CH661508A5 - 1,5-benzothiazepine mit cardiovascularer wirksamkeit, verfahren zu ihrer herstellung und pharmazeutische praeparate, welche diese verbindungen enthalten. - Google Patents
1,5-benzothiazepine mit cardiovascularer wirksamkeit, verfahren zu ihrer herstellung und pharmazeutische praeparate, welche diese verbindungen enthalten. Download PDFInfo
- Publication number
- CH661508A5 CH661508A5 CH3557/84A CH355784A CH661508A5 CH 661508 A5 CH661508 A5 CH 661508A5 CH 3557/84 A CH3557/84 A CH 3557/84A CH 355784 A CH355784 A CH 355784A CH 661508 A5 CH661508 A5 CH 661508A5
- Authority
- CH
- Switzerland
- Prior art keywords
- alkyl
- substituted
- alkoxy
- pharmaceutically acceptable
- salts
- Prior art date
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- 238000000034 method Methods 0.000 title claims description 8
- KJFRSZASZNLCDF-UHFFFAOYSA-N 1,5-benzothiazepine Chemical compound S1C=CC=NC2=CC=CC=C12 KJFRSZASZNLCDF-UHFFFAOYSA-N 0.000 title claims description 6
- 239000000825 pharmaceutical preparation Substances 0.000 title claims description 5
- 230000002526 effect on cardiovascular system Effects 0.000 title description 2
- 238000004519 manufacturing process Methods 0.000 title 1
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- 125000000217 alkyl group Chemical group 0.000 claims description 16
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- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 12
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- HDRXZJPWHTXQRI-BHDTVMLSSA-N diltiazem hydrochloride Chemical compound [Cl-].C1=CC(OC)=CC=C1[C@H]1[C@@H](OC(C)=O)C(=O)N(CC[NH+](C)C)C2=CC=CC=C2S1 HDRXZJPWHTXQRI-BHDTVMLSSA-N 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000035475 disorder Diseases 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000003937 drug carrier Substances 0.000 description 1
- 230000007831 electrophysiology Effects 0.000 description 1
- 238000002001 electrophysiology Methods 0.000 description 1
- 239000000796 flavoring agent Substances 0.000 description 1
- 235000019634 flavors Nutrition 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000012458 free base Substances 0.000 description 1
- 238000007429 general method Methods 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000000004 hemodynamic effect Effects 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229940071826 hydroxyethyl cellulose Drugs 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- PZOUSPYUWWUPPK-UHFFFAOYSA-N indole Natural products CC1=CC=CC2=C1C=CN2 PZOUSPYUWWUPPK-UHFFFAOYSA-N 0.000 description 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 238000007918 intramuscular administration Methods 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 125000002183 isoquinolinyl group Chemical class C1(=NC=CC2=CC=CC=C12)* 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 210000005240 left ventricle Anatomy 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 229960002900 methylcellulose Drugs 0.000 description 1
- 230000002107 myocardial effect Effects 0.000 description 1
- 208000010125 myocardial infarction Diseases 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 230000010412 perfusion Effects 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- ATBIAJXSKNPHEI-UHFFFAOYSA-N pyridine-3-carbonyl chloride Chemical compound ClC(=O)C1=CC=CN=C1 ATBIAJXSKNPHEI-UHFFFAOYSA-N 0.000 description 1
