ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

Base Information

Chemical Name:ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate
CAS No.:1614229-16-1
Molecular Formula:C₂₉H₂₄F₃N₃O₆S
Molecular Weight:599.587
Hs Code.:

Synonyms:ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

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Chemical Property of ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

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Technology Process of ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

There total 4 articles about ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-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: 58.0%

: 1418287-68-9
ethyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1-(2-[4-(trifluoromethoxy)phenoxy]ethyl)-1H-indole-2-carboxylate

: 1614229-15-0
3-bromo-1-(phenylsulfonyl)-1H-pyrazole

: 1614229-16-1
ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

Guidance literature:: With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; palladium diacetate; potassium carbonate; In 1,4-dioxane; water; at 80 ℃; Inert atmosphere;
DOI:10.1021/jm5006429

Reference yield:

: 627902-05-0
2-[4-(trifluoromethoxy)phenoxy]ethanol

: 1614229-16-1
ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 0 - 20 °C

2: potassium acetate; palladium diacetate; XPhos / 1,4-dioxane / 85 °C / Inert atmosphere

3: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium carbonate; palladium diacetate / water; 1,4-dioxane / 80 °C / Inert atmosphere

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; di-isopropyl azodicarboxylate; potassium acetate; palladium diacetate; potassium carbonate; triphenylphosphine; XPhos; In 1,4-dioxane; water; toluene;
DOI:10.1021/jm5006429

Reference yield:

: 16732-70-0
ethyl 5-bromoindolecarboxylate

: 1614229-16-1
ethyl 5-(1-(phenylsulfonyl)-1H-pyrazol-3-yl)-1-(2-(4-(trifluoromethoxy)phenoxy)ethyl)-1H-indole-2-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: triphenylphosphine; di-isopropyl azodicarboxylate / toluene / 0 - 20 °C

2: potassium acetate; palladium diacetate; XPhos / 1,4-dioxane / 85 °C / Inert atmosphere

3: dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; potassium carbonate; palladium diacetate / water; 1,4-dioxane / 80 °C / Inert atmosphere

With dicyclohexyl-(2',6'-dimethoxybiphenyl-2-yl)-phosphane; di-isopropyl azodicarboxylate; potassium acetate; palladium diacetate; potassium carbonate; triphenylphosphine; XPhos; In 1,4-dioxane; water; toluene;
DOI:10.1021/jm5006429