GB920623A - Substituted amino-alcohols - Google Patents
Substituted amino-alcoholsInfo
- Publication number
- GB920623A GB920623A GB4739/61A GB473961A GB920623A GB 920623 A GB920623 A GB 920623A GB 4739/61 A GB4739/61 A GB 4739/61A GB 473961 A GB473961 A GB 473961A GB 920623 A GB920623 A GB 920623A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydrogen
- formula
- compound
- replacing
- prepared
- 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
- 150000001414 amino alcohols Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 239000000839 emulsion Substances 0.000 abstract 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 abstract 2
- JPJALAQPGMAKDF-UHFFFAOYSA-N selenium dioxide Chemical compound O=[Se]=O JPJALAQPGMAKDF-UHFFFAOYSA-N 0.000 abstract 2
- LAXWRTNRGFBLOI-UHFFFAOYSA-N 1-(3,5-dihydroxyphenyl)-2-(propan-2-ylamino)propan-1-one hydrobromide Chemical compound Br.OC=1C=C(C=C(C1)O)C(C(C)NC(C)C)=O LAXWRTNRGFBLOI-UHFFFAOYSA-N 0.000 abstract 1
- YJKHOUIVWKQRSL-UHFFFAOYSA-N 1-(3,5-dimethoxyphenyl)ethanone Chemical compound COC1=CC(OC)=CC(C(C)=O)=C1 YJKHOUIVWKQRSL-UHFFFAOYSA-N 0.000 abstract 1
- KEYHDMNGLWYBMJ-UHFFFAOYSA-N 2-(3,5-dimethoxyphenyl)-2-oxoacetaldehyde Chemical compound COC1=CC(OC)=CC(C(=O)C=O)=C1 KEYHDMNGLWYBMJ-UHFFFAOYSA-N 0.000 abstract 1
- MZMMIPRTUCZMHT-UHFFFAOYSA-N 2-bromo-1-(3,5-dimethoxyphenyl)ethanol Chemical compound COC=1C=C(C=C(C1)OC)C(CBr)O MZMMIPRTUCZMHT-UHFFFAOYSA-N 0.000 abstract 1
- IXJNGTKIRPXZNO-UHFFFAOYSA-N Cl.COC=1C=C(C=C(C1)OC)C(C(C)NC(C)C)=O Chemical compound Cl.COC=1C=C(C=C(C1)OC)C(C(C)NC(C)C)=O IXJNGTKIRPXZNO-UHFFFAOYSA-N 0.000 abstract 1
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical class CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 239000002671 adjuvant Substances 0.000 abstract 1
- 230000001476 alcoholic effect Effects 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000001813 broncholytic effect Effects 0.000 abstract 1
- 239000002775 capsule Substances 0.000 abstract 1
- 239000000969 carrier Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 239000008298 dragée Substances 0.000 abstract 1
- 239000000796 flavoring agent Substances 0.000 abstract 1
- 238000001640 fractional crystallisation Methods 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- -1 inhalations Substances 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- VGPBPWRBXBKGRE-UHFFFAOYSA-N n-(oxomethylidene)hydroxylamine Chemical compound ON=C=O VGPBPWRBXBKGRE-UHFFFAOYSA-N 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 238000007911 parenteral administration Methods 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 239000001294 propane Substances 0.000 abstract 1
- 235000013849 propane Nutrition 0.000 abstract 1
- 239000002510 pyrogen Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 239000000829 suppository Substances 0.000 abstract 1
- 239000002511 suppository base Substances 0.000 abstract 1
- 239000000375 suspending agent Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 239000006188 syrup Substances 0.000 abstract 1
- 235000020357 syrup Nutrition 0.000 abstract 1
- 239000003826 tablet Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB56662A DE1275069B (de) | 1960-02-15 | 1960-02-15 | 1-(3', 5'-Dihydroxyphenyl)-1-hydroxy-2-isopropylaminoalkane und Verfahren zu ihrer Herstellung |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB920623A true GB920623A (en) | 1963-03-13 |
Family
ID=6971416
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4739/61A Expired GB920623A (en) | 1960-02-15 | 1961-02-08 | Substituted amino-alcohols |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US3341594A (en:Method) |
