ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

Base Information

Chemical Name:ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate
CAS No.:1421848-90-9
Molecular Formula:C₂₂H₁₈FN₃O₂S
Molecular Weight:407.468
Hs Code.:

Synonyms:ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

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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 ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

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Technology Process of ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

There total 7 articles about ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-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: 32.0%

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

: 1421848-88-5
5-(4-fluorophenyl)-1-phenyl-1H-pyrazole-4-carbothioamide

: 1421848-90-9
ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

Guidance literature:: In ethanol; for 12h; Reflux;

Reference yield:

: 1999-00-4
ethyl 3-(4'-fluorophenyl)-3-oxopropionate

: 1421848-90-9
ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene / 15 h / Reflux

1.2: 3 h / 20 °C / Reflux

2.1: sodium hydroxide; water / ethanol / 3 h / 20 °C / Reflux

3.1: ammonium chloride; benzotriazol-1-ol; triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 - 100 °C

4.1: Lawessons reagent / tetrahydrofuran / 1 h / Reflux

5.1: ethanol / 12 h / Reflux

With Lawessons reagent; water; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene;

Reference yield:

: 100-63-0
phenylhydrazine

: 1421848-90-9
ethyl {2-[5-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl]-1,3-thiazol-4-yl}acetate

Guidance literature:: Multi-step reaction with 5 steps

1.1: toluene / 15 h / Reflux

1.2: 3 h / 20 °C / Reflux

2.1: sodium hydroxide; water / ethanol / 3 h / 20 °C / Reflux

3.1: ammonium chloride; benzotriazol-1-ol; triethylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / N,N-dimethyl-formamide / 1 h / 20 - 100 °C

4.1: Lawessons reagent / tetrahydrofuran / 1 h / Reflux

5.1: ethanol / 12 h / Reflux

With Lawessons reagent; water; ammonium chloride; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; sodium hydroxide; In tetrahydrofuran; ethanol; N,N-dimethyl-formamide; toluene;