CL2010000973A1 - Procedimiento de preparacion de la sal de clorhidrato de ester metilico del acido (e)-3-(4-{[2-(2-metil-1h-indol-3-il)etilamino]metil}fenil)-acrilico por combinacion de 2-metiltriptamina y el ester metilico del acido (e)-3-(4-formil-fenil)-acrilico, y posterior reduccion de la imina formada ( divisional de la sol. n° 1691-2007). - Google Patents
Procedimiento de preparacion de la sal de clorhidrato de ester metilico del acido (e)-3-(4-{[2-(2-metil-1h-indol-3-il)etilamino]metil}fenil)-acrilico por combinacion de 2-metiltriptamina y el ester metilico del acido (e)-3-(4-formil-fenil)-acrilico, y posterior reduccion de la imina formada ( divisional de la sol. n° 1691-2007).Info
- Publication number
- CL2010000973A1 CL2010000973A1 CL2010000973A CL2010000973A CL2010000973A1 CL 2010000973 A1 CL2010000973 A1 CL 2010000973A1 CL 2010000973 A CL2010000973 A CL 2010000973A CL 2010000973 A CL2010000973 A CL 2010000973A CL 2010000973 A1 CL2010000973 A1 CL 2010000973A1
- Authority
- CL
- Chile
- Prior art keywords
- methyl
- phenyl
- acrylic
- acid
- methyl ester
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/16—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
- C07D209/16—Tryptamines
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/10—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
- C07D207/14—Nitrogen atoms not forming part of a nitro radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/18—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
- C07D207/20—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Procedimiento para preparar la sal de clorhidrato de ester metílico del ácido (e)-3-(4-{[2-(2-metil-1h-indol-3-il)etilamino]metil}fenil)-acrílico que comprende: a) Combinar 2-metiltriptamina y ester metilico del ácido (e)-3-(4-formil-fenil)-acrílico, b) Agitar para formar un intermediario de imina y c) Reducir este intermediario para formar la sal.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US80452706P | 2006-06-12 | 2006-06-12 | |
US86787806P | 2006-11-30 | 2006-11-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
CL2010000973A1 true CL2010000973A1 (es) | 2011-07-01 |
Family
ID=38832681
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL200701691A CL2007001691A1 (es) | 2006-06-12 | 2007-06-11 | Metodo para hacer n-hidroxi-3-(4(((2-(2-metil-1h-indol-3-il)etil)amino)metil)fenil)-2e-2-propenamida. |
CL2010000973A CL2010000973A1 (es) | 2006-06-12 | 2010-09-13 | Procedimiento de preparacion de la sal de clorhidrato de ester metilico del acido (e)-3-(4-{[2-(2-metil-1h-indol-3-il)etilamino]metil}fenil)-acrilico por combinacion de 2-metiltriptamina y el ester metilico del acido (e)-3-(4-formil-fenil)-acrilico, y posterior reduccion de la imina formada ( divisional de la sol. n° 1691-2007). |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CL200701691A CL2007001691A1 (es) | 2006-06-12 | 2007-06-11 | Metodo para hacer n-hidroxi-3-(4(((2-(2-metil-1h-indol-3-il)etil)amino)metil)fenil)-2e-2-propenamida. |
Country Status (32)
Country | Link |
---|---|
US (2) | US20090306405A1 (es) |
EP (2) | EP2394991B1 (es) |
JP (2) | JP5431926B2 (es) |
KR (2) | KR101493530B1 (es) |
CN (4) | CN103086944A (es) |
AR (1) | AR061296A1 (es) |
AU (1) | AU2007257883B2 (es) |
BR (1) | BRPI0712847A2 (es) |
CA (1) | CA2653657C (es) |
CL (2) | CL2007001691A1 (es) |
DK (1) | DK2032533T3 (es) |
EC (1) | ECSP088978A (es) |
ES (2) | ES2416286T3 (es) |
GT (1) | GT200800282A (es) |
HK (2) | HK1126759A1 (es) |
HR (1) | HRP20130798T1 (es) |
IL (2) | IL195211A (es) |
IN (1) | IN2015DN00910A (es) |
JO (1) | JO2900B1 (es) |
MA (1) | MA30513B1 (es) |
MX (2) | MX2008015898A (es) |
MY (1) | MY147576A (es) |
NO (1) | NO341870B1 (es) |
NZ (1) | NZ572707A (es) |
PE (2) | PE20080851A1 (es) |
PL (1) | PL2032533T3 (es) |
PT (1) | PT2032533E (es) |
