CH156933A - Process for the preparation of a double compound of the pyridine series. - Google Patents
Process for the preparation of a double compound of the pyridine series.Info
- Publication number
- CH156933A CH156933A CH156933DA CH156933A CH 156933 A CH156933 A CH 156933A CH 156933D A CH156933D A CH 156933DA CH 156933 A CH156933 A CH 156933A
- Authority
- CH
- Switzerland
- Prior art keywords
- double compound
- preparation
- pyridine
- pyridine series
- compound
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
Description
Verfahren zur Darstellung einer Doppelverbindung der Pyridinreihe. Es wurde gefunden, dass man zu einer Doppelverbindung der Pyridinreihe gelangen kann, wenn man 2 Mol Nicotinsäurediäthyl- amid auf 1 Mol Galciumbromid einwirken lässt. Die Reaktion kann in An- oder Ab wesenheit eines Lösungsmittels ausgeführt werden.
Die neue Doppelverbindung bildet weisse Kristalle. Sie ist in Wasser und warmem Alkohol löslich, in Aceton und Essigäther unlöslich.
Das neue Produkt soll sowohl zur Ab scheidung und Reinigung der zugrunde lie genden Pyridinverbindung, wie auch zu thera peutischen Zwecken Verwendung finden.
<I>Beispiel:</I> 35,6 Teile Nicotinsäurediäthylamid und 20 Teile Calciumbromid werden in Wasser gelöst und die Lösung zur Trockne verdampft. Die gebildete Doppelverbindung lässt sich aus Alkohol umkristallisieren.
Process for the preparation of a double compound of the pyridine series. It has been found that a double compound of the pyridine series can be obtained if 2 moles of diethyl nicotinic acid are allowed to act on 1 mole of calcium bromide. The reaction can be carried out in the presence or absence of a solvent.
The new double compound forms white crystals. It is soluble in water and warm alcohol, insoluble in acetone and vinegar ether.
The new product is intended to be used both for separating and purifying the underlying pyridine compound as well as for therapeutic purposes.
<I> Example: </I> 35.6 parts of nicotinic acid diethylamide and 20 parts of calcium bromide are dissolved in water and the solution is evaporated to dryness. The double compound formed can be recrystallized from alcohol.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH154815T | 1931-03-07 | ||
CH156933T | 1931-03-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH156933A true CH156933A (en) | 1932-08-31 |
Family
ID=25716503
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH156933D CH156933A (en) | 1931-03-07 | 1931-03-07 | Process for the preparation of a double compound of the pyridine series. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH156933A (en) |
-
1931
- 1931-03-07 CH CH156933D patent/CH156933A/en unknown
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