| BE (1) | BE611502Q (en:Method) |
| CH (3) | CH410009A (en:Method) |
| DE (1) | DE1275069B (en:Method) |
| FR (2) | FR1466215A (en:Method) |
| GB (1) | GB920623A (en:Method) |
| NL (1) | NL120608C (en:Method) |
| OA (1) | OA01090A (en:Method) |
| SE (2) | SE220245C1 (en:Method) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1670342A1 (de) * | 1966-04-23 | 1970-10-29 | Albert Ag Chem Werke | Verfahren zur Herstellung eines neuen nikotinsauren Salzes |
| US3937838A (en) * | 1966-10-19 | 1976-02-10 | Aktiebolaget Draco | Orally active bronchospasmolytic compounds and their preparation |
| US4138581A (en) * | 1969-04-01 | 1979-02-06 | Sterling Drugs Inc. | 3(Hydroxy or hydroxymethyl)-4(hydroxy)-α-(aminomethyl)benzyl alcohols |
| US4336400A (en) * | 1969-04-01 | 1982-06-22 | Sterling Drug Inc. | 3-(Hydroxy or hydroxymethyl)-4-hydroxy-alpha(aminomethyl)benzyl alcohols and methods of use |
| US4335124A (en) * | 1973-08-20 | 1982-06-15 | Sandoz, Inc. | 1-Alkyl, 1-phenyl-butenes |
| AR207639A1 (es) * | 1973-12-26 | 1976-10-22 | Pfizer | Un procedimiento para preparar pirido (3,2-d)1,3-dioxin-6-epoxietanos y compuestos intermediarios desprovistos de actividad terapeutica |
| US4017632A (en) * | 1975-10-22 | 1977-04-12 | Centre European De Recherches Pharmacologiques C.E.R.P.H.A. | Phenoxyacetic acid derivatives |
| EP0043807B1 (en) | 1980-07-09 | 1984-05-30 | Aktiebolaget Draco | 1-(dihydroxyphenyl)-2-amino-ethanol derivatives; preparation, compositions and intermediates |
| EP0103830A3 (de) * | 1982-09-22 | 1985-07-31 | Bayer Ag | Wachstumsfördernde Phenylethylamin-Derivate |
| US4479967A (en) * | 1982-09-30 | 1984-10-30 | Ciba-Geigy Corporation | Method of lowering intraocular pressure with ibuterol |
| US4525359A (en) * | 1982-12-10 | 1985-06-25 | Greenway Frank L Iii | Treatment for selective weight control |
| US5464387A (en) * | 1991-07-24 | 1995-11-07 | Alza Corporation | Transdermal delivery device |
| JP2008534611A (ja) | 2005-03-30 | 2008-08-28 | シェーリング コーポレイション | 抗コリン作用薬、コルチコステロイドおよび長時間作用性βアゴニストを合わせる薬物および方法 |
| AU2013353723B2 (en) | 2012-12-03 | 2018-02-22 | Pfizer Inc. | Novel selective androgen receptor modulators |
| WO2014108449A1 (en) | 2013-01-08 | 2014-07-17 | Atrogi Ab | A screening method, a kit, a method of treatment and a compound for use in a method of treatment |
| GB201714740D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714736D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714734D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201714745D0 (en) | 2017-09-13 | 2017-10-25 | Atrogi Ab | New compounds and uses |
| GB201903832D0 (en) | 2019-03-20 | 2019-05-01 | Atrogi Ab | New compounds and methods |
| GB202205895D0 (en) | 2022-04-22 | 2022-06-08 | Atrogi Ab | New medical uses |
| CN120583945A (zh) | 2023-01-20 | 2025-09-02 | 阿托基公司 | 用于治疗或预防肌肉消耗的β2-肾上腺素能受体激动剂 |
| GB202302225D0 (en) | 2023-02-16 | 2023-04-05 | Atrogi Ab | New medical uses |
| GB202303229D0 (en) | 2023-03-06 | 2023-04-19 | Atrogi Ab | New medical uses |
| GB202403169D0 (en) | 2024-03-05 | 2024-04-17 | Atrogi Ab | New medical uses |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE865315C (de) * | 1943-07-27 | 1953-02-02 | Albert Ag Chem Werke | Verfahren zur Herstellung von 3, 5-Dioxyphenylaethanolaminen |
| US2725399A (en) * | 1949-11-03 | 1955-11-29 | American Cyanamid Co | Tertiary dialkylamino propanols |
| US2765307A (en) * | 1953-02-11 | 1956-10-02 | Rohm & Haas | Hydroxyamines |
| US2766286A (en) * | 1953-07-15 | 1956-10-09 | Lepetit Spa | Process for the resolution of racemic threo-1-phenyl-2-amino-1. 3-propanediol |
