(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

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Chemical Name:(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester
CAS No.:466651-95-6
Molecular Formula:C₃₁H₄₇N₇O₇S₂Si
Molecular Weight:721.974
Hs Code.:

(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

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Chemical Property of (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

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Technology Process of (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

There total 2 articles about (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl 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:

: 20980-22-7
N-(2-pyridinyl)piperazine

: 466651-79-6
(2S,4R)-2-[3-(2-chloroethanesulfonyl)thiazolidin-2-yl]-4-(tert-butyldimethylsilanyloxy)-1-(p-nitrobenzyloxycarbonyl)pyrrolidine

: 466651-95-6
(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: With potassium carbonate; In N,N-dimethyl-formamide; at 90 ℃; for 10h;
DOI:10.1002/1521-4184(200204)335:4<152::AID-ARDP152>3.0.CO;2-B

Reference yield:

: 137049-21-9
(2S,4R)-2-formyl-4-tert-butyldimethylsilyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

: 466651-95-6
(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87.2 percent / NaHCO₃ / ethanol; H₂O / 24 h / 20 °C

2: 76.9 percent / Et₃N / CH₂Cl₂ / 1 h / 0 °C

3: K₂CO₃ / dimethylformamide / 10 h / 90 °C

With sodium hydrogencarbonate; potassium carbonate; triethylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1002/1521-4184(200204)335:4<152::AID-ARDP152>3.0.CO;2-B

Reference yield:

: 124-63-0
methanesulfonyl chloride

: 466651-95-6
(2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

: (2S,4R)-4-Methanesulfonyloxy-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester

Guidance literature:: (2S,4R)-4-(tert-Butyl-dimethyl-silanyloxy)-2-{3-[2-(4-pyrimidin-2-yl-piperazin-1-yl)-ethanesulfonyl]-thiazolidin-2-yl}-pyrrolidine-1-carboxylic acid 4-nitro-benzyl ester; With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃;

methanesulfonyl chloride; With triethylamine; In dichloromethane; at 0 ℃;
DOI:10.1002/1521-4184(200204)335:4<152::AID-ARDP152>3.0.CO;2-B