ES440767A2 - Phenylethylamine derivatives - Google Patents

Phenylethylamine derivatives

Info

Publication number
ES440767A2
ES440767A2 ES440767A ES440767A ES440767A2 ES 440767 A2 ES440767 A2 ES 440767A2 ES 440767 A ES440767 A ES 440767A ES 440767 A ES440767 A ES 440767A ES 440767 A2 ES440767 A2 ES 440767A2
Authority
ES
Spain
Prior art keywords
equal
formula
phenylethylamine
derivatives
see formula
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
ES440767A
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 ES440767A2 publication Critical patent/ES440767A2/en
Expired legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/13—Amines
    • A61K31/145—Amines having sulfur, e.g. thiurams (>N—C(S)—S—C(S)—N< and >N—C(S)—S—S—C(S)—N<), Sulfinylamines (—N=SO), Sulfonylamines (—N=SO2)
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
    • C07C319/14—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides
    • C07C319/20—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of sulfides by reactions not involving the formation of sulfide groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
    • C07C323/23—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton
    • C07C323/31—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton
    • C07C323/32—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having the sulfur atom of at least one of the thio groups bound to a carbon atom of a six-membered aromatic ring of the carbon skeleton having at least one of the nitrogen atoms bound to an acyclic carbon atom of the carbon skeleton

Abstract

Improvements introduced in the object of the main patent No. 415,405, filed on May 30, 1973, on: Procedure for the preparation of derivatives of phenylethylamine, of general formula (I): ** (See formula) ** in which n is equal to 0, 1 or 2 and m is an integer at least equal to 1 and at most equal to 4, in the form of racemates or Optical isomers, as well as their pharmaceutically acid addition salts acceptable, characterized in that (trifluoromethylthio-3 phenyl) -1 propanone-2 is first condensed with an amine of the formula: ** (See formula) ** and then the intermediate obtained is reduced. (Machine-translation by Google Translate, not legally binding)
ES440767A 1974-09-06 1975-09-05 Phenylethylamine derivatives Expired ES440767A2 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7430284A FR2283673A1 (en) 1974-09-06 1974-09-06 NEW M-TRIFLUOROMETHYLTHIO PHENETHYLAMINE DERIVATIVES, THEIR SALTS, THEIR PREPARATION AND THE MEDICINAL PRODUCTS CONTAINING IT

Publications (1)

Publication Number Publication Date
ES440767A2 true ES440767A2 (en) 1977-04-01

Family

ID=9142841

Family Applications (1)

Application Number Title Priority Date Filing Date
ES440767A Expired ES440767A2 (en) 1974-09-06 1975-09-05 Phenylethylamine derivatives

Country Status (9)

Country Link
JP (1) JPS5163153A (en)
BE (1) BE832999R (en)
DK (1) DK398675A (en)
ES (1) ES440767A2 (en)
FR (1) FR2283673A1 (en)
GB (1) GB1469745A (en)
NL (1) NL7510489A (en)
SE (1) SE7509884L (en)
ZA (1) ZA755417B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2447907A1 (en) * 1979-02-05 1980-08-29 Synthelabo Anorexics used to treat obesity - are 1-3-tri:fluoro:methyl-sulphonyl or sulphinyl-phenyl-2-amino-propane(s)

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1218135A (en) * 1967-07-28 1971-01-06 Abbott Lab Substituted phenethylamine derivatives
FR2186248B1 (en) * 1972-05-31 1975-11-28 Synthelabo

Also Published As

Publication number Publication date
FR2283673A1 (en) 1976-04-02
JPS5163153A (en) 1976-06-01
AU8428375A (en) 1977-03-03
BE832999R (en) 1976-03-02
NL7510489A (en) 1976-03-09
FR2283673B1 (en) 1978-08-18
GB1469745A (en) 1977-04-06
DE2538593A1 (en) 1976-03-25
SE7509884L (en) 1976-03-08
DE2538593B2 (en) 1977-02-03
ZA755417B (en) 1976-07-28
DK398675A (en) 1976-03-07

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