- 125000005400 pyridylcarbonyl group Chemical group N1=C(C=CC=C1)C(=O)* 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 235000015424 sodium Nutrition 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- IMCGHZIGRANKHV-AJNGGQMLSA-N tert-butyl (3s,5s)-2-oxo-5-[(2s,4s)-5-oxo-4-propan-2-yloxolan-2-yl]-3-propan-2-ylpyrrolidine-1-carboxylate Chemical compound O1C(=O)[C@H](C(C)C)C[C@H]1[C@H]1N(C(=O)OC(C)(C)C)C(=O)[C@H](C(C)C)C1 IMCGHZIGRANKHV-AJNGGQMLSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- AWLILQARPMWUHA-UHFFFAOYSA-M thiopental sodium Chemical compound [Na+].CCCC(C)C1(CC)C(=O)NC([S-])=NC1=O AWLILQARPMWUHA-UHFFFAOYSA-M 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 239000000080 wetting agent Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D281/00—Heterocyclic compounds containing rings of more than six members having one nitrogen atom and one sulfur atom as the only ring hetero atoms
- C07D281/02—Seven-membered rings
- C07D281/04—Seven-membered rings having the hetero atoms in positions 1 and 4
- C07D281/08—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems
- C07D281/10—Seven-membered rings having the hetero atoms in positions 1 and 4 condensed with carbocyclic rings or ring systems condensed with one six-membered ring
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT8322185A IT1206505B (it) | 1983-07-22 | 1983-07-22 | Nuovi derivati benzotiazepinonici, metodo per la loro preparazione e composizioni farmaceutiche che licontengono. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH661508A5 true CH661508A5 (de) | 1987-07-31 |
Family
ID=11192749
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH3557/84A CH661508A5 (de) | 1983-07-22 | 1984-07-20 | 1,5-benzothiazepine mit cardiovascularer wirksamkeit, verfahren zu ihrer herstellung und pharmazeutische praeparate, welche diese verbindungen enthalten. |
Country Status (24)
| Country | Link |
|---|---|
| US (1) | US4547495A (en, 2012) |
| JP (1) | JPS6042374A (en, 2012) |
| KR (1) | KR910005708B1 (en, 2012) |
| AT (1) | AT392070B (en, 2012) |
| AU (1) | AU560729B2 (en, 2012) |
| BE (1) | BE900192A (en, 2012) |
| CA (1) | CA1223583A (en, 2012) |
| CH (1) | CH661508A5 (en, 2012) |
| DE (1) | DE3426821A1 (en, 2012) |
| DK (1) | DK165117C (en, 2012) |
| ES (1) | ES534539A0 (en, 2012) |
| FI (1) | FI80881C (en, 2012) |
| FR (1) | FR2567882B1 (en, 2012) |
| GB (1) | GB2143532B (en, 2012) |
| GR (1) | GR79983B (en, 2012) |
| IE (1) | IE57663B1 (en, 2012) |
| IL (1) | IL72368A (en, 2012) |
| IT (1) | IT1206505B (en, 2012) |
| LU (1) | LU85473A1 (en, 2012) |
| NL (1) | NL8402255A (en, 2012) |
| NZ (1) | NZ208761A (en, 2012) |
| PT (1) | PT78955B (en, 2012) |
| SE (1) | SE461219B (en, 2012) |
| ZA (1) | ZA845095B (en, 2012) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4925837A (en) * | 1984-09-14 | 1990-05-15 | Synthelabo | Pharmaceutical compositions |
| GB2167063A (en) * | 1984-11-17 | 1986-05-21 | Tanabe Seiyaku Co | 6 or 9-chloro-1, 5-benzothiazepine derivatives |
| US4584131A (en) * | 1985-06-20 | 1986-04-22 | E. R. Squibb & Sons, Inc. | Benzothiazepine derivatives |
| USRE33072E (en) * | 1985-06-20 | 1989-09-26 | E. R. Squibb & Sons, Inc. | Benzothiazepine derivatives |
