AT342572B - PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS - Google Patents

PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Info

Publication number
AT342572B
AT342572B AT303977A AT303977A AT342572B AT 342572 B AT342572 B AT 342572B AT 303977 A AT303977 A AT 303977A AT 303977 A AT303977 A AT 303977A AT 342572 B AT342572 B AT 342572B
Authority
AT
Austria
Prior art keywords
sep
oximathers
aminoathyl
acylophenone
halogen
Prior art date
Application number
AT303977A
Other languages
German (de)
Other versions
ATA303977A (en
Original Assignee
Philips Nv
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
Priority claimed from NL7503312A external-priority patent/NL7503312A/en
Application filed by Philips Nv filed Critical Philips Nv
Priority to AT303977A priority Critical patent/AT342572B/en
Publication of ATA303977A publication Critical patent/ATA303977A/en
Application granted granted Critical
Publication of AT342572B publication Critical patent/AT342572B/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C249/00—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton
    • C07C249/04—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes
    • C07C249/12—Preparation of compounds containing nitrogen atoms doubly-bound to a carbon skeleton of oximes by reactions not involving the formation of oxyimino groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
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<tb> 
<tb> (2-amino-Verbindung <SEP> der <SEP> Formel <SEP> (1) <SEP> Noradr. <SEP> Serot. <SEP> MAO <SEP> Magen- <SEP> Broncho- <SEP> 
<tb> Ha. <SEP> l <SEP> R <SEP> pot. <SEP> pot. <SEP> Hemm. <SEP> ulcer. <SEP> striktur
<tb> Cl <SEP> OC2Hs* <SEP> 4, <SEP> 3 <SEP> 36 <SEP> > 215
<tb> Cl <SEP> CH2OCH3** <SEP> 5,3 <SEP> 36 <SEP> > 215
<tb> Cl <SEP> CH2OC2H5** <SEP> 7,4 <SEP> 54 <SEP> > 215
<tb> Cl <SEP> OC2H4OCH3* <SEP> 4, <SEP> 0 <SEP> 41 <SEP> > 215
<tb> Br <SEP> OC2H4OCH3* <SEP> 6,6 <SEP> 35 <SEP> > 215
<tb> Cl <SEP> CN** <SEP> 6, <SEP> 8 <SEP> 20 <SEP> > 215
<tb> Cl <SEP> CH2CN** <SEP> 11 <SEP> 38 <SEP> > 215
<tb> Br <SEP> CN** <SEP> 11, <SEP> 2 <SEP> 20 <SEP> > 215
<tb> Br <SEP> OCH3* <SEP> 6,6 <SEP> 22 <SEP> > 215
<tb> Cl <SEP> H <SEP> ** <SEP> 5,6 <SEP> 12 <SEP> > 215 <SEP> +
<tb> Cl <SEP> CH3*** <SEP> 1,

  9 <SEP> 14 <SEP> > 215 <SEP> + <SEP> +
<tb> Br <SEP> Chug** <SEP> 3, <SEP> 1 <SEP> 10 <SEP> > 215 <SEP> +
<tb> 
 
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**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 
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<tb>
<tb> (2-amino compound <SEP> of the <SEP> formula <SEP> (1) <SEP> noradr. <SEP> serot. <SEP> MAO <SEP> gastric <SEP> broncho- <SEP>
<tb> Ha. <SEP> l <SEP> R <SEP> pot. <SEP> pot. <SEP> inhib. <SEP> ulcer. <SEP> stricture
<tb> Cl <SEP> OC2Hs * <SEP> 4, <SEP> 3 <SEP> 36 <SEP>> 215
<tb> Cl <SEP> CH2OCH3 ** <SEP> 5,3 <SEP> 36 <SEP>> 215
<tb> Cl <SEP> CH2OC2H5 ** <SEP> 7.4 <SEP> 54 <SEP>> 215
<tb> Cl <SEP> OC2H4OCH3 * <SEP> 4, <SEP> 0 <SEP> 41 <SEP>> 215
<tb> Br <SEP> OC2H4OCH3 * <SEP> 6,6 <SEP> 35 <SEP>> 215
<tb> Cl <SEP> CN ** <SEP> 6, <SEP> 8 <SEP> 20 <SEP>> 215
<tb> Cl <SEP> CH2CN ** <SEP> 11 <SEP> 38 <SEP>> 215
<tb> Br <SEP> CN ** <SEP> 11, <SEP> 2 <SEP> 20 <SEP>> 215
<tb> Br <SEP> OCH3 * <SEP> 6,6 <SEP> 22 <SEP>> 215
<tb> Cl <SEP> H <SEP> ** <SEP> 5,6 <SEP> 12 <SEP>> 215 <SEP> +
<tb> Cl <SEP> CH3 *** <SEP> 1,

  9 <SEP> 14 <SEP>> 215 <SEP> + <SEP> +
<tb> Br <SEP> Chug ** <SEP> 3, <SEP> 1 <SEP> 10 <SEP>> 215 <SEP> +
<tb>
 
 EMI1.5
 

 <Desc / Clms Page number 2>

 
 EMI2.1
 
 EMI2.2
 
 EMI2.3
 

 <Desc / Clms Page number 3>

 
 EMI3.1
 
 EMI3.2
 
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** WARNING ** End of DESC field may overlap beginning of CLMS **.

Claims (1)

<Desc/Clms Page number 4> EMI4.1 EMI4.2 EMI4.3 EMI4.4 EMI4.5 <Desc / Clms Page number 4> EMI4.1 EMI4.2 EMI4.3 EMI4.4 EMI4.5
AT303977A 1975-03-20 1977-04-28 PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS AT342572B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT303977A AT342572B (en) 1975-03-20 1977-04-28 PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
NL7503312A NL7503312A (en) 1975-03-20 1975-03-20 CONNECTIONS WITH ANTIDEPRESSIVE ACTION.
AT195576A AT340896B (en) 1975-03-20 1976-03-17 METHOD FOR PRODUCING NEW P-HALOGEN-ACYLOPHENONE-O - (2-AMINOATHYL) -OXIMATHERS AND THEIR ACID ADDITION SALTS
AT303977A AT342572B (en) 1975-03-20 1977-04-28 PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Publications (2)

Publication Number Publication Date
ATA303977A ATA303977A (en) 1977-08-15
AT342572B true AT342572B (en) 1978-04-10

Family

ID=27148078

Family Applications (1)

Application Number Title Priority Date Filing Date
AT303977A AT342572B (en) 1975-03-20 1977-04-28 PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Country Status (1)

Country Link
AT (1) AT342572B (en)

Also Published As

Publication number Publication date
ATA303977A (en) 1977-08-15

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Legal Events

Date Code Title Description
EIH Change in the person of patent owner
ELJ Ceased due to non-payment of the annual fee
ELA Expired due to lapse of time