GB797448A - Novel piperidine compounds and their production - Google Patents

Novel piperidine compounds and their production

Info

Publication number
GB797448A
GB797448A GB3405155A GB3405155A GB797448A GB 797448 A GB797448 A GB 797448A GB 3405155 A GB3405155 A GB 3405155A GB 3405155 A GB3405155 A GB 3405155A GB 797448 A GB797448 A GB 797448A
Authority
GB
United Kingdom
Prior art keywords
norpethidine
hydrobromide
chloroethyl
phenoxyethyl
reacting
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
GB3405155A
Inventor
Peter Marshall Frearson
Edward Severin Stern
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.)
J F Macfarlan & Co Ltd
Original Assignee
J F Macfarlan & Co 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 J F Macfarlan & Co Ltd filed Critical J F Macfarlan & Co Ltd
Priority to GB3405155A priority Critical patent/GB797448A/en
Publication of GB797448A publication Critical patent/GB797448A/en
Expired legal-status Critical Current

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  • Hydrogenated Pyridines (AREA)

Abstract

The invention comprises norpethidines of the general formula: <FORM:0797448/IV (b)/1> in which X is a substituted or unsubstituted alkoxy, aralkoxy, aryloxy or cycloalkyloxy group or a heterocyclic residue containing an oxygen atom, and R is a straight or branched chain alkylene group which contains from one to six carbon atoms (preferred compounds being those in which R is -CH2.CH2- and X is ethoxy, isopropoxy, phenoxy or benzyloxy), and their manufacture by reacting norpethidine with a compound X-R-Hal in which Hal is a chlorine, bromine or iodine atom, or by reacting a di (chloroethyl)amine substituted by the group X-R with benzyl cyanide and hydrolysing and esterifying the resulting 4-phenyl-4-cyanopiperidine, or, when X is a substituted or unsubstituted alkoxy, aralkoxy, aryloxy or cycloalkyloxy group, by reacting a 1-(halogenoalkyl) norpethidine of the general formula: <FORM:0797448/IV (b)/2> with a compound X-Na. Examples describe the preparation of 1 - (21 - ethoxyethyl norpethidine, 1 - (21 - 411 - tetrahydropyranylethyl)norpethidine, 1 - (31 - ethoxypropyl) norpethidine hydrobromide, 1 - (41 - ethoxybutyl)norpethidine and its methiodide, 1 - (51-ethoxyamyl)norpethidine, 1 - (21 - 211 - ethoxy-ethoxyethyl)norpethidine, 1 - (21 - methoxyethyl)norpethidine, 1 - (21 - propoxyethyl) norpethidine, 1 - (21 - isopropoxyethyl)norpethidine, 1 - (21 - n - butoxyethyl)norpethidine, 1-(21 - cyclohexyloxyethyl)norpethidine hydrobromide, 1 - (21 - benzyloxyethyl)norpethidine and its hydrobromide, 1-(21-phenoxyethyl) norpethidine and its hydrobromide, 1-(21-p-chlorophenoxyethyl)norpethidine hydrobromide, 1 - (21 - m - chlorophenoxyethyl)norpethidine hydrobromide, 1 - (21 - p - methoxyphenoxyethyl)norpethidine hydrobromide, 1 - (21-m - methoxyphenoxyethyl)norpethidine hydrobromide, 1 - (21 - p - acetamidophenoxyethyl) norpethidine hydrobromide, 1 - (21 - p - aminophenoxyethyl)norpethidine and its dihydrochloride and dihydrobromide, 1 - (21 - p - carbethoxyphenoxyethyl)norpethidine hydrobromide, 1 - (21 - tetrahydrofurfuryloxyethyl) norpethidine, 1 - (21 - a - tetrahydropyranyl methoxy)ethylnorpethidine, 1 - (21 - phenoxyethyl)norpethidine hydrobromide, 1 - (21 - p-nitrophenoxyethyl)norpethidine hydrobromide, 1 - (21 - p - aminophenoxyethyl)norpethidine dihydrochloride, 1 - (21 - m - methylphenoxyethyl)norpethidine hydrobromide, 1 - (21 - o-methylphenoxyethyl)norpethidine hydrobromide and 1 - (21 - ethoxypropyl)norpethidine. The following are obtained as intermediates: 1 - (21 - chloroethyl)norpethidine (from the corresponding hydrochloride), 4 - (21 - chloroethyl) tetrahydropyran (by the action of thionyl chloride on 4-(21-hydroxyethyl) tetrahydropyran), di - (2 - chloroethyl) - 21 - phenoxyethylamine (by reacting 2-chloroethyl phenyl ether with diethanolamine and treating the product with thionyl chloride), and 4-carboxy-1-(21-phenoxyethyl) - 4 - phenyl - piperidine (by condensing di - (2 - chloroethyl) - 21 - phenoxyethylamine with benzyl cyanide and hydrolysing the 4-cyano - 1 - (21 - phenoxyethyl) - 4 - phenylpiperidine so formed. Specification 762,689 is referred to.
GB3405155A 1955-11-28 1955-11-28 Novel piperidine compounds and their production Expired GB797448A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3405155A GB797448A (en) 1955-11-28 1955-11-28 Novel piperidine compounds and their production

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3405155A GB797448A (en) 1955-11-28 1955-11-28 Novel piperidine compounds and their production

Publications (1)

Publication Number Publication Date
GB797448A true GB797448A (en) 1958-07-02

Family

ID=10360754

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3405155A Expired GB797448A (en) 1955-11-28 1955-11-28 Novel piperidine compounds and their production

Country Status (1)

Country Link
GB (1) GB797448A (en)

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