GB1071593A - Amido compounds derived from beta-phenyl propionic acids - Google Patents

Amido compounds derived from beta-phenyl propionic acids

Info

Publication number
GB1071593A
GB1071593A GB31377/64A GB3137764A GB1071593A GB 1071593 A GB1071593 A GB 1071593A GB 31377/64 A GB31377/64 A GB 31377/64A GB 3137764 A GB3137764 A GB 3137764A GB 1071593 A GB1071593 A GB 1071593A
Authority
GB
United Kingdom
Prior art keywords
nhac
nhme
oet
beta
compounds derived
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
GB31377/64A
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.)
FINANZ KOMPENSATIONS ANST
Original Assignee
FINANZ KOMPENSATIONS ANST
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 FINANZ KOMPENSATIONS ANST filed Critical FINANZ KOMPENSATIONS ANST
Publication of GB1071593A publication Critical patent/GB1071593A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/54—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
    • C07D213/56—Amides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises compounds of formula <FORM:1071593/C2/1> wherein (a) X=OH, Y=NH2 or NHMe; (b) X=NHAc, Y=OEt; and (c) X=NHAc, Y=NH2 or NHMe. R is H, Me or OMe, R1 is alkyl, aryl or 2- or 4-pyridyl and R11 is H or Me. The starting material of the above formula has X=OH, Y=OEt; this is reacted with aq. NH3 or MeNH2 to give (a), or with MeCN+H2SO4 to give (b), while (c) is made by reacting (b) with aq. NH3 or MeNH2. In exemplified compounds, R and R11=H and (1) R1=4-pyridyl, X=OH, Y=NHMe; (2) R1=Ph, X=NHAc, Y=OEt or NHMe; (3) R1=Me, X=NHAc, Y=OEt; (4) R1=Et, X=NHAc, Y=OEt or NHMe. Starting materials of formula <FORM:1071593/C2/2> X1 being Me, Et or 4-pyridyl, are prepared by reacting PhCOX1 with BrCH2CO2Et and activated
GB31377/64A 1963-08-01 1964-08-04 Amido compounds derived from beta-phenyl propionic acids Expired GB1071593A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR943475A FR3143M (en) 1963-08-01 1963-08-01 Amides of β-phenyl-β-oxypropionic and β-aceto-amido-β-phenylpropionic acids.

Publications (1)

Publication Number Publication Date
GB1071593A true GB1071593A (en) 1967-06-07

Family

ID=8809721

Family Applications (1)

Application Number Title Priority Date Filing Date
GB31377/64A Expired GB1071593A (en) 1963-08-01 1964-08-04 Amido compounds derived from beta-phenyl propionic acids

Country Status (4)

Country Link
BR (1) BR6461300D0 (en)
DE (1) DE1493669A1 (en)
FR (1) FR3143M (en)
GB (1) GB1071593A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003091201A1 (en) * 2002-04-26 2003-11-06 Sergio Enrique Meza Toledo Dl-hydroxy-alkyl-phenylamides having anticonvulsive activity

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003091201A1 (en) * 2002-04-26 2003-11-06 Sergio Enrique Meza Toledo Dl-hydroxy-alkyl-phenylamides having anticonvulsive activity

Also Published As

Publication number Publication date
DE1493669A1 (en) 1969-05-22
FR3143M (en) 1965-02-22
BR6461300D0 (en) 1973-08-07

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