ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

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Chemical Name:ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate
CAS No.:1318754-59-4
Molecular Formula:C₁₉H₁₇F₃N₄O₃S
Molecular Weight:438.43
Hs Code.:

Synonyms:ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

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Chemical Property of ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

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Technology Process of ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

There total 4 articles about ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate 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: 75.0%

: 1318757-55-9
ethyl 5-amino-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

: 84547-59-1
2-methyl-2H-pyrazole-3-carbonyl chloride

: 1318754-59-4
ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

Guidance literature:: In N,N-dimethyl acetamide; at 80 ℃; for 3h;

Reference yield:

: 1318757-54-8
ethyl 3-nitrilo-N-{[3-(trifluoromethyl)phenyl]acetyl}alaninate

: 1318754-59-4
ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: Lawessons reagent / toluene / 6 h / 80 °C

2: N,N-dimethyl acetamide / 3 h / 80 °C

With Lawessons reagent; In N,N-dimethyl acetamide; toluene;

Reference yield:

: 2003-14-7
(3-trifluoromethyl-phenyl)-acetyl chloride

: 1318754-59-4
ethyl 5-{[(1-methyl-1H-pyrazol-5-yl)carbonyl]amino}-2-[3-(trifluoromethyl)benzyl]-1,3-thiazole-4-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: sodium hydrogencarbonate; sodium dithionite / water / 2 h / 20 °C

1.2: 0 - 20 °C

2.1: Lawessons reagent / toluene / 6 h / 80 °C

3.1: N,N-dimethyl acetamide / 3 h / 80 °C

With Lawessons reagent; sodium dithionite; sodium hydrogencarbonate; In N,N-dimethyl acetamide; water; toluene;