5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

Base Information

Chemical Name:5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine
CAS No.:470699-90-2
Molecular Formula:C₃₅H₄₃IN₅O₉PS
Molecular Weight:867.699
Hs Code.:

Synonyms:5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

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Chemical Property of 5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

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Technology Process of 5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

There total 6 articles about 5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine 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:

: 2-benzyloxymethyl-5-(6-tert-butoxycarbonylamino-purin-9-yl)-3-(diethoxy-phosphanyloxy)-tetrahydro-furan-2-carbothioic acid S-[2-(2-iodo-phenyl)-ethyl] ester

: 470699-90-2
5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

Guidance literature:: With 2,6-dimethylpyridine; iodine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/S0040-4020(02)00557-4

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 470699-90-2
5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / triethylamine; DMAP / CH₂Cl₂ / 1 h / 20 °C

2: 66 percent / potassium tert-butoxide / tetrahydrofuran; H₂O

3: 95 percent / BOP-Cl; triethylamine / tetrahydrofuran; CH₂Cl₂ / 2 h / Heating

4: DMAP / CH₂Cl₂ / 0 °C

5: iodine; 2,6-lutidine / CH₂Cl₂; tetrahydrofuran; H₂O

With 2,6-dimethylpyridine; dmap; potassium tert-butylate; iodine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/S0040-4020(02)00557-4

Reference yield:

: 208175-48-8
5'-O-benzyl-6-N-benzoyl-3'-O-(tert-butyldimethylsilyl)-2'-deoxy-4'α-methoxycarbonyl-D-adenosine

: 470699-90-2
5'-O-benzyl-6-N-(tert-butyloxycarbonyl)-2'-deoxy-3'-O-diethylphosphoryl-4'α-{[(2-(2-iodophenyl)ethyl)thio]carbonyl}adenosine

Guidance literature:: Multi-step reaction with 5 steps

1: 100 percent / triethylamine; DMAP / CH₂Cl₂ / 1 h / 20 °C

2: 66 percent / potassium tert-butoxide / tetrahydrofuran; H₂O

3: 95 percent / BOP-Cl; triethylamine / tetrahydrofuran; CH₂Cl₂ / 2 h / Heating

4: DMAP / CH₂Cl₂ / 0 °C

5: iodine; 2,6-lutidine / CH₂Cl₂; tetrahydrofuran; H₂O

With 2,6-dimethylpyridine; dmap; potassium tert-butylate; iodine; bis-(2-oxo-3-oxazolidinyl)phosphoryl chloride; triethylamine; In tetrahydrofuran; dichloromethane; water;
DOI:10.1016/S0040-4020(02)00557-4