tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate
CAS No.:1449668-09-0
Molecular Formula:C₂₆H₃₅N₅O₂
Molecular Weight:449.596
Hs Code.:

Synonyms:tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

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Chemical Property of tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

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Technology Process of tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

There total 9 articles about tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-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:

: 607373-83-1
2-chloro-4-methoxy-5-nitro-pyridine

: 1449668-09-0
tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: tetrahydrofuran / 2 h / 20 °C

2.1: iron; acetic acid / 1 h / 50 - 80 °C

3.1: 4 h / 100 °C

4.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; sodium t-butanolate / 1,4-dioxane / 1.5 h / 100 °C / Inert atmosphere

5.1: sodium hexamethyldisilazane / N,N-dimethyl-formamide / 0.33 h / 0 °C

5.2: 0.5 h / 0 - 20 °C

6.1: palladium 10% on activated carbon; hydrogen / methanol / 60 °C / 45004.5 Torr

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium hexamethyldisilazane; iron; acetic acid; sodium t-butanolate; XPhos; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;

Reference yield:

: 1449506-74-4
tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)-5,6-dihydropyridine-1(2H)-carboxylate

: 1449668-09-0
tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: With palladium 10% on activated carbon; hydrogen; In methanol; at 60 ℃; under 45004.5 Torr;

Reference yield:

: 1449506-72-2
tert-butyl 4-(4-amino-3-ethylphenyl)-5,6-dihydropyridine-1(2H)-carboxylate

: 1449668-09-0
tert-butyl 4-(3-ethyl-4-(methyl(1-methyl-1H-imidazo[4,5-c]pyridin-6-yl)amino)phenyl)piperidine-1-carboxylate

Guidance literature:: Multi-step reaction with 3 steps

1.1: tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; XPhos; sodium t-butanolate / 1,4-dioxane / 1.5 h / 100 °C / Inert atmosphere

2.1: sodium hexamethyldisilazane / N,N-dimethyl-formamide / 0.33 h / 0 °C

2.2: 0.5 h / 0 - 20 °C

3.1: palladium 10% on activated carbon; hydrogen / methanol / 60 °C / 45004.5 Torr

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; palladium 10% on activated carbon; hydrogen; sodium hexamethyldisilazane; sodium t-butanolate; XPhos; In 1,4-dioxane; methanol; N,N-dimethyl-formamide;