GB919126A - Quaternary ammonium compounds and their preparation - Google Patents
Quaternary ammonium compounds and their preparationInfo
- Publication number
- GB919126A GB919126A GB2111758A GB2111758A GB919126A GB 919126 A GB919126 A GB 919126A GB 2111758 A GB2111758 A GB 2111758A GB 2111758 A GB2111758 A GB 2111758A GB 919126 A GB919126 A GB 919126A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methyl
- substituted
- prepared
- ethyl
- benzoyl
- 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
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises quaternary ammonium compounds containing a cation of the formula <FORM:0919126/IV (b)/1> (wherein R7 and R8 are methyl, ethyl or 2-hydroxyethyl groups, R9 is an acetyl, phenacetyl, propionyl, methoxycarbonyl, ethoxycarbonyl, isopropoxycarbonyl, acetamido or propionamido group when E is an ethylene radical, L and M are hydrogen or halogen atoms or methyl, ethyl or methoxy groups, and Z is a hydrogen atom, or R9 is a benzoyl, halobenzoyl, C1-4 alkylbenzoyl, C1-4 alkoxybenzoyl, nitro-benzoyl or aminobenzoyl radical when E is an ethylene, trimethylene, or 1- or 2-methylethylene radical, L and M have the values given above and Z is a hydrogen atom or a hydroxy group) and their preparation by reacting a tertiary amine (which may be formed in situ) with a reactive ester of a hydroxy derivative of the substituted-phenoxyalkyl, R7, R8 or methyl group, the aminobenzoyl compounds being prepared by subsequent reduction of the nitrobenzoyl compounds. Anions may be exchanged by metathesis. Reactive esters referred to are halides and p-toluenesulphonates, and these may be reacted either directly with the tertiary amine or with a suitable primary or secondary amine to form first the tertiary amine and then the quaternary derivative. Detailed examples are provided. p 2-L-4-R9-5-Z-6-M-phenoxyalkyl substituted secondary and tertiary amine starting materials wherein the other substituent or substituents on the nitrogen atom is or are one or two of the groups R7, R8 and CH3 are prepared from corresponding haloalkyl substituted secondary and tertiary amines and 2-L-4-R9-5-Z-6-M-phenols or from appropriate primary or secondary amines containing one or two of the groups R7, R8 and CH3 and 2-L-4-R9-5-Z-6-M-phenoxyalkyl halides, which in turn are prepared either from 2-L-4-R9-5-Z-6-M-phenols and alkylene dihalides or, when R9 is a benzoyl or substituted benzoyl group, from 2-L-5-Z-6-M-phenoxyalkyl halides and benzoyl or substituted benzoyl halides. 2-(21,61-Dimethylphenoxy)-propan-1-ol is prepared by reduction of ethyl a -(2,6-dimethylphenoxy)-propionate, in turn prepared from 2,6-dimethylphenol and ethyl a -bromopropionate. 3 - Bromo-4-hydroxy-5-methyl-benzophenone is prepared by bromination of 4-hydroxy-3-methyl-benzophenone. 3-Ethyl-4-hydroxy-5-methyl-benzophenone is prepared by heating aluminium chloride with 2-ethyl-6-methyl-phenyl benzoate, in turn prepared from 2 - ethyl - 6 - methyl - phenol and benzoyl chloride. 4 - hydroxy - 3,5 - dimethyldeoxybenzoin and the intermediate 2,6-dimethylphenyl phenacetate are prepared similarly. The compounds of the invention, which are stated to depress the peripheral sympathetic nervous system, may be formulated as pharmaceutical preparation with suitable carriers. Powders (which may contain dispersing and surface-active agents and which may be presented in a draught in water or in a syrup), capsules, or cachets (in the dry state or in nonaqueous suspension, which may contain a suspending agent), tablets, suspensions (which may contain flavouring, preserving, suspending, thickening or emulsifying agents), aqueous injection solutions (which may contain anti-oxidants, buffers, bacteriostats, solubilizing agents and salts to render the solutions isotonic), suppositories and pessaries are referred to. The first Provisional Specification describes quaternary ammonium compound containing a cation of the formula <FORM:0919126/IV (b)/2> wherein R1 and R2 are methyl or ethyl, A has the values of E detailed above, the a and b rings may be substituted by alkyl, alkenyl or alkoxy groups or halogen atoms, and the b ring may, in addition, be substituted by a nitro, amino or acylamino group. In the third Provisional Specification quaternary ammonium compounds containing a cation of the formula II wherein Z may additionally be a methoxy group, R6 may additionally be isobutyryl, R when benzoyl may additionally be substituted by acylamino groups and R6 when phenacetyl may additionally be substituted by acylamino, alkyl, alkoxy, nitro or amino groups or halogen atoms, are described. Specification 765,850 is referred to.
