(1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

Base Information

Chemical Name:(1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate
CAS No.:1616268-44-0
Molecular Formula:C₃₀H₃₅N₆O₈P
Molecular Weight:638.617
Hs Code.:

Synonyms:(1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

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Chemical Property of (1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

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Technology Process of (1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

There total 1 articles about (1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate 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: 95.0%

: 873550-85-7
dibenzyl (1S,2R,3R)-4-azido-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

: 264611-41-8
N-(1,2-dihydro-2-oxo-1-(prop-2-ynyl)pyrimidin-4-yl)acetamide

: 1616268-44-0
(1S,2R,3R)-dibenzyl 4-{[4-(4-acetylamino-2-oxopyrimidin-1-yl)methyl]-1H-1,2,3-triazol-1-yl}-1,2,3-trihydroxy-2,3-O-isopropylidenebutylphosphonate

Guidance literature:: With copper(ll) sulfate pentahydrate; sodium L-ascorbate; In ethanol; water; at 40 - 45 ℃; for 0.333333h; Microwave irradiation;
DOI:10.1016/j.bmc.2014.05.020