020-07-10 |
RS60408B1 (sr) | 2020-07-31 |
WO2014027330A1 (en) | 2014-02-20 |
JP6424250B2 (ja) | 2018-11-14 |
JP2017160223A (ja) | 2017-09-14 |
JP6322630B2 (ja) | 2018-05-09 |
KR20150042277A (ko) | 2015-04-20 |
CY1123300T1 (el) | 2021-12-31 |
US9340518B2 (en) | 2016-05-17 |
PL2885266T3 (pl) | 2020-11-16 |
EP2885266B1 (en) | 2020-03-18 |
CN104540800A (zh) | 2015-04-22 |
EP2885266A1 (en) | 2015-06-24 |
SI2885266T1 (sl) | 2020-10-30 |
HUE050733T2 (hu) | 2021-01-28 |
US20150203459A1 (en) | 2015-07-23 |
KR101731739B1 (ko) | 2017-05-11 |
DK2885266T3 (da) | 2020-06-08 |
IL237198A (en) | 2017-12-31 |
CN104540800B (zh) | 2017-05-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
MX350891B (es) | Proceso para la preparacion de (2z,5z)-5-(3-cloro-4-((r)-2,3-dihid roxipropoxi) bencilideno)-2-(propilimino)-3-(o-tolil) tiazolidin-4-ona y el intermediario usado en dicho proceso. | |
IL260297A (en) | Process for preparing n-[5-(5,3-difluoro-benzyl)-h1-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino )–benzamide | |
MY155317A (en) | Benzene sulfonamide thiazole and oxazole compounds | |
NI201500142A (es) | Derivados de 3-acetilamino-1 (fenil-heteroaril-aminocarbonil o fenil-heteroaril-carbonilamino) benceno para el tratamiento de desordenes hiperproliferativos. | |
NZ734516A (en) | Pharmaceutical compositions comprising n-(3,5-dimethoxyphenyl)-n’-(1-methylethyl)-n-[3-(1-methyl-1h-pyrazol-4-yl)quinoxalin-6-yl]ethane-1,2-diamine | |
CO7101245A2 (es) | Compuestos de benzaldehído sustituidos y métodos para su uso en incrementar la oxigenación del tejido | |
CR20210108A (es) | Benzamidas sustituidas con 1, 3-tiazol-2-ilo | |
MX370099B (es) | Combinación que comprende un inhibidor de fgfr y un inhibidor de cmet para el tratamiento del cáncer. | |
GB201212081D0 (en) | New polymorph | |
EP3292119A4 (en) | DIHYDRO-2H-BENZO[b][1,4]OXAZINE SULFONAMIDE AND RELATED COMPOUNDS FOR USE AS AGONISTS OF RORy AND THE TREATMENT OF DISEASE | |
CL2013000488A1 (es) | Co-cristales de compuestos derivados de (2r)-5-oxo-1-(bencilpiperidin-4-il)-n-(piridin-2-il)pirrolidin-2-carboxamida y un agente de formacion de co-cristales; sales de los compuestos; compuestos intermediarios; composicion farmaceutica; y su uso para el tratamiento de enfermedades inflamatorias e infecciosas. | |
CL2011001405A1 (es) | Procedimiento para la preparacion de n-[2-(7-metoxi-1-naftil)etil]acetamida, agometalina. | |
CL2013001643A1 (es) | Composicion farmaceutica que comprende: 1)n-[(2s)-2,3-dihidroxipropil]-3-(2-fluoro-4-iodoanilino)piridin-4-carboxamida y 2a)2-amino-n-[3-[[3-(2-cloro-5-metoxianilin)quinoxalin-2-yl]sulfamoil]fenil]-2-metilpropanamida o 2b) 2-amino-8-etil-4-metil-6-(1h-pirazol-5-il)pirido[2,3-d]pirimidin-7-ona ; su uso para el tratamiento del cancer; un kit | |
CL2012000097A1 (es) | Compuestos derivados de 3-fenoximetilpirrolidina, inhibidores de la recaptacion de serotonina-norepinefrina; procedimiento de preparacion; compuestos intermediarios; composicion farmaceutica que lo comprende; y su uso en el tratamiento de trastornos del dolor, depresion, entre otros. | |
CL2022000492A1 (es) | Proceso para la preparación de estetrol de alta pureza. | |
EA201401341A1 (ru) | Твердые формы n-((s)-2,3-дигидроксипропил)-3-(2-фтор-4-йодфениламино)изоникотинамида | |
CL2009001112A1 (es) | Compuestos derivados de cinolin-3-carboxamida, inhibidores de la quinasa csf-1r; procedimiento de preparacion; composicion farmaceutica; y uso para el tratamiento del cancer. | |
IL286834A (en) | Crystal form of nitro tetramethylpyrazine, method of preparation and use thereof | |
WO2012117334A8 (en) | Mglur5 positive allosteric modulators for use in the treatment of phelan-mcdermid syndrome | |
IL272034B (en) | Process for preparing n-((1r, 2s, 5r)-5-(tert-butylamino)-2-((s)-3-(7-tert-butylpyrazolo[1,a-5][1, 3, 5) Triazine-4-ylamino)-2-oxopyrrolidin-1-yl)cyclohexyl)acetamide | |
CL2009000496A1 (es) | Formas cristalina tipo iii de (3,5-bis trifluorometil)-n-[4-metil-3-(4-piridin-3-il)-pirimidin-2-ilamino)-fenil]-benzamida; proceso de preparacion de la forma cristalina iii; composion farmaceutica que compende la forma cristalina iii; y su uso como agente antitumoral. | |
AU2020901514A0 (en) | Use of aminoacetonitrile compounds for the treatment of disease | |
CL2016003357A1 (es) | Un nuevo uso de la molecula 2-octahidroisoquinolin-2(1h)-eletanamina. | |
AR106542A1 (es) | Inhibidor del receptor p2x7 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant or registration |