1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

Base Information

Chemical Name:1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea
CAS No.:1370256-57-7
Molecular Formula:C₁₀H₇F₃N₄OS₂
Molecular Weight:320.319
Hs Code.:

Synonyms:1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

Suppliers and Price of 1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

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Technology Process of 1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

There total 1 articles about 1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 94.6%

: 2349-67-9
2-Amino-5-mercapto-1,3,4-thiadiazole

: 1548-13-6
p-trifluoromethyl-phenylisocyanate

: 1370256-57-7
1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

Guidance literature:: With triethylamine; In acetonitrile; Reflux;

Reference yield: 91.5%

: 1193-21-1
4,6-dichloropyrimidine

: 1370256-57-7
1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

: C₁₄H₈ClF₃N₆OS₂

Guidance literature:: With potassium carbonate; In acetonitrile; Reflux;

Reference yield:

: 1370256-57-7
1-(5-mercapto-[1,3,4]thiadiazol-2-yl)-3-[4-(trifluoromethyl)phenyl]urea

: 3-{5-[(6-{[3-(morpholin-4-yl)propyl]amino}pyrimidin-4-yl)sulfanyl]-1,3,4-thiadiazol-2-yl}-1-[4-(trifluoromethyl)phenyl]urea

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / acetonitrile / Reflux

2: ethanol / Reflux

With potassium carbonate; In ethanol; acetonitrile;