DE617544C - Process for the preparation of nitrogen-containing products of the oxazole and imidazole series - Google Patents

Process for the preparation of nitrogen-containing products of the oxazole and imidazole series

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Publication number
DE617544C
DE617544C DEI48084D DEI0048084D DE617544C DE 617544 C DE617544 C DE 617544C DE I48084 D DEI48084 D DE I48084D DE I0048084 D DEI0048084 D DE I0048084D DE 617544 C DE617544 C DE 617544C
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DE
Germany
Prior art keywords
nitrogen
oxazole
preparation
ammonia
containing products
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
DEI48084D
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German (de)
Inventor
Dr Ernst Herdieckerhoff
Dr Werner Zerweck
Dr Heinrich Salkowski
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.)
IG Farbenindustrie AG
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IG Farbenindustrie 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 IG Farbenindustrie AG filed Critical IG Farbenindustrie AG
Priority to DEI48084D priority Critical patent/DE617544C/en
Application granted granted Critical
Publication of DE617544C publication Critical patent/DE617544C/en
Expired legal-status Critical Current

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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Description

Verfahren zur Darstellung von stickstoffhaltigen Produkten der Oxazol- und Imidazolreihe Durch das Hauptpatent 615 526 ist ein Verfahren zur Darstellung von 2-Aminoarylentl-iazolen geschützt, das darin besteht, daß man die sauerstofF- und schwefelhaltigen wasserlöslichen Arylenthiazolverb@indungen, denen die Konstitution von Arylentl@iazol-2-sulfonsäuren zukommt, mit Ammoniak oder Ammoniak abspaltenden Mitteln auf höhere Temperaturerhitzt. Das erste Zusatzpatent 617 188 betriffst eine Erweiterung des Verfahrens des Hauptpatents, dadurch gekennzeichnet, daß man die gleichen Ausgangsstoffe mit Aminen der aliphatischeav, aromatischen, hydroaromatischen oder heterocyclischen Reihe, die mindestens ein am Stickstoff gebundenes Wasserstoffatom tragen" auf höhere Temperatur erhitzt.Process for the preparation of nitrogen-containing products of the oxazole and imidazole series By the main patent 615 526 a process for the preparation of 2-aminoarylentl-iazoles is protected, which consists in that the oxygen- and sulfur-containing water-soluble arylene thiazole compounds, which have the constitution of arylene @iazole-2-sulfonic acids, heated to a higher temperature with ammonia or ammonia-releasing agents. The first additional patent 617 188 concerns an extension of the process of the main patent, characterized in that the same starting materials are heated to a higher temperature with amines of the aliphatic, aromatic, hydroaromatic or heterocyclic series which carry at least one hydrogen atom bonded to nitrogen.

In weiterer Ausbildung des Verfahrens wurde nun gefunden, daß man auch die sauerstoff- und schwefelhaltigen wasserlöslichen Oxydationsprodukte vom .Typus von Sulfonsäuren der Formel worin Y =Sauerstoff oder NR (R = H, Alkyl, Aralkyl oder Aryl) ist, wie sie z. B. durch Oxydation der entsprechenden Mercaptoverb,indung .erhalten werden, mit Ammoniak oder Ammoniak abspaltenden Mitteln sowie auch mit Aminen der oben angegebenen Art umsetzen kann.In a further development of the process, it has now been found that the oxygen- and sulfur-containing water-soluble oxidation products of the .Type of sulfonic acids of the formula wherein Y = oxygen or NR (R = H, alkyl, aralkyl or aryl), as described e.g. B. by oxidation of the corresponding mercapto verb, indung .erhalten, can react with ammonia or ammonia-releasing agents and also with amines of the type indicated above.

Man erhält auf diese Weise in glatter Umsetzung die 2-Aminokörp,er der Oxazol- und Imidazolreihe sowie deren N-subsltituierte Abkömmlinge.In this way, the 2-amino bodies, er, are obtained in a smooth reaction the oxazole and imidazole series and their N-substituted derivatives.

Der Erfolg des vorliegenden Verfahrens ist namentlich aus dem Grunde überraschend, weil die Aufspaltbarkeit der Oxazol- und Imydazolverbindungen durch Alkalien bekannt ist. (Vgl. Meyer-Jacobs,on, Lehrbuch der org. Chemie, z. Band, 3. Teil [192o], S.527.) Das Verfahren ist besonders geeignet zur Herstellung unsymmetrischer Verbindungen, bei denen der am Stickstoff haftende Rest nacht mit dem Arylenrest identisch ist und die bisher schwer zugänglich waren.The success of the present proceedings is due in particular to the reason Surprising because the oxazole and imydazole compounds can be split Alkalis is known. (Cf. Meyer-Jacobs, on, Textbook of Org.Chemistry, z. Volume, 3rd part [192o], p.527.) The process is particularly suitable for the production of asymmetrical Compounds in which the remainder adhering to the nitrogen coincides with the arylene remainder is identical and which were previously difficult to access.

