MXPA04004063A - Procedimientos para elaboracion de 3-hidroxi-n, 1, 6-trialquil-4 -oxo-1 ,4-dihidropiridin-2 -carboxamida. - Google Patents
Procedimientos para elaboracion de 3-hidroxi-n, 1, 6-trialquil-4 -oxo-1 ,4-dihidropiridin-2 -carboxamida.Info
- Publication number
- MXPA04004063A MXPA04004063A MXPA04004063A MXPA04004063A MXPA04004063A MX PA04004063 A MXPA04004063 A MX PA04004063A MX PA04004063 A MXPA04004063 A MX PA04004063A MX PA04004063 A MXPA04004063 A MX PA04004063A MX PA04004063 A MXPA04004063 A MX PA04004063A
- Authority
- MX
- Mexico
- Prior art keywords
- oxo
- dihydropyridine
- trialkyl
- carboxamide
- hydroxy
- Prior art date
Links
Classifications
-
- 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- A61K31/4412—Non condensed pyridines; Hydrogenated derivatives thereof having oxo groups directly attached to the heterocyclic ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/06—Antianaemics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
- C07D309/34—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D309/36—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with oxygen atoms directly attached to ring carbon atoms
- C07D309/40—Oxygen atoms attached in positions 3 and 4, e.g. maltol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Diabetes (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Hematology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
La presente invencion se refiere a un nuevo procedimiento para la preparacion de la 3-hidroxi-N,1,6-triaquil-4-oxo-1,4-dihidropiridin-2-carboxamida de la formula I: El metodo comprende la oxidacion con TEMPO de un alcohol primario de 2-hidroximetil-6-alquil-4H-piran-4-ona 3-0-protegida de la formula III al acido 6-alquil-4-oxo-4H-piran-2-carboxilico 3-0-protegido de la formula II. La reaccion del compuesto de la formula II con metilamina y 1,1-carbonildiimidazol en un solvente inerte proporciona la N,1,6-tri-alquil-4-oxo-1,4-dihidropiridin-2-carboxamida 3-0-protegida, la cual es desprotegida para proporcionar la 3-hidroxi-N,1,6-trialqul-4-oxo-1,4-dihidropiridin-2-carboxamida de la formula I.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/985,269 US6426418B1 (en) | 2001-11-02 | 2001-11-02 | Processes for the manufacturing of 3-hydroxy-N,1,6-trialkyl-4-oxo-1,4-dihydropyridine-2-carboxamide |
PCT/CA2002/001623 WO2003037867A1 (en) | 2001-11-02 | 2002-10-30 | Processes for the manufacturing of 3-hydroxy-n,1,6-trialkyl-4-oxo-1,4-dihydropyridine-2-carboxamide |
Publications (1)
Publication Number | Publication Date |
---|---|
MXPA04004063A true MXPA04004063A (es) | 2004-07-08 |
Family
ID=25531334
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MXPA04004063A MXPA04004063A (es) | 2001-11-02 | 2002-10-30 | Procedimientos para elaboracion de 3-hidroxi-n, 1, 6-trialquil-4 -oxo-1 ,4-dihidropiridin-2 -carboxamida. |
Country Status (11)
Country | Link |
---|---|
US (3) | US6426418B1 (es) |
EP (1) | EP1440061B1 (es) |
KR (1) | KR20050056908A (es) |
CN (1) | CN1282645C (es) |
AT (1) | ATE359272T1 (es) |
BR (1) | BR0213814A (es) |
DE (1) | DE60219501D1 (es) |
ES (1) | ES2284925T3 (es) |
MX (1) | MXPA04004063A (es) |
PL (1) | PL368722A1 (es) |
WO (1) | WO2003037867A1 (es) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6426418B1 (en) * | 2001-11-02 | 2002-07-30 | Apotex, Inc. | Processes for the manufacturing of 3-hydroxy-N,1,6-trialkyl-4-oxo-1,4-dihydropyridine-2-carboxamide |
NZ529657A (en) * | 2003-11-20 | 2004-07-30 | Apotex Inc | Iron chelating cycloalkyl derivatives of 3-hydroxy-4-pyridinones |
CA2488034C (en) | 2004-11-19 | 2009-10-06 | Apotex Inc. | Process for the manufacture of 3-hydroxy-n-alkyl-1-cycloalkyl-6-alkyl-4-oxo-1,4-dihydropyridine-2-carboxamide and its related analogues |
