HRP940182B1 - Enantioselective synthesis of 5,6-dihydro-(s)-4-(ethylamino)-(s)-6-methyl-4h-thieno(2,3-b)thiopyran-2-sulfonamide 7,7-dioxyde and related compounds - Google Patents
Enantioselective synthesis of 5,6-dihydro-(s)-4-(ethylamino)-(s)-6-methyl-4h-thieno(2,3-b)thiopyran-2-sulfonamide 7,7-dioxyde and related compoundsInfo
- Publication number
- HRP940182B1 HRP940182B1 HR08/195,886A HRP940182A HRP940182B1 HR P940182 B1 HRP940182 B1 HR P940182B1 HR P940182 A HRP940182 A HR P940182A HR P940182 B1 HRP940182 B1 HR P940182B1
- Authority
- HR
- Croatia
- Prior art keywords
- thiopyran
- thieno
- ethylamino
- sulfonamide
- dihydro
- Prior art date
Links
- 230000015572 biosynthetic process Effects 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 238000003786 synthesis reaction Methods 0.000 title abstract 2
- SNHBGEDHHQFRLN-XPUUQOCRSA-N CCN[C@H]1C[C@H](C)Sc2sc(cc12)S(N)(=O)=O Chemical compound CCN[C@H]1C[C@H](C)Sc2sc(cc12)S(N)(=O)=O SNHBGEDHHQFRLN-XPUUQOCRSA-N 0.000 title 1
- IAVUPMFITXYVAF-XPUUQOCRSA-N dorzolamide Chemical compound CCN[C@H]1C[C@H](C)S(=O)(=O)C2=C1C=C(S(N)(=O)=O)S2 IAVUPMFITXYVAF-XPUUQOCRSA-N 0.000 abstract 2
- 238000006434 Ritter amidation reaction Methods 0.000 abstract 1
- 229960003933 dorzolamide Drugs 0.000 abstract 1
- 230000014759 maintenance of location Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Ophthalmology & Optometry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Cephalosporin Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Seasonings (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US3552393A | 1993-03-22 | 1993-03-22 | |
| US19588694A | 1994-02-10 | 1994-02-10 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| HRP940182A2 HRP940182A2 (en) | 1996-08-31 |
| HRP940182B1 true HRP940182B1 (en) | 2000-02-29 |
Family
ID=26712200
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HR08/195,886A HRP940182B1 (en) | 1993-03-22 | 1994-03-21 | Enantioselective synthesis of 5,6-dihydro-(s)-4-(ethylamino)-(s)-6-methyl-4h-thieno(2,3-b)thiopyran-2-sulfonamide 7,7-dioxyde and related compounds |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US5688968A (cs) |
| EP (1) | EP0617037B1 (cs) |
| JP (1) | JP3273096B2 (cs) |
| KR (1) | KR0157162B1 (cs) |
| CN (1) | CN1046732C (cs) |
| AT (1) | ATE163291T1 (cs) |
| AU (1) | AU673409B2 (cs) |
| BR (1) | BR9406017A (cs) |
| CA (1) | CA2119218C (cs) |
| CY (1) | CY2108B1 (cs) |
| CZ (1) | CZ281390B6 (cs) |
| DE (1) | DE69408550T2 (cs) |
| DK (1) | DK0617037T3 (cs) |
| ES (1) | ES2112482T3 (cs) |
| FI (1) | FI107384B (cs) |
| GR (1) | GR3026178T3 (cs) |
| HK (1) | HK1009063A1 (cs) |
| HR (1) | HRP940182B1 (cs) |
| HU (1) | HU217363B (cs) |
| NO (1) | NO313240B1 (cs) |
| NZ (1) | NZ263092A (cs) |
| PL (1) | PL176373B1 (cs) |
| RO (1) | RO115264B1 (cs) |
| SI (1) | SI9420016B (cs) |
| SK (1) | SK280831B6 (cs) |
| TW (1) | TW265343B (cs) |
| UA (1) | UA41921C2 (cs) |
| WO (1) | WO1994021645A1 (cs) |
| YU (1) | YU48951B (cs) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5760249A (en) * | 1995-08-29 | 1998-06-02 | Merck & Co., Inc. | Synthesis of hydroxysulfone and related compounds |
| ES2177415B1 (es) * | 2000-09-04 | 2004-10-16 | Ragactives, S.L. | Procedimiento para la obtencion de 4-alquilamino-5, 6-dihidro-4h-tieno-(2,3b)-tiopiran-2-sulfonamida-7-dioxidos, e intermedios. |
| ES2204306B1 (es) * | 2002-08-16 | 2005-08-01 | Ragactives, S.L. | Formas polimorficas de clorhidrato de dorzolamida, su obtencion y composiciones farmaceuticas que las contienen. |
