AR019120A1 - Proceso para la fabricacion de ureas 1,3-disustituidas-4-oxociclicas - Google Patents
Proceso para la fabricacion de ureas 1,3-disustituidas-4-oxociclicasInfo
- Publication number
- AR019120A1 AR019120A1 ARP990101995A ARP990101995A AR019120A1 AR 019120 A1 AR019120 A1 AR 019120A1 AR P990101995 A ARP990101995 A AR P990101995A AR P990101995 A ARP990101995 A AR P990101995A AR 019120 A1 AR019120 A1 AR 019120A1
- Authority
- AR
- Argentina
- Prior art keywords
- oxocyclic
- disubstituted
- substituted
- group
- urea
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 2
- 150000003672 ureas Chemical class 0.000 title abstract 2
- 235000013877 carbamide Nutrition 0.000 abstract 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 abstract 4
- 239000004202 carbamide Substances 0.000 abstract 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 3
- 125000003342 alkenyl group Chemical group 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000003416 antiarrhythmic agent Substances 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- MREBEPTUUMTTIA-UHFFFAOYSA-N 1-[[5-(4-chlorophenyl)furan-2-yl]methylideneamino]-3-[4-(4-methylpiperazin-1-yl)butyl]imidazolidine-2,4-dione Chemical compound C1CN(C)CCN1CCCCN1C(=O)N(N=CC=2OC(=CC=2)C=2C=CC(Cl)=CC=2)CC1=O MREBEPTUUMTTIA-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 229910006069 SO3H Inorganic materials 0.000 abstract 1
- 125000004423 acyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- -1 alkylalkyl Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 230000003440 anti-fibrillation Effects 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004404 heteroalkyl group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 238000002955 isolation Methods 0.000 abstract 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/06—Antiarrhythmics
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Heart & Thoracic Surgery (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plural Heterocyclic 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)
- Furan Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Catalysts (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
Un proceso para la fabricacion de ureas 1,3-disustituidas-4-oxocíclicas de la formula general (I) donde R1, R2 y R3 se seleccionan independientemente delgrupo que consiste de H, Cl, F, Br, NH2, COOH, CH3SO2NH, SO3H, OH, alcoxi, alquilo alcoxicarbonilo, hidroxialquilo, carboxialquilo, y aciloxi, R4 se seleccionadel grupo que consiste de un alquilo sustituido o no sustituido, alquenilo, alquinilo, alquilacilo, y heteroalquilo; y A es un grupo alquilo o alquenilosustituido, saturado o insaturado, de cadena recta o ramificada que comprende 1-7 átomos de carbono; o A es un heterociclo sustituido o no sustituido, saturadoo insaturado que tiene 5, 6, o 7 miembros que contienen al menos un nitrogeno, y R4 se une a dicho nitrogeno; donde dicha urea1,3-disustituida-4-oxocíclica serealiza sin aislacion de intermedio y comprende los pasos: (Ia) reaccionar una urea 1-sustituida-4-oxocíclica con una cadena de carbono que contiene al menosdos grupos leaving en presencia de una base suave y un solvente para formar un aducto que contiene al menos un grupo leaving, y (Ib) condensar el aducto conuna amina para formar una urea 1,3-disustituida-4-oxocíclica, y (II) recuperar dicha urea 1,3-disustituida-4-oxocíclica, se revelan. Este método esparticularmente preferido para la realizacion de 1(([5-(4-clorofenil)-2-furanil]metileno)amino)-3-[4-(4-metil-1-piperazinil)butil]-2,4-imidazolidinediona. Loscompuestos citados tienen propiedades como agentes antifibrilatorios y antiarrítmicos.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8340698P | 1998-04-29 | 1998-04-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR019120A1 true AR019120A1 (es) | 2001-12-26 |