| US2937118A (en) * | 1956-06-27 | 1960-05-17 | Raschig Gmbh Dr F | Aminopyridine compositions |
| US2820739A (en) * | 1956-09-05 | 1958-01-21 | Merck & Co Inc | Antitussive compositions |
| US3048633A (en) * | 1960-12-02 | 1962-08-07 | American Home Prod | N-lower alkyl-2-(benzyloxatedphenyl)-glycolamide |
-
1960
- 1960-02-15 DE DEB56662A patent/DE1275069B/de active Pending
-
1961
- 1961-02-03 CH CH1736465A patent/CH410009A/de unknown
- 1961-02-03 CH CH130661A patent/CH413863A/de unknown
- 1961-02-03 CH CH1736365A patent/CH410008A/de unknown
- 1961-02-08 GB GB4739/61A patent/GB920623A/en not_active Expired
- 1961-02-10 FR FR852394A patent/FR1466215A/fr not_active Expired
- 1961-02-10 FR FR852395A patent/FR922M/fr not_active Expired
- 1961-02-15 NL NL261247A patent/NL120608C/nl active
- 1961-12-13 BE BE611502A patent/BE611502Q/fr active
-
1962
- 1962-09-21 SE SE1016762A patent/SE220245C1/sv unknown
- 1962-09-21 SE SE10166/62A patent/SE310889B/sv unknown
-
1964
- 1964-02-03 US US342290A patent/US3341594A/en not_active Expired - Lifetime
- 1964-12-30 OA OA51195A patent/OA01090A/fr unknown
-
1967
- 1967-07-19 US US654350A patent/US3422196A/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| OA01090A (fr) | 1968-08-07 |
| FR922M (en:Method) | 1961-10-20 |
| BE611502Q (fr) | 1962-03-30 |
| CH410009A (de) | 1966-03-31 |
| NL261247A (nl) | 1964-05-11 |
| CH413863A (de) | 1966-05-31 |
| SE220245C1 (sv) | 1968-04-30 |
| SE310889B (sv) | 1969-05-19 |
| CH410008A (de) | 1966-03-31 |
| NL120608C (nl) | 1966-02-15 |
| US3422196A (en) | 1969-01-14 |
| DE1275069B (de) | 1968-08-14 |
| FR1466215A (fr) | 1967-01-20 |
| US3341594A (en) | 1967-09-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| GB920623A (en) | Substituted amino-alcohols | |
| ES8104280A1 (es) | Procedimiento para la obtencion de derivados de tetrahidro- piridina y piperidina | |
| EP0233793A3 (en) | Decahydroquinoline derivatives, process for their preparation, intermediates for their preparation, their use as medicaments and compositions containing them | |
| US3875233A (en) | Bis-P-hydroxy-phenethyl amines | |
| US3755413A (en) | 1-cyanophenoxy-2-hydroxy-3-(cycloalkyl-amino)-propanes | |
| US4085114A (en) | 1,2-Benzoisoxazole derivatives and the production thereof | |
| US4024282A (en) | Pharmaceutically active 2-(3-alkylaminopropoxy)diphenylmethanes | |
| US2373299A (en) | Nitrogen derivatives of benzyl sulphonic acids | |
| US2336464A (en) | Urea and thiourea derivatives | |
| US2441576A (en) | Amino methyl phenols | |
| US4535159A (en) | Process for producing 1-position amino-derivatives of 1-(3',4'-methylenedioxyphenyl)propane-2-ol | |
| US2541473A (en) | Chzxchs | |
| US4562211A (en) | Pharmaceutically active 2-substituted-1-(omega-aminoalkoxy)benzenes | |
| US2497394A (en) | Alkylaminoalkyl benzoates | |
| US2500714A (en) | 4-phenyl-1-alkyl isonipecotic acid lactones | |
| US3691176A (en) | 1-(4-fluorophenoxypropyl)-4-anilino-piperidines | |
| Centolella et al. | Barbiturates Containing the▵ 2-Cyclopentenyl Group1 | |
| Huber et al. | Some dialkylaminoalkylamines | |
| US4048178A (en) | Novel N-allyl and N-propargyl benzmorphan derivatives | |
| DE3163567D1 (en) | Cycloheptindole derivatives and their acid-addition salts, their preparation, their use as medicaments and compositions containing them | |
| US4060641A (en) | Pharmaceutically active 2-(3-alkylaminopropoxy)diphenylmethanes | |
| US2993890A (en) | Beta-substituted indoles | |
| US2675408A (en) | Salts of dibenzyl beta-halopropylamines | |
| GB919126A (en) | Quaternary ammonium compounds and their preparation | |
| US3014912A (en) | Piperidine derivatives and method for preparing same |