HUP0202963A2 - Új benzol-szulfonamidok, valamint új eljárás ismert benzol-szulfonamid származék előállítására - Google Patents
Új benzol-szulfonamidok, valamint új eljárás ismert benzol-szulfonamid származék előállításáraInfo
- Publication number
- HUP0202963A2 HUP0202963A2 HU0202963A HUP0202963A HUP0202963A2 HU P0202963 A2 HUP0202963 A2 HU P0202963A2 HU 0202963 A HU0202963 A HU 0202963A HU P0202963 A HUP0202963 A HU P0202963A HU P0202963 A2 HUP0202963 A2 HU P0202963A2
- Authority
- HU
- Hungary
- Prior art keywords
- propyl
- benzyl
- benzenesulfonamides
- novel
- preparation
- Prior art date
Links
- 150000008331 benzenesulfonamides Chemical class 0.000 title 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical group NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 229960002613 tamsulosin Drugs 0.000 abstract 2
- VHNIORJSHIWCCH-UHFFFAOYSA-N 2-methoxy-3-propylbenzenesulfonamide Chemical compound CCCC1=CC=CC(S(N)(=O)=O)=C1OC VHNIORJSHIWCCH-UHFFFAOYSA-N 0.000 abstract 1
- MQQJFLHZXQRKKJ-UHFFFAOYSA-N 2-methoxy-5-(2-oxopropyl)benzenesulfonamide Chemical compound COC1=CC=C(CC(C)=O)C=C1S(N)(=O)=O MQQJFLHZXQRKKJ-UHFFFAOYSA-N 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 229940100198 alkylating agent Drugs 0.000 abstract 1
- 239000002168 alkylating agent Substances 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- 150000003840 hydrochlorides Chemical class 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 230000002829 reductive effect Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/30—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups
- C07C311/37—Sulfonamides, the carbon skeleton of the acid part being further substituted by singly-bound nitrogen atoms, not being part of nitro or nitroso groups having the sulfur atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/18—Sulfonamides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
- C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
- C07C303/40—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Az R-(-)-Tamsulosin HCl új előállítási eljárásában (R,S)-5-[2- (N-benzil-amino)propil)-2-metoxi.benzolszulfonsav-amid savaddiciós sói,valamint enantiomerjei, és az R-5-[2-[N-(2-etoxi-fenoxi)-etil)-N-benzil)-amino]-propil-2-metoxi-benzolszulfonamid új intermedierek. AzR-(-)-Tamsulosin HCl-t (I) úgy állítják elő, hogy a szekunderbenzilamint valamely alkilezőszerrel reagáltatva R-5-[2-[N-(2-etoxi-fenoxi)-etil]-N-benzil]-amino)-propil-2-metoxi-benzolszulfonamiddá N-alkilezik, ezt követően a benzil védőcsoportot eltávolítják, majd aHCl sót leválasztják. Az optikailag aktív vegyületet (4-metoxi-3-szulfamoil-fenil)-aceton és benzil-amin reduktív kondenzációjávalállítják elő, miután a kapott racémvegyületet királis savvalreszolválják. Ó
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0202963A HU225505B1 (en) | 2002-09-09 | 2002-09-09 | Process for the preparation of r-(-)-tamsulosin hydrochloride and novel intermediates |
DE60327220T DE60327220D1 (de) | 2002-09-09 | 2003-09-08 | Benzolsulfonamide und verfahren zu ihrer herstellung |
EP03793925A EP1539684B1 (en) | 2002-09-09 | 2003-09-08 | Benzenesulphonamides and process for their preparation |
PCT/HU2003/000071 WO2004022532A1 (en) | 2002-09-09 | 2003-09-08 | Benzenesulphonamides and process for their preparation |
AT03793925T ATE428689T1 (de) | 2002-09-09 | 2003-09-08 | Benzolsulfonamide und verfahren zu ihrer herstellung |
AU2003263378A AU2003263378A1 (en) | 2002-09-09 | 2003-09-08 | Benzenesulphonamides and process for their preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU0202963A HU225505B1 (en) | 2002-09-09 | 2002-09-09 | Process for the preparation of r-(-)-tamsulosin hydrochloride and novel intermediates |
Publications (3)
Publication Number | Publication Date |
---|---|
HU0202963D0 HU0202963D0 (hu) | 2002-10-28 |
HUP0202963A2 true HUP0202963A2 (hu) | 2004-10-28 |
HU225505B1 HU225505B1 (en) | 2007-01-29 |
Family
ID=89980754
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HU0202963A HU225505B1 (en) | 2002-09-09 | 2002-09-09 | Process for the preparation of r-(-)-tamsulosin hydrochloride and novel intermediates |
Country Status (6)
Country | Link |
---|---|
EP (1) | EP1539684B1 (hu) |
AT (1) | ATE428689T1 (hu) |
AU (1) | AU2003263378A1 (hu) |
DE (1) | DE60327220D1 (hu) |
HU (1) | HU225505B1 (hu) |
WO (1) | WO2004022532A1 (hu) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100545148C (zh) | 2004-08-16 | 2009-09-30 | 神隆新加坡私人有限公司 | 一种抗良性前列腺肥大药物坦索罗辛之合成方法 |
US8273918B2 (en) | 2005-09-12 | 2012-09-25 | Avrobindo Pharma Ltd. | Process for preparing tamsulosin hydrochloride |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR1429306A (fr) * | 1964-11-23 | 1966-02-25 | Soc Ind Fab Antibiotiques Sifa | Nouvelles benzylamines substituées et leurs sels, et procédé de préparation |
US3860647A (en) * | 1973-08-20 | 1975-01-14 | Smithkline Corp | {60 -Aminomethyl-4-hydroxy-3-sulfamyl-benzyl alcohols and 4-hydroxy-3-sulfamyl phenethylamines |
JPH066565B2 (ja) * | 1986-07-21 | 1994-01-26 | 山之内製薬株式会社 | 光学活性なベンゼンスルホンアミド誘導体の製造法 |
JP4342101B2 (ja) * | 1998-02-27 | 2009-10-14 | キッセイ薬品工業株式会社 | インドール誘導体および当該誘導体を含有する医薬品組成物 |
JP2000029901A (ja) * | 1998-07-14 | 2000-01-28 | Canon Inc | 画像検索装置及び方法 |
-
2002
- 2002-09-09 HU HU0202963A patent/HU225505B1/hu not_active IP Right Cessation
-
2003
- 2003-09-08 AT AT03793925T patent/ATE428689T1/de not_active IP Right Cessation
- 2003-09-08 AU AU2003263378A patent/AU2003263378A1/en not_active Abandoned
- 2003-09-08 WO PCT/HU2003/000071 patent/WO2004022532A1/en not_active Application Discontinuation
- 2003-09-08 EP EP03793925A patent/EP1539684B1/en not_active Expired - Lifetime
- 2003-09-08 DE DE60327220T patent/DE60327220D1/de not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
HU0202963D0 (hu) | 2002-10-28 |
DE60327220D1 (de) | 2009-05-28 |
HU225505B1 (en) | 2007-01-29 |
ATE428689T1 (de) | 2009-05-15 |
AU2003263378A1 (en) | 2004-03-29 |
EP1539684B1 (en) | 2009-04-15 |
EP1539684A1 (en) | 2005-06-15 |
WO2004022532A1 (en) | 2004-03-18 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
HC9A | Change of name, address |
Owner name: RICHTER GEDEON NYRT., HU Free format text: FORMER OWNER(S): RICHTER GEDEON VEGYESZETI GYAR RT., HU |
|
MH4A | Lapse of definitive patent protection due to relinquishment |