(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

Base Information

Chemical Name:(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester
CAS No.:1314945-44-2
Molecular Formula:C₂₆H₃₂N₆O₃
Molecular Weight:476.578
Hs Code.:

Synonyms:(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

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Chemical Property of (R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

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Technology Process of (R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

There total 7 articles about (R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester 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: 29.0%

: 1314945-35-1
(R)-1-[1-(2-cyano-benzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b] pyridin-7-yl] piperidin-3-yl tert-butyl carbamate

: 74-88-4
methyl iodide

: 1314945-44-2
(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

Guidance literature:: (R)-1-[1-(2-cyano-benzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b] pyridin-7-yl] piperidin-3-yl tert-butyl carbamate; With sodium hydride; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

methyl iodide; In N,N-dimethyl-formamide; at 0 - 20 ℃; for 4h;

Reference yield:

: 309956-78-3,172603-05-3
(R)-piperidin-3-ylcarbamic acid tert-butyl ester

: 1314945-44-2
(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / ethanol / 2 h / 20 °C

2.1: butan-1-ol; ethanol / 24 h / 110 °C

3.1: hydrogen / palladium 10% on activated carbon / methanol / 3 h / 20 °C

4.1: triethylamine / tetrahydrofuran / 0.5 h / -10 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / -10 - 20 °C

6.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

6.2: 4 h / 0 - 20 °C

With hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; butan-1-ol;

Reference yield:

: 5975-12-2
2,4-dichloro-3-nitro-pyridine

: 1314945-44-2
(R)-1-[1-(2-cyanobenzyl)-3-methyl-2-oxo-2,3-dihydro-1H-imidazo[4,5-b]pyridin-7-yl]piperidin-3-yl(methyl)carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1.1: triethylamine / ethanol / 2 h / 20 °C

2.1: butan-1-ol; ethanol / 24 h / 110 °C

3.1: hydrogen / palladium 10% on activated carbon / methanol / 3 h / 20 °C

4.1: triethylamine / tetrahydrofuran / 0.5 h / -10 °C

5.1: potassium carbonate / N,N-dimethyl-formamide / 1 h / -10 - 20 °C

6.1: sodium hydride / N,N-dimethyl-formamide / 0.5 h / 0 °C

6.2: 4 h / 0 - 20 °C

With hydrogen; sodium hydride; potassium carbonate; triethylamine; palladium 10% on activated carbon; In tetrahydrofuran; methanol; ethanol; N,N-dimethyl-formamide; butan-1-ol;