![](/StructureFile/ChemBookStructure4/GIF/CB5232824.gif)
2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE synthesis
- Product Name:2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE
- CAS Number:39181-55-0
- Molecular formula:C9H8FN3S
- Molecular Weight:209.24
![2-(2-(4-Fluorophenyl)acetyl)hydrazinecarbothioamide](/CAS/20210305/GIF/39203-09-3.gif)
39203-09-3
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![2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE](/StructureFile/ChemBookStructure4/GIF/CB5232824.gif)
39181-55-0
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$90.00/100mg
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
![thiosemicarbazide](/CAS/GIF/79-19-6.gif)
79-19-6
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![4-Fluorophenylacetic acid](/CAS/GIF/405-50-5.gif)
405-50-5
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$5.00/10g
![2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE](/StructureFile/ChemBookStructure4/GIF/CB5232824.gif)
39181-55-0
19 suppliers
$90.00/100mg
![4-Fluorophenylacetic acid](/CAS/GIF/405-50-5.gif)
405-50-5
419 suppliers
$5.00/10g
![2-AMINO-5-(4-FLUOROBENZYL)-1,3,4-THIADIAZOLE](/StructureFile/ChemBookStructure4/GIF/CB5232824.gif)
39181-55-0
19 suppliers
$90.00/100mg