Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE synthesis

3synthesis methods
-

Yield: 0.264 g

Reaction Conditions:

Stage #1:2-[(4-fluorophenyl)acetyl]hydrazinecarbothioamide with sulfuric acid at -10 - 0; for 3 h;
Stage #2: with sodium hydroxide in water at -10 - 0;

Steps:

1.2 1.2 Synthesis of 5-(4-fluorobenzyl)-1,3,4-thiadiazol-2-amine
[0256] 5 mL of sulfuric acid are placed in a round-bottomed flask, which is cooled to between 0 and -10° C. by placing it in a bath of ice and sodium chloride. 0.38 g of 2-[(4-fluorophenyl)acetyl]hydrazinecarbothioamide (1.67 mmol) is added portionwise with stirring. After stirring for 3 hours between 0 and -10° C., water is added dropwise and the mixture is then returned to basic pH with sodium hydroxide, while maintaining a temperature of between 0 and -10° C. The precipitate is filtered off, washed with water and dried. 0.264 g of 5-(4-fluorobenzyl)-1,3,4-thiadiazol-2-amine is obtained. [0257] M+H+=210.

References:

SANOFI;Fett, Eykmar;Mougenot, Patrick;Namane, Claudie;Nicolai, Eric;Philippo, Christophe US2012/40984, 2012, A1 Location in patent:Paragraph 0256; 0257