ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

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Chemical Name:ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate
CAS No.:1421849-61-7
Molecular Formula:C₂₂H₂₄FN₃O₂S
Molecular Weight:413.516
Hs Code.:

Synonyms:ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

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Chemical Property of ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

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Technology Process of ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

There total 3 articles about ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate 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: 84.0%

: 638-07-3
ethyl (2-chloroaceto)acetate

: 1421849-60-6
1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazole-4-carbothioamide

: 1421849-61-7
ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

Guidance literature:: In ethanol; at 90 ℃; for 18h;

Reference yield:

: 936084-51-4
1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid

: 1421849-61-7
ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: thionyl chloride; ammonium hydroxide / toluene / 2 h / 90 °C

1.2: 14 h / 20 °C

2.1: Lawessons reagent / tetrahydrofuran / 0.5 h / 60 °C

3.1: ethanol / 18 h / 90 °C

With Lawessons reagent; ammonium hydroxide; thionyl chloride; In tetrahydrofuran; ethanol; toluene;

Reference yield:

: 1421849-59-3
1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazole-4-carboxamide

: 1421849-61-7
ethyl 2-(2-(1-cyclohexyl-5-(4-fluorophenyl)-1H-pyrazol-4-yl)thiazol-4-yl)acetate

Guidance literature:: Multi-step reaction with 2 steps

1: Lawessons reagent / tetrahydrofuran / 0.5 h / 60 °C

2: ethanol / 18 h / 90 °C

With Lawessons reagent; In tetrahydrofuran; ethanol;