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CH437300A - Process for the preparation of benzo (a) -quinolizine derivatives - Google Patents

Process for the preparation of benzo (a) -quinolizine derivatives

Info

Publication number
CH437300A
CH437300A CH26564A CH26564A CH437300A CH 437300 A CH437300 A CH 437300A CH 26564 A CH26564 A CH 26564A CH 26564 A CH26564 A CH 26564A CH 437300 A CH437300 A CH 437300A
Authority
CH
Switzerland
Prior art keywords
formula
benzo
quinolizine
ethyl
preparation
Prior art date
Application number
CH26564A
Other languages
German (de)
Inventor
Tacon Openshaw Harry
Whittaker Norman
Original Assignee
Wellcome Found
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 CH1308460A external-priority patent/CH409969A/en
Priority claimed from GB247563A external-priority patent/GB1049181A/en
Application filed by Wellcome Found filed Critical Wellcome Found
Publication of CH437300A publication Critical patent/CH437300A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D455/00Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
    • C07D455/03Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine
    • C07D455/04Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine
    • C07D455/06Heterocyclic compounds containing quinolizine ring systems, e.g. emetine alkaloids, protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing quinolizine ring systems directly condensed with at least one six-membered carbocyclic ring, e.g. protoberberine; Alkylenedioxy derivatives of dibenzo [a, g] quinolizines, e.g. berberine containing a quinolizine ring system condensed with only one six-membered carbocyclic ring, e.g. julolidine containing benzo [a] quinolizine ring systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Description

  

  Verfahren zur Herstellung von Benzo(a)-chinolizinderivaten    Das Hauptpatent     betrifft        ein    Verfahren zur Herstel  lung von Verbindungen der Formel  
EMI0001.0002     
    oder von deren Spiegelbild, in welcher Formel R1 eine  Alkylgruppe mit 1 bis 4 Kohlenstoffatomen, R2 eine  niedere Alkoxygruppe und RS und R4 eine Methyl- oder  Äthylgruppe bedeuten, oder R3 und R4 zusammen eine  Alkylengruppe bilden, bei welchem Verfahren man ein  entsprechendes Keton der Formel  
EMI0001.0003     
    mit einem Alkoxycarbonylmethylen-triarylphosphoran  kondensiert.  



  Die Alkoxygruppe R2 kann anschliessend verseift  werden.  



       Dieses    Verfahren kann bei der Herstellung von  Emetin und dessen Analogen Verwendung finden.  



  Die vorliegende     Erfindung        betrifft    nun eine Verbesse  rung dieses Verfahrens. Das verbesserte Verfahren ist  dadurch gekennzeichnet, dass man bei Beendigung der    Kondensation überschüssiges Phosphoran durch Zufü  gung     eines    Aldehyds entfernt.  



  Als Aldehyd kann Benzaldehyd verwendet werden.    <I>Beispiel 1</I>  40 g racemisches 3-Äthyl-1,2,3,4,6,7-hexahydro-9,  10-dimethoxy-2-oxo-11b H-benzo(a)chinolizin (II) und  69,5 g (Methoxycarbonylmethylen)-triphenylphosphoran  werden innig     gemischt    und unter trockenem Stickstoff in  einem Bad bei<B>161'</B> C erhitzt. Die erhaltene Flüssigkeit  wird 3 Stunden bei 152  C gehalten. Das     abgekühlte          Reaktionsprodukt    behandelt man     mit    250     ml    heissem  Benzol und 29,4 g frischdestilliertem Benzaldehyd, lässt  das Gemisch 1 Stunde rückfliessen und extrahiert die  gekühlte Benzollösung mit 400 ml Wasser und ungefähr  150 ml n-Salzsäure. Man erhält so einen sauren Extrakt.

         Der    wässrige Extrakt wird mit Benzol gewaschen und  mit wässrigem Kaliumhydroxyd basisch gemacht, die aus,  gefallene Base     zweimal    mit je 200     ml    Chloroform extra  hiert, die Chloroformlösung mit Wasser gewaschen, über  wasserfreiem     Natriumsulfat    getrocknet und eingedampft.

    Den Rückstand befreit man von Chloroformspuren durch  Destillation mit Petroläther (Siedebereich 60-80  C) und  filtriert eine Lösung des erhaltenen Feststoffs in ungefähr  150 ml heissem Petroläther (Siedebereich 60-80  C)  vom Harz ab und dampft     ein.    Die Kristallisation des zu  rückbleibenden Feststoffs aus 80 ml Methanol unter  Kühlen auf 0  C liefert 25,6 g racemisches 3-Äthyl       1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-methoxycarb-          onylmethylen-11b    H-benzo(a)chinolizin(I) vom Schmelz  punkt<B>110-111'</B> C. Die     Umkristallisation    aus Methanol  erhöht den Schmelzpunkt auf     112-113'    C.  



