N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

Base Information

Chemical Name:N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide
CAS No.:1092394-91-6
Molecular Formula:C₂₀H₁₇N₅O₂
Molecular Weight:359.387
Hs Code.:

Synonyms:N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

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Chemical Property of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

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Technology Process of N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

There total 7 articles about N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-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: 22.0%

: 1092394-52-9
N-(3-{[1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl]oxy}phenyl)-6-methylpyridine-2-carboxamide

: 1092394-91-6
N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

Guidance literature:: N-(3-{[1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl]oxy}phenyl)-6-methylpyridine-2-carboxamide; With trifluoroacetic anhydride; In tetrahydrofuran; at 20 ℃; for 1h;

With ethanol; water; sodium carbonate; at 60 ℃; for 24h;

Reference yield:

: 39856-50-3
5-bromo2-nitropyridine

: 1092394-91-6
N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: caesium carbonate / N,N-dimethyl-formamide / 15 h / 50 °C

2.1: hydrogen / palladium on activated charcoal / methanol / 12 h / 20 °C

3.1: oxalyl dichloride / N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 0 - 20 °C

3.2: 65 h / 20 °C

4.1: pyridine / 2 h / 80 °C

5.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.33 h / 20 °C

5.2: 16 h / 20 °C

6.1: trifluoroacetic anhydride / tetrahydrofuran / 1 h / 20 °C

6.2: 24 h / 60 °C

With pyridine; oxalyl dichloride; hydrogen; caesium carbonate; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; palladium on activated charcoal; N,N-dimethyl-formamide; In tetrahydrofuran; methanol; N,N-dimethyl-formamide;

Reference yield:

: 1092393-85-5
5-(3-aminophenoxy)pyridin-2-amine

: 1092394-91-6
N-{3-[(2-aminoimidazo[1,2-a]pyridin-6-yl)oxy]phenyl}-6-methylpyridine-2-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: oxalyl dichloride / N,N-dimethyl-formamide / tetrahydrofuran / 2 h / 0 - 20 °C

1.2: 65 h / 20 °C

2.1: pyridine / 2 h / 80 °C

3.1: N-ethyl-N,N-diisopropylamine / N,N-dimethyl-formamide / 0.33 h / 20 °C

3.2: 16 h / 20 °C

4.1: trifluoroacetic anhydride / tetrahydrofuran / 1 h / 20 °C

4.2: 24 h / 60 °C

With pyridine; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; trifluoroacetic anhydride; N,N-dimethyl-formamide; In tetrahydrofuran; N,N-dimethyl-formamide;