CH91105A - Process for the preparation of a derivative of nicotinic acid. - Google Patents
Process for the preparation of a derivative of nicotinic acid.Info
- Publication number
- CH91105A CH91105A CH91105DA CH91105A CH 91105 A CH91105 A CH 91105A CH 91105D A CH91105D A CH 91105DA CH 91105 A CH91105 A CH 91105A
- Authority
- CH
- Switzerland
- Prior art keywords
- nicotinic acid
- derivative
- preparation
- piperidine
- water
- 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)
Description
Verfahren zur Herstellung eines Derivates der Nikotinsäure. Es wurde gefunden, dass man zu einem Derivat der Nikotinsäure gelangen kann, wenn man Verbindungen, welche den Nikotin säurerest enthalten, wie z. B. Nikotinsäure- halogenide, mit Piperidin behandelt.
Das so entstehende Nikotinsäurepiper-idid bildet ein dickes, bei 310 siedendes Öl, wel ches in Wasser und organischen Lösungs mitteln leicht löslich ist.
Die neue Verbindung besitzt wertvolle therapeutische Eigenschaften.
Beispiel: Nikotinsäurebromid wird mit der äqui valenten Menge Piperidinbromhydrat irn O1- bad während mehreren Stunden auf zirka <B>1601</B> erhitzt. Nach Beendigung der Brom wasserstoff-Entwicklung wird die Schmelze in Wasser gelöst, mit Kalitunhydroxydlösung 1 : 1 versetzt und mit Äther abdestilliert. Das zurückbleibende rohe Nikotinsäurepiperidid wird durch Destillation gereinigt.
Process for the preparation of a derivative of nicotinic acid. It has been found that a derivative of nicotinic acid can be obtained if compounds which contain the nicotine acid residue, such as. B. nicotinic acid halides, treated with piperidine.
The resulting nicotinic acid piperidide forms a thick oil boiling at 310 ° C, which is easily soluble in water and organic solvents.
The new compound has valuable therapeutic properties.
Example: Nicotinic acid bromide is heated with the equivalent amount of piperidine bromohydrate in an O1 bath for several hours to around <B> 1601 </B>. After the evolution of hydrogen bromide has ended, the melt is dissolved in water, 1: 1 potassium hydroxide solution is added and the mixture is distilled off with ether. The remaining crude nicotinic acid piperidide is purified by distillation.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90807T | 1920-07-21 | ||
CH91105T | 1920-07-21 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH91105A true CH91105A (en) | 1921-10-01 |
Family
ID=25704245
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH91105D CH91105A (en) | 1920-07-21 | 1920-07-21 | Process for the preparation of a derivative of nicotinic acid. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH91105A (en) |
-
1920
- 1920-07-21 CH CH91105D patent/CH91105A/en unknown
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