5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

Base Information

Chemical Name:5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one
CAS No.:1416308-78-5
Molecular Formula:C₁₈H₂₆N₄O
Molecular Weight:314.431
Hs Code.:

Synonyms:5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

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Chemical Property of 5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

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Technology Process of 5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

There total 6 articles about 5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one 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:

: 1416309-03-9
tert-butyl {4-[1-(2,2-dimethylpropyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-5-yl]cyclohex-3-en-1-yl}carbamate

: 1416308-78-5
5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

Guidance literature:: With hydrogenchloride; In methanol; dichloromethane; ethyl acetate;

Reference yield:

: 16013-85-7,136901-10-5
2,6-dicholoro-3-nitropyridine

: 1416308-78-5
5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

Guidance literature:: Multi-step reaction with 6 steps

1: sodium carbonate / ethanol; methanol / 3 h / 20 °C / Inert atmosphere

2: hydrogenchloride; tin(II) chloride dihdyrate / water / Reflux

3: N,N-dimethyl-formamide / 80 °C

4: caesium carbonate / 1-methyl-pyrrolidin-2-one / 90 °C / Inert atmosphere

5: caesium carbonate; water / bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 0.17 h / 100 °C / Microwave Irradiation

6: hydrogenchloride / dichloromethane; ethyl acetate; methanol

With hydrogenchloride; tin(II) chloride dihdyrate; water; sodium carbonate; caesium carbonate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; ethanol; dichloromethane; water; ethyl acetate; N,N-dimethyl-formamide;

Reference yield:

: 1276676-86-8
5-chloro-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

: 1416308-78-5
5-(4-aminocyclohex-1-en-1-yl)-1-(2,2-dimethylpropyl)-3-methyl-1,3-dihydro-2H-imidazo[4,5-b]pyridin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate; water / bis(tri-t-butylphosphine)palladium⁽⁰⁾ / 1,4-dioxane / 0.17 h / 100 °C / Microwave Irradiation

2: hydrogenchloride / dichloromethane; ethyl acetate; methanol

With hydrogenchloride; water; caesium carbonate; bis(tri-t-butylphosphine)palladium⁽⁰⁾; In 1,4-dioxane; methanol; dichloromethane; ethyl acetate;