5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Base Information

Chemical Name:5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester
CAS No.:1616670-36-0
Molecular Formula:C₃₀H₃₀ClF₃N₆O₃
Molecular Weight:615.055
Hs Code.:

5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

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

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

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

There total 5 articles about 5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-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: 37.0%

: 859027-02-4,859282-11-4
4-((4-methylpiperazin-1-yl)methyl)-3-(trifluoromethyl) benzoic acid

: 1643323-24-3
C₁₆H₁₅ClN₄O₂

: 1616670-36-0
5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-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:

: 116419-94-4
4-methyl-3-(trifluoromethyl)benzoic acid methyl ester

: 1616670-36-0
5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: N-Bromosuccinimide; Perbenzoic acid / tetrachloromethane; water / 6 h / Reflux

2: potassium carbonate / acetonitrile / Reflux; Inert atmosphere

3: lithium hydroxide; water / tetrahydrofuran / 4 h / Reflux

4: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 12 h / 20 °C

With N-Bromosuccinimide; Perbenzoic acid; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; tetrachloromethane; water; N,N-dimethyl-formamide; acetonitrile;

Reference yield:

: 261952-01-6
4-methyl-3-(trifluoromethyl)benzoic acid

: 1616670-36-0
5-{2-chloro-5-[4-(4-methylpiperazin-1-ylmethyl)-3-trifluoromethylbenzoylamino]-benzylamino}-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 5 steps

1: sulfuric acid / Reflux

2: N-Bromosuccinimide; Perbenzoic acid / tetrachloromethane; water / 6 h / Reflux

3: potassium carbonate / acetonitrile / Reflux; Inert atmosphere

4: lithium hydroxide; water / tetrahydrofuran / 4 h / Reflux

5: N-ethyl-N,N-diisopropylamine; HATU / N,N-dimethyl-formamide / 12 h / 20 °C

With N-Bromosuccinimide; Perbenzoic acid; sulfuric acid; water; potassium carbonate; N-ethyl-N,N-diisopropylamine; HATU; lithium hydroxide; In tetrahydrofuran; tetrachloromethane; water; N,N-dimethyl-formamide; acetonitrile;