1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

Base Information

Chemical Name:1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil
CAS No.:251296-70-5
Molecular Formula:C₃₅H₄₈N₂O₈Si₂
Molecular Weight:680.946
Hs Code.:

Synonyms:1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

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Chemical Property of 1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

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Technology Process of 1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

There total 1 articles about 1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil 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: 96.0%

: 98-88-4
benzoyl chloride

: 54925-66-5
2',5'-bis-O-(tert-butyldimethylsilyl)uridine

: 251296-70-5
1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

Guidance literature:: With pyridine; at 20 ℃;
DOI:10.1021/jo9908647

Reference yield: 81.0%

: 251296-70-5
1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

: 251296-71-6
1-[3-O-benzoyl-2-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

Guidance literature:: With water; trifluoroacetic acid; In dichloromethane; at 20 ℃; for 0.75h;
DOI:10.1021/jo9908647

Reference yield:

: 251296-70-5
1-[3-O-benzoyl-2,5-bis-O-(tert-butyldimethylsilyl)-β-D-ribofuranosyl]-3-N-(benzoyl)uracil

: 251296-74-9
5'-amino-3'-O-benzoyl-2'-O-(tert-butyldimethylsilyl)-5'-deoxyuridine

Guidance literature:: Multi-step reaction with 4 steps

1: 81 percent / TFA; H₂O / CH₂Cl₂ / 0.75 h / 20 °C

2: 70 percent / SOCl₂; pyridine / CH₂Cl₂ / 0 - 20 °C

3: 81 percent / LiN₃ / dimethylformamide / 2 h / 110 °C

4: 52 percent / SnCl₂*2H₂O / methanol / 0 - 20 °C

With pyridine; thionyl chloride; lithium azide; water; trifluoroacetic acid; tin(ll) chloride; In methanol; dichloromethane; N,N-dimethyl-formamide; 1: desilylation / 2: Substitution / 3: Substitution / 4: Reduction;
DOI:10.1021/jo9908647