N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

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Chemical Name:N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide
CAS No.:911313-02-5
Molecular Formula:C₂₇H₄₀ClN₃O₂Si
Molecular Weight:502.172
Hs Code.:

Synonyms:N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

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Chemical Property of N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

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Technology Process of N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

There total 3 articles about N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide 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:

: 911312-98-6
2-chloro-N-{2-[((R)-2-hydroxy-1-methylethylamino)methyl]-phenyl}-4-pyrrolidin-1-ylbenzamide

: 18162-48-6
tert-butyldimethylsilyl chloride

: 911313-02-5
N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

Guidance literature:: With 1H-imidazole; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 192513-60-3
2-chloro-(4-pyrrolidin-1-yl) benzoic acid

: 911313-02-5
N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

Guidance literature:: Multi-step reaction with 5 steps

1: thionyl chloride / 1-methyl-pyrrolidin-2-one / 1.5 h / 20 °C

2: triethylamine / dichloromethane / 66 h / 0 - 20 °C

3: potassium carbonate / ethanol / 1 h / Heating / reflux

4: sodium tetrahydroborate; ethanol / 20 °C / Heating / reflux

5: 1H-imidazole / N,N-dimethyl-formamide / 20 °C

With 1H-imidazole; sodium tetrahydroborate; thionyl chloride; ethanol; potassium carbonate; triethylamine; 1-methyl-pyrrolidin-2-one; In ethanol; dichloromethane; N,N-dimethyl-formamide;

Reference yield:

: 911312-93-1
2-chloro-4-pyrrolidin-1-ylbenzoyl chloride

: 911313-02-5
N-(2-{[(R)-2-(tert-butyldimethylsilanyloxy)-1-methylethylamino]methyl}phenyl)-2-chloro-4-pyrrolidin-1-ylbenzamide

Guidance literature:: Multi-step reaction with 4 steps

1: triethylamine / dichloromethane / 66 h / 0 - 20 °C

2: potassium carbonate / ethanol / 1 h / Heating / reflux

3: sodium tetrahydroborate; ethanol / 20 °C / Heating / reflux

4: 1H-imidazole / N,N-dimethyl-formamide / 20 °C

With 1H-imidazole; sodium tetrahydroborate; ethanol; potassium carbonate; triethylamine; In ethanol; dichloromethane; N,N-dimethyl-formamide;