1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

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Chemical Name:1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione
CAS No.:1333503-58-4
Molecular Formula:C₁₇H₂₀N₂O₆
Molecular Weight:348.356
Hs Code.:

Synonyms:1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

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Chemical Property of 1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

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Technology Process of 1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

There total 4 articles about 1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione 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: 78.0%

: 1333503-52-8
(2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-2-(3,4-dihydro-5-methyl-2,4-dioxopyrimidin-1(2H)-yl)furan-3-yl acetate

: 1333503-58-4
1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: With methanol; ammonia; at 20 ℃; for 6h; Inert atmosphere;
DOI:10.1016/j.ejmech.2011.05.036

Reference yield:

: 1333503-49-3
(3R,4S)-4-(4-methoxybenzyloxy)-tetrahydrofuran-2,3-diyl diacetate

: 1333503-58-4
1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 2 steps

1: trimethylsilyl trifluoromethanesulfonate / 1,2-dichloro-ethane / 4 h / 0 - 20 °C / Inert atmosphere

2: methanol; ammonia / 6 h / 20 °C / Inert atmosphere

With methanol; trimethylsilyl trifluoromethanesulfonate; ammonia; In 1,2-dichloro-ethane; 1: Vorbrüggen coupling;
DOI:10.1016/j.ejmech.2011.05.036

Reference yield:

: 65-71-4,28806-14-6,691841-57-3
thymin

: 1333503-58-4
1-((2R,3R,4S)-4-(4-methoxybenzyloxy)-tetrahydro-3-hydroxyfuran-2-yl)-5-methylpyrimidine-2,4(1H,3H)-dione

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / 135 °C / Inert atmosphere

2: trimethylsilyl trifluoromethanesulfonate / 1,2-dichloro-ethane / 4 h / 0 - 20 °C / Inert atmosphere

3: methanol; ammonia / 6 h / 20 °C / Inert atmosphere

With pyridine; methanol; trimethylsilyl trifluoromethanesulfonate; ammonia; In 1,2-dichloro-ethane; 2: Vorbrüggen coupling;
DOI:10.1016/j.ejmech.2011.05.036