GB809189A - Improvements in and relating to piperazine compounds - Google Patents

Improvements in and relating to piperazine compounds

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Publication number
GB809189A
GB809189A GB18030/57A GB1803057A GB809189A GB 809189 A GB809189 A GB 809189A GB 18030/57 A GB18030/57 A GB 18030/57A GB 1803057 A GB1803057 A GB 1803057A GB 809189 A GB809189 A GB 809189A
Authority
GB
United Kingdom
Prior art keywords
bis
methyl
chloride
compounds
dimethylpiperazine
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
GB18030/57A
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
Publication of GB809189A publication Critical patent/GB809189A/en
Expired legal-status Critical Current

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Abstract

The invention comprises piperazines of the following general formula <FORM:0809189/IV (b)/1> wherein R is a straight-chain alkyl radical containing 10-12 carbon atoms, and X- is the anion of a non-toxic acid. The compounds of the invention may be prepared by reacting 2,5-dimethylpiperazine with two equivalents of RX (X being iodide, bromide or toluenesulphonate) to give N,N1-diR-2,5-dimethylpiperazine which is then reacted with methyl iodide, toluenesulphonate, or sulphate to give the dimethiodide, dimethyl tosylate or dimethosulphate respectively. The iodide may be converted into the chloride by treatment with silver chloride or with methanolic hydrogen chloride. Other salts may be prepared by conventional methods. Alternatively 2,5-dimethylpiperazines may be reacted with formalin and formic acid to give N,N1 - bis - methyl - 2,5 - dimethylpiperazine which is then quaternized with R.X, where X is a halide. Examples describe the preparation, by the first method, of N,N1-bis-n - decyl -, n - undecyl -, and n - dodecyl - N,N1-bis - methyl - 2,5 - dimethylpiperazinium iodides and chlorides, and of N,N1 - bis - n - dodecyl-N,N1 - bis - methyl - 2,5 - dimethylpiperazinium lactate and methanesulphonate by reaction of the chloride with sodium lactate and silver methanesulphonate respectively. Compounds of the general formula wherein R is an alkyl radical containing 8, 13 and 14 carbon atoms as well as compounds of the general formula <FORM:0809189/IV (b)/2> where R is an alkyl group containing 8 or 10-14 carbon atoms, are also disclosed.
GB18030/57A 1956-06-11 1957-06-06 Improvements in and relating to piperazine compounds Expired GB809189A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US809189XA 1956-06-11 1956-06-11

Publications (1)

Publication Number Publication Date
GB809189A true GB809189A (en) 1959-02-18

Family

ID=22160493

Family Applications (1)

Application Number Title Priority Date Filing Date
GB18030/57A Expired GB809189A (en) 1956-06-11 1957-06-06 Improvements in and relating to piperazine compounds

Country Status (1)

Country Link
GB (1) GB809189A (en)

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