AT211299B - Process for the preparation of 1-phenyl-1 (o-chlorophenyl) -3-tert.aminopropanolen- (1) - Google Patents

Process for the preparation of 1-phenyl-1 (o-chlorophenyl) -3-tert.aminopropanolen- (1)

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Publication number
AT211299B
AT211299B AT247459A AT247459A AT211299B AT 211299 B AT211299 B AT 211299B AT 247459 A AT247459 A AT 247459A AT 247459 A AT247459 A AT 247459A AT 211299 B AT211299 B AT 211299B
Authority
AT
Austria
Prior art keywords
chlorophenyl
phenyl
tert
preparation
aminopropanolen
Prior art date
Application number
AT247459A
Other languages
German (de)
Inventor
Rudolf Dr Lorenz
Hans Dr Henecka
Rudolf Dr Goesswald
Original Assignee
Bayer Ag
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 Bayer Ag filed Critical Bayer Ag
Application granted granted Critical
Publication of AT211299B publication Critical patent/AT211299B/en

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  • Hydrogenated Pyridines (AREA)

Description

  

   <Desc/Clms Page number 1> 
 
 EMI1.1 
 (o-chlorphenyl)-3-tert. aminopropanolen- (l)l-Phenyl-l-   0 - chlorphenyl) -3-tert. aminopropa-   nole- (l) der Formel 
 EMI1.2 
 worin R und R'geradkettige oder verzweigte Alkylgruppen mit 1-5 Kohlenstoffatomen, die unter sich auch ringförmig, gegebenenfalls unter Zwischenschaltung eines Heteratoms, wie Sauerstoff, Schwefel oder Stickstoff, der seinerseits durch Alkylgruppen substituiert sein kann, verknüpft sein kann, bedeuten, zeichnen sich durch eine hervorragende hustenstillende Wirksamkeit aus. Es wurde bereits vorgeschlagen, das   1-Phenyl-   
 EMI1.3 
 - (1) mittels eines Grignard-Verfahrens herzustellen. 



  Die Schwierigkeiten eines solchen Verfahrens an sich sind allgemein bekannt. Ein solches Verfahren ist natürlich wesentlich umständlicher und in der Grosstechnik schwieriger auszuführen als das erfindungsgemässe Verfahren, bei dem die unangenehm zu handhabenden metallorganischen Verbindungen restlos vermieden werden. 



   Erfindungsgemäss kann man zur Herstellung der genannten Verbindungen so verfahren, dass man an o-Chlorbenzophenon in Gegenwart stark basischer Kondensationsmittel, wie z. B. 



  Natriumamid, Acetonitril addiert, das so er- 
 EMI1.4 
 (o-chlorphenyl)-hydracryl-nopropanol- (l) hydriert und diese Base am Stickstoff durch Alkylreste substituiert. 



   Man kann auch so vorgehen, dass man das aus o-Chlorbenzophenon und Acetonitril in Gegenwart stark basischer Kondensationsmittel erhaltene   ss-Phenyl-ss- (-o-chlorphenyl)-hydracryl-   säurenitril nach dem in der deutschen Patentschrift Nr. 1029380 beschriebenen Verfahren in Gegenwart von Salzen sekundärer Amine, wie z. B. Dimethylamin, Morpholin, Piperidin, Pyrrolidin, N-Methylpiperazin usw., katalytisch hydriert. 
 EMI1.5 
 

 <Desc/Clms Page number 2> 

 perazin durch die äquimolare Menge Morpholin ersetzt, so erhält man das nach Umkristallisieren aus Methanol bei 142  C schmelzende 
 EMI2.1 
 propanol- (l). Die analog hergestellte Piperidinoverbindung schmilzt bei 107   C. 



   PATENTANSPRÜCHE :
1. Verfahren zur Herstellung von l-Phenyl-   l- (o-chlorphenyl)-3-tert. aminopropanolen   der allgemeinen Formel : 
 EMI2.2 
   worin R und R'geradkettige oder verzweigte Alkylgruppen mit 1-5 Kohlenstoffatomen, die   unter sich auch ringförmig, gegebenenfalls unter Zwischenschaltung eines Heteroatoms, wie Sauerstoff, Schwefel oder Stickstoff, der seinerseits durch Alkylgruppen substituiert sein kann, verknüpft sein können, bedeuten, dadurch gekennzeichnet, dass man   o-Chlorbenzophenon   in Gegenwart stark basischer Kondensationsmittel Acetonitril addiert, das so erhaltene   ,-Phenyl-     ss- (o-chlorphenyl)-hydracrylsäurenitril   zum 1-Phenyl-1- (o-chlorphenyl)-3-amino-propanol-(1) hydriert und diese Base am Stickstoff durch Alkylreste substituiert.



