5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Chemical Name:5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester
CAS No.:1240322-52-4
Molecular Formula:C₃₂H₃₅F₃N₆O₃
Molecular Weight:608.664
Hs Code.:

5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Chemical Property of 5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Technology Process of 5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

There total 5 articles about 5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl 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: 28.0%

: 1240322-52-4
5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: 1616628-95-5
5-((2-methyl-5-nitrobenzyl)amino)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

: 1240322-52-4
5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: palladium 10% on activated carbon; hydrogen; hydrogenchloride / methanol; water / 48 h / 20 °C / 22502.3 Torr / Autoclave

2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 0.25 h / 20 °C

2.2: 20 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.6b00087

Reference yield:

: 952182-18-2
5-amino-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

: 1240322-52-4
5-{(5-[4-((3-(dimethylamino)pyrrolidin-1-yl)methyl)-3-(trifluoromethyl)benzoylamino]-2-methylbenzyl)amino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: acetic acid / methanol / 2 h / 20 °C

2.1: sodium cyanoborohydride / methanol / 48 h / 20 °C / Inert atmosphere

3.1: palladium 10% on activated carbon; hydrogen; hydrogenchloride / methanol; water / 48 h / 20 °C / 22502.3 Torr / Autoclave

4.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 0.25 h / 20 °C

4.2: 20 °C

With hydrogenchloride; palladium 10% on activated carbon; hydrogen; sodium cyanoborohydride; acetic acid; N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In methanol; water; N,N-dimethyl-formamide;
DOI:10.1021/acs.jmedchem.6b00087