CH292799A - Process for the preparation of 1-phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolone. - Google Patents
Process for the preparation of 1-phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolone.Info
- Publication number
- CH292799A CH292799A CH292799DA CH292799A CH 292799 A CH292799 A CH 292799A CH 292799D A CH292799D A CH 292799DA CH 292799 A CH292799 A CH 292799A
- Authority
- CH
- Switzerland
- Prior art keywords
- pyrazolone
- dimethyl
- phenyl
- isopropylamino
- preparation
- Prior art date
Links
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
Verfahren zur Herstellung von 1-Phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolon. Gegenstand der vorliegenden Erfindung ist ein Verfahren zur Herstellung von 1-Phe- iivl - 2,3 - dimethyl - 4- isopropylamino-5-pyrazo- lon, das dadurch gekennzeichnet ist, dass man 1-1'lienyl-2,3-dimethyl-4-amino-5-pyrazolon mit Aceton in Gegenwart von amalgamiertem Zink und Säure bei erhöhter Temperatur um setzt.
Das nach dem vorliegenden Verfahren er- lialtene 1-Pheii#,1-2,0'-dimeth-,y-1-4-isopropyl- z anAno -5-pyrazolon ist bereits bekannt. Es soll als Zwischenprodukt verwendet werden.
<I>Beispiel 1:</I> 20 Gewichtsteile 1-Phenyl-2,3-dimethyl-4- amino-5-pyrazolon werden mit 30 Gewichts teilen amalgamiertem Zink, 24 Gewichtsteilen _leeton und 120 Volumteilen verdünnter Salz- säure (1 :1) vier Stunden am Rückfluss er hitzt.
Dann wird mit konzentrierter Natron lauge alkalisch gemacht und ausgeäthert. Nach Trocknen und Verdampfen des Äthers erhält man 23,5 Gewichtsteile fast reines 1-Phenyl-2,3 -dimethyl -4-isopropylamino - 5- pyrazolon vom Schmelzpunkt 78 , das durch Umkristallisieren aus Essigester farblose Kri stalle vom Schmelzpunkt 80 ergibt.
Process for the preparation of 1-phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolone. The present invention relates to a process for the preparation of 1-phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolone, which is characterized in that 1-1'lienyl-2,3-dimethyl -4-amino-5-pyrazolone with acetone in the presence of amalgamated zinc and acid at elevated temperature.
The 1-Pheii #, 1-2,0'-dimeth-, y-1-4-isopropyl-z anAno -5-pyrazolone obtained by the present process is already known. It is intended to be used as an intermediate.
<I> Example 1: </I> 20 parts by weight of 1-phenyl-2,3-dimethyl-4-amino-5-pyrazolone are mixed with 30 parts by weight of amalgamated zinc, 24 parts by weight of leeton and 120 parts by volume of dilute hydrochloric acid (1: 1) He refluxed for four hours.
Then it is made alkaline with concentrated sodium hydroxide solution and etherified. After drying and evaporation of the ether, 23.5 parts by weight of almost pure 1-phenyl-2,3-dimethyl -4-isopropylamino-5-pyrazolone with a melting point of 78, which by recrystallization from ethyl acetate gives colorless crystals with a melting point of 80.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE292799X | 1950-03-06 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH292799A true CH292799A (en) | 1953-08-31 |
Family
ID=6075445
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH292799D CH292799A (en) | 1950-03-06 | 1951-02-13 | Process for the preparation of 1-phenyl-2,3-dimethyl-4-isopropylamino-5-pyrazolone. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH292799A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2864413A (en) * | 1956-02-21 | 1958-12-16 | Johnson Mfg Co | Gang saw |
-
1951
- 1951-02-13 CH CH292799D patent/CH292799A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2864413A (en) * | 1956-02-21 | 1958-12-16 | Johnson Mfg Co | Gang saw |
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