Family
ID=22178103
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP990101995A AR019120A1 (es) | 1998-04-29 | 1999-04-29 | Proceso para la fabricacion de ureas 1,3-disustituidas-4-oxociclicas |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US6420568B1 (es) |
| EP (1) | EP1075474B1 (es) |
| JP (1) | JP4514950B2 (es) |
| KR (1) | KR100400051B1 (es) |
| CN (1) | CN1298402A (es) |
| AR (1) | AR019120A1 (es) |
| AT (1) | ATE275563T1 (es) |
| AU (1) | AU747237B2 (es) |
| BR (1) | BR9910078A (es) |
| CA (1) | CA2330685A1 (es) |
| CO (1) | CO5050358A1 (es) |
| DE (1) | DE69920003T2 (es) |
| HU (1) | HUP0101356A3 (es) |
| ID (1) | ID27316A (es) |
| IL (1) | IL138405A (es) |
| MY (1) | MY133752A (es) |
| NO (1) | NO20005425L (es) |
| NZ (1) | NZ506773A (es) |
| PE (1) | PE20000439A1 (es) |
| PL (1) | PL198951B1 (es) |
| RU (1) | RU2194705C2 (es) |
| SK (1) | SK15832000A3 (es) |
| TR (1) | TR200003136T2 (es) |
| TW (1) | TW492965B (es) |
| WO (1) | WO1999055701A1 (es) |
| ZA (1) | ZA200004714B (es) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2194706C2 (ru) * | 1998-04-29 | 2002-12-20 | Дзе Проктер Энд Гэмбл Компани | Способ получения дигидрохлорида 1-[[[5-(4-хлорфенил)-2-фуранил]метилен]амино]-3-[4-(4-метил-1-пиперазинил) бутил]-2,4-имидазолидиндиона |
| CN100443473C (zh) * | 2005-04-30 | 2008-12-17 | 中国药科大学 | 1-氨基-3-(氮杂环基烷基)-2,4-咪唑二酮的合成方法 |
| TW200840578A (en) * | 2006-12-15 | 2008-10-16 | Procter & Gamble | Compositions of azimilide dihydrochloride |
| US20120178762A1 (en) | 2006-12-15 | 2012-07-12 | Warner Chilcott Company, Llc | Compositions of azimilide dihydrochloride |
| US8123815B2 (en) | 2008-11-24 | 2012-02-28 | Biomet Manufacturing Corp. | Multiple bearing acetabular prosthesis |
| US8308810B2 (en) | 2009-07-14 | 2012-11-13 | Biomet Manufacturing Corp. | Multiple bearing acetabular prosthesis |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL272960A (es) * | 1960-12-27 | |||
| US3919231A (en) | 1974-06-17 | 1975-11-11 | Morton Norwich Products Inc | Series of 5-aryl-2-furamidines |
| US3906010A (en) | 1974-06-17 | 1975-09-16 | Morton Norwich Products Inc | Series of 5-aryl-2-furamidines |
| US3946049A (en) | 1975-04-03 | 1976-03-23 | Morton-Norwich Products, Inc. | 5-phenyl-2-furamidoximes |
| US4001222A (en) | 1975-10-14 | 1977-01-04 | Morton-Norwich Products, Inc. | 3-(Aminoacyl)-1-{[5-(substituted phenyl)furfurylidene]amino}hydantoins and process for their preparation thereof |
| JPS5726653A (en) | 1980-05-09 | 1982-02-12 | Ciba Geigy Ag | Substituted phenyl ether |
| IL82856A0 (en) | 1986-06-26 | 1987-12-20 | Norwich Eaton Pharma | Pharmaceutical compositions containing 2-(5-phenyl-2-furanyl)imidazoles and certain such novel compounds |
| US4882354A (en) | 1987-12-16 | 1989-11-21 | Norwich Eaton Pharmaceuticals, Inc. | N-hydroxy-5-phenyl-2-furancarboximidamides useful as cardiotonic agents |
| US5019651A (en) | 1990-06-20 | 1991-05-28 | Merck & Co., Inc. | Process for preparing 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid (ABP) or salts thereof |
| JP3031973B2 (ja) * | 1990-08-16 | 2000-04-10 | 富士レビオ株式会社 | フェニトイン誘導体 |
| CA2115029C (en) | 1991-08-14 | 2002-03-26 | Stanford Salvatore Pelosi, Jr. | Cyclic urethanes useful as antiarrhythmic and antifibrillatory agents |
