Cytidine, N-benzoyl-2'-O-(tetrahydro-2H-pyran-2-yl)-

Base Information

Chemical Name:Cytidine, N-benzoyl-2'-O-(tetrahydro-2H-pyran-2-yl)-
CAS No.:31505-92-7
Molecular Formula:C21H25N3O7
Molecular Weight:431.445
Hs Code.:
Mol file:31505-92-7.mol

Synonyms:

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Chemical Property of Cytidine, N-benzoyl-2'-O-(tetrahydro-2H-pyran-2-yl)-

Chemical Property:

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MSDS Files:: SDS file from LookChem

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Technology Process of Cytidine, N-benzoyl-2'-O-(tetrahydro-2H-pyran-2-yl)-

There total 6 articles about Cytidine, N-benzoyl-2'-O-(tetrahydro-2H-pyran-2-yl)- 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:

: 110-87-2
3,4-dihydro-2H-pyran

: 31505-92-7
N⁴-benzoyl-2'-O-tetrahydropyranylcytidine

Guidance literature:: Multi-step reaction with 3 steps

1: p-toluenesulfonic acid monohydrate / CHCl₃ / 0.17 h / 0 °C

2: pyridine / 1.5 h / 0 °C

3: triethylamine hydrogen fluoride (TEAHF) / dioxane; tetrahydrofuran / Ambient temperature

With pyridine; toluene-4-sulfonic acid; triethylamine hydrofluoride; In tetrahydrofuran; 1,4-dioxane; chloroform;

Reference yield:

: 90742-20-4
2'-O-tetrahydropyranyl-3',5'-O-(tetraisopropyldisiloxane-1,3-diyl)cytidine

: 31505-92-7
N⁴-benzoyl-2'-O-tetrahydropyranylcytidine

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 1.5 h / 0 °C

2: triethylamine hydrogen fluoride (TEAHF) / dioxane; tetrahydrofuran / Ambient temperature

With pyridine; triethylamine hydrofluoride; In tetrahydrofuran; 1,4-dioxane;

Reference yield:

: 69304-42-3
3',5'-O-[(1,1,3,3-tetraisopropyl)-1,3-disiloxanediyl]cytidine

: 31505-92-7
N⁴-benzoyl-2'-O-tetrahydropyranylcytidine

Guidance literature:: Multi-step reaction with 3 steps

1: p-toluenesulfonic acid monohydrate / CHCl₃ / 0.17 h / 0 °C

2: pyridine / 1.5 h / 0 °C

3: triethylamine hydrogen fluoride (TEAHF) / dioxane; tetrahydrofuran / Ambient temperature

With pyridine; toluene-4-sulfonic acid; triethylamine hydrofluoride; In tetrahydrofuran; 1,4-dioxane; chloroform;