ES409565A1 - Procedimiento para la produccion de compuestos de aminoal- canol. - Google Patents
Procedimiento para la produccion de compuestos de aminoal- canol.Info
- Publication number
- ES409565A1 ES409565A1 ES409565A ES409565A ES409565A1 ES 409565 A1 ES409565 A1 ES 409565A1 ES 409565 A ES409565 A ES 409565A ES 409565 A ES409565 A ES 409565A ES 409565 A1 ES409565 A1 ES 409565A1
- Authority
- ES
- Spain
- Prior art keywords
- substituted phenoxy
- reacting
- new
- production
- methods
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- ANOUKFYBOAKOIR-UHFFFAOYSA-N 3,4-dimethoxyphenylethylamine Chemical compound COC1=CC=C(CCN)C=C1OC ANOUKFYBOAKOIR-UHFFFAOYSA-N 0.000 abstract 4
- -1 1-(3,4-Dimethoxyphenethylamino)-3-(substituted phenoxy)-2-propanols Chemical class 0.000 abstract 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 abstract 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 239000002876 beta blocker Substances 0.000 abstract 1
- 229940030611 beta-adrenergic blocking agent Drugs 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000002831 pharmacologic agent Substances 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- NESLWCLHZZISNB-UHFFFAOYSA-M sodium phenolate Chemical compound [Na+].[O-]C1=CC=CC=C1 NESLWCLHZZISNB-UHFFFAOYSA-M 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/22—Ethers with hydroxy compounds containing no oxirane rings with monohydroxy compounds
-
- 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
- A61P9/06—Antiarrhythmics
-
- 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
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Cardiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Heart & Thoracic Surgery (AREA)
- General Health & Medical Sciences (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US00207954A US3857891A (en) | 1971-12-14 | 1971-12-14 | New aminoalkanol compounds and methods for their production |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES409565A1 true ES409565A1 (es) | 1975-12-01 |
Family
ID=22772656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES409565A Expired ES409565A1 (es) | 1971-12-14 | 1972-12-13 | Procedimiento para la produccion de compuestos de aminoal- canol. |
Country Status (21)
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2119843B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1970-12-28 | 1974-03-22 | Laroche Navarro Labo | |
| JPS5653534B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1973-10-25 | 1981-12-19 | ||
| SE388849B (sv) * | 1974-02-14 | 1976-10-18 | Haessle Ab | Forfarande for framstellning av nya aminer med beta-receptorstimulerande verkan |
| US4081447A (en) * | 1975-04-09 | 1978-03-28 | Abbott Laboratories | 5-[2-Hydroxy-3-(3,4-dimethoxy phenethylamino)]-propoxy-3,4-dihydro carbostyril and pharmaceutically acceptable salts thereof |
| US4080471A (en) * | 1976-06-25 | 1978-03-21 | Aktiebolaget Hassle | Use of substituted isopropylaminopropanols for inducing inotropic effects of the human heart |
| JPS56158868A (en) * | 1980-05-13 | 1981-12-07 | Satake Eng Co Ltd | Ion nitriding treatment device |
| NZ211815A (en) * | 1984-05-15 | 1988-11-29 | Warner Lambert Co | Preparation of 1-((3,4-dimethoxyphenethyl)amino)-3- (3-tolyloxy)-2-propanol |
| US5095151A (en) * | 1985-05-21 | 1992-03-10 | American Home Products Corporation | Preparation of propranolol hydrochloride macrocrystals |
