ATE547410T1 - Verfahren zur herstellung von (s)-(+)-n-methyl-3- (1-naphthyloxy)-3-(2-thienyl)-propylamin mittels einer optisch aktiven methylhydroxylaminopropanolverbindung als zwischenprodukt - Google Patents
Verfahren zur herstellung von (s)-(+)-n-methyl-3- (1-naphthyloxy)-3-(2-thienyl)-propylamin mittels einer optisch aktiven methylhydroxylaminopropanolverbindung als zwischenproduktInfo
- Publication number
- ATE547410T1 ATE547410T1 AT10156142T AT10156142T ATE547410T1 AT E547410 T1 ATE547410 T1 AT E547410T1 AT 10156142 T AT10156142 T AT 10156142T AT 10156142 T AT10156142 T AT 10156142T AT E547410 T1 ATE547410 T1 AT E547410T1
- Authority
- AT
- Austria
- Prior art keywords
- methyl
- naphthyloxy
- thienyl
- propylamin
- producing
- Prior art date
Links
- -1 METHYLHYDROXYLAMINOPROPANOL COMPOUND Chemical class 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title abstract 3
- ZEUITGRIYCTCEM-KRWDZBQOSA-N (S)-duloxetine Chemical compound C1([C@@H](OC=2C3=CC=CC=C3C=CC=2)CCNC)=CC=CS1 ZEUITGRIYCTCEM-KRWDZBQOSA-N 0.000 title 1
- GUPBNSICSXFQNG-IBGZPJMESA-N (3s)-n-methyl-3-naphthalen-1-yloxy-3-thiophen-2-ylbutan-1-amine Chemical compound C1([C@@](C)(OC=2C3=CC=CC=C3C=CC=2)CCNC)=CC=CS1 GUPBNSICSXFQNG-IBGZPJMESA-N 0.000 abstract 2
Classifications
-
- 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
- C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US12/402,740 US8148549B2 (en) | 2009-03-12 | 2009-03-12 | Preparation of (S)-(+)-N-methyl-3-(1-naphthyloxy)-3-(2-thienyl) propylamine using optically active methylhydroxylaminopropanol compound as an intermediate |
| US12/718,289 US8614336B2 (en) | 2009-03-12 | 2010-03-05 | Process for preparing N-methyl-N-hydroxyl-3-(1-naphthyloxy)-3-(2-thienyl)propylamine derivative |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE547410T1 true ATE547410T1 (de) | 2012-03-15 |
Family
ID=42167649
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT10156142T ATE547410T1 (de) | 2009-03-12 | 2010-03-10 | Verfahren zur herstellung von (s)-(+)-n-methyl-3- (1-naphthyloxy)-3-(2-thienyl)-propylamin mittels einer optisch aktiven methylhydroxylaminopropanolverbindung als zwischenprodukt |
Country Status (5)
| Country | Link |
|---|---|
| US (2) | US8148549B2 (de) |
| EP (1) | EP2228372B1 (de) |
| JP (1) | JP5143167B2 (de) |
| AT (1) | ATE547410T1 (de) |
| ES (1) | ES2382604T3 (de) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8148549B2 (en) * | 2009-03-12 | 2012-04-03 | Sci Pharmtech, Inc. | Preparation of (S)-(+)-N-methyl-3-(1-naphthyloxy)-3-(2-thienyl) propylamine using optically active methylhydroxylaminopropanol compound as an intermediate |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4956388A (en) * | 1986-12-22 | 1990-09-11 | Eli Lilly And Company | 3-aryloxy-3-substituted propanamines |
| 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 |
| TWI306858B (en) * | 2004-12-23 | 2009-03-01 | Teva Pharma | Process for preparing pharmaceutically acceptable salts of duloxetine and intermediates thereof |
| US7538232B2 (en) * | 2006-01-19 | 2009-05-26 | Eli Lilly And Company | Process for the asymmetric synthesis of duloxetine |
| EP2114912B1 (de) * | 2006-12-22 | 2012-04-04 | Synthon B.V. | Verfahren zur herstellung von duloxetin und verwandten verbindungen |
| US7829731B2 (en) * | 2007-10-29 | 2010-11-09 | Sci Pharmtech, Inc. | Methylhydroxylaminopropanol derivative and its use as intermediate for preparation of 3-methylamino-1-(2-thienyl)propan-1-OL |
| US8148549B2 (en) * | 2009-03-12 | 2012-04-03 | Sci Pharmtech, Inc. | Preparation of (S)-(+)-N-methyl-3-(1-naphthyloxy)-3-(2-thienyl) propylamine using optically active methylhydroxylaminopropanol compound as an intermediate |
-
2009
- 2009-03-12 US US12/402,740 patent/US8148549B2/en active Active
-
2010
- 2010-03-05 US US12/718,289 patent/US8614336B2/en active Active
- 2010-03-10 ES ES10156142T patent/ES2382604T3/es active Active
- 2010-03-10 AT AT10156142T patent/ATE547410T1/de active
- 2010-03-10 EP EP10156142A patent/EP2228372B1/de active Active
- 2010-03-11 JP JP2010054505A patent/JP5143167B2/ja active Active
Also Published As
| Publication number | Publication date |
|---|---|
| ES2382604T3 (es) | 2012-06-11 |
| JP5143167B2 (ja) | 2013-02-13 |
| EP2228372B1 (de) | 2012-02-29 |
| EP2228372A1 (de) | 2010-09-15 |
| US20100234619A1 (en) | 2010-09-16 |
| US20100234620A1 (en) | 2010-09-16 |
| US8614336B2 (en) | 2013-12-24 |
| JP2010215623A (ja) | 2010-09-30 |
| US8148549B2 (en) | 2012-04-03 |
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