FI912280L - Kiral syntes av 1-aryl-3-aminopropan-1 -oler. - Google Patents
Kiral syntes av 1-aryl-3-aminopropan-1 -oler. Download PDFInfo
- Publication number
- FI912280L FI912280L FI912280A FI912280A FI912280L FI 912280 L FI912280 L FI 912280L FI 912280 A FI912280 A FI 912280A FI 912280 A FI912280 A FI 912280A FI 912280 L FI912280 L FI 912280L
- Authority
- FI
- Finland
- Prior art keywords
- oler
- synthes
- aminopropan
- chiral
- aryl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/02—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C215/22—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated
- C07C215/28—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being unsaturated and containing six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US52451290A | 1990-05-17 | 1990-05-17 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI912280A0 FI912280A0 (fi) | 1991-05-10 |
| FI912280A7 FI912280A7 (fi) | 1991-11-18 |
| FI912280L true FI912280L (fi) | 1991-11-18 |
Family
ID=24089523
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI912280A FI912280L (fi) | 1990-05-17 | 1991-05-10 | Kiral syntes av 1-aryl-3-aminopropan-1 -oler. |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0457559A3 (fi) |
| JP (1) | JPH04226948A (fi) |
| KR (1) | KR910019960A (fi) |
| CA (1) | CA2042346A1 (fi) |
| FI (1) | FI912280L (fi) |
| HU (1) | HUT57760A (fi) |
| IE (1) | IE911677A1 (fi) |
| IL (1) | IL98108A0 (fi) |
Families Citing this family (49)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0571685A1 (en) * | 1992-05-27 | 1993-12-01 | Novo Nordisk A/S | Aryloxyheteroarylpropylamines, their preparation and use |
| US5362886A (en) * | 1993-10-12 | 1994-11-08 | Eli Lilly And Company | Asymmetric synthesis |
| US6090950A (en) * | 1996-08-23 | 2000-07-18 | Zeeland Chemicals, Inc. | Chiral hydride complexes |
| US6008412A (en) * | 1997-10-14 | 1999-12-28 | Eli Lilly And Company | Process to make chiral compounds |
| TW514634B (en) * | 1997-10-14 | 2002-12-21 | Lilly Co Eli | Process to make chiral compounds |
| US5936124A (en) * | 1998-06-22 | 1999-08-10 | Sepacor Inc. | Fluoxetine process from benzoylpropionic acid |
| US6025517A (en) * | 1998-08-03 | 2000-02-15 | Sepracor Inc. | Fluoxetine process from benzoylacetonitrile |
| DE10207586A1 (de) * | 2002-02-22 | 2003-09-11 | Degussa | Herstellung von N-Methyl-3-hydroxy-3-(2-thienyl)propanamin über neue carbamatgruppenhaltige Thiophenderivate als Zwischenprodukte |
| EP1486493A4 (en) * | 2002-03-19 | 2007-04-04 | Mitsubishi Chem Corp | 3-HYDROXY-3- (2-THIENYL) PROPIONIC ACID AMID COMPOUND, METHOD FOR THE PRODUCTION THEREOF AND METHOD FOR PRODUCING A 3-AMINO-1- (2-THIENYL) -1-PROPANOL COMPOUND THEREFOR |
| US7659409B2 (en) | 2002-03-19 | 2010-02-09 | Mitsubishi Chemical Corporation | 3-Hydroxy-3-(2-thienyl) propionamides and production method thereof, and production method of 3-amino-1-(2-thienyl)-1-propanols using the same |
| JPWO2003097632A1 (ja) * | 2002-05-20 | 2005-09-15 | 三菱レイヨン株式会社 | プロパノールアミン誘導体、及び３−ｎ−メチルアミノ−１−（２−チエニル）−１−プロパノールの製造方法、並びにプロパノールアミン誘導体の製造方法 |
| EP1852415B1 (en) * | 2002-07-09 | 2009-10-07 | Lonza Ag | Process for the preparation of N-monosubstituted beta-amino alcohols |
