2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

Base Information

Chemical Name:2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid
CAS No.:1374645-76-7
Molecular Formula:C₁₆H₁₃FN₄O₂S
Molecular Weight:344.369
Hs Code.:

Synonyms:2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

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Chemical Property of 2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

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Technology Process of 2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

There total 6 articles about 2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid 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: 88.0%

: 1374645-75-6
2-{2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-2-hydroxy-ethyl}-4-methyl-thiazole-5-carboxylic acid methyl ester

: 1374645-76-7
2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

Guidance literature:: With sulfuric acid; at 160 ℃; for 2h; Inert atmosphere;

Reference yield:

: 766-98-3
1-ethynyl-4-fluorobenzene

: 1374645-76-7
2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: N-ethyl-N,N-diisopropylamine / copper(l) iodide / N,N-dimethyl-formamide / 18 h / 20 °C

2.1: water; tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 °C

3.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -75 °C / Inert atmosphere

3.2: 1 h / -75 - 20 °C

4.1: n-butyllithium / tetrahydrofuran; hexanes / 2 h / -75 °C / Inert atmosphere

4.2: 2 h / -75 °C

5.1: diethyl ether; methanol

6.1: sulfuric acid / 2 h / 160 °C / Inert atmosphere

With n-butyllithium; sulfuric acid; tetrabutyl ammonium fluoride; water; N-ethyl-N,N-diisopropylamine; copper(l) iodide; In tetrahydrofuran; methanol; hexanes; diethyl ether; hexane; N,N-dimethyl-formamide;

Reference yield:

: 1374645-72-3
4-(4-fluoro-phenyl)-1-trimethylsilanylmethyl-1H-[1,2,3]triazole

: 1374645-76-7
2-{(E)-2-[5-(4-fluoro-phenyl)-3-methyl-3H-[1,2,3]triazol-4-yl]-vinyl}-4-methyl-thiazole-5-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1.1: water; tetrabutyl ammonium fluoride / tetrahydrofuran / 1 h / 0 °C

2.1: n-butyllithium / hexane; tetrahydrofuran / 1 h / -75 °C / Inert atmosphere

2.2: 1 h / -75 - 20 °C

3.1: n-butyllithium / tetrahydrofuran; hexanes / 2 h / -75 °C / Inert atmosphere

3.2: 2 h / -75 °C

4.1: diethyl ether; methanol

5.1: sulfuric acid / 2 h / 160 °C / Inert atmosphere

With n-butyllithium; sulfuric acid; tetrabutyl ammonium fluoride; water; In tetrahydrofuran; methanol; hexanes; diethyl ether; hexane;