Beispi e1 i 8 kg 2-((3)-napthoxazolsulfonsaures Natrium werden mit etwa 4okg 2o%iggem Ammoniak 2 Stunden auf etwa i2o° unter Druck erhitzt. Es scheidet sich beim Erkalten in sehr guter Ausbeute das 2-Amin:)-(3-naphthoxazol der Formel in Form von weißen Kristallen aus. Es ist löslich in den üblichen organischen Lösungsmitteln und schmilzt in, reinem Zustande bei 19g bis 2oo°: Beispiel 2 15 kg 2-Benzimidazolsulfonsäure werden in etwa 5o kg Ammoniak 2 Stunden auf 12o bis 13o° unter Druck erhitzt. Es scheidet sich das 2-Aminob.enzimidazol in weißen schönen Kristallen vom Schmelzpunkt 225° in guter Ausbeute aus. Beispiel 3 3 kg 2-b,enzoxazolsulfonsaures Natrium wer- den mit 1, 5 kg Anilin: in etwa 15 kg Wasser bei; Zimmertemperatur gerührt. Es findet be- reits bei 15 bis 2o" unter Teanperatur.5tei;ge- rung die Umsetzung zum 2-Anilinob,enzooxazol statt. Man rührt noch einige Stunden bei 40 bis 5o° nach. Der gebildete weiße Niederschlag wird abgesaugt, alkalis ich gut gewaschen und gegebenenfalls; durch Dampfdestillation oder Umkristallisieren von anhaftendem Anilin befreit. Man erhält auf diese Weise in guter Ausbeute das 2-Anilinibenzoxazol, das nach dem UmkristalhsIeren aus z. B. Methanol in weißen Kristallen vom Schmelzpunkt 173 bis 17e erhalten wird:For example, 8 kg of 2 - ((3) -napthoxazolesulfonic acid sodium are heated under pressure with about 40 g of 20% ammonia for 2 hours to about 120 °. On cooling, the 2-amine separates in very good yield:) - (3 -naphthoxazole of the formula in the form of white crystals. It is soluble in the usual organic solvents and, in its pure state, melts at 19 g to 200 °: Example 2 15 kg of 2-benzimidazole sulfonic acid are heated in about 50 kg of ammonia for 2 hours to 120 to 130 ° under pressure. The 2-aminobenzimidazole separates out in good yield in white, beautiful crystals with a melting point of 225 °. Example 3 3 kg of 2-b, enzoxazolesulfonic acid sodium are the one with 1.5 kg of aniline: around 15 kg of water at; Stirred at room temperature. It takes place already at 15 to 2o "below the temperature. tion the conversion to 2-anilinob, enzooxazole instead of. The mixture is stirred for a few more hours 40 to 5o ° after. The white precipitate formed is filtered off with suction, washed thoroughly with alkalis and, if necessary; freed from adhering aniline by steam distillation or recrystallization. In this way, 2-anilinibenzoxazole is obtained in good yield. B. Methanol is obtained in white crystals from melting point 173 to 17e:

Claims (1)

PATRNTANSPRUCH:
Abänderung der Verfahren der Patente 615 526 und 617 188, dadurch gekennzeichnet, daß man hier Verbindungen der Zusammensetzung worin X - Sauerstoff oder N R (R=H, Alkyl, Aralkyl oder Aryl) ist, mit Ammoniak oder Ammoniak abspaltenden Mitteln oder mit Aminen der aliphatischen, aromatischen, hydroaromatischen oder heterocyclischen Reihe, die mindestens ,ein am Stickstoff gebundenes Wasserstoffatom tragen, umsetzt.
PATRN CLAIM:
Modification of the method of patents 615 526 and 617 188, characterized in that compounds of the composition where X - is oxygen or NR (R = H, alkyl, aralkyl or aryl), with ammonia or ammonia-releasing agents or with amines of the aliphatic, aromatic, hydroaromatic or heterocyclic series which carry at least one hydrogen atom bonded to nitrogen.
DEI48084D 1933-10-08 1933-10-08 Process for the preparation of nitrogen-containing products of the oxazole and imidazole series Expired DE617544C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEI48084D DE617544C (en) 1933-10-08 1933-10-08 Process for the preparation of nitrogen-containing products of the oxazole and imidazole series

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEI48084D DE617544C (en) 1933-10-08 1933-10-08 Process for the preparation of nitrogen-containing products of the oxazole and imidazole series

Publications (1)

Publication Number Publication Date
DE617544C true DE617544C (en) 1935-08-21

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Application Number Title Priority Date Filing Date
DEI48084D Expired DE617544C (en) 1933-10-08 1933-10-08 Process for the preparation of nitrogen-containing products of the oxazole and imidazole series

Country Status (1)

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DE (1) DE617544C (en)

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