N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

Base Information

Chemical Name:N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide
CAS No.:1186108-64-4
Molecular Formula:C₂₆H₂₅F₃N₈O₄S
Molecular Weight:602.597
Hs Code.:

Synonyms:N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

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Chemical Property of N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

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Technology Process of N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

There total 3 articles about N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide 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:

: 1186111-87-4
methyl 4'-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6'-(3-ethylureido)-3,3'-bipyridine-5-carboxylate

: 530-62-1
1,1'-carbonyldiimidazole

: 1186108-64-4
N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

Guidance literature:: methyl 4'-(5-(cyclohexylcarbamoyl)-4-(trifluoromethyl)thiazol-2-yl)-6'-(3-ethylureido)-3,3'-bipyridine-5-carboxylate; With hydrazine; In ethanol; for 3h; Reflux;

1,1'-carbonyldiimidazole; In tetrahydrofuran; at 20 ℃; for 2h;

Reference yield:

: 1025718-91-5
5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinecarboxylic acid methyl ester

: 1186108-64-4
N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 0.5 h / 110 °C / Microwave irradiation

2.1: hydrazine / ethanol / 3 h / Reflux

2.2: 2 h / 18 - 26 °C

With sodium hydrogencarbonate; hydrazine; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; ethanol; water; 1.1: Suzuki Coupling;

Reference yield:

: 1186111-60-3
2-(5-bromo-2-(3-ethylureido)pyridin-4-yl)-N-cyclohexyl-4-(trifluoromethyl)thiazole-5-carboxamide

: 1186108-64-4
N-cyclohexyl-2-(6-(3-ethylureido)-5'-(5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-3,3'-bipyridin-4-yl)-4-(trifluoromethyl)thiazole-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydrogencarbonate / bis-triphenylphosphine-palladium(II) chloride / 1,4-dioxane; water / 0.5 h / 110 °C / Microwave irradiation

2.1: hydrazine / ethanol / 3 h / Reflux

2.2: 2 h / 18 - 26 °C

With sodium hydrogencarbonate; hydrazine; bis-triphenylphosphine-palladium(II) chloride; In 1,4-dioxane; ethanol; water; 1.1: Suzuki Coupling;