| JP4546242B2 (ja) | 2002-07-09 | 2010-09-15 | ロンザ アーゲー | Ｎ−モノ置換β−アミノアルコールの製造方法 |
| DE10235206A1 (de) * | 2002-08-01 | 2004-02-19 | Basf Ag | Verfahren zur Herstellung von (S)-3-Methylmino-1-(thien-2-yl)propan-1-ol |
| CN100526290C (zh) * | 2002-08-27 | 2009-08-12 | 默克专利股份有限公司 | 氨基醇的对映选择性氢化方法 |
| GB0221438D0 (en) * | 2002-09-16 | 2002-10-23 | Avecia Ltd | Processes and compounds |
| US6846957B2 (en) | 2002-11-22 | 2005-01-25 | Board Of Regents, The University Of Texas System | Synthesis of 3-aminomethyl-1-propanol, a fluoxetine precursor |
| GB0229583D0 (en) * | 2002-12-19 | 2003-01-22 | Cipla Ltd | A process for preparing duloxetine and intermediates for use therein |
| DE10302595A1 (de) * | 2003-01-22 | 2004-07-29 | Basf Ag | 3-Methylamino-1-(2-thienyl)-1-proganon, seine Herstellung und Verwendung |
| DE10345772A1 (de) | 2003-10-01 | 2005-04-21 | Basf Ag | Verfahren zur Herstellung von 3-Methylamino-1-(thien-2-yl)-propan-1-ol |
| DE102004004719A1 (de) | 2004-01-29 | 2005-08-18 | Basf Ag | Verfahren zur Herstellung von enantiomerenreinen Aminoalkoholen |
| EP1566383A1 (en) * | 2004-02-19 | 2005-08-24 | Lonza AG | Process for the preparation of enantiomerically pure 1-substituted-3-aminoalcohols |
| CA2556891C (en) | 2004-02-19 | 2012-12-18 | Lonza Ag | Process for the preparation of enantiomerically pure 1-substituted-3-aminoalcohols |
| CN1300137C (zh) * | 2004-03-31 | 2007-02-14 | 上海医药工业研究院 | (s)－(+)－n,n－二甲基－3－(1－萘氧基)－3－(2－噻吩基)丙胺的制备方法 |
| DE102004022686A1 (de) | 2004-05-05 | 2005-11-24 | Basf Ag | Verfahren zur Herstellung optisch aktiver Alkohole |
| US20060194869A1 (en) * | 2004-12-23 | 2006-08-31 | Santiago Ini | Process for preparing pharmaceutically acceptable salts of duloxetine and intermediates thereof |
| KR20070104942A (ko) | 2005-02-21 | 2007-10-29 | 론자 아게 | 거울상적으로 순수한 1-치환-3-아미노알코올의 제조 방법 |
| US7399871B2 (en) | 2005-03-08 | 2008-07-15 | Teva Pharmaceutical Industries Ltd. | Crystal forms of (S)-(+)-N,N-dimethyl-3-(1-naphthalenyloxy)-3-(2-thienyl)propanamine oxalate and the preparation thereof |
| CA2599475A1 (en) | 2005-03-14 | 2006-09-21 | Teva Pharmaceutical Industries Ltd. | Pure duloxetine hydrochloride |
| EP1838692A2 (en) * | 2005-09-22 | 2007-10-03 | Teva Pharmaceutical Industries Ltd | Dnt-maleate and methods of preparation thereof |
| EP1863782A1 (en) | 2005-12-05 | 2007-12-12 | Teva Pharmaceutical Industries Ltd. | 2-(n-methyl-propanamine)-3-(2-naphtol) thiophene, an imputity of duloxetine hydrochloride |
| DE102005062662A1 (de) | 2005-12-23 | 2007-06-28 | Basf Ag | Verfahren zur Herstellung optisch aktiver Alkohole |
| DE102005062661A1 (de) | 2005-12-23 | 2007-08-16 | Basf Ag | Verfahren zur Herstellung von optisch aktivem (1S)-3-Chlor-(-thien-2-yl)-propan-1-ol |
| US8362279B2 (en) | 2006-01-06 | 2013-01-29 | Msn Laboratories Limited | Process for pure duloxetine hydrochloride |
| MX2007011676A (es) * | 2006-01-23 | 2007-11-15 | Teva Pharma | Dnt-bencensulfonato y metodos de preparacion de el. |
| WO2007084193A1 (en) * | 2006-01-23 | 2007-07-26 | Teva Pharmaceutical Industries Ltd. | Dnt-succinate and methods of preparation thereof |
| WO2007086948A1 (en) * | 2006-01-23 | 2007-08-02 | Teva Pharmaceutical Industries Ltd. | Dnt-fumarate and methods of preparation thereof |
