AU2290800A - 1-(6- methylpyridine- 3-yl)-2-(4- (methylsulfonyl) phenyl) ethanone and method for its preparation - Google Patents
1-(6- methylpyridine- 3-yl)-2-(4- (methylsulfonyl) phenyl) ethanone and method for its preparationInfo
- Publication number
- AU2290800A AU2290800A AU22908/00A AU2290800A AU2290800A AU 2290800 A AU2290800 A AU 2290800A AU 22908/00 A AU22908/00 A AU 22908/00A AU 2290800 A AU2290800 A AU 2290800A AU 2290800 A AU2290800 A AU 2290800A
- Authority
- AU
- Australia
- Prior art keywords
- preparation
- ethanone
- methylsulfonyl
- phenyl
- methylpyridin
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/54—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/57—Nitriles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- 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
- C07D213/24—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 substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pain & Pain Management (AREA)
- Pharmacology & Pharmacy (AREA)
- Rheumatology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1-(6-Methylpyridin-3-yl)-2-(4-methylsulfonyl-phenyl)-ethanone is new. 1-(6-methylpyridin-3-yl)-2-(4-methylsulfonyl-phenyl)-ethanone of formula (I) is new: Independent claims are also included for the following: (a) a 4-step preparation of (I) where the third step for the preparation of N,N-dialkylamino-(6-methyl-3-pyridyl)acetonitriles of formula (III) and the last step are claimed per se; (b) compounds (III); (c) alkali metal 1-hydroxy-(6-methylpyridin-3-yl)methanesulfonate intermediates of formula (II) (for preparing (III)); (d) preparation of (II) comprising treating 2-methyl-5-vinylpyridine with ozone followed by reduction with an alkali hydrogen sulfite. R1, R2 = 1-4C alkyl; M = alkali metal.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99100590 | 1999-01-14 | ||
EP99100590 | 1999-01-14 | ||
US14599699P | 1999-07-29 | 1999-07-29 | |
US60145996 | 1999-07-29 | ||
PCT/EP2000/000240 WO2000042014A2 (en) | 1999-01-14 | 2000-01-13 | 1-(6- methylpyridine- 3-yl)-2-[4- (methylsulfonyl) phenyl] ethanone and method for its preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2290800A true AU2290800A (en) | 2000-08-01 |
Family
ID=34089809
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU22908/00A Abandoned AU2290800A (en) | 1999-01-14 | 2000-01-13 | 1-(6- methylpyridine- 3-yl)-2-(4- (methylsulfonyl) phenyl) ethanone and method for its preparation |
Country Status (15)
Country | Link |
---|---|
EP (2) | EP1159270B1 (en) |
JP (1) | JP4765167B2 (en) |
CN (2) | CN1170820C (en) |
AT (2) | ATE253559T1 (en) |
AU (1) | AU2290800A (en) |
CA (2) | CA2485739C (en) |
CZ (1) | CZ302270B6 (en) |
DE (2) | DE50004327D1 (en) |
DK (2) | DK1394149T3 (en) |
ES (2) | ES2235138T3 (en) |
HU (1) | HUP0105124A3 (en) |
IL (1) | IL143981A0 (en) |
PT (2) | PT1394149E (en) |
SK (1) | SK284903B6 (en) |
WO (1) | WO2000042014A2 (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN104725300A (en) * | 2015-02-28 | 2015-06-24 | 宁波九胜创新医药科技有限公司 | Preparation method of 1-(6-methyl pyridine-3-yl)-2-(4-methylsulfonyl phenyl) ethanone |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3313683A (en) * | 1963-04-22 | 1967-04-11 | Lilly Co Eli | Nematocidal and fungicidal methods |
