CH161747A - Process for the preparation of 1-perhydrocarbazylethyl-5-methylpyrazoline. - Google Patents
Process for the preparation of 1-perhydrocarbazylethyl-5-methylpyrazoline.Info
- Publication number
- CH161747A CH161747A CH161747DA CH161747A CH 161747 A CH161747 A CH 161747A CH 161747D A CH161747D A CH 161747DA CH 161747 A CH161747 A CH 161747A
- Authority
- CH
- Switzerland
- Prior art keywords
- methylpyrazoline
- perhydrocarbazylethyl
- preparation
- monobromohydrate
- melts
- Prior art date
Links
Landscapes
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
Verfahren zur Darstellung von 1-Perhydrocarbazyläthyl-5-methylpyrazolin. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Darstellung von 1-Per- hydrocarbazyläthyl-5-methylpyrazolin, wel ches darin besteht, dass man N-Chloräthyl- perhydrocarbazol mit 5-Methylpyrazolin um setzt.
Die neue Verbindung ist als Heilmittel verwendbar und stellt ein gelbliches, unter 4 mm Druck bei l73-180 siedendes 01 dar; sie bildet ein farbloses, bei 187 schmel zendes Monobromhydrat.
<I>Beispiel:</I> 18 Teile N-_Chloräthylperhydrocarbazol (vergl. Beispiel des Hauptpatentes) und 13 Teile 5-Methylpyrazolin werden 1 Stunde lang auf dem Dampfbad erwärmt. Man ver setzt nach dem Erkalten mit Wasser und Natronlauge, nimmt das so erhaltene 1-Per- hydrocarbazyläthyl-5-methylpyrazolin
EMI0001.0013
in Äther auf und reinigt es durch Vakuum destillation. Das Produkt ist ein gelbliches 01, dessen Siedepunkt bei 4 mm Druck bei 173-180 liegt; es bildet ein farbloses Monobromhydrat, das bei 187<B>0 0</B> schmilzt.
Process for the preparation of 1-perhydrocarbazylethyl-5-methylpyrazoline. The present invention relates to a process for the preparation of 1-per-hydrocarbazylethyl-5-methylpyrazoline, which consists in that N-chloroethyl perhydrocarbazole is reacted with 5-methylpyrazoline.
The new compound can be used as a remedy and represents a yellowish oil boiling under 4 mm pressure at 173-180; it forms a colorless monobromohydrate that melts at 187.
<I> Example: </I> 18 parts of N-_Chloräthylperhydrocarbazol (see. Example of the main patent) and 13 parts of 5-methylpyrazoline are heated for 1 hour on the steam bath. After cooling, one sets ver with water and sodium hydroxide solution, takes the 1-perhydrocarbazylethyl-5-methylpyrazoline thus obtained
EMI0001.0013
in ether and purifies it by vacuum distillation. The product is a yellowish oil, the boiling point of which at 4 mm pressure is 173-180; it forms a colorless monobromohydrate that melts at 187 <B> 0 0 </B>.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE161747X | 1931-04-04 | ||
CH158827T | 1932-07-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH161747A true CH161747A (en) | 1933-05-15 |
Family
ID=25717158
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH161747D CH161747A (en) | 1931-04-04 | 1932-04-04 | Process for the preparation of 1-perhydrocarbazylethyl-5-methylpyrazoline. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH161747A (en) |
-
1932
- 1932-04-04 CH CH161747D patent/CH161747A/en unknown
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