| US4652561A (en) * | 1986-02-26 | 1987-03-24 | Hoffmann-La Roche Inc. | Naphtho[1,2-b]-1,4-thiazepinones |
| IL81954A0 (en) * | 1986-03-24 | 1987-10-20 | Hoffmann La Roche | Naphthothiazocinones,their manufacture and pharmaceutical compositions containing them |
| JPS63275572A (ja) * | 1987-05-01 | 1988-11-14 | Tanabe Seiyaku Co Ltd | １，５−ベンゾチアゼピン誘導体 |
| JP2703564B2 (ja) * | 1987-07-31 | 1998-01-26 | 田辺製薬株式会社 | １，５−ベンゾチアゼピン誘導体 |
| US4808580A (en) * | 1987-12-17 | 1989-02-28 | Hoffmann-La Roche Inc. | Naphtho[1,2-b][1,4]thiazepin-4(5H)-ones and use thereof in treatment of ischemia and blood pressure lowering |
| US4912102A (en) * | 1988-02-01 | 1990-03-27 | Hoffmann-La Roche Inc. | Analogs of naphtho[1,2-β] [1,4] thiazepin-4(5H)-one |
| JP2674232B2 (ja) * | 1989-08-31 | 1997-11-12 | 田辺製薬株式会社 | １，５―ベンゾチアゼピン誘導体 |
| US5001236A (en) * | 1989-11-22 | 1991-03-19 | Marion Laboratories, Inc. | Benzothiazepines |
| IT1240686B (it) * | 1990-04-27 | 1993-12-17 | Luso Farmaco Inst | Derivati 1,5-benzotiazepinonici, loro preparazione e uso farmaceutico |
| JP3151163B2 (ja) * | 1997-01-24 | 2001-04-03 | ソニーケミカル株式会社 | 記録用シート及びその記録用シートを使った記録方法 |
| KR100397799B1 (ko) * | 2001-07-11 | 2003-09-13 | 송기만 | 조명갓의 표면처리 방법 |
| KR100436262B1 (ko) * | 2002-01-04 | 2004-06-16 | 삼성전자주식회사 | 전자레인지용 램프의 제조방법 |
| WO2009100037A1 (en) * | 2008-02-01 | 2009-08-13 | The Scripps Research Institute | Methods for treating a condition characterized by dysfunction in protein homeostasis |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5899471A (ja) * | 1981-12-07 | 1983-06-13 | Tanabe Seiyaku Co Ltd | ベンゾチアゼピン誘導体の新規製造法 |
-
1983
- 1983-07-22 IT IT8322185A patent/IT1206505B/it active
-
1984
- 1984-07-03 NZ NZ208761A patent/NZ208761A/en unknown
- 1984-07-03 ZA ZA845095A patent/ZA845095B/xx unknown
- 1984-07-09 US US06/628,730 patent/US4547495A/en not_active Expired - Fee Related
- 1984-07-10 IL IL72368A patent/IL72368A/xx unknown
- 1984-07-17 NL NL8402255A patent/NL8402255A/nl not_active Application Discontinuation
- 1984-07-18 FR FR8411380A patent/FR2567882B1/fr not_active Expired
- 1984-07-18 KR KR1019840004202A patent/KR910005708B1/ko not_active Expired
- 1984-07-18 AT AT0232384A patent/AT392070B/de not_active IP Right Cessation
- 1984-07-20 BE BE2/60463A patent/BE900192A/fr not_active IP Right Cessation
- 1984-07-20 FI FI842927A patent/FI80881C/fi not_active IP Right Cessation
- 1984-07-20 LU LU85473A patent/LU85473A1/fr unknown
- 1984-07-20 PT PT78955A patent/PT78955B/pt not_active IP Right Cessation
- 1984-07-20 JP JP59149766A patent/JPS6042374A/ja active Pending
- 1984-07-20 CH CH3557/84A patent/CH661508A5/de not_active IP Right Cessation
- 1984-07-20 GR GR75393A patent/GR79983B/el unknown
- 1984-07-20 DE DE19843426821 patent/DE3426821A1/de active Granted
- 1984-07-20 CA CA000459353A patent/CA1223583A/en not_active Expired
- 1984-07-20 SE SE8403801A patent/SE461219B/sv not_active IP Right Cessation
- 1984-07-20 DK DK356484A patent/DK165117C/da not_active IP Right Cessation
- 1984-07-20 AU AU30923/84A patent/AU560729B2/en not_active Ceased
- 1984-07-20 IE IE1881/84A patent/IE57663B1/en not_active IP Right Cessation
- 1984-07-21 ES ES534539A patent/ES534539A0/es active Granted
- 1984-07-23 GB GB08418744A patent/GB2143532B/en not_active Expired
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| PL | Patent ceased | ||
| PL | Patent ceased |