2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

Base Information

Chemical Name:2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one
CAS No.:1415692-89-5
Molecular Formula:C₁₅H₁₁N₇O₂S₂
Molecular Weight:385.43
Hs Code.:

Synonyms:2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

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Chemical Property of 2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

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Technology Process of 2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

There total 8 articles about 2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one 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: 68.0%

: 3364-80-5
1,3-thiazole-4-carbaldehyde

: 1415692-80-6
4-amino-2-[4-(5-mercapto-[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-2,4-dihydro-[1,2,4]triazol-3-one

: 1415692-89-5
2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

Guidance literature:: With sulfuric acid; In dimethyl sulfoxide; at 80 ℃;
DOI:10.1007/s00044-012-0332-3

Reference yield:

: 619-45-4
4-methoxycarbonyl aniline

: 1415692-89-5
2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

Guidance literature:: Multi-step reaction with 8 steps

1.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 10 h / 110 °C

2.1: trifluoroacetic acid / dichloromethane / 12 h / 0 - 20 °C

3.1: hydrogenchloride / water / 0.17 h / Cooling

3.2: -5 - 0 °C

4.1: acetic anhydride / 1 h / 55 °C

5.1: bromine / 0 - 60 °C

6.1: hydrazine hydrate / ethanol / 4 h / Reflux

7.1: potassium hydroxide / 5 h / Reflux

8.1: sulfuric acid / dimethyl sulfoxide / 80 °C

With hydrogenchloride; sulfuric acid; bromine; acetic anhydride; hydrazine hydrate; N-ethyl-N,N-diisopropylamine; trifluoroacetic acid; potassium hydroxide; In ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;
DOI:10.1007/s00044-012-0332-3

Reference yield:

: 133273-94-6
4-(tert-butoxycarbonylmethylamino)-benzoic acid methyl ester

: 1415692-89-5
2-[4-(5-mercapto[1,3,4]oxadiazol-2-yl)phenyl]-5-methyl-4-[(thiazol-4-ylmethylene)-amino]-2,4-dihydro[1,2,4]triazol-3-one

Guidance literature:: Multi-step reaction with 7 steps

1.1: trifluoroacetic acid / dichloromethane / 12 h / 0 - 20 °C

2.1: hydrogenchloride / water / 0.17 h / Cooling

2.2: -5 - 0 °C

3.1: acetic anhydride / 1 h / 55 °C

4.1: bromine / 0 - 60 °C

5.1: hydrazine hydrate / ethanol / 4 h / Reflux

6.1: potassium hydroxide / 5 h / Reflux

7.1: sulfuric acid / dimethyl sulfoxide / 80 °C

With hydrogenchloride; sulfuric acid; bromine; acetic anhydride; hydrazine hydrate; trifluoroacetic acid; potassium hydroxide; In ethanol; dichloromethane; water; dimethyl sulfoxide;
DOI:10.1007/s00044-012-0332-3