CH156939A - 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
- CH156939A CH156939A CH156939DA CH156939A CH 156939 A CH156939 A CH 156939A CH 156939D A CH156939D A CH 156939DA CH 156939 A CH156939 A CH 156939A
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (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 a-Picolinsäurediäthyl- amid auf 1 Mol Caleiumrhodanid einwirken lässt. Die Reaktion kann in An- oder Ab wesenheit eines Lösungsmittels ausgeführt werden.
Die neue Doppelverbindung bildet weisse Kristalle. Sie ist in Wasser, Alkohol, Aceton und Essigäther sehr leicht löslich.
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> 23 Teile kristallwasserhaltiges Calcium- rhodanid, entsprechend 15 Teilen wasserfreiem, und 35 Teile a-Picolinsäurediäthylamid (was serlösliches Öl, Kp. s 120 ) werden in Alko hol gelöst. Nach kurzem Erhitzen auf dem Wasserbad wird der Alkohol abdestilliert, wobei die gebildete Doppelverbindung als ein fein kristallines, weisses Pulver zurückbleibt.
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 a-picolinic acid diethyl amide are allowed to act on 1 mole 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 very easily soluble in water, alcohol, acetone and vinegar ether.
The new product is intended to be used for separating and purifying the underlying pyridine compound as well as for therapeutic purposes.
<I> Example: </I> 23 parts of calcium rhodanide containing water of crystallization, corresponding to 15 parts of anhydrous, and 35 parts of a-picolinic acid diethylamide (soluble oil, b.p. s 120) are dissolved in alcohol. After brief heating on a water bath, the alcohol is distilled off, the double compound formed remaining as a finely crystalline, white powder.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH156939T | 1931-03-07 | ||
CH154815T | 1931-03-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH156939A true CH156939A (en) | 1932-08-31 |
Family
ID=25716509
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH156939D CH156939A (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) | CH156939A (en) |
-
1931
- 1931-03-07 CH CH156939D patent/CH156939A/en unknown
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