N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

Base Information

Chemical Name:N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide
CAS No.:1262414-17-4
Molecular Formula:C₂₁H₂₅ClN₄O₄S
Molecular Weight:464.973
Hs Code.:

Synonyms:N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

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Chemical Property of N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

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Technology Process of N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

There total 9 articles about N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide 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:

: 5398-44-7
2,6-dichloropyridine-4-carboxylic acid

: 1262414-17-4
N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: sodium hydroxide / water / 34 - 70 °C

1.2: 20 °C

2.1: sulfuric acid / 24 h / Reflux

3.1: Pd(dppf) / tetrahydrofuran / 18 h / 85 °C / Inert atmosphere

4.1: sodium hydroxide; water / ethanol / 1 h / 80 °C

5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.08 h / 20 °C

5.2: 18 h / 20 °C

6.1: 1,4-dioxane / 3 h / 80 °C

With water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; sulfuric acid; In tetrahydrofuran; 1,4-dioxane; ethanol; water; N,N-dimethyl-formamide; 3.1: Negishi Coupling Reaction;

Reference yield:

: 42521-10-8
2-chloro-6-methoxyisonicotinic acid methyl ester

: 1262414-17-4
N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: Pd(dppf) / tetrahydrofuran / 18 h / 85 °C / Inert atmosphere

2.1: sodium hydroxide; water / ethanol / 1 h / 80 °C

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 0.08 h / 20 °C

3.2: 18 h / 20 °C

4.1: 1,4-dioxane / 3 h / 80 °C

With water; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; Pd(dppf); In tetrahydrofuran; 1,4-dioxane; ethanol; N,N-dimethyl-formamide; 1.1: Negishi Coupling Reaction;

Reference yield:

: 1122089-63-7
2-methoxy-6-(pentan-3-yl)isonicotinic acid

: 1262413-98-8
3-chloro-N-hydroxy-4-methanesulfonylamino-5-methyl-benzamidine

: 1262414-17-4
N-(2-chloro-4-{5-[2-(1-ethyl-propyl)-6-methoxy-pyridin-4-yl]-[1,2,4]oxadiazol-3-yl}-6-methyl-phenyl)-methanesulfonamide

Guidance literature:: 2-methoxy-6-(pentan-3-yl)isonicotinic acid; With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In N,N-dimethyl-formamide; at 20 ℃; for 0.0833333h;

3-chloro-N-hydroxy-4-methanesulfonylamino-5-methyl-benzamidine; In N,N-dimethyl-formamide; at 20 ℃; for 18h;