5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Chemical Name:5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester
CAS No.:1616689-08-7
Molecular Formula:C₃₁H₃₅N₅O₃
Molecular Weight:525.651
Hs Code.:

Synonyms:5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Chemical Property of 5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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Technology Process of 5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

There total 5 articles about 5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-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: 42.0%

: 1616689-68-9
5-[2-(5-amino-2-methylphenyl)-ethyl]-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

: 106261-48-7
4-(4-methylpiperazin-1-ylmethyl)benzoic acid

: 1616689-08-7
5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-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 ℃; Schlenk technique; Inert atmosphere;
DOI:10.1021/acs.jmedchem.6b00087

Reference yield: 42.0%

: 1616689-08-7
5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: With N-ethyl-N,N-diisopropylamine; HATU; In N,N-dimethyl-formamide; at 20 ℃; for 12h;

Reference yield:

: 952182-16-0
5-cyano-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

: 1616689-08-7
5-(2-{2-methyl-5-[4-(4-methylpiperazin-1-ylmethyl)-benzoylamino]-phenyl}-ethyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine; water; acetic acid; hydrogen / 7500.75 Torr

2: lithium hydroxide / methanol / Reflux

3: palladium 10% on activated carbon; hydrogen / N,N-dimethyl-formamide / 24 h / 20 °C / 7500.75 Torr

4: 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 / 20 °C / Schlenk technique; Inert atmosphere

With pyridine; palladium 10% on activated carbon; water; hydrogen; 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; lithium hydroxide; In methanol; N,N-dimethyl-formamide; 2: |Wittig Olefination;
DOI:10.1021/acs.jmedchem.6b00087