KR101695807B1 (ko) | 2008-07-25 | 2017-01-13 | 비이브 헬쓰케어 컴퍼니 | 화합물 |
EP2376080B1 (en) | 2008-12-11 | 2017-09-13 | Shionogi&Co., Ltd. | Synthesis of carbamoylpyridone hiv integrase inhibitors and intermediates |
EP2370419B1 (en) * | 2008-12-11 | 2017-09-27 | Shionogi&Co., Ltd. | Maltol ether processes and intermediates |
SG171731A1 (en) | 2008-12-11 | 2011-07-28 | Glaxosmithkline Llc | Processes and intermediates for carbamoylpyridone hiv integrase inhibitors |
TWI518084B (zh) | 2009-03-26 | 2016-01-21 | 鹽野義製藥股份有限公司 | 哌喃酮與吡啶酮衍生物之製造方法 |
TWI582097B (zh) | 2010-03-23 | 2017-05-11 | Viiv醫療保健公司 | 製備胺甲醯吡啶酮衍生物及中間體之方法 |
CN105153421B (zh) * | 2015-07-28 | 2017-10-13 | 辽宁石油化工大学 | 一种制备四甲基哌啶氮氧自由基聚合物方法 |
CN105294413B (zh) * | 2015-09-17 | 2017-04-12 | 浙江工业大学 | 一种铁盐催化醇氧化制备醛/酮的方法 |
US11286262B2 (en) * | 2017-10-06 | 2022-03-29 | Shionogi & Co., Ltd. | Stereoselective process for preparing substituted polycyclic pyridone derivatives |
CN109438405B (zh) * | 2018-12-24 | 2023-04-07 | 广东莱佛士制药技术有限公司 | 一种3-(苄氧基)-4-氧代-4h-吡喃-2-羧酸的合成方法 |
PE20231939A1 (es) * | 2021-03-01 | 2023-12-05 | Orion Corp | Proceso para la preparacion de un inhibidor de cyp11a1 y sus intermedios |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3468915A (en) | 1966-04-18 | 1969-09-23 | Pfizer & Co C | Novel 2-substituted-6-methylpyromeconic acids |
GR78491B (es) | 1982-03-24 | 1984-09-27 | Nat Res Dev | |
GB9217099D0 (en) | 1992-08-12 | 1992-09-23 | British Tech Group | Pharmaceutical compositions |
EP0768302B1 (de) | 1995-09-29 | 2005-07-06 | Novartis AG | Hydroxypyridinone |
GB9711093D0 (en) | 1997-05-29 | 1997-07-23 | British Tech Group | Novel orally active iron (III) chelators |
JP2002511440A (ja) * | 1998-04-09 | 2002-04-16 | メルク エンド カムパニー インコーポレーテッド | Tempoを使用した酸化方法 |
US6426418B1 (en) * | 2001-11-02 | 2002-07-30 | Apotex, Inc. | Processes for the manufacturing of 3-hydroxy-N,1,6-trialkyl-4-oxo-1,4-dihydropyridine-2-carboxamide |
-
2001
- 2001-11-02 US US09/985,269 patent/US6426418B1/en not_active Expired - Fee Related
-
2002
- 2002-03-19 US US10/100,133 patent/US6472532B1/en not_active Expired - Fee Related
- 2002-03-19 US US10/100,107 patent/US6476229B1/en not_active Expired - Fee Related
- 2002-10-30 MX MXPA04004063A patent/MXPA04004063A/es active IP Right Grant
- 2002-10-30 WO PCT/CA2002/001623 patent/WO2003037867A1/en active IP Right Grant
- 2002-10-30 KR KR1020047006656A patent/KR20050056908A/ko not_active Application Discontinuation
- 2002-10-30 AT AT02771927T patent/ATE359272T1/de not_active IP Right Cessation
- 2002-10-30 ES ES02771927T patent/ES2284925T3/es not_active Expired - Lifetime
- 2002-10-30 EP EP02771927A patent/EP1440061B1/en not_active Expired - Lifetime
- 2002-10-30 PL PL02368722A patent/PL368722A1/xx not_active Application Discontinuation
- 2002-10-30 DE DE60219501T patent/DE60219501D1/de not_active Expired - Lifetime
- 2002-10-30 BR BR0213814-0A patent/BR0213814A/pt not_active Application Discontinuation
- 2002-10-30 CN CNB028215672A patent/CN1282645C/zh not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
BR0213814A (pt) | 2004-10-19 |
US6476229B1 (en) | 2002-11-05 |
CN1578769A (zh) | 2005-02-09 |
US6472532B1 (en) | 2002-10-29 |
DE60219501D1 (de) | 2007-05-24 |
US6426418B1 (en) | 2002-07-30 |
WO2003037867A1 (en) | 2003-05-08 |
EP1440061A1 (en) | 2004-07-28 |
KR20050056908A (ko) | 2005-06-16 |
ES2284925T3 (es) | 2007-11-16 |
PL368722A1 (en) | 2005-04-04 |
EP1440061B1 (en) | 2007-04-11 |
ATE359272T1 (de) | 2007-05-15 |
CN1282645C (zh) | 2006-11-01 |
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Legal Events
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FG | Grant or registration |