N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

Base Information

Chemical Name:N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide
CAS No.:1421373-50-3
Molecular Formula:C₂₆H₂₇ClN₈O₂
Molecular Weight:519.006
Hs Code.:

Synonyms:N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

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Chemical Property of N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

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Technology Process of N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

There total 8 articles about N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide 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: 73.0%

: 1421372-29-3
N'-(5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)-4-methoxy-6-(4-methylpiperazine-1-yl)benzene-1,3-diamine

: 814-68-6,25189-84-8
acryloyl chloride

: 1421373-50-3
N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 0.75h;

Reference yield:

: 1224709-13-0
3-(2,5-dichloropyrimidin-4-yl)pyrazolo[1,5-a]pyridine

: 1421373-50-3
N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 4 steps

1: toluene-4-sulfonic acid / 18 h / 125 °C

2: 2,2,2-trifluoroethanol / 1 h / 140 °C / Microwave irradiation

3: iron; ammonium chloride / water; ethanol / 2 h / Reflux

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.75 h / 20 °C

With iron; ammonium chloride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; 2,2,2-trifluoroethanol; water;

Reference yield:

: 1224708-12-6
4-[(E)-2-butoxyethenyl]-2,5-dichloropyrimidine

: 1421373-50-3
N-(5-((5-chloro-4-(pyrazolo[1,5-a]pyridin-3-yl)pyrimidin-2-yl)amino)-4-methoxy-2-(4-methylpiperazin-1-yl)phenyl)acrylamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium hydroxide; potassium carbonate / dimethyl sulfoxide / 5.5 h / 20 - 90 °C

2: toluene-4-sulfonic acid / 18 h / 125 °C

3: 2,2,2-trifluoroethanol / 1 h / 140 °C / Microwave irradiation

4: iron; ammonium chloride / water; ethanol / 2 h / Reflux

5: N-ethyl-N,N-diisopropylamine / dichloromethane / 0.75 h / 20 °C

With iron; potassium carbonate; ammonium chloride; toluene-4-sulfonic acid; N-ethyl-N,N-diisopropylamine; potassium hydroxide; In ethanol; dichloromethane; 2,2,2-trifluoroethanol; water; dimethyl sulfoxide;