5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Base Information

Chemical Name:5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide
CAS No.:138572-72-2
Molecular Formula:C₂₄H₃₃ClN₂O₃
Molecular Weight:432.991
Hs Code.:

Synonyms:5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Suppliers and Price of 5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of 5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

There total 8 articles about 5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)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:

: 321-14-2
5-chloro-2-hydroxybenzoic acid

: 138572-72-2
5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Guidance literature:: Multi-step reaction with 8 steps

1: 1.) thionyl chloride / 1.) 20 deg C, 1.5 h, 2.) reflux

2: 810.0 g / K₂CO₃ / acetone / 24 h / Heating

3: 71.2 percent / cesium carbonate / 4 h / 155 - 175 °C

4: 86 percent / H₂ / platinum dioxide / methanol / 1292.9 Torr

5: 67 percent / K₂CO₃ / dimethylformamide / 4 h / 80 °C

6: 80 percent / 1 N aq. NaOH / methanol / Ambient temperature

7: 1.5 g / thionyl chloride / CH₂Cl₂ / 2 h / Heating

8: CHCl₃ / 1 h / Heating

With sodium hydroxide; thionyl chloride; hydrogen; potassium carbonate; caesium carbonate; platinum(IV) oxide; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm00083a014

Reference yield:

: 4068-78-4
methyl 5-chloro-2-hydroxybenzoate

: 138572-72-2
5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1: 810.0 g / K₂CO₃ / acetone / 24 h / Heating

2: 71.2 percent / cesium carbonate / 4 h / 155 - 175 °C

3: 86 percent / H₂ / platinum dioxide / methanol / 1292.9 Torr

4: 67 percent / K₂CO₃ / dimethylformamide / 4 h / 80 °C

5: 80 percent / 1 N aq. NaOH / methanol / Ambient temperature

6: 1.5 g / thionyl chloride / CH₂Cl₂ / 2 h / Heating

7: CHCl₃ / 1 h / Heating

With sodium hydroxide; thionyl chloride; hydrogen; potassium carbonate; caesium carbonate; platinum(IV) oxide; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jm00083a014

Reference yield:

: 125341-28-8
methyl 5-chloro-2-(3'-cyclohexenyl)salicylate

: 138572-72-2
5-chloro-3-cyclohexyl-2-(2'-oxo-1'-methylpropoxy)-N-(1-azabicyclo<2.2.2>oct-3-yl)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1: 71.2 percent / cesium carbonate / 4 h / 155 - 175 °C

2: 86 percent / H₂ / platinum dioxide / methanol / 1292.9 Torr

3: 67 percent / K₂CO₃ / dimethylformamide / 4 h / 80 °C

4: 80 percent / 1 N aq. NaOH / methanol / Ambient temperature

5: 1.5 g / thionyl chloride / CH₂Cl₂ / 2 h / Heating

6: CHCl₃ / 1 h / Heating

With sodium hydroxide; thionyl chloride; hydrogen; potassium carbonate; caesium carbonate; platinum(IV) oxide; In methanol; dichloromethane; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm00083a014