GB837986A - New piperazine derivatives and process for the preparation thereof - Google Patents

New piperazine derivatives and process for the preparation thereof

Info

Publication number
GB837986A
GB837986A GB21624/57A GB2162457A GB837986A GB 837986 A GB837986 A GB 837986A GB 21624/57 A GB21624/57 A GB 21624/57A GB 2162457 A GB2162457 A GB 2162457A GB 837986 A GB837986 A GB 837986A
Authority
GB
United Kingdom
Prior art keywords
piperazine
chlorobenzhydryloxy
ethyl
mono
alkyl
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
GB21624/57A
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.)
Individual
Original Assignee
Individual
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 Individual filed Critical Individual
Publication of GB837986A publication Critical patent/GB837986A/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

The invention comprises compounds of the general formula <FORM:0837986/IV (b)/1> (wherein R is a halogen atom or an alkyl radical, R1 is an alkyl, hydroxyalkyl, hydroxyalkoxyalkyl, aralkoxyalkyl or aralkyl radical, any carbocyclic ring of which may be substituted by an alkyl or alkoxy radical or a halogen atom, or R1 is an alkanoyl radical or an aroyl radical which may be halogen substituted, and n is an integer of from 2 to 6), and acid-addition salts thereof; and their preparation by the following methods: (1) reaction of a 1 - mono - [omega - (o - R - benzhydryloxy)-alkyl]-piperazine with an R1-halide, optionally in the presence of a hydrohalic acid acceptor, or with an aldehyde with subsequent reduction of the intermediate product with hydrogen in the presence of Raney nickel, or with an acid chloride to form an N-acyl piperazine which may then be reduced with lithium aluminium hydride to the corresponding N-alkyl- or aralkyl-piperazine; (2) reaction of an omega-(o - R - benzhydryloxy) - alkyl halide with a 1 - mono - R1 - piperazine, optionally in the presence of a hydrohalic acid acceptor; (3) reaction of an o-R-benzhydryl halide with a 1-(omega - hydroxyalkyl) - 4 - R1 - piperazine, optionally in the presence of a hydrohalic acid acceptor; (4) reaction of an o-R-benzhydrol with a 1 - (omega - halogen - alkyl) - 4 - R1-piperazine, optionally in the presence of a hydrohalic acid acceptor; or (5) by building up the R1 chain in several steps, for example by condensing the compound wherein R1 is -(CH2)2OH with ethylene chlorohydrin or ethylene oxide. Examples illustrate the above processes, in which R1 has the values hydroxy-ethoxyethyl, isopropyl, m - methyl - benzyl, acetyl, ethyl, methyl, 2-(p-t-butylbenzyloxy)-ethyl, isopropyl, n- and iso-butyl, 2-hydroxy-ethyl, 2 :3 - dihydroxypropyl, cyclohexyl, 3-methyl - cyclohexyl, benzyl, o - chlorobenzyl, o - methylbenzyl, p - t - butylbenzyl, o - methoxybenzyl, R has the values of chloro and methyl and n the values of 2,3,4- and 6. Hydrochlorides of the products are also described. 2 - (o - Chlorobenzhydryloxy) - ethyl chloride, 2 - (o - methylbenzhydryloxy) - ethyl chloride, 3-(o - chlorobenzhydryloxy) - propyl chloride, 4-(o - chlorobenzhydryloxy) - butyl chloride and 6 - (o - chlorobenzhydryloxy) - hexyl chloride are prepared from the appropriate benzhydrol and chloro-alkanol in presence of concentrated sulphuric acid and benzene. 1 - Mono - [2 - (o - chlorobenzhydryloxy)-ethyl] - piperazine (dihydrochloride also described), is prepared from 2-(o-chlorobenzhydryloxy)-ethyl chloride and piperazine, and 1 - mono - [2 - (o - methylbenzhydryloxy) - ethyl]-1 - [3 - (o - chlorobenzhydryloxy) - propyl] -, 1 - [4 - (o - chlorobenzhydryloxybutyl] - and 1 - [6 - o - chlorobenzhydryloxy) - hexyl] - piperazines are prepared similarly. 1 - Mono - cyclohexyl - piperazine is prepared from cyclohexyl bromide and piperazine, and 1 - (3 - methylcyclohexyl) - and 1 - mono - (o - methylbenzyl) - piperazines are prepared similarly. 1 - Mono - (2 : 3 - dihydroxypropyl - piperazine) is prepared from piperazine and epoxypropanol. 1 - (4 - Hydroxybutyl) - 4 - (m - methylbenzyl)-piperazine is prepared from 1-(m-methylbenzyl)-piperazine and 4-chlorobutanol, and 1-(3-hydroxypropyl) - 4 - (o - methylbenzyl) - piperazine is prepared similarly.
GB21624/57A 1956-07-10 1957-07-08 New piperazine derivatives and process for the preparation thereof Expired GB837986A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
BE837986X 1956-07-10

