(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Name:(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS No.:850003-06-4
Molecular Formula:C₂₇H₄₁N₃O₄Si
Molecular Weight:499.726
Hs Code.:

Synonyms:(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

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Chemical Property of (2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

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Technology Process of (2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

There total 4 articles about (2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester 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: 67.0%

: 757247-71-5
tert-butyl (2S,3S)-3-{[tert-butyl(dimethyl)silyl]oxy}-2-formylpyrrolidine-1-carboxylate

: 13143-47-0
1-(4-aminophenyl)pyridin-2(1H)-one

: 850003-06-4
(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: With sodium tris(acetoxy)borohydride; In acetic acid; 1,2-dichloro-ethane; at 20 ℃; for 1h;

Reference yield:

: 142-08-5
2-hydroxypyridin

: 850003-06-4
(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: potassium phosphate; copper(l) iodide; N,N-dimethylethylenediamine / toluene / Heating / reflux

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

With potassium phosphate; copper(l) iodide; sodium tris(acetoxy)borohydride; N,N-dimethylethylenediamine; In acetic acid; 1,2-dichloro-ethane; toluene;

Reference yield:

: 4298-08-2
trans-3-hydroxy-L-proline

: 850003-06-4
(2R,3S)-3-(tert-butyl-dimethyl-silanyloxy)-2-{[4-(2-oxo-2H-pyridin-1-yl)-phenylamino]-methyl}-pyrrolidine-1-carboxylic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 6 steps

1: hydrogenchloride / 6.17 h / 0 - 20 °C

2: triethylamine / dichloromethane / 0 - 20 °C

3: 1H-imidazole / dichloromethane / 20 °C

4: lithium triethylborohydride / tetrahydrofuran / 3.67 h / -78 - 20 °C

5: Dess-Martin periodane / 2 - 4 h / 0 - 20 °C

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

With 1H-imidazole; hydrogenchloride; sodium tris(acetoxy)borohydride; lithium triethylborohydride; Dess-Martin periodane; triethylamine; In tetrahydrofuran; dichloromethane; acetic acid; 1,2-dichloro-ethane;