GB919126A - Quaternary ammonium compounds and their preparation - Google Patents

Quaternary ammonium compounds and their preparation

Info

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
Application number
GB2111758A
Inventor
Frederick Charles Copp
Albert Reginald Elphick
Geoffrey George Coker
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wellcome Foundation Ltd
Original Assignee
Wellcome Foundation Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Wellcome Foundation Ltd filed Critical Wellcome Foundation Ltd
Priority to GB2111758A priority Critical patent/GB919126A/en
Priority to FR798201A priority patent/FR1297710A/en
Priority to ES0250300A priority patent/ES250300A1/en
Priority to MC163A priority patent/MC150A1/en
Priority to FR837064A priority patent/FR372M/en
Publication of GB919126A publication Critical patent/GB919126A/en
Expired legal-status Critical Current

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  • 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.
GB2111758A 1958-07-01 1958-07-01 Quaternary ammonium compounds and their preparation Expired GB919126A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (8)

* Cited by examiner, † Cited by third party
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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