(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

Base Information

Chemical Name:(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine
CAS No.:1370411-83-8
Molecular Formula:C₂₆H₂₈N₂O₆
Molecular Weight:464.518
Hs Code.:

Synonyms:(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

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Chemical Property of (3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

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Technology Process of (3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

There total 7 articles about (3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine 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: 85.0%

: 1370411-81-6
(3'S,5'R)-1-(2'-O-methylsulfonyl-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

: 1370411-83-8
(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

Guidance literature:: With sodium hydroxide; In tetrahydrofuran; methanol; water; for 16h; Inert atmosphere; Reflux;
DOI:10.1021/jo300554w

Reference yield: 32.0%

: C₂₆H₂₆N₂O₆

: 1370411-83-8
(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

Guidance literature:: With potassium hydroxide; Reflux; Inert atmosphere;
DOI:10.1021/jo300554w

Reference yield:

: 1370411-72-5
(3'S,5'R)-1-(2'-acetoxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-ribofuranosyl)thymidine

: 1370411-83-8
(3'S, 5'R)-1-(2'-hydroxy-3',5'-O-dibenzyl-3',5'-ethano-β-D-arabinofuranosyl)thymidine

Guidance literature:: Multi-step reaction with 3 steps

1: sodium methylate / methanol / 4 h / 20 °C / Inert atmosphere

2: bis(phenyl) carbonate; sodium hydrogencarbonate / N,N-dimethyl-formamide / 1 h / 150 °C / Inert atmosphere

3: potassium hydroxide / Reflux; Inert atmosphere

With bis(phenyl) carbonate; sodium methylate; sodium hydrogencarbonate; potassium hydroxide; In methanol; N,N-dimethyl-formamide;
DOI:10.1021/jo300554w