(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

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Chemical Name:(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide
CAS No.:1604811-18-8
Molecular Formula:C₃₂H₂₈N₈O₂
Molecular Weight:556.627
Hs Code.:

Synonyms:(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

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Chemical Property of (E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

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Technology Process of (E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

There total 10 articles about (E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)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:

: 1604811-63-3
(E)-N-(3-(5-cyano-4-(1-(phenylsulfonyl)-1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

: 1604811-18-8
(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; at 70 ℃; for 3h;

Reference yield:

: 66493-39-8
4-(N-tert-butoxycarbonyl)aminobenzoic acid

: 1604811-18-8
(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

Guidance literature:: Multi-step reaction with 7 steps

1.1: N-ethyl-N,N-diisopropylamine; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / dichloromethane; N,N-dimethyl-formamide / 0.5 h / 20 °C

1.2: 20 °C

2.1: palladium 10% on activated carbon; hydrogen / methanol / 96 h / 760.05 Torr

3.1: 1-methyl-pyrrolidin-2-one / 0.5 h / 175 °C

4.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; zinc; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / N,N-dimethyl acetamide / 2 h / 95 °C

5.1: sodium hydroxide / 1,4-dioxane / 2 h / 75 °C

6.1: oxalyl dichloride / tetrahydrofuran; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

6.2: 3 h / 20 °C

7.1: sodium hydroxide / tetrahydrofuran / 3 h / 70 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; oxalyl dichloride; palladium 10% on activated carbon; hydrogen; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium hydroxide; zinc; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; dichloromethane; N,N-dimethyl acetamide; N,N-dimethyl-formamide;

Reference yield:

: 1604811-55-3
tert-butyl 4-(3-(2-oxo-2-phenylethylideneamino)phenylcarbamoyl)phenylcarbamate

: 1604811-18-8
(E)-N-(3-(5-cyano-4-(1H-indol-3-yl)pyrimidin-2-ylamino)phenyl)-4-(4-(dimethylamino)but-2-enamido)benzamide

Guidance literature:: Multi-step reaction with 6 steps

1.1: palladium 10% on activated carbon; hydrogen / methanol / 96 h / 760.05 Torr

2.1: 1-methyl-pyrrolidin-2-one / 0.5 h / 175 °C

3.1: 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; zinc; tris-(dibenzylideneacetone)dipalladium⁽⁰⁾ / N,N-dimethyl acetamide / 2 h / 95 °C

4.1: sodium hydroxide / 1,4-dioxane / 2 h / 75 °C

5.1: oxalyl dichloride / tetrahydrofuran; N,N-dimethyl-formamide / 2 h / 0 - 20 °C

5.2: 3 h / 20 °C

6.1: sodium hydroxide / tetrahydrofuran / 3 h / 70 °C

With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; oxalyl dichloride; palladium 10% on activated carbon; hydrogen; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; sodium hydroxide; zinc; In tetrahydrofuran; 1,4-dioxane; 1-methyl-pyrrolidin-2-one; methanol; N,N-dimethyl acetamide; N,N-dimethyl-formamide;