2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

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Chemical Name:2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole
CAS No.:1338725-39-5
Molecular Formula:C₂₈H₂₄N₆S
Molecular Weight:476.605
Hs Code.:

Synonyms:2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

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Chemical Property of 2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

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Technology Process of 2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

There total 4 articles about 2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole 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: 82.0%

: 1338725-29-3
4,5-dihydro-3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenylpyrazol-1-carbothioamide

: 70-11-1
α-bromoacetophenone

: 1338725-39-5
2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

Guidance literature:: In ethanol; for 2h; Reflux;
DOI:10.1002/jhet.706

Reference yield:

: 123-54-6,81235-32-7
acetylacetone

: 1338725-39-5
2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

Guidance literature:: Multi-step reaction with 4 steps

1.1: sodium methylate / methanol / 11 h / 0 °C / Reflux

2.1: potassium hydroxide / ethanol; water / 6 h / 25 °C / Cooling with ice

3.1: ethanol / 90 °C

3.2: 20 °C / Reflux

4.1: ethanol / 2 h / Reflux

With sodium methylate; potassium hydroxide; In methanol; ethanol; water; 2.1: Claisen Schmidt condensation;
DOI:10.1002/jhet.706

Reference yield:

: 1-[5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl]ethanone

: 1338725-39-5
2-(3-(5-methyl-1-(p-tolyl)-1H-1,2,3-triazol-4-yl)-5-phenyl-4,5-dihydro-1H-pyrazol-1-yl)-4-phenylthiazole

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide / ethanol; water / 6 h / 25 °C / Cooling with ice

2.1: ethanol / 90 °C

2.2: 20 °C / Reflux

3.1: ethanol / 2 h / Reflux

With potassium hydroxide; In ethanol; water; 1.1: Claisen Schmidt condensation;
DOI:10.1002/jhet.706