4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

Base Information

Chemical Name:4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile
CAS No.:1309431-03-5
Molecular Formula:C₁₅H₅ClF₂N₄O₃
Molecular Weight:362.68
Hs Code.:

Synonyms:4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

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Chemical Property of 4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

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Technology Process of 4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

There total 4 articles about 4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile 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:

: 920966-02-5
4-chloro-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

: 260552-98-5
2,6-difluoro-3-nitrobenzoic acid chloride

: 1309431-03-5
4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

Guidance literature:: With trifluorormethanesulfonic acid; at 0 - 20 ℃; for 96h;

Reference yield:

: 83141-10-0
2,6-difluoro-3-nitrobenzoic acid

: 1309431-03-5
4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / N,N-dimethyl-formamide / 80 °C

2: trifluorormethanesulfonic acid / 96 h / 0 - 20 °C

With thionyl chloride; trifluorormethanesulfonic acid; In N,N-dimethyl-formamide;

Reference yield:

: 446-35-5
2,4-Difluoronitrobenzene

: 1309431-03-5
4-chloro-3-(2,6-difluoro-3-nitro-benzoyl)-1H-pyrrolo[2,3-b]pyridine-5-carbonitrile

Guidance literature:: Multi-step reaction with 4 steps

1.1: tetrahydrofuran / 1 h / -78 °C

1.2: 3 h / -78 - 20 °C

2.1: sodium hydroxide; water / tetrahydrofuran / 2 h

3.1: thionyl chloride / N,N-dimethyl-formamide / 80 °C

4.1: trifluorormethanesulfonic acid / 96 h / 0 - 20 °C

With thionyl chloride; trifluorormethanesulfonic acid; water; sodium hydroxide; In tetrahydrofuran; N,N-dimethyl-formamide;