| EP1611138A1 (en) * | 2003-04-07 | 2006-01-04 | Hetero Drugs Limited | A novel crystalline form of dorzolamide hydrochloride |
| ATE380190T1 (de) * | 2004-07-09 | 2007-12-15 | Fdc Ltd | Verbessertes verfahren zur herstellung von 5,6 - dihydro -4h-4(s)-ethylamin-6(s)-methylthieno(2,3- b) thiopyran-2-sulfonamid- 7,7 -dioxid und seinen salzen |
| ES2253112B1 (es) * | 2004-11-05 | 2007-03-16 | Ragactives, S.L. | Procedimiento para la obtencion de derivados de 4-(n-alquilamino)-5, 6-dihidro-4h-tieno-(2,3-b)-tiopirano. |
| US7109353B2 (en) | 2004-12-28 | 2006-09-19 | Council Of Scientific And Industrial Research | Process for preparing 5,6-dihydro-4-(S)-(ethylamino)-6-(S) methyl-4H-thieno[2,3b]thiopyran-2-sulphonamide-7,7-dioxide HCl |
| BRPI0419257A (pt) * | 2004-12-28 | 2008-05-06 | Usv Ltd | processo para preparar cloridrato de 5,6-diidro-4-(s)-(ettilamino)-6-(s)-metil-4h-tieno{2,3b}tio pirano-2-sulfonamida-7,7-dióxido |
| US20060155132A1 (en) * | 2005-01-06 | 2006-07-13 | Kovacs Laszlo Z | Method of making dorzolamide hydrochloride |
| EP1838717A2 (en) * | 2005-01-18 | 2007-10-03 | Teva Gyógyszergyár Zártköruen Muködo Részvenytarsaság | Amorphous and crystalline forms of dorzolamide hydrochloride and processes of making same |
| AU2008247144B2 (en) * | 2007-05-07 | 2013-02-28 | Cipla Limited | Process for preparing dorzolamide |
| SI2683724T1 (sl) | 2011-03-10 | 2015-08-31 | Zach System S.P.A. | Asimetrični redukcijski proces |
| ITMI20121165A1 (it) * | 2012-07-03 | 2014-01-04 | Zach System Spa | Processo di riduzione asimmetrica |
| US9029554B1 (en) * | 2013-10-17 | 2015-05-12 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| US9102655B2 (en) * | 2013-10-17 | 2015-08-11 | Dow Agrosciences Llc | Processes for the preparation of pesticidal compounds |
| CN103497202B (zh) * | 2013-10-23 | 2015-12-02 | 武汉武药科技有限公司 | 盐酸多佐胺中间体的合成方法 |
| CN108822127B (zh) * | 2018-05-30 | 2020-05-15 | 沈阳药科大学 | 4-羟亚胺基噻吩并[2,3-b]噻喃-2-甲酰胺类化合物及其用途 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4797413A (en) * | 1986-05-14 | 1989-01-10 | Merck & Co., Inc. | Thieno thiopyran sulfonamide derivatives, pharmaceutical compositions and use |
| US4863922A (en) * | 1984-12-12 | 1989-09-05 | Merck & Co., Inc. | Substituted aromatic sulfonamides as antiglaucoma agents, compositions and use |
| US4968814A (en) * | 1990-04-18 | 1990-11-06 | Merck & Co., Inc. | (S)-Alkyl 3-(thien-2-ylthio)butyrate and analogs and synthesis thereof |
| US5091409A (en) * | 1990-05-17 | 1992-02-25 | Merck & Co., Inc. | 4-alkylamino-6-(C3-5 -hydrocarbyl)thieno[2,3-B]thiopyran-2-sulfonamide-7,7-dioxides |
-
1994
- 1994-03-15 TW TW083102219A patent/TW265343B/zh not_active IP Right Cessation
- 1994-03-16 KR KR1019950703996A patent/KR0157162B1/ko not_active Expired - Lifetime
- 1994-03-16 BR BR9406017A patent/BR9406017A/pt unknown
- 1994-03-16 CN CN94191502A patent/CN1046732C/zh not_active Expired - Lifetime
- 1994-03-16 CZ CZ952418A patent/CZ281390B6/cs not_active IP Right Cessation
- 1994-03-16 UA UA95094239A patent/UA41921C2/uk unknown
- 1994-03-16 SI SI9420016A patent/SI9420016B/sl unknown
- 1994-03-16 RO RO95-01639A patent/RO115264B1/ro unknown
- 1994-03-16 PL PL94310633A patent/PL176373B1/pl unknown
- 1994-03-16 HU HU9502772A patent/HU217363B/hu unknown
- 1994-03-16 NZ NZ263092A patent/NZ263092A/en not_active IP Right Cessation
- 1994-03-16 CA CA002119218A patent/CA2119218C/en not_active Expired - Fee Related
