ES407156A1 - Amino-esters - Google Patents

Amino-esters

Info

Publication number
ES407156A1
ES407156A1 ES407156A ES407156A ES407156A1 ES 407156 A1 ES407156 A1 ES 407156A1 ES 407156 A ES407156 A ES 407156A ES 407156 A ES407156 A ES 407156A ES 407156 A1 ES407156 A1 ES 407156A1
Authority
ES
Spain
Prior art keywords
naphthyl
methyl
ethyl
general formula
amino
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
ES407156A
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 ES407156A1 publication Critical patent/ES407156A1/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
    • C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D319/20—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring with substituents attached to the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/10—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/16—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D319/00—Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/10—1,4-Dioxanes; Hydrogenated 1,4-dioxanes
    • C07D319/14—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems
    • C07D319/16—1,4-Dioxanes; Hydrogenated 1,4-dioxanes condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D319/18—Ethylenedioxybenzenes, not substituted on the hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Compounds Containing Sulfur Atoms (AREA)
  • Furan Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Procedure for obtaining amino esters of the general formula: **(See formula)** wherein A and B are identical or different and are selected from the following radicals: α-naphthyl; β-naphthyl; β-dihydro-3,4 naphthyl; α-tetrahydro-5,6,7,8 naphthyl; β-tetrahydro-5,6,7,8 naphthyl; α-decahydronaphthyl; (benzodioxanil-1,4) -2; (benzodioxanil-1,4) -6; (dimethoxy-3,4 phenyl) -1; α-tetrahydrofuryl; α-thienyl; methyl-2α-thienyl; α-tetrahydrothienyl; indenyl-3; R is a residue selected from the following: β-dimethylamino-ethyl; β-methylethylamino-ethyl; β-methyl n-propyl-amino-ethyl; β-diethylamino-ethyl; β-di-n-propylaminoethyl; β-di-n-butylemino-ethyl; methyl-1 pyrrolidinyl-methyl-2; pyridinyl methyl-3; methyl-1 piperazinylethyl-4, compounds (I) for which A is an α-naphthyl residue when B is an α-tetrahydrofuryl radical and R is a β-dialkylamino-alkyl residue in which two of the Alkyl radicals, fixed on the nitrogen, can optionally form a nitrogenous heterocycle between them and the nitrogen atom, and their addition salts with pharmaceutically acceptable mineral or organic acids, characterized in that an acid of general formula (II) is condensed.) **(See formula)** with an amino alcohol of general formula (III) R-OH (III) where A, B and R have the meaning indicated above. (Machine-translation by Google Translate, not legally binding)
ES407156A 1971-09-30 1972-09-29 Amino-esters Expired ES407156A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR7135306A FR2154344B1 (en) 1971-09-30 1971-09-30

Publications (1)

Publication Number Publication Date
ES407156A1 true ES407156A1 (en) 1975-11-16

Family

ID=9083746

Family Applications (1)

Application Number Title Priority Date Filing Date
ES407156A Expired ES407156A1 (en) 1971-09-30 1972-09-29 Amino-esters

Country Status (11)

Country Link
JP (1) JPS4840757A (en)
AT (1) AT317884B (en)
AU (1) AU4718872A (en)
BE (1) BE789254A (en)
CA (1) CA980345A (en)
DE (1) DE2246709A1 (en)
ES (1) ES407156A1 (en)
FR (1) FR2154344B1 (en)
GB (1) GB1382699A (en)
NL (1) NL7213222A (en)
ZA (1) ZA726595B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5140159B1 (en) * 1969-11-26 1976-11-01
FR2455594A1 (en) * 1979-05-03 1980-11-28 Chauvin Blache Lab Vasodilatory and spasmolytic 2-aminoethyl iso-butyrate(s) - are substd. by furyl, thienyl, benzofuryl and benzo thienyl

Also Published As

Publication number Publication date
GB1382699A (en) 1975-02-05
BE789254A (en) 1973-03-26
FR2154344B1 (en) 1975-02-07
DE2246709A1 (en) 1973-04-05
AT317884B (en) 1974-09-25
JPS4840757A (en) 1973-06-15
CA980345A (en) 1975-12-23
ZA726595B (en) 1973-06-27
AU4718872A (en) 1974-04-04
FR2154344A1 (en) 1973-05-11
NL7213222A (en) 1973-04-03

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