IL69632A0 - Propylamine derivatives - Google Patents

Propylamine derivatives

Info

Publication number
IL69632A0
IL69632A0 IL69632A IL6963283A IL69632A0 IL 69632 A0 IL69632 A0 IL 69632A0 IL 69632 A IL69632 A IL 69632A IL 6963283 A IL6963283 A IL 6963283A IL 69632 A0 IL69632 A0 IL 69632A0
Authority
IL
Israel
Prior art keywords
compound
formula
lower alkyl
group
salt
Prior art date
Application number
IL69632A
Other versions
IL69632A (en
Original Assignee
Ciba Geigy Ag
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 Ciba Geigy Ag filed Critical Ciba Geigy Ag
Publication of IL69632A0 publication Critical patent/IL69632A0/en
Publication of IL69632A publication Critical patent/IL69632A/en

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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
    • C07D295/092Heterocyclic 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 with aromatic radicals attached to the chain
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/26Psychostimulants, e.g. nicotine, ***e
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/04Formation of amino groups in compounds containing carboxyl groups
    • C07C227/06Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid
    • C07C227/08Formation of amino groups in compounds containing carboxyl groups by addition or substitution reactions, without increasing the number of carbon atoms in the carbon skeleton of the acid by reaction of ammonia or amines with acids containing functional groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/16Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Hydrogenated Pyridines (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

For the Contracting States : BE, CH, DE, FR, GB, IT, LI, LU, NL, SE 1. A compound of the general formula I see diagramm : EP0102929,P33,F1 Wherein each of R1 and R2 independently of the other represents hydrogen or lower alkyl ; or R1 and R2 together with the adjacent nitrogen atom represent piperidino or pyrrolidino or a five- or six-membered saturated heterocyclic ring containing NH, N-lower alkyl, O or S ; R3 represents hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl ; Ar represents phenyl or phenyl substituted by one to three substituents selected from the group consisting of lower alkyl, lower alkoxy, lower alkenyloxy, lower alkynyloxy, lower alkylmercapto, lower alkylsulfinyl, lower alkylsulfonyl, halogen and trifluoromethyl, or by on lower alkylenedioxy ; and X represents O, S or N-lower alkyl ; and n represents an integer 1, 2 or 3 ; or an N-oxide thereof ; an acid addition salt thereof ; of an N-lower alkyl or N-benzyl quaternary salt thereof ; with the exception of the compound of formula I wherein R1 and R2 represent ethyl, R3 represents hydrogen, Ar represents phenyl, X represents O, and n is 3, or a salt thereof ; with the groups qualified by the term "lower" containing at most 7 carbon atoms. For the Contracting State : AT 1. A process for the preparation of a novel propylamine derivative of the general formula I see diagramm : EP0102929,P37,F1 Wherein each of R1 and R2 independently of the other represents hydrogen or lower alkyl ; or R1 and R2 together with the adjacent nitrogen atom represent piperidono or pyrrodino or a five- or six-membered saturated heterocyclic ring containing NH, N-lower alkyl, O or S ; R3 represents hydrogen, lower alkyl, lower alkoxy, halogen or trifluoromethyl ; Ar represents phenyl or phenyl substituted by one to three substituents selected from the group consisting of lower alkyl, lower alkoxy, lower alkenyloxy, lower alkynyloxy, lower alkylmercapto, lower alkylsulfinyl, lower alkylsulfonyl, halogen and trifluoromethyl, or by on lower alkylenedioxy ; and X represents O, S or N-lower alkyl ; and n represents an integer 1, 2 or 3 ; or of an N-oxide thereof ; an acid addition salt thereof ; of an N-lower alkyl or N-benzyl quaternary salt thereof ; with the exception of the compound of formula I wherein R1 and R2 represent ethyl, R3 represents hydrogen, Ar represents phenyl, X represents O, and n is 3, or a salt thereof ; with the groups qualified by the term "lower" containing at most 7 carbon atoms ; which process comprises a) condensing a compound of the formula II see diagramm : EP0102929,P37,F2 or an acid addition salt thereof, with a compound of the formula III AR-Y(III) wherein R1 , R2 , R3 , n and Ar are as defined above, one of the symbols W and Y represents a group XH or XH in a metal salt from, in which X is as defined above, and the other one represents the group XH in a reactive esterified form thereof or as an N,N'-disubstituted isourea or isothiourea derivative ; or b) alkylating an amine of the formula IV see diagramm : EP0102929,P37,F3 or an acid addition salt thereof, with a compound of the formula V see diagramm : EP0102929,P38,F4 in which Z is a hydrogen atom together with a reactive esterified hydroxyl group of the oxo group and Ar, X, R3 and n are as defined above, and if Z is the oxo group, said alkylation is carried out under reductive conditions ; or c) reducing a compound structurally analogous to a compound of formula I as defined above, wherein an oxo group is present on at least one carbon atom adjacent to the amino nitrogen ; or d) saturating with hydrogen a multiple bond or multiple bonds in a compound structurally analogous to the compound of formula I as defined above and wherein one or two double bonds are present in the aliphatic moiety of the molecule inclusive of the amino group ; or e) removing the radial R0 from a compound of the formula VI see diagramm : EP0102929,P38,F5 wherein R2 , R3 , X, n and Ar are as defined above and R0 is an amino proctective group, to obtain a compound of formula in which R1 is hyrogen ; or f) reducing a compound of the formula VII see diagramm : EP0102929,P38,F5 wherein T represents cyano or azidomethyl ; and R3 , X, n and Ar are as defined above to obtain a compound of formula I wherein R1 and R2 are hydrogen ; or g) condensing a compound of the formula VIIA see diagramm : EP0102929,P39,F6 with a compound of the formula VIIB see diagramm : EP0102929,P39,F6 wherein one of the groups Q and M represents a removable group, and the other represents a metal or halometal radical, and Ar, X, R1 to R3 and n are as defined above, if necesseray while temporarily protecting any interfering reactive group in all these processes, and isolating the resultant compound of formula ; and/or, if required, converting a resultant compound of formula I into another compound of formula I, and/or, if require, converting a resultant free compound into a salt or a resultant salt into the free compound or into another salt, and/or, if required, resolving a mixture of isomers or racemates obtained into the single isomers or racemates, and/or, if required, resolving a racemate obtained into the optical antipodes.
IL69632A 1982-09-07 1983-09-02 2-benzyl-3-phenoxypropylamines,their preparation and pharmaceutical compositions comprising them IL69632A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US41500082A 1982-09-07 1982-09-07

