AU2001269749A1 - Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazine - Google Patents
Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazineInfo
- Publication number
- AU2001269749A1 AU2001269749A1 AU2001269749A AU6974901A AU2001269749A1 AU 2001269749 A1 AU2001269749 A1 AU 2001269749A1 AU 2001269749 A AU2001269749 A AU 2001269749A AU 6974901 A AU6974901 A AU 6974901A AU 2001269749 A1 AU2001269749 A1 AU 2001269749A1
- Authority
- AU
- Australia
- Prior art keywords
- oxazine
- fluorophenyl
- trifluoromethyl
- ethoxy
- trans
- 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
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/28—1,4-Oxazines; Hydrogenated 1,4-oxazines
- C07D265/30—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
- C07D265/32—1,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings with oxygen atoms directly attached to ring carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US21050000P | 2000-06-09 | 2000-06-09 | |
US60210500 | 2000-06-09 | ||
PCT/US2001/018242 WO2001096319A1 (en) | 2000-06-09 | 2001-06-05 | Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-[1-(3,5-bis(trifluoromethyl)phenyl)ethoxy]-3-(4-fluorophenyl)-1,4-oxazine |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001269749A1 true AU2001269749A1 (en) | 2001-12-24 |
Family
ID=22783150
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001269749A Abandoned AU2001269749A1 (en) | 2000-06-09 | 2001-06-05 | Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazine |
Country Status (3)
Country | Link |
---|---|
US (1) | US6395898B1 (en) |
AU (1) | AU2001269749A1 (en) |
WO (1) | WO2001096319A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7985592B2 (en) * | 2004-02-13 | 2011-07-26 | Chevron Oronite Company Llc | High throughput screening methods for lubricating oil compositions |
WO2007044829A2 (en) * | 2005-10-06 | 2007-04-19 | Dr. Reddy's Laboratories Ltd. | Preparation of aprepitant |
KR101630884B1 (en) * | 2008-02-26 | 2016-06-15 | 산도즈 아게 | Preparation of morpholine derivatives |
WO2009116081A2 (en) * | 2008-03-03 | 2009-09-24 | Msn Laboratories Limited | An improved process for the preparation of aprepitant |
WO2012146692A1 (en) | 2011-04-29 | 2012-11-01 | Sandoz Ag | Novel intermediates for the preparation of highly pure aprepitant or fosaprepitant |
CN102675240B (en) | 2012-04-13 | 2015-01-14 | 浙江海正药业股份有限公司 | 4-substitute-2-hydroxy morpholine-3-ketone and preparation method thereof |
CN103193725A (en) * | 2013-04-12 | 2013-07-10 | 上海医药工业研究院 | Preparation method of (2R, 3R)-2-((1R)-1-(3, 5-bis (trifluoromethyl)phenyl)ethoxy)-3-(4-fluorophenyl) morpholine |
CN103214426A (en) * | 2013-04-12 | 2013-07-24 | 上海开义医药化工有限公司 | Production method of aprepitant morpholine key intermediate body or aprepitant morpholine salt |
CN113582982B (en) * | 2021-06-15 | 2023-06-16 | 山东罗欣药业集团股份有限公司 | Preparation method of NK1 receptor antagonist |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5719147A (en) * | 1992-06-29 | 1998-02-17 | Merck & Co., Inc. | Morpholine and thiomorpholine tachykinin receptor antagonists |
NZ277839A (en) * | 1993-12-29 | 1998-01-26 | Merck Sharp & Dohme | Substituted morpholine derivatives, preparation and pharmaceutical compositions thereof |
-
2001
- 2001-06-05 AU AU2001269749A patent/AU2001269749A1/en not_active Abandoned
- 2001-06-05 WO PCT/US2001/018242 patent/WO2001096319A1/en active Application Filing
- 2001-06-08 US US09/878,043 patent/US6395898B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
