AT224113B - Process for the preparation of the new 2- [1- (5-nitrofurfurylidene-amino) -2,4-dioxo-imidazolidyl- (3)] - ethylcarbamic acid ethyl ester - Google Patents
Process for the preparation of the new 2- [1- (5-nitrofurfurylidene-amino) -2,4-dioxo-imidazolidyl- (3)] - ethylcarbamic acid ethyl esterInfo
- Publication number
- AT224113B AT224113B AT938261A AT938261A AT224113B AT 224113 B AT224113 B AT 224113B AT 938261 A AT938261 A AT 938261A AT 938261 A AT938261 A AT 938261A AT 224113 B AT224113 B AT 224113B
- Authority
- AT
- Austria
- Prior art keywords
- imidazolidyl
- amino
- dioxo
- preparation
- new
- Prior art date
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Description
<Desc/Clms Page number 1>
Verfahren zur Herstellung des neuen 2-[1- (5-Nitrofurfuryliden-amino) - - 2, 4-dioxo-imidazolidyl- (3) j-äthylcarbaminsäure-äthylesters
Die Erfindung betrifft ein Verfahren zur Herstellung des neuen 2-[l- (fi-Nitrofurfuryliden-amino) - - 2, 4-dloxo-imidazolidyl- (3)]-äthylcarbaminsäure-äthylesters der Formel :
EMI1.1
EMI1.2
<Desc/Clms Page number 2>
Reaktionsprodukt wird abfiltriert, mit Wasser, Alkohol sowie Äther gewaschen und bei 1100C getrocknet..
Auf diese Weise erhält man 59 g (= 67tu0 d. Th.) des rohen 2-[1- (5-Nitrofurfuryliden-amino) -2, 4-dioxo- -imidazolidyl-(3)]-äthylcarbaminsäure-äthylesters. Nach zwei Umkristallisationen aus 100 cm3 Nitromethan unter Zugabe von Tierkohle schmilzt die Verbindung (46 g) bei 176-177 C.
<Desc / Clms Page number 1>
Process for the preparation of the new 2- [1- (5-nitrofurfurylidene-amino) - - 2, 4-dioxo-imidazolidyl- (3) j-ethylcarbamic acid ethyl ester
The invention relates to a process for the preparation of the new 2- [l- (fi-nitrofurfurylidene-amino) - - 2, 4-dloxo-imidazolidyl- (3)] - ethylcarbamic acid ethyl ester of the formula:
EMI1.1
EMI1.2
<Desc / Clms Page number 2>
The reaction product is filtered off, washed with water, alcohol and ether and dried at 1100C ..
In this way, 59 g (= 67tu0 of theory) of the crude ethyl 2- [1- (5-nitrofurfurylidene-amino) -2, 4-dioxo- imidazolidyl- (3)] ethylcarbamic acid are obtained. After two recrystallizations from 100 cm3 nitromethane with the addition of animal charcoal, the compound (46 g) melts at 176-177 C.
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US224113XA | 1960-12-27 | 1960-12-27 |
Publications (1)
Publication Number | Publication Date |
---|---|
AT224113B true AT224113B (en) | 1962-11-12 |
Family
ID=21809452
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT938261A AT224113B (en) | 1960-12-27 | 1961-12-12 | Process for the preparation of the new 2- [1- (5-nitrofurfurylidene-amino) -2,4-dioxo-imidazolidyl- (3)] - ethylcarbamic acid ethyl ester |
Country Status (1)
Country | Link |
---|---|
AT (1) | AT224113B (en) |
-
1961
- 1961-12-12 AT AT938261A patent/AT224113B/en active
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