DE459361C - Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid - Google Patents

Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid

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Publication number
DE459361C
DE459361C DEC37803D DEC0037803D DE459361C DE 459361 C DE459361 C DE 459361C DE C37803 D DEC37803 D DE C37803D DE C0037803 D DEC0037803 D DE C0037803D DE 459361 C DE459361 C DE 459361C
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DE
Germany
Prior art keywords
propionic acid
nuclear
preparation
oxine
sol
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
DEC37803D
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German (de)
Inventor
Dr Kurt Schmidt
Dr Walter Schoeller
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.)
Schering Kahlbaum AG
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Schering Kahlbaum 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.)
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Publication date
Application filed by Schering Kahlbaum AG filed Critical Schering Kahlbaum AG
Priority to DEC37803D priority Critical patent/DE459361C/en
Application granted granted Critical
Publication of DE459361C publication Critical patent/DE459361C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/30Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
    • C07D209/32Oxygen atoms
    • C07D209/34Oxygen atoms in position 2

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Indole Compounds (AREA)

Description

Verfahren zur Darstellung von Kernjodsubstitutionsprodukten der Oxindol-3-propionsäure. In analoger Weise wie bei der Darstellung kernhalogenierter Oxindol-3-essigsäuren nach dem Verfahren des Hauptpatents, Zusatz zum Patent 431 5 i o, gelangt man zu den entsprechenden jodsubstituierten Oxindol-3-propionsäuren, wenn man an Stelle der halogenierten Isatine hier die jodierten Oxindolaldehvde mit Malonsäure, zweckmäßig in molekularen Mengen, zusammenschmilzt und die hierdurch entstehenden jodoxindolacrylsäuren mit Reduktionsmitteln behandelt. Beispiel i.Process for the preparation of nuclear iodine substitution products of oxindole-3-propionic acid. In a manner analogous to the representation of nucleus-halogenated oxindole-3-acetic acids according to the procedure of the main patent, addition to patent 431 5 i o, one arrives at the corresponding iodine-substituted oxindole-3-propionic acids, if one in place of the halogenated isatins, here the iodinated oxindolaldehyde with malonic acid, is expedient in molecular quantities, melts together and the resulting jodoxindole acrylic acids treated with reducing agents. Example i.

Zur Darstellung der Mon0jOdOxindol-3-propionsäure geht man von jodoxindolaldehyd aus, den man in der Weise erhält, daß man Jodisatin mit Oxythionaphthencarbonsäure zum jodthioindigoscharlach kondensiert und letzteren durch alkoholische Natronlauge zum Aldehyd aufspaltet. Der jodoxindolaldehyd bildet, aus Eisessig umkristallisiert, gelbbraune Nädelchen, die sich oberhalb :25o° C unter Bräunung allmählich zersetzen. Der Aldehyd ist ziemlich leicht löslich in Alkohol, Eisessig, schwer in Aceton und sehr schwer in Äther und Wasser; in Alkalien und \Tatriumcarbonat ist er ziemlich leicht löslich unter Bildung der entsprechenden Natriumverbindüng.For the preparation of Mon0jOdOxindol-3-propionic acid one starts from iodoxindolaldehyde, which is obtained in such a way that iodisatin is condensed with oxythionaphthenecarboxylic acid to iodothioindigoscharlach and the latter is split up by alcoholic sodium hydroxide to form the aldehyde. The jodoxindolaldehyde, recrystallized from glacial acetic acid, forms yellow-brown needles, which gradually decompose above: 25o ° C while browning. The aldehyde is fairly soluble in alcohol and glacial acetic acid, difficult in acetone, and very difficult in ether and water; it is fairly readily soluble in alkalis and sodium carbonate, with the formation of the corresponding sodium compound.

i Mol. Jodoxindolaldehyd wird mit i Mol. Malonsäure im Metallbad bei i 5o bis 155 ° C so lange verschmolzen, bis keine Kohlensäure mehr entweicht; der Schmelzkuchen wird in verdünnter Natronlauge gelöst, das Filtrat mit verdünnter Salzsäure angesäuert und die ausgeschiedene jodoxindol-3-acrylsäure aus Alkohol und Eisessig umkristallisiert. Die reine Verbindung zeigt einen Zersetzungspunkt von -,io° C, ist leicht löslich in heißem Alkohol und Eisessig, schwerer in Äther und sehr schwer in Benzol, fast unlöslich in Wasser. Die Alkalisalze sind in Wasser leicht löslich. Aus Alkohol umkristallisiert, bildet die jodoxindol-3-acrylsäure kleine gelbliche Nadelbüschel.i. Mol Jodoxindolaldehyd is merged with i mole of malonic acid in the metal bath at 5o i to 1 55 ° C until no more carbon dioxide escapes. the melt cake is dissolved in dilute sodium hydroxide solution, the filtrate is acidified with dilute hydrochloric acid and the precipitated jodoxindole-3-acrylic acid is recrystallized from alcohol and glacial acetic acid. The pure compound has a decomposition point of -10 ° C, is easily soluble in hot alcohol and glacial acetic acid, more difficult in ether and very difficult in benzene, almost insoluble in water. The alkali salts are easily soluble in water. Recrystallized from alcohol, the jodoxindole-3-acrylic acid forms small, yellowish tufts of needles.

