4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

Base Information

Chemical Name:4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine
CAS No.:310434-48-1
Molecular Formula:C₄₆H₄₈F₃N₅O₁₀
Molecular Weight:887.91
Hs Code.:

Synonyms:4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

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Chemical Property of 4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

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Technology Process of 4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

There total 7 articles about 4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine 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: 84.0%

: 40615-36-9
4,4'-dimethoxytrityl chloride

: 310434-47-0
4-N-Benzoyl-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

: 310434-48-1
4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

Guidance literature:: With pyridine; at 20 ℃; for 4h;
DOI:10.1039/b004431h

Reference yield:

: 93-97-0
benzoic acid anhydride

: 310434-48-1
4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

Guidance literature:: Multi-step reaction with 6 steps

1: 91 percent / ethanol / Heating

2: 72 percent / pyridine

3: 80 percent / acetonitrile; CH₂Cl₂ / 2 h / 20 °C

4: 83 percent / CH₂Cl₂ / 1.5 h

5: 84 percent / TBAF / tetrahydrofuran / 0.33 h / 20 °C

6: 84 percent / pyridine / 4 h / 20 °C

With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; ethanol; dichloromethane; acetonitrile; 1: Acylation / 2: Cyclization / 3: Carbonylation / 4: Substitution / 5: Ring cleavage / 6: Substitution;
DOI:10.1039/b004431h

Reference yield:

: 13089-48-0
N₄-benzoylcytidine

: 310434-48-1
4-N-Benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-O-{[6-(trifluoroacetamido)hexyl]carbamoyl}cytidine

Guidance literature:: Multi-step reaction with 5 steps

1: 72 percent / pyridine

2: 80 percent / acetonitrile; CH₂Cl₂ / 2 h / 20 °C

3: 83 percent / CH₂Cl₂ / 1.5 h

4: 84 percent / TBAF / tetrahydrofuran / 0.33 h / 20 °C

5: 84 percent / pyridine / 4 h / 20 °C

With pyridine; tetrabutyl ammonium fluoride; In tetrahydrofuran; dichloromethane; acetonitrile; 1: Cyclization / 2: Carbonylation / 3: Substitution / 4: Ring cleavage / 5: Substitution;
DOI:10.1039/b004431h