ES425030A1 - Procedure for preparing piperazine derivatives. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for preparing piperazine derivatives. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES425030A1
ES425030A1 ES425030A ES425030A ES425030A1 ES 425030 A1 ES425030 A1 ES 425030A1 ES 425030 A ES425030 A ES 425030A ES 425030 A ES425030 A ES 425030A ES 425030 A1 ES425030 A1 ES 425030A1
Authority
ES
Spain
Prior art keywords
translation
procedure
machine
legally binding
google translate
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
ES425030A
Other languages
Spanish (es)
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.)
Synthelabo SA
Original Assignee
Synthelabo SA
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 Synthelabo SA filed Critical Synthelabo SA
Publication of ES425030A1 publication Critical patent/ES425030A1/en
Expired legal-status Critical Current

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

Procedure for preparing piperazine derivatives, characterized in that an amino alcohol responding to the formula is reacted: ** (See formula) ** in which R represents a halogen atom, or a CF3, OCF3 or SCF3 radical and R'represents a hydrogen atom or an alkyl radical of 1 to 3 carbon atoms, with a pharmaceutically acceptable acid in an organic solvent, and then the solvent is evaporated under reduced pressure. (Machine-translation by Google Translate, not legally binding)
ES425030A 1973-04-05 1974-04-05 Procedure for preparing piperazine derivatives. (Machine-translation by Google Translate, not legally binding) Expired ES425030A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7312278A FR2224464A1 (en) 1973-04-05 1973-04-05 N-Phenyl-N'-beta-hydroxy-ethyl piperazines - as analgesic and anti-inflammatory agents

Publications (1)

Publication Number Publication Date
ES425030A1 true ES425030A1 (en) 1976-11-01

Family

ID=9117462

Family Applications (1)

Application Number Title Priority Date Filing Date
ES425030A Expired ES425030A1 (en) 1973-04-05 1974-04-05 Procedure for preparing piperazine derivatives. (Machine-translation by Google Translate, not legally binding)

Country Status (2)

Country Link
ES (1) ES425030A1 (en)
FR (1) FR2224464A1 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2442234A2 (en) * 1978-08-01 1980-06-20 Synthelabo CNS-active 1-phenyl-piperazine cpds. - useful as analgesics and psychotropic agents
FR2459797A2 (en) * 1978-08-01 1981-01-16 Synthelabo PHENYL-1 PIPERAZINE DERIVATIVES AND THEIR THERAPEUTIC APPLICATION

Also Published As

Publication number Publication date
FR2224464A1 (en) 1974-10-31
FR2224464B1 (en) 1977-08-05

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