5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

Base Information

Chemical Name:5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)
CAS No.:1447970-02-6
Molecular Formula:C₅₀H₅₈N₅O₁₃P
Molecular Weight:968.01
Hs Code.:

Synonyms:5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

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Chemical Property of 5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

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Technology Process of 5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

There total 5 articles about 5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite) 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: 72.2%

: 1447970-01-5
5’-O-(4,4'-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine

: 124482-92-4,89992-70-1
2-cyanoethyl-N,N-(diisopropylamino)chlorophosphine

: 1447970-02-6
5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tetlet.2013.06.001

Reference yield:

: 1447969-98-3
3’,5’-O-di-tert-silyl-2’-O-[(methylthio)methyl]uridine

: 1447970-02-6
5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

Guidance literature:: Multi-step reaction with 4 steps

1: bromine; trimethylsilylacetylene; 18-crown-6 ether / 1,2-dichloro-ethane / 1 h / Cooling with ice; Inert atmosphere

2: triethylamine tris(hydrogen fluoride) / tetrahydrofuran / Inert atmosphere

3: pyridine / 20 °C / Inert atmosphere

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With pyridine; 18-crown-6 ether; bromine; triethylamine tris(hydrogen fluoride); N-ethyl-N,N-diisopropylamine; trimethylsilylacetylene; In tetrahydrofuran; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1016/j.tetlet.2013.06.001

Reference yield:

: 1447969-99-4
3’,5’-O-di-tert-silyl-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine

: 1447970-02-6
5’-O-(4,4’-dimethoxytrityl)-2’-O-[[2-methyl-2-(2-nitrophenyl)-1-oxopropoxy]methyl]uridine 3’-O-(2-cyanoethyl N,N-diisopropylphosphoramidite)

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine tris(hydrogen fluoride) / tetrahydrofuran / Inert atmosphere

2: pyridine / 20 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 20 °C / Inert atmosphere

With pyridine; triethylamine tris(hydrogen fluoride); N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1016/j.tetlet.2013.06.001