Zur Darstellung der jodoxindo1-3-propionsäure behandelt man eine Lösung des Natriumsalzes der jodoxindol-3-acrylsäure mit einem - Reduktionsmittel, zweckmäßig Aluminiumamalgam, und arbeitet das Reaktionsprodukt in bekannter Weise auf. Die so erhaltene jodoxindol-3-propionsäure entspricht in ihren Eigenschaften' der in der Patentschrift 433o99 der Klasse 12p beschriebenen Monoj odoxindol-3-propionsäure. Beispiel e. Dijodoxindolaldehyd (vgl. Ber.57 [192q.] S. 2116) wird mit Malonsäure unter den vorstehend angegebenen Bedingungen verschmolzen und aufgearbeitet. Die gebildete Dijodoxindol-3-acrylsäure ist leicht löslich in Alkalien, Alkohol, Essigester und Eisessig, schwerer in Äther und Aceton, fast unlöslich iii Wasser. Aus Alkohol umkristallisiert, zeigt sie einen Zersetzungspunkt von 2o4° C. Durch Behandlung mit Reduktionsmitteln gelangt man zur Dijodoxindol-3-propionsäure, die nach dem Umkristallisienen aus Eislessijg ein hellbraunes mikrokristallinisches Pulver vom Zersetzungspunkt 216° C bildet. Sie ist leicht löslich in Alkohol und Eisessig, schwerer in Aceton und Äther, fast unlöslich in Wasser, auch in heißem.A solution is treated to produce the jodoxindo1-3-propionic acid of the sodium salt of jodoxindole-3-acrylic acid with one - reducing agent, expediently aluminum amalgam, and the reaction product works in a known manner on. The properties of the jodoxindole-3-propionic acid obtained in this way correspond to ' the monoj odoxindole-3-propionic acid described in the patent specification 433o99 of class 12p. Example e. Dijodoxindolaldehyde (cf. Ber.57 [192q.] P. 2116) is mixed with malonic acid fused and worked up under the conditions given above. the Dijodoxindole-3-acrylic acid formed is easily soluble in alkalis, alcohol and ethyl acetate and glacial acetic acid, heavier in ether and acetone, almost insoluble iii water. From alcohol recrystallized, it shows a decomposition point of 204 ° C. By treatment with reducing agents one arrives at dijodoxindole-3-propionic acid, which after the Recrystallized from Eislessijg a light brown microcrystalline powder from Decomposition point forms 216 ° C. It is easily soluble in alcohol and glacial acetic acid, heavier in acetone and ether, almost insoluble in water, even in hot.

Claims (1)

PATENTANSPRUCH: Weitere Ausbildung des durch Patent 43 6 5 I $ (Zusatz zum Patent 431 5 10) .geschützten Verfahrens, dadurch gekennzeichnet, daß man zwecks Darstellung von Kernjodsubstitutionsprodukten der Oxindol-3-propionsäure hier die jodsubstituierten Oxindolaldehyde mit Malonsäure zusammenschmilzt und die so erhaltenen Acrylsäuren mit Reduktionsmitteln behandelt.PATENT CLAIM: Further development of the process protected by patent 43 6 5 I $ (addition to patent 431 5 1 0) , characterized in that the iodine-substituted oxindole aldehydes are melted together with malonic acid for the purpose of preparing nuclear iodine substitution products of oxindole-3-propionic acid and so obtained acrylic acids treated with reducing agents.
DEC37803D 1926-02-07 1926-02-07 Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid Expired DE459361C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEC37803D DE459361C (en) 1926-02-07 1926-02-07 Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEC37803D DE459361C (en) 1926-02-07 1926-02-07 Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid

Publications (1)

Publication Number Publication Date
DE459361C true DE459361C (en) 1928-05-02

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Family Applications (1)

Application Number Title Priority Date Filing Date
DEC37803D Expired DE459361C (en) 1926-02-07 1926-02-07 Process for the preparation of nuclear iodine substitution products of oxine sol-3-propionic acid

Country Status (1)

Country Link
DE (1) DE459361C (en)

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