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2111758A GB919126A (en) | 1958-07-01 | 1958-07-01 | Quaternary ammonium compounds and their preparation |
FR798201A FR1297710A (en) | 1958-07-01 | 1959-06-22 | Quaternary ammonium compounds and their preparation process |
ES0250300A ES250300A1 (en) | 1958-07-01 | 1959-06-23 | A method for the preparation of a compound of quaternary ammonium (Machine-translation by Google Translate, not legally binding) |
MC163A MC150A1 (en) | 1958-07-01 | 1959-06-24 | Quaternary ammonium compounds and their preparation process |
FR837064A FR372M (en) | 1958-07-01 | 1960-08-29 | Medicinal product based on quaternary ammonium compound. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2111758A GB919126A (en) | 1958-07-01 | 1958-07-01 | Quaternary ammonium compounds and their preparation |
Publications (1)
Publication Number | Publication Date |
---|---|
GB919126A true GB919126A (en) | 1963-02-20 |
Family
ID=10157494
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2111758A Expired GB919126A (en) | 1958-07-01 | 1958-07-01 | Quaternary ammonium compounds and their preparation |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB919126A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001044167A1 (en) * | 1999-12-15 | 2001-06-21 | Ucb Farchim S.A. | Quaternary ammonium compounds and their use as anti-tussive agents |
EP1736464A1 (en) * | 2004-03-31 | 2006-12-27 | Dainippon Ink and Chemicals, Incorporated | Quaternary ammonium compound, process for producing the same, therapeutic agent for cerebrovascular disorder, and therapeutic agent for heart disease |
WO2013170857A1 (en) | 2012-05-16 | 2013-11-21 | Coloplast A/S | Novel polymeric photoinitiators and photoinitiator monomers |
US8884061B2 (en) * | 2006-03-03 | 2014-11-11 | Colorado State University Research Foundation | Compositions and methods of use of electron transport system inhibitors |
-
1958
- 1958-07-01 GB GB2111758A patent/GB919126A/en not_active Expired
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001044167A1 (en) * | 1999-12-15 | 2001-06-21 | Ucb Farchim S.A. | Quaternary ammonium compounds and their use as anti-tussive agents |
EP1736464A1 (en) * | 2004-03-31 | 2006-12-27 | Dainippon Ink and Chemicals, Incorporated | Quaternary ammonium compound, process for producing the same, therapeutic agent for cerebrovascular disorder, and therapeutic agent for heart disease |
EP1736464A4 (en) * | 2004-03-31 | 2008-03-26 | Activus Pharma Co Ltd | Quaternary ammonium compound, process for producing the same, therapeutic agent for cerebrovascular disorder, and therapeutic agent for heart disease |
US7687546B2 (en) | 2004-03-31 | 2010-03-30 | Activus Pharma Co., Ltd. | Quaternary ammonium compound, process for producing the same, therapeutic agent for cerebrovascular disorder, and therapeutic agent for heart disease |
US8884061B2 (en) * | 2006-03-03 | 2014-11-11 | Colorado State University Research Foundation | Compositions and methods of use of electron transport system inhibitors |
WO2013170857A1 (en) | 2012-05-16 | 2013-11-21 | Coloplast A/S | Novel polymeric photoinitiators and photoinitiator monomers |
EP2850113B1 (en) * | 2012-05-16 | 2017-08-09 | Coloplast A/S | Novel polymeric photoinitiators and photoinitiator monomers |
US10040893B2 (en) | 2012-05-16 | 2018-08-07 | Coloplast A/S | Polymeric photoinitiators and photoinitiator monomers |
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