FR2074674A1 (en) * | 1970-01-16 | 1971-10-08 | Simafex | Sulphonamide/aldehyde-bisulphite complexes - antibacterials with very high solubility in water |
US4155909A (en) * | 1977-06-13 | 1979-05-22 | Philip Morris Incorporated | 2-Alkyl nicotinoids and processes for their production |
US5596008A (en) * | 1995-02-10 | 1997-01-21 | G. D. Searle & Co. | 3,4-Diaryl substituted pyridines for the treatment of inflammation |
SK283261B6 (en) * | 1996-07-18 | 2003-04-01 | Merck Frosst Canada & Co. / Merck Frosst Canada & Cie. | Substituted pyridines, pharmaceutical composition containing them and use |
TW492959B (en) * | 1997-04-18 | 2002-07-01 | Merck & Co Inc | Process for making 2-aryl-3-aryl-5-halo pyridines useful as cox-2 inhibitors |
AR015938A1 (en) * | 1997-09-25 | 2001-05-30 | Merck Sharp & Dohme | PROCEDURE TO PREPARE DIARIL PIRIDINES USEFUL AS COX-2 INHIBITORS AND INTERMEDIATE COMPOUND |
ATE272613T1 (en) * | 1998-04-24 | 2004-08-15 | Merck & Co Inc | METHOD FOR SYNTHESIS OF COX-2 INHIBITORS |
-
2000
- 2000-01-13 CA CA002485739A patent/CA2485739C/en not_active Expired - Fee Related
- 2000-01-13 WO PCT/EP2000/000240 patent/WO2000042014A2/en active Application Filing
- 2000-01-13 DK DK03024787T patent/DK1394149T3/en active
- 2000-01-13 CN CNB008027218A patent/CN1170820C/en not_active Expired - Fee Related
- 2000-01-13 ES ES03024787T patent/ES2235138T3/en not_active Expired - Lifetime
- 2000-01-13 IL IL14398100A patent/IL143981A0/en active IP Right Grant
- 2000-01-13 SK SK972-2001A patent/SK284903B6/en not_active IP Right Cessation
- 2000-01-13 CN CNB200410069946XA patent/CN1281589C/en not_active Expired - Fee Related
- 2000-01-13 EP EP00901555A patent/EP1159270B1/en not_active Expired - Lifetime
- 2000-01-13 DE DE50004327T patent/DE50004327D1/en not_active Expired - Lifetime
- 2000-01-13 AT AT00901555T patent/ATE253559T1/en active
- 2000-01-13 HU HU0105124A patent/HUP0105124A3/en unknown
- 2000-01-13 PT PT03024787T patent/PT1394149E/en unknown
- 2000-01-13 CA CA002359958A patent/CA2359958C/en not_active Expired - Fee Related
- 2000-01-13 DK DK00901555T patent/DK1159270T3/en active
- 2000-01-13 DE DE50009312T patent/DE50009312D1/en not_active Expired - Lifetime
- 2000-01-13 AT AT03024787T patent/ATE287396T1/en active
- 2000-01-13 ES ES00901555T patent/ES2209807T3/en not_active Expired - Lifetime
- 2000-01-13 EP EP03024787A patent/EP1394149B1/en not_active Expired - Lifetime
- 2000-01-13 CZ CZ20012457A patent/CZ302270B6/en not_active IP Right Cessation
- 2000-01-13 PT PT00901555T patent/PT1159270E/en unknown
- 2000-01-13 JP JP2000593582A patent/JP4765167B2/en not_active Expired - Fee Related
- 2000-01-13 AU AU22908/00A patent/AU2290800A/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
CN1583723A (en) | 2005-02-23 |
EP1159270B1 (en) | 2003-11-05 |
EP1159270A2 (en) | 2001-12-05 |
EP1394149B1 (en) | 2005-01-19 |
ES2235138T3 (en) | 2005-07-01 |
JP4765167B2 (en) | 2011-09-07 |
WO2000042014A2 (en) | 2000-07-20 |
CN1170820C (en) | 2004-10-13 |
DK1159270T3 (en) | 2004-02-23 |
