DE551870C - Process for the production of pellets of 1-benzyl-3-methylisoquinoline - Google Patents

Process for the production of pellets of 1-benzyl-3-methylisoquinoline

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Publication number
DE551870C
DE551870C DE1930551870D DE551870DD DE551870C DE 551870 C DE551870 C DE 551870C DE 1930551870 D DE1930551870 D DE 1930551870D DE 551870D D DE551870D D DE 551870DD DE 551870 C DE551870 C DE 551870C
Authority
DE
Germany
Prior art keywords
parts
methylisoquinoline
benzyl
pellets
production
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
DE1930551870D
Other languages
German (de)
Inventor
Dr Otto Wolfes
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Merck KGaA
Original Assignee
E Merck 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 E Merck AG filed Critical E Merck AG
Application granted granted Critical
Publication of DE551870C publication Critical patent/DE551870C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D217/00Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/12Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with radicals, substituted by hetero atoms, attached to carbon atoms of the nitrogen-containing ring
    • C07D217/18Aralkyl radicals
    • C07D217/20Aralkyl radicals with oxygen atoms directly attached to the aromatic ring of said aralkyl radical, e.g. papaverine

Description

Verfahren zur Herstellung von Abkömmlingen des 1-Benzyl-3-methylisochinolins In dem Hauptpatent 550 122 ist ein Verfahren zur Herstellung von Verbindungen mit Papaverinwirkung beschrieben, welches in seiner ersten Stufe in der Kondensation von Phenylessigsäure oder deren Ätherderivaten mit 1-(3, 4-Methylendioxyphenyl-) 2-aminopropan oder mit 1-(3, 4-Dimethoxyphenyl-) 2-aminopropan besteht; die so erhaltenen Säureamide werden darauf mit sauren Kondensationsmitteln zum Ring geschlossen und dehydriert. Man erhält hierdurch Abkömmlinge des i-Benzyl-3-methylisochinolins, welche die obenerwähnten therapeutisch wertvollen Eigenschaften besitzen. Es wurde nun gefunden, daß man an Stelle von Phenylessigsäure und deren Ätherderivaten Phenylacetaldehyd oder dessen Ätherderivate verwenden kann. Diese Reaktion ist deshalb bemerkenswert, weil die genannten Aldehyde neuerdings leicht zugänglich geworden sind. Beispiel i 18 Teile Safrylamin und 12 Teile Phenylacetaldehyd werden in je 2o Teilen Äther gelöst und die Lösungen unter Kühlung gemischt. Diese Lösung wird unter Rühren und Kühlung in ioo Teile Salzsäure (1,1g) eingetragen und einige Stunden aufbewahrt. Dann wird die Mischung mit 5o Teilen Wasser verdünnt und gekocht, bis der Äther völlig abdestilliert ist. Nach Zugabe von Zoo Teilen Wasser wird die Lösung von harzigen Nebenprodukten durch Filtration befreit und im Vakuum eingedampft. Der Rückstand wird in ioo Teilen heil?en Wassers gelöst, mit Kohle filtriert und mit Natronlauge stark alkalisch gemacht, wobei sich ein dickes basisches Öl abscheidet. Dieses wird von der Lauge getrennt, mehrfach mit Wasser gründlich gewaschen und dann mit Salzsäure (5°joig) verrührt, bis zur sauren Reaktion auf Kongopapier, heiß mit Kohle filtriert und mit i Teil Natriumchlorid verrührt. Das Hydrochlorid der neuen Base scheidet sich in kugeligen Kristallmassen ab. Schmelzpunkt 21q.'. Die freie Base kristallisiert langsam aus Äther. Schmelzpunkt etwa 78'.Process for the preparation of derivatives of 1-benzyl-3-methylisoquinoline In the main patent 550 122 a process for the preparation of compounds with papaverine action is described, which in its first stage in the condensation of phenylacetic acid or its ether derivatives with 1- (3, 4- Methylenedioxyphenyl-) 2-aminopropane or with 1- (3, 4-dimethoxyphenyl-) 2-aminopropane; the amides obtained in this way are then closed to form a ring with acidic condensing agents and dehydrated. This gives derivatives of i-benzyl-3-methylisoquinoline which have the therapeutically valuable properties mentioned above. It has now been found that phenylacetaldehyde or its ether derivatives can be used in place of phenylacetic acid and its ether derivatives. This reaction is remarkable because the aldehydes mentioned have recently become easily accessible. Example i 18 parts of safrylamine and 12 parts of phenylacetaldehyde are dissolved in 20 parts of ether each and the solutions are mixed with cooling. This solution is introduced into 100 parts of hydrochloric acid (1.1 g) with stirring and cooling and stored for a few hours. Then the mixture is diluted with 50 parts of water and boiled until the ether has completely distilled off. After adding zoo parts of water, the solution is freed from resinous by-products by filtration and evaporated in vacuo. The residue is dissolved in 100 parts of healing water, filtered with charcoal and made strongly alkaline with sodium hydroxide solution, a thick basic oil separating out. This is separated from the lye, washed thoroughly several times with water and then stirred with hydrochloric acid (5 ° joig), filtered hot with carbon until an acidic reaction on Congo paper and stirred with 1 part sodium chloride. The hydrochloride of the new base separates out in spherical crystal masses. Melting point 21q. '. The free base slowly crystallizes from ether. Melting point about 78 '.

