Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

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Chemical Name:Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester
CAS No.:166955-07-3
Molecular Formula:C₄₄H₅₀N₄O₁₁Si
Molecular Weight:838.987
Hs Code.:

Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

Synonyms:Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

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Chemical Property of Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

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Technology Process of Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

There total 5 articles about Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester 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:

: 154230-45-2
C₆₀H₆₆N₄O₁₃Si

: 166955-07-3
Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

Guidance literature:: With hydrogen; palladium dihydroxide; In methanol; acetone; at 23 ℃;
DOI:10.1021/jo00081a003

Reference yield:

: 101527-40-6
5'-O-tert-butyldiphenylsilylthymidine

: 166955-07-3
Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 5 steps

1: 88 percent / (i-Pr)2NEt / CH₂Cl₂ / 23 °C

2: 76 percent / NaH / dimethylformamide / 0 - 23 °C

3: 90 percent / NaBH₄ / methanol / 0 - 23 °C

4: 82 percent / TMSOTf, Et₃N / CH₂Cl₂ / -23 °C

5: H₂ / Pd(OH)2 / methanol; acetone / 23 °C

With sodium tetrahydroborate; trimethylsilyl trifluoromethanesulfonate; hydrogen; sodium hydride; triethylamine; N-ethyl-N,N-diisopropylamine; palladium dihydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo00081a003

Reference yield:

: 154230-32-7
5'-O-tert-butyldiphenylsilyl-N³-benzyloxymethyl-2'-deoxythymidine

: 166955-07-3
Benzoic acid (2S,3S,5R)-2-{2-[(2R,3S,5R)-2-(tert-butyl-diphenyl-silanyloxymethyl)-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yloxy]-ethoxy}-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 76 percent / NaH / dimethylformamide / 0 - 23 °C

2: 90 percent / NaBH₄ / methanol / 0 - 23 °C

3: 82 percent / TMSOTf, Et₃N / CH₂Cl₂ / -23 °C

4: H₂ / Pd(OH)2 / methanol; acetone / 23 °C

With sodium tetrahydroborate; trimethylsilyl trifluoromethanesulfonate; hydrogen; sodium hydride; triethylamine; palladium dihydroxide; In methanol; dichloromethane; N,N-dimethyl-formamide; acetone;
DOI:10.1021/jo00081a003