Publications (1)

Publication Number Publication Date
GB837986A true GB837986A (en) 1960-06-22

Family

ID=3881891

Family Applications (1)

Application Number Title Priority Date Filing Date
GB21624/57A Expired GB837986A (en) 1956-07-10 1957-07-08 New piperazine derivatives and process for the preparation thereof

Country Status (2)

Country Link
GB (1) GB837986A (en)
MY (1) MY6100003A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2374318A1 (en) * 1976-12-14 1978-07-13 Gist Brocades Nv 1-Benzhydryl:oxy-alkyl-4-phenylalkyl- or cinnamyl-piperazine derivs. - with dopaminergic, anticholinergic and antiparkinson activity (BE 14.6.78)
US4202896A (en) 1976-12-14 1980-05-13 Gist-Brocades N.V. N-Benzhydryloxyethyl-N-phenylpropyl-piperazines
EP0243903A1 (en) * 1986-04-28 1987-11-04 Richter Gedeon Vegyészeti Gyár R.T. Optionally substituted 1-(omega[bis(phenyl)-alcoxy]-alkyl)-4-(alkenyl)piperazines and -4-(alkynyl)piperazines, process for their preparation and medicines containing them
US4868184A (en) * 1986-04-28 1989-09-19 Richter Gedeon Vegyeszeti Gyar Benzhydrylpiperazines pharmaceutical compositions thereof and method of use
EP0566189A1 (en) * 1992-04-13 1993-10-20 Akzo N.V. Psychotropic piperazine derivative

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2374318A1 (en) * 1976-12-14 1978-07-13 Gist Brocades Nv 1-Benzhydryl:oxy-alkyl-4-phenylalkyl- or cinnamyl-piperazine derivs. - with dopaminergic, anticholinergic and antiparkinson activity (BE 14.6.78)
US4202896A (en) 1976-12-14 1980-05-13 Gist-Brocades N.V. N-Benzhydryloxyethyl-N-phenylpropyl-piperazines
US4874765A (en) * 1986-04-22 1989-10-17 Richter Gedeon Vegyeszeti Gyar 1,4-Disubstituted piperazines having dopaminergic activity
EP0243903A1 (en) * 1986-04-28 1987-11-04 Richter Gedeon Vegyészeti Gyár R.T. Optionally substituted 1-(omega[bis(phenyl)-alcoxy]-alkyl)-4-(alkenyl)piperazines and -4-(alkynyl)piperazines, process for their preparation and medicines containing them
US4868184A (en) * 1986-04-28 1989-09-19 Richter Gedeon Vegyeszeti Gyar Benzhydrylpiperazines pharmaceutical compositions thereof and method of use
EP0566189A1 (en) * 1992-04-13 1993-10-20 Akzo N.V. Psychotropic piperazine derivative
US5281598A (en) * 1992-04-13 1994-01-25 Akzo N.V. Piperazine derivatives

Also Published As

Publication number Publication date
MY6100003A (en) 1961-12-31

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