{3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester

Base Information

• Chemical Name: {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester
• CAS No.: 872315-98-5
• Molecular Formula: C₄₂H₆₃N₅O₉Si₂
• Molecular Weight: 838.161
• Mol file: 872315-98-5.mol

Synonyms:{3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester

Chemical Property of {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester

There total 3 articles about {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid 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: 83.0%

1-{(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(2S,3R)-3-(2,3-dihydro-indole-1-carbonyl)-oxiranyl]-tetrahydro-furan-2-yl}-1H-pyrimidine-2,4-dione (872315-95-2) + (3-aminopropyl)carbamic acid benzyl ester hydrochloride (17400-34-9) → {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester (872315-98-5)

Guidance literature:

(3-aminopropyl)carbamic acid benzyl ester hydrochloride; With triethylamine; In methanol; at 20 ℃; for 0.5h;

1-{(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(2S,3R)-3-(2,3-dihydro-indole-1-carbonyl)-oxiranyl]-tetrahydro-furan-2-yl}-1H-pyrimidine-2,4-dione; In methanol; for 48h; Heating;

DOI:10.1016/j.tet.2005.09.086

Reference yield:

(2S,3R,4R,5R)-3,4-bis(tert-butyldimethylsilanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydrofuran-2-carbaldehyde (161867-43-2) → {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester (872315-98-5)

Guidance literature:

Multi-step reaction with 2 steps

1.1: 0.76 g / aq. NaOH / CH₂Cl₂ / 1.5 h / 0 °C

2.1: Et₃N / methanol / 0.5 h / 20 °C

2.2: 83 percent / methanol / 48 h / Heating

With sodium hydroxide; triethylamine; In methanol; dichloromethane;

DOI:10.1016/j.tet.2005.09.086

Reference yield:

2',3'-bis-O-(tert-butyldimethylsilyl)uridine (87418-87-9,69504-12-7) → {3-[(1S,2R)-2-[(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propyl}-carbamic acid benzyl ester (872315-98-5)

Guidance literature:

Multi-step reaction with 3 steps

1.1: IBX

2.1: 0.76 g / aq. NaOH / CH₂Cl₂ / 1.5 h / 0 °C

3.1: Et₃N / methanol / 0.5 h / 20 °C

3.2: 83 percent / methanol / 48 h / Heating

With sodium hydroxide; triethylamine; 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In methanol; dichloromethane;

DOI:10.1016/j.tet.2005.09.086

upstream raw materials:

1-{(2R,3R,4R,5R)-3,4-Bis-(tert-butyl-dimethyl-silanyloxy)-5-[(2S,3R)-3-(2,3-dihydro-indole-1-carbonyl)-oxiranyl]-tetrahydro-furan-2-yl}-1H-pyrimidine-2,4-dione

(3-aminopropyl)carbamic acid benzyl ester hydrochloride

(2S,3R,4R,5R)-3,4-bis(tert-butyldimethylsilanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydrofuran-2-carbaldehyde

2',3'-bis-O-(tert-butyldimethylsilyl)uridine

Downstream raw materials:

(1-{3-[2-[3,4-bis-(tert-butyl-dimethyl-silanyloxy)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-yl]-1-(2,3-dihydro-indole-1-carbonyl)-2-hydroxy-ethylamino]-propylcarbamoyl}-3-methyl-butyl)-carbamic acid benzyl ester