CH253643A - Process for the preparation of 2- (3 ', 5'-dichloro-salicoylamino) -thiazole. - Google Patents
Process for the preparation of 2- (3 ', 5'-dichloro-salicoylamino) -thiazole.Info
- Publication number
- CH253643A CH253643A CH253643DA CH253643A CH 253643 A CH253643 A CH 253643A CH 253643D A CH253643D A CH 253643DA CH 253643 A CH253643 A CH 253643A
- Authority
- CH
- Switzerland
- Prior art keywords
- thiazole
- dichloro
- salicoylamino
- preparation
- amino
- Prior art date
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Description
Verfahren zur Herstellung von 2-(3',5'-Dichlor-salicoylamino)-thiazol. Das vorliegende Patent betrifft ein Ver- fJhren zur Herstellung von 2-(3',5'-Dichlor- .@llicoy lamino)-thiazol, welches dadurch ge kennzeichnet ist, dass man 3,5-Dichlor-sali- cvlsäurechloi-id auf 2-Amino-thiazol einwir ken lässt.
<I>Beispiel:</I> <B>10-</B> 2-Amino-thiazol werden in einer Mi- chiing von 40 em@ Äther und 10 cm3 Pyridin gelöst. In dieser Lösung gibt man tropfen wcie eine 3lischung von 19 g 3,5-Dichlor- salicyl@äiircchlorid, gelöst. in 115 cm' Chloro- forni. innerhalb 20 iVlinuten zu.
Die Reak tionsmischung wird darauf während 4 Stun den am Rückfluss zum Sieden erhitzt. Ein Teil des Lösungsmittels wird unter vermin dertem Druck a.bdestilliert, worauf das Re aktionsprodukt auskristallisiert.
Nach der Isolierung wird das Reaktionsprodukt wie- ilerholt aus Alkohol umkristallisiert und ge- troeknet. Smp. 275 C (korr.). Die Verbindung besitzt die Formel
EMI0001.0038
Analyse: Bruttozusammensetzung CIo' o02N2SC12. Ber. C41,5%; H2,1%; N9,7%.
Gef. <B>C41,75%;</B> 112,34%;<B>N9,64%.</B> Das 2-(3',5'-Dichlor-salicoylamino)-thiazol soll als F'ungicid Verwendung finden.
Process for the preparation of 2- (3 ', 5'-dichloro-salicoylamino) -thiazole. The present patent relates to a process for the preparation of 2- (3 ', 5'-dichloro-. @ Llicoy lamino) -thiazole, which is characterized in that one has 3,5-dichloro-salicylic acid chloride 2-Amino-thiazole can act.
<I> Example: </I> <B> 10- </B> 2-amino-thiazole are dissolved in a mixture of 40 em @ ether and 10 cm3 pyridine. A mixture of 19 g of 3,5-dichlorosalicylic chloride is added dropwise to this solution. in 115 cm 'chloroforni. within 20 minutes.
The reaction mixture is then heated to boiling under reflux for 4 hours. Some of the solvent is distilled off under reduced pressure, whereupon the reaction product crystallizes out.
After isolation, the reaction product is repeatedly recrystallized from alcohol and dried. M.p. 275 C (corr.). The compound has the formula
EMI0001.0038
Analysis: gross composition CIo 'o02N2SC12. Ber. C41.5%; H2.1%; N9.7%.
Found. <B> C41.75%; </B> 112.34%; <B> N9.64%. </B> The 2- (3 ', 5'-dichloro-salicoylamino) -thiazole is said to be F 'ungicid use.
Claims (1)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH253643T | 1945-12-07 | ||
CH246984T | 1945-12-07 |
Publications (1)
Publication Number | Publication Date |
---|---|
CH253643A true CH253643A (en) | 1948-03-15 |
Family
ID=25729152
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CH253643D CH253643A (en) | 1945-12-07 | 1945-12-07 | Process for the preparation of 2- (3 ', 5'-dichloro-salicoylamino) -thiazole. |
Country Status (1)
Country | Link |
---|---|
CH (1) | CH253643A (en) |
-
1945
- 1945-12-07 CH CH253643D patent/CH253643A/en unknown
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