| US20070238883A1 (en) * | 2006-02-13 | 2007-10-11 | Santiago Ini | Process for the preparation of(s)-(+)-N,N-dimethyl-3-(1-Naphthalenyloxy)-3-(2-Thienyl)propanamine, A duloxetine intermediate |
| WO2007098250A2 (en) | 2006-02-21 | 2007-08-30 | Teva Pharmaceutical Industries Ltd. | Process for the preparation of (s)-(-)-n,n-dimethyl-3-(2-thienyl)-3-hydroxypropanamine, a duloxetine intermediate |
| HU228458B1 (en) * | 2006-03-13 | 2013-03-28 | Egis Gyogyszergyar Nyrt | Duloxetine salts for producing pharmaceutical compositions |
| US20100280093A1 (en) | 2006-07-03 | 2010-11-04 | Ranbaxy Laboratories Limited | Process for the preparation enantiomerically pure salts of n-methyl-3-(1-naphthaleneoxy)-3-(2-thienyl)propanamine |
| WO2008077645A1 (en) | 2006-12-22 | 2008-07-03 | Synthon B.V. | Process for making duloxetine and related compounds |
| WO2009128057A2 (en) | 2008-04-18 | 2009-10-22 | UNIVERSITY COLLEGE DUBLIN, NATIONAL UNIVERSITY OF IRELAND, DUBLIN et al | Psycho-pharmaceuticals |
| HU230480B1 (hu) * | 2008-07-25 | 2016-07-28 | Egis Gyógyszergyár Nyilvánosan Működő Részvénytársaság | Eljárás N-metil-ariloxi-propánamin származékok előállítására |
| EP2329013B1 (en) | 2008-08-27 | 2015-10-28 | Codexis, Inc. | Ketoreductase polypeptides for the production of a 3-aryl-3-hydroxypropanamine from a 3-aryl-3-ketopropanamine |
| US8288141B2 (en) | 2008-08-27 | 2012-10-16 | Codexis, Inc. | Ketoreductase polypeptides for the production of 3-aryl-3-hydroxypropanamine from a 3-aryl-3-ketopropanamine |
| WO2010079404A2 (en) * | 2009-01-06 | 2010-07-15 | Alembic Limited | An improved process for the preparation of duloxetine and salts thereof |
| WO2011118625A1 (ja) * | 2010-03-24 | 2011-09-29 | 住友精化株式会社 | 光学活性なｎ－モノアルキル－３－ヒドロキシ－３－アリールプロピルアミン化合物の製造方法 |
| CN116640115A (zh) * | 2023-05-16 | 2023-08-25 | 浙江工业大学 | 一种3-甲氨基-1-(2-噻吩基)-1-丙酮盐酸盐的制备方法 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR880007433A (ko) * | 1986-12-22 | 1988-08-27 | 메리 앤 터커 | 3-아릴옥시-3-치환된 프로판아민 |
| DK630987D0 (da) * | 1987-12-01 | 1987-12-01 | Ferrosan As | Aryloxyphenylpropylaminer, deres fremstilling og anvendelse |
| ZA892517B (en) * | 1988-04-08 | 1990-12-28 | Lilly Co Eli | Propanamine derivatives |
-
1991
- 1991-05-10 IL IL98108A patent/IL98108A0/xx unknown
- 1991-05-10 FI FI912280A patent/FI912280L/fi unknown
- 1991-05-10 CA CA002042346A patent/CA2042346A1/en not_active Abandoned
- 1991-05-15 EP EP19910304345 patent/EP0457559A3/en not_active Withdrawn
- 1991-05-16 HU HU911648A patent/HUT57760A/hu unknown
- 1991-05-16 IE IE167791A patent/IE911677A1/en unknown
- 1991-05-17 JP JP3113034A patent/JPH04226948A/ja not_active Withdrawn
- 1991-05-17 KR KR1019910008023A patent/KR910019960A/ko not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| HU911648D0 (en) | 1991-11-28 |
| KR910019960A (ko) | 1991-12-19 |
| FI912280A7 (fi) | 1991-11-18 |
| FI912280A0 (fi) | 1991-05-10 |
| EP0457559A2 (en) | 1991-11-21 |
| IE911677A1 (en) | 1991-11-20 |
| HUT57760A (en) | 1991-12-30 |
| JPH04226948A (ja) | 1992-08-17 |
| EP0457559A3 (en) | 1993-05-12 |
| CA2042346A1 (en) | 1991-11-18 |
| IL98108A0 (en) | 1992-06-21 |
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