1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine

Base Information

• Chemical Name: 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine
• CAS No.: 194652-85-2
• Molecular Formula: C₂₅H₂₄N₂O₈
• Molecular Weight: 480.474
• Mol file: 194652-85-2.mol

Synonyms:1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine

Chemical Property of 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine

There total 4 articles about 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine 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:

3'-O-(tert-butyldimethylsilyl)-4'-(hydroxymethyl)-thymidine (139887-99-3) → 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine (194652-85-2)

Guidance literature:

Multi-step reaction with 4 steps

1: pyridine / Ambient temperature

2: Bu₄NF / tetrahydrofuran / 4 h / 40 °C

3: pyridine

4: 80percent aq. AcOH / 0.25 h / Heating

With pyridine; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran;

DOI:10.1135/cccc19971128

Reference yield:

1-[(2R,4S,5S)-4-(tert-Butyl-dimethyl-silanyloxy)-5-hydroxymethyl-5-trityloxymethyl-tetrahydro-furan-2-yl]-5-methyl-1H-pyrimidine-2,4-dione → 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine (194652-85-2)

Guidance literature:

Multi-step reaction with 3 steps

1: Bu₄NF / tetrahydrofuran / 4 h / 40 °C

2: pyridine

3: 80percent aq. AcOH / 0.25 h / Heating

With pyridine; tetrabutyl ammonium fluoride; acetic acid; In tetrahydrofuran;

DOI:10.1135/cccc19971128

Reference yield:

C44H38N2O8 → 1-(3-O-Benzoyl-4-C-benzoyloxymethyl-2-deoxy-α-L-threo-pentofuranosyl)thymine (194652-85-2)

Guidance literature:

With acetic acid; for 0.25h; Yield given; Heating;

DOI:10.1135/cccc19971128

upstream raw materials:

3'-O-(tert-butyldimethylsilyl)-4'-(hydroxymethyl)-thymidine

1-((2R,4S,5S)-4-Hydroxy-5-hydroxymethyl-5-trityloxymethyl-tetrahydro-furan-2-yl)-5-methyl-1H-pyrimidine-2,4-dione

Downstream raw materials:

N-[(Aminocarbonyl)methyl]-3',5'-di-O-benzoylthymidine-4'-carboxamide

N-(2-Hydroxymethyl)-3',5'-di-O-benzoylthymidine-4'-carboxamide

N,N-Dimethyl-3',5'-di-O-benzoylthymidine-4'-carboxamide

(2R,3S,5R)-3-Benzoyloxy-2-benzoyloxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-tetrahydro-furan-2-carboxylic acid