1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

Base Information

Chemical Name:1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine
CAS No.:159163-31-2
Molecular Formula:C₃₈H₃₈N₂O₇
Molecular Weight:634.729
Hs Code.:

Synonyms:1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

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Chemical Property of 1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

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Technology Process of 1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

There total 6 articles about 1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine 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: 68.6%

: 159163-25-4
1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-oxo-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

: 159163-41-4
1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-R-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

: 159163-31-2
1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

Guidance literature:: With sodium tetrahydroborate; In methanol; for 2h; Ambient temperature;
DOI:10.1016/S0040-4020(01)90435-1

Reference yield:

: 62593-92-4
phenylethynyl-N,N-diethylaminodimethylsilane

: 159163-31-2
1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / tetrahydrofuran / Heating

2: 93 percent / 0.7 M tributyltin hydride, AIBN / benzene / Heating

3: 57 percent / 30 percent aq. H₂O₂, KF, KHCO₃ / methanol; tetrahydrofuran / 2 h / Ambient temperature

4: 68.6 percent / sodium borohydride / methanol / 2 h / Ambient temperature

With potassium fluoride; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); dihydrogen peroxide; tri-n-butyl-tin hydride; potassium hydrogencarbonate; In tetrahydrofuran; methanol; benzene;
DOI:10.1016/S0040-4020(01)90435-1

Reference yield:

: 140134-77-6
1-<5'-O-(monomethoxytrityl)-2'-deoxy-2'-phenylseleno-β-D-ribofuranosyl>thymine

: 159163-31-2
1-<5'-O-(p-monomethoxytrityl)-2'-deoxy-2'-C-(1-S-hydroxy-2-phenyl)ethyl-β-D-ribofuranosyl>thymine

Guidance literature:: Multi-step reaction with 4 steps

1: 95 percent / tetrahydrofuran / Heating

2: 93 percent / 0.7 M tributyltin hydride, AIBN / benzene / Heating

3: 57 percent / 30 percent aq. H₂O₂, KF, KHCO₃ / methanol; tetrahydrofuran / 2 h / Ambient temperature

4: 68.6 percent / sodium borohydride / methanol / 2 h / Ambient temperature

With potassium fluoride; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); dihydrogen peroxide; tri-n-butyl-tin hydride; potassium hydrogencarbonate; In tetrahydrofuran; methanol; benzene;
DOI:10.1016/S0040-4020(01)90435-1