| US4789751A (en) * | 1985-10-01 | 1988-12-06 | University Patents, Inc. | Synthesis of new liquid crystal materials possessing phenylbenzoate or biphenyl core units and (2,3)-epoalkyloxirane methanol chiral tails |
| JP2587336B2 (ja) * | 1991-10-03 | 1997-03-05 | 日本ケミファ株式会社 | 塩酸ベバントロールの製造方法 |
| US5482964A (en) * | 1994-10-11 | 1996-01-09 | Warner-Lambert Company | Substituted phenoxyhydroxypropyl amines as central nervous system agents |
| TW467881B (en) * | 1997-07-31 | 2001-12-11 | Ying-Jiun Chen | Guaiacoxypropanolamines with Α/β-adrenergic blocking activity |
| AU8527798A (en) * | 1998-07-23 | 2000-02-14 | Ing-Jun Chen | Guaiacoxypropanolamine derivatives with alpha/beta-adrenergic blocking activity |
| PL375713A1 (en) | 2002-08-19 | 2005-12-12 | Pfizer Products Inc. | Combination therapy for hyperproliferative diseases |
| AU2004242777B2 (en) | 2003-05-30 | 2011-05-12 | Ranbaxy Laboratories Limited | Substituted pyrrole derivatives and their use as HMG-Co inhibitors |
| CN1884251B (zh) * | 2005-06-22 | 2010-06-23 | 北京德众万全医药科技有限公司 | 一种盐酸贝凡洛尔的精制方法 |
| KR101329112B1 (ko) | 2005-11-08 | 2013-11-14 | 랜박시 래보러터리스 리미티드 | (3ｒ,5ｒ)-7-〔2-(4-플루오로페닐)-5-이소프로필-3-페닐-4-〔(4-히드록시 메틸 페닐 아미노)카르보닐〕-피롤-1-일〕-3,5-디히드록시 헵탄산 헤미 칼슘염의 제조 방법 |
| EP3010543A1 (en) * | 2013-06-19 | 2016-04-27 | Som Innovation Biotech, S.L. | Therapeutic agents for use in the prophylaxis and/or treatment of hyperkinetic movement disorders |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL300886A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-11-23 | |||
| NL301580A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1962-12-11 | |||
| GB1069343A (en) * | 1963-09-10 | 1967-05-17 | Ici Ltd | Propanolamine derivatives |
-
0
- BE BE790165D patent/BE790165A/xx not_active IP Right Cessation
-
1971
- 1971-12-14 US US00207954A patent/US3857891A/en not_active Expired - Lifetime
-
1972
- 1972-10-03 ZA ZA727078A patent/ZA727078B/xx unknown
- 1972-11-10 CA CA156,190A patent/CA993889A/en not_active Expired
- 1972-11-14 FI FI3180/72A patent/FI55650C/fi active
- 1972-11-14 NO NO4113/72A patent/NO135244C/no unknown
- 1972-11-14 IE IE1562/72A patent/IE37701B1/xx unknown
- 1972-11-14 IL IL40833A patent/IL40833A/xx unknown
- 1972-11-23 GB GB5426172A patent/GB1344976A/en not_active Expired
- 1972-11-23 AU AU49186/72A patent/AU475446B2/en not_active Expired
- 1972-11-28 AT AT1010572A patent/AT317182B/de not_active IP Right Cessation
- 1972-11-30 NL NL727216281A patent/NL150101B/xx not_active IP Right Cessation
- 1972-11-30 CH CH1746772A patent/CH551371A/fr not_active IP Right Cessation
- 1972-12-06 YU YU3019/72A patent/YU35871B/xx unknown
- 1972-12-07 FR FR7243545A patent/FR2163486B1/fr not_active Expired
- 1972-12-11 AR AR245573A patent/AR195896A1/es active
- 1972-12-12 DK DK619172AA patent/DK134906B/da not_active IP Right Cessation
- 1972-12-12 JP JP47124055A patent/JPS5233621B2/ja not_active Expired
- 1972-12-13 SE SE7216240A patent/SE393104B/xx unknown
- 1972-12-13 HU HUPA1153A patent/HU164953B/hu unknown
- 1972-12-13 ES ES409565A patent/ES409565A1/es not_active Expired
-
1973
- 1973-10-15 AR AR250507A patent/AR198442A1/es active
-
1979
- 1979-12-03 YU YU2939/79A patent/YU36007B/xx unknown
Also Published As
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FD1A | Patent lapsed |
Effective date: 19950216 |