Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Base Information

Chemical Name:Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester
CAS No.:1027917-28-7
Molecular Formula:C₃₂H₃₂N₂O₇S
Molecular Weight:588.681
Hs Code.:

Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Synonyms:Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Suppliers and Price of Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

There total 4 articles about Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl 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:

: 132523-62-7
3-deoxy-3-<(phenylmethoxy)methyl>-5-O-(phenylmethyl)-α-D-ribofuranose diacetate

: 1027917-28-7
Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / HMDS, TCS, C₄F₉SO₃K / acetonitrile / 24 h / Heating

2: 95 percent / NH₃ / methanol / 24 h / Ambient temperature

3: (dimethylamino)pyridine / acetonitrile / a.) 0 deg C, 4 h, b.) RT, 12 h

With dmap; C₄F₉SO₃K; ammonia; 1,1,1,3,3,3-hexamethyl-disilazane; In methanol; acetonitrile;
DOI:10.1021/jm00055a006

Reference yield:

: 133713-77-6
1-<2-O-acetyl-5-O-benzyl-3-C-<(benzyloxy)methyl>-3-deoxy-β-D-erythro-pentofuranosyl>thymine

: 1027917-28-7
Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 95 percent / NH₃ / methanol / 24 h / Ambient temperature

2: (dimethylamino)pyridine / acetonitrile / a.) 0 deg C, 4 h, b.) RT, 12 h

With dmap; ammonia; In methanol; acetonitrile;
DOI:10.1021/jm00055a006

Reference yield:

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

: 1027917-28-7
Thiocarbonic acid O-[(2R,3R,4R,5S)-4,5-bis-benzyloxymethyl-2-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl] ester O-phenyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / HMDS, TCS, C₄F₉SO₃K / acetonitrile / 24 h / Heating

2: 95 percent / NH₃ / methanol / 24 h / Ambient temperature

3: (dimethylamino)pyridine / acetonitrile / a.) 0 deg C, 4 h, b.) RT, 12 h

With dmap; C₄F₉SO₃K; ammonia; 1,1,1,3,3,3-hexamethyl-disilazane; In methanol; acetonitrile;
DOI:10.1021/jm00055a006