N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

Base Information

Chemical Name:N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide
CAS No.:1439936-34-1
Molecular Formula:C₂₆H₂₅N₃O₃S
Molecular Weight:459.569
Hs Code.:

Synonyms:N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

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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 N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

Chemical Property:

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Technology Process of N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

There total 5 articles about N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide 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: 79.0%

: 1439936-37-4
4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-amine

: 39178-35-3
isonicotinoyl chloride hydrochloride

: 1439936-34-1
N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃;

Reference yield:

: 106-41-2
4-bromo-phenol

: 1439936-34-1
N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / dimethyl sulfoxide / 60 °C

2: caesium carbonate; copper(l) iodide; N,N-dimethylglycine hydrochoride / 1,4-dioxane / 48 h / 90 °C

3: tetrabutylammomium bromide / acetonitrile / 16 h / 20 °C

4: ethanol / 4 h / Reflux

5: triethylamine / dichloromethane / 20 °C

With copper(l) iodide; tetrabutylammomium bromide; N,N-dimethylglycine hydrochoride; potassium carbonate; caesium carbonate; triethylamine; In 1,4-dioxane; ethanol; dichloromethane; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 6967-88-0
1-bromo-4-isopropoxybenzene

: 1439936-34-1
N-{4-(4-(4-isopropoxyphenoxy)-2,6-dimethylphenyl)thiazol-2-yl}isonicotinamide

Guidance literature:: Multi-step reaction with 4 steps

1: caesium carbonate; copper(l) iodide; N,N-dimethylglycine hydrochoride / 1,4-dioxane / 48 h / 90 °C

2: tetrabutylammomium bromide / acetonitrile / 16 h / 20 °C

3: ethanol / 4 h / Reflux

4: triethylamine / dichloromethane / 20 °C

With copper(l) iodide; tetrabutylammomium bromide; N,N-dimethylglycine hydrochoride; caesium carbonate; triethylamine; In 1,4-dioxane; ethanol; dichloromethane; acetonitrile;