AT342566B - PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS - Google Patents

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

Info

Publication number
AT342566B
AT342566B AT27377A AT27377A AT342566B AT 342566 B AT342566 B AT 342566B AT 27377 A AT27377 A AT 27377A AT 27377 A AT27377 A AT 27377A AT 342566 B AT342566 B AT 342566B
Authority
AT
Austria
Prior art keywords
sep
oximathers
aminoathyl
acylophenone
methylthio
Prior art date
Application number
AT27377A
Other languages
German (de)
Other versions
ATA27377A (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 NL7503309A external-priority patent/NL7503309A/en
Application filed by Philips Nv filed Critical Philips Nv
Priority to AT27377A priority Critical patent/AT342566B/en
Publication of ATA27377A publication Critical patent/ATA27377A/en
Application granted granted Critical
Publication of AT342566B publication Critical patent/AT342566B/en

Links

Classifications

    • GPHYSICS
    • G10MUSICAL INSTRUMENTS; ACOUSTICS
    • G10LSPEECH ANALYSIS TECHNIQUES OR SPEECH SYNTHESIS; SPEECH RECOGNITION; SPEECH OR VOICE PROCESSING TECHNIQUES; SPEECH OR AUDIO CODING OR DECODING
    • G10L15/00Speech recognition
    • G10L15/22Procedures used during a speech recognition process, e.g. man-machine dialogue
    • G10L2015/223Execution procedure of a spoken command

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
 EMI1.1 
 
 EMI1.2 
 
 EMI1.3 
 

 <Desc/Clms Page number 2> 

 
 EMI2.1 
 
 EMI2.2 
 
<tb> 
<tb> 



  (2-aminoäthyl) <SEP> -oximäthernVerbindung <SEP> Noradr. <SEP> Serot. <SEP> s <SEP> MAG <SEP> Magen- <SEP> Broncho- <SEP> 
<tb> X <SEP> Pot. <SEP> Pot. <SEP> ,. <SEP> Hemmung <SEP> ulcer. <SEP> striktur
<tb> Noradr.
<tb> 



  (CHOCHg <SEP> ** <SEP> 26 <SEP> 12 <SEP> 0, <SEP> 5 <SEP> > 215
<tb> (CHOCH <SEP> * <SEP> 36 <SEP> 20 <SEP> 0, <SEP> 2 <SEP> > 215 <SEP> 
<tb> (CHjOCHOCHg <SEP> * <SEP> 45 <SEP> 34 <SEP> 0, <SEP> 8 <SEP> > <SEP> 215 <SEP> - <SEP> - <SEP> 
<tb> (CH2) <SEP> OCH <SEP> **-100 <SEP> 21-0, <SEP> 2 <SEP> > 215
<tb> (CHCN <SEP> ** <SEP> 33 <SEP> 16 <SEP> 0, <SEP> 5 <SEP> > 215
<tb> (CH2). <SEP> CN <SEP> **-100 <SEP> 29-0, <SEP> 3 <SEP> > 215
<tb> (CHCl <SEP> ** <SEP> > <SEP> 215 <SEP> 15 <SEP> > 0, <SEP> 1 <SEP> > 215 <SEP> 
<tb> CH <SEP> ** <SEP> 2, <SEP> 4 <SEP> 0, <SEP> 74 <SEP> 0, <SEP> 3 <SEP> 15 <SEP> - <SEP> 
<tb> (CH2) <SEP> CH <SEP> **-M <SEP> 10-0, <SEP> 2 <SEP> > 215 <SEP> + <SEP> + <SEP> 
<tb> 
   *     =     Fumarat   1 :

     1     **     =   Hydrochlorid 

 <Desc/Clms Page number 3> 

 
 EMI3.1 
 

 <Desc/Clms Page number 4> 

 
 EMI4.1 
 
 EMI4.2 




   <Desc / Clms Page number 1>
 
 EMI1.1
 
 EMI1.2
 
 EMI1.3
 

 <Desc / Clms Page number 2>

 
 EMI2.1
 
 EMI2.2
 
<tb>
<tb>



  (2-aminoethyl) <SEP> oxime ether compound <SEP> noradr. <SEP> serot. <SEP> s <SEP> MAG <SEP> gastric <SEP> bronchial <SEP>
<tb> X <SEP> Pot. <SEP> pot. <SEP>,. <SEP> inhibition <SEP> ulcer. <SEP> stricture
<tb> Noradr.
<tb>



  (CHOCHg <SEP> ** <SEP> 26 <SEP> 12 <SEP> 0, <SEP> 5 <SEP>> 215
<tb> (CHOCH <SEP> * <SEP> 36 <SEP> 20 <SEP> 0, <SEP> 2 <SEP>> 215 <SEP>
<tb> (CHjOCHOCHg <SEP> * <SEP> 45 <SEP> 34 <SEP> 0, <SEP> 8 <SEP>> <SEP> 215 <SEP> - <SEP> - <SEP>
<tb> (CH2) <SEP> OCH <SEP> ** - 100 <SEP> 21-0, <SEP> 2 <SEP>> 215
<tb> (CHCN <SEP> ** <SEP> 33 <SEP> 16 <SEP> 0, <SEP> 5 <SEP>> 215
<tb> (CH2). <SEP> CN <SEP> ** - 100 <SEP> 29-0, <SEP> 3 <SEP>> 215
<tb> (CHCl <SEP> ** <SEP>> <SEP> 215 <SEP> 15 <SEP>> 0, <SEP> 1 <SEP>> 215 <SEP>
<tb> CH <SEP> ** <SEP> 2, <SEP> 4 <SEP> 0, <SEP> 74 <SEP> 0, <SEP> 3 <SEP> 15 <SEP> - <SEP>
<tb> (CH2) <SEP> CH <SEP> ** - M <SEP> 10-0, <SEP> 2 <SEP>> 215 <SEP> + <SEP> + <SEP>
<tb>
   * = Fumarate 1:

     1 ** = hydrochloride

 <Desc / Clms Page number 3>

 
 EMI3.1
 

 <Desc / Clms Page number 4>

 
 EMI4.1
 
 EMI4.2


 

Claims (1)

EMI4.3 EMI4.4 EMI4.5 EMI4.6 EMI4.3 EMI4.4 EMI4.5 EMI4.6
AT27377A 1975-03-20 1977-01-19 PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS AT342566B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT27377A AT342566B (en) 1975-03-20 1977-01-19 PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
NL7503309A NL7503309A (en) 1975-03-20 1975-03-20 CONNECTIONS WITH ANTIDEPRESSIVE ACTION.
AT194876A AT340897B (en) 1975-03-20 1976-03-17 METHOD FOR PRODUCING NEW P-METHYLTHIOACYLOPHENONE-O- (2-AMINOATHYL) -OXIMATHERS AND THEIR ACID ADDITION SALTS
AT27377A AT342566B (en) 1975-03-20 1977-01-19 PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Publications (2)

Publication Number Publication Date
ATA27377A ATA27377A (en) 1977-08-15
AT342566B true AT342566B (en) 1978-04-10

Family

ID=27146079

Family Applications (1)

Application Number Title Priority Date Filing Date
AT27377A AT342566B (en) 1975-03-20 1977-01-19 PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS

Country Status (1)

Country Link
AT (1) AT342566B (en)

Also Published As

Publication number Publication date
ATA27377A (en) 1977-08-15

Similar Documents

Publication Publication Date Title
AT342566B (en) PROCESS FOR THE PREPARATION OF NEW P-METHYLTHIO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS
AT342501B (en) CONTAINER
ES458957A1 (en) 1-aryloxy-2 - hydroxy - 3 - aminopropanes and process for their preparation
AT342576B (en) PROCESS FOR THE PREPARATION OF NEW P-METHYLSULFINYL-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS
AT342573B (en) PROCESS FOR THE PREPARATION OF NEW P-NITRO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITIONAL SALTS
AT342569B (en) PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) -OXIMATHERS AND THEIR ACID ADDITION SALTS
AT342572B (en) PROCESS FOR THE PREPARATION OF NEW P-HALOGEN-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITION SALTS
AT342574B (en) PROCESS FOR THE PRODUCTION OF NEW P-TRIFLUOROMETHYL-ACYLOPHENONE-O- (2-AMINOATHYL) -OXIMATHERS AND THEIR ACID ADDITION SALTS
AT342567B (en) PROCESS FOR THE PREPARATION OF NEW P-NITRO-ACYLOPHENONE-O- (2-AMINOATHYL) OXIMATHERS AND THEIR ACID ADDITIONAL SALTS
ATE3972T1 (en) PROCESS FOR THE PRODUCTION OF BASIC SUBSTITUTED PHENYLACETONITRILES.
AT335429B (en) PROCESS FOR PREPARING CIS-2-HYDROXY-2-PHENYL-R-1-CYCLOHEXANECARBONIC ACID
AT348005B (en) METHOD FOR MANUFACTURING A BEAM SUPPORT, IN PARTICULAR A BRIDGE SUPPORT
AT343094B (en) PROCESS FOR MANUFACTURING THE NEW ALFA-AMINO-2-ADAMANTYL VINEGAR ACID
AT347927B (en) PROCESS FOR THE PREPARATION OF NEW 3-CYANAMINO-4-TRIFLUOROMETHYL-2,6-DINITROANILINES
AT347978B (en) PLANT FOR THE PRODUCTION OF HIGH QUALITY THINNING
AT347483B (en) PROCESS FOR THE PRODUCTION OF CHARACTERS FOR WREATH BOW LABELS
AT342608B (en) PROCESS FOR THE PREPARATION OF NEW DERIVATIVES OF (1,4) OXATHIINO (2,3-C) PYRROLE AND THE SALT THEREOF
AT340120B (en) RAILED FOR STAIRS
AT220622B (en) Process for the preparation of new, basic substituted oxodiazepines
AT347954B (en) PROCESS FOR THE PREPARATION OF NEW ISOTHIAZOLO-ISOCHINOLINE DERIVATIVES AND THEIR SALTS
AT335426B (en) PROCESS FOR THE MANUFACTURING OF NEW 1-ACYL-3-BIPHENYLYL-PROPANONE
AT250939B (en) Process for the preparation of new naphthalic acid imides
AT159953B (en) Process for the preparation of aminobenzenesulfonic acid amide compounds.
AT280498B (en) Process for the preparation of new 3-methyl-19-nor-3,5-androstadien-17β-ols
AT342395B (en) METHOD AND DEVICE FOR MANUFACTURING GRATING

Legal Events

Date Code Title Description
EIH Change in the person of patent owner
ELJ Ceased due to non-payment of the annual fee
REN Ceased due to non-payment of the annual fee
RZN Patent revoked