WO2001096319A1 (en) | 2001-12-20 |
US20020022725A1 (en) | 2002-02-21 |
US6395898B1 (en) | 2002-05-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HRP20020973A2 (en) | Process for the synthesis of (2r,2-alpha-r,3a)-2-[1-(3,5-bis(trifluoromethyl)phenyl)ethoxy]-3-(4-fluorophenyl)-1,4-oxazine | |
AU2001263399A1 (en) | 1-(pyrrlolidin-1-ylmethyl)-3-(pyrrol-2-ylmethylidene)-2-indo linone derivatives | |
AU2002224927A1 (en) | Use of substituted imidazoazines, novel imidazoazines, methods for the production thereof, and agents containing these compounds | |
AU2002237522A1 (en) | Beta-lactam compounds, process for reproducing the same and serum cholesterol-lowering agents containing the same | |
TWI341313B (en) | Process for the synthesis of 5-[[2(r)-[1(r)-[3,5-bis(trifluoromethyl)phenyl]ethoxy]-3(s)-(4-fluorophenyl)-4-morpholinyl]methyl]-1,2-dihydro-3h-1,2,4-triazol-3-one | |
AU2001269749A1 (en) | Trans-glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazine | |
AU2001266690A1 (en) | Process for the synthesis of (2r, 2-alpha-r)-4-benzyl-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-1,4-oxazin-3-one | |
AU2002352962A1 (en) | Novel-n-(4-(1h-imidazol-1-yl)-2-fluorophenyl)-3-(trifluoromethyl)-1-h-pyrazole-5-carboxamides as factor xa | |
AU2001268290A1 (en) | Intramolecular glycosidation process for the synthesis of (2r, 2-alpha-r, 3a)-2-(1-(3,5-bis(trifluoromethyl)phenyl) ethoxy)-3-(4-fluorophenyl)-1,4-oxazine | |
IL155706A0 (en) | Process for the preparation of (r)-5-(2-benzenesulfonylethyl)-3-(n-methylpyrrolidin-2-ylmethyl)-1h-indole | |
AU2001277801A1 (en) | Process for preparing 2,3-diaminopropanols and synthesis of other compounds using 2,3-diaminopropanols | |
AU2003222435A1 (en) | Process for the preparation of 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)- 1,3-dihydro-5-isobenzofuran carbonitrile | |
AU2002230961A1 (en) | Process for the synthesis of 1-(3,5-bis(trifluoromethyl)-phenyl)ethan-1-one | |
MXPA03006970A (en) | New use of iloperidone. | |
AU2003223098A1 (en) | Novel process for the preparation of substantially pure 5-(3,5-dimethylphenoxy)methyl-2-oxazolidinone | |
AU2003222399A1 (en) | Process for the synthesis of base addition salts of 2,3-0-isopropylidene-1-0-substituted-5,6-dideoxy-5-n- (4-(2-hydroxy-2-oxoethyl)-phenylaminocarbonyl) amino-l-gulofuranosides | |
HK1051190A1 (en) | Process for the preparation of 2-(4-alkyl-1-piperazinyl-benzaldehyde and -benzylidenyl compounds. | |
AU2002214977A1 (en) | Tetrahydrocarbazoles, a process for the preparation of those compounds, and the use thereof | |
EP1295882A4 (en) | Process for the preparation of a piperazine derivative | |
AU2003236207A1 (en) | The hydrochloride of (s)-(+)-3-(1-(2-(1-acetyl-2,3-dihydro-1h-indol-3-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-6-chloro-1h-indole | |
IL164377A0 (en) | Methods of preparation of the 2-(7-chloro-1,8-naphthyridine-2yl)-3-(5-methyl-2-oxo-hexyl)-1-isoindolinone | |
AU2001282744A1 (en) | Process for asymmetric synthesis of substituted 1,4-dihydropyridines | |
AU4595100A (en) | ((e),3(r))-enantiomer of 4-(3-chloro -4-cyanophenyl) -1-(p- methylsulphonyl -phenylsulphonyl) -2-trifluoromethylbut -trans-3-en-ol | |
AU2003243930A1 (en) | Pharmaceutical composition comprising (s)-(+)-3-(1-(2-(1-acetyl-2,3-dihydro-1h-indol-3-yl)ethyl)-1,2,3,6-tetrahydropyridin-4-yl)-6-chloro-1h-indole | |
WO2004099129A3 (en) | Intermediates useful in the synthesis of hiv-protease inhibitors and methods for preparing the same |