CH156932A - 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
- CH156932A CH156932A CH156932DA CH156932A CH 156932 A CH156932 A CH 156932A CH 156932D A CH156932D A CH 156932DA CH 156932 A CH156932 A CH 156932A
- Authority
- CH
- Switzerland
- Prior art keywords
- water
- double compound
- preparation
- pyridine
- pyridine series
- 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)
- Pyridine Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung einer Doppelverbindung der Pyridinr eihe. Es wurde gefunden, dass man zu einer Doppelverbindung der Pyridinreihe gelangen kann, wenn man 2 Mo1 Nieotinsäurediäthyl- amid auf 1 Dlol Calciumrhodanid einwirken lässt. Die Reaktion kann in An- oder in Ab wesenheit eines Lösungsmittels ausgeführt werden.
Die neue Doppelverbindung bildet weisse Kristalle. Sie ist in Alkohol und Wasser löslich, in Aceton und Essigäther schwer löslich. Aus Wasser kristallisiert sie mit 2 Mol Kristallwasser, das sie durch Erhitzen im Vakuum verliert.
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> 229 Teile kristallwasserhaltiges Calcium- rhodanid, entsprechend 156 Teilen wasser freiem, werden in 230 Teilen Wasser gelöst und mit 356 Teilen Nicotinsäurediäthylamid versetzt. Nachdem Lösung eingetreten ist, beginnt unter Erwärmung die Kristallisation der neuen Doppelverbindung. .plan erwärmt kurz auf dem Wasserbade, kühlt und saugt die weissen Kristalle ab.
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 mol of diethyl amide are allowed to act on 1 mol of calcium rhodanide. 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 alcohol and water, sparingly soluble in acetone and vinegar ether. It crystallizes from water with 2 moles of water of crystallization, which it loses by heating in a vacuum.
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> 229 parts of calcium rhodanide containing water of crystallization, corresponding to 156 parts of anhydrous, are dissolved in 230 parts of water and mixed with 356 parts of nicotinic acid diethylamide. After the solution has occurred, the crystallization of the new double compound begins with heating. .plan warms up briefly on the water bath, cools and sucks off the white crystals.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH154815T | 1931-03-07 | ||
CH156932T | 1931-03-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH156932A true CH156932A (en) | 1932-08-31 |
Family
ID=25716502
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH156932D CH156932A (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) | CH156932A (en) |
-
1931
- 1931-03-07 CH CH156932D patent/CH156932A/en unknown
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