  <I>Beispiel 2</I>  Man stellt     (+)-3-Äthyl-1,2,3,4,6,7-hexahydro-9,10-          dimethoxy-2-(äthoxycarbonylmethylen)-11b    H-benzo(a)  chinolizin (I) durch Umsetzung von 10 g     (-)-3-Äthyl-          1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-oxo-11b-benzo         (a)chinolizin (II) mit 27,1g     Äthoxy-carbonylmethylen-          triphenylphosphoran    in Abwesenheit eines Lösungsmit  tels bei 152  C in 21/2     Stunden    her. Das überschüssige  Phosphoran wird in der in Beispiel 1 beschriebenen  Weise mit Benzaldehyd zersetzt.

   Nach Umkristallisation  des Produkts aus Petroläther (Siedebereich 60-80  C)  und aus Äthanol erhält man 8,35 g (+)-3 Äthyl-1,2,3,4,       6,7-hexahydro-9,10-dimethoxy-2-(äthoxycarbonylmeth-          ylen)-11b    H-benzo(a)chinolizin (I) vom Schmelzpunkt  117-119  C, [a&alpha;D21 = +44  (c = 1 in Äthanol).



  Process for the preparation of benzo (a) quinolizine derivatives The main patent relates to a process for the preparation of compounds of the formula
EMI0001.0002
    or their mirror image, in which formula R1 is an alkyl group with 1 to 4 carbon atoms, R2 is a lower alkoxy group and RS and R4 are methyl or ethyl, or R3 and R4 together form an alkylene group, in which process a corresponding ketone of the formula
EMI0001.0003
    condensed with an alkoxycarbonylmethylene triarylphosphorane.



  The alkoxy group R2 can then be saponified.



       This process can be used in the manufacture of emetine and its analogs.



  The present invention now relates to an improvement of this method. The improved process is characterized in that, when the condensation has ended, excess phosphorane is removed by adding an aldehyde.



  Benzaldehyde can be used as the aldehyde. <I> Example 1 </I> 40 g of racemic 3-ethyl-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-oxo-11b H-benzo (a) quinolizine (II ) and 69.5 g (methoxycarbonylmethylene) triphenylphosphorane are intimately mixed and heated under dry nitrogen in a bath at <B> 161 '</B> C. The liquid obtained is kept at 152 ° C. for 3 hours. The cooled reaction product is treated with 250 ml of hot benzene and 29.4 g of freshly distilled benzaldehyde, the mixture is allowed to reflux for 1 hour and the cooled benzene solution is extracted with 400 ml of water and approximately 150 ml of n-hydrochloric acid. An acidic extract is obtained in this way.

         The aqueous extract is washed with benzene and made basic with aqueous potassium hydroxide, the precipitated base is extracted twice with 200 ml of chloroform each time, the chloroform solution is washed with water, dried over anhydrous sodium sulfate and evaporated.

    The residue is freed from traces of chloroform by distillation with petroleum ether (boiling range 60-80 C) and a solution of the solid obtained in about 150 ml of hot petroleum ether (boiling range 60-80 C) is filtered off from the resin and evaporated. Crystallization of the remaining solid from 80 ml of methanol with cooling to 0 C gives 25.6 g of racemic 3-ethyl 1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-methoxycarbonylmethylene 11b H-benzo (a) quinolizine (I) with a melting point of <B> 110-111 '</B> C. Recrystallization from methanol increases the melting point to 112-113' C.



  <I> Example 2 </I> (+) - 3-Ethyl-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2- (ethoxycarbonylmethylene) -11b H-benzo ( a) quinolizine (I) by reacting 10 g of (-) - 3-ethyl-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-oxo-11b-benzo (a) quinolizine (II) with 27.1g ethoxycarbonylmethylene triphenylphosphorane in the absence of a solvent at 152 ° C. in 21/2 hours. The excess phosphorane is decomposed in the manner described in Example 1 with benzaldehyde.

