5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

Base Information

Chemical Name:5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline
CAS No.:1345336-91-5
Molecular Formula:C₁₉H₁₂BrCl₂N₅O₃
Molecular Weight:509.146
Hs Code.:

Synonyms:5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

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Chemical Property of 5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

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Technology Process of 5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

There total 7 articles about 5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline 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:

: 1345336-85-7
5-(3-bromo-5-chlorophenoxy)-4-chloro-N-(4-methoxybenzyl)-2-nitroaniline

: 1345336-91-5
5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

Guidance literature:: Multi-step reaction with 3 steps

1: trifluoroacetic acid / 1 h / 75 °C / Inert atmosphere

2: caesium carbonate / N,N-dimethyl-formamide / 96 h / 20 °C / Inert atmosphere

3: trifluoroacetic acid / 0.5 h / Inert atmosphere

With caesium carbonate; trifluoroacetic acid; In N,N-dimethyl-formamide;
DOI:10.1021/jm2010173

Reference yield:

: 1345336-82-4
4,5-dichloro-N-(methoxybenzyl)-2-nitroaniline

: 1345336-91-5
5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

Guidance literature:: Multi-step reaction with 4 steps

1: potassium carbonate / 1-methyl-pyrrolidin-2-one / Heating; Inert atmosphere

2: trifluoroacetic acid / 1 h / 75 °C / Inert atmosphere

3: caesium carbonate / N,N-dimethyl-formamide / 96 h / 20 °C / Inert atmosphere

4: trifluoroacetic acid / 0.5 h / Inert atmosphere

With potassium carbonate; caesium carbonate; trifluoroacetic acid; In 1-methyl-pyrrolidin-2-one; N,N-dimethyl-formamide;
DOI:10.1021/jm2010173

Reference yield:

: 1345336-88-0
5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitroaniline

: 1345336-91-5
5-(3-bromo-5-chlorophenoxy)-4-chloro-2-nitro-N-(1H-pyrazolo[3,4-b]pyridin-3-ylmethyl)aniline

Guidance literature:: Multi-step reaction with 2 steps

1: caesium carbonate / N,N-dimethyl-formamide / 96 h / 20 °C / Inert atmosphere

2: trifluoroacetic acid / 0.5 h / Inert atmosphere

With caesium carbonate; trifluoroacetic acid; In N,N-dimethyl-formamide;
DOI:10.1021/jm2010173