1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

Base Information

Chemical Name:1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione
CAS No.:198703-67-2
Molecular Formula:C₂₈H₃₇N₃O₆Si
Molecular Weight:539.704
Hs Code.:

Synonyms:1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

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Chemical Property of 1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

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Technology Process of 1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

There total 4 articles about 1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-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:

: 55486-09-4
2'-O-Methyl-5-methyluridine

: 198703-67-2
1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 5 steps

1: PPh₃ / tetrahydrofuran

2: imidazole / dimethylformamide / 18 h

3: methylhydrazine / CH₂Cl₂ / 1 h / 0 °C

4: methanol; ethyl acetate / 0.5 h / 40 °C

5: NaBH₃CN / acetic acid / 2 h / 10 °C

With 1H-imidazole; sodium cyanoborohydride; triphenylphosphine; methylhydrazine; In tetrahydrofuran; methanol; dichloromethane; acetic acid; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1080/07328319708006242

Reference yield:

: 171176-42-4
2'-O-methyl-5'-O-phthalimido-5-methyluridine

: 198703-67-2
1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 4 steps

1: imidazole / dimethylformamide / 18 h

2: methylhydrazine / CH₂Cl₂ / 1 h / 0 °C

3: methanol; ethyl acetate / 0.5 h / 40 °C

4: NaBH₃CN / acetic acid / 2 h / 10 °C

With 1H-imidazole; sodium cyanoborohydride; methylhydrazine; In methanol; dichloromethane; acetic acid; ethyl acetate; N,N-dimethyl-formamide;
DOI:10.1080/07328319708006242

Reference yield:

: 171176-08-2
5'-O-amino-3'-O-tert-butyldiphenylsilyl-2'-O-methyl-5-methyluridine

: 198703-67-2
1-{(2R,3R,4R,5R)-4-(tert-Butyl-diphenyl-silanyloxy)-3-methoxy-5-[(N-methyl-aminooxy)-methyl]-tetrahydro-furan-2-yl}-5-methyl-1H-pyrimidine-2,4-dione

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; ethyl acetate / 0.5 h / 40 °C

2: NaBH₃CN / acetic acid / 2 h / 10 °C

With sodium cyanoborohydride; In methanol; acetic acid; ethyl acetate;
DOI:10.1080/07328319708006242