CU24049B1 - POLYMORPH B OF THE N- (2-AMINOPHENYL) -4- [N- (PIRIDIN-3-IL) METOXICARBONYLAMINE-METHYL] BENZAMIDE (MS-275) - Google Patents
POLYMORPH B OF THE N- (2-AMINOPHENYL) -4- [N- (PIRIDIN-3-IL) METOXICARBONYLAMINE-METHYL] BENZAMIDE (MS-275)Info
- Publication number
- CU24049B1 CU24049B1 CU2011000044A CU20110044A CU24049B1 CU 24049 B1 CU24049 B1 CU 24049B1 CU 2011000044 A CU2011000044 A CU 2011000044A CU 20110044 A CU20110044 A CU 20110044A CU 24049 B1 CU24049 B1 CU 24049B1
- Authority
- CU
- Cuba
- Prior art keywords
- aminophenyl
- benzamide
- methyl
- polymorph
- metoxicarbonylamine
- Prior art date
Links
- ZYHQGITXIJDDKC-UHFFFAOYSA-N 2-[2-(2-aminophenyl)ethyl]aniline Chemical class NC1=CC=CC=C1CCC1=CC=CC=C1N ZYHQGITXIJDDKC-UHFFFAOYSA-N 0.000 title abstract 2
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 title 3
- 208000023275 Autoimmune disease Diseases 0.000 abstract 1
- 201000011510 cancer Diseases 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 230000024241 parasitism Effects 0.000 abstract 1
Classifications
-
- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4406—Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 3, e.g. zimeldine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/62—Oxygen or sulfur atoms
- C07D213/63—One oxygen atom
- C07D213/65—One oxygen atom attached in position 3 or 5
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- 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
- A61P37/00—Drugs for immunological or allergic disorders
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/72—Nitrogen atoms
- C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Immunology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Abstract
El polimorfo B cristalino de N-(2-aminofenil)-4-[N-(piridin-3-il)metoxicarbonilamino-metil]benzamida (MS-275) de fórmula I ESPACIO PARA LA FÓRMULA el cual es útil para tratar tumores malignos, enfermedades autoinmunes, enfermedades dermatológicas y parasitismo. También se describe el proceso para producir dicho compuesto.The crystalline polymorph B of N- (2-aminophenyl) -4- [N- (pyridin-3-yl) methoxycarbonylamino-methyl] benzamide (MS-275) of formula I SPACE FOR FORMULA which is useful for treating malignant tumors , autoimmune diseases, dermatological diseases and parasitism. The process for producing said compound is also described.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US9304608P | 2008-08-29 | 2008-08-29 | |
PCT/EP2009/006381 WO2010022988A1 (en) | 2008-08-29 | 2009-08-27 | N-(2-aminophenyl)-4-[n-(pyridine-3-yl)-methoxycarbonyl-aminomethyl]-benzamide (ms-275)polymorph b |
Publications (2)
Publication Number | Publication Date |
---|---|
CU20110044A7 CU20110044A7 (en) | 2011-12-28 |
CU24049B1 true CU24049B1 (en) | 2014-12-26 |
Family
ID=40791975
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CU2011000044A CU24049B1 (en) | 2008-08-29 | 2011-02-28 | POLYMORPH B OF THE N- (2-AMINOPHENYL) -4- [N- (PIRIDIN-3-IL) METOXICARBONYLAMINE-METHYL] BENZAMIDE (MS-275) |
Country Status (2)
Country | Link |
---|---|
CU (1) | CU24049B1 (en) |
