CH134276A - Process for the preparation of a condensation product of the benzodiazine series. - Google Patents
Process for the preparation of a condensation product of the benzodiazine series.Info
- Publication number
- CH134276A CH134276A CH134276DA CH134276A CH 134276 A CH134276 A CH 134276A CH 134276D A CH134276D A CH 134276DA CH 134276 A CH134276 A CH 134276A
- Authority
- CH
- Switzerland
- Prior art keywords
- condensation product
- benzodiazine
- series
- preparation
- aminobenzene
- Prior art date
Links
Description
Verfahren zur Darstellung eines Kondensationsproduktes der Benzodiazinreihe. Gegenstand dieses Patentes ist ein Ver fahren zur Darstellung eines Kondensations produktes der Benzodiazinreihe von der Formel
EMI0001.0004
welches dadurch gekennzeichnet ist, dass man 1 Mol. 2.4-Dihalogenchinazolin mit 2 Mol. 4- Nitro-l-aminobenzol-3-sulfosäure kondensiert.
Das Kondensationsprodukt soll als Zwi schenprodukt für Farbstoffe oder auch für pharmazeutische Produkte gebraucht werden. <I>Beispiel:</I> 19,9 Gewichtsteile leinst gepulvertes 2.4- Dichlorchinazolin werden in 100 Gewichts teilen Wasser suspendiert. Man gibt dazu eine Lösung von 24,0 Gewichtsteilen des Natriumsalzes der 4-Nitro-l-aminobenzol-3- sulfosäure und erhitzt unter gutem Rühren auf 45 bis die 4-Nitro-l-aminobenzol-3-sulfo- säure nicht mehr nachweisbar ist.
Die lack mussaure Lösung enthält jetzt das noch chlorhaltige Kondensationsprodukt aus einem Molekül 2.4-Dichlorchinazolin und einem Molekül 4-Nitro -1-aminobenzol-3-sulfosäure, das man zum Beispiel durch .Gussalzen als gelbliches Pulver isolieren kann. Inzwischen hat man eine neutrale wässerige, auf 70-85 erhitzte Lösung von weiteren 24 Gewichts teilen des Natriumsalzes der 4-Nitro-l-amino- benzol-3-sulfosäure bereitet. Zu dieser Lösung tropft man unter sehr gutem Rühren langsam die auf schwach lackmussauer gestellte obige Lösung des chlorhaltigen Zwischenkörpers.
Nach beendigtem Zutropfen hält man noch einige Zeit auf 85 , lässt abkühlen, macht schwach kongosauer und salzt aus. Das Kondensationsprodukt aus 1 Mol. 2.4-Dichlor- chinazolin und 2 Mol. 4-Nitro-l-aminobenzol- 3-sulfosäure bildet ein schwach rötliches Pulver, das in Wasser mit gelber Farbe löslich ist.
Die neue Verbindung reagiert nicht mehr mit salpetriger Säure; sie lässt sich zum Beispiel durch Eisen und Essigsäure leicht zur entsprechenden Diaminoverbindung redu zieren.
Process for the preparation of a condensation product of the benzodiazine series. The subject of this patent is a process for the representation of a condensation product of the benzodiazine series of the formula
EMI0001.0004
which is characterized in that 1 mole of 2,4-dihaloquinazoline is condensed with 2 moles of 4-nitro-1-aminobenzene-3-sulfonic acid.
The condensation product should be used as an inter mediate product for dyes or for pharmaceutical products. <I> Example: </I> 19.9 parts by weight of powdered 2.4-dichloroquinazoline are suspended in 100 parts by weight of water. A solution of 24.0 parts by weight of the sodium salt of 4-nitro-1-aminobenzene-3-sulfonic acid is added and heated to 45 with thorough stirring until the 4-nitro-1-aminobenzene-3-sulfonic acid can no longer be detected .
The lacquer acidic solution now contains the condensation product still containing chlorine from a molecule of 2,4-dichloroquinazoline and a molecule of 4-nitro-1-aminobenzene-3-sulphonic acid, which can be isolated as a yellowish powder using cast salts, for example. In the meantime, a neutral aqueous solution, heated to 70-85, of a further 24 parts by weight of the sodium salt of 4-nitro-1-aminobenzene-3-sulfonic acid has been prepared. The above solution of the intermediate body containing chlorine is slowly added dropwise to this solution while stirring very well.
After the dropping is complete, hold at 85 for a while, let it cool down, make weak Congo acidic and salt out. The condensation product of 1 mole of 2,4-dichloroquinazoline and 2 moles of 4-nitro-1-aminobenzene-3-sulfonic acid forms a pale reddish powder which is soluble in water with a yellow color.
The new compound no longer reacts with nitrous acid; it can be easily reduced to the corresponding diamino compound, for example with iron and acetic acid.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE134276X | 1926-12-13 | ||
CH133192T | 1927-12-12 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH134276A true CH134276A (en) | 1929-07-15 |
Family
ID=25711987
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH134276D CH134276A (en) | 1926-12-13 | 1927-12-12 | Process for the preparation of a condensation product of the benzodiazine series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH134276A (en) |
-
1927
- 1927-12-12 CH CH134276D patent/CH134276A/en unknown
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