ATA203286A - METHOD FOR PRODUCING THE NEW R - (-) - 5- (2 - ((2- (O-ETHOXYPHENOXY)-ETHYL) -AMINO) - PROPYL) -2-METHOXYBENZENE SULPHONAMIDE - Google Patents

METHOD FOR PRODUCING THE NEW R - (-) - 5- (2 - ((2- (O-ETHOXYPHENOXY)-ETHYL) -AMINO) - PROPYL) -2-METHOXYBENZENE SULPHONAMIDE

Info

Publication number
ATA203286A
ATA203286A AT0203286A AT203286A ATA203286A AT A203286 A ATA203286 A AT A203286A AT 0203286 A AT0203286 A AT 0203286A AT 203286 A AT203286 A AT 203286A AT A203286 A ATA203286 A AT A203286A
Authority
AT
Austria
Prior art keywords
ethoxyphenoxy
propyl
ethyl
amino
producing
Prior art date
Application number
AT0203286A
Other languages
German (de)
Other versions
AT397960B (en
Inventor
Fujikura Takashi
Niigata Kunihiro
Original Assignee
Yamanouchi Pharma Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=17263445&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=ATA203286(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Yamanouchi Pharma Co Ltd filed Critical Yamanouchi Pharma Co Ltd
Publication of ATA203286A publication Critical patent/ATA203286A/en
Application granted granted Critical
Publication of AT397960B publication Critical patent/AT397960B/en

Links

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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
AT0203286A 1985-11-13 1986-07-28 METHOD FOR PRODUCING THE NEW R - (-) - 5- (2 - ((2- (O-ETHYXYPHENOXY) -THYL) -AMINO) - PROPYL) -2-METHOXYBENZENE SULPHONAMIDE AT397960B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60254326A JPS62114952A (en) 1985-11-13 1985-11-13 Production of substituted phenethylamine derivative

Publications (2)

Publication Number Publication Date
ATA203286A true ATA203286A (en) 1993-12-15
AT397960B AT397960B (en) 1994-08-25

Family

ID=17263445

Family Applications (1)

Application Number Title Priority Date Filing Date
AT0203286A AT397960B (en) 1985-11-13 1986-07-28 METHOD FOR PRODUCING THE NEW R - (-) - 5- (2 - ((2- (O-ETHYXYPHENOXY) -THYL) -AMINO) - PROPYL) -2-METHOXYBENZENE SULPHONAMIDE

Country Status (5)

Country Link
JP (1) JPS62114952A (en)
KR (1) KR940007746B1 (en)
AT (1) AT397960B (en)
CA (1) CA1282077C (en)
ES (1) ES2000382A6 (en)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4971990A (en) * 1988-02-19 1990-11-20 Hokuriku Pharmaceutical Co., Ltd. Phenoxyethylamine derivatives, for preparing the same and composition for exhibiting excellent α1 -blocking activity containing the same
US5288759A (en) * 1992-08-27 1994-02-22 Alcon Laboratories, Inc. Use of certain sulfamoyl-substituted phenethylamine derivatives to reverse drug-induced mydriasis
TW536402B (en) 1998-06-26 2003-06-11 Yamanouchi Pharma Co Ltd Pharmaceutical composition for the therapy of voiding dysfunction
KR100525493B1 (en) * 2001-02-23 2005-11-02 연성정밀화학(주) Process for preparing sulfamoyl-substituted phenethylamine derivatives
CZ20013848A3 (en) * 2001-10-25 2003-05-14 Léčiva, A.S. Process for preparing (R)-(-)-5-[2-[2-(2-ethoxyphenoxy)ethylamino]propyl]-2-methoxybenzene sulfonamide
ES2200699B1 (en) 2002-07-12 2005-10-01 Ragactives, S.L PROCEDURE FOR THE SEPARATION OF R (-) AND S (+) - 5- (2 - ((2- (ETOXIFENOXI) ETIL) AMINO) PROPIL-2-METOXIBENCENO-SULFONAMIDE.
WO2004016582A1 (en) * 2002-08-14 2004-02-26 Natco Pharma Limited An improved process for the preparation of tamsulosin hydrochloride
KR100503639B1 (en) 2003-02-12 2005-07-26 보령제약 주식회사 A purification process of Tamsulosin
JP2007513943A (en) 2003-12-09 2007-05-31 シージェイ コーポレーション Process for the preparation of optically pure phenethylamine derivatives
SI21656A (en) * 2003-12-29 2005-06-30 LEK farmacevtska družba d.d. Preparation of (r)-5-(2-(2-(2-ethoxyphenoxy)ethylamino)-1-propyl)-2-methoxybenzene sulphonamide hydrochloride of high chemical purity
SI21655A (en) * 2003-12-29 2005-06-30 LEK farmacevtska dru�ba d.d. Synthesis of optically pure (r)-5-(2-aminopropyl)-methoxybenzene sulphonamide
CZ2004197A3 (en) 2004-02-05 2005-08-17 Zentiva, A. S. Process for preparing (R)-(-)-5-(2-aminopropyl)-2-methoxybenzenesulfonamide
US20080033208A1 (en) * 2004-02-23 2008-02-07 Dilipkumar Chandubhai Ramolia Process for Manufacturing Optically Pure (R) or (S)-5-(2-Aminopropyl)-2-Methoxybenzene Sulfonamide
WO2006004093A1 (en) * 2004-07-07 2006-01-12 Hamari Chemicals, Ltd. Process for producing optically active phenylpropylamine derivative
CN100545148C (en) 2004-08-16 2009-09-30 神隆新加坡私人有限公司 Method for synthesizing tamsulosin medicine for resisting benign prostatic hyperplasia
US8273918B2 (en) 2005-09-12 2012-09-25 Avrobindo Pharma Ltd. Process for preparing tamsulosin hydrochloride
WO2008152653A2 (en) * 2007-06-11 2008-12-18 Matrix Laboratories Ltd An improved process for the preparation of tamsulosin hydrochloride
MY160652A (en) 2009-02-04 2017-03-15 Astellas Pharma Inc Pharmaceutical composition for oral administration
EP2255793A1 (en) 2009-05-28 2010-12-01 Krka Tovarna Zdravil, D.D., Novo Mesto Pharmaceutical composition comprising tamsulosin
JP5661773B2 (en) * 2009-09-12 2015-01-28 サンド・アクチエンゲゼルシヤフト Process for the preparation of indoline derivatives and intermediates thereof
DE202023102187U1 (en) 2023-04-25 2023-05-02 Nusrath Anjum Derivative formulation based on tamsulosin

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1147342A (en) * 1977-10-12 1983-05-31 Kazuo Imai Process of producing novel phenylethanolamine derivatives
JPS56110665A (en) * 1980-02-08 1981-09-01 Yamanouchi Pharmaceut Co Ltd Sulfamoyl-substituted phenetylamine derivative and its preparation
US4558156A (en) * 1980-02-08 1985-12-10 Yamanouchi Pharmaceutical Co., Ltd. Sulfamoyl-substituted phenethylamine derivatives

Also Published As

Publication number Publication date
JPH0137391B2 (en) 1989-08-07
AT397960B (en) 1994-08-25
JPS62114952A (en) 1987-05-26
KR870004949A (en) 1987-06-02
CA1282077C (en) 1991-03-26
KR940007746B1 (en) 1994-08-24
ES2000382A6 (en) 1988-02-16

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Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification
ELA Expired due to lapse of time