1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

Base Information

Chemical Name:1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil
CAS No.:208463-34-7
Molecular Formula:C₃₄H₃₆N₂O₇S
Molecular Weight:616.735
Hs Code.:

Synonyms:1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

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Chemical Property of 1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

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Technology Process of 1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

There total 11 articles about 1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil 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: 86.0%

: 208463-29-0
1-{(2R,3R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]-3-(1-imidazothiocarbonyloxy)tetrahydrofuran-2-yl}uracil

: 208463-34-7
1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In toluene; for 0.0833333h; Heating;
DOI:10.1021/jo0003910

Reference yield:

: 134056-17-0
(1R,5R,6R,7R)-6-<(benzoyloxy)methyl>-7-<<3-(trifluoromethyl)benzoyl>oxy>-2,8-dioxabicyclo<3.2.1>octane

: 208463-34-7
1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

Guidance literature:: Multi-step reaction with 5 steps

1.1: N-methyl-N-trimethylsilyltrifluoroacetamide / acetonitrile / 0.5 h / 20 °C

1.2: 96 percent / SnCl₄ / acetonitrile / 14 h / 20 °C

2.1: 85 percent / Photolysis

3.1: 100 percent / triethylamine / tetrahydrofuran

4.1: NaOH / methanol; H₂O

5.1: PPh₃; diisopropyl azodicarboxylate / tetrahydrofuran

With sodium hydroxide; di-isopropyl azodicarboxylate; N-methyl-N-trimethylsilyl-2,2,2-trifluoroacetamide; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; water; acetonitrile; 1.1: Vorbrueggen reaction / 5.1: Mitsunobu reaction;
DOI:10.1021/jo0003910

Reference yield:

: 134056-18-1
1-<(2R,3R,4R,5R)-3-<<3-(trifluoromethyl)benzoyl>oxy>-4-<(benzoyloxy)methyl>-5-(2-hydroxyethyl)tetrahydrofuran-2-yl>uracil

: 208463-34-7
1-{(2R,4R,5R)-4-acetylthiomethyl-5-[2-(4,4'-dimethoxytriphenylmethoxy)ethyl]tetrahydrofuran-2-yl}uracil

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / Photolysis

2: 100 percent / triethylamine / tetrahydrofuran

3: NaOH / methanol; H₂O

4: PPh₃; diisopropyl azodicarboxylate / tetrahydrofuran

With sodium hydroxide; di-isopropyl azodicarboxylate; triethylamine; triphenylphosphine; In tetrahydrofuran; methanol; water; 4: Mitsunobu reaction;
DOI:10.1021/jo0003910