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DE479349C - Process for the preparation of derivatives of 1, 3, 5-triazine - Google Patents

Process for the preparation of derivatives of 1, 3, 5-triazine

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Publication number
DE479349C
DE479349C DEM97282D DEM0097282D DE479349C DE 479349 C DE479349 C DE 479349C DE M97282 D DEM97282 D DE M97282D DE M0097282 D DEM0097282 D DE M0097282D DE 479349 C DE479349 C DE 479349C
Authority
DE
Germany
Prior art keywords
triazine
derivatives
preparation
formaldehyde
methylene
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
DEM97282D
Other languages
German (de)
Inventor
Dr Otto Diels
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
Priority to DEM97282D priority Critical patent/DE479349C/en
Application granted granted Critical
Publication of DE479349C publication Critical patent/DE479349C/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Description

Verfahren zur Darstellung von Derivaten des 1, 3, 5-Triazins Wie bekannt, führt die Einwirkung von Formaldehyd auf Harnstoff durch Reaktion beider Komponenten im Verhältnis i : i zum N, N-Methylenhamstoff Nun wurde die neue Beobachtung gemacht, daß acidylierte Harnstoffe und Thioharnstoffe mit Formaldehyd unter bestimmten Bedingungen, nämlich in konzentriert schwefelsaurer Lösung bei tiefen Temperaturen, in der Weise reagieren, daß i Formaldehyd mit 2 Acidylharn-Stoffresten bzw. Acidylthioharnstoffresten verknüpft wird. Es entstehen somit Verbindungen von nachstehendem Typus welche durch Verseifung der Acidylgruppen zu dem noch unbekannten N, N'-Methylendiharnstoff bzw. N, N'-Methylendithioharnstoff /NH#CO#NHz /NH.CS#NH2 CH2 \ NH , CO # NH2 und CH2\ NH # CS # NFI2 führen. Die Einwirkung starker Mineralsäure auf diese Harnstoffe bewirkt eine Abspaltung eines Moleküls Ammoniak aus den beiden end:"tändigen NH2 Gruppen, womit ein Ringschluß- zu Derivaten des hypothetischen i, 3, 5- Triazü.s (Cyanurwasserstoffes), nämlich dem 2, 4-Dioxohexahydro-i, 3, 5-triazin bzw. 2, 4-Dithiohexahydro-i, 3, 5-triazin erfolgt. Die neuen Verbindungen lassen sich auch als Xanthine der Cyanurreihe bezeichnen. Im Gegensatz zu dem recht reaktionsträgen Dioxoderivat bildet die geschwefelte Verbindung, in der isomeren Form reagierend, gut definierte Metallsalze, so mit Kupfer, Silber oder Quecksüber.Process for the preparation of derivatives of 1, 3, 5-triazine As is known, the action of formaldehyde on urea leads to N, N-methylenourea by reaction of the two components in the ratio i: i The new observation has now been made that acidylated ureas and thioureas react with formaldehyde under certain conditions, namely in concentrated sulfuric acid solution at low temperatures, in such a way that formaldehyde is linked to 2 acidylurea residues or acidylthiourea residues. Connections of the following type thus arise which by saponification of the acidyl groups to the as yet unknown N, N'-methylenediurea or N, N'-methylenedithiourea / NH # CO # NHz /NH.CS#NH2 CH2 \ NH, CO # NH2 and CH2 \ NH # CS # NFI2 to lead. The action of strong mineral acid on these ureas causes a molecule of ammonia to be split off from the two terminal NH2 groups, which leads to a ring closure to derivatives of the hypothetical i, 3, 5- triazide (cyanuric hydrogen), namely the 2, 4- Dioxohexahydro-1,3,5-triazine and 2, 4-dithiohexahydro-i, 3, 5-triazine he follows. The new compounds can also be referred to as xanthines of the cyanuric series. In contrast to the rather inert dioxoderivative, the sulfurized compound, reacting in the isomeric form, forms well-defined metal salts, for example with copper, silver or mercury.

Die Produkte sollen zur Herstellung therapeutischer Präparate dienen.The products are intended to be used in the manufacture of therapeutic preparations.

Beispiele i. Eine auf -i5 ° gekühlte Lösung von staubtrockenem Monoacetylharnstoff im 25fachen Gewicht konzentrierter Schwefelsäure wird unter Turbinieren langsam mit der berechneten Menge käuflicher 4oprozentiger Formaldehydlösung versetzt. Nach einer Viertelstunde läßt man noch langsam eiskaltes Wasser eintropfen, gießt darauf auf viel zerstoßenes Eis und saugt den sich alsbald ausscheidenden Kristallbrei schließlich ab. Der aus Wasser kristallisierte N,N'-Methylen-bis-(acetylharnstoff)bildetweiße, ! bei 255' schmelzende Nadeln.Examples i. A solution, cooled to -i5 °, of dust-dry monoacetylurea in 25 times the weight of concentrated sulfuric acid is slowly mixed with the calculated amount of commercially available 4% formaldehyde solution while rotating. After a quarter of an hour, ice-cold water is allowed to drip in slowly, poured onto a lot of crushed ice and finally the crystal pulp that soon separates is sucked off. The N, N'-methylenebis (acetylurea) crystallized from water forms white,! needles melting at 255 '.

Zur Überführung in das Triazinderivat wird der nach Verseifung der Acetylgruppen durch Erwärmen mit Kalilauge erhaltene, am besten nochmals aus Wasser gereinigte N, N'-Methy-" lendiharnstoff im 4l/2fachen Gewicht konzentrierter Salzsäure gelöst und einen Tag sich selbst überlassen. Nach dem Eindunsten im Vakuum erstarrt das hinterbleibende gelbrote -01 beim Verreiben mit Wasser zu weißen Kristallen des 2, ¢-Dioxohexahydro-i, 3, 5-triazins, die in reinem Zustande bei 245' schmelzen.To convert it into the triazine derivative, the N, N'-methylenediurea obtained after saponification of the acetyl groups by heating with potassium hydroxide solution, preferably purified again from water, is dissolved in 4 1/2 times the weight of concentrated hydrochloric acid and left to stand for one day in vacuo solidifies behind the permanent yellow - 01 on trituration with water to give white crystals of 2, ¢ -Dioxohexahydro-i, 3, 5-triazine, the 'melt in the pure state at the 245th

z. Beim Ersatz des Acetylhanistoffes durch Monoacetylthioharnstoff gelangt man in analoger Weise wie im Beispiel i zunächst zum N, N'-Methylen-bis-(acetylthioharnstoff) vom Schmelzpunkt 167' (weiße Nadeln aus Wasser).' Der nach Verseifung der Acetylreste erhältliche N, N'-Methylen-di-(thioharnstoff), der aus Aceton in Nadeln vom Schmelzpunkt 252' kristallisiert, wird in gleicher Weise wie nach Beispiel i mit konzentrierter Salzsäure in das 2, ¢-Dithiohexahydro-i, 3, 5-triazin verwandelt. Das Quecksilbersalz kristallisiert aus heißem Wasser in feinen, weißen Nädelchen, die sich beim Erhitzen im Röhrchen bei 23o' schwarz färben.z. When the acetylhanist is replaced by monoacetylthiourea, in a manner analogous to that in Example i, N, N'-methylenebis (acetylthiourea) with a melting point of 167 '(white needles of water) is obtained.' The N, N'-methylene-di- (thiourea), which is obtainable after saponification of the acetyl radicals and which crystallizes from acetone in needles with a melting point of 252 ' , is converted into the 2, [-dithiohexahydro-i] in the same way as in Example i with concentrated hydrochloric acid , 3, 5-triazine transformed. The mercury salt crystallizes from hot water in fine, white needles that turn black when heated in a tube at 23o '.

Claims (1)

PATENTANSPRUCH: Verfahren zur Darstellung von Derivaten des .1, 3, 5-Triazins, darin bestehend, daß man monoacidylierte Harnstoffe bzw. Thioharnstoffe mit Formaldehyd in, konzentriert schwefelsaurer Lösung bei tiefen Temperaturen zu N, N'-Methylen bis-(acidylharnstoff) bzw- N, N' - Methylen -bis - (acidylthioharnstoff) kondensiert und auf diese nach Verseifung der Acidylreste : starke Mineralsäure bei Zimmertemperatur einwirken läßt.PATENT CLAIM: Process for the preparation of derivatives of .1, 3, 5-triazines, consisting in the fact that one monoacidylated ureas or thioureas with formaldehyde in, concentrated sulfuric acid solution at low temperatures N, N'-methylene bis- (acidylurea) or- N, N'-methylene -bis - (acidylthiourea) condensed and on this after saponification of the acidyl residues: strong mineral acid lets act at room temperature.
DEM97282D 1926-12-05 1926-12-05 Process for the preparation of derivatives of 1, 3, 5-triazine Expired DE479349C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEM97282D DE479349C (en) 1926-12-05 1926-12-05 Process for the preparation of derivatives of 1, 3, 5-triazine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEM97282D DE479349C (en) 1926-12-05 1926-12-05 Process for the preparation of derivatives of 1, 3, 5-triazine

Publications (1)

Publication Number Publication Date
DE479349C true DE479349C (en) 1929-07-20

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Family Applications (1)

Application Number Title Priority Date Filing Date
DEM97282D Expired DE479349C (en) 1926-12-05 1926-12-05 Process for the preparation of derivatives of 1, 3, 5-triazine

Country Status (1)

Country Link
DE (1) DE479349C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3035055A (en) * 1962-05-15 Methylene diurea

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3035055A (en) * 1962-05-15 Methylene diurea

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