Zur Dehydrierung werden 1o Teile Base mit 1 Teil Palladiummoor eine halbe Stunde auf igo' erhitzt, die Schmelze in verdünnter heißer Salzsäure aufgenommen und diese mit Kohle gereinigte Lösung auf Base verarbeitet. Dieselbe schmilzt bei iog'.For dehydration, 1o parts of base and 1 part of palladium moor are used Heated to igo 'for half an hour, the melt taken up in dilute hot hydrochloric acid and base this coal-cleaned solution on. The same melts at iog '.

Beispiel 2 Nach dem in Beispiel i geschilderten Verfahren werden 5 Teile rohes Homopiperonal (aus Safrol durch Ozonisierung dargestellt) mit 6 Teilen Safrylamin gekuppelt und auf das entsprechende Tetrahydroisochinolinderivat verarbeitet. Farblose, länglich sechseckige Prismen ausÄther, F. 1x8°. Durch Dehydrierung mit Palladium wird das Isochinolinderivat obiger Zusammensetzung erhalten. Die Base schmilzt bei 1q.1° (aus Methanol).Example 2 According to the process described in Example i, 5 parts of crude homopiperonal (prepared from safrole by ozonization) are coupled with 6 parts of safrylamine and processed to the corresponding tetrahydroisoquinoline derivative. Colorless, elongated hexagonal prisms made of ether, F. 1x8 °. The isoquinoline derivative of the above composition is obtained by dehydration with palladium. The base melts at 1q.1 ° (from methanol).

Claims (1)

PATRNTANSPRUCH: Abänderung des Verfahrens nach Patent 550 122, dadurch gekennzeichnet, daß an Stelle von Phenylessigsäure oder derenÄtherderivaten hier Phenylacetaldehydoder dessen Ätherderivate verwendet werden.PATENT CLAIM: Modification of the process according to Patent 550 122, characterized in that phenylacetaldehyde or its ether derivatives are used here instead of phenylacetic acid or its ether derivatives.
DE1930551870D 1930-11-09 1930-11-09 Process for the production of pellets of 1-benzyl-3-methylisoquinoline Expired DE551870C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE551870T 1930-11-09

Publications (1)

Publication Number Publication Date
DE551870C true DE551870C (en) 1932-06-06

Family

ID=6563196

Family Applications (1)

Application Number Title Priority Date Filing Date
DE1930551870D Expired DE551870C (en) 1930-11-09 1930-11-09 Process for the production of pellets of 1-benzyl-3-methylisoquinoline

Country Status (1)

Country Link
DE (1) DE551870C (en)

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