Publications (2)

Publication Number Publication Date
IL69632A0 true IL69632A0 (en) 1983-12-30
IL69632A IL69632A (en) 1987-08-31

Family

ID=23643932

Family Applications (1)

Application Number Title Priority Date Filing Date
IL69632A IL69632A (en) 1982-09-07 1983-09-02 2-benzyl-3-phenoxypropylamines,their preparation and pharmaceutical compositions comprising them

Country Status (18)

Country Link
EP (1) EP0102929B1 (en)
JP (1) JPS5973546A (en)
AT (1) ATE28069T1 (en)
AU (1) AU566564B2 (en)
CA (1) CA1242728A (en)
DD (1) DD213208A5 (en)
DE (1) DE3372283D1 (en)
DK (1) DK405183A (en)
ES (4) ES525400A0 (en)
FI (1) FI83632C (en)
GR (1) GR78936B (en)
HU (1) HU194157B (en)
IE (1) IE55906B1 (en)
IL (1) IL69632A (en)
NO (1) NO157975C (en)
NZ (1) NZ205509A (en)
PT (1) PT77291B (en)
ZA (1) ZA836597B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005500371A (en) * 2001-08-08 2005-01-06 ニューロサーチ、アクティーゼルスカブ Substituted amine derivatives and methods of using them as monoamine neurotransmitter reuptake inhibitors

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1237352A (en) * 1969-01-03 1971-06-30 Ct Europ De Rech S Mauvernay Substituted propylamines
GB1343527A (en) * 1971-07-30 1974-01-10 Cerm Cent Europ Rech Mauvernay Amino-propanol derivatives
FR2460919A1 (en) * 1979-07-11 1981-01-30 Prod Synthese Ste Indle AMINO-ETHERS OXIDES, PROCESS FOR PREPARING THEM AND THEIR THERAPEUTIC APPLICATION

Also Published As

Publication number Publication date
ES8802010A1 (en) 1988-03-16
ES541259A0 (en) 1986-12-16
FI833150A (en) 1984-03-08
PT77291A (en) 1983-10-01
ES541260A0 (en) 1988-03-16
ATE28069T1 (en) 1987-07-15
CA1242728A (en) 1988-10-04
NO833178L (en) 1984-03-08
JPS5973546A (en) 1984-04-25
ES8506582A1 (en) 1985-08-01
DK405183D0 (en) 1983-09-06
FI83632C (en) 1991-08-12
HU194157B (en) 1988-01-28
FI83632B (en) 1991-04-30
AU1874683A (en) 1984-03-15
GR78936B (en) 1984-10-02
EP0102929A2 (en) 1984-03-14
NO157975C (en) 1988-06-28
IE55906B1 (en) 1991-02-14
NZ205509A (en) 1987-07-31
EP0102929A3 (en) 1984-09-12
AU566564B2 (en) 1987-10-22
PT77291B (en) 1986-07-14
IE832093L (en) 1984-03-07
DD213208A5 (en) 1984-09-05
ES8606244A1 (en) 1986-04-01
DE3372283D1 (en) 1987-08-06
IL69632A (en) 1987-08-31
NO157975B (en) 1988-03-14
ES541258A0 (en) 1986-04-01
ZA836597B (en) 1984-04-25
EP0102929B1 (en) 1987-07-01
ES8702335A1 (en) 1986-12-16
FI833150A0 (en) 1983-09-05
DK405183A (en) 1984-03-08
ES525400A0 (en) 1985-08-01

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