CH200914A - Process for the production of an imidazole. - Google Patents
Process for the production of an imidazole.Info
- Publication number
- CH200914A CH200914A CH200914DA CH200914A CH 200914 A CH200914 A CH 200914A CH 200914D A CH200914D A CH 200914DA CH 200914 A CH200914 A CH 200914A
- Authority
- CH
- Switzerland
- Prior art keywords
- imidazole
- production
- heptadecylimidazole
- heptadecylimidazoline
- colorless
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Herstellung eines Imidazols. Es wurde gefunden, dass man ein Imid- azol, das 2-Heptadecylimidazol, in sehr guter Ausbeute erhält, wenn man das 2.-Heptade- cylimidazolin mit Dehydrierungskatalysatoren in der Wärme behandelt. Das 2-Heptadecyl- imidazol, eine farblose, feste Masse vom Schmelzpunkt 83,5 bis 84 , kann als Aus gangsstoff zur Herstellung von Medikamenten verwendet werden.
<I>Beispiel:</I> 150 Teile 2-Heptadecylimidazolin werden mit 6 Teilen frisch reduziertem, fein ver teiltem Nickel unter Rühren auf 180 bis 240 erhitzt. Schon bei 190 tritt eine kräf tige Wasserstoffentwicklung ein. Nach etwa zweistündiger Reaktionsdauer wird das Re aktionsprodukt direkt bei 15 mm Druck vom Katalysator abdestilliert. Man erhält in guter Ausbeute ein farbloses, festes Destillat. Nach zweimaligem Umkristallisieren des Produk tes aus Methylalkohol besitzt das erhaltene 2-Heptadecylimidazol einen Schmelzpunkt von 83,5 bis 84 .
Process for the production of an imidazole. It has been found that an imidazole, 2-heptadecylimidazole, is obtained in very good yield if the 2.-heptadecylimidazoline is treated with hot dehydrogenation catalysts. The 2-heptadecyl imidazole, a colorless, solid mass with a melting point of 83.5 to 84, can be used as a starting material for the manufacture of drugs.
<I> Example: </I> 150 parts of 2-heptadecylimidazoline are heated to 180 to 240 with 6 parts of freshly reduced, finely divided nickel while stirring. A powerful evolution of hydrogen occurs as early as 190. After about two hours of reaction time, the reaction product is distilled off directly from the catalyst at 15 mm pressure. A colorless, solid distillate is obtained in good yield. After the product has been recrystallized twice from methyl alcohol, the 2-heptadecylimidazole obtained has a melting point of 83.5 to 84.
Claims (1)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH193338T | 1936-06-20 | ||
| CH200914T | 1936-06-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH200914A true CH200914A (en) | 1938-10-31 |
Family
ID=25722468
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH200914D CH200914A (en) | 1936-06-20 | 1936-06-20 | Process for the production of an imidazole. |
Country Status (1)
| Country | Link |
|---|---|
| CH (1) | CH200914A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116253684A (en) * | 2023-02-17 | 2023-06-13 | 天津工业大学 | A kind of 2-heptadecyl imidazole and its synthetic method |
-
1936
- 1936-06-20 CH CH200914D patent/CH200914A/en not_active IP Right Cessation
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN116253684A (en) * | 2023-02-17 | 2023-06-13 | 天津工业大学 | A kind of 2-heptadecyl imidazole and its synthetic method |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PL | Patent ceased |