4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

Base Information

Chemical Name:4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate
CAS No.:1575817-54-7
Molecular Formula:CH₂O₂*C₃₃H₄₁ClN₆O₂
Molecular Weight:635.206
Hs Code.:

4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

Synonyms:4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

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Chemical Property of 4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

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Technology Process of 4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

There total 10 articles about 4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate 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:

: 42564-51-2
4-fluoro-3-nitrobenzaldehyde

: 1575817-54-7
4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

Guidance literature:: Multi-step reaction with 9 steps

1.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 16 h / 20 °C

2.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C / Inert atmosphere

3.1: sodium hydroxide / 1,4-dioxane; water / 3 h / 10 - 20 °C

4.1: zinc; ammonium chloride / methanol / 2 h / 50 °C

5.1: ethanol / 16 h / 20 °C / Inert atmosphere

6.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

7.1: dichloromethane / 16 h / 0 - 20 °C

8.1: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 0.25 h / 0 °C / Inert atmosphere

9.1: hydrogen bromide; acetic acid / 0.5 h / 0 - 20 °C

9.2: 5 °C / pH Ca_. 11 - 12

With hydrogen bromide; sodium tris(acetoxy)borohydride; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; sodium hydroxide; zinc; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; 1,2-dichloro-ethane; acetonitrile;

Reference yield:

: 64-18-6
formic acid

: 1575819-65-6
benzyl (2-(4-chloro-benzamido)-1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-1H-benzo[d]imidazol-5-yl)methyl((S)-3,3-dimethylbutan-2-yl)carbamate

: 1575817-54-7
4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

Guidance literature:: benzyl (2-(4-chloro-benzamido)-1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-1H-benzo[d]imidazol-5-yl)methyl((S)-3,3-dimethylbutan-2-yl)carbamate; With hydrogen bromide; acetic acid; at 0 - 20 ℃; for 0.5h;

With sodium hydroxide; at 5 ℃; pH=Ca. 11 - 12;

formic acid;

Reference yield:

: 1575819-57-6
tert-butyl 2-((4-formyl-2-nitrophenylamino)methyl)pyrrolidine-1-carboxylate

: 1575817-54-7
4-chloro-N-(1-((1-(2-cyano-4-methylpent-2-enoyl)pyrrolidin-2-yl)methyl)-5-(((S)-3,3-dimethylbutan-2-ylamino)methyl)-1H-benzo[d]imidazol-2-yl)benzamide formate

Guidance literature:: Multi-step reaction with 8 steps

1.1: acetic acid; sodium tris(acetoxy)borohydride / 1,2-dichloro-ethane / 6 h / 20 °C / Inert atmosphere

2.1: sodium hydroxide / 1,4-dioxane; water / 3 h / 10 - 20 °C

3.1: zinc; ammonium chloride / methanol / 2 h / 50 °C

4.1: ethanol / 16 h / 20 °C / Inert atmosphere

5.1: benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine / dichloromethane / 4 h / 20 °C / Inert atmosphere

6.1: dichloromethane / 16 h / 0 - 20 °C

7.1: bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; triethylamine / dichloromethane / 0.25 h / 0 °C / Inert atmosphere

8.1: hydrogen bromide; acetic acid / 0.5 h / 0 - 20 °C

8.2: 5 °C / pH Ca_. 11 - 12

With hydrogen bromide; sodium tris(acetoxy)borohydride; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; sodium hydroxide; zinc; In 1,4-dioxane; methanol; ethanol; dichloromethane; water; 1,2-dichloro-ethane;