GB (1) | GB2462893B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2977492B1 (en) * | 2011-07-04 | 2013-07-05 | Servier Lab | NOVEL ASSOCIATION BETWEEN N-HYDROXY-4- {2- [3- (N, N-DIMETHYLAMINOMETHYL) BENZOFURAN-2-YLCARBONYLAMINO] ETHOXY} BENZAMIDE AND FOLFOX |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6174905B1 (en) * | 1996-09-30 | 2001-01-16 | Mitsui Chemicals, Inc. | Cell differentiation inducer |
US6794392B1 (en) * | 1996-09-30 | 2004-09-21 | Schering Aktiengesellschaft | Cell differentiation inducer |
JP2001064177A (en) * | 1999-08-16 | 2001-03-13 | Schering Ag | Pharmaceutical preparation including benzamide derivative as ingredient |
JP4360660B2 (en) * | 1999-11-09 | 2009-11-11 | 三井化学株式会社 | Purification method of monoacylphenylenediamine derivatives |
PE20050206A1 (en) * | 2003-05-26 | 2005-03-26 | Schering Ag | PHARMACEUTICAL COMPOSITION CONTAINING AN INHIBITOR OF HISTONE DEACETILASE |
-
2009
- 2009-04-29 GB GB0907347A patent/GB2462893B/en active Active
-
2011
- 2011-02-28 CU CU2011000044A patent/CU24049B1/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
CU20110044A7 (en) | 2011-12-28 |
GB0907347D0 (en) | 2009-06-10 |
GB2462893B (en) | 2010-10-13 |
GB2462893A (en) | 2010-03-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PH12015501585A1 (en) | Manufacturing process for pyrimidine derivatives | |
GEP20146131B (en) | Carbazole compounds and therapeutic uses thereof | |
CR20160465A (en) | POLYMORPH B OF THE N- (2-AMINOPHENYL) -4- [N- (PIRIDIN-3-IL) METOXICARBONYLAMINE-METHYL] BENZAMIDE (MS-275) | |
EA201000113A1 (en) | PYRAZOL COMPOUNDS | |
EA201690153A1 (en) | SUBSTITUTED PETROPHORANE AND BENZOXAZOLYL COMPOUNDS AND THEIR APPLICATIONS | |
EA201101650A1 (en) | NEW PYRIMIDINE DERIVATIVES AND THEIR APPLICATION IN THE TREATMENT OF MALIGNANT NONFORMS AND THE FOLLOWING DISEASES | |
EA201001848A1 (en) | DERIVATIVES OF PIRAZINE AS EPITELIAL SODIUM CHANNEL BLOCKS | |
EA201100299A1 (en) | ORGANIC COMPOUNDS | |
CU24269B1 (en) | 3- PIRIMIDIN- 4-IL- OXAZOLIDIN- 2- INHIBITING WAVES OF THE MUTANT HDI | |
EA201270752A1 (en) | KINASE INHIBITORS AND METHOD FOR TREATING MALIGNANT TUMOR WITH THEIR HELP | |
ECSP109987A (en) | METHODS AND USEFUL COMPOUNDS TO PREPARE INHIBITORS OF THE 2-GLUCOSE CO-TRANSPORTER SODIUM | |
EA201100503A1 (en) | GLUCOSIDE DERIVATIVES AND THEIR APPLICATIONS | |
EA201400245A1 (en) | INHIBITORS DYRK1 AND THEIR APPLICATION | |
EA201170154A1 (en) | DERIVATIVES OF PYRIDINOPIRIDINONES, METHOD OF THEIR RECEPTION AND APPLICATION IN THERAPY | |
EA201170617A1 (en) | PYRAZOLYLAMINOPIRIDINE AS FAK INHIBITORS | |
BR112022009390A2 (en) | IMPROVED SYNTHESIS OF KRAS INHIBITOR COMPOUND G12C | |
EA201291246A1 (en) | CONDENSED BICYCLIC KINASE INHIBITORS | |
NO20080445L (en) | New azetidine derivatives as neurokinin receptor antagonists for the treatment of gastrointestinal disorders | |
TW200635905A (en) | Processes for producing 4-aminoquinazolines | |
GT200600207A (en) | PROCESS FOR THE SYNTHESIS OF ORGANIC COMPOUNDS | |
EA201170672A1 (en) | COMPOUNDS SUITABLE FOR THE TREATMENT OF CELLULITE | |
EA201690755A1 (en) | SALT AND CRYSTAL FORMS OF PLK-4 INHIBITOR | |
TNSN06260A1 (en) | Process for the preparation of tryptase inhibitors | |
EA201001566A1 (en) | NEW CLASS OF SPYROPIPERIDINES FOR THE TREATMENT OF NEURODEGENERATIVE DISEASES | |
SG10201902903RA (en) | Synthesis and novel salt forms of (r)-5-((e)-2-(pyrrolidin-3-ylvinyl)pyrimidine |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG | Grant of patent |