   <Desc / Clms Page number 1>
 
 EMI1.1
 (o-chlorophenyl) -3-tert. aminopropanolen- (l) l-phenyl-l- 0-chlorophenyl) -3-tert. aminopropanols (l) of the formula
 EMI1.2
 wherein R and R 'mean straight-chain or branched alkyl groups with 1-5 carbon atoms, which can also be linked in a ring, optionally with the interposition of a heteratom such as oxygen, sulfur or nitrogen, which in turn may be substituted by alkyl groups, are distinguished due to its excellent cough suppressant effectiveness. It has already been suggested that 1-phenyl
 EMI1.3
 - (1) to be produced using a Grignard process.



  The difficulties inherent in such a process are well known. Such a method is of course much more complicated and more difficult to carry out in large-scale technology than the method according to the invention, in which the unpleasant-to-handle organometallic compounds are completely avoided.



   According to the invention, for the preparation of the compounds mentioned, the procedure is that o-chlorobenzophenone in the presence of strongly basic condensing agents, such as. B.



  Sodium amide, acetonitrile added, the so
 EMI1.4
 (o-chlorophenyl) -hydracryl-nopropanol- (l) hydrogenated and this base substituted on the nitrogen by alkyl radicals.



   You can also proceed in such a way that the ß-phenyl-ss- (-o-chlorophenyl) -hydracryl- säurenitril obtained from o-chlorobenzophenone and acetonitrile in the presence of strongly basic condensing agents by the method described in German Patent No. 1029380 in the presence of salts of secondary amines, such as. B. dimethylamine, morpholine, piperidine, pyrrolidine, N-methylpiperazine, etc., catalytically hydrogenated.
 EMI1.5
 

 <Desc / Clms Page number 2>

 perazine replaced by the equimolar amount of morpholine, the one which melts at 142 ° C. after recrystallization from methanol is obtained
 EMI2.1
 propanol- (l). The analogously prepared piperidino compound melts at 107 C.



   PATENT CLAIMS:
1. Process for the preparation of l-phenyl- l- (o-chlorophenyl) -3-tert. aminopropanols of the general formula:
 EMI2.2
   wherein R and R 'straight-chain or branched alkyl groups with 1-5 carbon atoms, which can also be linked in a ring, optionally with the interposition of a hetero atom such as oxygen, sulfur or nitrogen, which in turn may be substituted by alkyl groups, are characterized that one adds o-chlorobenzophenone in the presence of a strongly basic condensing agent acetonitrile, the -phenyl-ss- (o-chlorophenyl) -hydracrylic acid nitrile to 1-phenyl-1- (o-chlorophenyl) -3-aminopropanol- 1) hydrogenated and this base is substituted on the nitrogen by alkyl radicals.

 

Claims (1)

2. Verfahren nach Anspruch 1, dadurch gekennzeichnet, dass man als stark basisches Kondensationsmittel Natriumamid verwendet. EMI2.3 wart von Salzen sekundärer Amine katalytisch hydriert. 2. The method according to claim 1, characterized in that sodium amide is used as the strongly basic condensing agent. EMI2.3 was catalytically hydrogenated by salts of secondary amines.
AT247459A 1958-04-05 1959-04-01 Process for the preparation of 1-phenyl-1 (o-chlorophenyl) -3-tert.aminopropanolen- (1) AT211299B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE211299X 1958-04-05

Publications (1)

Publication Number Publication Date
AT211299B true AT211299B (en) 1960-09-26

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ID=5801903

Family Applications (1)

Application Number Title Priority Date Filing Date
AT247459A AT211299B (en) 1958-04-05 1959-04-01 Process for the preparation of 1-phenyl-1 (o-chlorophenyl) -3-tert.aminopropanolen- (1)

Country Status (1)

Country Link
AT (1) AT211299B (en)

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