RU (1) | RU2448090C2 (es) |
TN (1) | TNSN08507A1 (es) |
TW (1) | TWI395734B (es) |
WO (1) | WO2007146718A2 (es) |
ZA (1) | ZA200809490B (es) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT202000004075A1 (it) | 2020-02-27 | 2021-08-27 | Flamma Spa | Processo per la preparazione di panobinostat |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB146260A (en) | 1918-07-11 | 1921-08-11 | Elektro Osmose Ag | A process for preparing proteids charged with immune substances |
GB8531612D0 (en) * | 1985-12-23 | 1986-02-05 | Beecham Wuelfing Gmbh & Co Kg | Compounds |
PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
US20040067540A1 (en) | 2001-01-09 | 2004-04-08 | Piotr Lassota | Rapid method for screening compounds for in vivo activity |
BR0213932A (pt) | 2001-11-06 | 2004-08-31 | Novartis Ag | Combinação do inibidor da ciclooxigenase-2/inibidor da desacetilase histona |
MX2008015899A (es) * | 2006-06-12 | 2009-04-01 | Novartis Ag | Procedimiento para hacer sales de n-hidroxi-3-[4-[[[2-(2-metil-1h- indol-3-il)etil]amino]metil]fenil]-2e-2-propenamida. |
-
2007
- 2007-06-07 KR KR20087030232A patent/KR101493530B1/ko active Protection Beyond IP Right Term
- 2007-06-07 CN CN2012103501544A patent/CN103086944A/zh active Pending
- 2007-06-07 EP EP11179043.2A patent/EP2394991B1/en active Active
- 2007-06-07 EP EP07784350.6A patent/EP2032533B8/en active Active
- 2007-06-07 CN CN2011100629486A patent/CN102167678B/zh active Active
- 2007-06-07 IN IN910DEN2015 patent/IN2015DN00910A/en unknown
- 2007-06-07 MX MX2008015898A patent/MX2008015898A/es active IP Right Grant
- 2007-06-07 JP JP2009515575A patent/JP5431926B2/ja active Active
- 2007-06-07 AU AU2007257883A patent/AU2007257883B2/en not_active Ceased
- 2007-06-07 US US12/302,572 patent/US20090306405A1/en not_active Abandoned
- 2007-06-07 DK DK07784350.6T patent/DK2032533T3/da active
- 2007-06-07 RU RU2008151726/04A patent/RU2448090C2/ru active
- 2007-06-07 CN CN2011100630820A patent/CN102174008A/zh active Pending
- 2007-06-07 WO PCT/US2007/070564 patent/WO2007146718A2/en active Application Filing
- 2007-06-07 PT PT77843506T patent/PT2032533E/pt unknown
- 2007-06-07 NZ NZ572707A patent/NZ572707A/en not_active IP Right Cessation
- 2007-06-07 MX MX2012002221A patent/MX366213B/es unknown
- 2007-06-07 ES ES07784350T patent/ES2416286T3/es active Active
- 2007-06-07 CA CA2653657A patent/CA2653657C/en active Active
- 2007-06-07 PL PL07784350T patent/PL2032533T3/pl unknown
- 2007-06-07 ES ES11179043.2T patent/ES2553255T3/es active Active
- 2007-06-07 BR BRPI0712847-9A patent/BRPI0712847A2/pt not_active IP Right Cessation
- 2007-06-07 KR KR1020147026120A patent/KR101540194B1/ko active IP Right Grant
- 2007-06-07 CN CNA2007800217257A patent/CN101466674A/zh active Pending
- 2007-06-08 PE PE2007000720A patent/PE20080851A1/es active IP Right Grant
- 2007-06-08 PE PE2011002097A patent/PE20120221A1/es active IP Right Grant
- 2007-06-08 AR ARP070102498A patent/AR061296A1/es unknown
- 2007-06-11 TW TW096120985A patent/TWI395734B/zh not_active IP Right Cessation
- 2007-06-11 CL CL200701691A patent/CL2007001691A1/es unknown
- 2007-06-12 JO JO2007219A patent/JO2900B1/en active
-
2008
- 2008-11-06 ZA ZA200809490A patent/ZA200809490B/xx unknown
- 2008-11-10 IL IL195211A patent/IL195211A/en active IP Right Grant
- 2008-11-28 MY MYPI20084865A patent/MY147576A/en unknown
- 2008-12-05 TN TNP2008000507A patent/TNSN08507A1/en unknown
- 2008-12-10 GT GT200800282A patent/GT200800282A/es unknown
- 2008-12-12 EC EC2008008978A patent/ECSP088978A/es unknown
- 2008-12-12 MA MA31472A patent/MA30513B1/fr unknown
-
2009
- 2009-01-09 NO NO20090137A patent/NO341870B1/no not_active IP Right Cessation
- 2009-06-17 HK HK09105439.9A patent/HK1126759A1/xx not_active IP Right Cessation
- 2009-06-17 HK HK12102475.6A patent/HK1162029A1/xx not_active IP Right Cessation
-
2010
- 2010-09-13 CL CL2010000973A patent/CL2010000973A1/es unknown
-
2011
- 2011-09-23 US US13/243,001 patent/US8536346B2/en active Active
-
2013
- 2013-08-22 HR HRP20130798TT patent/HRP20130798T1/hr unknown
- 2013-10-25 JP JP2013222442A patent/JP5809223B2/ja active Active
-
2014
- 2014-07-28 IL IL233836A patent/IL233836A/en active IP Right Grant
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CY1124874T1 (el) | Διεργασια για την παρασκευη [(5-(3-χλωροφαινυλ)-3-υδροξυπυριδινο-2-καρβονυλ)-αμινο]οξικου οξεος απο 5-((3-χλωροφαινυλ)-3-χλωρο-πυριδιν-2-υλ)-νιτριλιο, και διεργασια για την παρασκευη παραγωγων 5-((αλογονοφαινυλ)-3-αλογονο-πυριδιν-2-υλ)-νιτριλιου | |
PH12013500745A1 (en) | Azaadamantane derivatives and methods of use | |
DE502006002659D1 (de) | Verfahren zur herstellung von 5-(4-ä4-(5-cyano-3-indolyl)-butylü-1-piperazinyl)-benzofuran-2-carboxamid | |
NZ593030A (en) | Pyridyloxyindoles inhibitors of vegf-r2 and use thereof for treatment of disease | |
MX2009003739A (es) | Derivados de hidrobenzamida como inhibidores de hsp90. | |
EA201070116A1 (ru) | Новые кристаллы и способ получения 5-({[2-амино-3-(4-карбамоил-2,6-диметилфенил)пропионил]-[1-(4-фенил-1н-имидазол-2-ил)этил]амино}метил)-2-метоксибензоевой кислоты | |
EA200870302A1 (ru) | 1,3-диоксанкарбоновые кислоты | |
WO2007103550A3 (en) | Substituted aminothiazole derivatives with anti-hcv activity | |
NO20083708L (no) | 4-Fenyl-tiazol-5-karboksylsyre og 4-fenyl-tiazol-5-karboksylmider som PLK1-inhibitorer | |
BR112014010401A8 (pt) | Inibidores do vírus da hepatite c rod-like que contêm o fragmento {2-[4-(bifenil-4-il)-1h-imidazo-2-il] pirrolidina-1-carbonilmetil}amina | |
CO6361988A2 (es) | Forma cristalina de un compuesto de 4-[2-(2-fluorofenoximetil)fenil]piperidina. | |
BRPI0607093A2 (pt) | polimorfo cristalino de monoidrato de sal monossódico de ácido 3-(n-metil-n-pentil)amino-1-hidroxipropano-1, 1-difosfÈnico, ibandronato, processo para a preparação de um polimorfo de ibandronato cristalino, e composição farmacêutica que o compreende | |
NO20090136L (no) | Fremgangsmate for fremstilling av salter av N-hydroksy-3-[4-[[[2-(2-metyl-1H-1ln-dol-3-yl)etyl]amino]metyl]fenyl]-2E-2-propenamid | |
EA200801893A1 (ru) | Производные тетрагидронафталина, способ их получения и их применение в качестве ингибиторов воспаления | |
ATE465152T1 (de) | Verfahren zum herstellen von alkylaniliden aus halogenbenzolderivaten | |
WO2011037833A3 (en) | Novel n-benzylamide substituted derivatives of 2-(acylamido)acetic acid and 2-(acylamido)propionic acids: potent neurological agents | |
MX2010009876A (es) | Nuevo proceso para la preparacion de derivados de acido ciclohexanocarboxilico por medio del derivado de ciclohexanocarboxamida correspondiente. | |
MX2010009926A (es) | Nuevo proceso para la preparacion de derivados de acido ciclohexancarboxilico. | |
CL2010000973A1 (es) | Procedimiento de preparacion de la sal de clorhidrato de ester metilico del acido (e)-3-(4-{[2-(2-metil-1h-indol-3-il)etilamino]metil}fenil)-acrilico por combinacion de 2-metiltriptamina y el ester metilico del acido (e)-3-(4-formil-fenil)-acrilico, y posterior reduccion de la imina formada ( divisional de la sol. n° 1691-2007). | |
TNSN08531A1 (en) | Phenylacetic acid derivatives as cox - 2 inhibitors | |
ATE512134T1 (de) | Verfahren zur herstellung von 5-benzyloxy-2-(4- benzyloxyphenyl)-3-methyl-1h-indol | |
EA201101014A1 (ru) | Сульфонамиды, предназначенные для лечения респираторных нарушений | |
DK1585728T3 (da) | Iminosyrederivater som inhibitorer af matrix-metalloproteinaser | |
UA98311C2 (ru) | Соединение 2-алкилиндазола для лечения определенных расстройств, связанных с цнс, способ его получения (варианты) и фармацевтическая композиция на его основе | |
WO2009019719A3 (en) | Process for the preparation of 3-aryloxy-3-arylpropanamines |