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 SALTSInfo
- 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
Links
- 239000002253 acid Substances 0.000 title 1
- 150000003839 salts Chemical class 0.000 title 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 description 1
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 208000031481 Pathologic Constriction Diseases 0.000 description 1
- 208000025865 Ulcer Diseases 0.000 description 1
- 230000002496 gastric effect Effects 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- -1 oxime ether compound Chemical class 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
Classifications
-
- G—PHYSICS
- G10—MUSICAL INSTRUMENTS; ACOUSTICS
- G10L—SPEECH ANALYSIS TECHNIQUES OR SPEECH SYNTHESIS; SPEECH RECOGNITION; SPEECH OR VOICE PROCESSING TECHNIQUES; SPEECH OR AUDIO CODING OR DECODING
- G10L15/00—Speech recognition
- G10L15/22—Procedures used during a speech recognition process, e.g. man-machine dialogue
- G10L2015/223—Execution procedure of a spoken command
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
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<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
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<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
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Claims (1)
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) |
-
1977
- 1977-01-19 AT AT27377A patent/AT342566B/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
ATA27377A (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 | ||
REN | Ceased due to non-payment of the annual fee | ||
RZN | Patent revoked |