- 1994-03-16 SK SK1169-95A patent/SK280831B6/sk not_active IP Right Cessation
- 1994-03-16 WO PCT/US1994/002852 patent/WO1994021645A1/en active IP Right Grant
- 1994-03-17 EP EP94301933A patent/EP0617037B1/en not_active Expired - Lifetime
- 1994-03-17 AT AT94301933T patent/ATE163291T1/de active
- 1994-03-17 JP JP04730794A patent/JP3273096B2/ja not_active Expired - Lifetime
- 1994-03-17 ES ES94301933T patent/ES2112482T3/es not_active Expired - Lifetime
- 1994-03-17 DE DE69408550T patent/DE69408550T2/de not_active Expired - Lifetime
- 1994-03-17 DK DK94301933.1T patent/DK0617037T3/da active
- 1994-03-18 AU AU57871/94A patent/AU673409B2/en not_active Expired
- 1994-03-21 HR HR08/195,886A patent/HRP940182B1/xx not_active IP Right Cessation
- 1994-03-21 YU YU13194A patent/YU48951B/sh unknown
-
1995
- 1995-01-06 US US08/369,557 patent/US5688968A/en not_active Expired - Fee Related
- 1995-09-20 FI FI954438A patent/FI107384B/fi not_active IP Right Cessation
- 1995-09-21 NO NO19953733A patent/NO313240B1/no not_active IP Right Cessation
-
1998
- 1998-02-19 GR GR980400202T patent/GR3026178T3/el unknown
- 1998-07-23 CY CY9800020A patent/CY2108B1/xx unknown
- 1998-08-07 HK HK98109764A patent/HK1009063A1/en not_active IP Right Cessation
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HRP940182B1 (en) | Enantioselective synthesis of 5,6-dihydro-(s)-4-(ethylamino)-(s)-6-methyl-4h-thieno(2,3-b)thiopyran-2-sulfonamide 7,7-dioxyde and related compounds | |
| DE69905652D1 (de) | Direkte Herstellung von Pyrrolo-(3,4-c)pyrrolpigmenten | |
| AU3317689A (en) | Thieno(2,3-e)(1,2,4)triazolo(3,4-c)(1,4)-diazepines | |
| ATE212408T1 (de) | Zylinderschloss mit zylinderkern und zylindergehäuse | |
| IL125035A0 (en) | Thieno (2,3-b) pyrazolo (3,4-d) pyridin-3-ones to enhance erythropoiesis | |
| AU8599491A (en) | Substituted thieno (3,2-b)pyran-5,7-diones | |
| GR3031294T3 (en) | Optically active 1,4-Dihydropyridine derivatives and methods of producing the same | |
| ES1023797U (es) | Llavero. | |
| HK1016091A (en) | Thieno(2,3-b)pyrazolo(3,4-d)pyridin-3-ones to enhance erythropoiesis | |
| DE3879235D1 (en) | Pyrazolothiopyranopyrazole. | |
| EP1039582A3 (de) | Modulartiges elektrisches Gerät | |
| TW300484U (en) | Production of 2,6-dichloro-4-nitroaniline | |
| IE842874L (en) | THIENO (2,3-b) PYRROLE DERIVATIVES | |
| AU5631790A (en) | Key using synthetic resin at grip part | |
| KR100199834B1 (en) | Tetrahydroisoquinolinylcarbamates of 1,2,3,3a,8,8a-hexahydro-1,3a,8-trimethylpyrrolo[2,3-b]indole | |
| IES940467A2 (en) | A faceplate | |
| AU119075S (en) | Artist's carry case | |
| LT97026A (en) | Lock with variety of keys | |
| WO1994028753A3 (de) | Verschlussglied für babykettchen | |
| YU36788A (en) | Certain derivatives of cycloalka-/b/-pyrazolo/3,4-d/-pyridin-3-ones |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A1OB | Publication of a patent application | ||
| AIPI | Request for the grant of a patent on the basis of a substantive examination of a patent application | ||
| B1PR | Patent granted | ||
| PNAN | Change of the applicant name, address/residence |
Owner name: MERCK SHARP & DOHME CORP., US |
|
| PNAN | Change of the applicant name, address/residence |
Owner name: MERCK SHARP & DOHME CORP., US Owner name: SCHERING CORPORATION, US |
|
| ODRP | Renewal fee for the maintenance of a patent |
Payment date: 20130319 Year of fee payment: 20 |
|
| PB20 | Patent expired after termination of 20 years |
Effective date: 20140321 |