N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

Base Information

Chemical Name:N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide
CAS No.:1383475-07-7
Molecular Formula:C₃₂H₃₆N₈O₃
Molecular Weight:580.69
Hs Code.:

Synonyms:N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

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Chemical Property of N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

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Technology Process of N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

There total 7 articles about N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-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:

: 1313408-94-4
7-[2-(4-methylpiperazin-1-yl)ethoxy]imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester

: 1383475-06-6
3-((4-amino-1H-indazol-1-yl)methyl)-N_.N-dimethylbenzamide

: 1383475-07-7
N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: 7-[2-(4-methylpiperazin-1-yl)ethoxy]imidazo[1,2-a]pyridine-3-carboxylic acid ethyl ester; 3-((4-amino-1H-indazol-1-yl)methyl)-N_.N-dimethylbenzamide; With lithium hexamethyldisilazane; In tetrahydrofuran; at -5 - 0 ℃; for 1h;

With ammonium chloride; Saturated solution;

Reference yield:

: 63024-77-1
3-(Chloromethyl)benzoyl chloride

: 1383475-07-7
N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: triethylamine / dichloromethane; tetrahydrofuran / 4 h / 0 - 20 °C

2.1: N,N,N′,N′-tetramethyl-N″-tert-butylguanidine / acetonitrile / 5 h / 20 °C

3.1: zinc; ammonium chloride / water; methanol / 0 - 20 °C / Saturated solution

4.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -5 - 0 °C

4.2: Saturated solution

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; ammonium chloride; triethylamine; lithium hexamethyldisilazane; zinc; In tetrahydrofuran; methanol; dichloromethane; water; acetonitrile;

Reference yield:

: 885521-22-2
3-iodo-4-nitro-1H-indazole

: 1383475-07-7
N-(1-(3-(dimethylcarbamoyl)benzyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: N,N,N′,N′-tetramethyl-N″-tert-butylguanidine / acetonitrile / 5 h / 20 °C

2.1: zinc; ammonium chloride / water; methanol / 0 - 20 °C / Saturated solution

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 1 h / -5 - 0 °C

3.2: Saturated solution

With N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; ammonium chloride; lithium hexamethyldisilazane; zinc; In tetrahydrofuran; methanol; water; acetonitrile;