N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

Base Information

Chemical Name:N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide
CAS No.:1333127-18-6
Molecular Formula:C₂₈H₂₄ClF₆N₅O₆
Molecular Weight:675.972
Hs Code.:

Synonyms:N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

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Chemical Property of N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

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Technology Process of N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

There total 7 articles about N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide 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:

: 280773-17-3
2-amino-N-(5-chloro-pyridin-2-yl)-5-methoxy-benzamide

: 1333127-11-9
2-[3-(trifluoroacetylamino)propoxy]-4-[trifluoroacetyl-(methyl)amino]benzoic acid

: 1333127-18-6
N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In tetrahydrofuran; for 48h;

Reference yield:

: 65-49-6
4-Aminosalicylic acid

: 1333127-18-6
N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium hydroxide / 1,4-dioxane; water / 24 h

2.1: potassium carbonate / 1 h / 110 °C

3.1: hydrogenchloride / ethanol; water / 2 h

4.1: zinc; sodium hydroxide / water / 4 h / 60 °C

4.2: pH 4 - 5

5.1: sodium hydroxide; water / ethanol / 10 h / 100 °C / Sealed ampoule

5.2: pH 8 - 9

6.1: 1 h

7.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 48 h

With hydrogenchloride; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; zinc; In tetrahydrofuran; 1,4-dioxane; ethanol; water;

Reference yield:

: 184033-42-9
4-[(tert-butoxycarbonyl)amino]-2-hydroxybenzoic acid

: 1333127-18-6
N-(5-chloropyridine-2-yl)-2-[4-(trifluoroacetyl(methyl)amino)-2-(3-(trifluoroacetylamino)propoxy)phenylcarbonylamino]-5-methoxybenzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium carbonate / 1 h / 110 °C

2.1: hydrogenchloride / ethanol; water / 2 h

3.1: zinc; sodium hydroxide / water / 4 h / 60 °C

3.2: pH 4 - 5

4.1: sodium hydroxide; water / ethanol / 10 h / 100 °C / Sealed ampoule

4.2: pH 8 - 9

5.1: 1 h

6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride / tetrahydrofuran / 48 h

With hydrogenchloride; water; potassium carbonate; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; zinc; In tetrahydrofuran; ethanol; water;