1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

Base Information

Chemical Name:1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine
CAS No.:148704-65-8
Molecular Formula:C₃₂H₂₇BrN₂O₉
Molecular Weight:663.478
Hs Code.:

Synonyms:1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

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Chemical Property of 1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

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Technology Process of 1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

There total 7 articles about 1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)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: 98.0%

: 148704-60-3
2,2'-anhydro-1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-α-L-ribofuranosyl)thymine

: 148704-65-8
1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

Guidance literature:: With hydrogen bromide; In N,N-dimethyl-formamide; at 100 ℃; for 0.333333h;
DOI:10.1135/cccc19930409

Reference yield:

: 98-88-4
benzoyl chloride

: 148704-65-8
1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

Guidance literature:: Multi-step reaction with 6 steps

1: 97 percent / pyridine / 5 h / Ambient temperature

2: 1.) sulfuric acid, 2.) SnCl₄ / 1.) AcOH, RT, overnight, 2.) CH₂Cl₂, RT, overnight

3: 95 percent / conc. HCl / dioxane / 144 h / 30 °C

4: 97 percent / pyridine / 4 h / Ambient temperature

5: 94 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / acetonitrile / Ambient temperature

6: 98 percent / HBr / dimethylformamide / 0.33 h / 100 °C

With pyridine; hydrogenchloride; sulfuric acid; hydrogen bromide; tin(IV) chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1135/cccc19930409

Reference yield:

: 55797-64-3,55797-65-4
1,2-O-isopropylidene-4-C-(hydroxymethyl)-β-L-threo-pento-1,4-furanose

: 148704-65-8
1-(3,5-O-benzoyl-4-C-benzoyloxymethyl-2-bromo-2-deoxy-α-L-arabinofuranosyl)thymine

Guidance literature:: Multi-step reaction with 6 steps

1: 97 percent / pyridine / 5 h / Ambient temperature

2: 1.) sulfuric acid, 2.) SnCl₄ / 1.) AcOH, RT, overnight, 2.) CH₂Cl₂, RT, overnight

3: 95 percent / conc. HCl / dioxane / 144 h / 30 °C

4: 97 percent / pyridine / 4 h / Ambient temperature

5: 94 percent / 1,8-diazabicyclo<5.4.0>undec-7-ene / acetonitrile / Ambient temperature

6: 98 percent / HBr / dimethylformamide / 0.33 h / 100 °C

With pyridine; hydrogenchloride; sulfuric acid; hydrogen bromide; tin(IV) chloride; 1,8-diazabicyclo[5.4.0]undec-7-ene; In 1,4-dioxane; N,N-dimethyl-formamide; acetonitrile;
DOI:10.1135/cccc19930409