tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

Base Information

Chemical Name:tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate
CAS No.:1426670-93-0
Molecular Formula:C₂₉H₃₁N₇O₄
Molecular Weight:541.61
Hs Code.:

Synonyms:tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

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Chemical Property of tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

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Technology Process of tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

There total 5 articles about tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-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: 56.0%

: 1426671-16-0
6-bromo-N-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl)imidazo[1,2-a]pyridine-3-carboxamide

: 1426671-41-1
tert-butyl 2-(3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetate

: 1426670-93-0
tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

Guidance literature:: With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; In 1,4-dioxane; at 135 ℃; for 1.33333h; Microwave irradiation;

Reference yield:

: 60710-80-7
5-cyano-2-methylaniline

: 1426670-93-0
tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydroxylamine / ethanol; water / 70 °C / Reflux

2.1: 1,1'-carbonyldiimidazole / 1-methyl-pyrrolidin-2-one / 0.5 h / 30 °C

2.2: 0.75 h / 30 - 125 °C / Microwave irradiation

3.1: 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / ethyl acetate / 65 °C

4.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / 1,4-dioxane / 1.33 h / 135 °C / Microwave irradiation

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; hydroxylamine; sodium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; 1,1'-carbonyldiimidazole; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethanol; water; ethyl acetate;

Reference yield:

: 1426671-14-8
3-amino-N-hydroxy-4-methylbenzimidamide

: 1426670-93-0
tert-butyl 2-(3,5-dimethyl-4-(3-(2-methyl-5-(5-methyl-1,2,4-oxadiazol-3-yl)phenylcarbamoyl)imidazo[1,2-a]pyridin-6-yl)-1H-pyrazol-1-yl)acetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1,1'-carbonyldiimidazole / 1-methyl-pyrrolidin-2-one / 0.5 h / 30 °C

1.2: 0.75 h / 30 - 125 °C / Microwave irradiation

2.1: 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide / ethyl acetate / 65 °C

3.1: (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate / 1,4-dioxane / 1.33 h / 135 °C / Microwave irradiation

With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; sodium carbonate; 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; 1,1'-carbonyldiimidazole; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; ethyl acetate;