| CZ282368B6 (cs) * | 1991-08-14 | 1997-07-16 | Procter And Gamble Pharmaceuticals | 4-Oxocyklické močoviny a faramceutický prostředek je obsahující |
| RU2194706C2 (ru) * | 1998-04-29 | 2002-12-20 | Дзе Проктер Энд Гэмбл Компани | Способ получения дигидрохлорида 1-[[[5-(4-хлорфенил)-2-фуранил]метилен]амино]-3-[4-(4-метил-1-пиперазинил) бутил]-2,4-имидазолидиндиона |
-
1999
- 1999-04-27 HU HU0101356A patent/HUP0101356A3/hu unknown
- 1999-04-27 NZ NZ506773A patent/NZ506773A/xx not_active Application Discontinuation
- 1999-04-27 PL PL343733A patent/PL198951B1/pl not_active IP Right Cessation
- 1999-04-27 IL IL13840599A patent/IL138405A/xx not_active IP Right Cessation
- 1999-04-27 CA CA002330685A patent/CA2330685A1/en not_active Abandoned
- 1999-04-27 RU RU2000129802/04A patent/RU2194705C2/ru not_active IP Right Cessation
- 1999-04-27 CN CN99805365A patent/CN1298402A/zh active Pending
- 1999-04-27 SK SK1583-2000A patent/SK15832000A3/sk unknown
- 1999-04-27 DE DE69920003T patent/DE69920003T2/de not_active Expired - Lifetime
- 1999-04-27 AU AU37644/99A patent/AU747237B2/en not_active Ceased
- 1999-04-27 ID IDW20002480A patent/ID27316A/id unknown
- 1999-04-27 TR TR2000/03136T patent/TR200003136T2/xx unknown
- 1999-04-27 JP JP2000545861A patent/JP4514950B2/ja not_active Expired - Fee Related
- 1999-04-27 US US09/674,228 patent/US6420568B1/en not_active Expired - Lifetime
- 1999-04-27 BR BR9910078-9A patent/BR9910078A/pt not_active IP Right Cessation
- 1999-04-27 KR KR10-2000-7011922A patent/KR100400051B1/ko not_active IP Right Cessation
- 1999-04-27 EP EP99920062A patent/EP1075474B1/en not_active Expired - Lifetime
- 1999-04-27 AT AT99920062T patent/ATE275563T1/de not_active IP Right Cessation
- 1999-04-27 WO PCT/US1999/009093 patent/WO1999055701A1/en not_active Application Discontinuation
- 1999-04-29 MY MYPI99001689A patent/MY133752A/en unknown
- 1999-04-29 CO CO99025955A patent/CO5050358A1/es unknown
- 1999-04-29 AR ARP990101995A patent/AR019120A1/es not_active Application Discontinuation
- 1999-04-29 PE PE1999000354A patent/PE20000439A1/es not_active Application Discontinuation
- 1999-07-28 TW TW088106940A patent/TW492965B/zh not_active IP Right Cessation
-
2000
- 2000-09-07 ZA ZA200004714A patent/ZA200004714B/en unknown
- 2000-10-27 NO NO20005425A patent/NO20005425L/no not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| EP1075474A1 (en) | 2001-02-14 |
| SK15832000A3 (sk) | 2001-06-11 |
| NZ506773A (en) | 2004-03-26 |
| JP2002513022A (ja) | 2002-05-08 |
| HUP0101356A2 (hu) | 2002-05-29 |
| TW492965B (en) | 2002-07-01 |
| KR20010043053A (ko) | 2001-05-25 |
| AU747237B2 (en) | 2002-05-09 |
| PE20000439A1 (es) | 2000-07-13 |
| BR9910078A (pt) | 2000-12-26 |
| IL138405A (en) | 2005-03-20 |
| KR100400051B1 (ko) | 2003-09-29 |
| MY133752A (en) | 2007-11-30 |
| EP1075474B1 (en) | 2004-09-08 |
| PL198951B1 (pl) | 2008-08-29 |
| ATE275563T1 (de) | 2004-09-15 |
| HUP0101356A3 (en) | 2003-08-28 |
| ZA200004714B (en) | 2002-01-30 |
| TR200003136T2 (tr) | 2001-03-21 |
| CO5050358A1 (es) | 2001-06-27 |
| DE69920003T2 (de) | 2005-09-15 |
| WO1999055701A1 (en) | 1999-11-04 |
| AU3764499A (en) | 1999-11-16 |
| IL138405A0 (en) | 2001-10-31 |
| NO20005425D0 (no) | 2000-10-27 |
| US6420568B1 (en) | 2002-07-16 |
| CA2330685A1 (en) | 1999-11-04 |
| PL343733A1 (en) | 2001-09-10 |
| CN1298402A (zh) | 2001-06-06 |
| DE69920003D1 (de) | 2004-10-14 |
| JP4514950B2 (ja) | 2010-07-28 |
| NO20005425L (no) | 2000-10-27 |
| ID27316A (id) | 2001-03-22 |
| RU2194705C2 (ru) | 2002-12-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |