AR061295A1 - Procedimiento para hacer sales de n-hidroxi-3- [4-[ [ [ 2- ( 2-metil-1h-indol-3-il) etil] amino] metil] fenil] -2e-2-propenamida - Google Patents
Procedimiento para hacer sales de n-hidroxi-3- [4-[ [ [ 2- ( 2-metil-1h-indol-3-il) etil] amino] metil] fenil] -2e-2-propenamidaInfo
- Publication number
- AR061295A1 AR061295A1 ARP070102497A ARP070102497A AR061295A1 AR 061295 A1 AR061295 A1 AR 061295A1 AR P070102497 A ARP070102497 A AR P070102497A AR P070102497 A ARP070102497 A AR P070102497A AR 061295 A1 AR061295 A1 AR 061295A1
- Authority
- AR
- Argentina
- Prior art keywords
- methyl
- phenyl
- ethyl
- amino
- propenamide
- Prior art date
Links
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/4045—Indole-alkylamines; Amides thereof, e.g. serotonin, melatonin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- 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
-
- 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)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Indole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
El compuesto es util como inhibidor de histona-desacetilasa, antiproliferativo. Reivindicacion 1: Un método para preparar una sal cristalina de N-hidroxi-3-[4-[[[2-(2-metil-1H-indol-3-il)etil]amino]metil]fenil]-2E-2-propenamida, que comprende los pasos de: (a) disolver o suspender la base libre de N-hidroxi-3-[4-[[[2-(2-metil-1H-indol-3-il)etil]amino]metil]fenil]-2E-2-propenamida en una cantidad de solvente apropiado; y (b) tratar la base libre de N-hidroxi-3-[4-[[[2-(2-metil-1H-indol-3- il)etil]amino]metil]fenil]-2E-2-propenamida a una temperatura apropiada con un agente formador de sal, en donde el agente formador de sal se selecciona del grupo que consiste de proveedores de iones de clorhidrato, lactato, maleato, mesilato, tartarato, acetato, benzoato, citrato, fumarato, gentisato, malato, malonato, oxalato, fosfato, propionato, sulfato, succinato, sodio, potasio, calcio y zinc.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US80452906P | 2006-06-12 | 2006-06-12 | |
US85325906P | 2006-10-20 | 2006-10-20 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR061295A1 true AR061295A1 (es) | 2008-08-20 |
Family
ID=38832680
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070102497A AR061295A1 (es) | 2006-06-12 | 2007-06-08 | Procedimiento para hacer sales de n-hidroxi-3- [4-[ [ [ 2- ( 2-metil-1h-indol-3-il) etil] amino] metil] fenil] -2e-2-propenamida |
Country Status (24)
Country | Link |
---|---|
US (1) | US7989639B2 (es) |
EP (1) | EP2032532B8 (es) |
JP (1) | JP2009540007A (es) |
KR (1) | KR20090026282A (es) |
AR (1) | AR061295A1 (es) |
AU (1) | AU2007257882B2 (es) |
BR (1) | BRPI0713653A2 (es) |
CA (1) | CA2654230C (es) |
CL (1) | CL2007001690A1 (es) |
EC (1) | ECSP088957A (es) |
GT (1) | GT200800281A (es) |
HK (1) | HK1126495A1 (es) |
IL (1) | IL195344A (es) |
JO (1) | JO3099B1 (es) |
MA (1) | MA30564B1 (es) |
MX (1) | MX2008015899A (es) |
MY (1) | MY147013A (es) |
NO (1) | NO20090136L (es) |
NZ (1) | NZ572744A (es) |
PE (1) | PE20080365A1 (es) |
RU (1) | RU2008151724A (es) |
TN (1) | TNSN08508A1 (es) |
TW (1) | TWI385142B (es) |
WO (1) | WO2007146717A2 (es) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2448090C2 (ru) * | 2006-06-12 | 2012-04-20 | Новартис Аг | Способ получения n-гидрокси-3-[4-[[[2-(2-метил-1н-индол-3-ил)этил]амино]метил]фенил]-2е-2-пропенамида и исходных материалов для него |
MX2008015901A (es) * | 2006-06-12 | 2009-01-12 | Novartis Ag | Sales de n-hidroxi-3-[4-[[[2-(2-metil-1h-indol-3-il)etil]amino]met il]fenil]-2e-2-propenamida. |
CA2674604A1 (en) * | 2007-01-10 | 2008-07-17 | Novartis Ag | Formulations of deacetylase inhibitors |
WO2009119785A1 (ja) * | 2008-03-28 | 2009-10-01 | 浜理薬品工業株式会社 | エチニルチミジン化合物の精製方法 |
AU2014358682B2 (en) * | 2013-12-02 | 2016-10-20 | Suven Life Sciences Limited | Process for large scale production of 1-[(2-bromophenyl)sulfonyl]-5-methoxy-3-[(4-methyl-1-piperazinyl)methyl]-1H-indole dimesylate monohydrate |
WO2017221163A1 (en) * | 2016-06-21 | 2017-12-28 | Alembic Pharmaceuticals Limited | Novel salts and polymorphic forms of panobinostat |
WO2018092151A1 (en) * | 2016-11-21 | 2018-05-24 | Msn Laboratories Private Limited, R&D Center | Process for the preparation of 2-(e)-n-hydroxy-3-[4-[[[2-(2-methyl-1h-indol-3-yl) ethyl]amino]methyl]phenyl]-2-propenamide 2-hydroxypropanoic acid (1:1) and its polymorphs thereof |
WO2018163114A1 (en) * | 2017-03-10 | 2018-09-13 | Shilpa Medicare Limited | Amorphous panobinostat and its lactate salt |
US10537585B2 (en) | 2017-12-18 | 2020-01-21 | Dexcel Pharma Technologies Ltd. | Compositions comprising dexamethasone |
US20230416255A1 (en) * | 2022-06-27 | 2023-12-28 | Abion Inc. | Mesylate salts of triazolopyrazine derivatives |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH342565A (de) | 1954-04-14 | 1959-11-30 | Thomae Gmbh Dr K | Verfahren zur Herstellung von basischen Äthern endocyclisch substituierter Carbinole oder ihren nicht quaternären Salzen |
GB891413A (en) | 1958-10-06 | 1962-03-14 | Smith Kline French Lab | Tris-(dialkylaminoalkyl) phosphates and a method for their preparation |
GB8600397D0 (en) | 1986-01-08 | 1986-02-12 | Glaxo Group Ltd | Chemical compounds |
PE20020354A1 (es) * | 2000-09-01 | 2002-06-12 | Novartis Ag | Compuestos de hidroxamato como inhibidores de histona-desacetilasa (hda) |
DE60215028T2 (de) | 2001-08-14 | 2007-03-15 | Eli Lilly And Co., Indianapolis | Indol derivate als beta-3-adrenerge agonisten zur behandlung von typ 2 diabetes |
CA2461373A1 (en) * | 2001-11-06 | 2003-05-15 | Novartis Ag | Cyclooxygenase-2 inhibitor/histone deacetylase inhibitor combination |
US20040224952A1 (en) * | 2003-05-07 | 2004-11-11 | Cowart Marlon D. | Fused bicyclic-substituted amines as histamine-3 receptor ligands |
CA2562627A1 (en) * | 2004-04-26 | 2005-11-10 | Santiago Ini | Preparation of tegaserod and tegaserod maleate |
TW200613275A (en) | 2004-08-24 | 2006-05-01 | Recordati Ireland Ltd | Lercanidipine salts |
-
2007
- 2007-06-07 AU AU2007257882A patent/AU2007257882B2/en not_active Ceased
- 2007-06-07 MX MX2008015899A patent/MX2008015899A/es active IP Right Grant
- 2007-06-07 MY MYPI20084895A patent/MY147013A/en unknown
- 2007-06-07 BR BRPI0713653-6A patent/BRPI0713653A2/pt not_active IP Right Cessation
- 2007-06-07 KR KR1020087030231A patent/KR20090026282A/ko not_active Application Discontinuation
- 2007-06-07 JP JP2009515574A patent/JP2009540007A/ja active Pending
- 2007-06-07 US US12/302,576 patent/US7989639B2/en active Active
- 2007-06-07 EP EP07812044.1A patent/EP2032532B8/en active Active
- 2007-06-07 NZ NZ572744A patent/NZ572744A/en not_active IP Right Cessation
- 2007-06-07 RU RU2008151724/04A patent/RU2008151724A/ru unknown
- 2007-06-07 WO PCT/US2007/070562 patent/WO2007146717A2/en active Application Filing
- 2007-06-07 CA CA2654230A patent/CA2654230C/en active Active
- 2007-06-08 PE PE2007000719A patent/PE20080365A1/es not_active Application Discontinuation
- 2007-06-08 AR ARP070102497A patent/AR061295A1/es unknown
- 2007-06-11 CL CL200701690A patent/CL2007001690A1/es unknown
- 2007-06-11 TW TW096120979A patent/TWI385142B/zh not_active IP Right Cessation
- 2007-06-12 JO JOP/2007/0221A patent/JO3099B1/ar active
-
2008
- 2008-11-17 IL IL195344A patent/IL195344A/en active IP Right Grant
- 2008-12-05 TN TNP2008000508A patent/TNSN08508A1/en unknown
- 2008-12-10 GT GT200800281A patent/GT200800281A/es unknown
- 2008-12-11 EC EC2008008957A patent/ECSP088957A/es unknown
- 2008-12-12 MA MA31474A patent/MA30564B1/fr unknown
-
2009
- 2009-01-09 NO NO20090136A patent/NO20090136L/no not_active Application Discontinuation
- 2009-06-17 HK HK09105412.0A patent/HK1126495A1/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
GT200800281A (es) | 2009-03-18 |
IL195344A0 (en) | 2009-08-03 |
AU2007257882B2 (en) | 2011-09-08 |
EP2032532A2 (en) | 2009-03-11 |
WO2007146717A3 (en) | 2008-03-27 |
BRPI0713653A2 (pt) | 2012-10-23 |
ECSP088957A (es) | 2009-01-30 |
TWI385142B (zh) | 2013-02-11 |
MY147013A (en) | 2012-10-15 |
PE20080365A1 (es) | 2008-05-07 |
TNSN08508A1 (en) | 2010-04-14 |
IL195344A (en) | 2014-11-30 |
CL2007001690A1 (es) | 2008-05-16 |
JP2009540007A (ja) | 2009-11-19 |
JO3099B1 (ar) | 2017-03-15 |
US20090187029A1 (en) | 2009-07-23 |
MX2008015899A (es) | 2009-04-01 |
RU2008151724A (ru) | 2010-07-20 |
EP2032532B1 (en) | 2015-04-22 |
EP2032532B8 (en) | 2015-07-01 |
MA30564B1 (fr) | 2009-07-01 |
CA2654230C (en) | 2012-09-11 |
HK1126495A1 (en) | 2009-09-04 |
CA2654230A1 (en) | 2007-12-21 |
NZ572744A (en) | 2011-05-27 |
NO20090136L (no) | 2009-03-06 |
WO2007146717A2 (en) | 2007-12-21 |
AU2007257882A1 (en) | 2007-12-21 |
US7989639B2 (en) | 2011-08-02 |
TW200808692A (en) | 2008-02-16 |
KR20090026282A (ko) | 2009-03-12 |
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