GB837986A - New piperazine derivatives and process for the preparation thereof - Google Patents
New piperazine derivatives and process for the preparation thereofInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic 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
- C07D295/04—Heterocyclic 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
- C07D295/08—Heterocyclic 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
- C07D295/084—Heterocyclic 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
- C07D295/088—Heterocyclic 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.
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)
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 |
-
1957
- 1957-07-08 GB GB21624/57A patent/GB837986A/en not_active Expired
-
1961
- 1961-12-30 MY MY3/61A patent/MY6100003A/en unknown
Cited By (7)
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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