ATE287396T1 (en) | 2005-02-15 |
CZ20012457A3 (en) | 2002-01-16 |
DK1394149T3 (en) | 2005-04-04 |
CA2359958A1 (en) | 2000-07-20 |
SK9722001A3 (en) | 2001-12-03 |
DE50009312D1 (en) | 2005-02-24 |
PT1394149E (en) | 2005-05-31 |
PT1159270E (en) | 2004-03-31 |
HUP0105124A2 (en) | 2002-04-29 |
DE50004327D1 (en) | 2003-12-11 |
WO2000042014A3 (en) | 2000-12-07 |
EP1394149A1 (en) | 2004-03-03 |
CA2485739A1 (en) | 2000-07-20 |
JP2003518002A (en) | 2003-06-03 |
CN1281589C (en) | 2006-10-25 |
CA2485739C (en) | 2009-09-22 |
IL143981A0 (en) | 2002-04-21 |
HUP0105124A3 (en) | 2002-05-28 |
CZ302270B6 (en) | 2011-01-19 |
SK284903B6 (en) | 2006-02-02 |
ATE253559T1 (en) | 2003-11-15 |
ES2209807T3 (en) | 2004-07-01 |
CA2359958C (en) | 2006-04-04 |
CN1359374A (en) | 2002-07-17 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EA200300067A1 (en) | CRYSTAL FORM OF TELECOXIB | |
AU2001263278A1 (en) | Cyclic gmp-specific phosphodiesterase inhibitors | |
MY147948A (en) | 4- imidazolin-2-one compounds | |
AU2290800A (en) | 1-(6- methylpyridine- 3-yl)-2-(4- (methylsulfonyl) phenyl) ethanone and method for its preparation | |
AU6220300A (en) | Benzofurylpiperazine serotonin agonists | |
ES8604170A1 (en) | Triazole antifungal agents. | |
AU2001293856A1 (en) | A process for the preparation of pantoprazole and intermediates therefor | |
NZ336091A (en) | Aqueous disinfecting cleaning composition | |
AP2001002045A0 (en) | FKBP inhibitors. | |
AU2001296699A1 (en) | Condensed pyrazindione derivatives as pde inhibitors | |
WO2003049698A3 (en) | Substituted hydrazones as inhibitors of cyclooxygenase-2 | |
NZ333854A (en) | Intermediates for the preparation of 2-imidazoline-5-ones | |
MXPA04003086A (en) | A process for the stereoselective synthesis of 2-hydroxymethyl-chromans. | |
EP1104756A4 (en) | Brassionosteroid biosynthesis inhibitors | |
MXPA01007169A (en) | 1-(6- methylpyridine- 3-yl)-2-[4- (methylsulfonyl) phenyl] ethanone and method for its preparation. | |
DK1370547T3 (en) | Benzoxathiepine derivatives and their use as pharmaceuticals | |
EP0618204A4 (en) | Heterocyclic compound and cardiotonic containing the same as active ingredient. | |
MX9703146A (en) | Heterocycle substituted propenoic acid derivatives as nmda antagonists. | |
AU6191599A (en) | Method for preparing trion-bis(oxime ether) derivatives andrion-mono and trion-bis(oxime ether) derivatives obtained therewith | |
DK0823907T3 (en) | Process for the preparation of (-) - trans-N-p-fluorobenzoylmethyl-4- (p-fluorophenyl) -3 - [[3,4- (methylenedioxy) phenoxy] methyl] | |
WO2002009520A1 (en) | Flowering regulators | |
JPS5515455A (en) | 2-substituted-methyl-1,4-benzodioxane | |
MXPA02012483A (en) | Method for producing 4-bromine-aniline derivatives. | |
GB9707643D0 (en) | 2-(3,5-Difluorophenyl)-3-(4-(methylsulfonyl)phenyl)-2-cyclopenten-1-one useful as an inhibitor of cox-2 | |
AU5044499A (en) | 2-ethyl-2,3-dihydrobenzofuran-carboxylic acid ester derivative, preparation method and use for preparing efaroxan derivatives |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MK6 | Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase |