2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

Base Information

Chemical Name:2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide
CAS No.:1125632-15-6
Molecular Formula:C₂₂H₁₄ClFN₄O₄
Molecular Weight:452.829
Hs Code.:

Synonyms:2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

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Chemical Property of 2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

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Technology Process of 2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

There total 7 articles about 2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide 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: 93.0%

: 4548-45-2
2-chloro-5-nitropyridine

: 1125632-14-5
2-chloro-3-(1-cyanocyclopropyl)-N-(2-fluoro-5-hydroxyphenyl)benzamide

: 1125632-15-6
2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 20 ℃; for 4h;
DOI:10.1021/jm300126x

Reference yield:

: 920759-93-9
methyl 2-chloro-3-methylbenzoate

: 1125632-15-6
2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile) / acetonitrile / 26 h / 90 °C

2.1: N,N-dimethyl-formamide / 1 h / 80 °C / Inert atmosphere

3.1: sodium hydride / dimethyl sulfoxide; mineral oil / 0.33 h / 20 °C / Cooling with ice

3.2: 16 h / 20 °C

4.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 18 h / 20 °C

5.1: thionyl chloride

6.1: sodium hydrogencarbonate / tetrahydrofuran; water / 20 °C

7.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C

With N-Bromosuccinimide; thionyl chloride; lithium hydroxide monohydrate; 2,2'-azobis(isobutyronitrile); water; sodium hydride; sodium hydrogencarbonate; potassium carbonate; In tetrahydrofuran; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1021/jm300126x

Reference yield:

: 920759-94-0
methyl 3-(bromomethyl)-2-chlorobenzoate

: 1125632-15-6
2-chloro-3-(1-cyanocycropropyl)-N-{2-fluoro-5-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: N,N-dimethyl-formamide / 1 h / 80 °C / Inert atmosphere

2.1: sodium hydride / dimethyl sulfoxide; mineral oil / 0.33 h / 20 °C / Cooling with ice

2.2: 16 h / 20 °C

3.1: lithium hydroxide monohydrate; water / tetrahydrofuran; methanol / 18 h / 20 °C

4.1: thionyl chloride

5.1: sodium hydrogencarbonate / tetrahydrofuran; water / 20 °C

6.1: potassium carbonate / N,N-dimethyl-formamide / 4 h / 20 °C

With thionyl chloride; lithium hydroxide monohydrate; water; sodium hydride; sodium hydrogencarbonate; potassium carbonate; In tetrahydrofuran; methanol; water; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;
DOI:10.1021/jm300126x