   After recrystallization of the product from petroleum ether (boiling range 60-80 ° C.) and from ethanol, 8.35 g of (+) - 3-ethyl-1,2,3,4, 6,7-hexahydro-9,10-dimethoxy-2 are obtained - (Ethoxycarbonylmethylene) -11b H-benzo (a) quinolizine (I), melting point 117-119 C, [aαD21 = +44 (c = 1 in ethanol).

 

Claims (1)

PATENTANSPRUCH Verfahren zur Herstellung von 11bH-Benzo(a) chinolizinderivaten der Formel EMI0002.0005 oder von deren Spiegelbild, in welcher Formel R1 eine Alkylgruppe mit 1 bis 4 Kohlenstoffatomen, R2 eine nie dere Alkoxygruppe und R3 und R4 eine Methyl- oder Äthylgruppe bedeuten oder R3 und R4 zusammen eine Alkylengruppe darstellen, wobei man ein entsprechendes Keton der Formel EMI0002.0006 mit einem Alkoxycarbonylmethylen-triarylphosphoran kondensiert, worin die Alkoxygruppe dem Rest R2 ent spricht, dadurch gekennzeichnet, dass man bei Beendi gung der Reaktion überschüssiges Phosphoran durch Zufügung eines Aldehyds entfernt. UNTERANSPRÜCHE 1. PATENT CLAIM Process for the preparation of 11bH-Benzo (a) quinolizine derivatives of the formula EMI0002.0005 or their mirror image, in which formula R1 is an alkyl group with 1 to 4 carbon atoms, R2 is a lower alkoxy group and R3 and R4 are methyl or ethyl or R3 and R4 together represent an alkylene group, where a corresponding ketone of the formula EMI0002.0006 condensed with an alkoxycarbonylmethylene-triarylphosphorane, in which the alkoxy group corresponds to the radical R2, characterized in that excess phosphorane is removed by adding an aldehyde at the end of the reaction. SUBCLAIMS 1. Verfahren nach Patentanspruch, dadurch gekenn zeichnet, dass man die Alkoxygruppe R2 in eine Hydr oxylgruppe überführt. 2. Verfahren nach Patentanspruch, dadurch gekenn zeichnet, dass man ein 3 Äthyl-1,2,3,4,6,7-hexahydro- 9,10-dimethoxy-2-oxo-11bH-benzo(a)chinolizin der For mel II in. ein 2 Alkoxycarbonylmethylen-3-äthyl-1,2,3,4, 6,7-hexahydro-9,10-dimethoxy-11b H-benzo(a)chinolizin überführt. 3. Verfahren nach Patentanspruch, dadurch gekenn zeichnet, dass man Äthoxycarbonylmethylen-triphenyl phosphoran verwendet. 4. Process according to patent claim, characterized in that the alkoxy group R2 is converted into a hydroxyl group. 2. The method according to claim, characterized in that a 3-ethyl-1,2,3,4,6,7-hexahydro-9,10-dimethoxy-2-oxo-11bH-benzo (a) quinolizine of the formula II converted into a 2-alkoxycarbonylmethylene-3-ethyl-1,2,3,4, 6,7-hexahydro-9,10-dimethoxy-11b H-benzo (a) quinolizine. 3. The method according to claim, characterized in that Äthoxycarbonylmethylen-triphenyl phosphoran is used. 4th Verfahren nach Patentanspruch, dadurch gekenn zeichnet, dass man durch Verwendung des (-)-Enantio- meren des Ketons der Formel II das (+)-Enantiomere des ungesättigten Esters der Formel I herstellt. 5. Verfahren nach Patentanspruch, dadurch gekenn zeichnet, dass man Benzaldehyd verwendet. Process according to patent claim, characterized in that the (+) - enantiomer of the unsaturated ester of the formula I is prepared by using the (-) - enantiomer of the ketone of the formula II. 5. The method according to claim, characterized in that benzaldehyde is used.
CH26564A 1960-11-22 1964-01-10 Process for the preparation of benzo (a) -quinolizine derivatives CH437300A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
CH1308460A CH409969A (en) 1959-11-24 1960-11-22 Process for the preparation of benzo (a) quinolizines
GB247563A GB1049181A (en) 1963-01-21 1963-01-21 Method for making benzo(a)quinolizine derivatives

Publications (1)

Publication Number Publication Date
CH437300A true CH437300A (en) 1967-06-15

Family

ID=25711513

Family Applications (1)

Application Number Title Priority Date Filing Date
CH26564A CH437300A (en) 1960-11-22 1964-01-10 Process for the preparation of benzo (a) -quinolizine derivatives

Country Status (1)

Country Link
CH (1) CH437300A (en)

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